Page last updated: 2024-08-17

lysine and Neurodevelopmental Disorders

lysine has been researched along with Neurodevelopmental Disorders in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (37.50)24.3611
2020's5 (62.50)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
Hou, Y; Huang, T; Li, M; Lin, Q; Shao, G; Sun, A; Zhang, B; Zhang, Z1
Azzarà, A; Cassano, I; Facchiano, A; Galasso, C; Gurrieri, F; Lintas, C; Tabolacci, C1
Assaraf, YG; Wiesel-Motiuk, N1
Banka, S; Chung, WK; Kar, RK; Park, MH; Ziegler, A1
Cho, KS; Kim, JH; Lee, IS; Lee, JH; Lee, SB1
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
Tapias, A; Wang, ZQ1

Reviews

5 review(s) available for lysine and Neurodevelopmental Disorders

ArticleYear
Structure, activity and function of the lysine methyltransferase SETD5.
    Frontiers in endocrinology, 2023, Volume: 14

    Topics: Histones; Humans; Lysine; Methyltransferases; Neurodevelopmental Disorders

2023
The key roles of the lysine acetyltransferases KAT6A and KAT6B in physiology and pathology.
    Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy, 2020, Volume: 53

    Topics: Acetylation; Animals; Disease Models, Animal; Embryonic Development; Histone Acetyltransferases; Histone Code; Histones; Humans; Lysine; Mice; Neurodevelopmental Disorders; Protein Processing, Post-Translational

2020
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
Histone Lysine Methylation and Neurodevelopmental Disorders.
    International journal of molecular sciences, 2017, Jun-30, Volume: 18, Issue:7

    Topics: Animals; Epigenesis, Genetic; Histones; Humans; Lysine; Methylation; Neurodevelopmental Disorders; Protein Processing, Post-Translational

2017
Lysine Acetylation and Deacetylation in Brain Development and Neuropathies.
    Genomics, proteomics & bioinformatics, 2017, Volume: 15, Issue:1

    Topics: Acetylation; Brain; Carboxy-Lyases; Chromatin Assembly and Disassembly; Humans; Lysine; Lysine Acetyltransferases; Neural Stem Cells; Neurodevelopmental Disorders; Neurogenesis

2017

Other Studies

3 other study(ies) available for lysine and Neurodevelopmental 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
Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability.
    Genes, 2023, 06-27, Volume: 14, Issue:7

    Topics: Brain Diseases; Calcium-Calmodulin-Dependent Protein Kinase Type 2; Female; Humans; Intellectual Disability; Lysine; Neurodevelopmental Disorders; Protein Serine-Threonine Kinases

2023
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