Integrated treatment guided by RNA-seq–based endometrial receptivity assessment for infertility complicated by MEN1

Preimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in endocrinology (Lausanne) Vol. 14; p. 1224574
Main Authors Huang, Xi, Fu, Jing, Zhang, Qiong, Zhao, Jing, Yao, Zhongyuan, Xia, Qiuping, Tang, Hongying, Xu, Aizhuang, He, Aihua, Liang, Shaolin, Lu, Sijia, Li, Yanping
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 20.10.2023
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Preimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.BackgroundPreimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.We validated our newly developed RNA-seq-based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).MethodsWe validated our newly developed RNA-seq-based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).Significant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.ResultsSignificant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.Applying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.ConclusionsApplying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.Reproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010.Trial RegistrationReproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010.
AbstractList BackgroundPreimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.MethodsWe validated our newly developed RNA-seq–based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).ResultsSignificant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.ConclusionsApplying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.Trial RegistrationReproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010.
Preimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.BackgroundPreimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is transferred, implantation success is attained independent of embryo quality. Using PGT alone is unable to tackle implantation failure caused by endometrial receptivity (ER) abnormalities in these patients.We validated our newly developed RNA-seq-based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).MethodsWe validated our newly developed RNA-seq-based ER test (rsERT) in a retrospective cohort study including 511 PGT cycles and reported experience in treating an infertile female patient complicated by multiple endocrine neoplasia type 1 (MEN1).Significant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.ResultsSignificant improvement in the clinical pregnancy rate was found in the performed personalized embryo transfer (pET) group (CR, 69.7%; P = 0.035). In the rare MEN1 case, pET was done according to the prediction of the optimal time of window of implantation after unaffected blastocysts were obtained by PGT-M, which ultimately led to a healthy live birth. However, none of the mRNA variants identified in the patient showed a strong association with the MEN1 gene.Applying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.ConclusionsApplying the new rsERT along with PGT improved ART outcomes and brought awareness of the importance of the ER examination in MEN1 infertile female patients. MEN1-induced endocrine disorder rather than MEN1 mutation contributes to the ER abnormality.Reproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010.Trial RegistrationReproductive Medicine Ethics Committee of Xiangya Hospital Registry No.: 2022010.
Author Tang, Hongying
Yao, Zhongyuan
Xu, Aizhuang
He, Aihua
Zhang, Qiong
Lu, Sijia
Zhao, Jing
Li, Yanping
Huang, Xi
Liang, Shaolin
Fu, Jing
Xia, Qiuping
AuthorAffiliation 4 National Comprehensive Utilization of Science and Technology Information Resources and Public Service Center, Scientific and Technical Information (STI)-Zhilian Research Institute for Innovation and Digital Health , Beijing , China
3 Department of Reproductive Medicine Center, The Third Xiangya Hospital, Central South University , Changsha, Hunan , China
6 Institute for Six-sector Economy, Fudan University , Shanghai , China
5 ”Mobile Health” Ministry of Education-China Mobile Joint Laboratory, Xiangya Hospital, Central South University , Changsha , China
1 Department of Reproductive Medicine, Xiangya Hospital, Central South University , Changsha, Hunan , China
2 Clinical Research Center for Women’s Reproductive Health in Hunan Province , Changsha, Hunan , China
7 Department of Clinical Research, Yikon Genomics Company, Ltd. , Suzhou, Jiangsu , China
AuthorAffiliation_xml – name: 5 ”Mobile Health” Ministry of Education-China Mobile Joint Laboratory, Xiangya Hospital, Central South University , Changsha , China
– name: 7 Department of Clinical Research, Yikon Genomics Company, Ltd. , Suzhou, Jiangsu , China
– name: 3 Department of Reproductive Medicine Center, The Third Xiangya Hospital, Central South University , Changsha, Hunan , China
– name: 2 Clinical Research Center for Women’s Reproductive Health in Hunan Province , Changsha, Hunan , China
– name: 1 Department of Reproductive Medicine, Xiangya Hospital, Central South University , Changsha, Hunan , China
– name: 4 National Comprehensive Utilization of Science and Technology Information Resources and Public Service Center, Scientific and Technical Information (STI)-Zhilian Research Institute for Innovation and Digital Health , Beijing , China
– name: 6 Institute for Six-sector Economy, Fudan University , Shanghai , China
Author_xml – sequence: 1
  givenname: Xi
  surname: Huang
  fullname: Huang, Xi
– sequence: 2
  givenname: Jing
  surname: Fu
  fullname: Fu, Jing
– sequence: 3
  givenname: Qiong
  surname: Zhang
  fullname: Zhang, Qiong
– sequence: 4
  givenname: Jing
  surname: Zhao
  fullname: Zhao, Jing
– sequence: 5
  givenname: Zhongyuan
  surname: Yao
  fullname: Yao, Zhongyuan
– sequence: 6
  givenname: Qiuping
  surname: Xia
  fullname: Xia, Qiuping
– sequence: 7
  givenname: Hongying
  surname: Tang
  fullname: Tang, Hongying
– sequence: 8
  givenname: Aizhuang
  surname: Xu
  fullname: Xu, Aizhuang
– sequence: 9
  givenname: Aihua
  surname: He
  fullname: He, Aihua
– sequence: 10
  givenname: Shaolin
  surname: Liang
  fullname: Liang, Shaolin
– sequence: 11
  givenname: Sijia
  surname: Lu
  fullname: Lu, Sijia
– sequence: 12
  givenname: Yanping
  surname: Li
  fullname: Li, Yanping
BookMark eNpVkU1uFDEQhS0UJMKQC7DqJZsZ_Nc99gpFUYCRQpAQrK1quzw46m5PbHek2XEHbshJ8PwIEW9celX-XlnvNbmY4oSEvGV0JYTS7z1OLq445WLFOJftWr4gl6zr5JILzS_-q1-Rq5wfaD2SMq3VJZk3U8FtgoKuKQmhjDiVZjsHV4V-33y7v15mfPzz63cPuUoHqxFLCjA0CS3uSngKZd9Azpjz8bGPqQmTx1TCcGjZOO6GYI8Wlfjl9p69IS89DBmvzveC_Ph4-_3m8_Lu66fNzfXd0gq9LksLnmkhKe1Ui8JSpWQLSnOv0WqOrqOtbdeWtc4LBGulRSU7x6EWmnZULMjmxHURHswuhRHS3kQI5ijEtDVQ17QDmsplTmnwqqeS0R4ca71mzGmQvKNYWR9OrN3cj-hs_WqC4Rn0eWcKP802PhlGOy4kY5Xw7kxI8XHGXMwYssVhgAnjnA1Xqmu1FnV8Qfhp1KaYc0L_z4dRcwjdHEM3h9DNOXTxF8s3ppM
Cites_doi 10.1016/S0140-6736(20)32475-2
10.1111/cen.13890
10.1016/j.fertnstert.2010.04.063
10.1093/hropen/hoab010
10.1093/hropen/hoab011
10.3390/medicina47110092
10.1158/0008-5472.CAN-05-4461
10.1038/sj.onc.1204529
10.5935/1518-0557.20180010
10.1016/B978-0-323-47912-7.00022-6
10.1186/s12967-021-02837-y
10.4103/jhrs.JHRS_164_19
10.1210/jc.2012-1230
10.1016/s0015-0282(02)04670-8
10.1080/09513590.2021.1974382
10.1093/humrep/14.1.252
10.1054/bjoc.2000.1380
10.1016/j.fertnstert.2012.09.046
ContentType Journal Article
Copyright Copyright © 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li.
Copyright © 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li
Copyright_xml – notice: Copyright © 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li.
– notice: Copyright © 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li 2023 Huang, Fu, Zhang, Zhao, Yao, Xia, Tang, Xu, He, Liang, Lu and Li
DBID AAYXX
CITATION
7X8
5PM
DOA
DOI 10.3389/fendo.2023.1224574
DatabaseName CrossRef
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1664-2392
ExternalDocumentID oai_doaj_org_article_a891d89af8b0410bad15f911d9a4260e
PMC10623411
10_3389_fendo_2023_1224574
GroupedDBID 53G
5VS
9T4
AAFWJ
AAKDD
AAYXX
ACGFO
ACGFS
ACXDI
ADBBV
ADRAZ
AFPKN
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BCNDV
CITATION
DIK
EMOBN
GROUPED_DOAJ
GX1
HYE
KQ8
M48
M~E
OK1
PGMZT
RPM
7X8
5PM
ID FETCH-LOGICAL-c397t-caf193400685e3c08845a892f9ec92ed605c57c15df3eacc4ce846d2a4ce90603
IEDL.DBID M48
ISSN 1664-2392
IngestDate Wed Aug 27 01:29:44 EDT 2025
Thu Aug 21 18:36:23 EDT 2025
Thu Jul 10 17:13:46 EDT 2025
Tue Jul 01 01:41:47 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Language English
License This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c397t-caf193400685e3c08845a892f9ec92ed605c57c15df3eacc4ce846d2a4ce90603
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
These authors have contributed equally to this work and share first authorship
Edited by: Zhen-Gao Sun, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, China
Reviewed by: Xiushan Feng, Fujian Medical University, China; Qingzhen Xie, Renmin Hospital of Wuhan University, China
OpenAccessLink https://doaj.org/article/a891d89af8b0410bad15f911d9a4260e
PQID 2886599362
PQPubID 23479
ParticipantIDs doaj_primary_oai_doaj_org_article_a891d89af8b0410bad15f911d9a4260e
pubmedcentral_primary_oai_pubmedcentral_nih_gov_10623411
proquest_miscellaneous_2886599362
crossref_primary_10_3389_fendo_2023_1224574
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2023-10-20
PublicationDateYYYYMMDD 2023-10-20
PublicationDate_xml – month: 10
  year: 2023
  text: 2023-10-20
  day: 20
PublicationDecade 2020
PublicationTitle Frontiers in endocrinology (Lausanne)
PublicationYear 2023
Publisher Frontiers Media S.A
Publisher_xml – name: Frontiers Media S.A
References Brandi (B9) 1993; 53
Barbieri (B3) 2019
Tatum (B2) 2020; 396
Díaz-Gimeno (B5) 2013; 99
Dreijerink (B19) 2006; 66
Schuppe (B10) 1999; 14
Juodelė (B11) 2011; 47
Heppner (B20) 2001; 20
He (B8) 2021; 19
Bergman (B18) 2000; 83
Dhiman (B15) 2020; 13
Díaz-Gimeno (B4) 2011; 95
Thakker (B17) 2012; 97
Troncoso (B1) 2003; 79
Daglar (B14) 2016; 11
Ruiz-Alonso (B7) 2021; 2021
Li (B16) 2021; 38
Thompson (B12) 2019; 90
Lima (B13) 2018; 22
Ben Rafael (B6) 2021; 2021
References_xml – volume: 396
  year: 2020
  ident: B2
  article-title: China’s fertility treatment boom
  publication-title: Lancet
  doi: 10.1016/S0140-6736(20)32475-2
– volume: 90
  year: 2019
  ident: B12
  article-title: No evidence of adverse fertility and pregnancy outcomes in patients with unrecognized and untreated multiple endocrine neoplasia type 1
  publication-title: Clin Endocrinol (Oxf)
  doi: 10.1111/cen.13890
– volume: 95
  start-page: 50
  year: 2011
  ident: B4
  article-title: A genomic diagnostic tool for human endometrial receptivity based on the transcriptomic signature
  publication-title: Fertility Sterility
  doi: 10.1016/j.fertnstert.2010.04.063
– volume: 2021
  start-page: hoab010
  year: 2021
  ident: B6
  article-title: Endometrial Receptivity Analysis (ERA) test: an unproven technology
  publication-title: Hum Reprod Open
  doi: 10.1093/hropen/hoab010
– volume: 2021
  start-page: hoab011
  year: 2021
  ident: B7
  article-title: Endometrial Receptivity Analysis (ERA): data versus opinions
  publication-title: Hum Reprod Open
  doi: 10.1093/hropen/hoab011
– volume: 47
  year: 2011
  ident: B11
  article-title: Carcinoma of two parathyroid glands caused by a novel MEN1 gene mutation – a rare feature of the MEN 1 syndrome
  publication-title: Medicina
  doi: 10.3390/medicina47110092
– volume: 53
  year: 1993
  ident: B9
  article-title: Homozygotes for the autosomal dominant neoplasia syndrome (MEN1)
  publication-title: Am J Hum Genet
– volume: 66
  year: 2006
  ident: B19
  article-title: Menin links estrogen receptor activation to histone H3K4 trimethylation
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-05-4461
– volume: 20
  year: 2001
  ident: B20
  article-title: The tumor suppressor protein menin interacts with NF-κB proteins and inhibits NF-κB-mediated transactivation
  publication-title: Oncogene
  doi: 10.1038/sj.onc.1204529
– volume: 22
  start-page: 67
  year: 2018
  ident: B13
  article-title: Preimplantation genetic diagnosis for a patient with multiple endocrine neoplasia type 1: case report
  publication-title: JBRA Assist Reprod
  doi: 10.5935/1518-0557.20180010
– start-page: 556
  volume-title: Yen and Jaffe’s Reproductive Endocrinology
  year: 2019
  ident: B3
  article-title: Yen & Jaffe’s reproductive endocrinology : physiology, pathophysiology, and clinical management
  doi: 10.1016/B978-0-323-47912-7.00022-6
– volume: 19
  start-page: 176
  year: 2021
  ident: B8
  article-title: The role of transcriptomic biomarkers of endometrial receptivity in personalized embryo transfer for patients with repeated implantation failure
  publication-title: J Transl Med
  doi: 10.1186/s12967-021-02837-y
– volume: 11
  start-page: 217
  year: 2016
  ident: B14
  article-title: Management of a multiple endocrine neoplasia type 1 during pregnancy: A case report and review of the literature
  publication-title: J Exp Ther Oncol
– volume: 13
  year: 2020
  ident: B15
  article-title: Management of a multiple endocrine neoplasia 1 patient in pregnancy
  publication-title: J Hum Reprod Sci
  doi: 10.4103/jhrs.JHRS_164_19
– volume: 97
  start-page: 2990
  year: 2012
  ident: B17
  article-title: Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1)
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/jc.2012-1230
– volume: 79
  year: 2003
  ident: B1
  article-title: The origin of biochemical pregnancies: lessons learned from preimplantation genetic diagnosis
  publication-title: Fertil Steril
  doi: 10.1016/s0015-0282(02)04670-8
– volume: 38
  start-page: 1
  year: 2021
  ident: B16
  article-title: Management of a multiple endocrine neoplasia type 1 during pregnancy: a case with primary hypertension
  publication-title: Gynecol Endocrinol
  doi: 10.1080/09513590.2021.1974382
– volume: 14
  year: 1999
  ident: B10
  article-title: Case Report: Secondary infertility as early symptom in a man with multiple endocrine neoplasia-type 1
  publication-title: Hum Reprod
  doi: 10.1093/humrep/14.1.252
– volume: 83
  year: 2000
  ident: B18
  article-title: Identification of MEN1 gene mutations in families with MEN 1 and related disorders
  publication-title: Br J Cancer
  doi: 10.1054/bjoc.2000.1380
– volume: 99
  year: 2013
  ident: B5
  article-title: The accuracy and reproducibility of the endometrial receptivity array is superior to histology as a diagnostic method for endometrial receptivity
  publication-title: Fertil Steril
  doi: 10.1016/j.fertnstert.2012.09.046
SSID ssj0000401998
Score 2.315136
Snippet Preimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected embryo is...
BackgroundPreimplantation genetic testing (PGT) serves as a tool to avoid genetic disorders in patients with known genetic conditions. However, once a selected...
SourceID doaj
pubmedcentral
proquest
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
StartPage 1224574
SubjectTerms Endocrinology
endometrial receptivity
MEN1
personalized embryo transfer
PGT-M
RNA-seq
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV07T8MwELZQB8SCeIrykpHYUGjiRxOPgEAFqR0QSGyWY1-gA-HVDmz8B_4hv4S7JK2aiYUtcqLEuTvffSefv2PsWIoUlCzySGvnIlUI9IPO60hIJ6SXoHRGZ4eHo_7gXt086IeFVl9UE1bTA9eC67nMJCEzrsjyWCVx7kKiC1yhwTgiVwfyvhjzFpKpygdj2oCJRH1KBrMw0yugDHTYT8hT2kzSqWpFooqwv4Uy2zWSC0Hnao2tNmiRn9WzXGdLUG6w5WGzH77JptcztofA5yXj_HE6DjiQf_Lb0Vn0AW8_X98UrQKn2T1D1amDo6ujihbqHcHdnJ-TI4jlVKGFnySEzuc15_Ubh5ejZIvdX13eXQyippFC5BFuTCLvCsRpio6DaJAeHYvSKFdRGPBGQMCUxuvUJzoUEh2xVx4QlgTh8MLE_Vhus075UsIO48IkqAHpdAZOpbHJYylTQJgQEP-Cll12MhOqfa35MizmGaQCW6nAkgpso4IuOye5z58krutqAC3ANhZg_7KALjuaac3i2qAND1fCy_TDiizrawRgfdFlWUudrS-275Tjp4plG3NlgSE-2f2POe6xFfpvCnoi3medyfsUDhDNTPLDynB_AUKl9sw
  priority: 102
  providerName: Directory of Open Access Journals
Title Integrated treatment guided by RNA-seq–based endometrial receptivity assessment for infertility complicated by MEN1
URI https://www.proquest.com/docview/2886599362
https://pubmed.ncbi.nlm.nih.gov/PMC10623411
https://doaj.org/article/a891d89af8b0410bad15f911d9a4260e
Volume 14
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3da9RAEB9qBfFF_MTTtqzgm6Qm-5FkH4q00lqFuwfx4N6Wze6kLWjO3gfY_96ZvdxhQMGXEDZhdrOzO_Ob7HwAvFWyQq3aJjPG-0y3kuSgDyaTyksVFGpTc-zweFJeTvWXmZntwbbcUT-By7-adlxParr4fvzr9u4DbfgTtjhJ375vsYscxyfVMZ8TmUrfg_ukmSreqOMe7ifJTMaETeVxi7LUNB4rN3E0_yAz0FUppf8Ahw69KP9QSxeP4VGPJ8XpZgE8gT3snsKDcX9i_gyWn7f5IKLYOZWLq_VNpIbmTnydnGZLvM1Ym0XBY_uBqZKHIFHIHi9cW0L4Xf5OQSBXsAcXdcgIXux80jf0xueT4jlML86_fbzM-kILWSA4ssqCbwnHaQ4XMagCCR5tfG1lazFYiZFMnmCqUJjYKhLUQQck2BKlpxubl7l6AfvdvMOXIKQtfCyUNzV6XeW2yZWqkGBEJHyMRo3g3XZK3c9NPg1HdggzwCUGOGaA6xkwgjOe9d2bnAs7NcwXV67fWo5GStStb-sm10XeUP-mJRkeref0-ziCN1ueOdo7fCDiO5yvl07WdWkIoJVyBPWAmYMeh0-6m-uUhZtsaUkQoHj1H-Rfw0P-LNZ5Mj-A_dVijYcEZlbNUfoJQNdPs-Iordbf4Rn2WA
linkProvider Scholars Portal
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=Integrated+treatment+guided+by+RNA-seq-based+endometrial+receptivity+assessment+for+infertility+complicated+by+MEN1&rft.jtitle=Frontiers+in+endocrinology+%28Lausanne%29&rft.au=Huang%2C+Xi&rft.au=Fu%2C+Jing&rft.au=Zhang%2C+Qiong&rft.au=Zhao%2C+Jing&rft.date=2023-10-20&rft.issn=1664-2392&rft.eissn=1664-2392&rft.volume=14&rft.spage=1224574&rft_id=info:doi/10.3389%2Ffendo.2023.1224574&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-2392&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-2392&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-2392&client=summon