Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
about
Gametic but not somatic instability of CAG repeat length in Huntington's disease.Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset.The Nature, Extent, and Consequences of Genetic Variation in the opa Repeats of Notch in Drosophila.Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease.Microsatellite alterations as clonal markers for the detection of human cancerDecrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmissionA third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locusMolecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.Androgen receptor trinucleotide polymorphism in leiomyomaPhysical chemistry of polyglutamine: intriguing tales of a monotonous sequence.Onset Manifestations of Spinal and Bulbar Muscular Atrophy (Kennedy's Disease).Identification of two novel cis-elements in the promoter of the prostate-specific antigen gene that are required to enhance androgen receptor-mediated transactivation.Inherited neuropathies: the interface between molecular genetics and pathology.Androgen receptor and mechanism of androgen action.Differential effects of simple repeating DNA sequences on gene expression from the SV40 early promoter.Clinical aspects of CAG repeat diseases.The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.Trinucleotide repeat instability: genetic features and molecular mechanisms.Nuclear inclusions and pseudoinclusions: friends or foes of the surgical pathologist?A phenotypic-genetic study of a group of Polish patients with spinal and bulbar muscular atrophy.Polymorphic CAG repeat numbers in the androgen receptor gene of female pattern hair loss patients.
P2860
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P2860
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
description
1992 nî lūn-bûn
@nan
1992 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@ast
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@en
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@nl
type
label
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@ast
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@en
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@nl
prefLabel
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@ast
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@en
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@nl
P2093
P356
P1476
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
@en
P2093
P304
P356
10.1093/HMG/1.4.255
P577
1992-07-01T00:00:00Z