Compounds > isoleucine

isoleucine and Amyloidosis

isoleucine has been researched along with Amyloidosis in 14 studies

Research

Studies (14)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (7.14)	18.7374
1990's	10 (71.43)	18.2507
2000's	1 (7.14)	29.6817
2010's	2 (14.29)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Almeida, MR; de Carvalho, M; Esperante, S; Ferreira, P; Foguel, D; Gallego, P; Palhano, FL; Pereira-Henriques, A; Reverter, D; Sant'Anna, R; Saraiva, MJ; Varejāo, N; Ventura, S	1
Alexander, A; Buxbaum, J; Fox, E; Kitzman, D; Koziol, J; Tagoe, C	1
Benson, MD; Liepnieks, JJ; Wilson, DL	1
Buxbaum, JN; Gertz, MA; Jacobson, DR	1
Altland, K; Blätzinger, P; Denzel, K; Jenne, DE; Linke, RP; Obermaier, B; Winter, P	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
Canet, D; Dobson, CM; Last, AM; Miranker, A; Robinson, CV; Spencer, A; Sunde, M	1
Cohen, AS; Harding, J; Jones, LA; Milunsky, A; Skare, I; Skare, J; Skinner, M	1
Harada, H; Hayashi, Y; Kimura, A; Nakamura, M; Nishi, H; Sasazuki, T	1
Saeki, Y; Soga, F; Takahashi, N; Ueno, S; Yanagihara, T	1
Jacobson, DR	1
Benson, MD; Liepnieks, JJ; Nichols, WC; Snyder, EL	1
Cohen, AS; Connors, LH; Gertz, MA; Kyle, RA; Skinner, M	1

Other Studies

14 other study(ies) available for isoleucine and Amyloidosis

Article	Year
Cavity filling mutations at the thyroxine-binding site dramatically increase transthyretin stability and prevent its aggregation. Scientific reports, 2017, 03-24, Volume: 7 Topics: Aged; Alanine; Amino Acid Substitution; Amyloidosis; Asymptomatic Diseases; Binding Sites; Crystallography, X-Ray; Female; Gene Expression; Humans; Isoleucine; Models, Molecular; Prealbumin; Protein Binding; Protein Conformation, alpha-Helical; Protein Conformation, beta-Strand; Protein Interaction Domains and Motifs; Protein Multimerization; Protein Stability; Recombinant Proteins; Thermodynamics; Valine	2017
Significance of the amyloidogenic transthyretin Val 122 Ile allele in African Americans in the Arteriosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies. American heart journal, 2010, Volume: 159, Issue:5 Topics: Adult; Aged; Aged, 80 and over; Amyloidosis; Black or African American; Female; Gene Frequency; Heart Diseases; Humans; Isoleucine; Kaplan-Meier Estimate; Male; Middle Aged; Mutation; Prealbumin; Ultrasonography; Valine	2010
Biochemical characterization of vitreous and cardiac amyloid in Ile84Ser transthyretin amyloidosis. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2006, Volume: 13, Issue:3 Topics: Amino Acid Substitution; Amyloid; Amyloidosis; Isoleucine; Myocardium; Prealbumin; Vitreous Body	2006
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
A new isoleucine substitution of Val-20 in transthyretin tetramers selectively impairs dimer-dimer contacts and causes systemic amyloidosis. Proceedings of the National Academy of Sciences of the United States of America, 1996, Jun-25, Volume: 93, Issue:13 Topics: Amino Acid Sequence; Amyloidosis; Base Sequence; Biopolymers; Female; Genetic Carrier Screening; Humans; Isoleucine; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Prealbumin; Valine	1996
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
Mechanistic studies of the folding of human lysozyme and the origin of amyloidogenic behavior in its disease-related variants. Biochemistry, 1999, May-18, Volume: 38, Issue:20 Topics: Amyloid; Amyloidosis; Aspartic Acid; Histidine; Humans; Isoleucine; Kinetics; Mass Spectrometry; Models, Molecular; Muramidase; Protein Folding; Protons; Recombinant Proteins; Spectrometry, Fluorescence; Threonine	1999
A new transthyretin mutation associated with amyloidotic vitreous opacities. Asparagine for isoleucine at position 84. Ophthalmology, 1992, Volume: 99, Issue:4 Topics: Aged; Amyloidosis; Asparagine; Base Sequence; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Eye Diseases; Female; Humans; Isoleucine; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Prealbumin; Vitreous Body	1992
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 novel mutant (transthyretin Ile-50) related to amyloid polyneuropathy. Single-strand conformation polymorphism as a new genetic marker. FEBS letters, 1992, Aug-10, Volume: 308, Issue:1 Topics: Amyloidosis; Autoradiography; Base Sequence; DNA Mutational Analysis; DNA, Single-Stranded; Genetic Markers; Humans; Isoleucine; Molecular Sequence Data; Mutation; Nervous System Diseases; Polymerase Chain Reaction; Polymorphism, Genetic; Prealbumin	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
Isolation and characterization of a kappa amyloid fibril protein. Scandinavian journal of immunology, 1985, Volume: 22, Issue:3 Topics: Amino Acid Sequence; Amyloid; Amyloidosis; Animals; Antibody Formation; Electrophoresis, Polyacrylamide Gel; Female; Glutamates; Glutamic Acid; Histidine; Humans; Immunodiffusion; Isoleucine; Methionine; Middle Aged; Rabbits; Serine	1985