Myo5b knockout mice as a model of microvillus inclusion disease. (Q35880786)

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20 February 2020

title

Myo5b knockout mice as a model of microvillus inclusion disease (English)

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Irati Macaya

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20 February 2020

Stefania Landolfi

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20 February 2020

Javier Hernandez-Losa

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Simo Schwartz

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Santiago Ramon y Cajal

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20 February 2020

Diego Arango

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20 February 2020

Sven C D van IJzendoorn

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object named as

Sven C D van Ijzendoorn

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20 February 2020

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Josipa Bilic

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20 February 2020

author name string

Fernando Cartón-García

1

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20 February 2020

Arend W Overeem

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20 February 2020

Rocio Nieto

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20 February 2020

Sarah Bazzocco

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20 February 2020

language of work or name

English

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publication date

23 July 2015

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20 February 2020

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20 February 2020

volume

5

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20 February 2020

page(s)

12312

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Creative Commons Attribution 4.0 International

20 February 2020

copyright license

start time

23 July 2015

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4511872/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease

27 July 2018

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Microvillus inclusion disease: loss of Myosin vb disrupts intracellular traffic and cell polarity.

27 July 2018

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An overview and online registry of microvillus inclusion disease patients and their MYO5B mutations.

27 July 2018

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Cdc42 and Rab8a are critical for intestinal stem cell division, survival, and differentiation in mice

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Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease

27 July 2018

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Recycling endosomes in apical plasma membrane domain formation and epithelial cell polarity

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Interpreting neonatal lethal phenotypes in mouse mutants: insights into gene function and human diseases

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MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity.

27 July 2018

1 reference

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Microvillous inclusion disease (microvillous atrophy)

27 July 2018

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Stearoyl-CoA desaturase-2 gene expression is required for lipid synthesis during early skin and liver development

27 July 2018

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Translational control is required for the unfolded protein response and in vivo glucose homeostasis

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Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation

27 July 2018

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Familial enteropathy: A syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy

27 July 2018

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Myosin Vb and Rab11a regulate phosphorylation of ezrin in enterocytes.

27 July 2018

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Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model.

24 September 2018

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24 September 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/26201991

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/SREP12312

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26201991 AND SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26201991 AND SRC:MED&resulttype=core&format=json

20 February 2020

PubMed publication ID

26201991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26201991 AND SRC:MED&resulttype=core&format=json