J. Castro

发表

Lysosomal vitamin E accumulation in Niemann-Pick type C disease.

F. Leighton, S. Zanlungo, A. Álvarez, 2012, Biochimica et biophysica acta.

Relevance of Niemann‐Pick type C1 protein expression in controlling plasma cholesterol and biliary lipid secretion in mice

J. Miquel, S. Zanlungo, L. Amigo, 2002, Hepatology.

Niemann-Pick C2 Protein Expression Regulates Lithogenic Diet-Induced Gallstone Formation and Dietary Cholesterol Metabolism in Mice

A. Rigotti, Gonzalo Carrasco, S. Zanlungo, 2011, Lipids.

Deficiency of Niemann‐Pick C1 protein protects against diet‐induced gallstone formation in mice

A. Rigotti, J. Miquel, F. Nervi, 2010, Liver international : official journal of the International Association for the Study of the Liver.

Inactivation of hepatic microsomal triglyceride transfer protein protects mice from diet-induced gallstones.

J. Miquel, F. Nervi, S. Zanlungo, 2006, Gastroenterology.

Increased activity of hepatic microsomal triglyceride transfer protein and bile acid synthesis in gallstone disease

J. Miquel, F. Nervi, M. Rudling, 2007, Hepatology.

Transgenic overexpression of Niemann-Pick C2 protein promotes cholesterol gallstone formation in mice.

Juan I. Young, J. Miquel, A. Groen, 2016, Journal of hepatology.

Spermatozoa from mice deficient in Niemann-Pick disease type C2 (NPC2) protein have defective cholesterol content and reduced in vitro fertilising ability.

D. Busso, C. Lizama, S. Zanlungo, 2014, Reproduction, fertility, and development.

Npc1 deficiency in the C57BL/6J genetic background enhances Niemann-Pick disease type C spleen pathology.

María Gabriela Morales, A. Rigotti, M. Morales, 2011, Biochemical and biophysical research communications.

Imatinib therapy blocks cerebellar apoptosis and improves neurological symptoms in a mouse model of Niemann‐Pick type C disease

Julio D Amigo, S. Zanlungo, A. Álvarez, 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Structural and functional analysis of the ASM p.Ala359Asp mutant that causes acid sphingomyelinase deficiency.

Mauricio González, M. Latorre, E. Schuchman, 2016, Biochemical and biophysical research communications.

c-Abl Inhibition Activates TFEB and Promotes Cellular Clearance in a Lysosomal Disorder

A. Ballabio, D. Medina, F. Platt, 2020, iScience.

MLN64 induces mitochondrial dysfunction associated with increased mitochondrial cholesterol content

J. Fernandez-Checa, C. Garcia-Ruiz, S. Zanlungo, 2017, Redox biology.

c-Abl Activation Linked to Autophagy-Lysosomal Dysfunction Contributes to Neurological Impairment in Niemann-Pick Type A Disease

Noel Southall, Wei Zheng, J. Marugan, 2022, Frontiers in Cell and Developmental Biology.

Vitamin E Dietary Supplementation Improves Neurological Symptoms and Decreases c-Abl/p73 Activation in Niemann-Pick C Mice

M. Bosch-Morató, F. J. Muñoz, S. Zanlungo, 2014, Nutrients.

Disruption in Connexin-Based Communication Is Associated with Intracellular Ca2+ Signal Alterations in Astrocytes from Niemann-Pick Type C Mice

Jean X. Jiang, J. Sáez, J. Orellana, 2013, PloS one.

Relevance of Niemann‐Pick type C1 protein expression in controlling plasma cholesterol and biliary lipid secretion in mice

J. Miquel, S. Zanlungo, L. Amigo, 2002, Hepatology.

Spermatozoa from mice deficient in Niemann-Pick disease type C2 (NPC2) protein have defective cholesterol content and reduced in vitro fertilising ability.

D. Busso, C. Lizama, S. Zanlungo, 2014, Reproduction, fertility, and development.