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Article

Implications of the phenotype of POMC deficiency for the role of POMC-derived peptides in skin physiology.

Annals of the New York Academy of Sciences - 20 Oct 1999

Krude H, Schnabel D, Luck W, Grüters A

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 10816678
DOI: 10.1111/j.1749-6632.1999.tb08702.x

Genes

POMC

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Implications of the phenotype of POMC deficiency for the role of POMC-derived peptides in skin physiology.PMID 10816678Read ↗

Proopiomelanocortin (POMC): the cutaneous roles of its melanocortin products and receptors.Semantic proximity Read ↗

Implications of proopiomelanocortin (POMC) mutations in humans: the POMC deficiency syndrome.Semantic proximity Read ↗

A case of early-onset obesity, hypocortisolism, and skin pigmentation problem due to a novel homozygous mutation in the proopiomelanocortin (POMC) gene in an Indian boy.Semantic proximity Read ↗

Gene expression analysis of the corticotrophin-releasing hormone-proopiomelanocortin system in psoriasis skin biopsies.Semantic proximity Read ↗

The expression of proopiomelanocortin (POMC) and of corticotropin releasing hormone receptor (CRH-R) genes in mouse skinSemantic proximity Read ↗

60 YEARS OF POMC: The proopiomelanocortin gene: discovery, deletion and disease.Semantic proximity Read ↗

The melanocortin system and insulin resistance in humans: insights from a patient with complete POMC deficiency and type 1 diabetes mellitus.Semantic proximity Read ↗

Differential expression of proopiomelanocortin (POMC) transcriptional variants in human skin cells.Semantic proximity Read ↗

A novel missense mutation in the signal peptide of the human POMC gene: a possible additional link between early-onset type 2 diabetes and obesitySemantic proximity Read ↗

Identification and sequencing of a putative variant of proopiomelanocortin in human epidermis and epidermal cells in culture.Semantic proximity Read ↗

Preservation of eumelanin hair pigmentation in proopiomelanocortin-deficient mice on a nonagouti (a/a) genetic background.Semantic proximity Read ↗

Delayed diagnosis of proopiomelanocortin (POMC) deficiency with type 1 diabetes in a 9-year-old girl and her infant sibling.Semantic proximity Read ↗

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