Pages that link to "Q30985374"
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The following pages link to Human genes containing polymorphic trinucleotide repeats (Q30985374):
Displaying 50 items.
- Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy (Q24308826) (← links)
- Purification of nuclear proteins from human HeLa cells that bind specifically to the unstable tandem repeat (CGG)n in the human FMR1 gene (Q24310425) (← links)
- Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats (Q24317096) (← links)
- Identification of a human achaete-scute homolog highly expressed in neuroendocrine tumors (Q24562643) (← links)
- Isolation and characterization of novel CAG repeat containing genes expressed in human brain (Q28138069) (← links)
- Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p (Q28250966) (← links)
- Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) (Q28250990) (← links)
- Polyglycine expansions in eRF3/GSPT1 are associated with gastric cancer susceptibility (Q28259039) (← links)
- Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle (Q28288313) (← links)
- Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle (Q29303096) (← links)
- Issues in searching molecular sequence databases (Q30421088) (← links)
- Molecular cloning and characterization of a human brain-specific gene implicated in neuronal differentiation (Q32076745) (← links)
- CAG-encoded polyglutamine length polymorphism in the human genome (Q33285435) (← links)
- Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13. (Q33678843) (← links)
- Possible role of natural selection in the formation of tandem-repetitive noncoding DNA. (Q33962229) (← links)
- Length variation of CAG/CAA trinucleotide repeats in natural populations of Drosophila melanogaster and its relation to the recombination rate. (Q33968147) (← links)
- Obesity and cortisol (Q34071860) (← links)
- Structure of the leukemia-associated human CBFB gene (Q34299691) (← links)
- Direct detection of novel expanded trinucleotide repeats in the human genome (Q34352411) (← links)
- Identification of the gene FMR2, associated with FRAXE mental retardation (Q34385889) (← links)
- Northern blot analysis of simple repetitive sequence transcription in plants (Q34401500) (← links)
- Amino acid repeats cause extraordinary coding sequence variation in the social amoeba Dictyostelium discoideum (Q34430895) (← links)
- Simple sequence repeats as a source of quantitative genetic variation (Q34738348) (← links)
- Codon reiteration and the evolution of proteins (Q35226136) (← links)
- Structures of trinucleotide repeats in human transcripts and their functional implications. (Q35538754) (← links)
- Quantitative comparison of FMR1 gene expression in normal and premutation alleles (Q35643830) (← links)
- Search for unstable DNA in schizophrenia families with evidence for genetic anticipation (Q35882141) (← links)
- LAR tyrosine phosphatase receptor: alternative splicing is preferential to the nervous system, coordinated with cell growth and generates novel isoforms containing extensive CAG repeats (Q36235220) (← links)
- Characterization of the 5'-flanking region and chromosomal assignment of the human brain natriuretic peptide gene (Q36787129) (← links)
- Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22. (Q36836960) (← links)
- Identification and chromosomal localization of human genes containing CAG/CTG repeats expressed in testis and brain. (Q36875797) (← links)
- A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1. (Q36883370) (← links)
- The biological effects of simple tandem repeats: lessons from the repeat expansion diseases (Q37204533) (← links)
- Sequence specific binding of cytosolic proteins to a 12 nucleotide sequence in the 5' untranslated region of FMR1 mRNA. (Q38350625) (← links)
- Cloning (CAG/GTC)n STSs by an Alu-(CAG/GTC)n PCR method: an approach to human chromosome 12 and spinocerebellar ataxia 2 (SCA2) (Q39717360) (← links)
- Multivariate analysis of factors influencing repeat expansion detection (Q40413696) (← links)
- A rapid method for sequencing trinucleotide repeats (Q40416769) (← links)
- Genes with triplet repeats: candidate mediators of neuropsychiatric disorders (Q40489620) (← links)
- The insertion of foreign DNA into mammalian genomes and its consequences: a concept in oncogenesis (Q40551592) (← links)
- Genetic anticipation. Expanding tandem repeats. (Q40585513) (← links)
- Biological significance of minisatellites (Q40959185) (← links)
- Clinical implications of unstable DNA repeat sequences (Q41025202) (← links)
- Are ABL and BCR imprinted? (Q41167757) (← links)
- Differential effects of simple repeating DNA sequences on gene expression from the SV40 early promoter (Q41368750) (← links)
- CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome (Q41492637) (← links)
- Screening for fragile X syndrome: information needs for health planners (Q41579814) (← links)
- The lean woman (Q42166510) (← links)
- The gene for Huntington's disease (Q42552052) (← links)
- The exact numbers of possible microsatellite motifs (Q42557256) (← links)
- Central and peripheral glucocorticoid receptor function in abdominal obesity (Q43949701) (← links)