Výsledky vyhledávání - Santhi K. Ganesh
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SARS-CoV-2 Spike Protein S1-Mediated Endothelial Injury and Pro-Inflammatory State Is Amplified by Dihydrotestosterone and Prevented by Mineralocorticoid Antagonism Autor Nitin Kumar, Yu Zuo, Srilakshmi Yalavarthi, Kristina L. Hunker, Jason S. Knight, Yogendra Kanthi, T. Andrea, Santhi K. Ganesh
Vydáno 2021Artigo -
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Differences in Demographics and Outcomes Between Men and Women With Spontaneous Coronary Artery Dissection Autor Cameron McAlister, Mesfer Alfadhel, Rohit Samuel, Andrew Starovoytov, Johandra Argote Parolis, Tejana Grewal, Eve Aymong, Tara Sedlak, Santhi K. Ganesh, Jacqueline Saw
Vydáno 2022Artigo -
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The in vivo endothelial cell translatome is highly heterogeneous across vascular beds Autor Audrey Cleuren, Martijn A. van der Ent, Hui Jiang, Kristina L. Hunker, Andrew Yee, David Siemieniak, Grietje Molema, William C. Aird, Santhi K. Ganesh, David Ginsburg
Vydáno 2019Artigo -
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Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes Autor Xiaoling Zhang, Andrew D. Johnson, Audrey E. Hendricks, Shih-Jen Hwang, Kahraman Tanrıverdi, Santhi K. Ganesh, Nicholas L. Smith, Patricia A. Peyser, Jane E. Freedman, Christopher J. O’Donnell
Vydáno 2013Artigo -
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Relevance of Genetics and Genomics for Prevention and Treatment of Cardiovascular Disease Autor Donna K. Arnett, Alison E. Baird, Ruth Ann Barkley, Craig T. Basson, Eric Boerwinkle, Santhi K. Ganesh, David M. Herrington, Yuling Hong, Cashell E. Jaquish, Deborah A. McDermott, Christopher J. O’Donnell
Vydáno 2007Artigo -
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Spontaneous Coronary Artery Dissection: Current State of the Science: A Scientific Statement From the American Heart Association Autor Sharonne N. Hayes, Esther Kim, Jacqueline Saw, David Adlam, Cynthia Arslanian‐Engoren, Katherine E. Economy, Santhi K. Ganesh, Rajiv Gulati, Mark E. Lindsay, Jennifer H. Mieres, Sahar Naderi, Svati Shah, David E. Thaler, Marysia S. Tweet, Malissa J. Wood
Vydáno 2018Revisão -
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A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model Autor Brian C. Capell, Michelle Olive, Michael R. Erdos, Kan Cao, Dina A. Faddah, Urraca Tavarez, Karen N. Conneely, Xuan Qu, Hong San, Santhi K. Ganesh, Xiaohong Chen, Hedwig Avallone, Frank D. Kolodgie, Renu Virmani, Elizabeth G. Nabel, Francis S. Collins
Vydáno 2008Artigo -
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Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF‐β expression and connective tissue features Autor Santhi K. Ganesh, Rachel Morissette, Xu Zhi, Florian Schoenhoff, Benjamin F. Griswold, Jiandong Yang, Lan Tong, Min‐Lee Yang, Kristina L. Hunker, Leslie Sloper, Shinie Kuo, Rafi Raza, Dianna M. Milewicz, Clair A. Francomano, Harry C. Dietz, Jennifer E. Van Eyk, Nazli B. McDonnell
Vydáno 2014Artigo -
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Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans Autor Ken Sin Lo, James G. Wilson, Leslie A. Lange, Aaron R. Folsom, Geneviève Galarneau, Santhi K. Ganesh, Struan F.A. Grant, Brendan J. Keating, Steven A. McCarroll, Emile R. Mohler, Christopher J. O’Donnell, Walter Palmas, Weihong Tang, Russell P. Tracy, Alexander P. Reiner, Guillaume Lettre
Vydáno 2010Artigo -
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Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson–Gilford progeria syndrome Autor Renée Varga, Maria Eriksson, Michael R. Erdos, Michelle Olive, Ingrid A. Harten, Frank D. Kolodgie, Brian C. Capell, Jun Cheng, Dina A. Faddah, Stacie Perkins, Hedwig Avallone, Hong San, Xuan Qu, Santhi K. Ganesh, Leslie B. Gordon, Renu Virmani, Thomas N. Wight, Elizabeth G. Nabel, Francis S. Collins
Vydáno 2006Artigo -
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Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease Autor Dongchuan Guo, Xue-Yan Duan, Ellen S. Regalado, Lauren Mellor-Crummey, Callie Kwartler, Dong Kim, Kenneth V. Lieberman, Bert B.A. de Vries, Rolph Pfundt, Albert Schinzel, Dieter Kotzot, Xuetong Shen, Min-Lee Yang, Michael J. Bamshad, Deborah A. Nickerson, Heather L. Gornik, Santhi K. Ganesh, Alan C. Braverman, Dorothy K. Grange, Dianna M. Milewicz
Vydáno 2016Artigo -
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IFN-γ and TNF-α synergism may provide a link between psoriasis and inflammatory atherogenesis Autor Nehal N. Mehta, Heather Teague, William R. Swindell, Yvonne Baumer, Nicole L. Ward, Xianying Xing, Brooke Baugous, Andrew Johnston, Aditya A. Joshi, Joanna I Silverman, Drew H. Barnes, Liza Wolterink, Rajan P. Nair, Philip E. Stuart, Martin P. Playford, John J. Voorhees, Mrinal K. Sarkar, James T. Elder, Katherine Gallagher, Santhi K. Ganesh, Jóhann E. Guðjónsson
Vydáno 2017Artigo -
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Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project Autor Paul L. Auer, Jill M. Johnsen, Andrew D. Johnson, Benjamin A. Logsdon, Leslie A. Lange, Michael A. Nalls, Guosheng Zhang, Nora Franceschini, Keolu Fox, Ethan M. Lange, Stephen S. Rich, Christopher J. O’Donnell, Rebecca D. Jackson, Robert B. Wallace, Zhao Chen, Timothy A. Graubert, James Wilson, Hua Tang, Guillaume Lettre, Alex P. Reiner, Santhi K. Ganesh, Yun Li
Vydáno 2012Artigo -
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Canadian spontaneous coronary artery dissection cohort study: in-hospital and 30-day outcomes Autor Jacqueline Saw, Andrew Starovoytov, Karin H. Humphries, Tej Sheth, Derek So, Kunal Minhas, Neil Brass, Andrea Lavoie, Helen Bishop, Shahar Lavi, Colin Pearce, Suzanne Renner, Mina Madan, Robert C. Welsh, Sohrab Lutchmedial, Ram Vijayaraghavan, Eve Aymong, Bryan Har, Réda Ibrahim, Heather L. Gornik, Santhi K. Ganesh, Christopher E. Buller, Alexis Matteau, Giuseppe Martucci, Dennis T. Ko, G.B. John Mancini
Vydáno 2019Artigo -
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Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk Autor Oddgeir L. Holmen, He Zhang, Yanbo Fan, Daniel H. Hovelson, Ellen M. Schmidt, Wei Zhou, Yanhong Guo, Ji Zhang, Arnulf Langhammer, Maja‐Lisa Løchen, Santhi K. Ganesh, Lars J. Vatten, Frank Skorpen, Håvard Dalen, Jifeng Zhang, Subramaniam Pennathur, Jin Chen, Carl G. P. Platou, Ellisiv B. Mathiesen, Tom Wilsgaard, Inger Njølstad, Michael Boehnke, Yongzhen Chen, Gonçalo R. Abecasis, Kristian Hveem, Cristen J. Willer
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Internal medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Endocrinology
Genetic association
Phenotype
Quantitative trait locus
Bioinformatics
Cardiology
Computational biology
Exome sequencing
Locus (genetics)
Blood pressure
Disease
Kidney
Exome
Fibromuscular dysplasia
Myocardial infarction
Renal artery
Coronary artery disease
Pathology
Surgery
Candidate gene
Immunology
Mutation