cysteine and Nephritis, Hereditary

cysteine has been researched along with Nephritis, Hereditary in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kobayashi, T; Uchiyama, M1
Eccles, MR; Walker, RJ; Wilson, JC; Yoon, HS1
Hertz, JM; Leinonen, A; Tryggvason, K; Zhou, J1
Atkin, CL; Barker, DF; Gregory, MC; Hostikka, SL; Tryggvason, K; Zhou, J1

Other Studies

4 other study(ies) available for cysteine and Nephritis, Hereditary

ArticleYear
Characterization of assembly of recombinant type IV collagen alpha3, alpha4, and alpha5 chains in transfected cell strains.
    Kidney international, 2003, Volume: 64, Issue:6

    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.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2007, Volume: 22, Issue:5

    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.
    The Journal of biological chemistry, 1992, Jun-25, Volume: 267, Issue:18

    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.
    Genomics, 1991, Volume: 9, Issue:1

    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