Genetic alterations of ascus development in Neurospora tetrasperma

Two-dimensional electrophoresis of plasma membranes, showing differences among wild-type and abnormal ascospore mutant strains of Neurospora crassa.

Journal of bacteriology·1983

Molecular alteration in a Neurospora crassa morphological mutant and its phenocopy.

Proceedings of the National Academy of Sciences of the United States of America·1978

Occurrence of a major protein associated with fruiting body development in Neurospora and related Ascomycetes.

Proceedings of the National Academy of Sciences of the United States of America·1977

Genetically related protein variants specifically associated with fruiting body maturation in Neurospora.

Proceedings of the National Academy of Sciences of the United States of America·1973

Evidence for the differentiation of wild-type alleles in different species of neurospora.

Genetics·1972

Dominance modifiers in neurospora crassa: phenocopy selection and influence of certain ascus mutants.

Genetics·1972

The transcription factor CLAMP is required for neurogenesis in Drosophila melanogaster.

Genetics·2026

Starve-Feed Cycles Direct Quiescence to Proliferation Transitions in Drosophila Follicle Stem Cells via Transcriptional Regulation.

Genetics·2026

Cell adhesion molecules CadN, DIP-α and klg regulate axon targeting and dendritic elaboration through synergistic and opposing effects.

Genetics·2026

Autophagy, the Ubiquitin proteasome system, and the MAPK pathway control the temperature dependence of synaptic growth.

Genetics·2026

An Essential Role of the AMPK-Related Kinase Snrk in Regulating Drosophila Sleep.

Genetics·2026

Cave evolution on repeat: reuse of the same genomic regions across lineages of Astyanax mexicanus.

Genetics·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Related Experiment Videos

Genetic alterations of ascus development in Neurospora tetrasperma

Related Concept Videos

Two-dimensional electrophoresis of plasma membranes, showing differences among wild-type and abnormal ascospore mutant strains of Neurospora crassa.

Molecular alteration in a Neurospora crassa morphological mutant and its phenocopy.

Occurrence of a major protein associated with fruiting body development in Neurospora and related Ascomycetes.

Genetically related protein variants specifically associated with fruiting body maturation in Neurospora.

Evidence for the differentiation of wild-type alleles in different species of neurospora.

Dominance modifiers in neurospora crassa: phenocopy selection and influence of certain ascus mutants.

The transcription factor CLAMP is required for neurogenesis in Drosophila melanogaster.

Starve-Feed Cycles Direct Quiescence to Proliferation Transitions in Drosophila Follicle Stem Cells via Transcriptional Regulation.

Cell adhesion molecules CadN, DIP-α and klg regulate axon targeting and dendritic elaboration through synergistic and opposing effects.

Autophagy, the Ubiquitin proteasome system, and the MAPK pathway control the temperature dependence of synaptic growth.

An Essential Role of the AMPK-Related Kinase Snrk in Regulating Drosophila Sleep.

Cave evolution on repeat: reuse of the same genomic regions across lineages of Astyanax mexicanus.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Related Experiment Videos

Genetic alterations of ascus development in Neurospora tetrasperma

Related Concept Videos

Related Articles