Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Thomas J. Balmat"'
Autor:
Liuyang Wang, Thomas J. Balmat, Alejandro L. Antonia, Florica J. Constantine, Ricardo Henao, Thomas W. Burke, Andy Ingham, Micah T. McClain, Ephraim L. Tsalik, Emily R. Ko, Geoffrey S. Ginsburg, Mark R. DeLong, Xiling Shen, Christopher W. Woods, Elizabeth R. Hauser, Dennis C. Ko
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-19 (2021)
Abstract Background While genome-wide associations studies (GWAS) have successfully elucidated the genetic architecture of complex human traits and diseases, understanding mechanisms that lead from genetic variation to pathophysiology remains an impo
Externí odkaz:
https://doaj.org/article/39fc59f51cab48dda86b587f7fe9ca79
Autor:
Shaul, Lerner, Raya, Eilam, Lital, Adler, Julien, Baruteau, Topaz, Kreiser, Michael, Tsoory, Alexander, Brandis, Tevie, Mehlman, Mina, Ryten, Juan A, Botia, Sonia Garcia, Ruiz, Alejandro Cisterna, Garcia, Carlo, Dionisi-Vici, Giusy, Ranucci, Marco, Spada, Ram, Mazkereth, Robert, McCarter, Rima, Izem, Thomas J, Balmat, Rachel, Richesson, Ehud, Gazit, Sandesh C S, Nagamani, Marc, Yudkoff
Publikováno v:
Human Genetics
Argininosuccinate lyase (ASL) is essential for the NO-dependent regulation of tyrosine hydroxylase (TH) and thus for catecholamine production. Using a conditional mouse model with loss of ASL in catecholamine neurons, we demonstrate that ASL is expre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b55b04fcb401eba776e6c8db6bbac0e0
https://pubmed.ncbi.nlm.nih.gov/34417872
https://pubmed.ncbi.nlm.nih.gov/34417872
Autor:
Ephraim L. Tsalik, Alejandro L. Antonia, Liuyang Wang, Micah T. McClain, Elizabeth R. Hauser, Thomas J Balmat, Mark R. DeLong, Thomas W. Burke, Xiling Shen, Andy Ingham, Emily R Ko, Dennis C. Ko, Christopher W. Woods, Florica J Constantine, Geoffrey S. Ginsburg, Ricardo Henao
Publikováno v:
medRxiv
article-version (status) pre
article-version (number) 1
Genome Medicine
Genome Medicine, Vol 13, Iss 1, Pp 1-19 (2021)
article-version (status) pre
article-version (number) 1
Genome Medicine
Genome Medicine, Vol 13, Iss 1, Pp 1-19 (2021)
Background While genome-wide associations studies (GWAS) have successfully elucidated the genetic architecture of complex human traits and diseases, understanding mechanisms that lead from genetic variation to pathophysiology remains an important cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::746fc7b1a6c15759a266e26aadcaf580
https://doi.org/10.1101/2020.12.20.20248572
https://doi.org/10.1101/2020.12.20.20248572
