Genetics and development of the nervous system

Xenopus fibrillin is expressed in the organizer and is the earliest component of matrix at the developing notochord-somite boundary.

Developmental dynamics : an official publication of the American Association of Anatomists·2006

The role of combinational coding by homeodomain and bHLH transcription factors in retinal cell fate specification.

Developmental biology·2005

The zebrafish as a tool for understanding the biology of visual disorders.

Seminars in cell & developmental biology·2003

Temporal coordinates: the genes that fix cell fate with birth order.

Developmental cell·2001

Semaphorin 3A elicits stage-dependent collapse, turning, and branching in Xenopus retinal growth cones.

The Journal of neuroscience : the official journal of the Society for Neuroscience·2001

Cellular competence plays a role in photoreceptor differentiation in the developing Xenopus retina.

Journal of neurobiology·2001

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

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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Genetics and development of the nervous system

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Xenopus fibrillin is expressed in the organizer and is the earliest component of matrix at the developing notochord-somite boundary.

The role of combinational coding by homeodomain and bHLH transcription factors in retinal cell fate specification.

The zebrafish as a tool for understanding the biology of visual disorders.

Temporal coordinates: the genes that fix cell fate with birth order.

Semaphorin 3A elicits stage-dependent collapse, turning, and branching in Xenopus retinal growth cones.

Cellular competence plays a role in photoreceptor differentiation in the developing Xenopus retina.

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.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

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Genetics and development of the nervous system

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