Spontaneous mutability in Drosophila melanogaster, in natural and laboratory environments

Linkage disequilibria and the site frequency spectra in the su(s) and su(w(a)) regions of the Drosophila melanogaster X chromosome.

Genetics·2000

Both naturally occurring insertions of transposable elements and intermediate frequency polymorphisms at the achaete-scute complex are associated with variation in bristle number in Drosophila melanogaster.

Genetics·2000

Contrasting patterns of nucleotide polymorphism at the alcohol dehydrogenase locus in the outcrossing Arabidopsis lyrata and the selfing Arabidopsis thaliana.

Molecular biology and evolution·2000

The power of association studies to detect the contribution of candidate genetic loci to variation in complex traits.

Genome research·1999

Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster.

Genetics·1999

Classic Weinstein: tetrad analysis, genetic variation and achiasmate segregation in Drosophila and humans.

Genetics·1999

In silico analysis of missense variants in functional domains of PWWP2A and PWWP2B proteins.

Mutation research·2026

The role of KIT mutations in oral melanoma and disease progression: A literature review on early detection and targeted therapy.

Mutation research·2026

Mothers against decapentaplegic homolog 3-activated FAT atypical cadherin 2 regulates programmed death ligand-1 to mediate immune evasion in lung squamous cell carcinoma.

Mutation research·2026

Potential targets and molecular mechanisms of curcumin in treating Laryngeal and Pharyngeal Carcinoma throat cancer based on network pharmacology and bioinformatics analysis.

Mutation research·2026

Non-clonal interphase markers of chromosomal instability in malignancy acquisition and cancer progression.

Mutation research·2026

miR-145-5p induces ferroptosis by targeting Notch2 to suppress melanoma progression.

Mutation research·2026

Yunis Varon Syndrome: Characteristic Limb Abnormalities and Refining of the Phenotype.

American journal of medical genetics. Part A·2026

Genetic control of local mutation rates.

Proceedings of the National Academy of Sciences of the United States of America·2026

Deep Sequencing of Hepatitis B Virus Reveals Clinically Relevant Low-Frequency Variants Among People Living with HIV in Botswana.

Viruses·2026

Diverse Genomic Mechanisms of cfiA Activation in Carbapenem-Resistant Bacteroides fragilis Clinical Isolates from Korea.

Antibiotics (Basel, Switzerland)·2026

Updating the RZooRoH Package for the Analysis of Inbreeding, Identity-By-Descent and Relatedness From Genomic Data.

Molecular ecology resources·2026

A single-cell transcriptome atlas reveals paradoxical monoallelic expression of RNA editing and heterozygous SNPs.

Nucleic acids research·2026

Related Experiment Videos

Spontaneous mutability in Drosophila melanogaster, in natural and laboratory environments

Related Concept Videos

Linkage disequilibria and the site frequency spectra in the su(s) and su(w(a)) regions of the Drosophila melanogaster X chromosome.

Both naturally occurring insertions of transposable elements and intermediate frequency polymorphisms at the achaete-scute complex are associated with variation in bristle number in Drosophila melanogaster.

Contrasting patterns of nucleotide polymorphism at the alcohol dehydrogenase locus in the outcrossing Arabidopsis lyrata and the selfing Arabidopsis thaliana.

The power of association studies to detect the contribution of candidate genetic loci to variation in complex traits.

Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster.

Classic Weinstein: tetrad analysis, genetic variation and achiasmate segregation in Drosophila and humans.

In silico analysis of missense variants in functional domains of PWWP2A and PWWP2B proteins.

The role of KIT mutations in oral melanoma and disease progression: A literature review on early detection and targeted therapy.

Mothers against decapentaplegic homolog 3-activated FAT atypical cadherin 2 regulates programmed death ligand-1 to mediate immune evasion in lung squamous cell carcinoma.

Potential targets and molecular mechanisms of curcumin in treating Laryngeal and Pharyngeal Carcinoma throat cancer based on network pharmacology and bioinformatics analysis.

Non-clonal interphase markers of chromosomal instability in malignancy acquisition and cancer progression.

miR-145-5p induces ferroptosis by targeting Notch2 to suppress melanoma progression.

Yunis Varon Syndrome: Characteristic Limb Abnormalities and Refining of the Phenotype.

Genetic control of local mutation rates.

Deep Sequencing of Hepatitis B Virus Reveals Clinically Relevant Low-Frequency Variants Among People Living with HIV in Botswana.

Diverse Genomic Mechanisms of cfiA Activation in Carbapenem-Resistant Bacteroides fragilis Clinical Isolates from Korea.

Updating the RZooRoH Package for the Analysis of Inbreeding, Identity-By-Descent and Relatedness From Genomic Data.

A single-cell transcriptome atlas reveals paradoxical monoallelic expression of RNA editing and heterozygous SNPs.

Related Experiment Videos

Spontaneous mutability in Drosophila melanogaster, in natural and laboratory environments

Related Concept Videos

Related Articles