High-resolution physical map for chromosome 16q12.1-q13, the Blau syndrome locus

Yazar: Wang, Xiaoju, Kuivaniemi, Helena, Bonavita, Gina, Williams, Charlene J, Tromp, Gerard
Baskı/Yayın Bilgisi 2002

P5L mutation in Ank results in an increase in extracellular inorganic pyrophosphate during proliferation and nonmineralizing hypertrophy in stably transduced ATDC5 cells

Yazar: Zaka, Raihana, Stokes, David, Dion, Arnold S, Kusnierz, Anna, Han, Fei, Williams, Charlene J
Baskı/Yayın Bilgisi 2006

Oxygen Tension Regulates the Expression of ANK (Progressive Ankylosis) in an HIF-1–Dependent Manner in Growth Plate Chondrocytes

Yazar: Zaka, Raihana, Dion, Arnold S., Kusnierz, Anna, Bohensky, Jolene, Srinivas, Vickram, Freeman, Theresa, Williams, Charlene J.
Baskı/Yayın Bilgisi 2009

The TNFRSF11B mutation associated with calcium pyrophosphate deposition disease results in ineffective osteoclast suppression

Yazar: Mitton-Fitzgerald, Elizabeth, Gohr, Claudia M., Williams, Charlene J, Ortiz, Amaryllis, Mbalaviele, Gabriel, Rosenthal, Ann K.
Yayımlandı Arthritis Rheumatol (2021)

HIF Regulation of ANK Expression in Nucleus Pulposus Cells: Possible Implications in Controlling Dystrophic Mineralization in the Intervertebral Disc

Yazar: Skubutyte, Renata, Markova, Dessislava, Freeman, Theresa A., Anderson, D. Greg, Dion, Arnold S., Williams, Charlene J., Shapiro, Irving M., Risbud, Makarand V.
Baskı/Yayın Bilgisi 2010

Regulatory regions and critical residues of NOD2 involved in muramyl dipeptide recognition

Yazar: Tanabe, Tsuyoshi, Chamaillard, Mathias, Ogura, Yasunori, Zhu, Li, Qiu, Su, Masumoto, Junya, Ghosh, Partho, Moran, Anthony, Predergast, Martina M, Tromp, Gerard, Williams, Charlene J, Inohara, Naohiro, Núñez, Gabriel
Baskı/Yayın Bilgisi 2004

The membrane protein ANKH is crucial for bone mechanical performance by mediating cellular export of citrate and ATP

Yazar: Szeri, Flora, Lundkvist, Stefan, Donnelly, Sylvia, Engelke, Udo F. H., Rhee, Kyu, Williams, Charlene J., Sundberg, John P., Wevers, Ron A., Tomlinson, Ryan E., Jansen, Robert S., van de Wetering, Koen
Yayımlandı PLoS Genet (2020)

Autosomal Dominant Familial Calcium Pyrophosphate Dihydrate Deposition Disease Is Caused by Mutation in the Transmembrane Protein ANKH

Yazar: Williams, Charlene J., Zhang, Yun, Timms, Andrew, Bonavita, Gina, Caeiro, Francisco, Broxholme, John, Cuthbertson, Jonathan, Jones, Yvonne, Marchegiani, Raul, Reginato, Antonio, Russell, R. Graham G., Wordsworth, B. Paul, Carr, Andrew J., Brown, Matthew A.
Baskı/Yayın Bilgisi 2002