-
1
-
-
0036801569
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|