Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model. (Q34617207)

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18 January 2020

title

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

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18 January 2020

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microvillus inclusion disease

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inferred from title

author

Natalia Schiefermeier

3

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18 January 2020

Hannes Ebner

4

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Geneviève de Saint Basile

18 January 2020

16

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18 January 2020

Michael W. Hess

21

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18 January 2020

Andreas Janecke

22

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18 January 2020

Lukas Alfons Huber

23

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18 January 2020

14

Danielle Canioni

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18 January 2020

author name string

Frank M Ruemmele

1

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18 January 2020

Thomas Müller

2

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18 January 2020

Silvia Lechner

5

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18 January 2020

Kristian Pfaller

6

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18 January 2020

Cornelia E Thöni

7

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18 January 2020

Olivier Goulet

8

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18 January 2020

Florence Lacaille

9

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18 January 2020

Jacques Schmitz

10

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18 January 2020

Virginie Colomb

11

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18 January 2020

Frédérique Sauvat

12

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18 January 2020

Yann Revillon

13

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18 January 2020

Nicole Brousse

15

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18 January 2020

Juliette Lefebvre

17

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18 January 2020

Peter Heinz-Erian

18

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18 January 2020

Axel Enninger

19

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18 January 2020

Gerd Utermann

20

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18 January 2020

publication date

1 May 2010

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18 January 2020

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18 January 2020

volume

31

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18 January 2020

issue

5

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18 January 2020

page(s)

544-551

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Myosin vb is associated with plasma membrane recycling systems

18 January 2020

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The intracellular lumen: origin, role and implications of a cytoplasmic neostructure

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Role of microtubules in polarized delivery of apical membrane proteins to the brush border of the intestinal epithelium

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7 January 2021

Microvillus inclusion disease: a genetic defect affecting apical membrane protein traffic in intestinal epithelium

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7 January 2021

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

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7 January 2021

Navajo microvillous inclusion disease is due to a mutation in MYO5B.

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7 January 2021

Subcellular fractionation of polarized epithelial cells and identification of organelle-specific proteins by two-dimensional gel electrophoresis

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7 January 2021

CD10: a valuable tool for the light microscopic diagnosis of microvillous inclusion disease (familial microvillous atrophy)

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7 January 2021

Fusion pore expansion is a slow, discontinuous, and Ca2+-dependent process regulating secretion from alveolar type II cells

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7 January 2021

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7 January 2021

In migrating fibroblasts, recycling receptors are concentrated in narrow tubules in the pericentriolar area, and then routed to the plasma membrane of the leading lamella

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7 January 2021

Microvillous inclusion disease: ultrastructural variability

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7 January 2021

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

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7 January 2021

The constitutive exocytotic pathway in microvillous atrophy

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7 January 2021

Periodic acid-Schiff staining abnormality in microvillous atrophy: photometric and ultrastructural studies

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7 January 2021

Autophagocytosis of the apical membrane in microvillus inclusion disease

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7 January 2021

An epithelial cell destined for apoptosis signals its neighbors to extrude it by an actin- and myosin-dependent mechanism

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7 January 2021

Microvillous inclusion disease (microvillous atrophy)

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7 January 2021

The Rab8 GTPase regulates apical protein localization in intestinal cells

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7 January 2021

The Fate of Effete Epithelial Cells at the Villus Tips of the Human Small Intestine

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7 January 2021

P115 RhoGEF and microtubules decide the direction apoptotic cells extrude from an epithelium

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7 January 2021

Myosin Vb is required for trafficking of the cystic fibrosis transmembrane conductance regulator in Rab11a-specific apical recycling endosomes in polarized human airway epithelial cells

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021