Epidermolysis bullosa simplex (Koebner) is a keratin disorder. Ultrastructural and immunohistochemical study.
about
Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skinMapping of epidermolysis bullosa simplex mutation to chromosome 12Defining keratin protein function in skin epithelia: epidermolysis bullosa simplex and its aftermathDiscovery of keratin function and role in genetic diseases: the year that 1991 was.Linkage of epidermolysis bullosa simplex to keratin gene loci.Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.A function for keratins and a common thread among different types of epidermolysis bullosa simplex diseasesEpidermolysis bullosa simplex: a paradigm for disorders of tissue fragility.Epidermolysis bullosa simplex with mottled pigmentation.Inherited epidermolysis bullosa.Epidermolysis bullosa simplex, Dowling-Meara type. A report of two cases with different types of tonofilament clumping.Immunohistochemical detection of keratin with the monoclonal antibody MNF116 is useful in the diagnosis of epidermolysis bullosa simplex.
P2860
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P2860
Epidermolysis bullosa simplex (Koebner) is a keratin disorder. Ultrastructural and immunohistochemical study.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
1991年學術文章
@zh
1991年學術文章
@zh-hant
name
Epidermolysis bullosa simplex ...... and immunohistochemical study.
@en
type
label
Epidermolysis bullosa simplex ...... and immunohistochemical study.
@en
prefLabel
Epidermolysis bullosa simplex ...... and immunohistochemical study.
@en
P2093
P1433
P1476
Epidermolysis bullosa simplex ...... and immunohistochemical study.
@en
P2093
P304
P356
10.1001/ARCHDERM.127.3.367
P577
1991-03-01T00:00:00Z