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One or more keywords matched the following items that are connected to Mcgrath, John
Item TypeName
Concept Photosensitivity Disorders
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 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 Kindlin-1 controls Wnt and TGF-? availability to regulate cutaneous stem cell proliferation.
Academic Article Five new homozygous mutations in the KIND1 gene in Kindler syndrome.
Academic Article Questioning the Clinical Utility of Exome Sequencing in Developing Countries.
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 Pathogenesis of solar urticaria: Classic perspectives and emerging concepts.
Academic Article The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndrome.
Academic Article Colocalization of kindlin-1, kindlin-2, and migfilin at keratinocyte focal adhesion and relevance to the pathophysiology of Kindler syndrome.
Academic Article An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene.
Academic Article Genetic analysis in Egyptian patients with Chediak-Higashi syndrome reveals new LYST mutations.
Academic Article Kindler syndrome: a focal adhesion genodermatosis.
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  • Photosensitivity Disorders