Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic control of caudal development.

Clinical genetics - 1 Feb 2002

Catala M

Abstract excerpt

Several lines of evidence suggest that caudal development involves a distinct programme. This is illustrated by the fact that a specific pattern of malformations affects the caudal end of the human embryo. In addition, neurulation, the process leading to the formation of the neural tube, proceeds through different morphogenetic movements caudally. In mammals, as in birds, the caudal neural tube arises from...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Mice, Knockout
Share to Models, Biological
Share to Neural Crest

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Neurons

Share to Homeodomain Proteins

Share to Gene Expression Regulation, Developmental

Share to Heterozygote

Source

Identifiers

PMID: 11940082
DOI: 10.1034/j.1399-0004.2002.610202.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic control of caudal development.PMID 11940082Read ↗

Neurulation in the cranial region--normal and abnormal.Semantic proximity Read ↗

Embryonic development of the mammalian caudal Neural TubeSemantic proximity Read ↗

Genetic patterning of the posterior neuropore region of curly tail mouse embryos: deficiency of Wnt5a expression.Semantic proximity Read ↗

Caudal duplication syndromeSemantic proximity Read ↗

HLXB9 homeobox gene and caudal regression syndrome.Semantic proximity Read ↗

Lhx2 regulates the development of the forebrain hem system.Semantic proximity Read ↗

Posterior axis formation requires <i>Dlx5/Dlx6</i> expression at the neural plate borderSemantic proximity Read ↗

Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in mice.Semantic proximity Read ↗

Biomechanical coupling facilitates spinal neural tube closure in mouse embryosSemantic proximity Read ↗

Congenital abnormalities of body patterning: embryology revisited.Semantic proximity Read ↗

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.Semantic proximity Read ↗

Caudal <i>Fgfr1</i> disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in miceSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.