Cholestatic Liver Disease due to Novel USP53 Mutations: A Case Series of Three Indian Children-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Cholestatic Liver Disease due to Novel USP53 Mutations: A Case Series of Three Indian Children

Published:2024-03 Issue:2 Volume:14 Page:101290
ISSN:0973-6883
Container-title:Journal of Clinical and Experimental Hepatology
language:en
Short-container-title:Journal of Clinical and Experimental Hepatology

Author:

Samanta Arghya^ORCID,Parveen Neha,Sen Sarma Moinak^ORCID,Poddar Ujjal^ORCID,Srivastava Anshu^ORCID

Publisher

Elsevier BV

Subject

Hepatology

Reference13 articles.

1. Mining the idiopathic genetic cholestasis syndrome;Chen;J Gastroenterol Hepatol,2013

2. Individual exome analysis in diagnosis and management of paediatric liver failure of indeterminate aetiology;Vilarinho;J Hepatol,2014

3. Cloning and enzymatic analysis of 22 novel human ubiquitin-specific proteases;Quesada;Biochem Biophys Res Commun,2004

4. Low-GGT intrahepatic cholestasis associated with biallelic USP53 variants: clinical, histological and ultrastructural characterization;Zhang;Liver Int,2020

5. Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT;Carlton;Nat Genet,2003

Cited by 2 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. Discovery and mechanism of K63-linkage-directed deubiquitinase activity in USP53;2024-07-07

2. Emerging drugs for the treatment of progressive familial intrahepatic cholestasis: a focus on phase II and III trials;Expert Opinion on Emerging Drugs;2024-07-04

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP