Page last updated: 2024-08-24

5-methylcytosine and Intellectual Disability

5-methylcytosine has been researched along with Intellectual Disability in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (33.33)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bansal, D; Frye, M; Garone, C; Gleeson, JG; Kim, JS; Lee, SY; McCann, BJ; Minczuk, M; Miska, EA; Powell, CA; Rhee, HW; Shin, S; Van Haute, L; Vasiliauskaitė, L	1
Ali, G; Ansar, M; Ayub, M; Doherty, D; Flores, JV; Frye, M; Hussain, S; Ibrahim, S; Ishak, GE; Khan, FS; Khan, MA; Malli, R; Noor, A; Rafiq, MA; Rupp, V; Vincent, AK; Vincent, JB; Weksberg, R; Windpassinger, C	1
Camerino, G; Goodfellow, P	1

Reviews

1 review(s) available for 5-methylcytosine and Intellectual Disability

Article	Year
A fragile understanding. Trends in genetics : TIG, 1991, Volume: 7, Issue:8 Topics: 5-Methylcytosine; Brain; Cytosine; Female; Fetal Diseases; Fragile X Syndrome; Gene Expression Regulation; Genetic Carrier Screening; Humans; Intellectual Disability; Male; Meiosis; Methylation; Models, Genetic; Organ Specificity; Prenatal Diagnosis; Repetitive Sequences, Nucleic Acid; X Chromosome	1991

Other Studies

2 other study(ies) available for 5-methylcytosine and Intellectual Disability

Article	Year
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs. Nucleic acids research, 2019, 09-19, Volume: 47, Issue:16 Topics: 5-Methylcytosine; Animals; CRISPR-Cas Systems; Eczema; Facies; Fibroblasts; Gene Editing; Gene Knockout Techniques; Growth Disorders; HEK293 Cells; Humans; Intellectual Disability; Methylation; Methyltransferases; Mice; Mice, Knockout; Microcephaly; Mitochondria; Nucleic Acid Conformation; Oxidative Phosphorylation; Primary Cell Culture; Protein Transport; RNA Processing, Post-Transcriptional; RNA, Messenger; RNA, Mitochondrial; RNA, Transfer	2019
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability. American journal of human genetics, 2012, May-04, Volume: 90, Issue:5 Topics: 5-Methylcytosine; Adolescent; Amino Acid Sequence; Animals; Asian People; Cell Line, Tumor; Child; Chromosome Mapping; Disease Models, Animal; Female; Genes, Recessive; Genetic Heterogeneity; Genotype; Homozygote; Humans; Intellectual Disability; Lod Score; Male; Methyltransferases; Mice; Molecular Sequence Data; Pakistan; Pedigree; Polymorphism, Single Nucleotide; RNA	2012

Article

Year

NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs.

Nucleic acids research, 2019, 09-19, Volume: 47, Issue:16

Topics: 5-Methylcytosine; Animals; CRISPR-Cas Systems; Eczema; Facies; Fibroblasts; Gene Editing; Gene Knockout Techniques; Growth Disorders; HEK293 Cells; Humans; Intellectual Disability; Methylation; Methyltransferases; Mice; Mice, Knockout; Microcephaly; Mitochondria; Nucleic Acid Conformation; Oxidative Phosphorylation; Primary Cell Culture; Protein Transport; RNA Processing, Post-Transcriptional; RNA, Messenger; RNA, Mitochondrial; RNA, Transfer

2019

Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability.

American journal of human genetics, 2012, May-04, Volume: 90, Issue:5

Topics: 5-Methylcytosine; Adolescent; Amino Acid Sequence; Animals; Asian People; Cell Line, Tumor; Child; Chromosome Mapping; Disease Models, Animal; Female; Genes, Recessive; Genetic Heterogeneity; Genotype; Homozygote; Humans; Intellectual Disability; Lod Score; Male; Methyltransferases; Mice; Molecular Sequence Data; Pakistan; Pedigree; Polymorphism, Single Nucleotide; RNA

2012