alanine has been researched along with Nephritis, Hereditary in 1 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Nephritis, Hereditary: A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Autosomal recessive Alport syndrome is a progressive hematuric glomerulonephritis characterized by glomerular basement membrane abnormalities and associated with mutations in either the COL4A3 or the COL4A4 gene, which encode the alpha3 and alpha4 type IV collagen chains, respectively." | 1.30 | Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome. ( Antignac, C; Boye, E; Cochat, P; Cohen-Solal, L; Forestier, L; Grünfeld, JP; Gubler, MC; Heidet, L; Mollet, G; Palcoux, JB, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Boye, E | 1 |
| Mollet, G | 1 |
| Forestier, L | 1 |
| Cohen-Solal, L | 1 |
| Heidet, L | 1 |
| Cochat, P | 1 |
| Grünfeld, JP | 1 |
| Palcoux, JB | 1 |
| Gubler, MC | 1 |
| Antignac, C | 1 |
1 other study available for alanine and Nephritis, Hereditary
| Article | Year |
|---|---|
Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.
Topics: Alanine; Amino Acid Substitution; Base Sequence; Basement Membrane; Collagen; DNA Primers; Exons; Fe | 1998 |