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Capturing schizophrenia-like prodromal symptoms in a spinocerebellar ataxia-17 transgenic rat.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Symptomatic treatment options for Huntington's disease (guidelines of the German Neurological Society).
- Published in:
- Neurological Research & Practice, 2023, v. 5, n. 1, p. 1, doi. 10.1186/s42466-023-00285-1
- By:
- Publication type:
- Article
Differential diagnosis of chorea (guidelines of the German Neurological Society).
- Published in:
- Neurological Research & Practice, 2023, v. 5, n. 1, p. 1, doi. 10.1186/s42466-023-00292-2
- By:
- Publication type:
- Article
Age at onset in Huntington’s disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 453, doi. 10.1007/s00439-010-0873-9
- By:
- Publication type:
- Article
Patent Signals of IPO Performance: Evidence from High- and Low-Tech Industries in Japan.
- Published in:
- Asian Journal of Technology Management (AJTM), 2022, v. 15, n. 1, p. 21, doi. 10.12695/ajtm.2022.15.1.2
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- Publication type:
- Article
Optical Genome Mapping Reveals Genomic Alterations upon Gene Editing in hiPSCs: Implications for Neural Tissue Differentiation and Brain Organoid Research.
- Published in:
- Cells (2073-4409), 2024, v. 13, n. 6, p. 507, doi. 10.3390/cells13060507
- By:
- Publication type:
- Article
Intravenous MSC-Treatment Improves Impaired Brain Functions in the R6/2 Mouse Model of Huntington's Disease via Recovered Hepatic Pathological Changes.
- Published in:
- Cells (2073-4409), 2024, v. 13, n. 6, p. 469, doi. 10.3390/cells13060469
- By:
- Publication type:
- Article
Evidences for Mutant Huntingtin Inducing Musculoskeletal and Brain Growth Impairments via Disturbing Testosterone Biosynthesis in Male Huntington Disease Animals.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 23, p. 3779, doi. 10.3390/cells11233779
- By:
- Publication type:
- Article
The Diverse Calpain Family in Trypanosomatidae: Functional Proteins Devoid of Proteolytic Activity?
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 2, p. 299, doi. 10.3390/cells10020299
- By:
- Publication type:
- Article
Intranasal Administration of Mesenchymal Stem Cells Ameliorates the Abnormal Dopamine Transmission System and Inflammatory Reaction in the R6/2 Mouse Model of Huntington Disease.
- Published in:
- Cells (2073-4409), 2019, v. 8, n. 6, p. 595, doi. 10.3390/cells8060595
- By:
- Publication type:
- Article
bHLH Transcription Factor Math6 Antagonizes TGF-β Signalling in Reprogramming, Pluripotency and Early Cell Fate Decisions.
- Published in:
- Cells (2073-4409), 2019, v. 8, n. 6, p. 529, doi. 10.3390/cells8060529
- By:
- Publication type:
- Article
Sexual behavior and testis morphology in the BACHD rat model.
- Published in:
- PLoS ONE, 2018, v. 13, n. 6, p. 1, doi. 10.1371/journal.pone.0198338
- By:
- Publication type:
- Article
BACHD rats expressing full-length mutant huntingtin exhibit differences in social behavior compared to wild-type littermates.
- Published in:
- PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0192289
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- Publication type:
- Article
Loss of BAF Complex in Developing Cortex Perturbs Radial Neuronal Migration in a WNT Signaling-Dependent Manner.
- Published in:
- Frontiers in Molecular Neuroscience, 2021, v. 14, p. 1, doi. 10.3389/fnmol.2021.687581
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- Publication type:
- Article
A Novel Transgenic Rat Model for Spinocerebellar Ataxia Type 17 Recapitulates Neuropathological Changes and Supplies In Vivo Imaging Biomarkers.
- Published in:
- Journal of Neuroscience, 2013, v. 33, n. 21, p. 9068, doi. 10.1523/JNEUROSCI.5622-12.2013
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- Publication type:
- Article
A Novel BACHD Transgenic Rat Exhibits Characteristic Neuropathological Features of Huntington Disease.
- Published in:
- Journal of Neuroscience, 2012, v. 32, n. 44, p. 15426, doi. 10.1523/JNEUROSCI.1148-12.2012
- By:
- Publication type:
- Article
Behavioral and In Vivo Electrophysiological Evidence for Presymptomatic Alteration of Prefrontostriatal Processing in the Transgenic Rat Model for Huntington Disease.
- Published in:
- Journal of Neuroscience, 2011, v. 31, n. 24, p. 8986, doi. 10.1523/JNEUROSCI.1238-11.2011
- By:
- Publication type:
- Article
Cholesterol Defect Is Marked across Multiple Rodent Models of Huntington's Disease and Is Manifest in Astrocytes.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 32, p. 10844, doi. 10.1523/JNEUROSCI.0917-10.2010
- By:
- Publication type:
- Article
Low Risk of Severe Acute Respiratory Syndrome Coronavirus 2 Transmission by Fomites: A Clinical Observational Study in Highly Infectious Coronavirus Disease 2019 Patients.
- Published in:
- Journal of Infectious Diseases, 2022, v. 226, n. 9, p. 1608, doi. 10.1093/infdis/jiac170
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- Publication type:
- Article
Safeguarding transcriptional memory: a mitotic bookmarking role for chromatin remodelers.
- Published in:
- Signal Transduction & Targeted Therapy, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41392-023-01610-5
- By:
- Publication type:
- Article
Huntingtin forms toxic NH2-terminal fragment complexes that are promoted by the age-dependent decrease in proteasome activity.
- Published in:
- Journal of Cell Biology, 2003, v. 163, n. 1, p. 109, doi. 10.1083/jcb.200306038
- By:
- Publication type:
- Article
Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3).
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. 508, doi. 10.1093/hmg/dds449
- By:
- Publication type:
- Article
Sex differences in a transgenic rat model of Huntington's disease: decreased 17β-estradiol levels correlate with reduced numbers of DARPP32+ neurons in males.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 17, p. 2595, doi. 10.1093/hmg/ddn159
- By:
- Publication type:
- Article
Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 8, p. 1137, doi. 10.1093/hmg/ddn003
- By:
- Publication type:
- Article
Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 21, p. 3177, doi. 10.1093/hmg/ddl394
- By:
- Publication type:
- Article
Huntington disease update: new insights into the role of repeat instability in disease pathogenesis.
- Published in:
- Medizinische Genetik, 2021, v. 33, n. 4, p. 293, doi. 10.1515/medgen-2021-2101
- By:
- Publication type:
- Article
Huntington-Erkrankung.
- Published in:
- Medizinische Genetik, 2018, v. 30, n. 2, p. 246, doi. 10.1007/s11825-018-0190-6
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- Publication type:
- Article
DYT6 mutated THAP1 is a cell type dependent regulator of the SP1 family.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 19, p. 14716, doi. 10.3390/ijms241914716
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- Publication type:
- Article
Mitochondria and Energetic Depression in Cell Pathophysiology.
- Published in:
- International Journal of Molecular Sciences, 2009, v. 10, n. 5, p. 2252, doi. 10.3390/ijms10052252
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- Publication type:
- Article
Detection of a heterozygous germline APC mutation in a three-generation family with familial adenomatous polyposis using targeted massive parallel sequencing in Vietnam.
- Published in:
- BMC Medical Genetics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12881-018-0701-y
- By:
- Publication type:
- Article
Polygenic Scores for Cognitive Abilities and Their Association with Different Aspects of General Intelligence—A Deep Phenotyping Approach.
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 8, p. 4145, doi. 10.1007/s12035-021-02398-7
- By:
- Publication type:
- Article
Context-specific chromatin remodeling activity of mSWI/SNF complexes depends on the epigenetic landscape.
- Published in:
- Signal Transduction & Targeted Therapy, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41392-021-00770-6
- By:
- Publication type:
- Article
Optical Genome Mapping Reveals Disruption of the RASGRF2 Gene in a Patient with Developmental Delay Carrying a De Novo Balanced Reciprocal Translocation.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Optical Genome Mapping Reveals and Characterizes Recurrent Aberrations and New Fusion Genes in Adult ALL.
- Published in:
- Genes, 2023, v. 14, n. 3, p. 686, doi. 10.3390/genes14030686
- By:
- Publication type:
- Article
Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy.
- Published in:
- Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101752
- By:
- Publication type:
- Article
Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease.
- Published in:
- Molecular Neurodegeneration, 2011, v. 6, n. 1, p. 1, doi. 10.1186/1750-1326-6-1
- By:
- Publication type:
- Article
AAV-Mediated CAG-Targeting Selectively Reduces Polyglutamine-Expanded Protein and Attenuates Disease Phenotypes in a Spinocerebellar Ataxia Mouse Model.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 8, p. 4354, doi. 10.3390/ijms25084354
- By:
- Publication type:
- Article
Novel variants in a patient with late-onset hyperprolinemia type II: diagnostic key for status epilepticus and lactic acidosis.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Normal-Weight 14-Year-Old Girl with Acanthosis Nigricans and Markedly Increased Hepatic Steatosis: Evidence for the Important Role of Ectopic Fat Deposition in the Pathogenesis of Insulin Resistance in Childhood and Adolescence.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
Phoenix from the ashes: dramatic improvement in severe late-onset methylenetetrahydrofolate reductase (MTHFR) deficiency with a complete loss of vision.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 4, p. 2206, doi. 10.1007/s00415-021-10841-x
- By:
- Publication type:
- Article
Killing Two Angry Birds with One Stone: Autophagy Activation by Inhibiting Calpains in Neurodegenerative Diseases and Beyond.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/4741252
- By:
- Publication type:
- Article
Reduced Motivation in the BACHD Rat Model of Huntington Disease Is Dependent on the Choice of Food Deprivation Strategy.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0105662
- By:
- Publication type:
- Article
Early Deficits in Glycolysis Are Specific to Striatal Neurons from a Rat Model of Huntington Disease.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0081528
- By:
- Publication type:
- Article
Reversal Learning and Associative Memory Impairments in a BACHD Rat Model for Huntington Disease.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0071633
- By:
- Publication type:
- Article
The V471A Polymorphism in Autophagy-Related Gene <i>ATG7</i> Modifies Age at Onset Specifically in Italian Huntington Disease Patients.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068951
- By:
- Publication type:
- Article
Assessment of Motor Function, Sensory Motor Gating and Recognition Memory in a Novel BACHD Transgenic Rat Model for Huntington Disease.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068584
- By:
- Publication type:
- Article
Cerebellar Soluble Mutant Ataxin-3 Level Decreases during Disease Progression in Spinocerebellar Ataxia Type 3 Mice.
- Published in:
- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062043
- By:
- Publication type:
- Article
The Guanine Nucleotide Exchange Factor Kalirin-7 Is a Novel Synphilin-1 Interacting Protein and Modifies Synphilin-1 Aggregate Transport and Formation.
- Published in:
- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051999
- By:
- Publication type:
- Article
Regulation of Cell Delamination During Cortical Neurodevelopment and Implication for Brain Disorders.
- Published in:
- Frontiers in Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnins.2022.824802
- By:
- Publication type:
- Article