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Page 1
Mapping the human genetic architecture of COVID-19.
COVID-19 Host Genetics Initiative. COVID-19 Host Genetics Initiative. Nature. 2021 Dec;600(7889):472-477. doi: 10.1038/s41586-021-03767-x. Epub 2021 Jul 8. Nature. 2021. PMID: 34237774 Free PMC article.
Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase.
Koiwai O, Nishizawa M, Hasada K, Aono S, Adachi Y, Mamiya N, Sato H. Koiwai O, et al. Hum Mol Genet. 1995 Jul;4(7):1183-6. doi: 10.1093/hmg/4.7.1183. Hum Mol Genet. 1995. PMID: 8528206
Gilbert's syndrome, which is characterized by chronic, non-hemolytic unconjugated hyperbilirubinemia, is caused by a reduction in the activity of hepatic bilirubin UDP-glucuronosyltransferase (UGT). ...An expression study in COS cells in vitro, using the expression …
Gilbert's syndrome, which is characterized by chronic, non-hemolytic unconjugated hyperbilirubinemia, is caused by a reduction …
[Constitutional jaundice].
Adachi Y, Kamisako T. Adachi Y, et al. Nihon Naika Gakkai Zasshi. 1997 Apr 10;86(4):574-81. Nihon Naika Gakkai Zasshi. 1997. PMID: 9198647 Review. Japanese. No abstract available.
The genetic basis of Gilbert's syndrome.
Sato H, Adachi Y, Koiwai O. Sato H, et al. Lancet. 1996 Mar 2;347(9001):557-8. doi: 10.1016/s0140-6736(96)91266-0. Lancet. 1996. PMID: 8596313 No abstract available.
Nonreciprocal Phonon Propagation in a Metallic Chiral Magnet.
Nomura T, Zhang XX, Takagi R, Karube K, Kikkawa A, Taguchi Y, Tokura Y, Zherlitsyn S, Kohama Y, Seki S. Nomura T, et al. Phys Rev Lett. 2023 Apr 28;130(17):176301. doi: 10.1103/PhysRevLett.130.176301. Phys Rev Lett. 2023. PMID: 37172228
From the ultrasound and microwave-spectroscopy experiments, we conclude that the magnitude of the phonon MChE of Co_{9}Zn_{9}Mn_{2} mostly depends on the Gilbert damping, which increases at low temperatures and hinders the magnon-phonon hybridization. ...
From the ultrasound and microwave-spectroscopy experiments, we conclude that the magnitude of the phonon MChE of Co_{9}Zn_{9}Mn_{2} mostly d …
Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.
Aono S, Adachi Y, Uyama E, Yamada Y, Keino H, Nanno T, Koiwai O, Sato H. Aono S, et al. Lancet. 1995 Apr 15;345(8955):958-9. doi: 10.1016/s0140-6736(95)90702-5. Lancet. 1995. PMID: 7715297
Gilbert's and Crigler-Najjar syndromes are characterised by unconjugated hyperbilirubinaemia due to complete and partial absence of bilirubin UDP-glucuronosyltransferase (UGT). ...These results suggest that Gilbert's syndrome is inherited as a dominant …
Gilbert's and Crigler-Najjar syndromes are characterised by unconjugated hyperbilirubinaemia due to complete and partial absen …
Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.
Takeuchi K, Kobayashi Y, Tamaki S, Ishihara T, Maruo Y, Araki J, Mifuji R, Itani T, Kuroda M, Sato H, Kaito M, Adachi Y. Takeuchi K, et al. J Gastroenterol Hepatol. 2004 Sep;19(9):1023-8. doi: 10.1111/j.1440-1746.2004.03370.x. J Gastroenterol Hepatol. 2004. PMID: 15304120
To clarify the incidence of this gene mutation in the Japanese population, the presence of UGT1A1 mutation was investigated in a group of Japanese patients with Crigler-Najjar syndrome type 2 (CNS2) and Gilbert's syndrome (GS), as well as in healthy anicteric subjec …
To clarify the incidence of this gene mutation in the Japanese population, the presence of UGT1A1 mutation was investigated in a group of Ja …
28 results