-
3
-
-
18744433901
-
Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
-
(1999)
J Clin Invest
, vol.103
, pp. 39-43
-
-
Mogensen, J.1
Klausen, I.C.2
Pedersen, A.K.3
Egeblad, H.4
Bross, P.5
Kruse, T.A.6
Gregersen, N.7
Hansen, P.S.8
Baandrup, U.9
Borglum, A.D.10
-
4
-
-
0029143611
-
Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3
-
(1995)
J Clin Invest
, vol.96
, pp. 1216-1220
-
-
MacRae, C.A.1
Ghaisas, N.2
Kass, S.3
Donnelly, S.4
Basson, C.T.5
Watkins, H.6
Anan, R.7
Thierfelder, L.H.8
McGarry, K.9
Rowland, E.10
McKenna, W.J.11
Seidman, J.G.12
Seidman, C.E.13
-
5
-
-
15644366960
-
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy
-
(1998)
J Mol Med
, vol.76
, pp. 208-214
-
-
Flavigny, J.1
Richard, P.2
Isnard, R.3
Carrier, L.4
Charron, P.5
Bonne, G.6
Forissier, J.F.7
Desnos, M.8
Dubourg, O.9
Komajda, M.10
Schwartz, K.11
Hainque, B.12
-
6
-
-
0031066438
-
Symposium on gene abnormalities in medical diseases. 3. Molecular genetics of hypertrophic cardiomyopathy in Japan
-
(1997)
Intern Med
, vol.36
, pp. 152-154
-
-
Kimura, A.1
-
8
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy
-
(1995)
N Engl J Med
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.J.2
Thierfelder, L.3
Suk, H.J.4
Anan, R.5
O'Donoghue, A.6
Spirito, P.7
Matsumori, A.8
Moravec, C.S.9
Seidman, J.G.10
Seidman, C.E.11
-
9
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
(1997)
Nat Genet
, vol.16
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park, J.E.3
Nishi, H.4
Satoh, M.5
Takahashi, M.6
Hiroi, S.7
Sasaoka, T.8
Ohbuchi, N.9
Nakamura, T.10
Koyanagi, T.11
Hwang, T.H.12
Choo, J.A.13
Chung, K.S.14
Hasegawa, A.15
Nagai, R.16
Okazaki, O.17
Nakamura, H.18
Matsuzaki, M.19
Sakamoto, T.20
Toshima, H.21
Koga, Y.22
Imaizumi, T.23
Sasazuki, T.24
more..
-
11
-
-
0346315804
-
Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T gene
-
(1998)
J Mol Cell Cardiol
, vol.30
, pp. 1247-1253
-
-
Farza, H.1
Townsend, P.J.2
Carrier, L.3
Barton, P.J.4
Mesnard, L.5
Bahrend, E.6
Forissier, J.F.7
Fiszman, M.8
Yacoub, M.H.9
Schwartz, K.10
-
12
-
-
0028178083
-
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
MacRae, C.3
Lamas, R.4
McKenna, W.5
Vosberg, H.P.6
Seidman, J.G.7
Seidman, C.E.8
-
13
-
-
0027420155
-
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3
-
(1993)
Nat Genet
, vol.3
, pp. 333-337
-
-
Watkins, H.1
MacRae, C.2
Thierfelder, L.3
Chou, Y.H.4
Frenneaux, M.5
McKenna, W.6
Seidman, J.G.7
Seidman, C.E.8
-
16
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
17
-
-
0028302366
-
Human cardiac troponin T: Identification of fetal isoforms and assignment of the TNNT2 locus to chromosome 1q
-
(1994)
Genomics
, vol.21
, pp. 311-316
-
-
Townsend, P.J.1
Farza, H.2
MacGeoch, C.3
Spurr, N.K.4
Wade, R.5
Gahlmann, R.6
Yacoub, M.H.7
Barton, P.J.8
-
18
-
-
0005556446
-
-
Database
-
-
-
-
19
-
-
0005555988
-
-
Database
-
-
-
-
23
-
-
0028886136
-
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
-
(1995)
Nat Genet
, vol.11
, pp. 438-440
-
-
Bonne, G.1
Carrier, L.2
Bercovici, J.3
Cruaud, C.4
Richard, P.5
Hainque, B.6
Gautel, M.7
Labeit, S.8
James, M.9
Beckmann, J.10
Weissenbach, J.11
Vosberg, H.P.12
Fiszman, M.13
Komajda, M.14
Schwartz, K.15
-
24
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
(1995)
Nat Genet
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
Jarcho, J.A.4
MacRae, C.5
McKenna, W.J.6
Maron, B.J.7
Seidman, J.G.8
Seidman, C.E.9
-
25
-
-
0027161005
-
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11
-
(1993)
Nat Genet
, vol.4
, pp. 311-313
-
-
Carrier, L.1
Hengstenberg, C.2
Beckmann, J.S.3
Guicheney, P.4
Dufour, C.5
Bercovici, J.6
Dausse, E.7
Berebbi Bertrand, I.8
Wisnewsky, C.9
Pulvenis, D.10
Fetler, L.11
Vignal, A.12
Weissenbach, J.13
Hillaire, D.14
Feingold, J.15
Bouhour, J.B.16
Hagège, A.A.17
Desnos, M.18
Isnard, R.19
Dubourg, O.20
Komajda, M.21
Schwartz, K.22
more..
-
26
-
-
0031055854
-
Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy
-
(1997)
Circ Res
, vol.80
, pp. 427-434
-
-
Carrier, L.1
Bonne, G.2
Bährend, E.3
Yu, B.4
Richard, P.5
Niel, F.6
Hainque, B.7
Cruaud, C.8
Gary, F.9
Labeit, S.10
Bouhour, J.B.11
Dubourg, O.12
Desnos, M.13
Hagège, A.A.14
Trent, R.J.15
Komajda, M.16
Fiszman, M.17
Schwartz, K.18
-
29
-
-
0024514081
-
A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene
-
(1989)
Am J Hum Genet
, vol.44
, pp. 397-401
-
-
Litt, M.1
Luty, J.A.2
-
31
-
-
0033119752
-
Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain
-
(1999)
J Mol Cell Cardiol
, vol.31
, pp. 745-750
-
-
Bundgaard, H.1
Havndrup, O.2
Andersen, P.S.3
Larsen, L.A.4
Brandt, N.J.5
Vuust, J.6
Kjeldsen, K.7
Christiansen, M.8
-
32
-
-
0027180678
-
A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 6270-6274
-
-
Thierfelder, L.1
MacRae, C.2
Watkins, H.3
Tomfohrde, J.4
Williams, M.5
McKenna, W.6
Bohm, K.7
Noeske, G.8
Schlepper, M.9
Bowcock, A.10
Vosberg, H.P.11
Seidman, J.G.12
Seidman, C.E.13
-
33
-
-
0031883848
-
A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity
-
(1998)
Circ Res
, vol.82
, pp. 106-115
-
-
Bottinelli, R.1
Coviello, D.A.2
Redwood, C.S.3
Pellegrino, M.A.4
Maron, B.J.5
Spirito, P.6
Watkins, H.7
Reggiani, C.8
-
34
-
-
0031042881
-
Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin gene
-
(1997)
J Am Coll Cardiol
, vol.29
, pp. 635-640
-
-
Coviello, D.A.1
Maron, B.J.2
Spirito, P.3
Watkins, H.4
Vosberg, H.P.5
Thierfelder, L.6
Schoen, F.J.7
Seidman, J.G.8
Seidman, C.E.9
-
35
-
-
0344878860
-
The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population
-
(1998)
J Am Coll Cardiol
, vol.32
, pp. 1709-1716
-
-
Jaaskelainen, P.1
Soranta, M.2
Miettinen, R.3
Saarinen, L.4
Pihlajamaki, J.5
Silvennoinen, K.6
Tikanoja, T.7
Laakso, M.8
Kuusisto, J.9
-
36
-
-
0033538612
-
Mouse model of a familial hypertrophic cardiomyopathy mutation in alpha-tropomyosin manifests cardiac dysfunction
-
(1999)
Circ Res
, vol.85
, pp. 47-56
-
-
Muthuchamy, M.1
Pieples, K.2
Rethinasamy, P.3
Hoit, B.4
Grupp, I.L.5
Boivin, G.P.6
Wolska, B.7
Evans, C.8
Solaro, R.J.9
Wieczorek, D.F.10
-
39
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
(1995)
Nat Genet
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
|