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alanine and Alport Syndrome

alanine has been researched along with Alport Syndrome 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.

Research Excerpts

ExcerptRelevanceReference
"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."1.30Determination 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)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boye, E1
Mollet, G1
Forestier, L1
Cohen-Solal, L1
Heidet, L1
Cochat, P1
Grünfeld, JP1
Palcoux, JB1
Gubler, MC1
Antignac, C1

Other Studies

1 other study available for alanine and Alport Syndrome

ArticleYear
Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.
    American journal of human genetics, 1998, Volume: 63, Issue:5

    Topics: Alanine; Amino Acid Substitution; Base Sequence; Basement Membrane; Collagen; DNA Primers; Exons; Fe

1998