Resultats de la cerca - Sumantra Chatterjee
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Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms per Ashish Kapoor, Qian Jiang, Sumantra Chatterjee, Prakash Chakraborty, Maria X. Sosa, Courtney Berrios, Aravinda Chakravarti
Publicat 2015Artigo -
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<i>Ret</i> deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development per Elizabeth Vincent, Sumantra Chatterjee, Gabrielle H. Cannon, Dallas R. Auer, Holly Ross, Aravinda Chakravarti, Loyal A. Goff
Publicat 2023Artigo -
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Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease per Sumantra Chatterjee, Ashish Kapoor, Jennifer A. Akiyama, Dallas R. Auer, Dongwon Lee, Stacey Gabriel, Courtney Berrios, L Pennacchio, Aravinda Chakravarti
Publicat 2016Artigo -
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Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease per Joseph M. Tilghman, Albee Y. Ling, Tychele N. Turner, Maria X. Sosa, Niklas Krumm, Sumantra Chatterjee, Ashish Kapoor, Bradley P. Coe, Khanh-Dung H. Nguyen, Namrata Gupta, Stacey Gabriel, Evan E. Eichler, Courtney Berrios, Aravinda Chakravarti
Publicat 2019Artigo -
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An Enhancer Polymorphism at the Cardiomyocyte Intercalated Disc Protein NOS1AP Locus Is a Major Regulator of the QT Interval per Ashish Kapoor, Rajesh B. Sekar, Nancy F. Hansen, Karen Fox-Talbot, Michael P. Morley, Vasyl Pihur, Sumantra Chatterjee, Jeffrey Brandimarto, Christine S. Moravec, Sara L. Pulit, Arne Pfeufer, Jim Mullikin, Mark T. Ross, Eric D. Green, David Bentley, Christopher Newton‐Cheh, Eric Boerwinkle, Gordon F. Tomaselli, Thomas P. Cappola, Dan E. Arking, Marc K. Halushka, Aravinda Chakravarti
Publicat 2014Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Medicine
Transcription factor
Disease
Gene expression
Internal medicine
Neuroscience
Population
Anatomy
Cell biology
Enhancer
Environmental health
Genetic variation
Regulation of gene expression
Regulatory sequence
Allele
Aphidicolin
CRISPR
Cell fate determination
Computational biology
DLX5
DNA
DNA damage
DNA replication
Demography
Electrophysiology
Embryo
Embryonic stem cell