4.6 Article

Rescuing Trafficking Mutants of the ATP-binding Cassette Protein, ABCA4, with Small Molecule Correctors as a Treatment for Stargardt Eye Disease

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Pharmacology & Pharmacy

Searching for Combinations of Small-Molecule Correctors to Restore F508del-Cystic Fibrosis Transmembrane Conductance Regulator Function and Processing

Clement Boinot et al.

JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2014)

Review Biochemistry & Molecular Biology

Molecular Chaperone Functions in Protein Folding and Proteostasis

Yujin E. Kim et al.

ANNUAL REVIEW OF BIOCHEMISTRY, VOL 82 (2013)

Article Cell Biology

Regulated recycling of mutant CFTR is partially restored by pharmacological treatment

John P. Holleran et al.

JOURNAL OF CELL SCIENCE (2013)

Article Biochemistry & Molecular Biology

Requirements for Efficient Correction of ΔF508 CFTR Revealed by Analyses of Evolved Sequences

Juan L. Mendoza et al.

Article Biochemistry & Molecular Biology

The Role of Intrinsically Disordered Regions in the Structure and Functioning of Small Heat Shock Proteins

Maria V. Sudnitsyna et al.

CURRENT PROTEIN & PEPTIDE SCIENCE (2012)

Editorial Material Cell Biology

Fixing cystic fibrosis by correcting CFTR domain assembly

Tsukasa Okiyoneda et al.

JOURNAL OF CELL BIOLOGY (2012)

Article Multidisciplinary Sciences

ABCA4 is an N-retinylidene-phosphatidylethanolamine and phosphatidylethanolamine importer

Faraz Quazi et al.

NATURE COMMUNICATIONS (2012)

Review Biochemistry & Molecular Biology

ABC transporters, mechanisms and biology: an overview

I. Barry Holland

ESSAYS IN BIOCHEMISTRY: ABC TRANSPORTERS (2011)

Review Biochemistry & Molecular Biology

The role of the photoreceptor ABC transporter ABCA4 in lipid transport and Stargardt macular degeneration

Robert S. Molday et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2009)

Article Biochemistry & Molecular Biology

Cystic fibrosis transmembrane regulator missing the first four transmembrane segments increases wild type and ΔF508 processing

Liudmila Cebotaru et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2008)

Article Cell Biology

Small heat-shock proteins select ΔF508-CFTR for endoplasmic reticulum-associated degradation

Annette Ahner et al.

MOLECULAR BIOLOGY OF THE CELL (2007)

Review Physiology

The ABCA subfamily - gene and protein structures, functions and associated hereditary diseases

Christiane Albrecht et al.

PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2007)

Review Physiology

CFTR (ABCC7) is a hydrolyzable-ligand-gated channel

Andrei A. Aleksandrov et al.

PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2007)

Article Biochemistry & Molecular Biology

HDAC6-p97/VCP controlled polyubiquitin chain turnover

Cyril Boyault et al.

EMBO JOURNAL (2006)

Article Physiology

Rescue of ΔF508-CFTR trafficking and gating in human cystic fibrosis airway primary cultures by small molecules

F Van Goor et al.

AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY (2006)

Article Medicine, Research & Experimental

Small-molecule correctors of defective ΔF508-CFTR cellular processing identified by high-throughput screening

N Pedemonte et al.

JOURNAL OF CLINICAL INVESTIGATION (2005)

Article Biochemistry & Molecular Biology

Modulation of mature cystic fibrosis transmembrane regulator protein by the PDZ domain protein CAL

J Cheng et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2004)

Article Biochemistry & Molecular Biology

CFTR and chaperones - Processing and degradation

MD Amaral

JOURNAL OF MOLECULAR NEUROSCIENCE (2004)

Article Genetics & Heredity

Further evidence for an association of ABCR alleles with age-related macular degeneration

R Allikmets

AMERICAN JOURNAL OF HUMAN GENETICS (2000)