D. Château

发表

Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy

A. Helbling-Leclerc, M. Fardeau, F. Tomé, 1997, Neuromuscular Disorders.

Requirement of cellular prion protein for intestinal barrier function and mislocalization in patients with inflammatory bowel disease.

B. Riveau, D. Château, M. Rousset, 2012, Gastroenterology.

The lipoatrophic caveolin-1 deficient mouse model reveals autophagy in mature adipocytes

N. Briand, É. Hajduch, D. Château, 2010, Autophagy.

Intestinal invalidation of the glucose transporter GLUT2 delays tissue distribution of glucose and reveals an unexpected role in gut homeostasis

B. Tavitian, N. Kapel, M. le Gall, 2016, Molecular metabolism.

Autophagosomes contribute to intracellular lipid distribution in enterocytes

E. Morel, D. Château, M. Rousset, 2014, Molecular biology of the cell.

Lipid-dependent bidirectional traffic of apolipoprotein B in polarized enterocytes.

E. Morel, D. Château, M. Rousset, 2003, Molecular biology of the cell.

Apolipoprotein A-II is catabolized in the kidney as a function of its plasma concentration Published, JLR Papers in Press, July 24, 2007.

P. Verroust, C. Klein, D. Château, 2007, Journal of Lipid Research.

Mutations in SLC2A2 reveal hGLUT2 function in pancreatic ß cell development

M. Gall, A. Leturque, É. Brot-Laroche, 2013 .

Adaptation of enterocytic Caco-2 cells to glucose modulates triacylglycerol-rich lipoprotein secretion through triacylglycerol targeting into the endoplasmic reticulum lumen.

D. Château, Julien Bouchoux, M. Rousset, 2006, The Biochemical journal.

The Cellular Prion Protein PrPc Is Expressed in Human Enterocytes in Cell-Cell Junctional Domains*

T. Pillot, E. Morel, Y. Frobert, 2004, Journal of Biological Chemistry.

Yersinia pseudotuberculosis disrupts intestinal barrier integrity through hematopoietic TLR-2 signaling.

J. Hugot, N. Cerf-Bensussan, D. Château, 2012, The Journal of clinical investigation.

Muscle as a putative producer of acid α-glucosidase for glycogenosis type II gene therapy

A. Orlacchio, C. Emiliani, A. Kahn, 2002 .

Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic).

B. Eymard, E. Krejci, M. Fardeau, 1998, American journal of human genetics.

Regulation of differentiation and keratin 10 expression by all-trans retinoic acid during the estrous cycle in the rat vaginal epithelium

D. Château, N. Boehm, D. Château, 1996, Cell and Tissue Research.

Asporin and the Mineralization Process in Fluoride‐Treated Rats

A. Dessombz, A. Berdal, D. Château, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Multi‐minicore disease–searching for boundaries: Phenotype analysis of 38 cases

A. Toutain, N. Romero, B. Estournet, 2000, Annals of neurology.

A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy

M. Prevost, F. Chapon, M. Fardeau, 1998, Nature Genetics.

Adult onset reducing body myopathy

D. Figarella-Branger, J. Pouget, M. Fardeau, 1999, Neuromuscular Disorders.

Retinoid receptors in rat vaginal and uterine epithelia: changes with ovarian steroids

D. Château, C. Rochette-Egly, N. Boehm, 1997, Molecular and Cellular Endocrinology.