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alanine and Bullous Congenital Ichthyosiform Erythroderma

alanine has been researched along with Bullous Congenital Ichthyosiform Erythroderma 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
"We report a mutation in a case of epidermolytic hyperkeratosis that results in a proline for alanine substitution in the residue position 12 of the 1A subdomain of the keratin 10 chain (codon 158)."1.30An alanine to proline mutation in the 1A rod domain of the keratin 10 chain in epidermolytic hyperkeratosis. ( Imamura, S; Lee, ES; Morita, E; Nam, K; Steinert, PM; Yang, JM; Yoneda, K, 1997)

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
Yang, JM1
Yoneda, K1
Morita, E1
Imamura, S1
Nam, K1
Lee, ES1
Steinert, PM1

Other Studies

1 other study available for alanine and Bullous Congenital Ichthyosiform Erythroderma

ArticleYear
An alanine to proline mutation in the 1A rod domain of the keratin 10 chain in epidermolytic hyperkeratosis.
    The Journal of investigative dermatology, 1997, Volume: 109, Issue:5

    Topics: Adolescent; Adult; Aged; Alanine; Female; Humans; Hyperkeratosis, Epidermolytic; Intermediate Filame

1997