Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes. - Wikidata - awgldk - TriplyDB

Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes.

Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes.

http://www.wikidata.org/entity/Q36740601

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Non-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomes The AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertility Recombination between the mouse Y chromosome short arm and an additional Y short arm-derived chromosomal segment attached distal to the X chromosome PAR Dicentric chromosomes: unique models to study centromere function and inactivation Clinical genetic testing for male factor infertility: current applications and future directions How to make a sex chromosome Multicopy gene family evolution on primate Y chromosomes Microarray Analysis of Copy Number Variants on the Human Y Chromosome Reveals Novel and Frequent Duplications Overrepresented in Specific Haplogroups The role of sex chromosomes in sexual dimorphism: discordance between molecular and phenotypic data.Fusion of nearby inverted repeats by a replication-based mechanism leads to formation of dicentric and acentric chromosomes that cause genome instability in budding yeast.A novel universal multiplex PCR improves detection of AZFc Y-chromosome microdeletions Patterns of Inter-Chromosomal Gene Conversion on the Male-Specific Region of the Human Y Chromosome Structural maintenance of chromosomes (SMC) proteins promote homolog-independent recombination repair in meiosis crucial for germ cell genomic stability.Telomere disruption results in non-random formation of de novo dicentric chromosomes involving acrocentric human chromosomes.Pseudosynapsis and decreased stringency of meiotic repair pathway choice on the hemizygous sex chromosome of Caenorhabditis elegans males Clinical evaluation of the infertile male with respect to genetic etiologies.EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013.Origin-dependent inverted-repeat amplification: a replication-based model for generating palindromic amplicons.A genetic and structural study of genome rearrangements mediated by high copy repeat Ty1 elements Inter- and intraspecies phylogenetic analyses reveal extensive X-Y gene conversion in the evolution of gametologous sequences of human sex chromosomes.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.A W-linked palindrome and gene conversion in New World sparrows and blackbirds.Evaluation of the azoospermic male Gene duplication, gene conversion and the evolution of the Y chromosome.Heat shock transcription factor 1 localizes to sex chromatin during meiotic repression.AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.Recombination dynamics of a human Y-chromosomal palindrome: rapid GC-biased gene conversion, multi-kilobase conversion tracts, and rare inversions.Can intra-Y gene conversion oppose the degeneration of the human Y chromosome? A simulation study Sequencing the mouse Y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes.Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions.Genome destabilization by homologous recombination in the germ line Conflict on the sex chromosomes: cause, effect, and complexity.Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication.The scope and strength of sex-specific selection in genome evolution.Function of the sex chromosomes in mammalian fertility.Structural variation of the human genome: mechanisms, assays, and role in male infertility Step-by-step evolution of neo-sex chromosomes in geographical populations of wild silkmoths, Samia cynthia ssp.Small but mighty: the evolutionary dynamics of W and Y sex chromosomes.W chromosome expression responds to female-specific selection.Mechanisms for recurrent and complex human genomic rearrangements.

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P2860

Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes.

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P2860

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

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

Origins of chromosomal rearrangement hotspots in the human genome: evidence from the AZFa deletion hotspots

Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis.

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11

High mutation rates have driven extensive structural polymorphism among human Y chromosomes

Formation of de novo centromeres and construction of first-generation human artificial microchromosomes

Crossover and noncrossover pathways in mouse meiosis

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