Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Crossover patterns under meiotic chromosome program

25 Jan 2021

Abstract excerpt

Repairing DNA double-strand breaks (DSBs) with homologous chromosomes as templates is the hallmark of meiosis. The critical outcome of meiotic homologous recombination is crossovers, which ensure faithful chromosome segregation and promote genetic diversity of progenies. Crossover patterns are tightly controlled and exhibit three characteristics: obligatory crossover, crossover interference, and crossover...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomal and Genetic Variations
Share to DNA Repair Mechanisms
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 33533735
DOI: 10.4103/aja.aja_86_20

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 16 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Crossover patterns under meiotic chromosome programPMID 33533735Read ↗

Crossover Interference, Crossover Maturation, and Human AneuploidySemantic proximity Read ↗

Meiotic and mitotic recombination in meiosis.Semantic proximity Read ↗

Genetic control of meiosis surveillance mechanisms in mammalsSemantic proximity Read ↗

Insights about variation in meiosis from 31,228 human sperm genomesSemantic proximity Read ↗

Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermiaSemantic proximity Read ↗

Common variation in meiosis genes shapes human recombination and aneuploidy.Semantic proximity Read ↗

Common variation in meiosis genes shapes human recombination phenotypes and aneuploidy riskSemantic proximity Read ↗

Inefficient Crossover Maturation Underlies Elevated Aneuploidy in Human Female MeiosisSemantic proximity Read ↗

Meiosis: the chromosomal foundation of reproductionSemantic proximity Read ↗

Missed connections: recombination and human aneuploidySemantic proximity Read ↗

Meiotic Recombination in Human OocytesSemantic proximity Read ↗

Insights into variation in meiosis from 31,228 human sperm genomes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.