Zobrazeno 1 - 4
of 4
pro vyhledávání: '"JASMINE REID"'
Autor:
Yuki Matsumura, Katie M. Stiles, Jasmine Reid, Esther Z. Frenk, Samantha Cronin, Odelya E. Pagovich, Ronald G. Crystal
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss , Pp 72-82 (2019)
Aldehyde dehydrogenase 2 (ALDH2) deficiency causes “Asian flush syndrome,” presenting as alcohol-induced facial flushing, tachycardia, nausea, and headaches. One of the most common hereditary enzyme deficiencies, it affects 35%–40% of East Asia
Externí odkaz:
https://doaj.org/article/5da7c1a7b8d048de9d3148f3829970aa
Autor:
JASMINE REID
Publikováno v:
Heritage and Democracy ISBN: 9780813070360
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::097e5607940902f487af5764f7bdeafd
https://doi.org/10.2307/jj.2299524.14
https://doi.org/10.2307/jj.2299524.14
Autor:
Odelya E. Pagovich, Katie M. Stiles, Jasmine Reid, Yuki Matsumura, Esther Z Frenk, Samantha Cronin, Ronald G. Crystal
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 72-82 (2019)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
Aldehyde dehydrogenase 2 (ALDH2) deficiency causes “Asian flush syndrome,” presenting as alcohol-induced facial flushing, tachycardia, nausea, and headaches. One of the most common hereditary enzyme deficiencies, it affects 35%–40% of East Asia
Autor:
Philip L. Leopold, Odelya E. Pagovich, Ronald G. Crystal, Jasmine Reid, Clarisse Jose, Sandra Markmann, Bishnu P. De, Dolan Sondhi, Jonathan B. Rosenberg, Stephen M. Kaminsky
Publikováno v:
Human gene therapy. 29(4)
Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder occurring in 1:10,000 to 1:20,000 live births. In >95% of the cases, CAH results from mutations in the CYP21A2 gene, encoding the adrenal steroid enzyme 21-hydroxylase (21OH). Ca