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1. Lang, Lockhart and biography
by Grierson, Herbert John Clifford, Sir, 1866-1960
1934, Andrew Lang Lecture, 1933, 38
Lockhart, J. G. 1794-1854 | Lang, Andrew, 1844-1912
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2. Full Text The C9orf72 protein interacts with Rab1a and the ULK1 complex to regulate initiation of autophagy
by Webster, Christopher P and Smith, Emma F and Bauer, Claudia S and Moller, Annekathrin and Hautbergue, Guillaume M and Ferraiuolo, Laura and Myszczynska, Monika A and Higginbottom, Adrian and Walsh, Matthew J and Whitworth, Alexander J and Kaspar, Brian K and Meyer, Kathrin and Shaw, Pamela J and Grierson, Andrew J and De Vos, Kurt J
The EMBO journal, ISSN 0261-4189, 08/2016, Volume 35, Issue 15, pp. 1656 - 1676
Rab GTPase | frontotemporal dementia | autophagy | amyotrophic lateral sclerosis | C9orf72 | Amyotrophic lateral sclerosis | Frontotemporal dementia | Autophagy | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Proteins - metabolism | Neurons - chemistry | rab1 GTP-Binding Proteins - metabolism | Humans | Cell Physiological Phenomena | Cells, Cultured | Autophagy-Related Protein-1 Homolog - metabolism | C9orf72 Protein | Intracellular Signaling Peptides and Proteins - metabolism | Neurons - metabolism | Frontotemporal Dementia - pathology | Proteins | Pathology | Genetics | Index Medicus | Neuroscience
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3. Full Text Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis
by Ferraiuolo, Laura and Kirby, Janine and Grierson, Andrew J and Sendtner, Michael and Shaw, Pamela J
Nature reviews. Neurology, ISSN 1759-4758, 11/2011, Volume 7, Issue 11, pp. 616 - 630
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amyotrophic Lateral Sclerosis - pathology | Amyotrophic Lateral Sclerosis - genetics | Humans | Amyotrophic Lateral Sclerosis - metabolism | Nerve Degeneration - genetics | Motor Neurons - pathology | Nerve Degeneration - metabolism | Nerve Degeneration - pathology | Physiological aspects | Complications and side effects | Amyotrophic lateral sclerosis | Genetic aspects | Research | Genes | Index Medicus
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4. Full Text Systemic Delivery of scAAV9 Expressing SMN Prolongs Survival in a Model of Spinal Muscular Atrophy
by Chiara F. Valori and Ke Ning and Matthew Wyles and Richard J. Mead and Andrew J. Grierson and Pamela J. Shaw and Mimoun Azzouz
Science translational medicine, ISSN 1946-6234, 06/2010, Volume 2, Issue 35, pp. 35ra42 - 35ra42
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Cell Biology | Research & Experimental Medicine | Animals, Newborn | Dependovirus - genetics | Gene Transfer Techniques | Genetic Therapy | Motor Activity - physiology | Molecular Sequence Data | Fibroblasts - pathology | Mutation - genetics | Muscular Atrophy, Spinal - genetics | Phenotype | Animals | Survival of Motor Neuron 1 Protein - therapeutic use | Base Sequence | Muscular Atrophy, Spinal - therapy | Survival Analysis | Survival of Motor Neuron 1 Protein - genetics | Mice | Codon - genetics | Muscular Atrophy, Spinal - physiopathology | Disease Models, Animal | Fibroblasts - metabolism | Index Medicus
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5. Full Text Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content
by De Vos, Kurt J and Chapman, Anna L and Tennant, Maria E and Manser, Catherine and Tudor, Elizabeth L and Lau, Kwok-Fai and Brownlees, Janet and Ackerley, Steven and Shaw, Pamela J and McLoughlin, Declan M and Shaw, Christopher E and Leigh, P. Nigel and Miller, Christopher C.J and Grierson, Andrew J
Human molecular genetics, ISSN 0964-6906, 11/2007, Volume 16, Issue 22, pp. 2720 - 2728
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Neurology | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Mitochondria - enzymology | Axonal Transport | Superoxide Dismutase - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Mice, Inbred C57BL | Male | Mice, Transgenic | Mitochondria - pathology | Mutation - genetics | Amyotrophic Lateral Sclerosis - pathology | Animals | Axons - pathology | Fluorescent Antibody Technique | Female | Amyotrophic Lateral Sclerosis - enzymology | Mice | Superoxide Dismutase-1 | Superoxide Dismutase - metabolism | Index Medicus
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6. Full Text Direct evidence for axonal transport defects in a novel mouse model of mutant spastin‐induced hereditary spastic paraplegia (HSP) and human HSP patients
by Kasher, Paul R and De Vos, Kurt J and Wharton, Stephen B and Manser, Catherine and Bennett, Ellen J and Bingley, Megan and Wood, Jonathan D and Milner, Roy and McDermott, Christopher J and Miller, Christopher C. J and Shaw, Pamela J and Grierson, Andrew J
Journal of neurochemistry, ISSN 0022-3042, 07/2009, Volume 110, Issue 1, pp. 34 - 44
axonal transport | spastin | hereditary spastic paraplegia | mouse model | axonal spheroid | Hereditary spastic paraplegia | Axonal spheroid | Mouse model | Spastin | Axonal transport | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Cerebrospinal fluid. Meninges. Spinal cord | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Nervous system (semeiology, syndromes) | Spastic Paraplegia, Hereditary - genetics | Axonal Transport - genetics | Spinal Cord - metabolism | Wallerian Degeneration - pathology | Humans | Spastic Paraplegia, Hereditary - metabolism | Mice, Neurologic Mutants | Motor Neurons - pathology | Microtubules - metabolism | Spinal Cord - pathology | Lameness, Animal - metabolism | Amyloid beta-Protein Precursor - metabolism | Spastic Paraplegia, Hereditary - physiopathology | Disease Models, Animal | Wallerian Degeneration - genetics | Genetic Predisposition to Disease - genetics | Wallerian Degeneration - metabolism | Cells, Cultured | Axons - metabolism | Lameness, Animal - pathology | Mitochondria - metabolism | Microtubules - pathology | Mutation - genetics | Down-Regulation - genetics | Motor Neurons - metabolism | Animals | Microtubules - genetics | Axons - pathology | Adenosine Triphosphatases - genetics | Mice | Spinal Cord - physiopathology | Lameness, Animal - genetics | Heat shock proteins | Mitochondrial DNA | Cytoskeletal proteins | Analysis | Paralysis, Spastic | Amyloid beta-protein | Biochemistry | Genetic disorders | Mutation | Paralysis | Index Medicus
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7. Full Text Role of axonal transport in neurodegenerative diseases
by De Vos, Kurt J and Grierson, Andrew J and Ackerley, Steven and Miller, Christopher C. J
Annual review of neuroscience, ISSN 0147-006X, 2008, Volume 31, Issue 1, pp. 151 - 173
Amyotrophic lateral sclerosis | Parkinson's disease | Huntington's disease | Alzheimer's disease | Charcot-Marie-tooth disease | Motor neuron disease | Neurology | Organic mental disorders. Neuropsychology | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Psychopathology. Psychiatry | Biological and medical sciences | Medical sciences | Axonal Transport - genetics | Central Nervous System - metabolism | Humans | Central Nervous System - pathology | Charcot-Marie-Tooth Disease - genetics | Motor Neuron Disease - metabolism | Motor Neuron Disease - genetics | Parkinson Disease - metabolism | Motor Neuron Disease - physiopathology | Charcot-Marie-Tooth Disease - metabolism | Huntington Disease - physiopathology | Alzheimer Disease - physiopathology | Axons - metabolism | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - metabolism | Parkinson Disease - genetics | Parkinson Disease - physiopathology | Huntington Disease - metabolism | Animals | Neurodegenerative Diseases - physiopathology | Axons - pathology | Alzheimer Disease - metabolism | Huntington Disease - genetics | Central Nervous System - physiopathology | Charcot-Marie-Tooth Disease - physiopathology | Alzheimer Disease - genetics | Nervous system | Degeneration | Axonal transport | Analysis | Index Medicus
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8. Full Text A manually annotated Actinidia chinensis var. chinensis (kiwifruit) genome highlights the challenges associated with draft genomes and gene prediction in plants
by Pilkington, Sarah M and Crowhurst, Ross and Hilario, Elena and Nardozza, Simona and Fraser, Lena and Peng, Yongyan and Gunaseelan, Kularajathevan and Simpson, Robert and Tahir, Jibran and Deroles, Simon C and Templeton, Kerry and Luo, Zhiwei and Davy, Marcus and Cheng, Canhong and McNeilage, Mark and Scaglione, Davide and Liu, Yifei and Zhang, Qiong and Datson, Paul and De Silva, Nihal and Gardiner, Susan E and Bassett, Heather and Chagné, David and McCallum, John and Dzierzon, Helge and Deng, Cecilia and Wang, Yen-Yi and Barron, Lorna and Manako, Kelvina and Bowen, Judith and Foster, Toshi M and Erridge, Zoe A and Tiffin, Heather and Waite, Chethi N and Davies, Kevin M and Grierson, Ella P and Laing, William A and Kirk, Rebecca and Chen, Xiuyin and Wood, Marion and Montefiori, Mirco and Brummell, David A and Schwinn, Kathy E and Catanach, Andrew and Fullerton, Christina and Li, Dawei and Meiyalaghan, Sathiyamoorthy and Nieuwenhuizen, Niels and Read, Nicola and Prakash, Roneel and Hunter, Don and Zhang, Huaibi and McKenzie, Marian and Knäbel, Mareike and Harris, Alastair and Allan, Andrew C and Gleave, Andrew and Chen, Angela and Janssen, Bart J and Plunkett, Blue and Ampomah-Dwamena, Charles and Voogd, Charlotte and Leif, Davin and Lafferty, Declan and Souleyre, Edwige J.F and Varkonyi-Gasic, Erika and Gambi, Francesco and Hanley, Jenny and Yao, Jia-Long and Cheung, Joey and David, Karine M and Warren, Ben and Marsh, Ken and Snowden, Kimberley C and Lin-Wang, Kui and Brian, Lara and Martinez-Sanchez, Marcela and Wang, Mindy and Ileperuma, Nadeesha and Macnee, Nikolai and Campin, Robert and McAtee, Peter and Drummond, Revel S.M and Espley, Richard V and Ireland, Hilary S and Wu, Rongmei and Atkinson, Ross G and Karunairetnam, Sakuntala and Bulley, Sean and Chunkath, Shayhan and Hanley, Zac and Storey, Roy and Thrimawithana, Amali H and Thomson, Susan and David, Charles and Testolin, Raffaele and Huang, Hongwen and Hellens, Roger P and Schaffer, Robert J
BMC genomics, ISSN 1471-2164, 04/2018, Volume 19, Issue 1, pp. 257 - 257
Genome sequencing | Actinidia chinensis | Manual annotation | Genetics & Heredity | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Index Medicus
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