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Select item 87127791.

Human myocardial mitochondrial oxidative capacity is impaired in mild acute heart transplant rejection

Daniel Scheiber, Elric Zweck, Sophie Albermann, Tomas Jelenik, Maximilian Spieker, Florian Bönner, Patrick Horn, Heinz‐Peter Schultheiss, Ganna Aleshcheva, Felicitas Escher, Udo Boeken, Payam Akhyari, Michael Roden, Malte Kelm, Julia Szendroedi, Ralf Westenfeld

ESC Heart Fail. 2021 Dec; 8(6): 4674–4684. Published online 2021 Sep 6. doi: 10.1002/ehf2.13607

PMCID:: PMC8712779

Article PDF–5.6M

Select item 78654922.

Cardiomyocytes Derived from Induced Pluripotent Stem Cells as a Disease Model for Propionic Acidemia

Esmeralda Alonso-Barroso, Belén Pérez, Lourdes Ruiz Desviat, Eva Richard

Int J Mol Sci. 2021 Feb; 22(3): 1161. Published online 2021 Jan 25. doi: 10.3390/ijms22031161

PMCID:: PMC7865492

Article PDF–2.6M

Select item 72482043.

PTX3 Predicts Myocardial Damage and Fibrosis in Duchenne Muscular Dystrophy

Andrea Farini, Chiara Villa, Dario Di Silvestre, Pamela Bella, Luana Tripodi, Rossana Rossi, Clementina Sitzia, Stefano Gatti, Pierluigi Mauri, Yvan Torrente

Front Physiol. 2020; 11: 403. Published online 2020 May 19. doi: 10.3389/fphys.2020.00403

PMCID:: PMC7248204

Article PDF–4.3M

Select item 53406624.

Combined therapy with melatonin and exendin-4 effectively attenuated the deterioration of renal function in rat cardiorenal syndrome

Kuan-Hung Chen, Chih-Hung Chen, Christopher Glenn Wallace, Yen-Ta Chen, Chih-Chao Yang, Pei-Hsun Sung, Hsin-Ju Chiang, Yi-Ling Chen, Sarah Chua, Hon-Kan Yip, Jiin-Tsuey Cheng

Am J Transl Res. 2017; 9(2): 214–229. Published online 2017 Feb 15.

PMCID:: PMC5340662

Article PDF–4.2M

Select item 38594085.

Insulin receptor substrate signaling suppresses neonatal autophagy in the heart

Christian Riehle, Adam R. Wende, Sandra Sena, Karla Maria Pires, Renata Oliveira Pereira, Yi Zhu, Heiko Bugger, Deborah Frank, Jack Bevins, Dong Chen, Cynthia N. Perry, Xiaocheng C. Dong, Steven Valdez, Monika Rech, Xiaoming Sheng, Bart C. Weimer, Roberta A. Gottlieb, Morris F. White, E. Dale Abel

J Clin Invest. 2013 Dec 2; 123(12): 5319–5333. Published online 2013 Nov 1. doi: 10.1172/JCI71171

PMCID:: PMC3859408

Article PDF–7.4M

Select item 27653236.

Emerging cardiovascular actions of the incretin hormone glucagon-like peptide-1: potential therapeutic benefits beyond glycaemic control?

David J Grieve, Roslyn S Cassidy, Brian D Green

Br J Pharmacol. 2009 Aug; 157(8): 1340–1351. doi: 10.1111/j.1476-5381.2009.00376.x

PMCID:: PMC2765323

Article PDF–438K

Select item 27638497.

Cardiac insulin-like growth factor-1 and cyclins gene expression in canine models of ischemic or overpacing cardiomyopathy

Maryam Mahmoudabady, Myrielle Mathieu, Karim Touihri, Ielham Hadad, Agnes Mendes Da Costa, Robert Naeije, Kathleen Mc Entee

BMC Cardiovasc Disord. 2009; 9: 49. Published online 2009 Oct 9. doi: 10.1186/1471-2261-9-49

PMCID:: PMC2763849

Article PDF–302K

Select item 106144048.

Genetic heterogeneity of cardiomyopathy and its correlation with patient care

Mi Jin Kim, Seulgi Cha, Jae Suk Baek, Jeong Jin Yu, Go Hun Seo, Minji Kang, Hyo-Sang Do, Sang Eun Lee, Beom Hee Lee

BMC Med Genomics. 2023; 16: 270. Published online 2023 Oct 30. doi: 10.1186/s12920-023-01639-z

PMCID:: PMC10614404

Article PDF–1.1M

Select item 103451609.

Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects

Jessica X. Chong, Matthew Carter Childers, Colby T. Marvin, Anthony J. Marcello, Hernan Gonorazky, Lili-Naz Hazrati, James J. Dowling, Fatema Al Amrani, Yasemin Alanay, Yolanda Nieto, Miguel Á Marín Gabriel, Arthur S. Aylsworth, Kati J. Buckingham, Kathryn M. Shively, Olivia Sommers, Kailyn Anderson, University of Washington Center for Mendelian Genomics, University of Washington Center for Rare Disease Research, Michael Regnier, Michael J. Bamshad

HGG Adv. 2023 Jul 13; 4(3): 100213. Published online 2023 Jun 15. doi: 10.1016/j.xhgg.2023.100213

PMCID:: PMC10345160

Article PDF–3.9M

Select item 1028414010.

Missense Mutation in Human CHD4 Causes Ventricular Noncompaction by Repressing ADAMTS1

Wei Shi, Angel P. Scialdone, James I. Emerson, Liu Mei, Lauren K. Wasson, Haley A. Davies, Christine E. Seidman, Jonathan G. Seidman, Jeanette G. Cook, Frank L. Conlon

Circ Res. 2023 Jun 23; 133(1): 48–67. Published online 2023 May 31. doi: 10.1161/CIRCRESAHA.122.322223

PMCID:: PMC10284140

Article PDF–26M

Select item 946238911.

Longitudinal Observational Study of Cardiac Outcome Risk Factor Prediction in Children, Adolescents, and Adults with Barth Syndrome

Shahryar Chowdhury, Lanier Jackson, Barry J. Byrne, Randall M. Bryant, W. Todd Cade, Tammy Lane Churchill, Julia Buchanan, Carolyn Taylor

Pediatr Cardiol. Author manuscript; available in PMC 2023 Aug 1.

Published in final edited form as: Pediatr Cardiol. 2022 Aug; 43(6): 1251–1263. Published online 2022 Mar 3. doi: 10.1007/s00246-022-02846-8

PMCID:: PMC9462389

Article PDF–1.3M

Select item 933214212.

Genetic Profile of Left Ventricular Noncompaction Cardiomyopathy in Children—A Single Reference Center Experience

Dorota Piekutowska-Abramczuk, Agata Paszkowska, Elżbieta Ciara, Kamila Frączak, Alicja Mirecka-Rola, Dorota Wicher, Agnieszka Pollak, Karolina Rutkowska, Jędrzej Sarnecki, Lidia Ziółkowska

Genes (Basel) 2022 Aug; 13(8): 1334. Published online 2022 Jul 26. doi: 10.3390/genes13081334

PMCID:: PMC9332142

Article PDF–1008K

Select item 898468313.

ErbB/integrin signaling interactions in regulation of myocardial cell-cell and cell-matrix interactions

Laura Pentassuglia, Douglas B. Sawyer

Biochim Biophys Acta. Author manuscript; available in PMC 2022 Apr 6.

Published in final edited form as: Biochim Biophys Acta. 2013 Apr; 1833(4): 909–916. Published online 2012 Dec 20. doi: 10.1016/j.bbamcr.2012.12.007

PMCID:: PMC8984683

Article PDF–668K

Select item 876283114.

Family screening in black patients with isolated left ventricular non-compaction: the Chris Hani Baragwanath experience

Anneen L Basson, Mohammed R Essop, Elena Libhaber, Ferande Peters

Cardiovasc J Afr. 2020 Jul-Aug; 31(4): 180–184. Published online 2020 Mar 11. doi: 10.5830/CVJA-2020-003

PMCID:: PMC8762831

Article PDF–81K

Select item 812372815.

Co‐occurrence of orofacial clefts and clubfoot phenotypes in a sub‐Saharan African cohort: Whole‐exome sequencing implicates multiple syndromes and genes

Lord J. J. Gowans, Noura Al Dhaheri, Mary Li, Tamara Busch, Solomon Obiri‐Yeboah, Alexander A. Oti, Daniel K. Sabbah, Fareed K. N. Arthur, Waheed O. Awotoye, Azeez A. Alade, Peter Twumasi, Pius Agbenorku, Gyikua Plange‐Rhule, Thirona Naicker, Peter Donkor, Jeffrey C. Murray, Nara L. M. Sobreira, Azeez Butali

Mol Genet Genomic Med. 2021 Apr; 9(4): e1655. Published online 2021 Mar 14. doi: 10.1002/mgg3.1655

PMCID:: PMC8123728

Article PDF–1.1M

Select item 810516516.

Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies

Francesco Mazzarotto, Megan H. Hawley, Matteo Beltrami, Leander Beekman, Antonio de Marvao, Kathryn A. McGurk, Ben Statton, Beatrice Boschi, Francesca Girolami, Angharad M. Roberts, Elisabeth M. Lodder, Mona Allouba, Soha Romeih, Yasmine Aguib, A. John Baksi, Antonis Pantazis, Sanjay K. Prasad, Elisabetta Cerbai, Magdi H. Yacoub, Declan P. O’Regan, Stuart A. Cook, James S. Ware, Birgit Funke, Iacopo Olivotto, Connie R. Bezzina, Paul J. R. Barton, Roddy Walsh

Genet Med. 2021; 23(5): 856–864. Published online 2021 Jan 26. doi: 10.1038/s41436-020-01049-x

PMCID:: PMC8105165

Article PDF–918K

Select item 750742917.

Expanding the phenotype of STRA6‐related disorder to include left ventricular non‐compaction

Hairui Sun, Shaomei Yu, Xiaoxue Zhou, Lu Han, Hongjia Zhang, Yihua He

Mol Genet Genomic Med. 2020 Sep; 8(9): e1377. Published online 2020 Jun 29. doi: 10.1002/mgg3.1377

PMCID:: PMC7507429

Article PDF–515K

Select item 719645318.

Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction

Sai Suma K. Samudrala, Lauren M. North, Karl D. Stamm, Michael G. Earing, Michele A. Frommelt, Richard Willes, Swarnendu Tripathi, Nikita R. Dsouza, Michael T. Zimmermann, Donna K. Mahnke, Huan Ling Liang, Michael Lund, Chien‐Wei Lin, Gabrielle C. Geddes, Michael E. Mitchell, Aoy Tomita‐Mitchell

Mol Genet Genomic Med. 2020 Apr; 8(4): e1152. Published online 2020 Jan 27. doi: 10.1002/mgg3.1152

PMCID:: PMC7196453

Article PDF–840K

Select item 711217319.

TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway

Nariaki Miyao, Yukiko Hata, Hironori Izumi, Ryo Nagaoka, Yuko Oku, Ichiro Takasaki, Taisuke Ishikawa, Shinya Takarada, Mako Okabe, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Tomoyuki Yoshida, Hideyuki Hasegawa, Naomasa Makita, Naoki Nishida, Hisashi Mori, Fukiko Ichida, Keiichi Hirono

PLoS One. 2020; 15(4): e0227393. Published online 2020 Apr 1. doi: 10.1371/journal.pone.0227393

PMCID:: PMC7112173

Article PDF–2.0M

Select item 677781120.

Semaphorin 3E/PlexinD1 signaling is required for cardiac ventricular compaction

Reddemma Sandireddy, Dasan Mary Cibi, Priyanka Gupta, Anamika Singh, Nicole Tee, Akiyoshi Uemura, Jonathan A. Epstein, Manvendra K. Singh

JCI Insight. 2019 Aug 22; 4(16): e125908. Published online 2019 Aug 22. doi: 10.1172/jci.insight.125908

PMCID:: PMC6777811

Article PDF–21M

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