Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ondine, Atwa"'
Autor:
Bridget Simonson, Mark Chaffin, Matthew C. Hill, Ondine Atwa, Yasmine Guedira, Harshit Bhasin, Amelia W. Hall, Sikander Hayat, Simon Baumgart, Kenneth C. Bedi, Jr., Kenneth B. Margulies, Carla A. Klattenhoff, Patrick T. Ellinor
Publikováno v:
Cell Reports, Vol 42, Iss 2, Pp 112086- (2023)
Summary: Ischemic cardiomyopathy (ICM) is the leading cause of heart failure worldwide, yet the cellular and molecular signature of this disease is largely unclear. Using single-nucleus RNA sequencing (snRNA-seq) and integrated computational analyses
Externí odkaz:
https://doaj.org/article/20970c7a3b5845f094b6b93928416d12
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248532 (2021)
The human FBN1 gene encodes fibrillin-1 (FBN1); the main component of the 10-12 nm diameter extracellular matrix microfibrils. Marfan syndrome (MFS) is a common inherited connective tissue disorder, caused by FBN1 mutations. It features a wide spectr
Externí odkaz:
https://doaj.org/article/381176441eb0470fa733d77b84567ed6
Autor:
Mark Chaffin, Irinna Papangeli, Bridget Simonson, Amer-Denis Akkad, Matthew C. Hill, Alessandro Arduini, Stephen J. Fleming, Michelle Melanson, Sikander Hayat, Maria Kost-Alimova, Ondine Atwa, Jiangchuan Ye, Kenneth C. Bedi, Matthias Nahrendorf, Virendar K. Kaushik, Christian M. Stegmann, Kenneth B. Margulies, Nathan R. Tucker, Patrick T. Ellinor
Publikováno v:
Nature. 608:174-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3953303da37730099f0ab2b5ff9e6a36
https://doi.org/10.1038/s41586-022-04817-8
https://doi.org/10.1038/s41586-022-04817-8
Autor:
Mark, Chaffin, Irinna, Papangeli, Bridget, Simonson, Amer-Denis, Akkad, Matthew C, Hill, Alessandro, Arduini, Stephen J, Fleming, Michelle, Melanson, Sikander, Hayat, Maria, Kost-Alimova, Ondine, Atwa, Jiangchuan, Ye, Kenneth C, Bedi, Matthias, Nahrendorf, Virendar K, Kaushik, Christian M, Stegmann, Kenneth B, Margulies, Nathan R, Tucker, Patrick T, Ellinor
Publikováno v:
Nature. 608(7921)
Heart failure encompasses a heterogeneous set of clinical features that converge on impaired cardiac contractile function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f97f4a16987cefc7247f8f3be3b4547b
https://pubmed.ncbi.nlm.nih.gov/35732739
https://pubmed.ncbi.nlm.nih.gov/35732739
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248532 (2021)
PLoS ONE
PLoS ONE
The human FBN1 gene encodes fibrillin-1 (FBN1); the main component of the 10–12 nm diameter extracellular matrix microfibrils. Marfan syndrome (MFS) is a common inherited connective tissue disorder, caused by FBN1 mutations. It features a wide spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02de311453de7ae69786035eecf2963f
https://doaj.org/article/381176441eb0470fa733d77b84567ed6
https://doaj.org/article/381176441eb0470fa733d77b84567ed6