Rowan Digital Works

Hypoxia‐inducible factor regulation of ANK expression in nucleus pulposus cells: Possible implications in controlling dystrophic mineralization in the intervertebral disc, Renata Skubutyte, Dessislava Markova, Theresa A. Freeman, D. Greg Anderson, Arnold S. Dion, Charlene J. Williams, Irving M. Shapiro, Makarand V. Risbud
Charlene Williams

Oxygen Tension Regulates the Expression of ANK (Progressive Ankylosis) in an HIF-1-Dependent Manner in Growth Plate Chondrocytes†‡, Raihana Zaka, Arnold S. Dion, Anna Kusnierz, Jolene Bohensky, Vickram Srinivas, Theresa Freeman, Charlene J. Williams
Charlene Williams

The genetics of osteoarthritis., Charlene J. Williams
Charlene Williams

New developments in the epidemiology and genetics of gout, Raihana Zaka, Charlene J. Williams
Charlene Williams

Genetics of chondrocalcinosis, Raihana Zaka, Charlene J. Williams
Charlene Williams

Regulatory regions and critical residues of NOD2 involved in muramyl dipeptide recognition, Tsuyoshi Tanabe, Mathias Chamaillard, Yasunori Ogura, Li Zhu, Su Qiu, Junya Masumoto, Partho Ghosh, Anthony Moran, Martina M. Predergast, Gerard Tromp, Charlene J. Williams, Naohiro Inohara, Gabriel Núñez
Charlene Williams

Skeletal dysplasias and the osteoarthritic phenotype, Charlene J. Williams, Sergio A. Jimenez
Charlene Williams

CARD15 mutations in familial granulomatosis syndromes: A study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy, Xiaoju Wang, Helena Kuivaniemi, Gina Bonavita, Lysette Mutkus, Ulrike Mau, Edward Blau, Naohiro Inohara, Gabriel Nunez, Gerard Tromp, Charlene J. Williams
Charlene Williams

Exclusion of the gene for human cartilage intermediate layer protein in currently mapped calcium pyrophosphate dihydrate deposition syndromes, R. Catrinel Marinescu, Kristin Nyce, Lourdes Serrano De La Peñaa, Joan Overhauser, Charlene J. Williams
Charlene Williams

FIVE FAMILIES WITH ARGININE519-CYSTEINE MUTATION IN COL2A1 : EVIDENCE FOR THREE DISTINCT FOUNDERS, Jane F. Bleasel, Daniel Holderbaum, Valeria Brancolini, Roland W. Moskowitz, Eileen L. Considine, Darwin J. Prockop, Marcella Devoto, Charlene J. Williams
Charlene Williams

Identification of Incidental Sequence Polymorphisms and Absence of the db/db Mouse and fa/fa Rat Mutations, Robert V. Considine, Jose F. Caro, Eileen L. Considine, Charlene J. Williams, Thomas M. Hyde
Charlene Williams

Mutation screening and identification of a sequence variation in the human ob gene coding region., Robert V. Considine, Eileen L. Considine, Charlene J. Williams, Mark R. Nyce, Peili Zhang, Irina Opentanova, Joanna P. Ohannesian, Jerzy W. Kolaczynski, Thomas L. Bauer, John H. Moore, Jose F. Caro
Charlene Williams

Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity., Robert V. Considine, Eileen L. Considine, Charlene J. Williams, Mark R. Nyce, Susan A. Magosin, Thomas L. Bauer, Ernest L. Rosato, James Colberg, Jose F. Caro
Charlene Williams

Three new point mutations in type II procollagen (COL2A1) and identification of a fourth family with the COL2A1 Arg519→Cys base substitution using conformation sensitive gel electrophoresis, Charlene J. Williams, Matthew Rock, Eileen Considine, Seamus McCarron, Peter Gow, Roger Ladda, David McLain, Virginia M. Michels, William Murphy, Darwin J. Prockop, Arupa Ganguly
Charlene Williams

The Molecular Genetics and Clinical Manifestations of Heritable Osteoarthritis A Rheumatologist's Guide., Charlene J. Williams, Antonio J. Reginato
Charlene Williams

Familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis associated with an arginine 75 → cysteine mutation in the procollagen type ii gene in a kindred of chiloe islanders., Antonio J. Reginato, Gian M. Passano, Guillermo Neumann, Gerald F. Falasca, Marcelo Diaz‐Valdez, Sergio A. Jimenez, Charlene J. Williams
Charlene Williams

Primers and methods for detecting mutations in the procollagen II gene (COL2A1) that indicate a genetic predisposition for a COL2A1-associated disease, Darwin J. Prockop, Leena Ala-Kokko, Charlene J. Williams, Pertti Ritvaniemi, Clinton Baldwin, Ian Hopkinson, Nilofer Nina Ahmad
Charlene Williams

Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75→Cys mutation in the procollagen type II gene (COL2A1), Charlene J. Williams, Eileen L. Considine, Robert G. Knowlton, Antonio Reginato, Guillermo Neumann, David Harrison, Paul Buxton, Sergio Jimenez, Darwin J. Prockop
Charlene Williams

Detection of sequence variants in the gene for human type II procollagen (COL2A1) by direct sequencing of polymerase chain reaction-amplified genomic DNA, Charlene J. Williams, David A. Harrison, Ian Hopkinson, Clinton T. Baldwin, N. Nina Ahmad, Leena Ala‐Kokko, Richard M. Korn, Paul G. Buxton, Jeffrey Dimascio, Eileen L. Considine, Darwin J. Prockop
Charlene Williams

Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta, Mon-Li Chu, Charlene J. Williams, Gugliemina Pepe, Jeffrey L. Hirsch, Darwin J. Prockop, Francesco Ramirez
Charlene Williams