Human skeletal dysplasia caused by a constitutive activated transient receptor potential vanilloid 4 (TRPV4) cation channel mutation-Reference-Cited by-同舟云学术

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Human skeletal dysplasia caused by a constitutive activated transient receptor potential vanilloid 4 (TRPV4) cation channel mutation

Published:2012 Issue:12 Volume:44 Page:707
ISSN:1226-3613
Container-title:Experimental & Molecular Medicine
language:en
Short-container-title:Exp Mol Med

Author:

Kang Sang Sun¹,Shin Sung Hwa¹,Auh Chung-Kyoon²,Chun Jaesun³

Affiliation:

1. Department of Biology Education, Chungbuk National University, Cheongju 361-763, Korea.

2. Department of Biological Science, Mokpo National University, Muan 534-729, Korea.

3. Department of Biology Education, Korea National University of Education, Cheongwon 363-791, Korea.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Biochemistry,Molecular Biology,Molecular Medicine,Biochemistry

Reference79 articles.

1. Expression of transient receptor potential (TRP) channels in human and murine osteoblast-like cells

2. Hypotonicity Induces TRPV4-Mediated Nociception in Rat

3. Familial digital arthropathy-brachydactyly

4. TRPV4 channel is involved in the coupling of fluid viscosity changes to epithelial ciliary activity

5. TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families

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1. High-viscosity driven modulation of biomechanical properties of human mesenchymal stem cells promotes osteogenic lineage;Materials Today Bio;2024-06

2. TRPV4-dependent Ca2+ influx determines cholesterol dynamics at the plasma membrane;Biophysical Journal;2024-04

3. TRPV Channels in Osteoarthritis: A Comprehensive Review;Biomolecules;2024-02-29

4. Identification and Properties of TRPV4 Mutant Channels Present in Polycystic Kidney Disease Patients;Function;2024

5. Homozygous TRPV4 Mutation Broadens the Phenotypic Spectrum of Congenital Spinal Muscular Atrophy and Arthrogryposis: A Case Report;Cureus;2023-08-13

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