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1. Full Text Genomics, Circuits, and Pathways in Clinical Neuropsychiatry
by Lehner, Thomas and Miller, Bruce L and State, Matthew W
2016, ISBN 9780128001059, 798
Neuropsychiatry
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2. Full Text Literature of Luther: Receptions of the Reformer ed. by A. Edward Wesley and J. Christopher Edwards (review)
by Miller, Joshua C
Lutheran Quarterly, ISSN 0024-7499, 2016, Volume 30, Issue 1, pp. 123 - 124
Edwards, J. Christopher, ǂd 1982- ǂe editor | Northeast Regional Meeting | Conference on Christianity and Literature (U.S.) | St. Francis College | Awards | Congresses | 2013 | 1483-1546 $vCongresses | Luther, Martin | Wesley, Edward, ǂe editor | 1483-1546 | Theology | Lewis, C S (1898-1963) | McCarthy, Cormac (1933- ) | Kleist, Heinrich von (1777-1811) | Henry VIII, King of England (1491-1547)
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3. Full Text Noise Constraints Effecting Optimal Propeller Designs
by Miller, Christopher J., author
SAE technical paper series, Volume 850871.
Noise | Aerodynamics
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4. Handbook of consumer psychology
by Haugtvedt, Curtis P., 1958 and Herr, Paul, 1956 and Kardes, Frank R
2008, Marketing and consumer psychology series, ISBN 080585603X, Volume 4, xvi, 1273
Psychological aspects | Consumer behavior | Decision making | Advertising | Marketing
Book
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5. WJ IV clinical use and interpretation
: scientist-practitioner perspectives
by Flanagan, Dawn P., editor and Alfonso, Vincent C., editor
2016, ISBN 9780128020760, xvi, 420 pages
Woodcock-Johnson Psycho-Educational Battery | Woodcock-Johnson Tests of Cognitive Ability
Book
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6. 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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7. Full Text ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43
by Stoica, Radu and De Vos, Kurt J and Paillusson, Sébastien and Mueller, Sarah and Sancho, Rosa M and Lau, Kwok-Fai and Vizcay-Barrena, Gema and Lin, Wen-Lang and Xu, Ya-Fei and Lewis, Jada and Dickson, Dennis W and Petrucelli, Leonard and Mitchell, Jacqueline C and Shaw, Christopher E and Miller, Christopher C. J
Nature communications, ISSN 2041-1723, 06/2014, Volume 5, Issue 1, pp. 3996 - 3996
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Cell Line | Calcium - metabolism | Vesicular Transport Proteins - metabolism | Humans | Endoplasmic Reticulum - metabolism | Glycogen Synthase Kinase 3 beta | Protein Tyrosine Phosphatases - metabolism | Mitochondria - metabolism | Glycogen Synthase Kinase 3 - metabolism | DNA-Binding Proteins - metabolism | Frontotemporal Dementia - metabolism | Animals | Mitochondrial Proteins - metabolism | Amyotrophic Lateral Sclerosis - metabolism | HEK293 Cells | Membrane Proteins - metabolism | Mice | Index Medicus
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8. Full Text The importance of tau phosphorylation for neurodegenerative diseases
by Noble, Wendy and Hanger, Diane P and Miller, Christopher C.J and Lovestone, Simon
Frontiers in neurology, ISSN 1664-2295, 2013, Volume 4, pp. 83 - 83
Oligomers | Function | Tau | Phosphorylation | Alzheimer's disease | Extracellular | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Aggregation | neurodegeneration | Alzheimer’s disease | dendritic | oligomers
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9. A new literary history of America
by Marcus, Greil and Sollors, Werner
2009, Harvard University Press reference library, ISBN 9780674035942, xxvii, 1095
United States Civilization | History and criticism | American literature
Book
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10. 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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11. Full Text There's Something Wrong with my MAM; the ER–Mitochondria Axis and Neurodegenerative Diseases
by Paillusson, Sebastien and Stoica, Radu and Gomez-Suaga, Patricia and Lau, Dawn H.W and Mueller, Sarah and Miller, Tanya and Miller, Christopher C.J
Trends in neurosciences (Regular ed.), ISSN 0166-2236, 2016, Volume 39, Issue 3, pp. 146 - 157
Neurology | amyotrophic lateral sclerosis/fronto-temporal dementia | Parkinson's disease | Alzheimer's disease | mitochondria associated ER membranes | mitochondria | endoplasmic reticulum | Amyotrophic lateral sclerosis/fronto-temporal dementia | Mitochondria | Endoplasmic reticulum | Mitochondria associated ER membranes | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Animals | Neurodegenerative Diseases - pathology | Humans | Endoplasmic Reticulum - metabolism | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - therapy | Mitochondria - metabolism | Neurodegenerative Diseases - metabolism | Mitochondria - ultrastructure | Endoplasmic Reticulum - ultrastructure | Nervous system diseases | Mitochondrial DNA | Amyotrophic lateral sclerosis | Membranes | Alzheimers disease | Medical treatment | Parkinsons disease | Index Medicus | fronto-temporal dementia | Review | amyotrophic lateral sclerosis
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