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

The IgSF Cell Adhesion Protein CLMP and Congenital Short Bowel Syndrome (CSBS)

16 Mar 2023

Abstract excerpt

The immunoglobulin-like cell adhesion molecule CLMP is a member of the CAR family of cell adhesion proteins and is implicated in human congenital short-bowel syndrome (CSBS). CSBS is a rare but very severe disease for which no cure is currently available. In this review, we compare data from human CSBS patients and a mouse knockout model. These data indicate that CSBS is characterized by a defect in intestinal...

Read the complete abstract on PubMed

Topics

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

Share to Connexins and lens biology
Share to Erythrocyte Function and Pathophysiology
Share to Escherichia coli research studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36982793
DOI: 10.3390/ijms24065719

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The IgSF Cell Adhesion Protein CLMP and Congenital Short Bowel Syndrome (CSBS)PMID 36982793Read ↗

CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome.Semantic proximity Read ↗

Loss-of-Function of CLMP Is Associated With Congenital Short Bowel Syndrome and Impaired Intestinal Development.Semantic proximity Read ↗

Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder.Semantic proximity Read ↗

Clinical and Pathological Features of Severe Gut Dysmotility.Semantic proximity Read ↗

Visceral myopathy: clinical syndromes, genetics, pathophysiology, and fall of the cytoskeleton.Semantic proximity Read ↗

Two new mutations of the CLMP gene identified in a newborn presenting congenital short-bowel syndrome.Semantic proximity Read ↗

De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis.Semantic proximity Read ↗

A genetic mechanism for cecal atresia: the role of the Fgf10 signaling pathway.Semantic proximity Read ↗

Functional consequences of EpCam mutation in mice and men.Semantic proximity Read ↗

The long Filamin-A isoform is required for intestinal development and motility: implications for chronic intestinal pseudo-obstructionSemantic proximity Read ↗

Mutation of EpCAM leads to intestinal barrier and ion transport dysfunction.Semantic proximity Read ↗

Loss of Lsc/p115 protein leads to neuronal hypoplasia in the esophagus and an achalasia-like phenotype in mice.Semantic proximity Read ↗

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