Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and ABCB6[original query] |
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| ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis. American journal of medical genetics 2002 May 109 (3): 202-5. Visapää Ilona, Fellman Vineta, Lanyi Lisa, Peltonen Lee |
| Screening the expression of ABCB6 in erythrocytes reveals an unexpectedly high frequency of Lan mutations in healthy individuals. PloS one 2014 9 (10): e111590. Koszarska Magdalena, Kucsma Nora, Kiss Katalin, Varady Gyorgy, Gera Melinda, Antalffy Geza, Andrikovics Hajnalka, Tordai Attila, Studzian Maciej, Strapagiel Dominik, Pulaski Lukasz, Tani Yoshihiko, Sarkadi Balazs, Szakacs Gerge |
| ABCB6 polymorphisms are not overly represented in patients with porphyria. Blood advances 2021 11 6 (3): 760-766. Farrell Colin P, Nicolas Gäel, Desnick Robert J, Parker Charles J, Lamoril Jerome, Gouya Laurent, Karim Zoubida, Tchernitchko Dimitri, Chan Brenden, Puy Herve, Phillips John |
| Identification of a glycolysis-related gene signature for predicting prognosis in patients with hepatocellular carcinoma. BMC cancer 2022 2 22 (1): 142. Kong Junjie, Yu Guangsheng, Si Wei, Li Guangbing, Chai Jiawei, Liu Yong, Liu J |
| Development and validation of metabolic models for predicting survival and immune status of hepatocellular carcinoma patients. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2023 5 . Xueying Li, Mengli Gu, Qiying Hu, Yihui Weng, Xianlei C |
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