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Volumn 169, Issue 2, 2003, Pages 345-346

A new ABCA1 mutation associated with low HDL cholesterol but without coronary artery disease [1]

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; HIGH DENSITY LIPOPROTEIN CHOLESTEROL;

EID: 0142124350     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0021-9150(03)00151-5     Document Type: Letter
Times cited : (4)

References (11)
  • 1
    • 0036801569 scopus 로고    scopus 로고
    • Alabama: A novel variant associated with HDL deficiency and premature coronary artery disease
    • Alabama: a novel variant associated with HDL deficiency and premature coronary artery disease. Atherosclerosis. 164:2002;245-250.
    • (2002) Atherosclerosis , vol.164 , pp. 245-250
    • Hong, S.H.1    Rhyne, J.2    Zeller, K.3    Miller, M.4
  • 2
    • 0032813809 scopus 로고    scopus 로고
    • The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
    • Bodzioch M., Orso E., Klucken J., et al. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat. Genet. 22:1999;347-351.
    • (1999) Nat. Genet. , vol.22 , pp. 347-351
    • Bodzioch, M.1    Orso, E.2    Klucken, J.3
  • 3
    • 0032813808 scopus 로고    scopus 로고
    • Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
    • Brook-Wilson A., Marcil M., Clee S.M., et al. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat. Genet. 22:1999;336-345.
    • (1999) Nat. Genet. , vol.22 , pp. 336-345
    • Brook-Wilson, A.1    Marcil, M.2    Clee, S.M.3
  • 4
    • 0016431779 scopus 로고
    • The pathology of Tangier disease. A light and electron microscopic study
    • Ferrans V.J., Fredrickson D.S. The pathology of Tangier disease. A light and electron microscopic study. Am. J. Pathol. 78:1975;101-158.
    • (1975) Am. J. Pathol. , vol.78 , pp. 101-158
    • Ferrans, V.J.1    Fredrickson, D.S.2
  • 6
    • 0018953911 scopus 로고
    • Coronary heart disease prevalence and other clinical features in familial high-density lipoprotein deficiency (Tangier disease)
    • Schaefer E.J., Zech L.A., Schwartz D.E., Brewer H.B. Coronary heart disease prevalence and other clinical features in familial high-density lipoprotein deficiency (Tangier disease). Ann. Int. Med. 93:1980;261-266.
    • (1980) Ann. Int. Med. , vol.93 , pp. 261-266
    • Schaefer, E.J.1    Zech, L.A.2    Schwartz, D.E.3    Brewer, H.B.4
  • 7
    • 0025060889 scopus 로고
    • Dyslipidemias with desirable plasma total cholesterol levels and angiographically demonstrated coronary artery disease
    • Miller M., Mead L., Kwiterovich P.O., et al. Dyslipidemias with desirable plasma total cholesterol levels and angiographically demonstrated coronary artery disease. Am. J. Cardiol. 65:1990;1-5.
    • (1990) Am. J. Cardiol. , vol.65 , pp. 1-5
    • Miller, M.1    Mead, L.2    Kwiterovich, P.O.3
  • 10
    • 0037031835 scopus 로고    scopus 로고
    • Naturally occurring mutations in ABCA1's largest extracellular loops can disrupt its direct interaction with apolipoprotein A-I
    • Fitzgerald M.L., Morris A.L., Rhee J.S., Andersson L.P., Mendez A.J., Freeman M.W. Naturally occurring mutations in ABCA1's largest extracellular loops can disrupt its direct interaction with apolipoprotein A-I. J. Biol. Chem. 277:(36):2002;33178-33187.
    • (2002) J. Biol. Chem. , vol.277 , Issue.36 , pp. 33178-33187
    • Fitzgerald, M.L.1    Morris, A.L.2    Rhee, J.S.3    Andersson, L.P.4    Mendez, A.J.5    Freeman, M.W.6
  • 11
    • 0032813660 scopus 로고    scopus 로고
    • Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
    • Rust S., Rosier M., Funke H., et al. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat. Genet. 22:1999;352-355.
    • (1999) Nat. Genet. , vol.22 , pp. 352-355
    • Rust, S.1    Rosier, M.2    Funke, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.