CLDN4: Difference between revisions

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m (→‎Further reading: task, replaced: journal = J Proteome Res. → journal = J Proteome Res using AWB)
 
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*{{cite journal  | vauthors=Michl P, Barth C, Buchholz M |title=Claudin-4 expression decreases invasiveness and metastatic potential of pancreatic cancer. |journal=Cancer Res. |volume=63 |issue= 19 |pages= 6265–71 |year= 2003 |pmid= 14559813 |doi=  |display-authors=etal}}
*{{cite journal  | vauthors=Michl P, Barth C, Buchholz M |title=Claudin-4 expression decreases invasiveness and metastatic potential of pancreatic cancer. |journal=Cancer Res. |volume=63 |issue= 19 |pages= 6265–71 |year= 2003 |pmid= 14559813 |doi=  |display-authors=etal}}
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* {{cite journal | vauthors = Liu F, Koval M, Ranganathan S, Fanayan S, Hancock WS, Lundberg EK, Beavis RC, Lane L, Duek P, McQuade L, Kelleher NL, Baker MS | title = A systems proteomics view of the endogenous human claudin protein family | journal = J Proteome Res | date= 2015 | pmid = 26680015 | doi = 10.1021/acs.jproteome.5b00769 }}
* {{cite journal | vauthors = Liu F, Koval M, Ranganathan S, Fanayan S, Hancock WS, Lundberg EK, Beavis RC, Lane L, Duek P, McQuade L, Kelleher NL, Baker MS | title = A systems proteomics view of the endogenous human claudin protein family | journal = J Proteome Res | volume = 15 | issue = 2 | pages = 339–59 | date= 2015 | pmid = 26680015 | pmc = 4777318 | doi = 10.1021/acs.jproteome.5b00769 }}
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Latest revision as of 10:56, 23 October 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Claudin 4, also known as CLDN4, is a protein which in humans is encoded by the CLDN4 gene. It belongs to the group of claudins.

This gene encodes an integral membrane protein, which belongs to the claudin family. The protein is a component of tight junction strands and may play a role in internal organ development and function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems.[1]

References

  1. "Entrez Gene: CLDN4 claudin 4".

External links

Further reading