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Nature, ISSN 0028-0836, 12/2009, Volume 462, Issue 7273, pp. 669 - 673
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2011, Volume 108, Issue 52, pp. 20881 - 20890
Amyotrophic lateral sclerosis (ALS) is a devastating and universally fatal neurodegenerative disease. Mutations in two related RNA-binding proteins, TDP-43 and... 
Aggregation | Proteins | Yeasts | Nervous system diseases | Neurodegenerative diseases | Neurons | Drosophila | Prions | Amyotrophic lateral sclerosis | Genetic mutation | WILD-TYPE | TDP-43 PROTEINOPATHY | DROSOPHILA MODEL | MULTIDISCIPLINARY SCIENCES | NEURODEGENERATION | AMYLOID PORES | TOXICITY | AMYOTROPHIC-LATERAL-SCLEROSIS | FUS MUTATIONS | FRONTOTEMPORAL LOBAR DEGENERATION | AGGREGATION | Immunohistochemistry | Protein Structure, Tertiary | RNA-Binding Proteins - genetics | TATA-Binding Protein Associated Factors - metabolism | Saccharomyces cerevisiae - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Cells, Cultured | Computational Biology | Genetic Association Studies - methods | TATA-Binding Protein Associated Factors - genetics | Drosophila melanogaster - genetics | Mutation, Missense - genetics | Motor Neurons - metabolism | Animals | Spinal Cord - cytology | Yeast fungi | Gene mutations | Physiological aspects | Development and progression | Genetic aspects | Research | Binding proteins | Health aspects | Biological Sciences | amyotrophic-lateral-sclerosis; frontotemporal lobar degeneration; drosophila model; fus mutations; tdp-43 proteinopathy; amyloid pores; wild-type; toxicity; neurodegeneration; aggregation | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
Frontiers in Physiology, ISSN 1664-042X, 2013, Volume 4, p. 353
The insulin/insulin-like growth factor signaling (IIS) pathway is well-established as a critical regulator of growth and metabolic homeostasis across the... 
Locomotion | Behavior | Drosophila melanogaster | Feeding | Insulin signaling | NERVOUS-SYSTEM | PHYSIOLOGY | RECEPTOR HOMOLOG | DROSOPHILA-MELANOGASTER | NEUROPEPTIDE-Y-LIKE | CIRCADIAN-RHYTHMS | locomotion | SEXUALLY DIMORPHIC BEHAVIOR | LOCOMOTOR-ACTIVITY | insulin signaling | RHODNIUS-PROLIXUS | feeding | FEEDING-BEHAVIOR | NEUROSECRETORY-CELLS | behavior
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 07/2012, Volume 21, Issue 13, pp. 2899 - 2911
Journal Article
Genes & Development, ISSN 0890-9369, 12/2016, Volume 30, Issue 23, pp. 2596 - 2606
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 09/2012, Volume 287, Issue 39, pp. 32406 - 32414
Journal Article
01/2014, ISBN 9781321479423
The increasing prevalence of metabolic disease in modern society has accelerated our need to understand factors that may be contributing to its development.... 
Neurosciences | Molecular biology
Dissertation
Nature, ISSN 0028-0836, 12/2009, Volume 462, Issue 7273, pp. 669 - 673
A longstanding challenge is to understand at the atomic level how protein dynamics contribute to enzyme catalysis. X-ray crystallography can provide snapshots... 
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2011, Volume 108, Issue 52, p. 20881
Amyotrophic lateral sclerosis (ALS) is a devastating and universally fatal neurodegenerative disease. Mutations in two related RNA-binding proteins, TDP-43 and... 
Immunohistochemistry | Proteins | Yeast | Genes | Amyotrophic lateral sclerosis | Ribonucleic acid--RNA
Journal Article
01/2014, ISBN 9781321479423, Volume 76, Issue 5
The increasing prevalence of metabolic disease in modern society has accelerated our need to understand factors that may be contributing to its development.... 
Book Chapter
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