Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene-Reference-Cited by-同舟云学术

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Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene

Published:2014 Issue:1 Volume:13 Page:670-679
ISSN:1676-5680
Container-title:Genetics and Molecular Research
language:
Short-container-title:Genet. Mol. Res.

Author:

Hsieh T.-Y.,Shiu T.-Y.,Chu N.-F.,Chao T.-Y.,Chu H.-C.,Chang W.-K.,Chao Y.-C.,Huang H.-H.

Publisher

Genetics and Molecular Research

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.funpecrp.com.br/gmr/year2014/vol13-1/pdf/gmr2955.pdf

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Rapid detection of the irinotecan‐related UGT1A1 *28 polymorphism by asymmetric PCR melting curve analysis using one fluorescent probe;Journal of Clinical Laboratory Analysis;2022-06-29

2. Rapid detection of the ugt1a1 single nucleotide polymorphism G211A using TaqMAMA real-time PCR;Minerva Biotechnology and Biomolecular Research;2022-03

3. Effect of gilbert's syndrome associated polymorphic alleles (rs8175347 and rs4148323) of UDP-glucuronyl transferase on serum bilirubin level;Meta Gene;2020-12

4. Genetic lesions in the UGT1A1 genes among Gilbert’s syndrome patients from India;Molecular Biology Reports;2018-08-13

5. Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II;Medicine;2017-11

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