Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y - Test2 - elhamkhani - TriplyDB

Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y

Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y

http://www.wikidata.org/entity/Q24652487

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Review and theory of handedness, birth order, and homosexuality in men Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome Dental enamel development: proteinases and their enamel matrix substrates Human Y chromosome copy number variation in the next generation sequencing era and beyond.Genetic integrity of the human Y chromosome exposed to groundwater arsenic.A one-step real-time multiplex PCR for screening Y-chromosomal microdeletions without downstream amplicon size analysis.Sex determination in highly fragmented human DNA by high-resolution melting (HRM) analysis The Low Prevalence of Y Chromosomal Microdeletions is Observed in the Oligozoospermic Men in the Area of Mato Grosso State and Amazonian Region of Brazilian Patients.Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators Genetic basis of Y-linked hearing impairment.The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades.Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.Fate of the human Y chromosome linked genes and loci in prostate cancer cell lines DU145 and LNCaP.Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH.Structural variation of the human genome: mechanisms, assays, and role in male infertility Structural variation on the human Y chromosome from population-scale resequencing.MSY Breakpoint Mapper, a database of sequence-tagged sites useful in defining naturally occurring deletions in the human Y chromosome.Great ape Y Chromosome and mitochondrial DNA phylogenies reflect subspecies structure and patterns of mating and dispersal An evolutionary perspective on Y-chromosomal variation and male infertility.Unique signatures of natural background radiation on human Y chromosomes from Kerala, India.The fine-scale and complex architecture of human copy-number variation Genomic complexity of the Y-STR DYS19: inversions, deletions and founder lineages carrying duplications.Intrachromosomal homologous recombination between inverted amplicons on opposing Y-chromosome arms.Dynamic nature of the proximal AZFc region of the human Y chromosome: multiple independent deletion and duplication events revealed by microsatellite analysis.Remarkably little variation in proteins encoded by the Y chromosome's single-copy genes, implying effective purifying selection.An Exceptional Gene: Evolution of the TSPY Gene Family in Humans and Other Great Apes The Y chromosomes of the great apes.Human Y-chromosome variation in the genome-sequencing era.TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages.Identification of new susceptibility regions for X;Y translocations in patients with testicular disorder of sex development.A real-time PCR-based amelogenin Y allele dropout assessment model in gender typing of degraded DNA samples.Genetics of the human Y chromosome and its association with male infertility."YFlag"--a single-base extension primer based method for gender determination.A tremendous expansion of copy number in crossbred bulls ( × ).HSFY genes and the P4 palindrome in the AZFb interval of the human Y chromosome are not required for spermatocyte maturation.Mutational landscape of the human Y chromosome-linked genes and loci in patients with hypogonadism.Differential pattern of genetic variability at the DXYS156 locus on homologous regions of X and Y chromosomes in Indian population and its forensic implications.

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Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y

http://www.wikidata.org/entity/Q24652487

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2007 nî lūn-bûn

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2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի փետրվարին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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Human Molecular Genetics

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Matthew E Hurles

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R John Mitchell

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P2860

Deletions in the Y-derived amelogenin gene fragment in the Indian population

X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats

The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes

A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)

The effective mutation rate at Y chromosome short tandem repeats, with application to human population-divergence time.

Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure

Y-chromosomal DNA variation in Pakistan

A nomenclature system for the tree of human Y-chromosomal binary haplogroups

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Median-joining networks for inferring intraspecific phylogenies

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10.1093/HMG/DDL465

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