Learning to "think like a geneticist" with the de Serres ad-3 forward-mutation test in Neurospora crassa

Comparison of the spectra of genetic damage in formaldehyde-induced ad-3 mutations between DNA repair-proficient and -deficient heterokaryons of Neurospora crassa.

Mutation research·1999

Quantitative and qualitative comparison of spontaneous and chemical-induced specific-locus mutation in the ad-3 region of heterokaryon 12 of Neurospora crassa.

Mutation research·1997

Utility of a test for chromosomal malsegregation in Saccharomyces cerevisiae strain D61.M for the detection of antianeugens: test of the model combination of chlorophyllin and nocodazole.

Mutation research·1996

Activity profiles of antimutagens: in vitro and in vivo data.

Mutation research·1996

Interpretation of short-term test data: implications for assessment of chemopreventive activity.

IARC scientific publications·1996

Quantitative and qualitative aspects of spontaneous specific-locus mutation in the ad-3 region of heterokaryon 12 of Neurospora crassa.

Mutation research·1995

A crosslinking positive control for any in vivo comet assay tissue.

Mutation research·2026

Molecular characterisation and mutational analysis of antimicrobial resistance genes in Helicobacter pylori isolates in Erbil, Iraq.

Mutation research·2026

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

Synergistic Variants in C-terminal Binding Protein 1 and Alkaline Phosphatase Lead to Mandibular Hypoplasia Through Impaired Wnt Signaling: An Oligogenic Model.

bioRxiv : the preprint server for biology·2026

Point mutations and complex variants impact gene expression and addiction-related behaviors in Heterogeneous Stock rats.

bioRxiv : the preprint server for biology·2026

Developmental Cerebellar Pathology in Mouse Models of SCN2A Premature Termination Codon Variants.

bioRxiv : the preprint server for biology·2026

Single-nucleus transcriptome-wide association study of human brain disorders.

Nature·2026

A Genetic Risk Variant Associated With the Risk of Primary Biliary Cholangitis Is Inherited From Neanderthals.

Liver international : official journal of the International Association for the Study of the Liver·2026

Clinical and Genetic Analysis of Pediatric Neurodevelopmental Disorders With Complex Chromosomal Rearrangements in Two Cases.

Molecular genetics & genomic medicine·2026

Related Experiment Videos

Learning to "think like a geneticist" with the de Serres ad-3 forward-mutation test in Neurospora crassa

Related Concept Videos

Comparison of the spectra of genetic damage in formaldehyde-induced ad-3 mutations between DNA repair-proficient and -deficient heterokaryons of Neurospora crassa.

Quantitative and qualitative comparison of spontaneous and chemical-induced specific-locus mutation in the ad-3 region of heterokaryon 12 of Neurospora crassa.

Utility of a test for chromosomal malsegregation in Saccharomyces cerevisiae strain D61.M for the detection of antianeugens: test of the model combination of chlorophyllin and nocodazole.

Activity profiles of antimutagens: in vitro and in vivo data.

Interpretation of short-term test data: implications for assessment of chemopreventive activity.

Quantitative and qualitative aspects of spontaneous specific-locus mutation in the ad-3 region of heterokaryon 12 of Neurospora crassa.

A crosslinking positive control for any in vivo comet assay tissue.

Molecular characterisation and mutational analysis of antimicrobial resistance genes in Helicobacter pylori isolates in Erbil, Iraq.

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.

Synergistic Variants in C-terminal Binding Protein 1 and Alkaline Phosphatase Lead to Mandibular Hypoplasia Through Impaired Wnt Signaling: An Oligogenic Model.

Point mutations and complex variants impact gene expression and addiction-related behaviors in Heterogeneous Stock rats.

Developmental Cerebellar Pathology in Mouse Models of SCN2A Premature Termination Codon Variants.

Single-nucleus transcriptome-wide association study of human brain disorders.

A Genetic Risk Variant Associated With the Risk of Primary Biliary Cholangitis Is Inherited From Neanderthals.

Clinical and Genetic Analysis of Pediatric Neurodevelopmental Disorders With Complex Chromosomal Rearrangements in Two Cases.

Related Experiment Videos

Learning to "think like a geneticist" with the de Serres ad-3 forward-mutation test in Neurospora crassa

Related Concept Videos

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