Molecular neurogenetics of biological rhythms

Chemical, morphological, and genetic characterization of the floral scent and scent-releasing structures of Gynandropsis gynandra (Cleomaceae, Brassicales).

Plant biology (Stuttgart, Germany)·2025

Diversification and the evolution of dispersal ability in the tribe Brassiceae (Brassicaceae).

Annals of botany·2014

Learning and memory mutations impair acoustic priming of mating behaviour in Drosophila.

Nature·2011

Quantification of epididymal retinoic acid-binding protein (ERABP) mRNA in different anatomical regions of the adult rat epididymis.

Biochemistry and molecular biology international·2009

Assessment of exposure to secondhand smoke at outdoor bars and family restaurants in Athens, Georgia, using salivary cotinine.

Journal of occupational and environmental hygiene·2009

Principles and problems revolving around rhythm-related genetic variants.

Cold Spring Harbor symposia on quantitative biology·2008

Fine mapping of a putative genomic element that mediates the induction of a male-specific muscle in Drosophila.

Journal of neurogenetics·2026

Psilocybin-induced behavioral and cellular effects.

Journal of neurogenetics·2026

Novel Variants in PLPBP, SCN1A, and SLC6A1: Genetics, Bioinformatics, and clinical Elucidation of Three Distinct Cases of Developmental and Epileptic Encephalopathy.

Journal of neurogenetics·2026

D-ribose-L-cysteine protects against rotenone-induced neurotoxicity in Drosophila via redox, neurotransmitter, and DDC gene regulation.

Journal of neurogenetics·2026

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Journal of neurogenetics·2026

Expression of sulfate pathway genes in human neurodevelopment.

Journal of neurogenetics·2026

Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

European journal of human genetics : EJHG·2026

Genetic Etiology and Neurodevelopmental Outcomes in Children With Craniosynostosis: A 15-Year Single-Center Retrospective Study.

The Journal of craniofacial surgery·2026

Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human Populations.

Annals of human genetics·2026

Gerstmann-Straussler-Scheinker Disease With F198S Mutation Diagnosis on Repeat Genetic Testing: A Case Report.

Cureus·2026

Update and recommendations on genetic testing for amyotrophic lateral sclerosis in clinical practice: a Brazilian expert view.

Frontiers in neurology·2026

Characterisation of the Novel HLA-DRB1*10:52 Allele by Next-Generation Sequencing and Oxford Nanopore Sequencing.

HLA·2026

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Molecular neurogenetics of biological rhythms

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Chemical, morphological, and genetic characterization of the floral scent and scent-releasing structures of Gynandropsis gynandra (Cleomaceae, Brassicales).

Diversification and the evolution of dispersal ability in the tribe Brassiceae (Brassicaceae).

Learning and memory mutations impair acoustic priming of mating behaviour in Drosophila.

Quantification of epididymal retinoic acid-binding protein (ERABP) mRNA in different anatomical regions of the adult rat epididymis.

Assessment of exposure to secondhand smoke at outdoor bars and family restaurants in Athens, Georgia, using salivary cotinine.

Principles and problems revolving around rhythm-related genetic variants.

Fine mapping of a putative genomic element that mediates the induction of a male-specific muscle in Drosophila.

Psilocybin-induced behavioral and cellular effects.

Novel Variants in PLPBP, SCN1A, and SLC6A1: Genetics, Bioinformatics, and clinical Elucidation of Three Distinct Cases of Developmental and Epileptic Encephalopathy.

D-ribose-L-cysteine protects against rotenone-induced neurotoxicity in Drosophila via redox, neurotransmitter, and DDC gene regulation.

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Expression of sulfate pathway genes in human neurodevelopment.

Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

Genetic Etiology and Neurodevelopmental Outcomes in Children With Craniosynostosis: A 15-Year Single-Center Retrospective Study.

Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human Populations.

Gerstmann-Straussler-Scheinker Disease With F198S Mutation Diagnosis on Repeat Genetic Testing: A Case Report.

Update and recommendations on genetic testing for amyotrophic lateral sclerosis in clinical practice: a Brazilian expert view.

Characterisation of the Novel HLA-DRB1*10:52 Allele by Next-Generation Sequencing and Oxford Nanopore Sequencing.

Related Experiment Videos

Molecular neurogenetics of biological rhythms

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