Page last updated: 2024-08-24

hypusine and Child Mental Disorders

hypusine has been researched along with Child Mental Disorders in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's2 (66.67)2.80

Authors

AuthorsStudies
Bézieau, S; Boland, A; Bonneau, D; Chung, WK; Coubes, C; Deleuze, JF; Faivre, L; Hanner, AS; Kar, RK; Küry, S; Le Mao, M; Lenaers, G; Maystadt, I; Navet, B; Park, MH; Prouteau, C; Rauch, A; Steindl, K; Tran Mau-Them, F; Zanoni, P; Ziegler, A1
Banka, S; Chung, WK; Kar, RK; Park, MH; Ziegler, A1
Au, PB; Chung, WK; Deng, L; Devinsky, O; Ganapathi, M; Hanner, A; Karlowicz, D; LeDuc, CA; Lee, J; Mastracci, TL; McDonald, M; Mirmira, RG; Okur, V; Padgett, LR; Park, MH; Person, R; Shen, Y; Tagoe, J; Wang, J; Willaert, R; Wolf, B; Yamada, K1

Reviews

1 review(s) available for hypusine and Child Mental Disorders

ArticleYear
Post-translational formation of hypusine in eIF5A: implications in human neurodevelopment.
    Amino acids, 2022, Volume: 54, Issue:4

    Topics: Animals; Eukaryotic Translation Initiation Factor 5A; Humans; Lysine; Mice; Neurodevelopmental Disorders; Oxidoreductases Acting on CH-NH Group Donors; Peptide Initiation Factors; Protein Biosynthesis; Protein Processing, Post-Translational; RNA-Binding Proteins

2022

Other Studies

2 other study(ies) available for hypusine and Child Mental Disorders

ArticleYear
Bi-allelic variants in DOHH, catalyzing the last step of hypusine biosynthesis, are associated with a neurodevelopmental disorder.
    American journal of human genetics, 2022, 08-04, Volume: 109, Issue:8

    Topics: Alleles; Gene Expression; Humans; Lysine; Mixed Function Oxygenases; Neurodevelopmental Disorders

2022
Recessive Rare Variants in Deoxyhypusine Synthase, an Enzyme Involved in the Synthesis of Hypusine, Are Associated with a Neurodevelopmental Disorder.
    American journal of human genetics, 2019, 02-07, Volume: 104, Issue:2

    Topics: Alleles; Amino Acid Sequence; Child; Child, Preschool; Developmental Disabilities; Eukaryotic Translation Initiation Factor 5A; Female; Genes, Recessive; Haplotypes; Humans; Lysine; Male; Metabolism, Inborn Errors; Mutation; Neurodevelopmental Disorders; Oxidoreductases Acting on CH-NH Group Donors; Pedigree; Peptide Initiation Factors; RNA-Binding Proteins; Seizures; Young Adult

2019