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1دورية أكاديمية
المؤلفون: Morrison, Jack, Watts, Giles, Hobbs, Glyn, Dawnay, Nick
المصدر: In Forensic Science International April 2018 285:147-160
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2دورية أكاديمية
المؤلفون: Nalbandian, Angèle, Llewellyn, Katrina J, Badadani, Mallikarjun, Yin, Hong Z, Nguyen, Christopher, Katheria, Veeral, Watts, Giles, Mukherjee, Jogeshwar, Vesa, Jouni, Caiozzo, Vincent, Mozaffar, Tahseen, Weiss, John H, Kimonis, Virginia E
المصدر: Muscle & Nerve. 47(2)
مصطلحات موضوعية: Neurosciences, Neurodegenerative, Genetics, Aging, Brain Disorders, Rare Diseases, Aetiology, 2.1 Biological and endogenous factors, Neurological, Musculoskeletal, Adenosine Triphosphatases, Animals, Brain, Cell Cycle Proteins, Disease Models, Animal, Disease Progression, Frontotemporal Dementia, Mice, Mice, Transgenic, Motor Neurons, Myositis, Inclusion Body, Osteitis Deformans, Spinal Cord, Valosin Containing Protein, amyotrophic lateral sclerosis, cytoplasmic inclusions, frontotemporal dementia, inclusion body myopathy, molecular genetics, motor neuron degeneration, Paget disease of bone, pathology, valosin-containing protein, Medical and Health Sciences, Neurology & Neurosurgery
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/6fv693w5
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3دورية أكاديمية
المؤلفون: Mehta, Sarju G., Khare, Manaswitha, Ramani, Rupal, Watts, Giles J., Simon, Mariella, Osann, Kathryn E., Donkervoort, Sandra, Dec, Eric, Nalbandian, Angele, Platt, Julia, Pasquali, Marzia, Wang, Annabel, Mozaffar, Tahseen, Smith, Charles D., Kimonis, Virginia E.
المصدر: Clinical genetics. 83(5)
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/1j2017bg
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4دورية أكاديمية
المؤلفون: Nalbandian, Angele, Llewellyn, Katrina J., Kitazawa, Masashi, Yin, Hong Z., Badadani, Mallikarjun, Khanlou, Negar, Edwards, Robert, Nguyen, Christopher, Mukherjee, Jogeshwar, Mozaffar, Tahseen, Watts, Giles, Weiss, John, Kimonis, Virginia E.
المصدر: PLoS ONE. 7(9)
مصطلحات موضوعية: inclusion-body myopathy, valosin-containing protein, paget-disease, frontotemporal dementia, cell-death, bone, mutations, autophagy, family, degradation
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/4tq368h0
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5دورية أكاديمية
المؤلفون: Camacho-Vanegas, Olga, Camacho, Sandra Catalina, Till, Jacob, Miranda-Lorenzo, Irene, Terzo, Esteban, Ramirez, Maria Celeste, Schramm, Vern, Cordovano, Grace, Watts, Giles, Mehta, Sarju, Kimonis, Virginia, Hoch, Benjamin, Philibert, Keith D, Raabe, Carsten A, Bishop, David F, Glucksman, Marc J, Martignetti, John A
المصدر: American Journal of Human Genetics. 90(4)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Human Genome, Cancer, Stem Cell Research, Rare Diseases, Biotechnology, Aetiology, 2.1 Biological and endogenous factors, Alternative Splicing, Animals, Base Sequence, Biological Evolution, Bone Diseases, Developmental, Bone Neoplasms, Chromosomes, Human, Pair 9, Exons, Genome, Histiocytoma, Benign Fibrous, Humans, Isoenzymes, Molecular Sequence Data, Muscular Dystrophies, Mutation, Neoplastic Syndromes, Hereditary, Primates, Purine-Nucleoside Phosphorylase, Retroviridae, Sarcoma, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/40t5r6fw
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6دورية أكاديمية
المؤلفون: Nalbandian, Angèle, Donkervoort, Sandra, Dec, Eric, Badadani, Mallikarjun, Katheria, Veeral, Rana, Prachi, Nguyen, Christopher, Mukherjee, Jogeshwar, Caiozzo, Vincent, Martin, Barbara, Watts, Giles D, Vesa, Jouni, Smith, Charles, Kimonis, Virginia E
المصدر: Journal of Molecular Neuroscience. 45(3)
مصطلحات موضوعية: Neurosciences, Dementia, Brain Disorders, Genetics, Rare Diseases, Neurodegenerative, Aging, Acquired Cognitive Impairment, 2.1 Biological and endogenous factors, Aetiology, Musculoskeletal, Neurological, Adenosine Triphosphatases, Amyotrophic Lateral Sclerosis, Animals, Autophagy, Cell Cycle Proteins, DNA-Binding Proteins, Disease Models, Animal, Frontotemporal Dementia, Genetic Association Studies, Humans, Mutation, Myositis, Inclusion Body, Osteitis Deformans, Valosin Containing Protein, Valosin containing protein, Amyotrophic lateral sclerosis, Inclusion body myopathy, Paget's disease of bone, Frontotemporal dementia, NFKB, Ubiquitin, TAR DNA Binding Protein-43, Endoplasmic reticulum associated degradation, Cognitive Sciences, Neurology & Neurosurgery
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/6j39b9w6
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7دورية أكاديمية
المؤلفون: Badadani, Mallikarjun, Nalbandian, Angele, Watts, Giles D., Vesa, Jouni, Kitazawa, Masashi, Su, Hailing, Tanaja, Jasmin, Dec, Eric, Wallace, Douglas C., Mukherjee, Jogeshwar, Caiozzo, Vincent, Warman, Matthew, Kimonis, Virginia E.
المصدر: PLoS ONE. 5(10)
مصطلحات موضوعية: valosin-containing protein, frontotemporal dementia, aaa-atpase, endoplasmic-reticulum, cell-death, autophagic vacuoles, gene-expression, mice, ubiquitin, p97
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/8b2742z1
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8دورية أكاديمية
المؤلفون: Vesa, Jouni, Su, Hailing, Watts, Giles D, Krause, Sabine, Walter, Maggie C, Martin, Barbara, Smith, Charles, Wallace, Douglas C, Kimonis, Virginia E
المصدر: Neuromuscular Disorders. 19(11)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Biological Psychology, Clinical Sciences, Neurosciences, Psychology, Rare Diseases, Aging, 2.1 Biological and endogenous factors, Aetiology, Musculoskeletal, Neurological, Adenosine Triphosphatases, Adult, Apoptosis, Autophagy, Caspase 3, Cell Cycle Proteins, Cell Fusion, Cells, Cultured, Down-Regulation, Female, Frontotemporal Dementia, Humans, In Situ Nick-End Labeling, Lysosomal-Associated Membrane Protein 2, Lysosome-Associated Membrane Glycoproteins, Male, Microscopy, Electron, Transmission, Middle Aged, Muscle Fibers, Skeletal, Mutation, Myoblasts, Myositis, Inclusion Body, Osteitis Deformans, Valosin Containing Protein, IBMPFD, Inclusion body myopathy, Paget's disease of the bone, Frontotemporal dementia, VCP, Vacuoles, Medical Physiology, Neurology & Neurosurgery, Clinical sciences, Biological psychology
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/54c8h882
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9دورية أكاديمية
المؤلفون: Kimonis, Virginia E, Fulchiero, Erin, Vesa, Jouni, Watts, Giles
المصدر: Biochimica et Biophysica Acta. 1782(12)
مصطلحات موضوعية: Rare Diseases, Acquired Cognitive Impairment, Brain Disorders, Dementia, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Neurodegenerative, Aging, Neurosciences, Aetiology, 2.1 Biological and endogenous factors, Neurological, Musculoskeletal, Adenosine Triphosphatases, Cell Cycle Proteins, Frontal Lobe, Genetic Predisposition to Disease, Humans, Muscular Diseases, Mutation, Osteitis Deformans, Valosin Containing Protein, Inclusion body, Vacuolar myopathy, ALS, FSH, Alzheimer, TDP-43, Ubiquitin, AAA protein, Physical Sciences, Biological Sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/987704pr
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10دورية أكاديمية
المؤلفون: Kimonis, Virginia E, Mehta, Sarju G, Fulchiero, Erin C, Thomasova, Dana, Pasquali, Marzia, Boycott, Kym, Neilan, Edward G, Kartashov, Alex, Forman, Mark S, Tucker, Stuart, Kimonis, Katerina, Mumm, Steven, Whyte, Michael P, Smith, Charles D, Watts, Giles DJ
المصدر: American Journal of Medical Genetics Part A, vol 146A. (6)
مصطلحات موضوعية: Intellectual and Developmental Disabilities (IDD), Neurodegenerative, Muscular Dystrophy, Dementia, Brain Disorders, Neurosciences, Genetics, Rare Diseases, Aging, Acquired Cognitive Impairment, 2.1 Biological and endogenous factors, Aetiology, Neurological, Musculoskeletal, Adenosine Triphosphatases, Adult, Cell Cycle Proteins, Cross-Sectional Studies, Family, Female, Humans, Inclusion Bodies, Male, Middle Aged, Muscle, Skeletal, Muscular Diseases, Osteitis Deformans, Pedigree, Retrospective Studies, Valosin Containing Protein, autosomal dominant, hereditary inclusion body myopathy, limb-girdle muscular dystrophy, Paget disease of bone, frontotemporal dementia, chromosome 9p13.3-12, VCP, Clinical Sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/3t13p9jp