-
1
-
-
0031885093
-
Familial dilated cardiomyopathy: Cardiac abnormalities are common in asymptomatic relatives and may represent early disease
-
Baig MK, Goldman JH, Caforio AL, Coonar AS, Keeling PJ, McKenna WJ (1998) Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease. J Am Coll Cardiol 31:195-201
-
(1998)
J Am Coll Cardiol
, vol.31
, pp. 195-201
-
-
Baig, M.K.1
Goldman, J.H.2
Caforio, A.L.3
Coonar, A.S.4
Keeling, P.J.5
McKenna, W.J.6
-
2
-
-
0020974404
-
An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes
-
Barth PG, Scholte HR, Berden JA, Van der Klei-Van Moorsel JM, Luyt-Houwen IE, Van 't Veer-Korthof ET, Van der Harten JJ, Sobotka-Plojhar MA (1983) An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes. J Neurol Sci 62:327-355
-
(1983)
J Neurol Sci
, vol.62
, pp. 327-355
-
-
Barth, P.G.1
Scholte, H.R.2
Berden, J.A.3
Van Der Klei-Van Moorsel, J.M.4
Luyt-Houwen, I.E.5
Van 'T Veer-Korthof, E.T.6
Van Der Harten, J.J.7
Sobotka-Plojhar, M.A.8
-
3
-
-
0026344545
-
The cyclophilin multigene family of peptidyl-prolyl isomerases. Characterization of three separate human isoforms
-
Bergsma DJ, Eder C, Gross M, Kersten H, Sylvester D, Appelbaum E, Cusimano D, Livi GP, McLaughlin MM, Kasyan K, et al (1991) The cyclophilin multigene family of peptidyl-prolyl isomerases. Characterization of three separate human isoforms. J Biol Chem 266:23204-23214
-
(1991)
J Biol Chem
, vol.266
, pp. 23204-23214
-
-
Bergsma, D.J.1
Eder, C.2
Gross, M.3
Kersten, H.4
Sylvester, D.5
Appelbaum, E.6
Cusimano, D.7
Livi, G.P.8
McLaughlin, M.M.9
Kasyan, K.10
-
4
-
-
0023215347
-
X-linked dilated cardiomyopathy
-
Berko BA, Swift M (1987) X-linked dilated cardiomyopathy. N Engl J Med 316:1186-1191
-
(1987)
N Engl J Med
, vol.316
, pp. 1186-1191
-
-
Berko, B.A.1
Swift, M.2
-
5
-
-
0029963145
-
A novel X-linked gene, G4.5, is responsible for Barth syndrome
-
Bione S, D'Adamo P, Maestrini E, Gedeon AK, Bolhuis PA, Toniolo D (1996) A novel X-linked gene, G4.5, is responsible for Barth syndrome. Nat Genet 12:385-389
-
(1996)
Nat Genet
, vol.12
, pp. 385-389
-
-
Bione, S.1
D'Adamo, P.2
Maestrini, E.3
Gedeon, A.K.4
Bolhuis, P.A.5
Toniolo, D.6
-
6
-
-
0030774767
-
Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome
-
Bleyl SB, Mumford BR, Thompson V, Carey JC, Pysher TJ, Chin TK, Ward K (1997) Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome. Am J Hum Genet 61:868-872
-
(1997)
Am J Hum Genet
, vol.61
, pp. 868-872
-
-
Bleyl, S.B.1
Mumford, B.R.2
Thompson, V.3
Carey, J.C.4
Pysher, T.J.5
Chin, T.K.6
Ward, K.7
-
7
-
-
0027359722
-
Natural history and patterns of current practice in heart failure. The studies of left ventricular dysfunction (SOLVD) investigators
-
Bourassa MG, Gurne O, Bangdiwala SI, Ghali JK, Young JB, Rousseau M, Johnstone DE, Yusuf S (1993) Natural history and patterns of current practice in heart failure. The studies of left ventricular dysfunction (SOLVD) investigators. J Am Coll Cardiol 22[Suppl A]: 14A-19A
-
(1993)
J Am Coll Cardiol
, vol.22
, Issue.SUPPL. A
-
-
Bourassa, M.G.1
Gurne, O.2
Bangdiwala, S.I.3
Ghali, J.K.4
Young, J.B.5
Rousseau, M.6
Johnstone, D.E.7
Yusuf, S.8
-
8
-
-
0022600645
-
Detection of Coxsackie-B-virus-specific RNA sequences in myocardial biopsy samples from patients with myocarditis and dilated cardiomyopathy
-
Bowles NE, Richardson PJ, Olsen EGJ, Archard LC (1986) Detection of Coxsackie-B-virus-specific RNA sequences in myocardial biopsy samples from patients with myocarditis and dilated cardiomyopathy. Lancet i: 1120-1123
-
(1986)
Lancet
, vol.1
, pp. 1120-1123
-
-
Bowles, N.E.1
Richardson, P.J.2
Olsen, E.G.J.3
Archard, L.C.4
-
9
-
-
0029784361
-
Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23
-
Bowles KR, Gajarski R, Porter P, Goytia V, Bachinski L, Roberts R, Pignatelli R, Towbin JA (1996) Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23. J Clin Invest 98:1355-1360
-
(1996)
J Clin Invest
, vol.98
, pp. 1355-1360
-
-
Bowles, K.R.1
Gajarski, R.2
Porter, P.3
Goytia, V.4
Bachinski, L.5
Roberts, R.6
Pignatelli, R.7
Towbin, J.A.8
-
11
-
-
0032401567
-
Cyclophilin-D binds strongly to complexes of the voltage-dependent anion channel and the adenine nucleotide translocase to form the permeability transition pore
-
Crompton M, Virji S, Ward JM (1998) Cyclophilin-D binds strongly to complexes of the voltage-dependent anion channel and the adenine nucleotide translocase to form the permeability transition pore. Eur J Biochem 258:729-735
-
(1998)
Eur J Biochem
, vol.258
, pp. 729-735
-
-
Crompton, M.1
Virji, S.2
Ward, J.M.3
-
12
-
-
16944366521
-
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies
-
D'Adamo P, Fassone L, Gedeon A, Janssen EA, Bione S, Bolhuis PA, Barth PG, Wilson M, Haan E, Orstavik KH, Patton MA, Green AJ, Zammarchi E, Donati MA, Toniolo D (1997) The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. Am J Hum Genet 61:862-867
-
(1997)
Am J Hum Genet
, vol.61
, pp. 862-867
-
-
D'Adamo, P.1
Fassone, L.2
Gedeon, A.3
Janssen, E.A.4
Bione, S.5
Bolhuis, P.A.6
Barth, P.G.7
Wilson, M.8
Haan, E.9
Orstavik, K.H.10
Patton, M.A.11
Green, A.J.12
Zammarchi, E.13
Donati, M.A.14
Toniolo, D.15
-
13
-
-
0028116218
-
Idiopathic dilated cardiomyopathy
-
Dec GW, Fuster V (1994) Idiopathic dilated cardiomyopathy. N Engl J Med 331:1564-1575
-
(1994)
N Engl J Med
, vol.331
, pp. 1564-1575
-
-
Dec, G.W.1
Fuster, V.2
-
14
-
-
0032561502
-
A physical map of 30,000 human genes
-
Deloukas P, Schuler GD, Gyapay G, et al (1998) A physical map of 30,000 human genes. Science 282:744-746
-
(1998)
Science
, vol.282
, pp. 744-746
-
-
Deloukas, P.1
Schuler, G.D.2
Gyapay, G.3
-
15
-
-
0028801254
-
Localization of a gene responsible for familial dilated cardiomyopathy to chromosome Iq32
-
Durand JB, Bachinski LL, Bieling LC, Czernuszewicz GZ, Abchee AB, Yu QT, Tapscolt T, Hill R, Ifeqwu J, Marian AJ, Brugada R, Daiger S, Gregoritch JM, Anderson JL, Quinones M, Towbin JA, Roberts R (1995) Localization of a gene responsible for familial dilated cardiomyopathy to chromosome Iq32. Circulation 92:3387-3389
-
(1995)
Circulation
, vol.92
, pp. 3387-3389
-
-
Durand, J.B.1
Bachinski, L.L.2
Bieling, L.C.3
Czernuszewicz, G.Z.4
Abchee, A.B.5
Yu, Q.T.6
Tapscolt, T.7
Hill, R.8
Ifeqwu, J.9
Marian, A.J.10
Brugada, R.11
Daiger, S.12
Gregoritch, J.M.13
Anderson, J.L.14
Quinones, M.15
Towbin, J.A.16
Roberts, R.17
-
16
-
-
0015222453
-
Dominant and recessive modes of inheritance in idiopathic cardiomyopathy
-
Emanuel R, Withers R, O'Brien K (1971) Dominant and recessive modes of inheritance in idiopathic cardiomyopathy. Lancet 2:1065-1067
-
(1971)
Lancet
, vol.2
, pp. 1065-1067
-
-
Emanuel, R.1
Withers, R.2
O'Brien, K.3
-
17
-
-
0024959449
-
Cydophilin and peptidyl-prolyl cis-trans isomerase are probably identical proteins
-
Fischer G, Wittmann-Liebold B. Lang K, Kiefhaber T, Schmid FX (1989) Cydophilin and peptidyl-prolyl cis-trans isomerase are probably identical proteins. Nature 337:476-478
-
(1989)
Nature
, vol.337
, pp. 476-478
-
-
Fischer, G.1
Wittmann-Liebold, B.2
Lang, K.3
Kiefhaber, T.4
Schmid, F.X.5
-
18
-
-
0026499641
-
Isomerase and chaperone activity of prolyl isomerase in the folding of carbonic anhydrase
-
Freskgard PO, Bergenhem N, Jonsson BH, Svensson M, Carlsson U (1992) Isomerase and chaperone activity of prolyl isomerase in the folding of carbonic anhydrase. Science 258:466-468
-
(1992)
Science
, vol.258
, pp. 466-468
-
-
Freskgard, P.O.1
Bergenhem, N.2
Jonsson, B.H.3
Svensson, M.4
Carlsson, U.5
-
19
-
-
0023150788
-
Autosomal recessive inheritance of idiopathic dilated cardiomyopathy in a Madeira Portuguese kindred
-
Goldblatt J, Melmed J, Rose AG (1987) Autosomal recessive inheritance of idiopathic dilated cardiomyopathy in a Madeira Portuguese kindred. Clin Genet 31:249-254
-
(1987)
Clin Genet
, vol.31
, pp. 249-254
-
-
Goldblatt, J.1
Melmed, J.2
Rose, A.G.3
-
20
-
-
0031951537
-
Frequency and phenotypes of familial dilated cardiomyopathy
-
Grunig E, Tasman JA, Kucherer H, Franz W, Kubler W, Katus HA (1998) Frequency and phenotypes of familial dilated cardiomyopathy. J Am Coll Cardiol 31:186-194
-
(1998)
J Am Coll Cardiol
, vol.31
, pp. 186-194
-
-
Grunig, E.1
Tasman, J.A.2
Kucherer, H.3
Franz, W.4
Kubler, W.5
Katus, H.A.6
-
21
-
-
0032504709
-
Elucidating the molecular mechanism of the permeability transition pore and its role in reperfusion injury of the heart
-
Halestrap AP, Kerr PM, Javadov S, Woodfield KY (1998) Elucidating the molecular mechanism of the permeability transition pore and its role in reperfusion injury of the heart. Biochim Biophys Acta 1366:79-94
-
(1998)
Biochim Biophys Acta
, vol.1366
, pp. 79-94
-
-
Halestrap, A.P.1
Kerr, P.M.2
Javadov, S.3
Woodfield, K.Y.4
-
22
-
-
0021159379
-
Cyclophilin: A specific cytosolic binding protein for cyclosporin A
-
Handschumacher RE, Harding MW, Rice J, Drugge RJ, Speicher DW (1984) Cyclophilin: a specific cytosolic binding protein for cyclosporin A. Science 226:544-547
-
(1984)
Science
, vol.226
, pp. 544-547
-
-
Handschumacher, R.E.1
Harding, M.W.2
Rice, J.3
Drugge, R.J.4
Speicher, D.W.5
-
23
-
-
0030741693
-
Nitric oxide induces apoptosis via triggering mitochondrial permeability transition
-
Hortelano S, Dallaporta B, Zamzami N, Hirsch T, Susin SA, Marzo I, Bosca L, Kroemer G (1997) Nitric oxide induces apoptosis via triggering mitochondrial permeability transition. FEBS Lett 410:373-377
-
(1997)
FEBS Lett
, vol.410
, pp. 373-377
-
-
Hortelano, S.1
Dallaporta, B.2
Zamzami, N.3
Hirsch, T.4
Susin, S.A.5
Marzo, I.6
Bosca, L.7
Kroemer, G.8
-
24
-
-
0030728921
-
Mutation characterization and genotype-phenotype correlation in Barth syndrome
-
Johnston J, Kelley RI, Feigenbaum A, Cox GF, Iyer GS, Funanage VL, Proujansky R (1997) Mutation characterization and genotype-phenotype correlation in Barth syndrome. Am J Hum Genet 61:1053-1058
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1053-1058
-
-
Johnston, J.1
Kelley, R.I.2
Feigenbaum, A.3
Cox, G.F.4
Iyer, G.S.5
Funanage, V.L.6
Proujansky, R.7
-
25
-
-
0028295899
-
The causes of dilated cardiomyopathy: A clinicopathologic review of 673 consecutive patients
-
Kasper EK, Agena WRP, Hutchins GM, Deckers JW, Hare JM, Baughman KL (1994) The causes of dilated cardiomyopathy: a clinicopathologic review of 673 consecutive patients. J Am Coll Cardiol 23:586-590
-
(1994)
J Am Coll Cardiol
, vol.23
, pp. 586-590
-
-
Kasper, E.K.1
Agena, W.R.P.2
Hutchins, G.M.3
Deckers, J.W.4
Hare, J.M.5
Baughman, K.L.6
-
26
-
-
0028145745
-
A genetic defect that causes conduction system disease and dilated cardiomyopathy maps to 1p1-1q1
-
Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB, Cody RJ, Fishman MC, Cox N, Kong A, Wooley CT, Seidman JG, Seidman CE (1994) A genetic defect that causes conduction system disease and dilated cardiomyopathy maps to 1p1-1q1. Nat Genet 7:546-551
-
(1994)
Nat Genet
, vol.7
, pp. 546-551
-
-
Kass, S.1
MacRae, C.2
Graber, H.L.3
Sparks, E.A.4
McNamara, D.5
Boudoulas, H.6
Basson, C.T.7
Baker, P.B.8
Cody, R.J.9
Fishman, M.C.10
Cox, N.11
Kong, A.12
Wooley, C.T.13
Seidman, J.G.14
Seidman, C.E.15
-
27
-
-
0029009393
-
Familial dilated cardiomyopathy in the United Kingdom
-
Keeling PJ, Gang Y, Smith G, Seo H, Bent SE, Murday V, Caforio AL, McKenna WJ (1995) Familial dilated cardiomyopathy in the United Kingdom. Br Heart J 73:417-421
-
(1995)
Br Heart J
, vol.73
, pp. 417-421
-
-
Keeling, P.J.1
Gang, Y.2
Smith, G.3
Seo, H.4
Bent, S.E.5
Murday, V.6
Caforio, A.L.7
McKenna, W.J.8
-
28
-
-
0028347574
-
Inherited cardiomyopathies
-
Kelly DP, Strauss AW (1994) Inherited cardiomyopathies. N Engl J Med 330:930-932
-
(1994)
N Engl J Med
, vol.330
, pp. 930-932
-
-
Kelly, D.P.1
Strauss, A.W.2
-
29
-
-
0029151478
-
Linkage of familial dilated cardiomyopathy to chromosome 9
-
Krajinovic M, Pinamonti B, Sinagra G, Vatta M, Severini GM, Milasin J, Filaschi A, Camerini F, Giacci M, Mestroni L (1995) Linkage of familial dilated cardiomyopathy to chromosome 9. Am J Hum Genet 57:846-852
-
(1995)
Am J Hum Genet
, vol.57
, pp. 846-852
-
-
Krajinovic, M.1
Pinamonti, B.2
Sinagra, G.3
Vatta, M.4
Severini, G.M.5
Milasin, J.6
Filaschi, A.7
Camerini, F.8
Giacci, M.9
Mestroni, L.10
-
30
-
-
0031918742
-
The mitochondrial death/life regulator in apoptosis and necrosis
-
Kroemer G, Dallaporta B, Resche-Rigon M (1998) The mitochondrial death/life regulator in apoptosis and necrosis. Annu Rev Physiol 60:619-642
-
(1998)
Annu Rev Physiol
, vol.60
, pp. 619-642
-
-
Kroemer, G.1
Dallaporta, B.2
Resche-Rigon, M.3
-
31
-
-
0026629099
-
Prevalence and etiology of idiopathic dilated cardiomyopathy
-
Manolio TA, Baughman KL, Rodeheffer R, Pearson TA, Bristow JD, Michels VV, Abelman WH, Harlan WR (1992) Prevalence and etiology of idiopathic dilated cardiomyopathy. (Summary of a National Heart, Lung, and Blood Institute Workshop) Am J Cardiol 69:1458-1466
-
(1992)
(Summary of a National Heart, Lung, and Blood Institute Workshop) Am J Cardiol
, vol.69
, pp. 1458-1466
-
-
Manolio, T.A.1
Baughman, K.L.2
Rodeheffer, R.3
Pearson, T.A.4
Bristow, J.D.5
Michels, V.V.6
Abelman, W.H.7
Harlan, W.R.8
-
32
-
-
0031420903
-
Map integration at human chromosome 10: Molecular and cytogenetic analysis of a chromosome-specific somatic cell hybrid panel and genomic clones, based on a well-supported genetic map
-
Marzella R, Kokkinaki MA, Kapsetaki M, Ricco A, Argyrokastritis A, Kamakari S, Sarafidou T, Archidiacono N, Roussou A, Pasparaki A, Rocchi M, Moschonas NK (1997) Map integration at human chromosome 10: molecular and cytogenetic analysis of a chromosome-specific somatic cell hybrid panel and genomic clones, based on a well-supported genetic map. Cytogenet Cell Genet 79:257-265
-
(1997)
Cytogenet Cell Genet
, vol.79
, pp. 257-265
-
-
Marzella, R.1
Kokkinaki, M.A.2
Kapsetaki, M.3
Ricco, A.4
Argyrokastritis, A.5
Kamakari, S.6
Sarafidou, T.7
Archidiacono, N.8
Roussou, A.9
Pasparaki, A.10
Rocchi, M.11
Moschonas, N.K.12
-
33
-
-
0026319459
-
The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
-
Michels VV, Moll PP, Miller FA, Tajik AJ, Chu JS, Driscoll DJ, Burnett JC, Rodeheffer RJ, Chesebro JH, Tazelaar HD (1992) The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. N Engl J Med 326:77-82
-
(1992)
N Engl J Med
, vol.326
, pp. 77-82
-
-
Michels, V.V.1
Moll, P.P.2
Miller, F.A.3
Tajik, A.J.4
Chu, J.S.5
Driscoll, D.J.6
Burnett, J.C.7
Rodeheffer, R.J.8
Chesebro, J.H.9
Tazelaar, H.D.10
-
34
-
-
0027265702
-
Brief report: Deletion of the dystrophin muscle-specific promoter region associated with X-linked dilated cardiomyopathy
-
Muntoni F, Cau M, Ganau A, Congiu R, Arvedi G, Mateddu A, Marrosu MG, Cianchetti C, Realdi G, Cao A, Antonietta M (1993) Brief report: deletion of the dystrophin muscle-specific promoter region associated with X-linked dilated cardiomyopathy. N Engl J Med 329:921-925
-
(1993)
N Engl J Med
, vol.329
, pp. 921-925
-
-
Muntoni, F.1
Cau, M.2
Ganau, A.3
Congiu, R.4
Arvedi, G.5
Mateddu, A.6
Marrosu, M.G.7
Cianchetti, C.8
Realdi, G.9
Cao, A.10
Antonietta, M.11
-
35
-
-
10244254975
-
Apoptosis in myocytes in end-stage heart disease
-
Narula J, Haider N, Virmani R, DiSalvo TG, Kolodgie FD, Hajjar RJ, Schmidt U, Semigran MJ, Dec GW, Khaw B-A (1996) Apoptosis in myocytes in end-stage heart disease. N Engl J Med 335:1182-1189
-
(1996)
N Engl J Med
, vol.335
, pp. 1182-1189
-
-
Narula, J.1
Haider, N.2
Virmani, R.3
DiSalvo, T.G.4
Kolodgie, F.D.5
Hajjar, R.J.6
Schmidt, U.7
Semigran, M.J.8
Dec, G.W.9
Khaw, B.-A.10
-
36
-
-
0028041629
-
Economic impact of heart failure in the United States: Time for a different approach
-
O'Connell JB, Bristow MR (1994) Economic impact of heart failure in the United States: time for a different approach. J Heart Lung Transplant 13:S107-S112
-
(1994)
J Heart Lung Transplant
, vol.13
-
-
O'Connell, J.B.1
Bristow, M.R.2
-
37
-
-
0030031004
-
Mapping a cardiomyopathy locus to chromosome 3p22-p25
-
Olson TM, Keating MT (1996) Mapping a cardiomyopathy locus to chromosome 3p22-p25. J Clin Invest 97:528-532
-
(1996)
J Clin Invest
, vol.97
, pp. 528-532
-
-
Olson, T.M.1
Keating, M.T.2
-
38
-
-
0032076955
-
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
-
Olson TM, Michels VV, Thibodeau SN, Tai YS, Keating MT (1998) Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 280:750-752
-
(1998)
Science
, vol.280
, pp. 750-752
-
-
Olson, T.M.1
Michels, V.V.2
Thibodeau, S.N.3
Tai, Y.S.4
Keating, M.T.5
-
39
-
-
0030922569
-
Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy
-
Ortiz-Lopez R, Li H, Su J, Goytia V, Towbin JA (1997) Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy. Circulation 95:2434-2440
-
(1997)
Circulation
, vol.95
, pp. 2434-2440
-
-
Ortiz-Lopez, R.1
Li, H.2
Su, J.3
Goytia, V.4
Towbin, J.A.5
-
40
-
-
0030932502
-
Recognition of 3'-processing sites of human mRNA precursors
-
Salamov AA, Solovyev VV (1997) Recognition of 3'-processing sites of human mRNA precursors. Comput Appl Biosci 13: 23-28
-
(1997)
Comput Appl Biosci
, vol.13
, pp. 23-28
-
-
Salamov, A.A.1
Solovyev, V.V.2
-
41
-
-
0029565008
-
Genetic heterogeneity in familial dilated cardiomyopathy
-
Schultz KR, Gajarski RJ, Pignatelli R, Goytia V, Roberts R, Bachinski L, Towbin JA (1995) Genetic heterogeneity in familial dilated cardiomyopathy. Biochem Mol Med 56:87-93
-
(1995)
Biochem Mol Med
, vol.56
, pp. 87-93
-
-
Schultz, K.R.1
Gajarski, R.J.2
Pignatelli, R.3
Goytia, V.4
Roberts, R.5
Bachinski, L.6
Towbin, J.A.7
-
42
-
-
0026729835
-
Mitochondrial genetics: Principles and practice
-
Shoffner JM, Wallace DC (1992) Mitochondrial genetics: principles and practice. Am J Hum Genet 51:1179-1186
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1179-1186
-
-
Shoffner, J.M.1
Wallace, D.C.2
-
43
-
-
0033514986
-
Familial dilated cardiomyopathy locus maps to chromosome 2q31
-
Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE (1999) Familial dilated cardiomyopathy locus maps to chromosome 2q31. Circulation 99:1022-1026
-
(1999)
Circulation
, vol.99
, pp. 1022-1026
-
-
Siu, B.L.1
Niimura, H.2
Osborne, J.A.3
Fatkin, D.4
MacRae, C.5
Solomon, S.6
Benson, D.W.7
Seidman, J.G.8
Seidman, C.E.9
-
44
-
-
0030627562
-
The Gene-Finder computer tools for analysis of human and model organisms genome sequences
-
Solovyev V, Salamov A (1997) The Gene-Finder computer tools for analysis of human and model organisms genome sequences. Ismb 5:294-302
-
(1997)
Ismb
, vol.5
, pp. 294-302
-
-
Solovyev, V.1
Salamov, A.2
-
45
-
-
0027215234
-
Molecular genetic aspects of cardiomyopathy
-
Towbin JA (1993) Molecular genetic aspects of cardiomyopathy. Biochem Med Metab Biol 49:285-320
-
(1993)
Biochem Med Metab Biol
, vol.49
, pp. 285-320
-
-
Towbin, J.A.1
-
46
-
-
0028762447
-
X-linked dilated cardiomyopathy
-
Towbin JA, Ortiz-Lopez R (1994) X-linked dilated cardiomyopathy. N Engl J Med 330:369-370
-
(1994)
N Engl J Med
, vol.330
, pp. 369-370
-
-
Towbin, J.A.1
Ortiz-Lopez, R.2
-
47
-
-
0027193330
-
X-linked dilated cardiomyopathy: Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
-
Towbin JA, Hejtmancik JF, Brink P, Gelb BD, Zhu XM, Chamberlain JS, McCabe ERB, Swift M (1993) X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation 87:1854-1865
-
(1993)
Circulation
, vol.87
, pp. 1854-1865
-
-
Towbin, J.A.1
Hejtmancik, J.F.2
Brink, P.3
Gelb, B.D.4
Zhu, X.M.5
Chamberlain, J.S.6
McCabe, E.R.B.7
Swift, M.8
-
48
-
-
0028807019
-
Guidelines for the evaluation and management of heart failure. Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on Evaluation and Management of Heart Failure)
-
Williams JF, Bristow MR, Fowler MB, et al (1995) Guidelines for the evaluation and management of heart failure. Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on Evaluation and Management of Heart Failure). J Am Coll Cardiol 26: 1376-1398
-
(1995)
J Am Coll Cardiol
, vol.26
, pp. 1376-1398
-
-
Williams, J.F.1
Bristow, M.R.2
Fowler, M.B.3
-
50
-
-
0032387842
-
Direct demonstration of a specific interaction between cyclophilin-D and the adenine nucleotide translocase confirms their role in the mitochondrial permeability transition
-
Woodfield K, Ruck A, Brdiczka D, Halestrap AP (1998) Direct demonstration of a specific interaction between cyclophilin-D and the adenine nucleotide translocase confirms their role in the mitochondrial permeability transition. Biochem J 336:287-290
-
(1998)
Biochem J
, vol.336
, pp. 287-290
-
-
Woodfield, K.1
Ruck, A.2
Brdiczka, D.3
Halestrap, A.P.4
-
51
-
-
0019201765
-
Viral myocarditis. A review
-
Woodruff JF (1980) Viral myocarditis. A review. Am J Pathol 101: 425-484
-
(1980)
Am J Pathol
, vol.101
, pp. 425-484
-
-
Woodruff, J.F.1
|