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index medicus (462) 462
autophagy (426) 426
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article (93) 93
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analysis (51) 51
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cells (51) 51
expression (49) 49
physiological aspects (49) 49
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cells, cultured (47) 47
mice, inbred c57bl (46) 46
activation (45) 45
research (45) 45
autophagosomes - ultrastructure (44) 44
mechanisms (44) 44
models, biological (44) 44
multidisciplinary sciences (44) 44
phagosomes - metabolism (44) 44
autophagosomes - pathology (42) 42
neurons (41) 41
endoplasmic-reticulum (39) 39
inhibition (39) 39
signal transduction - drug effects (39) 39
homeostasis (38) 38
mitophagy (38) 38
death (37) 37
disease models, animal (36) 36
macroautophagy (36) 36
mitochondria - metabolism (36) 36
ubiquitin (36) 36
lysosomes - drug effects (35) 35
immunology (34) 34
oncology (34) 34
pathway (34) 34
rodents (34) 34
binding (33) 33
calcium (33) 33
metabolism (33) 33
microtubule-associated proteins - genetics (33) 33
reactive oxygen species - metabolism (33) 33
endoplasmic-reticulum stress (32) 32
microscopy, electron, transmission (32) 32
phosphorylation (32) 32
health aspects (31) 31
kinases (31) 31
neurons - metabolism (31) 31
protein binding (31) 31
selective autophagy (31) 31
starvation (31) 31
cell survival - drug effects (30) 30
lysosomes - pathology (30) 30
medicine (30) 30
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pharmacology & pharmacy (30) 30
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inflammation (29) 29
physiology (29) 29
alpha-synuclein (28) 28
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1. Full Text Autophagy in liver diseases
by Rautou, Pierre-Emmanuel and Mansouri, Abdellah and Lebrec, Didier and Durand, François and Valla, Dominique and Moreau, Richard
Journal of Hepatology, ISSN 0168-8278, 2010, Volume 53, Issue 6, pp. 1123 - 1134
Autophagy, or cellular self-digestion, is a cellular pathway crucial for development, differentiation, survival, and homeostasis. Its implication in human... 
Gastroenterology and Hepatology | Hepatitis | Starvation | Autophagic vacuole | Hepatocellular carcinoma | Autophagosome | LC3 | Survival | RAT HEPATOCYTES | ALPHA-ANTITRYPSIN DEFICIENCY | ENDOPLASMIC-RETICULUM STRESS | STARVATION-INDUCED AUTOPHAGY | HEPATOCELLULAR-CARCINOMA | HEPATITIS-C VIRUS | INSULIN-RESISTANCE | GASTROENTEROLOGY & HEPATOLOGY | MALLORY-DENK BODIES | INTRACELLULAR INCLUSIONS | MUTANT ALPHA-ANTITRYPSIN-Z | Liver - pathology | Fatty Liver - pathology | Humans | Liver Diseases - pathology | Male | Autophagy - physiology | Liver - physiopathology | Liver Diseases, Alcoholic - physiopathology | Liver Neoplasms - physiopathology | Female | Liver Neoplasms - pathology | alpha 1-Antitrypsin Deficiency - pathology | Liver Diseases, Alcoholic - pathology | Acute Lung Injury - physiopathology | Carcinoma, Hepatocellular - physiopathology | Reperfusion Injury - pathology | Fatty Liver - physiopathology | Acute Lung Injury - pathology | Hepatitis, Viral, Human - pathology | Hepatitis, Viral, Human - physiopathology | Animals | Models, Biological | Carcinoma, Hepatocellular - pathology | Reperfusion Injury - physiopathology | alpha 1-Antitrypsin Deficiency - physiopathology | Mice | Liver Diseases - physiopathology | Proteins | Liver cancer | Leukemia | Lymphomas | Hepatitis C | Hepatitis C virus | Health aspects | Protein kinases
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2. Full Text Autophagy in mammalian neurodevelopment and implications for childhood neurological disorders
by Marsh, Derek and Dragich, Joanna M
Neuroscience Letters, ISSN 0304-3940, 04/2019, Volume 697, pp. 29 - 33
Here we explore the neurodevelopmental aspects of macroautophagy (henceforth known as autophagy), the process by which cells remove and remodel their structure... 
Brain | Neurological | Lysosome | Childhood | Neurodevelopment | Axon | Autophagy | AXONS | EMBRYONIC-DEVELOPMENT | PROTEIN | NEURODEGENERATION | NEUROSCIENCES | DEGENERATION | DELETION | MEMORY | NEURONS | MUTATIONS | SPASTIZIN | Neurons - pathology | Humans | Central Nervous System - pathology | Autophagy - physiology | Brain - growth & development | Endosomes - pathology | Neurodevelopmental Disorders - pathology | Autophagosomes - pathology | Central Nervous System - growth & development | Animals | Brain - pathology | Lysosomes - pathology | Child | Nervous System Diseases - pathology | Lipids | Nervous system diseases | Disease susceptibility | Neurons | Analysis
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3. Full Text Autophagy in Spinal Cord Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis
by Sasaki, Shoichi
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 05/2011, Volume 70, Issue 5, pp. 349 - 359
To assess the potential role of autophagy in amyotrophic lateral sclerosis (ALS), lumbar spinal cords in a total of 19 sporadic ALS cases and 27 age-matched... 
Autolysosome | Amyotrophic lateral sclerosis | Autophagosome | Electron microscopy | Autophagy | LC3 | p62 | NEURODEGENERATIVE DISEASE | POLYGLUTAMINE | INDUCTION | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | CELL-DEATH | INHIBITION | PROTEIN-DEGRADATION | PATHWAY | LITHIUM | TRANSGENIC MICE | SELF-DIGESTION | Immunohistochemistry | Spinal Cord - metabolism | Humans | Middle Aged | Male | Microscopy, Electron | Motor Neurons - pathology | Nerve Degeneration - metabolism | Nerve Degeneration - pathology | Motor Neurons - metabolism | Amyotrophic Lateral Sclerosis - pathology | Spinal Cord - pathology | Amyotrophic Lateral Sclerosis - metabolism | Aged, 80 and over | Inclusion Bodies - pathology | Female | Aged | Lewy Bodies - metabolism | Lumbar Vertebrae | Inclusion Bodies - metabolism | Lewy Bodies - pathology
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4. Full Text Two novel Tau antibodies targeting the 396/404 region are primarily taken up by neurons and reduce Tau protein pathology
by Gu, Jiaping and Congdon, Erin E and Sigurdsson, Einar M
Journal of Biological Chemistry, ISSN 0021-9258, 11/2013, Volume 288, Issue 46, pp. 33081 - 33095
Background: Tau immunotherapy is an emerging approach to treat Alzheimer disease. Results: Two novel Tau antibodies targeting the 396/404 region are primarily... 
NEUROFIBRILLARY TANGLES | Phosphorylation | AMYLOID-BETA 25-35 | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | Antibodies | Lysosomes | Tau | Alzheimer Disease | CEREBROSPINAL-FLUID | PASSIVE-IMMUNIZATION | Autophagosomes | Immunotherapy | MOUSE MODEL | CENTRAL-NERVOUS-SYSTEM | PROPAGATION | Endosomes | TRANSGENIC MICE | Endosomes - immunology | Neurons - pathology | Antibodies, Monoclonal, Murine-Derived - immunology | tau Proteins - immunology | Neurons - immunology | Alzheimer Disease - drug therapy | Mice, Transgenic | Endosomes - pathology | Immunoglobulin Fab Fragments - pharmacology | Alzheimer Disease - pathology | Phosphorylation - genetics | Animals | tau Proteins - genetics | Models, Biological | Lysosomes - pathology | Mice | Phosphorylation - immunology | Immunoglobulin Fab Fragments - immunology | Alzheimer Disease - genetics | Alzheimer Disease - immunology | Antibodies, Monoclonal, Murine-Derived - pharmacology | Lysosomes - immunology | Index Medicus | Neurobiology
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5. Full Text Enhanced autophagy in pulmonary endothelial cells on exposure to HIV-Tat and morphine: Role in HIV-related pulmonary arterial hypertension
by Dalvi, Pranjali and Sharma, Himanshu and Chinnappan, Mahendran and Sanderson, Miles and Allen, Julie and Zeng, Ruoxi and Choi, Augustine and O'Brien-Ladner, Amy and Dhillon, Navneet K
Autophagy, ISSN 1554-8627, 12/2016, Volume 12, Issue 12, pp. 2420 - 2438
Intravenous drug use is one of the major risk factors for HIV-infection in HIV-related pulmonary arterial hypertension patients. We previously demonstrated... 
apoptosis | endothelial cells | autophagy | HIV-Tat | proliferation | morphine | CANCER-CELLS | OXIDATIVE STRESS | ANGIOGENESIS | PERMEABILITY | RECEPTOR | CELL BIOLOGY | PROTEIN-LEVELS | INHIBITION | INFECTION | GROWTH-FACTOR | Substance Abuse, Intravenous - pathology | Apoptosis - drug effects | Recombinant Fusion Proteins - adverse effects | Humans | Microvessels - pathology | Apoptosis - genetics | RNA, Messenger - metabolism | Autophagy - drug effects | Autophagosomes - drug effects | Endothelial Cells - ultrastructure | Simian Acquired Immunodeficiency Syndrome - virology | tat Gene Products, Human Immunodeficiency Virus - adverse effects | Lysosomes - metabolism | HIV Infections - pathology | Macaca | Autophagy - genetics | Substance Abuse, Intravenous - complications | Simian Acquired Immunodeficiency Syndrome - pathology | Biomarkers - metabolism | Lysosomes - drug effects | Lung - pathology | Endothelial Cells - metabolism | RNA, Messenger - genetics | Autophagosomes - metabolism | Autophagosomes - ultrastructure | Simian Immunodeficiency Virus - physiology | Lysosomes - ultrastructure | Animals | Models, Biological | HIV Infections - complications | Substance Abuse, Intravenous - virology | Endothelium, Vascular - pathology | Cell Proliferation - drug effects | Hypertension, Pulmonary - virology | Oxidative Stress - drug effects | Endothelial Cells - pathology | Hypertension, Pulmonary - pathology | Morphine - adverse effects | Apoptosis Regulatory Proteins - adverse effects | Hypertension, Pulmonary - complications
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6. Full Text Autophagosome–lysosome fusion in neurons requires INPP5E, a protein associated with Joubert syndrome
by Hasegawa, Junya and Iwamoto, Ryo and Otomo, Takanobu and Nezu, Akiko and Hamasaki, Maho and Yoshimori, Tamotsu
The EMBO Journal, ISSN 0261-4189, 09/2016, Volume 35, Issue 17, pp. 1853 - 1867
Autophagy is a multistep membrane traffic pathway. In contrast to autophagosome formation, the mechanisms underlying autophagosome–lysosome fusion remain... 
lysosomes | autophagosomes | Joubert syndrome | phosphoinositides | Lysosomes | Autophagosomes | Phosphoinositides | Abnormalities, Multiple - pathology | Membrane Fusion | Humans | Autophagosomes - metabolism | Cerebellum - abnormalities | Cerebellum - pathology | Kidney Diseases, Cystic - pathology | Lysosomes - metabolism | Eye Abnormalities - pathology | Neurons - physiology | Retina - abnormalities | Phosphoric Monoester Hydrolases - metabolism | Retina - pathology | Proteins | Enzymes | Neurons | Autophagy | Neurological disorders | Membrane & Intracellular Transport | Autophagy & Cell Death | Molecular Biology of Disease
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7. Full Text Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement
by Hori, Ikumi and Otomo, Takanobu and Nakashima, Mitsuko and Miya, Fuyuki and Negishi, Yutaka and Shiraishi, Hideaki and Nonoda, Yutaka and Magara, Shinichi and Tohyama, Jun and Okamoto, Nobuhiko and Kumagai, Takeshi and Shimoda, Konomi and Yukitake, Yoshiya and Kajikawa, Daigo and Morio, Tomohiro and Hattori, Ayako and Nakagawa, Motoo and Ando, Naoki and Nishino, Ichizo and Kato, Mitsuhiro and Tsunoda, Tatsuhiko and Saitsu, Hirotomo and Kanemura, Yonehiro and Yamasaki, Mami and Kosaki, Kenjiro and Matsumoto, Naomichi and Yoshimori, Tamotsu and Saitoh, Shinji
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 3552 - 11
Vici syndrome (VICIS) is a rare, autosomal recessive neurodevelopmental disorder with multisystem involvement characterized by agenesis of the corpus callosum,... 
SENSORINEURAL HEARING-LOSS | MULTIDISCIPLINARY SCIENCES | CORPUS-CALLOSUM | MUTATION | AGENESIS | EPG5 | NEURODEGENERATION | DEVELOPMENTAL DELAY | MUSCLE BIOPSY | OF-THE-LITERATURE | IMMUNODEFICIENCY | Brain - diagnostic imaging | Humans | Cataract - pathology | Epithelial Cells - pathology | Family Health | Neurodevelopmental Disorders - genetics | Autophagosomes - metabolism | Fibroblasts - pathology | Gene Knockout Techniques | Agenesis of Corpus Callosum - pathology | Muscles - pathology | Neurodevelopmental Disorders - pathology | Gene Knockdown Techniques | Proteins - genetics | Magnetic Resonance Imaging | Asian Continental Ancestry Group | Lysosomes - metabolism | Biopsy | Agenesis of Corpus Callosum - genetics | Brain - pathology | Cataract - genetics | HeLa Cells | Mutation | Cataracts | CRISPR | Splicing | Cardiomyopathy | Immunodeficiency | siRNA | Neurodevelopmental disorders | Pigmentation | Corpus callosum | Hereditary diseases | Magnetic resonance imaging | Clonal deletion | Fibroblasts | Skin | Phagocytosis
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8. Full Text Autophagy in Hepatocytes during Distant Tumor Growth
by Bgatova, N P and Bakhbaeva, S A and Taskaeva, Yu S and Makarova, V V and Borodin, Yu I
Bulletin of Experimental Biology and Medicine, ISSN 0007-4888, 7/2018, Volume 165, Issue 3, pp. 390 - 393
Structural changes in the liver of CBA mice were studied during the development of experimental hepatocarcinoma-29 inoculated into the hip. A decrease in the... 
Biomedicine, general | Pathology | Biomedicine | Internal Medicine | Laboratory Medicine | impaired structure of hepatocytes | distant tumor growth | Cell Biology | non-selective autophagy | MEDICINE, RESEARCH & EXPERIMENTAL | PHYSIOLOGY | LIVER | THERAPEUTIC TARGETS | MECHANISMS | CANCER | Hepatocytes - pathology | Male | Liver Neoplasms, Experimental - ultrastructure | Autophagy | Mitochondria - ultrastructure | Endoplasmic Reticulum - ultrastructure | Endoplasmic Reticulum - pathology | Lipid Droplets - ultrastructure | Mice, Inbred CBA | Lysosomes - pathology | Carcinoma, Hepatocellular - ultrastructure | Liver Neoplasms, Experimental - pathology | Lipid Droplets - pathology | Injections, Intramuscular | Mitochondria - pathology | Microscopy, Electron | Autophagosomes - pathology | Autophagosomes - ultrastructure | Lysosomes - ultrastructure | Animals | Carcinoma, Hepatocellular - pathology | Cell Line, Tumor | Hepatocytes - ultrastructure | Mice | Muscle, Skeletal | Glycogen | Tumors | Liver | Ribosomes | Homeostasis | Phagosomes | Lysosomes | Electron microscopy | Hip | Mitochondria | Hepatocytes | Intracellular | Endoplasmic reticulum | Cytoplasm | Phagocytosis
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9. Full Text Defective ciliogenesis in INPP5E‐related Joubert syndrome
by Hardee, Isabel and Soldatos, Ariane and Davids, Mariska and Vilboux, Thierry and Toro, Camilo and David, Karen L and Ferreira, Carlos R and Nehrebecky, Michele and Snow, Joseph and Thurm, Audrey and Heller, Theo and Macnamara, Ellen F and Gunay‐Aygun, Meral and Zein, Wadih M and Gahl, William A and Malicdan, May Christine V
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2017, Volume 173, Issue 12, pp. 3231 - 3237
Joubert syndrome is a neurodevelopmental disorder, characterized by malformation of the mid and hindbrain leading to the pathognomonic molar tooth appearance... 
rare disorders | Joubert syndrome | INPP5E | molar‐tooth sign | ciliopathy | molar-tooth sign | INPP5E MUTATIONS | AUTOPHAGOSOME-LYSOSOME FUSION | CILIOPATHIES | DISEASE | GENETICS & HEREDITY | DISORDERS | Abnormalities, Multiple - pathology | Eye Abnormalities - diagnostic imaging | Humans | Kidney Diseases, Cystic - diagnostic imaging | Cerebellum - abnormalities | Ciliopathies - diagnosis | Young Adult | Ciliopathies - genetics | Cerebellum - diagnostic imaging | Kidney Diseases, Cystic - genetics | Female | Abnormalities, Multiple - genetics | Phosphoric Monoester Hydrolases - genetics | Cilia - pathology | Abnormalities, Multiple - diagnostic imaging | Eye Abnormalities - genetics | Fibroblasts - pathology | Cerebellum - pathology | Kidney Diseases, Cystic - pathology | Homozygote | Magnetic Resonance Imaging | Retina - diagnostic imaging | Phenotype | Eye Abnormalities - pathology | Pedigree | Adolescent | Retina - abnormalities | Mutation | Retina - pathology | Ciliopathies - pathology | Medicine, Experimental | Medical research | Inositol | Phosphatases | RNA | Analysis | Cerebellum | Brain | Brain stem | Congenital defects | Teeth | Cognitive ability | Inositol polyphosphate | Retina | mRNA | Neurodevelopmental disorders | Sleep disorders | Apnea | Magnetic resonance imaging | Polydactyly | Fibroblasts | Retinal degeneration | Hindbrain | Ataxia | Dystrophy | Inositol-1,4,5-trisphosphate 5-phosphatase | Cilia
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10. Full Text Dysfunctional autophagy in RPE, a contributing factor in age-related macular degeneration
by Golestaneh, Nady and Chu, Yi and Xiao, Yang-Yu and Stoleru, Gianna L and Theos, Alexander C
Cell Death and Disease, ISSN 2041-4889, 01/2017, Volume 8, Issue 1, pp. e2537 - e2537
Age-related macular degeneration (AMD) is a devastating neurodegenerative disease and a major cause of blindness in the developed world. Owing to its... 
DRUSEN FORMATION | PATHOGENESIS | OXIDATIVE STRESS | P62/SQSTM1 | DISEASE | MITOCHONDRIAL DYSFUNCTION | ENDOPLASMIC-RETICULUM STRESS | RETINAL-PIGMENT EPITHELIUM | MOLECULAR-MECHANISMS | CELL-DEATH | CELL BIOLOGY | Retinal Pigment Epithelium - metabolism | Reactive Oxygen Species - metabolism | Humans | Cells, Cultured | Oxidative Stress - genetics | Lipid Droplets - pathology | Lysosome-Associated Membrane Glycoproteins - biosynthesis | Mitochondria - metabolism | Autophagosomes - metabolism | Mitochondria - pathology | Retinal Pigment Epithelium - growth & development | Autophagosomes - pathology | Macular Degeneration - metabolism | Retinal Pigment Epithelium - pathology | Glycogen - metabolism | Lysosome-Associated Membrane Glycoproteins - genetics | Lipid Droplets - metabolism | Macular Degeneration - pathology | Macular degeneration | Oxidative stress | Retina | Pathogenesis | Autophagy | Original
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11. Full Text Endophilin-A Deficiency Induces the Foxo3a-Fbxo32 Network in the Brain and Causes Dysregulation of Autophagy and the Ubiquitin-Proteasome System
by Murdoch, John D and Rostosky, Christine M and Gowrisankaran, Sindhuja and Arora, Amandeep S and Soukup, Sandra-Fausia and Vidal, Ramon and Capece, Vincenzo and Freytag, Siona and Fischer, Andre and Verstreken, Patrik and Bonn, Stefan and Raimundo, Nuno and Milosevic, Ira
Cell Reports, ISSN 2211-1247, 10/2016, Volume 17, Issue 4, pp. 1071 - 1086
Endophilin-A, a well-characterized endocytic adaptor essential for synaptic vesicle recycling, has recently been linked to neurodegeneration. We report here... 
endophilin | ubiquitin-proteasome system | autophagy | ataxia | next-generation sequencing | protein homeostasis | neurodegeneration | endocytosis | FBXO32 | Parkinson’s disease | Parkinson's disease | NEURODEGENERATIVE DISEASE | COMPLEX | DOMAIN | PATHWAY | SYNAPTIC VESICLE ENDOCYTOSIS | DOWN-REGULATION | TRAFFICKING | PROTEINS | PLASMA-MEMBRANE | PARKINSONS-DISEASE | CELL BIOLOGY | Up-Regulation | SKP Cullin F-Box Protein Ligases - genetics | Acyltransferases - deficiency | Humans | Ubiquitin - metabolism | Male | Acyltransferases - metabolism | Autophagy | Brain - metabolism | Forkhead Box Protein O3 - genetics | Muscle Proteins - metabolism | Transcription, Genetic | Ataxia - genetics | Ataxia - pathology | Parkinson Disease - pathology | Movement Disorders - pathology | Hippocampus - pathology | SKP Cullin F-Box Protein Ligases - metabolism | Autophagosomes - metabolism | Parkinson Disease - genetics | Mutation - genetics | Nerve Degeneration - complications | Forkhead Box Protein O3 - metabolism | Nerve Degeneration - pathology | Aging - pathology | Mice, Knockout | Movement Disorders - complications | Muscle Proteins - genetics | Hippocampus - metabolism | Animals | Protein Binding | Mice | HeLa Cells | Proteasome Endopeptidase Complex - metabolism | Homeostasis - genetics | Apoptosis
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12. Full Text Lipid-Induced Endoplasmic Reticulum Stress Impairs Selective Autophagy at the Step of Autophagosome-Lysosome Fusion in Hepatocytes
by Miyagawa, Koichiro and Oe, Shinji and Honma, Yuichi and Izumi, Hiroto and Baba, Ryoko and Harada, Masaru
American Journal of Pathology, The, ISSN 0002-9440, 2016, Volume 186, Issue 7, pp. 1861 - 1873
Blockage of hepatic autophagic degradation system occurs in obesity and is associated with the development of nonalcoholic fatty liver disease. However, the... 
Pathology | NEURODEGENERATIVE DISEASE | INCLUSION FORMATION | CELLS | PROTEIN | ACIDS | FATTY LIVER-DISEASE | INSULIN-RESISTANCE | ER STRESS | PATHOLOGY | MALLORY-DENK BODIES | UP-REGULATION | Non-alcoholic Fatty Liver Disease - pathology | Humans | Mice, Inbred C57BL | Diet, High-Fat - adverse effects | Hepatocytes - pathology | Immunoblotting | Male | Autophagy - physiology | Non-alcoholic Fatty Liver Disease - physiopathology | Fatty Acids - toxicity | Autophagosomes - pathology | Animals | Fluorescent Antibody Technique | Cell Line, Tumor | Lysosomes - pathology | Mice | Fatty Acids, Monounsaturated - toxicity | Disease Models, Animal | Endoplasmic Reticulum Stress - physiology
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13. Full Text Lysosomes, autophagosomes and Alzheimer pathology in dementia with Lewy body disease
by Gurney, Rowan and Davidson, Yvonne S and Robinson, Andrew C and Richardson, Anna and Jones, Matthew and Snowden, Julie S and Mann, David M.A
Neuropathology, ISSN 0919-6544, 08/2018, Volume 38, Issue 4, pp. 347 - 360
A failure of protein degradation may underpin Lewy body disease (LBD) where α‐synuclein is assimilated into the pathognomic Lewy bodies and Lewy neurites. We... 
autophagosomes | Lewy body disease | lysosomes | DIAGNOSIS | MULTICENTER | MANAGEMENT | DLB CONSORTIUM | CHAPERONE-MEDIATED AUTOPHAGY | ALPHA-SYNUCLEIN | PATHOLOGY | A-BETA-DEPOSITION | GLUCOCEREBROSIDASE MUTATIONS | NEUROSCIENCES | CLINICAL NEUROLOGY | BODIES | SPORADIC PARKINSONS-DISEASE | Proteolysis | Alzheimer's disease | Membrane proteins | Substantia nigra | Phagosomes | Lysosomes | Glial cells | Synuclein | Autophagy | Lewy bodies | Proteins | Axons | Dementia disorders | Cathepsin D | Mutation | Immunoreactivity | Plaques | Structure-function relationships
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