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MYO5B gene

Known as: KIAA1119, MYO5B, MYOSIN VB 
National Institutes of Health

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1 relation
MYO3A gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Knockdown Rab11‐FIP2 inhibits migration and invasion of nasopharyngeal carcinoma via suppressing Rho GTPase signaling
Rab11 family interacting protein 2 (Rab11‐FIP2) is a conserved protein and effector molecule for the small GTPase Rab11. By… 
2019
2019
Faculty Opinions recommendation of MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update.
2018
2018
New Study Suggests MYO5B As a Prognostic Marker for Colorectal Cancer
Investigators found a methylation-independent loss of MYO5B expression in CRC that matched disease progression, which indicates… 
2017
2017
[Clinical features and MYO5B mutations of a family affected by microvillus inclusion disease].
Microvillus inclusion disease (MVID) is an autosomal recessive disorder caused by biallelic mutations in the MYO5B or STX3 gene… 
2016
2016
Identification of the Isoform-specific Interactions between the Tail and the Head of Class V Myosin*
Vertebrates have three isoforms of class V myosin (Myo5), Myo5a, Myo5b, and Myo5c, which are involved in transport of multiple… 
2016
2016
Myosin Vb mediates copper export in polarized hepatocytes
The cellular machinery responsible for copper-stimulated delivery of the Wilson Disease protein ATP7B to the apical domain of… 
2016
2016
New Mouse Models for Microvillus Inclusion Disease (MVID): Where Do the Inclusions Come From and Are They Cause or Consequence?
2014
2014
Apical vesicle trafficking takes center stage in neonatal enteropathies.
2014
2014
PS-076 Novel Mutations Underlying Rare Familial Enteropathies
Background Microvillous Inclusion Disease (MVID) and Congenital Tufting Enteropathy (CTE) are congenital disorders of the… 
2014
2014
Genetic risk variants for dyslexia on chromosome 18 in a German cohort
Dyslexia is characterized by impaired reading and spelling. The disorder has a prevalence of about 5% in Germany, and a strong… 
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