hypusine has been researched along with Neurodevelopmental Disorders in 3 studies
*Neurodevelopmental Disorders: These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5). [MeSH]
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 2 (66.67) | 2.80 |
Authors | Studies |
---|---|
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, A | 1 |
Banka, S; Chung, WK; Kar, RK; Park, MH; Ziegler, A | 1 |
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, K | 1 |
1 review(s) available for hypusine and Neurodevelopmental Disorders
Article | Year |
---|---|
Post-translational formation of hypusine in eIF5A: implications in human neurodevelopment.
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 |
2 other study(ies) available for hypusine and Neurodevelopmental Disorders
Article | Year |
---|---|
Bi-allelic variants in DOHH, catalyzing the last step of hypusine biosynthesis, are associated with a neurodevelopmental disorder.
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.
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 |