cysteine has been researched along with Nephritis, Hereditary in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (50.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Kobayashi, T; Uchiyama, M | 1 |
Eccles, MR; Walker, RJ; Wilson, JC; Yoon, HS | 1 |
Hertz, JM; Leinonen, A; Tryggvason, K; Zhou, J | 1 |
Atkin, CL; Barker, DF; Gregory, MC; Hostikka, SL; Tryggvason, K; Zhou, J | 1 |
4 other study(ies) available for cysteine and Nephritis, Hereditary
Article | Year |
---|---|
Characterization of assembly of recombinant type IV collagen alpha3, alpha4, and alpha5 chains in transfected cell strains.
Topics: Amino Acid Substitution; Animals; Arginine; Autoantigens; Cell Line; Collagen Type IV; Cysteine; Gene Deletion; Glycine; Humans; Mice; Nephritis, Hereditary; Protein Processing, Post-Translational; Recombinant Proteins; Transfection | 2003 |
A novel Cys1638Tyr NC1 domain substitution in alpha5(IV) collagen causes Alport syndrome with late onset renal failure without hearing loss or eye abnormalities.
Topics: Adult; Aged; Biopsy; Collagen Type IV; Cysteine; Eye Abnormalities; Female; Genetic Linkage; Glomerular Basement Membrane; Hearing Loss; Humans; Kidney; Male; Middle Aged; Mutation; Nephritis, Hereditary; New Zealand; Pedigree; Renal Insufficiency; Tyrosine | 2007 |
Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient.
Topics: Adolescent; Adult; Amino Acid Sequence; Base Sequence; Collagen; Cysteine; Deoxyribonuclease HindIII; DNA; DNA Mutational Analysis; Exons; Female; Glycine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Nephritis, Hereditary; Pedigree; Polymorphism, Restriction Fragment Length | 1992 |
Single base mutation in alpha 5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome.
Topics: Bacterial Proteins; Base Sequence; Blotting, Southern; Collagen; Cysteine; Deoxyribonucleases, Type II Site-Specific; Female; Genes; Humans; Male; Molecular Sequence Data; Mutation; Nephritis, Hereditary; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Restriction Mapping; Serine | 1991 |