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Insulinlike Growth Factor (IGF)-1 Administration Ameliorates Disease Manifestations in a Mouse Model of Spinal and Bulbar Muscular Atrophy.
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- Molecular Medicine, 2012, v. 18, n. 12, p. 1261, doi. 10.2119/molmed.2012.00271
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- Article
Insulinlike Growth Factor (IGF)-1 Administration Ameliorates Disease Manifestations in a Mouse Model of Spinal and Bulbar Muscular Atrophy.
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- Molecular Medicine, 2012, v. 18, n. 9, p. 1261, doi. 10.2119/molmed.2012.00271
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- Article
Introduction to the Special Issue "Skeletal Muscle Atrophy: Mechanisms at a Cellular Level".
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- Cells (2073-4409), 2023, v. 12, n. 3, p. 502, doi. 10.3390/cells12030502
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- Article
Skeletal Muscle Pathogenesis in Polyglutamine Diseases.
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- Cells (2073-4409), 2022, v. 11, n. 13, p. N.PAG, doi. 10.3390/cells11132105
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- Article
Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism.
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- Cells (2073-4409), 2020, v. 9, n. 2, p. 325, doi. 10.3390/cells9020325
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- Article
Post-translational modifications of expanded polyglutamine proteins: impact on neurotoxicity.
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- Human Molecular Genetics, 2009, v. 18, n. R1, p. R40, doi. 10.1093/hmg/ddn412
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- Article
Mitochondrial abnormalities in spinal and bulbar muscular atrophy.
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- Human Molecular Genetics, 2009, v. 18, n. 1, p. 27, doi. 10.1093/hmg/ddn310
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- Article
Akt blocks ligand binding and protects against expanded polyglutamine androgen receptor toxicity.
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- Human Molecular Genetics, 2007, v. 16, n. 13, p. 1593, doi. 10.1093/hmg/ddm109
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- Article
Adenylyl cyclase activating polypeptide reduces phosphorylation and toxicity of the polyglutamine-expanded androgen receptor in spinobulbar muscular atrophy.
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- Science Translational Medicine, 2016, v. 8, n. 370, p. 1, doi. 10.1126/scitranslmed.aaf9526
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- Article
Identification and Expression of Acetylcholinesterase in Octopus vulgaris Arm Development and Regeneration: a Conserved Role for ACHE?
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- Molecular Neurobiology, 2015, v. 52, n. 1, p. 45, doi. 10.1007/s12035-014-8842-2
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- Article
AR cooperates with SMAD4 to maintain skeletal muscle homeostasis.
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- Acta Neuropathologica, 2022, v. 143, n. 6, p. 713, doi. 10.1007/s00401-022-02428-1
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- Article
MEF2 impairment underlies skeletal muscle atrophy in polyglutamine disease.
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- Acta Neuropathologica, 2020, v. 140, n. 1, p. 63, doi. 10.1007/s00401-020-02156-4
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- Article
Androgen-dependent impairment of myogenesis in spinal and bulbar muscular atrophy.
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- Acta Neuropathologica, 2013, v. 126, n. 1, p. 109, doi. 10.1007/s00401-013-1122-9
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- Article
Synaptophysin: leading actor or walk-on role in synaptic vesicle exocytosis?
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- BioEssays, 2004, v. 26, n. 4, p. 445, doi. 10.1002/bies.20012
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- Article
Autophagic and Proteasomal Mediated Removal of Mutant Androgen Receptor in Muscle Models of Spinal and Bulbar Muscular Atrophy.
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- Frontiers in Endocrinology, 2019, p. 1, doi. 10.3389/fendo.2019.00569
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- Article
Clenbuterol-sensitive delayed outward potassium currents in a cell model of spinal and bulbar muscular atrophy.
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- Pflügers Archiv: European Journal of Physiology, 2021, v. 473, n. 8, p. 1213, doi. 10.1007/s00424-021-02559-6
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- Article
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice.
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- Frontiers in Cellular Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fncel.2013.00234
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- Article
Mutational Screening of Androgen Receptor Gene in 8224 Men of Infertile Couples.
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 5, p. 1181, doi. 10.1210/clinem/dgac671
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- Article
Protein Arginine Methyltransferase 1 and 8 Interact with FUS to Modify Its Sub-Cellular Distribution and Toxicity <i>In Vitro</i> and <i>In Vivo</i>.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0061576
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- Article
Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubes.
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- Scientific Reports, 2017, p. 41046, doi. 10.1038/srep41046
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- Article
NURR1 and ERR1 Modulate the Expression of Genes of a DRD2 Coexpression Network Enriched for Schizophrenia Risk.
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- Journal of Neuroscience, 2020, v. 40, n. 4, p. 932, doi. 10.1523/JNEUROSCI.0786-19.2019
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- Article
The E3 ubiquitin-protein ligase MDM2 is a novel interactor of the von Hippel–Lindau tumor suppressor.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-72683-3
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- Article
Motor Neuron Diseases and Neuroprotective Peptides: A Closer Look to Neurons.
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- Frontiers in Aging Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnagi.2021.723871
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- Article
Decoding distinctive features of plasma extracellular vesicles in amyotrophic lateral sclerosis.
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- Molecular Neurodegeneration, 2021, v. 16, n. 1, p. 1, doi. 10.1186/s13024-021-00470-3
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- Article
Different Intracellular Pathomechanisms Produce Diverse Myelin Protein Zero Neuropathies in Transgenic Mice.
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- Journal of Neuroscience, 2006, v. 26, n. 8, p. 2358, doi. 10.1523/JNEUROSCI.3819-05.2006
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- Article
Editorial Comment to Castration‐resistant prostate cancer diagnosed during leuprorelin treatment for spinal and bulbar muscular atrophy.
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- 2022
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- Publication type:
- Editorial
Muscleblind acts as a modifier of FUS toxicity by modulating stress granule dynamics and SMN localization.
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- Nature Communications, 2019, p. 1, doi. 10.1038/s41467-019-13383-z
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- Article
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot–Marie–Tooth disease type 1B.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 7, p. 2032, doi. 10.1093/brain/aws140
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- Article
ClC-2-like Chloride Current Alterations in a Cell Model of Spinal and Bulbar Muscular Atrophy, a Polyglutamine Disease.
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- Journal of Molecular Neuroscience, 2021, v. 71, n. 3, p. 662, doi. 10.1007/s12031-020-01687-5
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- Article
In Vitro and In Vivo Modeling of Spinal and Bulbar Muscular Atrophy.
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- Journal of Molecular Neuroscience, 2016, v. 58, n. 3, p. 365, doi. 10.1007/s12031-015-0677-4
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- Article
Introduction to the Special Issue on Spinal and Bulbar Muscular Atrophy.
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- 2016
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- Publication type:
- Editorial
New Routes to Therapy for Spinal and Bulbar Muscular Atrophy.
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- Journal of Molecular Neuroscience, 2013, v. 50, n. 3, p. 514, doi. 10.1007/s12031-013-9978-7
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- Article
The E3 ubiquitin ligase TRIM11 mediates the degradation of congenital central hypoventilation syndrome-associated polyalanine-expanded PHOX2B.
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- Journal of Molecular Medicine, 2012, v. 90, n. 9, p. 1025, doi. 10.1007/s00109-012-0868-1
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- Article
Mutations in TGM6 induce the unfolded protein response in SCA35.
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- Human Molecular Genetics, 2017, v. 26, n. 19, p. 3749, doi. 10.1093/hmg/ddx259
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- Article
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients.
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- Human Molecular Genetics, 2017, v. 26, n. 6, p. 1087, doi. 10.1093/hmg/ddx019
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- Article
The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA).
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-44419-6
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- Article
The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA).
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-44419-6
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- Publication type:
- Article
Post-translational Modifications and Protein Quality Control in Motor Neuron and Polyglutamine Diseases.
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- Frontiers in Molecular Neuroscience, 2017, v. 10, p. 1, doi. 10.3389/fnmol.2017.00082
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- Article
Proteostasis and Diseases of the Motor Unit.
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- Frontiers in Molecular Neuroscience, 2016, v. 9, p. 1, doi. 10.3389/fnmol.2016.00164
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- Article
NGF-dependent and tissue-specific transcription of vgf is regulated by a CREB-p300 and bHLH factor interaction.
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- FEBS Letters, 2002, v. 510, n. 1-2, p. 50, doi. 10.1016/S0014-5793(01)03227-6
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- Article