Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects,

door Wilcox, William R.
Gepubliceerd in 2003

Changing paradigm of cancer therapy: precision medicine by next-generation sequencing

door Xue, Yuan, Wilcox, William R.
Gepubliceerd in Cancer Biol Med (2016)

Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing

door Stanislaw, Christine, Xue, Yuan, Wilcox, William R.
Gepubliceerd in Cancer Biol Med (2016)

Sixteen years and counting: the current understanding of fibroblast growth factor receptor 3 (FGFR3) signaling in skeletal dysplasias

door Foldynova-Trantirkova, Silvie, Wilcox, William R., Krejci, Pavel
Gepubliceerd in 2011

Molecular pathology of the fibroblast growth factor family

door Krejci, Pavel, Prochazkova, Jirina, Bryja, Vitezslav, Kozubik, Alois, Wilcox, William R.
Gepubliceerd in 2009

A Second Locus for Schneckenbecken Dysplasia Identified by a Mutation in the Gene Encoding Inositol Polyphosphate Phosphatase-Like 1 (INPPL1)

door Lee, Hane, Nevarez, Lisette, Lachman, Ralph S., Wilcox, William R., Krakow, Deborah, Cohn, Daniel H.
Gepubliceerd in Am J Med Genet A (2015)

Two-Tiered Newborn Screening with Post-Analytical Tools for Pompe Disease and Mucopolysaccharidosis Type I Results in Performance Improvement and Future Direction

door Hall, Patricia L., Sanchez, Rossana, Hagar, Arthur F., Jerris, S. Caleb, Wittenauer, Angela, Wilcox, William R.
Gepubliceerd in Int J Neonatal Screen (2020)

A novel interaction between fibroblast growth factor receptor 3 and the p85 subunit of phosphoinositide 3-kinase: activation-dependent regulation of ERK by p85 in multiple myeloma...

door Salazar, Lisa, Kashiwada, Tamara, Krejci, Pavel, Muchowski, Paul, Donoghue, Daniel, Wilcox, William R., Thompson, Leslie Michels
Gepubliceerd in 2009

Evaluation of Prenatal-Onset Osteochondrodysplasias by Ultrasonography: A Retrospective and Prospective Analysis

door Krakow, Deborah, Alanay, Yasemin, Rimoin, Lauren P., Lin, Victoria, Wilcox, William R., Lachman, Ralph S., Rimoin, David L.
Gepubliceerd in 2008

FGFR3 mutation frequency in 324 cases from the International Skeletal Dysplasia Registry

door Xue, Yuan, Sun, Angela, Mekikian, P Betty, Martin, Jorge, Rimoin, David L, Lachman, Ralph S, Wilcox, William R
Gepubliceerd in Mol Genet Genomic Med (2014)

Fibroblast growth factor inhibits interferon γ-STAT1 and interleukin 6-STAT3 signaling in chondrocytes

door Krejci, Pavel, Prochazkova, Jirina, Bryja, Vitezslav, Jelinkova, Petra, Pejchalova, Katerina, Kozubik, Alois, Thompson, Leslie Michels, Wilcox, William R.
Gepubliceerd in 2008

FGFR3 signaling induces a reversible senescence phenotype in chondrocytes similar to oncogene-induced premature senescence

door Krejci, Pavel, Prochazkova, Jirina, Smutny, Jiri, Chlebova, Katarina, Lin, Patricia, Aklian, Anie, Bryja, Vitezslav, Kozubik, Alois, Wilcox, William R.
Gepubliceerd in 2010

Long-Term Safety and Efficacy of Enzyme Replacement Therapyfor Fabry Disease

door Wilcox, William R., Banikazemi, Maryam, Guffon, Nathalie, Waldek, Stephen, Lee, Philip, Linthorst, Gabor E., Desnick, Robert J., Germain, Dominique P.
Gepubliceerd in 2004

Mitogen-Activated Protein Kinases Promote WNT/β-Catenin Signaling via Phosphorylation of LRP6

door Červenka, Igor, Wolf, Joshua, Mašek, Jan, Krejci, Pavel, Wilcox, William R., Kozubík, Alois, Schulte, Gunnar, Gutkind, J. Silvio, Bryja, Vítězslav
Gepubliceerd in 2011

A Novel ZRS Mutation Leads to Preaxial Polydactyly Type 2 in a Heterozygous Form and Werner Mesomelic Syndrome in a Homozygous Form

door VanderMeer, Julia E., Lozano, Reymundo, Sun, Miao, Xue, Yuan, Daentl, Donna, Jabs, Ethylin Wang, Wilcox, William R., Ahituv, Nadav
Gepubliceerd in 2014

Analysis of STAT1 Activation by Six FGFR3 Mutants Associated with Skeletal Dysplasia Undermines Dominant Role of STAT1 in FGFR3 Signaling in Cartilage

door Krejci, Pavel, Salazar, Lisa, Kashiwada, Tamara A., Chlebova, Katarina, Salasova, Alena, Thompson, Leslie Michels, Bryja, Vitezslav, Kozubik, Alois, Wilcox, William R.
Gepubliceerd in 2008

Cardiovascular manifestations of Fabry disease: relationships between left ventricular hypertrophy, disease severity, and α-galactosidase A activity

door Wu, Justina C., Ho, Carolyn Y., Skali, Hicham, Abichandani, Rekha, Wilcox, William R., Banikazemi, Maryam, Packman, Seymour, Sims, Katherine, Solomon, Scott D.
Gepubliceerd in 2010

Fibroblast Growth Factor Receptor 3 Interacts with and Activates TGFβ-Activated Kinase 1 Tyrosine Phosphorylation and NFκB Signaling in Multiple Myeloma and Bladder Cancer

door Salazar, Lisa, Kashiwada, Tamara, Krejci, Pavel, Meyer, April N., Casale, Malcolm, Hallowell, Matthew, Wilcox, William R., Donoghue, Daniel J., Thompson, Leslie Michels
Gepubliceerd in 2014

Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy

door Schiffmann, Raphael, Warnock, David G., Banikazemi, Maryam, Bultas, Jan, Linthorst, Gabor E., Packman, Seymour, Sorensen, Sven Asger, Wilcox, William R., Desnick, Robert J.
Gepubliceerd in 2009

NF449 Is a Novel Inhibitor of Fibroblast Growth Factor Receptor 3 (FGFR3) Signaling Active in Chondrocytes and Multiple Myeloma Cells

door Krejci, Pavel, Murakami, Shunichi, Prochazkova, Jirina, Trantirek, Lukas, Chlebova, Katarina, Ouyang, Zhufeng, Aklian, Anie, Smutny, Jiri, Bryja, Vitezslav, Kozubik, Alois, Wilcox, William R.
Gepubliceerd in 2010