Zobrazeno 1 - 10
of 342
pro vyhledávání: '"Fah"'
Publikováno v:
Publishers Weekly. 12/4/2023, Vol. 270 Issue 50, p97-97. 1/5p.
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-7 (2022)
Abstract Background Hereditary tyrosinemia type 1 (HT1; OMIM# 276700) is a genetic metabolism disorder caused by disease-causing variants in the fumarylacetoacetate hydrolase (FAH) gene encoding the last enzyme of the tyrosine catabolic pathway. Here
Externí odkaz:
https://doaj.org/article/5a3546440f25472799b978ce5550f8f6
Akademický článek
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Autor:
Mars-Jones, Adam
Publikováno v:
London Review of Books. 1/4/2024, Vol. 46 Issue 1, p23-25. 3p.
Autor:
Moran, Alexander
Publikováno v:
Booklist. 1/1/2024-1/15/2024, Vol. 120 Issue 9/10, p23-23. 1/7p.
Publikováno v:
Kirkus Reviews. 11/1/2023, Vol. 91 Issue 21, pN.PAG-N.PAG. 1p.
Autor:
Anna Georgina Kopasz, Dávid Zsolt Pusztai, Réka Karkas, Liza Hudoba, Khaldoon Sadiq Ahmed Abdullah, Gergely Imre, Gabriella Pankotai-Bodó, Ede Migh, Andrea Nagy, András Kriston, Péter Germán, Andrea Bakné Drubi, Anna Molnár, Ildikó Fekete, Virág Éva Dani, Imre Ocsovszki, László Géza Puskás, Péter Horváth, Farkas Sükösd, Lajos Mátés
Publikováno v:
BMC Biology, Vol 20, Iss 1, Pp 1-16 (2022)
Abstract Background Understanding the contribution of gene function in distinct organ systems to the pathogenesis of human diseases in biomedical research requires modifying gene expression through the generation of gain- and loss-of-function phenoty
Externí odkaz:
https://doaj.org/article/35efc12f86b64a41872e0eaea3368b04
Autor:
Chenhui Zou, Imane El Dika, Koen O. A. Vercauteren, Marinela Capanu, Joanne Chou, Jinru Shia, Jill Pilet, Corrine Quirk, Gadi Lalazar, Linda Andrus, Mohammad Kabbani, Amin Yaqubie, Danny Khalil, Taha Mergoub, Luis Chiriboga, Charles M. Rice, Ghassan K. Abou‐Alfa, Ype P. de Jong
Publikováno v:
Cancer Medicine, Vol 11, Iss 3, Pp 602-617 (2022)
Abstract Background Hepatocellular carcinoma (HCC) patient‐derived xenograft (PDX) models hold potential to advance knowledge in HCC biology to help improve systemic therapies. Beside hepatitis B virus‐associated tumors, HCC is poorly established
Externí odkaz:
https://doaj.org/article/94c89770dd5544638da6f30f878a4838
Autor:
Jihong Ma, Xinping Tan, Yongkook Kwon, Evan R. Delgado, Arman Zarnegar, Marie C. DeFrances, Andrew W. Duncan, Reza Zarnegar
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 13, Iss 2, Pp 565-582 (2022)
Background & Aims: Nonalcoholic fatty liver disease is a frequent cause of hepatic dysfunction and is now a global epidemic. This ailment can progress to an advanced form called nonalcoholic steatohepatitis (NASH) and end-stage liver disease. Current
Externí odkaz:
https://doaj.org/article/7e58c9b02e0346ed9b58c9790204be6a
Autor:
Marwa ALMahroos, Mohammed AlMannai
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 5, Iss 1, Pp 17-19 (2022)
Background: Hereditary tyrosinemia type 1 (HT1) is an autosomal recessive inherited metabolic disorder caused by the fumerylacetoacetate hydrolase enzyme deficiency. It is characterized by liver dysfunction and/ or failure, renal tubular dysfunction.
Externí odkaz:
https://doaj.org/article/16f2cfe38b6e47aeaf0341ec4eb393a8