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Volumn 129, Issue 12, 2009, Pages 2772-2776

In vitro analysis of LIPH mutations causing hypotrichosis simplex: Evidence confirming the role of lipase H and lysophosphatidic acid in hair growth

Author keywords

[No Author keywords available]

Indexed keywords

LIPH PROTEIN, HUMAN; LYSOPHOSPHATIDIC ACID; LYSOPHOSPHOLIPID; TRIACYLGLYCEROL LIPASE;

EID: 79958140945     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2009.154     Document Type: Article
Times cited : (28)

References (11)
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    • A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis
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  • 2
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    • Structure and function of extracellular phospholipase A1 belonging to the pancreatic lipase gene family
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  • 3
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    • Involvement of basic amino acid residues in transmembrane regions 6 and 7 in agonist and antagonist recognition of the human platelet P2Y(12)-receptor
    • Hoffmann K, Sixel U, Di Pasquale F, von Kügelgen I (2008) Involvement of basic amino acid residues in transmembrane regions 6 and 7 in agonist and antagonist recognition of the human platelet P2Y(12)-receptor. Biochem Pharmacol 76:1201-13
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  • 4
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    • A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2)
    • Jelani M, Wasif N, Ali G, Chishti M, Ahmad W (2008) A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2). Clin Genet 74:184-8
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  • 6
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    • Desmoglein 4 in hair follicle differentiation and epidermal adhesion: Evidence from inherited hypotrichosis and acquired pemphigus vulgaris
    • Kljuic A, Bazzi H, Sundberg JP, Martinez-Mir A, O'Shaughnessy R, Mahoney MG et al. (2003) Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell 113:249-60
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    • Kljuic, A.1    Bazzi, H.2    Sundberg, J.P.3    Martinez-Mir, A.4    O'Shaughnessy, R.5    Mahoney, M.G.6
  • 7
    • 0037941582 scopus 로고    scopus 로고
    • Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin
    • Levy-Nissenbaum E, Betz RC, Frydman M, Simon M, Lahat H, Bakhan T et al. (2003) Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin. Nat Genet 34:151-3
    • (2003) Nat Genet , vol.34 , pp. 151-153
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  • 8
    • 0031577327 scopus 로고    scopus 로고
    • The 6H1 orphan receptor, claimed to be the p2y5 receptor, does not mediate nucleotide-promoted second messenger responses
    • Li Q, Schachter JB, Harden TK, Nicholas RA (1997) The 6H1 orphan receptor, claimed to be the p2y5 receptor, does not mediate nucleotide-promoted second messenger responses. Biochem Biophys Res Commun 236:455-60
    • (1997) Biochem Biophys Res Commun , vol.236 , pp. 455-460
    • Li, Q.1    Schachter, J.B.2    Harden, T.K.3    Nicholas, R.A.4
  • 9
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    • A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families
    • Nahum S, Pasternack SM, Pforr J, Indelman M, Wollnik B, Bergman R et al. (2008) A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families. Arch Dermatol Res. 301:391-3
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  • 10
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    • G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth
    • Pasternack SM, von Kügelgen I, Al Aboud K, Lee YA, Rüschendorf F, Voss K et al. (2008) G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. Nat Genet 40:329-34
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.