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Nature Genetics, ISSN 1061-4036, 2012, Volume 44, Issue 5, pp. 581 - 585
Journal Article
Brain, ISSN 0006-8950, 10/2007, Volume 130, Issue 10, pp. 2725 - 2735
Journal Article
Neurology, ISSN 0028-3878, 05/2009, Volume 72, Issue 21, pp. 1802 - 1809
Journal Article
Annals of Neurology, ISSN 0364-5134, 11/2008, Volume 64, Issue 5, pp. 573 - 582
Journal Article
Brain Pathology, ISSN 1015-6305, 10/2009, Volume 19, Issue 4, pp. 596 - 611
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 12/2017, Volume 214, Issue 12, pp. 3707 - 3729
The biogenesis of the multi-subunit vacuolar-type H+-ATPase (V-ATPase) is initiated in the endoplasmic reticulum with the assembly of the proton pore V0, which... 
MEDICINE, RESEARCH & EXPERIMENTAL | RENIN/PRORENIN RECEPTOR | ENDOSOMAL TRAFFICKING | PRORENIN RECEPTOR | DROSOPHILA OPTIC LOBE | ABNORMAL PROTEIN GLYCOSYLATION | CONGENITAL DISORDERS | COGNITIVE IMPAIRMENT | ENDOPLASMIC-RETICULUM | IMMUNOLOGY | VACUOLAR H+-ATPASE | DEFICIENCY CAUSES | Endoplasmic Reticulum-Associated Degradation | Vacuolar Proton-Translocating ATPases - genetics | Brain - embryology | Liver - pathology | Humans | Liver Diseases - pathology | Infant | Male | Psychomotor Disorders - complications | Blood Proteins - metabolism | Drosophila Proteins - metabolism | Neural Stem Cells - cytology | Autophagy | Drosophila melanogaster - metabolism | Proton-Translocating ATPases - metabolism | Young Adult | Lipids - chemistry | Genes, X-Linked | Proton-Translocating ATPases - genetics | Base Sequence | Cutis Laxa - complications | Liver Diseases - complications | Receptors, Cell Surface - chemistry | Membrane Proteins - metabolism | Amino Acid Sequence | Membrane Proteins - genetics | Proton-Translocating ATPases - deficiency | Psychomotor Disorders - pathology | Receptors, Cell Surface - metabolism | Glycosylation | Fibroblasts - pathology | Mutation - genetics | Animals | Receptors, Cell Surface - deficiency | Vacuolar Proton-Translocating ATPases - chemistry | Adolescent | Brain - pathology | Protein Binding | Mice | Protein Processing, Post-Translational | Drosophila Proteins - genetics | Vacuolar Proton-Translocating ATPases - deficiency | Cutis Laxa - pathology | Neural Stem Cells - metabolism | Receptors, Cell Surface - genetics | TOR protein | Liver | Impairment | Acidification | Serum proteins | Defects | Proteins | Missense mutation | Renin | Rodents | Evolution | Lipid metabolism | Fat body | Assembly | H+-transporting ATPase | Liver diseases | Drosophila | Immunodeficiency | Rapamycin | Metabolism | Signaling | Skin | Mutation | Auditory defects | Endoplasmic reticulum | Adenosine triphosphatase | Phagocytosis | Index Medicus | 316 | 310 | 321
Journal Article
Alcoholism: Clinical and Experimental Research, ISSN 0145-6008, 12/2016, Volume 40, Issue 12, pp. 2573 - 2590
Journal Article