Որոնման արդյունքները - Daniel Quiat
- Ցուցադրվում են 1 - 8 արդյունքները 8
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Genomic frontiers in congenital heart disease Sarah U. Morton, Daniel Quiat, Jonathan G. Seidman, Christine E. Seidman
Հրապարակվել է 2021Revisão -
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Concerted regulation of myofiber-specific gene expression and muscle performance by the transcriptional repressor Sox6 Daniel Quiat, Kevin A. Voelker, Jimin Pei, Nick V. Grishin, Robert W. Grange, Rhonda Bassel‐Duby, Eric N. Olson
Հրապարակվել է 2011Artigo -
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A Family of microRNAs Encoded by Myosin Genes Governs Myosin Expression and Muscle Performance Eva van Rooij, Daniel Quiat, Brett A. Johnson, Lillian B. Sutherland, Xiaoxia Qi, James A. Richardson, Robert J. Kelm, Eric N. Olson
Հրապարակվել է 2009Artigo -
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Population Prevalence of Premature Truncating Variants in Plakophilin-2 and Association With Arrhythmogenic Right Ventricular Cardiomyopathy: A UK Biobank Analysis Robyn J. Hylind, Alexandre C. Pereira, Daniel Quiat, Stephanie F. Chandler, Thomas M. Roston, William T. Pu, Vassilios J. Bezzerides, Jonathan G. Seidman, Christine E. Seidman, Dominic J. Abrams
Հրապարակվել է 2022Artigo -
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Discordant clinical features of identical hypertrophic cardiomyopathy twins Giuliana G. Repetti, Yuri Kim, Alexandre C. Pereira, Jodie Ingles, Mark W. Russell, Neal K. Lakdawala, Carolyn Y. Ho, Sharlene M. Day, Christopher Semsarian, Barbara McDonough, Steven R. DePalma, Daniel Quiat, Eric M. Green, Christine E. Seidman, Jonathan G. Seidman
Հրապարակվել է 2021Artigo -
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An ancient founder mutation located between<i>ROBO1</i>and<i>ROBO2</i>is responsible for increased microtia risk in Amerindigenous populations Daniel Quiat, Seong Won Kim, Qi Zhang, Sarah U. Morton, Alexandre C. Pereira, Steven R. DePalma, Jon A. L. Willcox, Barbara McDonough, Daniel M. DeLaughter, Joshua M. Gorham, Justin J. Curran, Melissa Tumblin, Yamileth Nicolau, Maria A. Artunduaga, Lourdes Quintanilla‐Dieck, Gabriel Osorno, Luís Serrano, Usama S. Hamdan, Roland D. Eavey, Christine E. Seidman, Jonathan G. Seidman
Հրապարակվել է 2022Artigo -
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Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease Sarah U. Morton, Akiko Shimamura, Peter E. Newburger, Alexander R. Opotowsky, Daniel Quiat, Alexandre C. Pereira, Sheng Chih Jin, Michelle Gurvitz, Martina Brueckner, Wendy K. Chung, Yufeng Shen, Daniel Bernstein, Bruce D. Gelb, Anna Giardini, Elizabeth Goldmuntz, Richard W. Kim, Richard P. Lifton, George A. Porter, Deepak Srivastava, Martin Tristani‐Firouzi, Jane W. Newburger, Jonathan G. Seidman, Christine E. Seidman
Հրապարակվել է 2020Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Medicine
Cell biology
Disease
Gene expression
Internal medicine
Allele
Anatomy
Bioinformatics
Cardiomyopathy
Environmental health
Genotype
Heart failure
Mutation
Myocyte
Pathology
Phenotype
Population
Single-nucleotide polymorphism
microRNA
Allele frequency
Arrhythmogenic right ventricular dysplasia
Atrial fibrillation
Biobank
Biochemistry
Cancer
Cardiology
Case-control study