Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia)
Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high prevalence of mitochondrial disorders (MIDs) urges the clinician to diagnose these disorders accurately, which is difficult in the light of highly var...
Saved in:
Published in | Molecular biology reports Vol. 40; no. 11; pp. 6495 - 6499 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
01.11.2013
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high prevalence of mitochondrial disorders (MIDs) urges the clinician to diagnose these disorders accurately, which is difficult in the light of highly variable and overlapping phenotypes, transmission patterns and molecular backgrounds. Fibroblast growth factor 21 (FGF-21) is an important endocrine and paracrine regulator of metabolic homeostasis. The FGF-21 transcript is reported to be abundantly expressed in liver, but little is known about the regulation of FGF-21 expression in other tissues. FGF-21 could play a role in the metabolic alterations that are often associated with mitochondrial diseases. The aim of this study was to show the association of the FGF-21 biomarker with human primary MIDs and secondary MIDs in suspected patients in Iran. Serum FGF-21 levels were determined using ELISA in 47 mitochondrial patients, including 32 with primary MIDs, 15 patients with Friedreich ataxia as a secondary MID and 30 control subjects. Serum FGF-21 levels were significantly higher in subjects with the primary MIDs (
p
< 0.05), compared to subjects without MIDs. However, serum FGF-21 levels did not show significant increase in subjects with FA as a secondary MID. There is an association between increasing concentrations of FGF-21 with mitochondrial diseases, suggesting FGF-21 as a biomarker for diagnosis of primary MIDs in humans. However, this biomarker is not appropriate for the diagnosis of FA. |
---|---|
AbstractList | Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high prevalence of mitochondrial disorders (MIDs) urges the clinician to diagnose these disorders accurately, which is difficult in the light of highly variable and overlapping phenotypes, transmission patterns and molecular backgrounds. Fibroblast growth factor 21 (FGF-21) is an important endocrine and paracrine regulator of metabolic homeostasis. The FGF-21 transcript is reported to be abundantly expressed in liver, but little is known about the regulation of FGF-21 expression in other tissues. FGF-21 could play a role in the metabolic alterations that are often associated with mitochondrial diseases. The aim of this study was to show the association of the FGF-21 biomarker with human primary MIDs and secondary MIDs in suspected patients in Iran. Serum FGF-21 levels were determined using ELISA in 47 mitochondrial patients, including 32 with primary MIDs, 15 patients with Friedreich ataxia as a secondary MID and 30 control subjects. Serum FGF-21 levels were significantly higher in subjects with the primary MIDs (
p
< 0.05), compared to subjects without MIDs. However, serum FGF-21 levels did not show significant increase in subjects with FA as a secondary MID. There is an association between increasing concentrations of FGF-21 with mitochondrial diseases, suggesting FGF-21 as a biomarker for diagnosis of primary MIDs in humans. However, this biomarker is not appropriate for the diagnosis of FA. Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high prevalence of mitochondrial disorders (MIDs) urges the clinician to diagnose these disorders accurately, which is difficult in the light of highly variable and overlapping phenotypes, transmission patterns and molecular backgrounds. Fibroblast growth factor 21 (FGF-21) is an important endocrine and paracrine regulator of metabolic homeostasis. The FGF-21 transcript is reported to be abundantly expressed in liver, but little is known about the regulation of FGF-21 expression in other tissues. FGF-21 could play a role in the metabolic alterations that are often associated with mitochondrial diseases. The aim of this study was to show the association of the FGF-21 biomarker with human primary MIDs and secondary MIDs in suspected patients in Iran. Serum FGF-21 levels were determined using ELISA in 47 mitochondrial patients, including 32 with primary MIDs, 15 patients with Friedreich ataxia as a secondary MID and 30 control subjects. Serum FGF-21 levels were significantly higher in subjects with the primary MIDs (p < 0.05), compared to subjects without MIDs. However, serum FGF-21 levels did not show significant increase in subjects with FA as a secondary MID. There is an association between increasing concentrations of FGF-21 with mitochondrial diseases, suggesting FGF-21 as a biomarker for diagnosis of primary MIDs in humans. However, this biomarker is not appropriate for the diagnosis of FA. Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high prevalence of mitochondrial disorders (MIDs) urges the clinician to diagnose these disorders accurately, which is difficult in the light of highly variable and overlapping phenotypes, transmission patterns and molecular backgrounds. Fibroblast growth factor 21 (FGF-21) is an important endocrine and paracrine regulator of metabolic homeostasis. The FGF-21 transcript is reported to be abundantly expressed in liver, but little is known about the regulation of FGF-21 expression in other tissues. FGF-21 could play a role in the metabolic alterations that are often associated with mitochondrial diseases. The aim of this study was to show the association of the FGF-21 biomarker with human primary MIDs and secondary MIDs in suspected patients in Iran. Serum FGF-21 levels were determined using ELISA in 47 mitochondrial patients, including 32 with primary MIDs, 15 patients with Friedreich ataxia as a secondary MID and 30 control subjects. Serum FGF-21 levels were significantly higher in subjects with the primary MIDs (p < 0.05), compared to subjects without MIDs. However, serum FGF-21 levels did not show significant increase in subjects with FA as a secondary MID. There is an association between increasing concentrations of FGF-21 with mitochondrial diseases, suggesting FGF-21 as a biomarker for diagnosis of primary MIDs in humans. However, this biomarker is not appropriate for the diagnosis of FA.[PUBLICATION ABSTRACT] Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high prevalence of mitochondrial disorders (MIDs) urges the clinician to diagnose these disorders accurately, which is difficult in the light of highly variable and overlapping phenotypes, transmission patterns and molecular backgrounds. Fibroblast growth factor 21 (FGF-21) is an important endocrine and paracrine regulator of metabolic homeostasis. The FGF-21 transcript is reported to be abundantly expressed in liver, but little is known about the regulation of FGF-21 expression in other tissues. FGF-21 could play a role in the metabolic alterations that are often associated with mitochondrial diseases. The aim of this study was to show the association of the FGF-21 biomarker with human primary MIDs and secondary MIDs in suspected patients in Iran. Serum FGF-21 levels were determined using ELISA in 47 mitochondrial patients, including 32 with primary MIDs, 15 patients with Friedreich ataxia as a secondary MID and 30 control subjects. Serum FGF-21 levels were significantly higher in subjects with the primary MIDs (p < 0.05), compared to subjects without MIDs. However, serum FGF-21 levels did not show significant increase in subjects with FA as a secondary MID. There is an association between increasing concentrations of FGF-21 with mitochondrial diseases, suggesting FGF-21 as a biomarker for diagnosis of primary MIDs in humans. However, this biomarker is not appropriate for the diagnosis of FA.Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high prevalence of mitochondrial disorders (MIDs) urges the clinician to diagnose these disorders accurately, which is difficult in the light of highly variable and overlapping phenotypes, transmission patterns and molecular backgrounds. Fibroblast growth factor 21 (FGF-21) is an important endocrine and paracrine regulator of metabolic homeostasis. The FGF-21 transcript is reported to be abundantly expressed in liver, but little is known about the regulation of FGF-21 expression in other tissues. FGF-21 could play a role in the metabolic alterations that are often associated with mitochondrial diseases. The aim of this study was to show the association of the FGF-21 biomarker with human primary MIDs and secondary MIDs in suspected patients in Iran. Serum FGF-21 levels were determined using ELISA in 47 mitochondrial patients, including 32 with primary MIDs, 15 patients with Friedreich ataxia as a secondary MID and 30 control subjects. Serum FGF-21 levels were significantly higher in subjects with the primary MIDs (p < 0.05), compared to subjects without MIDs. However, serum FGF-21 levels did not show significant increase in subjects with FA as a secondary MID. There is an association between increasing concentrations of FGF-21 with mitochondrial diseases, suggesting FGF-21 as a biomarker for diagnosis of primary MIDs in humans. However, this biomarker is not appropriate for the diagnosis of FA. |
Author | Salehi, Mohammad Hossein Houshmand, Massoud Sadeghizadeh, Majid Kamalidehghan, Behnam Aryani, Omid Mossalaeie, Mir Majid |
Author_xml | – sequence: 1 givenname: Mohammad Hossein surname: Salehi fullname: Salehi, Mohammad Hossein email: m_h_salehi@yahoo.com organization: Molecular Genetics Department, Tarbiat Modares University, Medical Genetics Department, National Institute for Genetic Engineering and Biotechnology (NIGEB) – sequence: 2 givenname: Behnam surname: Kamalidehghan fullname: Kamalidehghan, Behnam organization: Pharmacy Department, Faculty of Medicine, University of Malaya (UM) – sequence: 3 givenname: Massoud surname: Houshmand fullname: Houshmand, Massoud organization: Medical Genetics Department, National Institute for Genetic Engineering and Biotechnology (NIGEB), Medical Genetics Department, Special Medical Center – sequence: 4 givenname: Omid surname: Aryani fullname: Aryani, Omid organization: Medical Genetics Department, Special Medical Center – sequence: 5 givenname: Majid surname: Sadeghizadeh fullname: Sadeghizadeh, Majid organization: Molecular Genetics Department, Tarbiat Modares University – sequence: 6 givenname: Mir Majid surname: Mossalaeie fullname: Mossalaeie, Mir Majid organization: Parseh Medical Laboratory |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24078096$$D View this record in MEDLINE/PubMed |
BookMark | eNqNktFuFCEUhompsdvqA3hjSLxpE0c5MMDMTZNN41aTJt7oNWGA2aXODhUYq2_kY8o6a1Ob2PSKEL7_HP5z_iN0MIbRIfQSyFsgRL5LAISxigCrqBSyIk_QArhkVd3K5gAtCCNQ1Q2HQ3SU0hUhpAbJn6FDWhPZkFYs0K9lSsF4nX0Ycehx77sYukGnjNcx3OQN7rXJIeKT1cWqonCKdcIadz5sdfzqIr7xhbmOvlx_4q3PwWzCaKPXA7Y-hWhdTG9wN2U8hjzTyZmCPMCXZtE7G503G7zM-ofXp8_R014Pyb3Yn8foy-r95_MP1eWni4_ny8vKcCZyZayVvWwtB9oRoLYXrZWNI9IIoIJB19W051DzhnIQzjkhRd8zShzrhCYNO0Znc93rqds6a9yYox7U3qEK2qt_X0a_UevwXbGG1rQlpcDJvkAM3yaXstr6ZNww6NGFKSmQQCiTrXgEWrdUlIVy9ghU8LJbDrygr--hV2GKYxlaoWomQDZsR7266_PW4N9oFABmwMSQUnT9LQJE7eKn5vipEj-1i5_aGZL3NMbnP9kqo_LDg0o6K1PpMq5dvPPp_4p-A6hy74U |
CitedBy_id | crossref_primary_10_1002_acn3_51104 crossref_primary_10_1016_j_jpeds_2017_08_077 crossref_primary_10_3892_mmr_2017_8100 crossref_primary_10_2119_molmed_2015_00168 crossref_primary_10_1016_j_mito_2021_08_011 crossref_primary_10_1002_jimd_12307 crossref_primary_10_1212_WNL_0000000000003374 crossref_primary_10_3389_fped_2022_851534 crossref_primary_10_1038_s41598_024_80273_w crossref_primary_10_1093_mutage_gead010 crossref_primary_10_3389_fendo_2015_00154 crossref_primary_10_3892_etm_2018_5840 crossref_primary_10_1016_j_cyto_2018_05_020 crossref_primary_10_1016_j_ymgme_2021_12_001 crossref_primary_10_1210_er_2017_00016 crossref_primary_10_1016_j_mito_2021_10_008 crossref_primary_10_1016_j_neurot_2024_e00325 crossref_primary_10_1212_WNL_0000000000000578 |
Cites_doi | 10.1053/j.gastro.2009.07.064 10.1023/A:1015629912477 10.1172/JCI23606 10.1126/science.1144837 10.1016/j.febslet.2008.10.021 10.1210/jc.2010-1326 10.1016/j.cmet.2007.05.010 10.1016/j.cmet.2007.05.002 10.1016/j.cmet.2007.05.003 10.1186/gb-2001-2-3-reviews3005 10.1093/hmg/ddq310 10.1093/brain/awg170 10.1007/s00415-009-5028-3 10.2337/db07-1476 10.1007/s10545-010-9222-3 10.1056/NEJMra022567 10.1073/pnas.0906039107 10.2337/db05-1435 10.1128/MCB.00992-07 10.1002/ana.21217 10.1038/nrg1606 10.1007/s10545-006-0362-4 10.1530/EJE-10-0454 10.1016/S0167-4781(00)00067-1 10.1016/j.tig.2004.08.007 10.1210/me.2010-0142 10.1055/s-2007-985148 10.1023/A:1024489218004 10.1210/jc.2008-2331 |
ContentType | Journal Article |
Copyright | The Author(s) 2013 Springer Science+Business Media Dordrecht 2013 |
Copyright_xml | – notice: The Author(s) 2013 – notice: Springer Science+Business Media Dordrecht 2013 |
DBID | C6C AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7TK 7TM 7X7 7XB 88A 88E 88I 8AO 8FD 8FE 8FH 8FI 8FJ 8FK ABUWG AFKRA AZQEC BBNVY BENPR BHPHI CCPQU DWQXO FR3 FYUFA GHDGH GNUQQ HCIFZ K9. LK8 M0S M1P M2P M7P P64 PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS Q9U RC3 7X8 7S9 L.6 5PM |
DOI | 10.1007/s11033-013-2767-0 |
DatabaseName | Springer Nature OA Free Journals CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Neurosciences Abstracts Nucleic Acids Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Biology Database (Alumni Edition) Medical Database (Alumni Edition) Science Database (Alumni Edition) ProQuest Pharma Collection Technology Research Database ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials Biological Science Collection ProQuest Natural Science Collection ProQuest One ProQuest Central Korea Engineering Research Database Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) ProQuest Biological Science Collection ProQuest Health & Medical Collection Medical Database Science Database Biological Science Database Biotechnology and BioEngineering Abstracts ProQuest Central Premium ProQuest One Academic (New) ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest Central Basic Genetics Abstracts MEDLINE - Academic AGRICOLA AGRICOLA - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Central Student Technology Research Database ProQuest One Academic Middle East (New) ProQuest Central Essentials Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest One Health & Nursing ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central China ProQuest Biology Journals (Alumni Edition) ProQuest Central ProQuest One Applied & Life Sciences ProQuest Health & Medical Research Collection Genetics Abstracts Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Health & Medical Research Collection Biological Science Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Science Journals (Alumni Edition) ProQuest Biological Science Collection ProQuest Central Basic ProQuest Science Journals ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection Neurosciences Abstracts ProQuest Hospital Collection (Alumni) Biotechnology and BioEngineering Abstracts ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition Engineering Research Database ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic AGRICOLA AGRICOLA - Academic |
DatabaseTitleList | MEDLINE Neurosciences Abstracts ProQuest Central Student MEDLINE - Academic AGRICOLA |
Database_xml | – sequence: 1 dbid: C6C name: Springer Nature OA Free Journals url: http://www.springeropen.com/ sourceTypes: Publisher – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 4 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry Biology |
EISSN | 1573-4978 |
EndPage | 6499 |
ExternalDocumentID | PMC3824290 3104896661 24078096 10_1007_s11033_013_2767_0 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GeographicLocations | Iran |
GeographicLocations_xml | – name: Iran |
GroupedDBID | --- -4W -56 -5G -BR -EM -Y2 -~C .86 .GJ .VR 06C 06D 0R~ 0VY 123 1SB 203 28- 29M 29~ 2J2 2JN 2JY 2KG 2KM 2LR 2P1 2VQ 2~H 30V 3SX 3V. 4.4 406 408 409 40E 53G 5QI 5RE 5VS 67N 67Z 6NX 78A 7X7 88A 88E 88I 8AO 8FE 8FH 8FI 8FJ 8TC 8UJ 95- 95. 95~ 96X AAAVM AABHQ AACDK AAHBH AAHNG AAIAL AAJBT AAJKR AANXM AANZL AARHV AARTL AASML AATNV AATVU AAUYE AAWCG AAYIU AAYQN AAYTO AAYZH ABBBX ABBXA ABDZT ABECU ABFTV ABHLI ABHQN ABJNI ABJOX ABKCH ABKTR ABMNI ABMQK ABNWP ABPLI ABQBU ABQSL ABSXP ABTEG ABTHY ABTKH ABTMW ABULA ABUWG ABWNU ABXPI ACAOD ACBXY ACDTI ACGFS ACGOD ACHSB ACHXU ACKNC ACMDZ ACMLO ACOKC ACOMO ACPIV ACPRK ACZOJ ADBBV ADHHG ADHIR ADIMF ADINQ ADKNI ADKPE ADRFC ADTPH ADURQ ADYFF ADYPR ADZKW AEBTG AEFIE AEFQL AEGAL AEGNC AEJHL AEJRE AEKMD AEMSY AENEX AEOHA AEPYU AESKC AETLH AEVLU AEXYK AFBBN AFEXP AFGCZ AFKRA AFLOW AFQWF AFWTZ AFZKB AGAYW AGDGC AGGDS AGJBK AGMZJ AGQEE AGQMX AGRTI AGWIL AGWZB AGYKE AHAVH AHBYD AHMBA AHSBF AHYZX AIAKS AIGIU AIIXL AILAN AITGF AJBLW AJRNO AJZVZ AKMHD ALIPV ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AMYQR AOCGG ARMRJ ASPBG AVWKF AXYYD AZFZN AZQEC B-. BA0 BBNVY BBWZM BDATZ BENPR BGNMA BHPHI BPHCQ BSONS BVXVI C6C CAG CCPQU COF CS3 CSCUP DDRTE DL5 DNIVK DPUIP DU5 DWQXO EBD EBLON EBS EIOEI EJD EMOBN EN4 EPAXT ESBYG F5P FEDTE FERAY FFXSO FIGPU FINBP FNLPD FRRFC FSGXE FWDCC FYUFA G-Y G-Z GGCAI GGRSB GJIRD GNUQQ GNWQR GQ6 GQ7 GQ8 GXS H13 HCIFZ HF~ HG5 HG6 HMCUK HMJXF HQYDN HRMNR HVGLF HZ~ I09 IHE IJ- IKXTQ ITM IWAJR IXC IZIGR IZQ I~X I~Z J-C J0Z JBSCW JCJTX JZLTJ KDC KOV KOW KPH LAK LK8 LLZTM M0L M1P M2P M4Y M7P MA- N2Q NB0 NDZJH NPVJJ NQJWS NU0 O9- O93 O9G O9I O9J OAM OVD P19 PF0 PQQKQ PROAC PSQYO PT4 PT5 Q2X QOK QOR QOS R4E R89 R9I RHV RIG RNI RNS ROL RPX RRX RSV RZC RZE RZK S16 S1Z S26 S27 S28 S3A S3B SAP SBL SBY SCLPG SDH SDM SHX SISQX SJYHP SNE SNPRN SNX SOHCF SOJ SPISZ SRMVM SSLCW SSXJD STPWE SV3 SZN T13 T16 TEORI TSG TSK TSV TUC TUS U2A U9L UG4 UKHRP UOJIU UTJUX UZXMN VC2 VFIZW W23 W48 WH7 WJK WK6 WK8 YLTOR Z45 Z7U Z7V Z7W Z7Y Z82 Z83 Z87 Z8O Z8P Z8Q Z8S Z8V Z8W Z91 ZMTXR ZOVNA ZXP ~A9 ~EX ~KM AAPKM AAYXX ABAKF ABBRH ABDBE ABFSG ACSTC ADHKG AEZWR AFDZB AFHIU AFOHR AGQPQ AHPBZ AHWEU AIXLP ATHPR AYFIA CITATION PHGZM PHGZT CGR CUY CVF ECM EIF NPM 7TK 7TM 7XB 8FD 8FK ABRTQ FR3 K9. P64 PJZUB PKEHL PPXIY PQEST PQGLB PQUKI PRINS Q9U RC3 7X8 7S9 L.6 5PM |
ID | FETCH-LOGICAL-c536t-cdd7f79d512b012df69d78e07c612631bb42f514582516eee676ff320e3b6a083 |
IEDL.DBID | 7X7 |
ISSN | 0301-4851 1573-4978 |
IngestDate | Thu Aug 21 18:19:50 EDT 2025 Thu Jul 10 17:42:06 EDT 2025 Thu Jul 10 22:59:27 EDT 2025 Tue Aug 05 11:33:36 EDT 2025 Fri Jul 25 18:52:29 EDT 2025 Thu Apr 03 07:07:28 EDT 2025 Thu Apr 24 23:05:36 EDT 2025 Tue Jul 01 03:17:42 EDT 2025 Fri Feb 21 02:31:43 EST 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 11 |
Keywords | Mitochondrial disorders (MIDs) OXPHOS Respiratory chain deficiency (RCD) Friedreich ataxia (FA) Fibroblast growth factor 21 (FGF-21) |
Language | English |
License | http://creativecommons.org/licenses/by/2.0 Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c536t-cdd7f79d512b012df69d78e07c612631bb42f514582516eee676ff320e3b6a083 |
Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | https://link.springer.com/10.1007/s11033-013-2767-0 |
PMID | 24078096 |
PQID | 1443617835 |
PQPubID | 54080 |
PageCount | 5 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_3824290 proquest_miscellaneous_1710237960 proquest_miscellaneous_1492615753 proquest_miscellaneous_1465175515 proquest_journals_1443617835 pubmed_primary_24078096 crossref_primary_10_1007_s11033_013_2767_0 crossref_citationtrail_10_1007_s11033_013_2767_0 springer_journals_10_1007_s11033_013_2767_0 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2013-11-01 |
PublicationDateYYYYMMDD | 2013-11-01 |
PublicationDate_xml | – month: 11 year: 2013 text: 2013-11-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | Dordrecht |
PublicationPlace_xml | – name: Dordrecht – name: Netherlands |
PublicationSubtitle | An International Journal on Molecular and Cellular Biology |
PublicationTitle | Molecular biology reports |
PublicationTitleAbbrev | Mol Biol Rep |
PublicationTitleAlternate | Mol Biol Rep |
PublicationYear | 2013 |
Publisher | Springer Netherlands Springer Nature B.V |
Publisher_xml | – name: Springer Netherlands – name: Springer Nature B.V |
References | Itoh, Ornitz (CR1) 2004; 20 Taylor, Turnbull (CR19) 2005; 6 Di Donato (CR25) 2009; 256 Li, Bao, Xu, Pan, Lu, Wu, Lu, Xiang, Jia (CR6) 2009; 94 Tacer, Bookout, Ding, Kurosu, John, Wang, Goetz, Mohammadi, Kuro-o, Mangelsdorf (CR15) 2010; 24 Janssen, Nijtmans, Heuvel, Smeitink (CR29) 2006; 29 Suomalainen (CR18) 2011; 34 Shaham, Slate, Goldberger, Xu, Ramanathan, Souza, Clish, Sims, Mootha (CR27) 2010; 107 Moore (CR8) 2007; 316 Reitman (CR9) 2007; 5 Wente, Efanov, Brenner, Kharitonenkov, Köster, Sandusky, Sewing, Treinies, Zitzer, Gromada (CR13) 2006; 55 DiMauro, Schon (CR24) 2003; 348 Kharitonenkov, Shiyanova, Koester, Ford, Micanovic, Galbreath, Sandusky, Hammond, Moyers, Owens (CR3) 2005; 115 Tyynismaa, Raivio, Hakkarainen, Ortega-Alonso, Lundbom, Kaprio, Rissanen, Suomalainen, Pietiläinen (CR4) 2011; 96 Badman, Pissios, Kennedy, Koukos, Flier, Maratos-Flier (CR16) 2007; 5 Schaefer, McFarland, Blakely, He, Whittaker, Taylor, Chinnery, Turnbull (CR23) 2007; 63 Cuevas-Ramos, Almeda-Valdes, Gómez-Pérez, Meza-Arana, Cruz-Bautista, Arellano-Campos, Navarrete-López, Aguilar-Salinas (CR28) 2010; 163 Smeitink (CR26) 2003; 26 Skladal, Halliday, Thorburn (CR20) 2003; 126 Nishimura, Nakatake, Konishi, Itoh (CR5) 2000; 1492 CR21 Johnson, Weston, Chadi, Fazio, Huff, Kharitonenkov, Köester, Pin (CR14) 2009; 137 Tyynismaa, Carroll, Raimundo, Ahola-Erkkilä, Wenz, Ruhanen, Guse, Hemminki, Peltola-Mjøsund, Tulkki (CR30) 2010; 19 Inagaki, Dutchak, Zhao, Ding, Gautron, Parameswara, Li, Goetz, Mohammadi, Esser (CR17) 2007; 5 Chen, Li, Yang, Li, Qi, Zhu, Tang, Liu, Boden (CR7) 2008; 116 Zhang, Yeung, Karpisek, Stejskal, Zhou, Liu, Wong, Chow, Tso, Lam (CR10) 2008; 57 Izumiya, Bina, Ouchi, Akasaki, Kharitonenkov, Walsh (CR12) 2008; 582 Schapira (CR22) 2002; 25 Ornitz, Itoh (CR2) 2001; 2 Wang, Qiang, Farmer (CR11) 2008; 28 2767_CR21 AM Schaefer (2767_CR23) 2007; 63 H Tyynismaa (2767_CR4) 2011; 96 H Li (2767_CR6) 2009; 94 ML Reitman (2767_CR9) 2007; 5 T Inagaki (2767_CR17) 2007; 5 MK Badman (2767_CR16) 2007; 5 X Zhang (2767_CR10) 2008; 57 CL Johnson (2767_CR14) 2009; 137 Y Izumiya (2767_CR12) 2008; 582 KF Tacer (2767_CR15) 2010; 24 DM Ornitz (2767_CR2) 2001; 2 W Wente (2767_CR13) 2006; 55 H Wang (2767_CR11) 2008; 28 T Nishimura (2767_CR5) 2000; 1492 W Chen (2767_CR7) 2008; 116 H Tyynismaa (2767_CR30) 2010; 19 N Itoh (2767_CR1) 2004; 20 S DiMauro (2767_CR24) 2003; 348 D Cuevas-Ramos (2767_CR28) 2010; 163 DD Moore (2767_CR8) 2007; 316 O Shaham (2767_CR27) 2010; 107 RJRJ Janssen (2767_CR29) 2006; 29 A Kharitonenkov (2767_CR3) 2005; 115 S Di Donato (2767_CR25) 2009; 256 RW Taylor (2767_CR19) 2005; 6 A Schapira (2767_CR22) 2002; 25 JAM Smeitink (2767_CR26) 2003; 26 D Skladal (2767_CR20) 2003; 126 A Suomalainen (2767_CR18) 2011; 34 19252802 - J Neurol. 2009 May;256(5):693-710 17550778 - Cell Metab. 2007 Jun;5(6):426-37 15861210 - Nat Rev Genet. 2005 May;6(5):389-402 21123446 - J Clin Endocrinol Metab. 2011 Feb;96(2):E351-5 15475116 - Trends Genet. 2004 Nov;20(11):563-9 12137229 - J Inherit Metab Dis. 2002 May;25(3):207-14 16838076 - J Inherit Metab Dis. 2006 Aug;29(4):499-515 20566587 - Eur J Endocrinol. 2010 Sep;163(3):469-77 17954559 - Mol Cell Biol. 2008 Jan;28(1):188-200 12805096 - Brain. 2003 Aug;126(Pt 8):1905-12 18948104 - FEBS Lett. 2008 Nov 12;582(27):3805-10 12889661 - J Inherit Metab Dis. 2003;26(2-3):199-207 16936195 - Diabetes. 2006 Sep;55(9):2470-8 12826641 - N Engl J Med. 2003 Jun 26;348(26):2656-68 19318452 - J Clin Endocrinol Metab. 2009 Jun;94(6):2151-6 20656789 - Hum Mol Genet. 2010 Oct 15;19(20):3948-58 17886296 - Ann Neurol. 2008 Jan;63(1):35-9 18252893 - Diabetes. 2008 May;57(5):1246-53 17556573 - Science. 2007 Jun 8;316(5830):1436-8 10858549 - Biochim Biophys Acta. 2000 Jun 21;1492(1):203-6 20941643 - J Inherit Metab Dis. 2011 Apr;34(2):277-82 17550773 - Cell Metab. 2007 Jun;5(6):405-7 11276432 - Genome Biol. 2001;2(3):REVIEWS3005 19664632 - Gastroenterology. 2009 Nov;137(5):1795-804 15902306 - J Clin Invest. 2005 Jun;115(6):1627-35 17550777 - Cell Metab. 2007 Jun;5(6):415-25 20080599 - Proc Natl Acad Sci U S A. 2010 Jan 26;107(4):1571-5 17926232 - Exp Clin Endocrinol Diabetes. 2008 Jan;116(1):65-8 20667984 - Mol Endocrinol. 2010 Oct;24(10):2050-64 |
References_xml | – volume: 137 start-page: 1795 issue: 5 year: 2009 end-page: 1804 ident: CR14 article-title: Fibroblast growth factor 21 reduces the severity of cerulein-induced pancreatitis in mice publication-title: Gastroenterology doi: 10.1053/j.gastro.2009.07.064 – volume: 25 start-page: 207 issue: 3 year: 2002 end-page: 214 ident: CR22 article-title: Primary and secondary defects of the mitochondrial respiratory chain publication-title: J Inherit Metab Dis doi: 10.1023/A:1015629912477 – volume: 115 start-page: 1627 issue: 6 year: 2005 end-page: 1635 ident: CR3 article-title: FGF-21 as a novel metabolic regulator publication-title: J Clin Inv doi: 10.1172/JCI23606 – volume: 316 start-page: 1436 issue: 5830 year: 2007 end-page: 1438 ident: CR8 article-title: Sister act publication-title: Science doi: 10.1126/science.1144837 – volume: 582 start-page: 3805 issue: 27 year: 2008 end-page: 3810 ident: CR12 article-title: FGF21 is an Akt-regulated myokine publication-title: FEBS Lett doi: 10.1016/j.febslet.2008.10.021 – volume: 96 start-page: E351 issue: 2 year: 2011 end-page: E355 ident: CR4 article-title: Liver fat but not other adiposity measures influence circulating FGF21 levels in healthy young adult twins publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2010-1326 – volume: 5 start-page: 405 issue: 6 year: 2007 end-page: 407 ident: CR9 article-title: FGF21: a missing link in the biology of fasting publication-title: Cell Metab doi: 10.1016/j.cmet.2007.05.010 – volume: 5 start-page: 426 issue: 6 year: 2007 end-page: 437 ident: CR16 article-title: Hepatic fibroblast growth factor 21 is regulated by PPARα and is a key mediator of hepatic lipid metabolism in ketotic states publication-title: Cell Metab doi: 10.1016/j.cmet.2007.05.002 – volume: 5 start-page: 415 issue: 6 year: 2007 end-page: 425 ident: CR17 article-title: Endocrine regulation of the fasting response by PPARα-mediated induction of fibroblast growth factor 21 publication-title: Cell Metab doi: 10.1016/j.cmet.2007.05.003 – volume: 2 start-page: 3005.3001 issue: 3 year: 2001 end-page: 3005.3012 ident: CR2 article-title: Fibroblast growth factors publication-title: Gen Biol doi: 10.1186/gb-2001-2-3-reviews3005 – volume: 19 start-page: 3948 issue: 20 year: 2010 end-page: 3958 ident: CR30 article-title: Mitochondrial myopathy induces a starvation-like response publication-title: Hum Mol Gen doi: 10.1093/hmg/ddq310 – volume: 126 start-page: 1905 issue: 8 year: 2003 end-page: 1912 ident: CR20 article-title: Minimum birth prevalence of mitochondrial respiratory chain disorders in children publication-title: Brain doi: 10.1093/brain/awg170 – volume: 256 start-page: 693 issue: 5 year: 2009 end-page: 710 ident: CR25 article-title: Multisystem manifestations of mitochondrial disorders publication-title: J Neurol doi: 10.1007/s00415-009-5028-3 – volume: 57 start-page: 1246 issue: 5 year: 2008 end-page: 1253 ident: CR10 article-title: Serum FGF21 levels are increased in obesity and are independently associated with the metabolic syndrome in humans publication-title: Diabetes doi: 10.2337/db07-1476 – volume: 34 start-page: 277 issue: 2 year: 2011 end-page: 282 ident: CR18 article-title: Biomarkers for mitochondrial respiratory chain disorders publication-title: J Inherit Metab Dis doi: 10.1007/s10545-010-9222-3 – ident: CR21 – volume: 348 start-page: 2656 issue: 26 year: 2003 end-page: 2668 ident: CR24 article-title: Mitochondrial respiratory-chain diseases publication-title: N Engl J Med doi: 10.1056/NEJMra022567 – volume: 107 start-page: 1571 issue: 4 year: 2010 end-page: 1575 ident: CR27 article-title: A plasma signature of human mitochondrial disease revealed through metabolic profiling of spent media from cultured muscle cells publication-title: Proc Natl Acad Sci doi: 10.1073/pnas.0906039107 – volume: 55 start-page: 2470 issue: 9 year: 2006 end-page: 2478 ident: CR13 article-title: Fibroblast growth factor-21 improves pancreatic β-cell function and survival by activation of extracellular signal-regulated kinase 1/2 and Akt signaling pathways publication-title: Diabetes doi: 10.2337/db05-1435 – volume: 28 start-page: 188 issue: 1 year: 2008 end-page: 200 ident: CR11 article-title: Identification of a domain within peroxisome proliferator-activated receptor γ regulating expression of a group of genes containing fibroblast growth factor 21 that are selectively repressed by SIRT1 in adipocytes publication-title: Mol Cell Biol doi: 10.1128/MCB.00992-07 – volume: 63 start-page: 35 issue: 1 year: 2007 end-page: 39 ident: CR23 article-title: Prevalence of mitochondrial DNA disease in adults publication-title: Ann Neurol doi: 10.1002/ana.21217 – volume: 6 start-page: 389 issue: 5 year: 2005 end-page: 402 ident: CR19 article-title: Mitochondrial DNA mutations in human disease publication-title: Nat Rev Gen doi: 10.1038/nrg1606 – volume: 29 start-page: 499 issue: 4 year: 2006 end-page: 515 ident: CR29 article-title: Mitochondrial complex I: structure, function and pathology publication-title: J Inherit Metab Dis doi: 10.1007/s10545-006-0362-4 – volume: 163 start-page: 469 issue: 3 year: 2010 end-page: 477 ident: CR28 article-title: Daily physical activity, fasting glucose, uric acid, and body mass index are independent factors associated with serum fibroblast growth factor 21 levels publication-title: Eur J Endocrinol doi: 10.1530/EJE-10-0454 – volume: 1492 start-page: 203 issue: 1 year: 2000 end-page: 206 ident: CR5 article-title: Identification of a novel FGF FGF-21 preferentially expressed in the liver publication-title: Biochimica et Biophysica Acta (BBA)-Gen Struct Exp doi: 10.1016/S0167-4781(00)00067-1 – volume: 20 start-page: 563 issue: 11 year: 2004 end-page: 569 ident: CR1 article-title: Evolution of the Fgf and Fgfr gene families publication-title: Tren Gen doi: 10.1016/j.tig.2004.08.007 – volume: 24 start-page: 2050 issue: 10 year: 2010 end-page: 2064 ident: CR15 article-title: Research resource: comprehensive expression atlas of the fibroblast growth factor system in adult mouse publication-title: Mol Endocrinol doi: 10.1210/me.2010-0142 – volume: 116 start-page: 65 issue: 1 year: 2008 end-page: 68 ident: CR7 article-title: Circulating FGF-21 levels in normal subjects and in newly diagnose patients with type 2 diabetes mellitus publication-title: Exp Clin Endocrinol Diabet doi: 10.1055/s-2007-985148 – volume: 26 start-page: 199 issue: 2 year: 2003 end-page: 207 ident: CR26 article-title: Mitochondrial disorders: clinical presentation and diagnostic dilemmas publication-title: J Inherit Metab Dis doi: 10.1023/A:1024489218004 – volume: 94 start-page: 2151 issue: 6 year: 2009 end-page: 2156 ident: CR6 article-title: Serum fibroblast growth factor 21 is associated with adverse lipid profiles and γ-glutamyltransferase but not insulin sensitivity in Chinese subjects publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2008-2331 – volume: 57 start-page: 1246 issue: 5 year: 2008 ident: 2767_CR10 publication-title: Diabetes doi: 10.2337/db07-1476 – volume: 2 start-page: 3005.3001 issue: 3 year: 2001 ident: 2767_CR2 publication-title: Gen Biol doi: 10.1186/gb-2001-2-3-reviews3005 – volume: 28 start-page: 188 issue: 1 year: 2008 ident: 2767_CR11 publication-title: Mol Cell Biol doi: 10.1128/MCB.00992-07 – volume: 63 start-page: 35 issue: 1 year: 2007 ident: 2767_CR23 publication-title: Ann Neurol doi: 10.1002/ana.21217 – volume: 26 start-page: 199 issue: 2 year: 2003 ident: 2767_CR26 publication-title: J Inherit Metab Dis doi: 10.1023/A:1024489218004 – volume: 34 start-page: 277 issue: 2 year: 2011 ident: 2767_CR18 publication-title: J Inherit Metab Dis doi: 10.1007/s10545-010-9222-3 – volume: 24 start-page: 2050 issue: 10 year: 2010 ident: 2767_CR15 publication-title: Mol Endocrinol doi: 10.1210/me.2010-0142 – volume: 6 start-page: 389 issue: 5 year: 2005 ident: 2767_CR19 publication-title: Nat Rev Gen doi: 10.1038/nrg1606 – volume: 1492 start-page: 203 issue: 1 year: 2000 ident: 2767_CR5 publication-title: Biochimica et Biophysica Acta (BBA)-Gen Struct Exp doi: 10.1016/S0167-4781(00)00067-1 – volume: 256 start-page: 693 issue: 5 year: 2009 ident: 2767_CR25 publication-title: J Neurol doi: 10.1007/s00415-009-5028-3 – volume: 29 start-page: 499 issue: 4 year: 2006 ident: 2767_CR29 publication-title: J Inherit Metab Dis doi: 10.1007/s10545-006-0362-4 – volume: 5 start-page: 405 issue: 6 year: 2007 ident: 2767_CR9 publication-title: Cell Metab doi: 10.1016/j.cmet.2007.05.010 – volume: 94 start-page: 2151 issue: 6 year: 2009 ident: 2767_CR6 publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2008-2331 – volume: 55 start-page: 2470 issue: 9 year: 2006 ident: 2767_CR13 publication-title: Diabetes doi: 10.2337/db05-1435 – volume: 316 start-page: 1436 issue: 5830 year: 2007 ident: 2767_CR8 publication-title: Science doi: 10.1126/science.1144837 – volume: 5 start-page: 415 issue: 6 year: 2007 ident: 2767_CR17 publication-title: Cell Metab doi: 10.1016/j.cmet.2007.05.003 – volume: 582 start-page: 3805 issue: 27 year: 2008 ident: 2767_CR12 publication-title: FEBS Lett doi: 10.1016/j.febslet.2008.10.021 – volume: 25 start-page: 207 issue: 3 year: 2002 ident: 2767_CR22 publication-title: J Inherit Metab Dis doi: 10.1023/A:1015629912477 – volume: 115 start-page: 1627 issue: 6 year: 2005 ident: 2767_CR3 publication-title: J Clin Inv doi: 10.1172/JCI23606 – volume: 163 start-page: 469 issue: 3 year: 2010 ident: 2767_CR28 publication-title: Eur J Endocrinol doi: 10.1530/EJE-10-0454 – volume: 5 start-page: 426 issue: 6 year: 2007 ident: 2767_CR16 publication-title: Cell Metab doi: 10.1016/j.cmet.2007.05.002 – volume: 107 start-page: 1571 issue: 4 year: 2010 ident: 2767_CR27 publication-title: Proc Natl Acad Sci doi: 10.1073/pnas.0906039107 – volume: 96 start-page: E351 issue: 2 year: 2011 ident: 2767_CR4 publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2010-1326 – volume: 116 start-page: 65 issue: 1 year: 2008 ident: 2767_CR7 publication-title: Exp Clin Endocrinol Diabet doi: 10.1055/s-2007-985148 – ident: 2767_CR21 – volume: 348 start-page: 2656 issue: 26 year: 2003 ident: 2767_CR24 publication-title: N Engl J Med doi: 10.1056/NEJMra022567 – volume: 137 start-page: 1795 issue: 5 year: 2009 ident: 2767_CR14 publication-title: Gastroenterology doi: 10.1053/j.gastro.2009.07.064 – volume: 20 start-page: 563 issue: 11 year: 2004 ident: 2767_CR1 publication-title: Tren Gen doi: 10.1016/j.tig.2004.08.007 – volume: 126 start-page: 1905 issue: 8 year: 2003 ident: 2767_CR20 publication-title: Brain doi: 10.1093/brain/awg170 – volume: 19 start-page: 3948 issue: 20 year: 2010 ident: 2767_CR30 publication-title: Hum Mol Gen doi: 10.1093/hmg/ddq310 – reference: 20566587 - Eur J Endocrinol. 2010 Sep;163(3):469-77 – reference: 18252893 - Diabetes. 2008 May;57(5):1246-53 – reference: 12889661 - J Inherit Metab Dis. 2003;26(2-3):199-207 – reference: 15861210 - Nat Rev Genet. 2005 May;6(5):389-402 – reference: 17556573 - Science. 2007 Jun 8;316(5830):1436-8 – reference: 17954559 - Mol Cell Biol. 2008 Jan;28(1):188-200 – reference: 12137229 - J Inherit Metab Dis. 2002 May;25(3):207-14 – reference: 19252802 - J Neurol. 2009 May;256(5):693-710 – reference: 19318452 - J Clin Endocrinol Metab. 2009 Jun;94(6):2151-6 – reference: 10858549 - Biochim Biophys Acta. 2000 Jun 21;1492(1):203-6 – reference: 17886296 - Ann Neurol. 2008 Jan;63(1):35-9 – reference: 12805096 - Brain. 2003 Aug;126(Pt 8):1905-12 – reference: 20080599 - Proc Natl Acad Sci U S A. 2010 Jan 26;107(4):1571-5 – reference: 16838076 - J Inherit Metab Dis. 2006 Aug;29(4):499-515 – reference: 16936195 - Diabetes. 2006 Sep;55(9):2470-8 – reference: 17550773 - Cell Metab. 2007 Jun;5(6):405-7 – reference: 15475116 - Trends Genet. 2004 Nov;20(11):563-9 – reference: 17550777 - Cell Metab. 2007 Jun;5(6):415-25 – reference: 17926232 - Exp Clin Endocrinol Diabetes. 2008 Jan;116(1):65-8 – reference: 12826641 - N Engl J Med. 2003 Jun 26;348(26):2656-68 – reference: 15902306 - J Clin Invest. 2005 Jun;115(6):1627-35 – reference: 11276432 - Genome Biol. 2001;2(3):REVIEWS3005 – reference: 18948104 - FEBS Lett. 2008 Nov 12;582(27):3805-10 – reference: 20941643 - J Inherit Metab Dis. 2011 Apr;34(2):277-82 – reference: 21123446 - J Clin Endocrinol Metab. 2011 Feb;96(2):E351-5 – reference: 20656789 - Hum Mol Genet. 2010 Oct 15;19(20):3948-58 – reference: 17550778 - Cell Metab. 2007 Jun;5(6):426-37 – reference: 19664632 - Gastroenterology. 2009 Nov;137(5):1795-804 – reference: 20667984 - Mol Endocrinol. 2010 Oct;24(10):2050-64 |
SSID | ssj0004175 |
Score | 2.1028662 |
Snippet | Mitochondrial respiratory chain deficiencies are a group of more than 100 disorders of adults and children, with highly variable phenotypes. The high... |
SourceID | pubmedcentral proquest pubmed crossref springer |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 6495 |
SubjectTerms | adults Animal Anatomy Animal Biochemistry ataxia (disorder) Biomarkers Biomarkers - blood Biomedical and Life Sciences blood serum children Diagnosis, Differential electron transport chain enzyme-linked immunosorbent assay Female fibroblast growth factors Fibroblast Growth Factors - blood Friedreich Ataxia - blood Friedreich Ataxia - diagnosis Histology homeostasis Humans Iran Life Sciences liver Male Mitochondria Mitochondrial Diseases - blood Mitochondrial Diseases - diagnosis Molecular biology Morphology patients phenotype Proteins |
SummonAdditionalLinks | – databaseName: SpringerLink Journals (ICM) dbid: U2A link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lb9QwELZQEYILgvJa2qJB4kCBSIkd28lxVbFUSHBipd4iO7bZlUqCNlkJ_hE_szN57HZbWImzJy_PjP19Gc8MY29ywz3X1kTOI3xLjcnQ57yKgsgM7gguLrsI_pev6nyefr6QF0MedzOedh9Dkt1KvU12S6jvGHUj4Bq9G3n6XUnUHY14zqfbZMikq65LUD9KEU-Mocy_3WJ3M7qFMG8flLwRLe02odkj9nBAjzDt1f2Y3fHVIbvX95P8fcjun43t256wP9cmHuoAAXlxbRErt_AdqXe7gL7VDrydfZpFPDkF04ABSsenEzsroD-08LMvRgE_0PFxoawc2Su4oWRn8wHsuoWqbnvphti12yOPD0Nq7lZ-WS5g2ppfS3P6lM1nH7-dnUdDW4aolEK1UemcDjp3CBUsbm8uqNzpzMe6RLSkRGJtygPiMElZscp7r7QKQfDYC6sMQr5n7KCqK_-CQUjyTOZeGm2SVIfMBi6FUTo3iRbGywmLR_0U5VCznFpnXBbbasuk0gJVWpBKi3jC3m0uGeZon_DxqPRi8N0GyVAqKHFS4ONfb4ZRexRKMZWv1ySjJNoZgsF9MjnSU4TDYo8MATyhkUZO2PPe1jZvTVw7Q4Y5YXrHCjcCVBl8d6RaLroK4SJDP8vxnu9He732ef-ajJf_JX3EHnBypC4t85gdtKu1P0F81tpXnT9eASBsM3I priority: 102 providerName: Springer Nature |
Title | Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia) |
URI | https://link.springer.com/article/10.1007/s11033-013-2767-0 https://www.ncbi.nlm.nih.gov/pubmed/24078096 https://www.proquest.com/docview/1443617835 https://www.proquest.com/docview/1465175515 https://www.proquest.com/docview/1492615753 https://www.proquest.com/docview/1710237960 https://pubmed.ncbi.nlm.nih.gov/PMC3824290 |
Volume | 40 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9NAEB5BK0QvCMrLUKpF4kABC9tr79onFKKkFYgKISKFk7X27pJIxS6xI8E_4mcy40fSUOFLLMXj185jv9nZmQF4kajABDJTrjYI30KlYtQ5I1zLY4UzgvbyJoL_6VyczcIP82jeLbhV3bbK3iY2hlqXOa2Rv0XgzymdjUfvLn-61DWKoqtdC42bsE-ly2hLl5zLbV6k3xTaJdTvhggt-qhmkzrnUxcz6m0QSLQV3u68dA1sXt8z-U_gtJmPpnfhTgck2ajl_D24YYpDuNW2lvx9CLfHfSe3-_DnCg9YaZlFF7nMEDbX7Dt64fWCtV132Mvp6dQN_BOmKqYYZebT5p0Vo8VadtnWpWA_0AagzSw0iS7TXfXO6g3L1jUryrqlrsjR1gP0-DD00vXKLPMFG9Xq11KdPIDZdPJ1fOZ2HRrcPOKidnOtpZWJRtSQ4UynrUi0jI0ncwROgvtZFgYWIVlECbLCGCOksJYHnuGZUIj-HsJeURbmMTDrJ3GUmEhJ5YfSxpkNIq6ETJQvuTKRA17PnzTvypdTF42LdFt4mViaIktTYmnqOfBqc0k3RkPERz3T006Nq3QrdA4835xG7lFURRWmXBONiFDOEBcO0SToqSIy5gM0hPW4RI_SgUetrG3emtzuGJ1NB-SOFG4IqEj47pliuWiKhfMYVS7Be77u5fXK5_1vMJ4MD8ZTOAhIc5qUzCPYq1dr8wyxWZ0dNwp4DPuj028fJ3h8Pzn__AX_HYsx_s6C0V_FHzv3 |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEB6VVqhcEJRXoMAigUQBC9sb79oHhEppSGkbIdRKvZm1d5dEArvEjqD_iBO_kRk_koYK33r2-LXz-mZnZwbgaaR848tEOdogfOsrFaLOGeFYHir0CNpNqwz-4UgMj_sfT4KTFfjT1sLQscrWJlaGWucp7ZG_RuDPqZyNB29Pfzg0NYqyq-0IjVos9s3ZTwzZijd775G_z3x_sHu0M3SaqQJOGnBROqnW0spIo6dL0DprKyItQ-PKFJ294F6S9H2LMCKgok5hjBFSWMt91_BEKEQs-NwrsIZf46IhWHu3O_r0eVGJ6VWtfSnOcPoIZto8alWs59HcNJqm4Eu0Tu6yJ7wAby-e0vwnVVt5wMENuN5AV7Zdy9pNWDHZBlyth1mebcD6Tjs77hb8Psd1lltmMSjPEwTqJfuKcX85ZvWcH_Z88GHg-N4WUwVTjHoB0HGhKaPtYXZad8Jg39HqoJXONCkL002_0OIVS2Yly_Kypi4otNcd9PiyKQLuqZmkY7Zdql8TtXUbji-Fe3dgNcszcw-Y9aIwiEygpPL60oaJ9QOuhIyUJ7kyQQ_clj9x2jRMp7kd3-JFq2diaYwsjYmlsduDF_NbmjXqIt5smR43hqOIF2Legyfzy8g9yuOozOQzohEByhki0S6aCGNjxOK8g4bQJZcYw_bgbi1r86-mQD_E8LYHckkK5wTUlnz5SjYZV-3JeYhKHuEzX7byeu73_rcY97sX4zGsD48OD-KDvdH-A7jmkxZVBaGbsFpOZ-YhIsMyedSoI4Mvl20B_gK063RS |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwEB6VIh4XBAXKQgEjgUShUZM4sZMDQlXL0lKoOFBpb8GJbXYlSMomq9J_xG_g1zGTx26Xitx6zuTleX3j8cwAPI-Vb3yZKkcbhG-BUhHqnBGO5ZFCj6DdrM7gfzoS-8fBh1E4WoE_XS0MHavsbGJtqHWR0R75NgJ_TuVsPNy27bGIz3vDtyc_HZogRZnWbpxGIyKH5uwUw7fyzcEe8vqF7w_ffdndd9oJA04WclE5mdbSylij10vRUmsrYi0j48oMHb_gXpoGvkVIEVKBpzDGCCms5b5reCoUohd87hW4KnnokY7JkVzUZHp1k1-KOJwAYU2XUa3L9jyaoEZzFXyJdspd9okXgO7F85r_JG1rXzi8DbdaEMt2Gqm7AysmX4NrzVjLszW4sdtNkbsLv8_xnxWWWQzPixQhe8W-TYvTasyaiT_s5fD90PG9TaZKphh1BaCDQ1NGG8XspOmJwX6g_UF7nWtSG6bbzqHlFktnFcuLqqEuKcjXPfT4silC76mZZGO2U6lfE7V5D44vhXf3YTUvcvMAmPXiKIxNqKTyAmmj1PohV0LGypNcmXAAbsefJGtbp9MEj-_JoukzsTRBlibE0sQdwKv5Le0a9RFvdExPWhNSJguBH8Cz-WXkHmV0VG6KGdGIEOUMMWkfTYxRMqJy3kNDOJNLjGYHsN7I2vyrKeSPMNAdgFySwjkBNShfvpJPxnWjch6husf4zNedvJ77vf8txsP-xXgK11Hvk48HR4eP4KZPSlRXhm7AajWdmccIEav0Sa2LDL5etvL_BewmdyI |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Association+of+fibroblast+growth+factor+%28FGF-21%29+as+a+biomarker+with+primary+mitochondrial+disorders%2C+but+not+with+secondary+mitochondrial+disorders+%28Friedreich+Ataxia%29&rft.jtitle=Molecular+biology+reports&rft.au=Salehi%2C+Mohammad+Hossein&rft.au=Kamalidehghan%2C+Behnam&rft.au=Houshmand%2C+Massoud&rft.au=Aryani%2C+Omid&rft.date=2013-11-01&rft.pub=Springer+Nature+B.V&rft.issn=0301-4851&rft.eissn=1573-4978&rft.volume=40&rft.issue=11&rft.spage=6495&rft_id=info:doi/10.1007%2Fs11033-013-2767-0&rft.externalDBID=HAS_PDF_LINK&rft.externalDocID=3104896661 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0301-4851&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0301-4851&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0301-4851&client=summon |