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Arthritis Research & Therapy|October 28, 2006
P5L mutation in Ank results in an increase in extracellular inorganic pyrophosphate during proliferation and nonmineralizing hypertrophy in stably transduced ATDC5 cellsRaihana Zaka, David Stokes, Arnold S Dion, et al.Arthritis & Rheumatology (Hoboken, N.J.)|February 9, 2021
Effects of the TNFRSF11B Mutation Associated With Calcium Pyrophosphate Deposition Disease in Osteoclastogenesis in a Murine ModelElizabeth Mitton-Fitzgerald, Claudia M Gohr, Charlene J Williams, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 8, 2009
Oxygen tension regulates the expression of ANK (progressive ankylosis) in an HIF-1-dependent manner in growth plate chondrocytesRaihana Zaka, Arnold S Dion, Anna Kusnierz, et al.Arthritis and Rheumatism|November 13, 2002
CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathyXiaoju Wang, Helena Kuivaniemi, Gina Bonavita, et al.Journal of Cellular Biochemistry|April 16, 2005
Transforming growth factor-beta1 (TGF-beta1) regulates ATDC5 chondrogenic differentiation and fibronectin isoform expressionFei Han, Christopher S Adams, Zhuliang Tao, et al.Arthritis and Rheumatism|May 25, 2010
Hypoxia-inducible factor regulation of ANK expression in nucleus pulposus cells: possible implications in controlling dystrophic mineralization in the intervertebral discRenata Skubutyte, Dessislava Markova, Theresa A Freeman, et al.Arthritis and Rheumatism|September 18, 2003
Mutations in the amino terminus of ANKH in two US families with calcium pyrophosphate dihydrate crystal deposition diseaseCharlene J Williams, Adrian Pendleton, Gina Bonavita, et al.The EMBO Journal|March 27, 2004
Regulatory regions and critical residues of NOD2 involved in muramyl dipeptide recognitionTsuyoshi Tanabe, Mathias Chamaillard, Yasunori Ogura, et al.Plos Genetics|July 9, 2020
The membrane protein ANKH is crucial for bone mechanical performance by mediating cellular export of citrate and ATPFlora Szeri, Stefan Lundkvist, Sylvia Donnelly, et al.American Journal of Human Genetics|September 26, 2002
Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKHCharlene J Williams, Yun Zhang, Andrew Timms, et al.Pageof 2