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  • Uniparental Disomy

Nondisjunction, GeneticFollow by RSS 

You've reached a pubget topic page. Below are the latest papers on this topic, with subtopics on the left.

keywords > Pathological Conditions, Signs and Symptoms > Pathologic Processes > Chromosome Aberrations > Nondisjunction, Genetic

Latest papers

Evolution from heterozygous to homozygous KIT mutation in gastrointestinal stromal tumor correlates with the mechanism of mitotic nondisjunction and significant tumor progression.

Genomic plasticity and the diversity of polyploid plants.

Trichlorfon-induced polyploidy and nondisjunction in mouse oocytes from preantral follicle culture.

The chemotherapeutic agents nocodazole and amsacrine cause meiotic delay and non-disjunction in spermatocytes of mice.

Enhanced polarizing microscopy as a new tool in aneuploidy research in oocytes.

New insights into human nondisjunction of chromosome 21 in oocytes.

[Chromosome nondisjunction in Drosophila strains mutant for tumor suppressor Merlin].

Dissection of rye B chromosomes, and nondisjunction properties of the dissected segments in a common wheat background.

Acrocentric cryptic translocation associated with nondisjunction of chromosome 21.

Trisomy 18: a case study.

Chromosomes with a life of their own.

The mouse A/HeJ Y chromosome: another good Y gone bad.

Testing and estimating the non-disjunction fraction in Meiosis I using reference priors.

The origin of trisomy 13.

The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction.

Drosophila BubR1 is essential for meiotic sister-chromatid cohesion and maintenance of synaptonemal complex.

Non-disjunction of chromosome 13.

Role of the mod(mdg4) common region in homolog segregation in Drosophila male meiosis.

Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects.

Chromosome malorientations after meiosis II arrest cause nondisjunction.

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