Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aravindakshan Jagadeesan"'
Autor:
Shiv Kumar Viswanathan, Heather K Sanders, James W McNamara, Aravindakshan Jagadeesan, Arshad Jahangir, A Jamil Tajik, Sakthivel Sadayappan
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187948 (2017)
Over 1,500 gene mutations are known to cause hypertrophic cardiomyopathy (HCM). Previous studies suggest that cardiac β-myosin heavy chain (MYH7) gene mutations are commonly associated with a more severe phenotype, compared to cardiac myosin binding
Externí odkaz:
https://doaj.org/article/9a72e977d7ca4aa7967fdee2db754771
Autor:
Sakthivel Sadayappan, Elizabeth M. McNally, Philip Wong, Michael J. Zilliox, Thriveni Sanagala, Ashish Mehta, Regina Fritsche-Danielson, Megan J. Puckelwartz, Winston Shim, U. Nalla B. Durai, Hak Chiaw Tang, Rama Shanker Verma, Gina Kuffel, Domodhar P. Suresh, Philip R. Khoury, Shiv Kumar Viswanathan, Ratan Bhat, Sangeetha Kandoi, Ralph Knöll, Richard C. Becker, Aravindakshan Jagadeesan, Chrishan J A Ramachandra, Robert E. Molokie, Jennifer A. Schwanekamp, Annie Thomas, Lorenzo L. Pesce
Publikováno v:
JAMA cardiology. 3(6)
IMPORTANCE: The genetic variant MYBPC3(Δ25bp) occurs in 4% of South Asian descendants, with an estimated 100 million carriers worldwide. MYBPC3 (Δ25bp) has been linked to cardiomyopathy and heart failure. However, the high prevalence of MYBPC3(Δ25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5c5ed4469f149d04266afb99d8bf7ba
https://pubmed.ncbi.nlm.nih.gov/29641836
https://pubmed.ncbi.nlm.nih.gov/29641836
Autor:
Aravindakshan Jagadeesan, Shiv Kumar Viswanathan, Arshad Jahangir, James W. McNamara, Sakthivel Sadayappan, A. Jamil Tajik, Heather Sanders
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187948 (2017)
PLoS ONE
PLoS ONE
Over 1,500 gene mutations are known to cause hypertrophic cardiomyopathy (HCM). Previous studies suggest that cardiac β-myosin heavy chain (MYH7) gene mutations are commonly associated with a more severe phenotype, compared to cardiac myosin binding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bc5692349a8cfe0e0105df2aa734359
http://europepmc.org/articles/PMC5679632?pdf=render
http://europepmc.org/articles/PMC5679632?pdf=render
Autor:
David Y, Barefield, Thomas L, Lynch, Aravindakshan, Jagadeesan, Thriveni, Sanagala, Sakthivel, Sadayappan
Publikováno v:
Journal of molecular biomarkers & diagnosis
A 25-basepair deletion variant of MYBPC3 occurs at high frequency in individuals of South Asian descent and is estimated to affect 55 million people worldwide, carrying an increased likelihood of cardiomyopathy. Since this variant is prevalent and se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::529ede96c61841f88d70848e20fe990c
https://pubmed.ncbi.nlm.nih.gov/27990320
https://pubmed.ncbi.nlm.nih.gov/27990320
Autor:
Thriveni Sanagala, Aravindakshan Jagadeesan, Thomas L. Lynch, Sakthivel Sadayappan, David Y. Barefield
Publikováno v:
Journal of Molecular Biomarkers & Diagnosis.
A 25-basepair deletion variant of MYBPC3 occurs at high frequency in individuals of South Asian descent and is estimated to affect 55 million people worldwide, carrying an increased likelihood of cardiomyopathy. Since this variant is prevalent and se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::555184ece4d4483f78ec171877bc87f0
https://doi.org/10.4172/2155-9929.1000303
https://doi.org/10.4172/2155-9929.1000303
Autor:
Sakthivel Sadayappan, David Y. Barefield, Diederik W. D. Kuster, Aravindakshan Jagadeesan, Suresh Govindan
Publikováno v:
The FASEB Journal. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::879450d95b13c3ce1b82aeba345a6bb6
https://doi.org/10.1096/fasebj.28.1_supplement.1073.8
https://doi.org/10.1096/fasebj.28.1_supplement.1073.8