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Life Science Journal, ISSN 1097-8135, 2014, Volume 11, Issue 2, pp. 424 - 430
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 01/2009, Volume 94, Issue 1, pp. 277 - 284
Journal Article
Journal Article
Journal Article
Neuron, ISSN 0896-6273, 2009, Volume 63, Issue 3, pp. 316 - 328
Expansion of a polyglutamine tract in the androgen receptor (AR) causes spinal and bulbar muscular atrophy (SBMA). We previously showed that Akt-mediated... 
PROTEINS | HUMDISEASE | MOLNEURO | INSULIN | SURVIVAL | ANDROGEN RECEPTOR | SKELETAL-MUSCLE | HYPERTROPHY | KENNEDY-DISEASE | DEGRADATION | FOXO TRANSCRIPTION FACTORS | EXPRESSION | NEUROSCIENCES | GROWTH-FACTOR-I | Insulin-Like Growth Factor I - pharmacology | Humans | Receptors, Androgen - metabolism | Peptides - genetics | Ubiquitin - metabolism | Cercopithecus aethiops | Trinucleotide Repeat Expansion - physiology | Muscle, Skeletal - metabolism | Insulin-Like Growth Factor I - genetics | Phosphatidylinositol 3-Kinases - metabolism | Muscular Atrophy, Spinal - genetics | Phosphorylation - genetics | Muscular Atrophy - physiopathology | Peptides - metabolism | Transfection - methods | Time Factors | Muscle, Skeletal - drug effects | Muscle Proteins - metabolism | Behavior, Animal - drug effects | Phosphorylation - drug effects | Trinucleotide Repeat Expansion - drug effects | Oncogene Protein v-akt - metabolism | Disease Models, Animal | Muscular Atrophy, Spinal - mortality | Gene Expression Regulation - genetics | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Behavior, Animal - physiology | Mice, Transgenic | Mutation - genetics | Muscular Atrophy, Spinal - pathology | Serine - metabolism | Gene Expression Regulation - drug effects | Muscle Proteins - genetics | Animals | Receptors, Androgen - genetics | Muscular Atrophy, Spinal - therapy | Mice | Cell Line, Transformed | Insulin-Like Growth Factor I - metabolism | Medical colleges | Neurosciences | Peptide hormones | Neurons | Atrophy, Muscular | Growth factors | Cell culture | Phosphorylation | Statistical analysis | Disease | Insulin-like growth factors | Muscular system | Kinases | Molecular weight | Pathology | Musculoskeletal system | Rodents | Ligands | Index Medicus | Polyglutamine disease | spinal and bulbar muscular atrophy | androgen receptor | insulin-like growth factor 1 | skeletal muscle
Journal Article
National Medical Journal of China, ISSN 0376-2491, 10/2016, Volume 96, Issue 37, pp. 2965 - 2968
Journal Article
Annals of Neurology, ISSN 0364-5134, 02/2009, Volume 65, Issue 2, pp. 140 - 150
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 02/2018, Volume 48, pp. 90 - 92
Spinobulbar muscular atrophy (SBMA) is an X-linked recessive disease, presenting motor weakness and wasting of facial, bulbar and limb muscles. Hereditary... 
Hereditary neuropathy with liability to pressure palsy | Phenotypic variability | Spinobulbar muscular atrophy | Co-existence of two genetic disorders | PMP22 gene mutation | KENNEDY-DISEASE | MARIE-TOOTH NEUROPATHY | HNPP | BULBAR | NEUROSCIENCES | CLINICAL NEUROLOGY | DELETION | MOTOR
Journal Article
Journal Article
Neurological Sciences, ISSN 1590-1874, 4/2018, Volume 39, Issue 4, pp. 777 - 779
We report the case of a 54-year-old right-handed man who presented with a 2-year history of progressive upper-limb weakness with mild dysarthria and prominent... 
Neurology | Medicine & Public Health | Motor neuron disease | Fasciculations | Neurosurgery | Psychiatry | Neuroradiology | Movement disorders | Kennedy disease | Polymerase chain reaction | Atrophy | Handedness | Tongue | Gynecomastia | Polyglutamine | Motor neuron diseases | Trinucleotide repeats | Diagnosis | EMG | Genetic screening
Journal Article