CFTR processing, trafficking and interactions-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

CFTR processing, trafficking and interactions

Published:2020-03 Issue: Volume:19 Page:S33-S36
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Amaral Margarida D.,Hutt Darren M,Tomati Valeria,Botelho Hugo M.^ORCID,Pedemonte Nicoletta^ORCID

Funder

Ministero della Salute

Fondazione per la Ricerca sulla Fibrosi Cistica

Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference28 articles.

1. Genetics of cystic fibrosis: CFTR mutation classifications toward genotype-based CF therapies;Fanen;Int J Biochem Cell Biol,2014

2. Hallmarks of therapeutic management of the cystic fibrosis functional landscape;Amaral;J Cyst Fibros,2015

3. Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene;Sosnay;Nat Genet,2013

4. Peripheral protein quality control removes unfolded CFTR from the plasma membrane;Okiyoneda;Science,2010

5. A proteomic variant approach (ProVarA) for personalized medicine of inherited and somatic disease;Hutt;J Mol Biol,2018

Cited by 22 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. The role of CFTR in the eye, and the effect of early highly effective modulator treatment for cystic fibrosis on eye health;Progress in Retinal and Eye Research;2024-09

2. Targeting ubiquitination machinery in cystic fibrosis: Where do we stand?;Cellular and Molecular Life Sciences;2024-06-18

3. Point of care lung ultrasound in preschool children with cystic fibrosis: a case-controlled, prospective, pilot study;Journal of Ultrasound;2024-01-19

4. CTNNAL1 deficiency suppresses CFTR expression in HDM-induced asthma mouse model through ROCK1-CAL signaling pathway;Acta Biochimica et Biophysica Sinica;2023-09-15

5. L1077P CFTR pathogenic variant function rescue by Elexacaftor–Tezacaftor–Ivacaftor in cystic fibrosis patient-derived air–liquid interface (ALI) cultures and organoids: in vitro guided personalized therapy of non-F508del patients;Respiratory Research;2023-09-06

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

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3