Compounds > glutamic acid

glutamic acid and Hair Diseases

glutamic acid has been researched along with Hair Diseases in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (75.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bickers, DR; Christiano, AM; Djabali, K; Garzon, MC; Lalin, T; Longley, BJ; Panteleyev, AA; Zlotogorski, A1
Butterworth, RF; Qureshi, IA; Ratnakumari, L1
Krieg, T; Labrèze, C; Langbein, L; Leigh, IM; Rogers, MA; Roul, S; Schweizer, J; Stevens, HP; Taieb, A; Winter, H1
Chapalain, V; Labrèze, C; Mercier, M; Rogers, MA; Schweizer, J; Surlève-Bazeille, JE; Taieb, A; Winter, H1

Other Studies

4 other study(ies) available for glutamic acid and Hair Diseases

ArticleYear
Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix.
    Clinical and experimental dermatology, 2003, Volume: 28, Issue:2

    Topics: Colombia; DNA Mutational Analysis; Female; Glutamic Acid; Hair Diseases; Humans; Keratins; Lysine; Male; Mutation, Missense; Pedigree; Russia

2003
Effect of L-carnitine on cerebral and hepatic energy metabolites in congenitally hyperammonemic sparse-fur mice and its role during benzoate therapy.
    Metabolism: clinical and experimental, 1993, Volume: 42, Issue:8

    Topics: Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Benzoates; Benzoic Acid; Body Weight; Brain; Brain Chemistry; Carnitine; Coenzyme A; Dose-Response Relationship, Drug; Energy Metabolism; Genetic Linkage; Glutamates; Glutamic Acid; Glutamine; Hair Diseases; Ketoglutaric Acids; Lactates; Liver; Male; Mice; Mice, Mutant Strains; Ornithine Carbamoyltransferase; Pyruvates; Time Factors; Urea

1993
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix.
    Nature genetics, 1997, Volume: 16, Issue:4

    Topics: Adolescent; Child; Female; Glutamic Acid; Hair Diseases; Heterozygote; Humans; Keratins; Lysine; Male; Middle Aged; Mutation; Pedigree

1997
A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1.
    The Journal of investigative dermatology, 1998, Volume: 111, Issue:1

    Topics: Adult; Child, Preschool; Female; Glutamic Acid; Hair Diseases; Humans; Keratins; Lysine; Phenotype; Point Mutation

1998