Compounds > isoleucine

isoleucine and Cardiomyopathies

isoleucine has been researched along with Cardiomyopathies in 10 studies

Research

Studies (10)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (10.00)	18.7374
1990's	6 (60.00)	18.2507
2000's	3 (30.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Gefter, W; Groot, PH; O'Brien, EJ; Rader, DJ; Rut, A; Spurr, NK; Valdes, AM; Wolfe, ML	1
Hattori, T; Ikeda, S; Kanai, S; Takei, Y; Tokuda, T; Urasawa, N; Yazaki, M	1
Bergesio, F; Del Pace, S; Frusconi, S; Miliani, A; Minuti, B; Pelo, E; Perfetto, F; Tarquini, R; Torricelli, F	1
Henry, CG; Hillman, RE; Keating, JP; Strauss, AW	1
Buxbaum, JN; Gertz, MA; Jacobson, DR	1
Ballas, SK; Buxbaum, JN; Embury, SH; Jacobson, DR; Kane, I; Malendowicz, S; Pastore, R; Pool, S; Shivji, A	1
Hayashi, Y; Nakamura, M; Sadamatsu, K	1
Harada, H; Hayashi, Y; Kimura, A; Nakamura, M; Nishi, H; Sasazuki, T	1
Jacobson, DR	1
Benson, MD; Liepnieks, JJ; Nichols, WC; Snyder, EL	1

Other Studies

10 other study(ies) available for isoleucine and Cardiomyopathies

Article	Year
Val64Ile polymorphism in the C-C chemokine receptor 2 is associated with reduced coronary artery calcification. Arteriosclerosis, thrombosis, and vascular biology, 2002, Nov-01, Volume: 22, Issue:11 Topics: Adult; Aged; Amino Acid Substitution; Calcinosis; Cardiomyopathies; Coronary Vessels; Female; Genotype; Humans; Isoleucine; Male; Middle Aged; Models, Statistical; Polymorphism, Genetic; Receptors, CCR2; Receptors, Chemokine; Sex Factors; Valine	2002
Transthyretin Tyr69-to-Ile mutation (double-nucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2003, Volume: 10, Issue:1 Topics: Amyloidosis, Familial; Cardiomyopathies; Carpal Tunnel Syndrome; Female; Humans; Isoleucine; Japan; Middle Aged; Mutation; Phenotype; Prealbumin; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Tyrosine	2003
A new ATTR Phe64Ile mutation with late-onset multiorgan involvement. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2007, Volume: 14, Issue:4 Topics: Aged; Amyloidosis, Familial; Base Sequence; Cardiomyopathies; Codon; DNA Mutational Analysis; Echocardiography; Exons; Humans; Isoleucine; Male; Molecular Sequence Data; Mutation, Missense; Phenylalanine; Prealbumin	2007
Congestive cardiomyopathy associated with beta-ketothiolase deficiency. The Journal of pediatrics, 1981, Volume: 99, Issue:5 Topics: Acetyl-CoA C-Acyltransferase; Acyltransferases; Cardiomyopathies; Child; Echocardiography; Fatty Acids; Female; Heart Failure; Humans; Isoleucine; Mitochondria, Heart	1981
Transthyretin VAL107, a new variant associated with familial cardiac and neuropathic amyloidosis. Human mutation, 1994, Volume: 3, Issue:4 Topics: Amyloid Neuropathies; Amyloidosis; Base Sequence; Cardiomyopathies; DNA Mutational Analysis; Humans; Isoleucine; Male; Middle Aged; Molecular Sequence Data; Point Mutation; Polymerase Chain Reaction; Prealbumin; Valine	1994
Revised transthyretin Ile 122 allele frequency in African-Americans. Human genetics, 1996, Volume: 98, Issue:2 Topics: Alleles; Amyloidosis; Black People; Cardiomyopathies; Gene Frequency; Genetic Variation; Heterozygote; Homozygote; Humans; Isoleucine; Point Mutation; Prealbumin; United States	1996
Three siblings of familial amyloid cardiomyopathy with isoleucine-50 transthyretin mutation. International journal of cardiology, 1997, Sep-19, Volume: 61, Issue:2 Topics: Amyloidosis; Cardiac Pacing, Artificial; Cardiomyopathies; Codon; Electrocardiography; Fatal Outcome; Female; Heart Block; Humans; Isoleucine; Male; Middle Aged; Point Mutation; Prealbumin	1997
Novel variant transthyretin gene (Ser50 to Ile) in familial cardiac amyloidosis. Biochemical and biophysical research communications, 1992, Aug-31, Volume: 187, Issue:1 Topics: Amyloidosis; Base Sequence; Cardiomyopathies; Cloning, Molecular; DNA; Electrophoresis, Polyacrylamide Gel; Humans; Isoleucine; Japan; Male; Middle Aged; Molecular Sequence Data; Mutation; Nucleic Acid Conformation; Nucleic Acid Hybridization; Polymerase Chain Reaction; Polymorphism, Genetic; Prealbumin; Serine	1992
A specific test for transthyretin 122 (Val----Ile), based on PCR-primer-introduced restriction analysis (PCR-PIRA): confirmation of the gene frequency in blacks. American journal of human genetics, 1992, Volume: 50, Issue:1 Topics: Alleles; Amyloidosis; Base Sequence; Black People; Cardiomyopathies; Deoxyribonucleases, Type II Site-Specific; DNA; Homozygote; Humans; Isoleucine; Male; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Prealbumin; Restriction Mapping; Valine	1992
Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (ILE-122). The Journal of laboratory and clinical medicine, 1991, Volume: 117, Issue:3 Topics: Aged; Amyloid; Amyloidosis; Base Sequence; Cardiomyopathies; Chromatography, High Pressure Liquid; DNA; Genetic Variation; Heterozygote; Humans; Isoleucine; Male; Molecular Sequence Data; Polymerase Chain Reaction; Prealbumin	1991