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Bone marrow cell transfer into fetal circulation can ameliorate genetic skin diseases by providing fibroblasts to the skin and inducing immune tolerance.Academic Article Why?
Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in children.Academic Article Why?
Livedoid vasculopathy associated with plasminogen activator inhibitor-1 promoter homozygosity (4G/4G) treated successfully with tissue plasminogen activator.Academic Article Why?
Molecular therapies for heritable blistering diseases.Academic Article Why?
Progress in heritable skin diseases: translational implications of mutation analysis and prospects of molecular therapies*.Academic Article Why?
A central role for transcription factor C/EBP-beta in regulating CD1d gene expression in human keratinocytes.Academic Article Why?
Divergent effects of two sequence variants of GJB3 (G12D and R32W) on the function of connexin 31 in vitro.Academic Article Why?
Progress in epidermolysis bullosa: from eponyms to molecular genetic classification.Academic Article Why?
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