Thomas Jefferson University

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McGrath, John
One or more keywords matched the following items that are connected to McGrath, John
Item TypeName
Concept Neoplasm Proteins
Academic Article Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.
Academic Article Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.
Academic Article Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation.
Academic Article Neonatal diagnosis of Kindler syndrome.
Academic Article Novel and recurrent FERMT1 gene mutations in Kindler syndrome.
Academic Article Case of Kindler syndrome resulting from mutation in the FERMT1 gene.
Academic Article Is adermatoglyphia an additional feature of Kindler Syndrome?
Academic Article Sporadic Kindler syndrome with a novel mutation.
Academic Article Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.
Academic Article Five new homozygous mutations in the KIND1 gene in Kindler syndrome.
Academic Article Revertant mosaicism in Kindler syndrome.
Academic Article What is Kindler syndrome?
Academic Article Kindlin-1 Regulates Keratinocyte Electrotaxis.
Academic Article Kindler syndrome: a new mutation and new diagnostic possibilities.
Academic Article Kindlin-1 Regulates Epidermal Growth Factor?Receptor Signaling.
Academic Article EMSY expression affects multiple components of the skin barrier with relevance to atopic dermatitis.
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  • Neoplasm Proteins