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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2019/05/15 09:56:22」(JST)

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A plakin is a protein that associates with junctional complexes and the cytoskeleton.^[1]

Types include desmoplakin, envoplakin, periplakin, plectin, bullous pemphigoid antigen 1, corneodesmosin, and microtubule actin cross-linking factor.^[2]

References

^ Plakins at the US National Library of Medicine Medical Subject Headings (MeSH)
^ William B. Coleman; Gregory J. Tsongalis (2009). Molecular pathology: the molecular basis of human disease. Academic Press. pp. 531–. ISBN 978-0-12-374419-7. Retrieved 29 December 2010.

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1. 水疱性類天疱瘡および粘膜類天疱瘡の疫学および病因 epidemiology and pathogenesis of bullous pemphigoid and mucous membrane pemphigoid
2. 腫瘍随伴性天疱瘡 paraneoplastic pemphigus

English Journal

A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia.

Jan A1, Basit S, Wakil SM, Ramzan K, Ahmad W.
Archives of dermatological research.Arch Dermatol Res.2015 Jul 7. [Epub ahead of print]
Autosomal recessive forms of hair loss (alopecia) disorders have previously been associated with variants in at least five different genes including hairless (HR), desmoglein-4 (DSG4), desmocollin-3 (DSC3), lipase-H (LIPH), and lysophosphatidic acid receptor 6 (LPAR6). Here, we report the first fami
PMID 26148547

Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin.

McAleer MA1, Pohler E2, Smith FJ2, Wilson NJ2, Cole C3, MacGowan S3, Koetsier JL4, Godsel LM5, Harmon RM4, Gruber R6, Crumrine D7, Elias PM7, McDermott M8, Butler K9, Broderick A10, Sarig O11, Sprecher E12, Green KJ5, McLean WH2, Irvine AD13.
The Journal of allergy and clinical immunology.J Allergy Clin Immunol.2015 Jun 12. pii: S0091-6749(15)00653-3. doi: 10.1016/j.jaci.2015.05.002. [Epub ahead of print]
BACKGROUND: Severe dermatitis, multiple allergies, and metabolic wasting (SAM) syndrome is a recently recognized syndrome caused by mutations in the desmoglein 1 gene (DSG1). To date, only 3 families have been reported.OBJECTIVE: We studied a new case of SAM syndrome known to have no mutations in DS
PMID 26073755

Japanese Journal

Expression patterns of epiplakin1 in pancreas,pancreatic cancer and regenerating pancreas

Yoshida Tetsu,Shiraki Nobuaki,Baba Hideo,Goto Mizuki,Fujiwara Sakuhei,Kume Kazuhiko,Kume Shoen,クメショウエン,クメカズヒコ,粂昭苑,粂和彦
Genes to cells 13(7), 667-678, 2008-07
… Epiplakin1 (Eppk1) is a plakin family gene with its function remains largely unknown, although the plakin genes are known to function in interconnecting cytoskeletal filaments and anchoring them at plasma membrane-associated adhesive junction. …
NAID 120002468595