Investigation of androgen receptor CAG repeats length in polycystic ovary syndrome diagnosed using the new international evidence-based guideline [PDF]
Background To study whether CAG repeat polymorphism of androgen receptor (AR) contributes to the risk of polycystic ovarian morphology (PCOM) with antral follicle count (AFC) ≥ 20 in the context of new international guideline of polycystic ovary syndrome
Xueqi Yan +12 more
doaj +2 more sources
The Effect of CAG Repeats within the Non-Pathological Range in the HTT Gene on Cognitive Functions in Patients with Subjective Cognitive Decline and Mild Cognitive Impairment [PDF]
The Huntingtin gene (HTT) is within a class of genes containing a key region of CAG repeats. When expanded beyond 39 repeats, Huntington disease (HD) develops. Individuals with less than 35 repeats are not associated with HD.
Valentina Bessi +9 more
doaj +2 more sources
CAG Repeats Within the Non-pathological Range in the HTT Gene Influence Personality Traits in Patients With Subjective Cognitive Decline: A 13-Year Follow-Up Study [PDF]
Objective:HTT is a gene containing a key region of CAG repeats. When expanded beyond 39 repeats, Huntington disease (HD) develops. HTT genes with <35 repeats are not associated with HD.
Valentina Moschini +18 more
doaj +2 more sources
The effect of CAG repeats length on differences in hirsutism among healthy Israeli women of different ethnicities. [PDF]
PURPOSE:Variations in the degree of hirsutism among women of different ethnic backgrounds may stem from multiple etiologies. Shorter length of the polymorphic CAG repeats of the androgen receptor (AR) gene may be associated with increased activity of the
Naomi Weintrob +7 more
doaj +2 more sources
Comparison of NGS panel and Sanger sequencing for genotyping CAG repeats in the AR gene [PDF]
Background The androgen receptor (AR) is a nuclear receptor, encoded by the AR gene on the X chromosome. Within the first exon of the AR gene, two short tandem repeats (STR), CAG and GGC, are a source of polymorphism in the population.
Maria Santa Rocca +7 more
doaj +2 more sources
Short CAG repeat variation as a regulatory factor in health and disease [PDF]
Short cytosine-adenine-guanine (CAG) trinucleotide repeats, which encode polyglutamine (polyQ) tracts, are prevalent features of genes enriched in transcriptional and regulatory functions, including the androgen receptor (AR) and huntingtin (HTT).
Jacob R. Manjarrez
doaj +2 more sources
Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population. [PDF]
Spinocerebellar ataxia type 3 (SCA3), also called Machado-Joseph disease (MJD), is one of the most common SCAs worldwide and caused by a CAG repeat expansion located in ATXN3 gene.
Shi-Rui Gan +4 more
doaj +2 more sources
Mutant CAG Repeats Effectively Targeted by RNA Interference in SCA7 Cells [PDF]
Agnieszka Fiszer +2 more
exaly +2 more sources
Long tract of untranslated CAG repeats is deleterious in transgenic mice. [PDF]
The most frequent trinucleotide repeat found in human disorders is the CAG sequence. Expansion of CAG repeats is mostly found in coding regions and is thought to cause diseases through a protein mechanism.
Ren-Jun Hsu +6 more
doaj +1 more source
Identification of Proteins Specifically Assembled on a Stem-Loop Composed of a CAG Triplet Repeat
Human genomic DNA contains a number of diverse repetitive sequence motifs, often identified as fragile sites leading to genetic instability. Among them, expansion events occurring at triplet repeats have been extensively studied due to their association ...
Robert P. Fuchs +3 more
doaj +1 more source

