-
1
-
-
0030716498
-
Shattuck lecture-cardiovascular medicine at the turn of the millennium: Triumphs, concerns, and opportunities
-
(1997)
N Engl J Med
, vol.337
, pp. 1360-1369
-
-
Braunwald, E.1
-
3
-
-
0032554671
-
Statin trials and goals of cholesterol-lowering therapy
-
(1998)
Circulation
, vol.97
, pp. 1436-1439
-
-
Grundy, S.M.1
-
8
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
(2000)
N Engl J Med
, vol.343
, pp. 1688-1696
-
-
Kamisago, M.1
Sharma, S.D.2
DePalma, S.R.3
Solomon, S.4
Sharma, P.5
McDonough, B.6
Smoot, L.7
Mullen, M.P.8
Woolf, P.K.9
Wigle, E.D.10
Seidman, J.G.11
Seidman, C.E.12
-
11
-
-
0030883787
-
The genetics of dilated cardiomyopathy - Emerging clues to the puzzle
-
(1997)
N Engl J Med
, vol.337
, pp. 1080-1081
-
-
Leiden, J.M.1
-
12
-
-
0028908119
-
The cellular basis of dilated cardiomyopathy in humans
-
(1995)
J Mol Cell Cardiol
, vol.27
, pp. 291-305
-
-
Beltrami, C.A.1
Finato, N.2
Rocco, M.3
Feruglio, G.A.4
Puricelli, C.5
Cigola, E.6
Sonnenblick, E.H.7
Olivetti, G.8
Anversa, P.9
-
14
-
-
0006100572
-
-
Online Mendelian Inheritance in Man, OMIM (TM) McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD)
-
(2000)
-
-
-
15
-
-
0032540267
-
A calcineurin-dependent transcriptional pathway for cardiac hypertrophy
-
(1998)
Cell
, vol.93
, pp. 215-228
-
-
Molkentin, J.D.1
Lu, J.R.2
Antos, C.L.3
Markham, B.4
Richardson, J.5
Robbins, J.6
Grant, S.R.7
Olson, E.N.8
-
17
-
-
19244386873
-
CaM kinase signaling induces cardiac hypertrophy and activates the MEF2 transcription factor in vivo
-
(2000)
J Clin Invest
, vol.105
, pp. 1395-1406
-
-
Passier, R.1
Zeng, H.2
Frey, N.3
Naya, F.J.4
Nicol, R.L.5
McKinsey, T.A.6
Overbeek, P.7
Richardson, J.A.8
Grant, S.R.9
Olson, E.N.10
-
19
-
-
0033667464
-
Transcriptional regulation of cardiac development: Implications for congenital heart disease and DiGeorge syndrome
-
(2000)
Pediatr Res
, vol.48
, pp. 717-724
-
-
Epstein, J.A.1
Buck, C.A.2
-
23
-
-
0032479573
-
Congenital heart disease caused by mutations in the transcription factor NKX2-5
-
(1998)
Science
, vol.281
, pp. 108-111
-
-
Schott, J.J.1
Benson, D.W.2
Basson, C.T.3
Pease, W.4
Silberbach, G.M.5
Moak, J.P.6
Maron, B.J.7
Seidman, C.E.8
Seidman, J.G.9
-
24
-
-
0033430230
-
Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
-
(1999)
J Clin Invest
, vol.104
, pp. 1567-1573
-
-
Benson, D.W.1
Silberbach, G.M.2
Kavanaugh-McHugh, A.3
Cottrill, C.4
Zhang, Y.5
Riggs, S.6
Smalls, O.7
Johnson, M.C.8
Watson, M.S.9
Seidman, J.G.10
Seidman, C.E.11
Plowden, J.12
Kugler, J.D.13
-
28
-
-
17444434198
-
Frequency of 22q11 deletions in patients with conotruncal defects
-
(1998)
J Am Coll Cardiol
, vol.32
, pp. 492-498
-
-
Goldmuntz, E.1
Clark, B.J.2
Mitchell, L.E.3
Jawad, A.F.4
Cuneo, B.F.5
Reed, L.6
McDonald-McGinn, D.7
Chien, P.8
Feuer, J.9
Zackai, E.H.10
Emanuel, B.S.11
Driscoll, D.A.12
-
30
-
-
0033598389
-
Congenital heart disease in mice deficient for the DiGeorge syndrome region
-
(1999)
Nature
, vol.401
, pp. 379-383
-
-
Lindsay, E.A.1
Botta, A.2
Jurecic, V.3
Carattini-Rivera, S.4
Cheah, Y.C.5
Rosenblatt, H.M.6
Bradley, A.7
Baldini, A.8
-
31
-
-
0035263599
-
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice
-
(2001)
Nature
, vol.410
, pp. 97-101
-
-
Lindsay, E.A.1
Vitelli, F.2
Su, H.3
Morishima, M.4
Huynh, T.5
Pramparo, T.6
Jurecic, V.7
Ogunrinu, G.8
Sutherland, H.F.9
Scambler, P.J.10
Bradley, A.11
Baldini, A.12
-
32
-
-
17744395906
-
TBX1 is responsible for cardiovascular defects in velo-cardio- facial/DiGeorge syndrome
-
(2001)
Cell
, vol.104
, pp. 619-629
-
-
Merscher, S.1
Funke, B.2
Epstein, J.A.3
Heyer, J.4
Puech, A.5
Lu, M.M.6
Xavier, R.J.7
Demay, M.B.8
Russell, R.G.9
Factor, S.10
Tokooya, K.11
Jore, B.S.12
Lopez, M.13
Pandita, R.K.14
Lia, M.15
Carrion, D.16
Xu, H.17
Schorle, H.18
Kobler, J.B.19
Scambler, P.20
Wynshaw-Boris, A.21
Skoultchi, A.I.22
Morrow, B.E.23
Kucherlapati, R.24
more..
-
34
-
-
0035653927
-
Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects
-
(2001)
J Med Genet
, vol.38
-
-
Gong, W.1
Gottlieb, S.2
Collins, J.3
Blescia, A.4
Dietz, H.5
Goldmuntz, E.6
McDonald-McGinn, D.M.7
Zackai, E.H.8
Emanuel, B.S.9
Driscoll, D.A.10
Budarf, M.L.11
-
35
-
-
0030636780
-
Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome
-
(1997)
Nat Genet
, vol.15
, pp. 30-35
-
-
Basson, C.T.1
Bachinsky, D.R.2
Lin, R.C.3
Levi, T.4
Elkins, J.A.5
Soults, J.6
Grayzel, D.7
Kroumpouzou, E.8
Traill, T.A.9
Leblanc-Straceski, J.10
Renault, B.11
Kucherlapati, R.12
Seidman, J.G.13
Seidman, C.E.14
-
36
-
-
0030986873
-
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
-
(1997)
Nat Genet
, vol.16
, pp. 311-315
-
-
Bamshad, M.1
Lin, R.C.2
Law, D.J.3
Watkins, W.C.4
Krakowiak, P.A.5
Moore, M.E.6
Franceschini, P.7
Lala, R.8
Holmes, L.B.9
Gebuhr, T.C.10
Bruneau, B.G.11
Schinzel, A.12
Seidman, J.G.13
Seidman, C.E.14
Jorde, L.B.15
-
37
-
-
17944378083
-
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease
-
(2001)
Cell
, vol.106
, pp. 709-721
-
-
Bruneau, B.G.1
Nemer, G.2
Schmitt, J.P.3
Charron, F.4
Robitaille, L.5
Caron, S.6
Conner, D.A.7
Gessler, M.8
Nemer, M.9
Seidman, C.E.10
Seidman, J.G.11
-
46
-
-
0024996141
-
Plasma high density lipoproteins. Metabolism and relationship to atherogenesis
-
(1990)
J Clin Invest
, vol.86
, pp. 379-384
-
-
Tall, A.R.1
-
50
-
-
0033692757
-
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes
-
(2000)
J Clin Invest
, vol.106
, pp. 1263-1270
-
-
Clee, S.M.1
Kastelein, J.J.2
Van Dam, M.3
Marcil, M.4
Roomp, K.5
Zwarts, K.Y.6
Collins, J.A.7
Roelants, R.8
Tamasawa, N.9
Stulc, T.10
Suda, T.11
Ceska, R.12
Boucher, B.13
Rondeau, C.14
DeSouich, C.15
Brooks-Wilson, A.16
Molhuizen, H.O.17
Frohlich, J.18
Genest J., Jr.19
Hayden, M.R.20
more..
-
51
-
-
0343717914
-
High density lipoprotein deficiency and foam cell accumulation in mice with targeted disruption of ATP-binding cassette transporter-1
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 4245-4250
-
-
McNeish, J.1
Aiello, R.J.2
Guyot, D.3
Turi, T.4
Gabel, C.5
Aldinger, C.6
Hoppe, K.L.7
Roach, M.L.8
Royer, L.J.9
De Wet, J.10
Broccardo, C.11
Chimini, G.12
Francone, O.L.13
-
54
-
-
0025104275
-
Increased high-density lipoprotein levels caused by a common cholesteryl-ester transfer protein gene mutation
-
(1990)
N Engl J Med
, vol.323
, pp. 1234-1238
-
-
Inazu, A.1
Brown, M.L.2
Hesler, C.B.3
Agellon, L.B.4
Koizumi, J.5
Takata, K.6
Maruhama, Y.7
Mabuchi, H.8
Tall, A.R.9
-
56
-
-
0027162816
-
Hepatic lipase deficiency. Clinical, biochemical, and molecular genetic characteristics
-
(1993)
Arterioscler Thromb
, vol.13
, pp. 720-728
-
-
Hegele, R.A.1
Little, J.A.2
Vezina, C.3
Maguire, G.F.4
Tu, L.5
Wolever, T.S.6
Jenkins, D.J.7
Connelly, P.W.8
-
58
-
-
18544375474
-
Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans
-
(2002)
Nat Genet
, vol.30
, pp. 102-105
-
-
Arya, R.1
Duggirala, R.2
Almasy, L.3
Rainwater, D.L.4
Mahaney, M.C.5
Cole, S.6
Dyer, T.D.7
Williams, K.8
Leach, R.J.9
Hixson, J.E.10
MacCluer, J.W.11
O'Connell, P.12
Stern, M.P.13
Blangero, J.14
|