274 related articles for article (PubMed ID: 10330430)
1. Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy.
Mogensen J; Klausen IC; Pedersen AK; Egeblad H; Bross P; Kruse TA; Gregersen N; Hansen PS; Baandrup U; Borglum AD
J Clin Invest; 1999 May; 103(10):R39-43. PubMed ID: 10330430
[TBL] [Abstract][Full Text] [Related]
2. A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.
Watkins H; MacRae C; Thierfelder L; Chou YH; Frenneaux M; McKenna W; Seidman JG; Seidman CE
Nat Genet; 1993 Apr; 3(4):333-7. PubMed ID: 7981753
[TBL] [Abstract][Full Text] [Related]
3. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure.
Olson TM; Michels VV; Thibodeau SN; Tai YS; Keating MT
Science; 1998 May; 280(5364):750-2. PubMed ID: 9563954
[TBL] [Abstract][Full Text] [Related]
4. No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy.
Kärkkäinen S; Peuhkurinen K; Jääskeläinen P; Miettinen R; Kärkkäinen P; Kuusisto J; Laakso M
Am Heart J; 2002 Jun; 143(6):E6. PubMed ID: 12075240
[TBL] [Abstract][Full Text] [Related]
5. Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy.
Olson TM; Doan TP; Kishimoto NY; Whitby FG; Ackerman MJ; Fananapazir L
J Mol Cell Cardiol; 2000 Sep; 32(9):1687-94. PubMed ID: 10966831
[TBL] [Abstract][Full Text] [Related]
6. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
Kamisago M; Sharma SD; DePalma SR; Solomon S; Sharma P; McDonough B; Smoot L; Mullen MP; Woolf PK; Wigle ED; Seidman JG; Seidman CE
N Engl J Med; 2000 Dec; 343(23):1688-96. PubMed ID: 11106718
[TBL] [Abstract][Full Text] [Related]
7. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.
Kaski JP; Syrris P; Burch M; Tomé-Esteban MT; Fenton M; Christiansen M; Andersen PS; Sebire N; Ashworth M; Deanfield JE; McKenna WJ; Elliott PM
Heart; 2008 Nov; 94(11):1478-84. PubMed ID: 18467357
[TBL] [Abstract][Full Text] [Related]
8. Malignant familial hypertrophic cardiomyopathy in a family with a 453Arg-->Cys mutation in the beta-myosin heavy chain gene: coexistence of sudden death and end-stage heart failure.
Ko YL; Chen JJ; Tang TK; Cheng JJ; Lin SY; Liou YC; Kuan P; Wu CW; Lien WP; Liew CC
Hum Genet; 1996 May; 97(5):585-90. PubMed ID: 8655135
[TBL] [Abstract][Full Text] [Related]
9. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.
Watkins H; Conner D; Thierfelder L; Jarcho JA; MacRae C; McKenna WJ; Maron BJ; Seidman JG; Seidman CE
Nat Genet; 1995 Dec; 11(4):434-7. PubMed ID: 7493025
[TBL] [Abstract][Full Text] [Related]
10. Novel locus for an inherited cardiomyopathy maps to chromosome 7.
Song L; DePalma SR; Kharlap M; Zenovich AG; Cirino A; Mitchell R; McDonough B; Maron BJ; Seidman CE; Seidman JG; Ho CY
Circulation; 2006 May; 113(18):2186-92. PubMed ID: 16651466
[TBL] [Abstract][Full Text] [Related]
11. Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.
Dausse E; Komajda M; Fetler L; Dubourg O; Dufour C; Carrier L; Wisnewsky C; Bercovici J; Hengstenberg C; al-Mahdawi S
J Clin Invest; 1993 Dec; 92(6):2807-13. PubMed ID: 8254035
[TBL] [Abstract][Full Text] [Related]
12. Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
Thierfelder L; Watkins H; MacRae C; Lamas R; McKenna W; Vosberg HP; Seidman JG; Seidman CE
Cell; 1994 Jun; 77(5):701-12. PubMed ID: 8205619
[TBL] [Abstract][Full Text] [Related]
13. Genetic heterogeneity of familial hypertrophic cardiomyopathy.
Dausse E; Schwartz K
Neuromuscul Disord; 1993; 3(5-6):483-6. PubMed ID: 8186698
[TBL] [Abstract][Full Text] [Related]
14. Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.
Selvi Rani D; Nallari P; Dhandapany PS; Rani J; Meraj K; Ganesan M; Narasimhan C; Thangaraj K
DNA Cell Biol; 2015 May; 34(5):350-9. PubMed ID: 25607779
[TBL] [Abstract][Full Text] [Related]
15. Mapping the locus for familial hypertrophic cardiomyopathy to chromosome 11 in a family with a case of apical hypertrophic cardiomyopathy of the Japanese type.
Ko YL; Chen JJ; Tang TK; Teng MS; Lin SY; Kuan P; Wu CW; Lien WP; Liew CC
Hum Genet; 1996 Apr; 97(4):457-61. PubMed ID: 8834242
[TBL] [Abstract][Full Text] [Related]
16. Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy.
Frank D; Yusuf Rangrez A; Friedrich C; Dittmann S; Stallmeyer B; Yadav P; Bernt A; Schulze-Bahr E; Borlepawar A; Zimmermann WH; Peischard S; Seebohm G; Linke WA; Baba HA; Krüger M; Unger A; Usinger P; Frey N; Schulze-Bahr E
Circ Genom Precis Med; 2019 Aug; 12(8):e002491. PubMed ID: 31430208
[TBL] [Abstract][Full Text] [Related]
17. Novel α-Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical-Pathologic Correlation.
Frustaci A; De Luca A; Guida V; Biagini T; Mazza T; Gaudio C; Letizia C; Russo MA; Galea N; Chimenti C
J Am Heart Assoc; 2018 Feb; 7(4):. PubMed ID: 29440008
[TBL] [Abstract][Full Text] [Related]
18. Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
Solomon SD; Jarcho JA; McKenna W; Geisterfer-Lowrance A; Germain R; Salerni R; Seidman JG; Seidman CE
J Clin Invest; 1990 Sep; 86(3):993-9. PubMed ID: 1975599
[TBL] [Abstract][Full Text] [Related]
19. Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.
Yu B; French JA; Carrier L; Jeremy RW; McTaggart DR; Nicholson MR; Hambly B; Semsarian C; Richmond DR; Schwartz K; Trent RJ
J Med Genet; 1998 Mar; 35(3):205-10. PubMed ID: 9541104
[TBL] [Abstract][Full Text] [Related]
20. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X
Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]