about
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hairEarly stages of we/we wal/wal mouse hair morphogenesis: light and fluorescent microscopy of the whole-mount epidermisTo the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat BreedSelkirk Rex: morphological and genetic characterization of a new cat breed.Harnessing neuroendocrine controls of keratin expression: a new therapeutic strategy for skin diseases?Inherited desmosomal disorders.Keratins and skin disease.The biology and genetics of curly hair.Epistatic interactions between at least three loci determine the "rat-tail" phenotype in cattleSegregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan.Two cases of autosomal recessive woolly hair with LIPH gene mutations.An Autotaxin/Lysophosphatidic Acid/Interleukin-6 Amplification Loop Drives Scleroderma Fibrosis.Expression studies of a novel splice site mutation in the LIPH gene identified in a Japanese patient with autosomal recessive woolly hair.Novel mutation in LIPH in a Lebanese patient with autosomal recessive woolly hair/hypotrichosis.Comparative structures and evolution of vertebrate lipase H (LIPH) genes and proteins: a relative of the phospholipase A1 gene families.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
Congenital hair loss disorders: rare, but not too rare.
@en
Congenital hair loss disorders: rare, but not too rare.
@nl
type
label
Congenital hair loss disorders: rare, but not too rare.
@en
Congenital hair loss disorders: rare, but not too rare.
@nl
prefLabel
Congenital hair loss disorders: rare, but not too rare.
@en
Congenital hair loss disorders: rare, but not too rare.
@nl
P2860
P1476
Congenital hair loss disorders: rare, but not too rare.
@en
P2093
Yutaka Shimomura
P2860
P356
10.1111/J.1346-8138.2011.01395.X
P577
2011-11-02T00:00:00Z