Compounds > valine

valine and Cardiomyopathy, Hypertrophic

valine has been researched along with Cardiomyopathy, Hypertrophic in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (25.00)18.2507
2000's5 (62.50)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aguiar-Pulido, V; Huang, W; Kazmierczak, K; Narasimhan, G; Szczesna-Cordary, D; Zhou, Z1
Fujita, T; Goto, A; Hirata, Y; Nagai, R; Nishimatsu, H; Oba, S; Omata, M; Satonaka, H; Suzuki, E; Takeda, R1
Kawano, H; Koide, Y; Nakamizo, R; Seto, S; Toda, G; Yano, K1
Gong, HP; Li, L; Ma, X; Miao, Y; Sun, H; Zhang, W; Zhang, Y; Zhong, M1
Cohn, G; Cyran, F; Dalakas, MC; Epstein, ND; Fananapazir, L1
Azuma, J; Kishimoto, T; Nagata, S; Nakajima-Taniguchi, C; Yamauchi-Takihara, K1
Andersen, PS; Bundgaard, H; Christiansen, M; Havndrup, O; Kjeldsen, K; Larsen, LA; Vuust, J2

Trials

1 trial(s) available for valine and Cardiomyopathy, Hypertrophic

ArticleYear
Valsartan decreases type I collagen synthesis in patients with hypertrophic cardiomyopathy.
    Circulation journal : official journal of the Japanese Circulation Society, 2005, Volume: 69, Issue:10

    Topics: Adult; Aged; Angiotensin II Type 1 Receptor Blockers; Cardiomyopathy, Hypertrophic; Collagen Type I; Female; Fibrosis; Humans; Male; Middle Aged; Myocardium; Tetrazoles; Valine; Valsartan

2005

Other Studies

7 other study(ies) available for valine and Cardiomyopathy, Hypertrophic

ArticleYear
Gene expression patterns in transgenic mouse models of hypertrophic cardiomyopathy caused by mutations in myosin regulatory light chain.
    Archives of biochemistry and biophysics, 2016, 07-01, Volume: 601

    Topics: Algorithms; Animals; Arginine; Cardiomyopathy, Hypertrophic; Computational Biology; Gene Expression Profiling; Gene Expression Regulation; Glutamic Acid; Glutamine; Lysine; Mice; Mice, Transgenic; Multigene Family; Mutation; Myocardium; Myosin Light Chains; Oligonucleotide Array Sequence Analysis; Phenotype; Principal Component Analysis; Valine

2016
Calcineurin promotes the expression of monocyte chemoattractant protein-1 in vascular myocytes and mediates vascular inflammation.
    Circulation research, 2004, Mar-19, Volume: 94, Issue:5

    Topics: Angiotensin II; Animals; Calcineurin; Calcium Signaling; Calcium-Calmodulin-Dependent Protein Kinases; Cardiomyopathy, Hypertrophic; Cells, Cultured; Chemokine CCL2; Cyclosporine; Femoral Artery; Gene Expression Regulation; Humans; Hyperplasia; Imidazoles; Macrophages; MAP Kinase Kinase 6; Muscle, Smooth, Vascular; Myocytes, Smooth Muscle; Promoter Regions, Genetic; Protein Biosynthesis; Proteins; Pyridines; Rats; Recombinant Fusion Proteins; RNA, Messenger; Signal Transduction; Tetrazoles; Transcription, Genetic; Tunica Intima; Valine; Valsartan; Vasculitis

2004
[Mechanism of reversion of myocardial interstitial fibrosis in diabetic cardiomyopathy by valsartan].
    Zhonghua yi xue za zhi, 2006, Jan-24, Volume: 86, Issue:4

    Topics: Animals; Antihypertensive Agents; Blood Pressure; Blotting, Western; Cardiomyopathy, Hypertrophic; Diabetes Mellitus, Experimental; Fibrosis; Heart; Male; Myocardium; Random Allocation; Rats; Rats, Wistar; Receptors, Angiotensin; Reverse Transcriptase Polymerase Chain Reaction; Signal Transduction; Tetrazoles; Thrombospondin 1; Transforming Growth Factor beta; Valine; Valsartan

2006
Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.
    Proceedings of the National Academy of Sciences of the United States of America, 1993, May-01, Volume: 90, Issue:9

    Topics: Adolescent; Adult; Amino Acid Sequence; Arginine; Base Sequence; Cardiomyopathy, Hypertrophic; Child, Preschool; Codon; DNA; Exons; Female; Glutamine; Humans; Introns; Leucine; Leukocytes; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Muscles; Myosins; Oligodeoxyribonucleotides; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Valine

1993
A missense mutation in the beta-myosin heavy chain gene in a Japanese patient with hypertrophic cardiomyopathy.
    Japanese circulation journal, 1995, Volume: 59, Issue:12

    Topics: Cardiomyopathy, Hypertrophic; Exons; Humans; Japan; Male; Methionine; Middle Aged; Myosin Heavy Chains; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Valine

1995
A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy.
    Scandinavian cardiovascular journal : SCJ, 2000, Volume: 34, Issue:6

    Topics: Adolescent; Adult; Aged; Cardiomegaly; Cardiomyopathy, Hypertrophic; Electrocardiography; Exons; Humans; Leucine; Middle Aged; Mutation, Missense; Myosin Heavy Chains; Pedigree; Phenotype; Polymorphism, Single-Stranded Conformational; Sarcomeres; Valine

2000
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.
    The American journal of cardiology, 2001, Jun-01, Volume: 87, Issue:11

    Topics: Adolescent; Adult; Age Factors; Cardiomyopathy, Hypertrophic; Child; Cohort Studies; Death, Sudden, Cardiac; DNA Glycosylases; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Myosin Heavy Chains; N-Glycosyl Hydrolases; Nonmuscle Myosin Type IIB; Pedigree; Risk; Survival Analysis; Valine

2001