Association between inhaled nitric oxide treatment and long-term pulmonary function in survivors of acute respiratory distress syndrome
Dellinger, R Phillip, Trzeciak, Stephen W, Criner, Gerard J, Zimmerman, Janice L, Taylor, Robert W, Usansky, Helen, Young, Joseph, Goldstein, Brahm
Published in Critical care (London, England) (02.03.2012)
Published in Critical care (London, England) (02.03.2012)
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Journal Article
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular muscles
Yu-Wai-Man, Patrick, Lai-Cheong, Joey, Borthwick, Gillian M, He, Langping, Taylor, Geoffrey A, Greaves, Laura C, Taylor, Robert W, Griffiths, Philip G, Turnbull, Douglass M
Published in Investigative ophthalmology & visual science (01.07.2010)
Published in Investigative ophthalmology & visual science (01.07.2010)
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Journal Article
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO
Greaves, Laura C, Yu-Wai-Man, Patrick, Blakely, Emma L, Krishnan, Kim J, Beadle, Nina E, Kerin, Jamie, Barron, Martin J, Griffiths, Philip G, Dickinson, Alison J, Turnbull, Douglass M, Taylor, Robert W
Published in Investigative ophthalmology & visual science (01.07.2010)
Published in Investigative ophthalmology & visual science (01.07.2010)
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Journal Article
SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey
Kose, Melis, Canda, Ebru, Kagnici, Mehtap, Aykut, Ayça, Adebali, Ogün, Durmaz, Asude, Bircan, Aylin, Diniz, Gulden, Eraslan, Cenk, Kose, Engin, Ünalp, Aycan, Yılmaz, Ünsal, Ozyilmaz, Berk, Özdemir, Taha Reşid, Atik, Tahir, Uçar, Sema Kalkan, McFarland, Robert, Taylor, Robert W., Brown, Garry K., Çoker, Mahmut, Özkınay, Ferda
Published in Molecular genetics and metabolism reports (01.12.2020)
Published in Molecular genetics and metabolism reports (01.12.2020)
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Journal Article
The molecular pathology of pathogenic mitochondrial tRNA variants
Richter, Uwe, McFarland, Robert, Taylor, Robert W., Pickett, Sarah J.
Published in FEBS letters (01.04.2021)
Published in FEBS letters (01.04.2021)
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Journal Article
Over-expression of catalase in myeloid cells confers acute protection following myocardial infarction
Cabigas, E Bernadette, Somasuntharam, Inthirai, Brown, Milton E, Che, Pao Lin, Pendergrass, Karl D, Chiang, Bryce, Taylor, W Robert, Davis, Michael E
Published in International journal of molecular sciences (21.05.2014)
Published in International journal of molecular sciences (21.05.2014)
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Journal Article
Cardiomyopathies due to homoplasmic mitochondrial tRNA mutations: morphologic and molecular features
Giordano, Carla, MD, PhD, Perli, Elena, PhD, Orlandi, Maurizia, BSc, Pisano, Annalinda, BSc, Tuppen, Helen A., PhD, He, Langping, PhD, Ierinò, Rocco, BSc, Petruzziello, Luciano, BSc, Terzi, Amedeo, MD, Autore, Camillo, MD, Petrozza, Vincenzo, MD, Gallo, Pietro, MD, Taylor, Robert W., PhD, d'Amati, Giulia, MD, PhD
Published in Human pathology (01.07.2013)
Published in Human pathology (01.07.2013)
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Journal Article
Biomechanical modeling and morphology analysis indicates plaque rupture due to mechanical failure unlikely in atherosclerosis-prone mice
Campbell, Ian C, Weiss, Daiana, Suever, Jonathan D, Virmani, Renu, Veneziani, Alessandro, Vito, Raymond P, Oshinski, John N, Taylor, W Robert
Published in American journal of physiology. Heart and circulatory physiology (01.02.2013)
Published in American journal of physiology. Heart and circulatory physiology (01.02.2013)
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Journal Article
A Methodological Approach to Tracing Cell Lineage in Human Epithelial Tissues
Fellous, Tariq G., McDonald, Stuart A.C., Burkert, Julia, Humphries, Adam, Islam, Shahriar, De‐Alwis, Nemantha M.W., Gutierrez‐Gonzalez, Lydia, Tadrous, Paul J., Elia, George, Kocher, Hemant M., Bhattacharya, Satyajit, Mears, Lisa, El‐Bahrawy, Mona, Turnbull, Douglas M., Taylor, Robert W., Greaves, Laura C., Chinnery, Patrick F., Day, Christopher P., Wright, Nicholas A., Alison, Malcolm R.
Published in Stem cells (Dayton, Ohio) (01.06.2009)
Published in Stem cells (Dayton, Ohio) (01.06.2009)
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Journal Article
Developmental and pathological changes in the human cardiac muscle mitochondrial DNA organization, replication and copy number
Pohjoismäki, Jaakko L O, Goffart, Steffi, Taylor, Robert W, Turnbull, Douglas M, Suomalainen, Anu, Jacobs, Howard T, Karhunen, Pekka J
Published in PloS one (03.05.2010)
Published in PloS one (03.05.2010)
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Journal Article
A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families
Aldosary, Mazhor, Alsagob, Maysoon, AlQudairy, Hanan, González-Álvarez, Ana C, Arold, Stefan T, Dababo, Mohammad Anas, Alharbi, Omar A, Almass, Rawan, AlBakheet, AlBandary, AlSarar, Dalia, Qari, Alya, Al-Ansari, Mysoon M, Oláhová, Monika, Al-Shahrani, Saif A, AlSayed, Moeenaldeen, Colak, Dilek, Taylor, Robert W, AlOwain, Mohammed, Kaya, Namik
Published in Cells (Basel, Switzerland) (07.10.2022)
Published in Cells (Basel, Switzerland) (07.10.2022)
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Journal Article
SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion
Aldosary, Mazhor, Baselm, Shahad, Abdulrahim, Maha, Almass, Rawan, Alsagob, Maysoon, AlMasseri, Zainab, Huma, Rozeena, AlQuait, Laila, Al‐Shidi, Tarfa, Al‐Obeid, Eman, AlBakheet, Albandary, Alahideb, Basma, Alahaidib, Lujane, Qari, Alya, Taylor, Robert W., Colak, Dilek, AlSayed, Moeenaldeen D., Kaya, Namik
Published in JIMD reports (01.07.2021)
Published in JIMD reports (01.07.2021)
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Journal Article
Fibronectin and Cyclic Strain Improve Cardiac Progenitor Cell Regenerative Potential In Vitro
Davis, Michael E., Taylor, W. Robert, Johnson, Todd D., Fierro, Marcos J., Ghosh-Choudhary, Shohini, Bhutani, Srishti, Maxwell, Joshua T., French, Kristin M., Christman, Karen L.
Published in Stem cells international (01.01.2016)
Published in Stem cells international (01.01.2016)
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Journal Article
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number
Thompson, Kyle, Majd, Homa, Dallabona, Cristina, Reinson, Karit, King, Martin S., Alston, Charlotte L., He, Langping, Lodi, Tiziana, Jones, Simon A., Fattal-Valevski, Aviva, Fraenkel, Nitay D., Saada, Ann, Haham, Alon, Isohanni, Pirjo, Vara, Roshni, Barbosa, Inês A., Simpson, Michael A., Deshpande, Charu, Puusepp, Sanna, Bonnen, Penelope E., Rodenburg, Richard J., Suomalainen, Anu, Õunap, Katrin, Elpeleg, Orly, Ferrero, Ileana, McFarland, Robert, Kunji, Edmund R.S., Taylor, Robert W.
Published in American journal of human genetics (01.12.2016)
Published in American journal of human genetics (01.12.2016)
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Journal Article
Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease
Thompson, Kyle, Bianchi, Lucas, Rastelli, Francesca, Piron-Prunier, Florence, Ayciriex, Sophie, Besmond, Claude, Hubert, Laurence, Barth, Magalie, Barbosa, Inês A., Deshpande, Charu, Chitre, Manali, Mehta, Sarju G., Wever, Eric J.M., Marcorelles, Pascale, Donkervoort, Sandra, Saade, Dimah, Bönnemann, Carsten G., Chao, Katherine R., Cai, Chunyu, Iannaccone, Susan T., Dean, Andrew F., McFarland, Robert, Vaz, Frédéric M., Delahodde, Agnès, Taylor, Robert W., Rötig, Agnès
Published in HGG advances (14.04.2022)
Published in HGG advances (14.04.2022)
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Journal Article