arginine has been researched along with Nephritis, Hereditary in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (80.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kobayashi, T; Uchiyama, M | 1 |
| Atkin, C; Barker, DF; Gregory, MC; Hertz, JM; Spencer, ES; Tryggvason, K; Zhou, J | 1 |
| Fukushima, T; Harano, K; Harano, T; Kawai, S; Nomura, S; Osawa, G; Shimizu, B; Wago, M | 1 |
| Atkin, CL; Barker, DF; Denison, JC; Gregory, MC | 1 |
| Antignac, C; Deschenes, G; Gros, F; Grünfeld, JP; Gubler, MC; Hors, MC; Knebelmann, B; Tryggvason, K; Zhou, J | 1 |
5 other study(ies) available for arginine 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 |
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndrome.
Topics: Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Codon; Collagen; Conserved Sequence; DNA; DNA Mutational Analysis; Exons; Female; Humans; Male; Middle Aged; Molecular Sequence Data; Nephritis, Hereditary; Pedigree; Point Mutation; Polymerase Chain Reaction | 1993 |
A single-base mutation in exon 31 converting glycine 852 to arginine in the collagenous domain in an Alport syndrome patient.
Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Basement Membrane; Child; Collagen; Deoxyribonucleases, Type II Site-Specific; DNA Primers; Exons; Female; Glycine; Humans; Kidney Glomerulus; Male; Nephritis, Hereditary; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Protein Structure, Secondary | 1996 |
Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q.
Topics: Adult; Arginine; Base Sequence; Collagen; Dinucleotide Repeats; Europe; Family; Female; Genetic Markers; Glutamine; Humans; Jews; Male; Nephritis; Nephritis, Hereditary; Pedigree; Point Mutation; Trinucleotide Repeats; Utah | 1997 |
Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragments.
Topics: Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Collagen; Deoxyribonuclease HpaII; Deoxyribonucleases, Type II Site-Specific; Female; Gene Library; Genetic Linkage; Glycine; Humans; Lymphocytes; Male; Middle Aged; Molecular Sequence Data; Mutation; Nephritis, Hereditary; Pedigree; Polymerase Chain Reaction; X Chromosome | 1992 |