Pages that link to "Q54523047"

The following pages link to Meiotic chromosome pairing in the normal human female. (Q54523047):

Displaying 34 items.

• Meiotic chromosomes: it takes two to tango (Q27930023) (← links)
• ATR, BRCA1 and gammaH2AX localize to unsynapsed chromosomes at the pachytene stage in human oocytes (Q28609116) (← links)
• THE COMPLEX STRUCTURE AND DYNAMIC EVOLUTION OF HUMAN SUBTELOMERES (Q29393384) (← links)
• Apoptosis in mouse fetal and neonatal oocytes during meiotic prophase one. (Q33291584) (← links)
• Genome-wide crossover distribution in Arabidopsis thaliana meiosis reveals sex-specific patterns along chromosomes (Q34071405) (← links)
• Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human male (Q34114502) (← links)
• High-Resolution Crossover Maps for Each Bivalent of Zea mays Using Recombination Nodules (Q34618622) (← links)
• A sequence-based integrated map of chromosome 22. (Q35033383) (← links)
• XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region (Q35197098) (← links)
• The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications (Q35881781) (← links)
• The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2. (Q36021709) (← links)
• Molecular aspects of meiotic chromosome synapsis and recombination (Q36226840) (← links)
• Telomeres cluster de novo before the initiation of synapsis: a three-dimensional spatial analysis of telomere positions before and during meiotic prophase (Q36274072) (← links)
• The synaptonemal complex and meiotic recombination in humans: new approaches to old questions (Q36425570) (← links)
• The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes (Q36449560) (← links)
• A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis (Q36723618) (← links)
• Patterns of meiotic recombination in human fetal oocytes (Q37217307) (← links)
• The mammalian synaptonemal complex: protein components, assembly and role in meiotic recombination (Q37991045) (← links)
• The proterminal regions and telomeres of human chromosomes. (Q40519621) (← links)
• Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features (Q40550174) (← links)
• Future of germ cell cytogenetics (Q40743163) (← links)
• Recombination Hot Spots and Human Disease (Q41574990) (← links)
• The relationship between synaptonemal complex length and genome size in four vertebrate classes (Osteicthyes, Reptilia, Aves, Mammalia). (Q47379008) (← links)
• Analysis of meiotic chromosome pairing in the female mouse using a novel minichromosome (Q47750129) (← links)
• Sex-specific telomere redistribution and synapsis initiation in cattle oogenesis (Q48023252) (← links)
• Predicting gene networks in human oocyte meiosis. (Q48708236) (← links)
• Synaptonemal complex karyotype of zebrafish (Q48831956) (← links)
• Synaptic process in the rat (Rattus norvegicus): Influence of methodology on results (Q48835769) (← links)
• Sex-dependent synaptic behaviour in triploid turbot, Scophthalmus maximus (Pisces, Scophthalmidae). (Q48843915) (← links)
• Synaptonemal complex analysis in spermatocytes and oocytes of rainbow trout, Oncorhynchus mykiss (Pisces, Salmonidae): the process of autosome and sex chromosome synapsis. (Q49053498) (← links)
• Altered patterns of meiotic recombination in human fetal oocytes with asynapsis and/or synaptonemal complex fragmentation at pachytene (Q50647345) (← links)
• Sequential study of the synaptonemal complex in rat (Rattus norvegicus) oocytes by light and electron microscopy (Q61818873) (← links)
• Development of the first meiotic prophase stages in human fetal oocytes observed by light and electron microscopy (Q61818875) (← links)
• Morphology of a human-derived YAC in yeast meiosis (Q70806576) (← links)