Mutations in TRPV4 cause an inherited arthropathy of hands and feet
Published 2011 View Full Article
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Title
Mutations in TRPV4 cause an inherited arthropathy of hands and feet
Authors
Keywords
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Journal
NATURE GENETICS
Volume 43, Issue 11, Pages 1142-1146
Publisher
Springer Nature
Online
2011-10-03
DOI
10.1038/ng.945
References
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Related references
Note: Only part of the references are listed.- Mutant TRPV4-mediated Toxicity Is Linked to Increased Constitutive Function in Axonal Neuropathies
- (2011) Faisal Fecto et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies
- (2011) C. J. Klein et al. NEUROLOGY
- TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families
- (2011) Elena Andreucci et al. Orphanet Journal of Rare Diseases
- Increased Basal Activity Is a Key Determinant in the Severity of Human Skeletal Dysplasia Caused by TRPV4 Mutations
- (2011) Stephen Loukin et al. PLoS One
- De novo deletion of 1q24.3-q31.2 in a patient with severe growth retardation
- (2010) Akira Nishimura et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- DominantTRPV4mutations in nonlethal and lethal metatropic dysplasia
- (2010) Natalia Camacho et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Chondroprotective role of the osmotically sensitive ion channel transient receptor potential vanilloid 4: Age- and sex-dependent progression of osteoarthritis in Trpv4-deficient mice
- (2010) Andrea L. Clark et al. ARTHRITIS AND RHEUMATISM
- Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies
- (2010) Magdalena Zimoń et al. BRAIN
- Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family
- (2010) J. Dai et al. JOURNAL OF MEDICAL GENETICS
- CMT2C with vocal cord paresis associated with short stature and mutations in the TRPV4 gene
- (2010) D.- H. Chen et al. NEUROLOGY
- S100A8 and S100A9 in experimental osteoarthritis
- (2010) Hala Zreiqat et al. ARTHRITIS RESEARCH & THERAPY
- Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia
- (2009) Deborah Krakow et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia
- (2009) Ana Belinda Campos-Xavier et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Functional characterization of TRPV4 as an osmotically sensitive ion channel in porcine articular chondrocytes
- (2009) Mimi N. Phan et al. ARTHRITIS AND RHEUMATISM
- Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C
- (2009) Michaela Auer-Grumbach et al. NATURE GENETICS
- Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4
- (2009) Han-Xiang Deng et al. NATURE GENETICS
- Mutations in TRPV4 cause Charcot-Marie-Tooth disease type 2C
- (2009) Guida Landouré et al. NATURE GENETICS
- N-((1S)-1- -3-hydroxypropanoyl)-1-piperazinyl]carbonyl}-3-methylbutyl)-1-benzothiophene-2-carboxamide (GSK1016790A), a Novel and Potent Transient Receptor Potential Vanilloid 4 Channel Agonist Induces Urinary Bladder Contraction and Hyperactivity: Part I
- (2008) K. S. Thorneloe et al. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
- Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia
- (2008) Matthew J Rock et al. NATURE GENETICS
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