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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Gallstones and NPC1L1[original query]
Role of the ABCG8 19H risk allele in cholesterol absorption and gallstone disease.
BMC gastroenterology 2013 13 (1): 30.
Renner Olga, Lütjohann Dieter, Richter Dominique, Strohmeyer André, Schimmel Silke, Müller Oliver, Stange Eduard F, Harsch Simo
The NPC1L1 Polymorphism 1679C>G Is Associated with Gallstone Disease in Chinese Patients.
PloS one 2016 11 (1): e0147562.
Wu Jian, Cui Wei, Cai Qu, Fei Jian, Zhang Sheng-Dao, Han Tian-Quan, Hu Hai, Jiang Zhao-Y
Genetic polymorphism of sterol transporters in children with future gallstones.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2018 5 50 (9): 954-960.
Nissinen Markku J, Pitkänen Niina, Simonen Piia, Gylling Helena, Viikari Jorma, Raitakari Olli, Lehtimäki Terho, Juonala Markus, Pakarinen Mikko
Common variant p.D19H of the hepatobiliary sterol transporter ABCG8 increases the risk of gallstones in children.
Liver international : official journal of the International Association for the Study of the Liver 2022 Feb .
Krawczyk Marcin, Niewiadomska Olga, Jankowska Irena, Jankowski Krzysztof, Wi?ckowski Sebastian, Lebensztejn Dariusz, Wi?cek Sabina, Gozdowska Jolanta, Ku?aga Zbigniew, Weber Susanne N, Lütjohann Dieter, Lammert Frank, Socha Pio
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