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

Characterization of connexin31.1-deficient mice reveals impaired placental development.

Developmental biology - 1 Dec 2007

Zheng-Fischhöfer Qingyi, Kibschull Mark, Schnichels Marc, Kretz Markus, Petrasch-Parwez Elisabeth, Strotmann Jörg, Reucher Harald, Lynn Bruce D, Nagy James I, Lye Stephen J, Winterhager Elke, Willecke Klaus

Abstract excerpt

The gap junction gene Connexin31.1 has been reported to be expressed predominantly in the epidermis of murine skin. To study the function of this gene, we generated mice in which the coding DNA of the Connexin31.1 gene was replaced by lacZ reporter coding DNA. Using beta-galactosidase staining, we have shown that lacZ/Connexin31.1 was expressed in the spinous and granular layers of the epidermis, in cells of...

Read the complete abstract on PubMed

Topics

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

Share to beta-Galactosidase
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Embryo Implantation

Share to Embryonic Development

Share to Gene Targeting

Share to Placenta

Share to Placentation

Share to Sensation

Source

Identifiers

PMID: 17961533
DOI: 10.1016/j.ydbio.2007.09.025

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characterization of connexin31.1-deficient mice reveals impaired placental development.PMID 17961533Read ↗

Connexin31-deficiency in mice causes transient placental dysmorphogenesis but does not impair hearing and skin differentiation.Semantic proximity Read ↗

Cx31 and Cx43 double-deficient mice reveal independent functions in murine placental and skin development.Semantic proximity Read ↗

Connexinplexity: The spatial and temporal expression of <i>connexin</i> genes during vertebrate organogenesisSemantic proximity Read ↗

Diverse functions of vertebrate gap junctions.Semantic proximity Read ↗

Pannexin 1 Transgenic Mice: Human Diseases and Sleep-Wake Function Revision.Semantic proximity Read ↗

Connexin-caused genetic diseases and corresponding mouse models.Semantic proximity Read ↗

Connexin gene pathology.Semantic proximity Read ↗

Gap junctions and the connexin protein family.Semantic proximity Read ↗

Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice.Semantic proximity Read ↗

Unique and shared functions of different connexins in mice.Semantic proximity Read ↗

The connexin 30.3 of zebrafish homologue of human connexin 26 may play similar role in the inner ear.Semantic proximity Read ↗

Trafficking abnormality and ER stress underlie functional deficiency of hearing impairment-associated connexin-31 mutants.Semantic proximity Read ↗

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