Wendy E. Kutz

ADAMTS10 Protein Interacts with Fibrillin-1 and Promotes Its Deposition in Extracellular Matrix of Cultured Fibroblasts

Wendy E. Kutz, Lauren W. Wang, Hannah L. Bader et al. · Journal of Biological Chemistry · 2011 · 145 citations · Full text

Molecular Biology, Cytoskeleton, Cellular Physiology +18

Further delineation of the phenotype resulting from <i>BRAF</i> or <i>MEK1</i> germline mutations helps differentiate cardio‐facio‐cutaneous syndrome from Costello syndrome

Karen W. Gripp, Angela E. Lin, Linda K. Nicholson et al. · American Journal of Medical Genetics Part A · 2007 · 94 citations

<i>WISP3</i>, the Gene Responsible for the Human Skeletal Disease Progressive Pseudorheumatoid Dysplasia, Is Not Essential for Skeletal Function in Mice

Wendy E. Kutz, Yaoqin Gong, Matthew L. Warman · Molecular and Cellular Biology · 2004 · 65 citations · Full text

Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani syndrome demonstrates a long-range effect on secretion of the full-length enzyme

Wendy E. Kutz, Lauren W. Wang, Nathalie Dagoneau et al. · Human Mutation · 2008 · 52 citations

Protein Secretion, Genetics, Molecular Biology +22

Adamts10 inactivation in mice leads to persistence of ocular microfibrils subsequent to reduced fibrillin-2 cleavage

Lauren W. Wang, Wendy E. Kutz, Timothy J. Mead et al. · Matrix Biology · 2018 · 49 citations · Full text

Ocular Disease, Signal Transduction, Adamts10 Inactivation +10