Found: 19
Select item for more details and to access through your institution.
AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect.
- Published in:
- Human Genetics, 2020, v. 139, n. 10, p. 1247, doi. 10.1007/s00439-020-02168-w
- By:
- Publication type:
- Article
Advanced Microscopy for Liver and Gut Ultrastructural Pathology in Patients with MVID and PFIC Caused by MYO5B Mutations.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 9, p. 1901, doi. 10.3390/jcm10091901
- By:
- Publication type:
- Article
Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 3, p. 481, doi. 10.3390/jcm10030481
- By:
- Publication type:
- Article
Recruitment dynamics of ESCRT-III and Vps4 to endosomes and implications for reverse membrane budding.
- Published in:
- eLife, 2017, p. 1, doi. 10.7554/eLife.31652
- By:
- Publication type:
- Article
Development of an Innovative 3D Cell Culture System to Study Tumour - Stroma Interactions in Non-Small Cell Lung Cancer Cells.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092511
- By:
- Publication type:
- Article
FlgM as a Secretion Moiety for the Development of an Inducible Type III Secretion System.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059034
- By:
- Publication type:
- Article
Natural history of Wolcott‐Rallison syndrome: A systematic review and follow‐up study.
- Published in:
- Liver International, 2024, v. 44, n. 3, p. 811, doi. 10.1111/liv.15834
- By:
- Publication type:
- Article
Interleukin-like epithelial-to-mesenchymal transition inducer activity is controlled by proteolytic processing and plasminogen-urokinase plasminogen activator receptor system-regulated secretion during breast cancer progression.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Internal Ileal Diversion as Treatment for Progressive Familial Intrahepatic Cholestasis Type 1-Associated Graft Inflammation and Steatosis after Liver Transplantation.
- Published in:
- Children, 2022, v. 9, n. 12, p. 1964, doi. 10.3390/children9121964
- By:
- Publication type:
- Article
Biogenesis of lysosome‐related organelles complex‐1 (BORC) regulates late endosomal/lysosomal size through PIKfyve‐dependent phosphatidylinositol‐3,5‐bisphosphate.
- Published in:
- Traffic, 2019, v. 20, n. 9, p. 674, doi. 10.1111/tra.12679
- By:
- Publication type:
- Article
Combining high‐pressure freezing with pre‐embedding immunogold electron microscopy and tomography.
- Published in:
- Traffic, 2018, v. 19, n. 8, p. 639, doi. 10.1111/tra.12575
- By:
- Publication type:
- Article
Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion disease.
- Published in:
- Traffic, 2017, v. 18, n. 7, p. 453, doi. 10.1111/tra.12486
- By:
- Publication type:
- Article
Ultrastructural Morphometry Points to a New Role for LAMTOR2 in Regulating the Endo/Lysosomal System.
- Published in:
- Traffic, 2015, v. 16, n. 6, p. 617, doi. 10.1111/tra.12271
- By:
- Publication type:
- Article
Microvillus Inclusion Disease: Loss of Myosin Vb Disrupts Intracellular Traffic and Cell Polarity.
- Published in:
- Traffic, 2014, v. 15, n. 1, p. 22, doi. 10.1111/tra.12131
- By:
- Publication type:
- Article
Cryo-Immunoelectron Microscopy of Adherent Cells Improved by the Use of Electrospun Cell Culture Substrates.
- Published in:
- Traffic, 2013, v. 14, n. 8, p. 886, doi. 10.1111/tra.12080
- By:
- Publication type:
- Article
Impact of citrulline substitution on clinical outcome after liver transplantation in carbamoyl phosphate synthetase 1 and ornithine transcarbamylase deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 2024, v. 47, n. 2, p. 220, doi. 10.1002/jimd.12717
- By:
- Publication type:
- Article
A CRISPR screen in intestinal epithelial cells identifies novel factors for polarity and apical transport.
- Published in:
- eLife, 2023, p. 1, doi. 10.7554/eLife.80135
- By:
- Publication type:
- Article
SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption.
- Published in:
- Genes, 2023, v. 14, n. 7, p. 1359, doi. 10.3390/genes14071359
- By:
- Publication type:
- Article
The Phospholipid Flippase ATP8B1 is Involved in the Pathogenesis of Ulcerative Colitis via Establishment of Intestinal Barrier Function.
- Published in:
- Journal of Crohn's & Colitis, 2024, v. 18, n. 7, p. 1134, doi. 10.1093/ecco-jcc/jjae024
- By:
- Publication type:
- Article