[HTML][HTML] Organoid models of human gastrointestinal development and disease

PH Dedhia, N Bertaux-Skeirik, Y Zavros, JR Spence - Gastroenterology, 2016 - Elsevier
We have greatly advanced our ability to grow a diverse range of tissue-derived and
pluripotent stem cell–derived gastrointestinal (GI) tissues in vitro. These systems, broadly …

The myosin superfamily at a glance

MA Hartman, JA Spudich - Journal of cell science, 2012 - journals.biologists.com
The cytoskeleton is an interconnected network that provides support and organization to
cells. In eukaryotes, its main components include actin and microtubules, two types of …

The endosomal recycling pathway—at the crossroads of the cell

MJ O'sullivan, AJ Lindsay - International journal of molecular sciences, 2020 - mdpi.com
The endosomal recycling pathway lies at the heart of the membrane trafficking machinery in
the cell. It plays a central role in determining the composition of the plasma membrane and …

[PDF][PDF] MYO5B mutations cause cholestasis with normal serum gamma‐glutamyl transferase activity in children without microvillous inclusion disease

E Gonzales, SA Taylor, A Davit‐Spraul, A Thébaut… - …, 2017 - Wiley Online Library
Some patients with microvillus inclusion disease due to myosin 5B (MYO5B) mutations may
develop cholestasis characterized by a progressive familial intrahepatic cholestasis‐like …

Loss of syntaxin 3 causes variant microvillus inclusion disease

CL Wiegerinck, AR Janecke, K Schneeberger… - Gastroenterology, 2014 - Elsevier
Microvillus inclusion disease (MVID) is a disorder of intestinal epithelial differentiation
characterized by life-threatening intractable diarrhea. MVID can be diagnosed based on loss …

[PDF][PDF] Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

YL Qiu, JY Gong, JY Feng, RX Wang, J Han, T Liu… - …, 2017 - Wiley Online Library
Hereditary cholestasis in childhood and infancy with normal serum gamma‐
glutamyltransferase (GGT) activity is linked to several genes. Many patients, however …

Unravelling the genetic basis of schizophrenia and bipolar disorder with GWAS: A systematic review

DP Prata, B Costa-Neves, G Cosme… - Journal of psychiatric …, 2019 - Elsevier
Objectives To systematically review findings of GWAS in schizophrenia (SZ) and in bipolar
disorder (BD); and to interpret findings, with a focus on identifying independent replications …

The myosin family of mechanoenzymes: from mechanisms to therapeutic approaches

DV Trivedi, S Nag, A Spudich… - Annual review of …, 2020 - annualreviews.org
Myosins are among the most fascinating enzymes in biology. As extremely allosteric
chemomechanical molecular machines, myosins are involved in myriad pivotal cellular …

Intestinal epithelial cell polarity defects in disease: lessons from microvillus inclusion disease

K Schneeberger, S Roth… - Disease models & …, 2018 - journals.biologists.com
The intestinal epithelium is a highly organized tissue. The establishment of epithelial cell
polarity, with distinct apical and basolateral plasma membrane domains, is pivotal for both …

Mechanisms of apical–basal axis orientation and epithelial lumen positioning

AW Overeem, DM Bryant, SCD van IJzendoorn - Trends in cell biology, 2015 - cell.com
In epithelial cells, the polarized orientation of the apical–basal axis determines the position
of the apical lumen and, thereby, the collective tubular tissue architecture. From recent …