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Huntingtin
Regulation of SETD2 Stability Is Important for the Fidelity Of
The Huntington's Disease Protein Interacts with P53 and CREB
Transglutaminase-Catalyzed Inactivation Of
A Dissertation Entitled the Androgen Receptor
The Isolation and Characterization of Huntingtin Interacting
Phosphorylation of Huntingtin at Residue T3 Is Decreased In
Allele-Specific Regulation of Mutant Huntingtin by Wig1, a Downstream
Sequence Specificity Analysis of the SETD2 Protein Lysine Methyltransferase and Discovery of a SETD2 Super-Substrate
Datasheet: VMA00449 Product Details
The Ataxin-1 Interactome Reveals Direct Connection with Multiple Disrupted Nuclear Transport Pathways
Caenorhabditis Elegans Dnj-14, the Orthologue of the DNAJC5 Gene
Anti-KMT3A / SETD2 Antibody (ARG64368)
HUNTINGTIN: ITS ROLE in GENE EXPRESSION Synapse Experiences Over Time
Serum- and Glucocorticoid-Inducible Kinase 1 and the Response to Cell Stress
Huntingtin Modulates Transcription, Occupies Gene Promotersin Vivo, and Binds Directly to DNA in a Polyglutamine-Dependent Manne
And P53 in Neuronal Apoptosis: Evidence That GAPDH Is Upregulated by P53
Extensive Changes in DNA Methylation Are Associated with Expression of Mutant Huntingtin
CRE-Mediated Transcription Is Increased in Huntington's Disease
Top View
Insulin and Exendin-4 Reduced Mutated Huntingtin Accumulation in Neuronal Cells
Probing the Interaction Between Huntingtin and Nmda Receptors
Identification of Palmitoyl Protein Thioesterase 1 Substrates Defines Roles for Synaptic Depalmitoylation
Identification and Localization of Huntingtin in Brain and Human Lymphoblastoid Cell Lines with Anti-Fusion Protein Antibodies CLAIRE-ANNE GUTEKUNST*, ALLAN I
The Role of P53 in Oxidative Stress and Polyglutamine Neurotoxicity
Glyceraldehyde-3-Phosphate Dehydrogenase Is a Multifaceted Therapeutic Target
The Role of Cysteine String Protein Α Phosphorylation at Serine 10 And
Title: Proteomic Analysis of Zebrafish Brain Tissue Following Exposure to the Pesticide Prochloraz
Inactivation of Drosophila Huntingtin Affects Long-Term Adult Functioning and the Pathogenesis of a Huntington’S Disease Model
Autoinhibitory Structure of the WW Domain of HYPB/SETD2 Regulates Its Interaction with the Proline-Rich Region of Huntingtin
Network Organization of the Huntingtin Proteomic Interactome in Mammalian Brain
Huntington´S Disease
A Brain-Specific SGK1 Splice Isoform Regulates Expression of ASIC1 in Neurons
Mutant Huntingtin Impairs the Post-Golgi Trafficking of Brain-Derived Neurotrophic Factor but Not Its Val66met Polymorphism
Tric Subunits Enhance BDNF Axonal Transport and Rescue Striatal Atrophy
Datasheet: VMA00449K Product Details
Huntingtin: a Protein with a Peculiar Solvent Accessible Surface
Brain-Derived Neurotrophic Factor in Cerebrospinal Fluid and Plasma Is
Cargo-Loading of Misfolded Proteins Into Extracellular Vesicles
Increased Glucose Metabolism and ATP Level in Brain Tissue Of
Glyceraldehyde-3-Phosphate Dehydrogenase: Nuclear Translocation Participates in Neuronal and Nonneuronal Cell Death
HIP2 Antibody Cat
Mutant Huntingtin Causes Context-Dependent Neurodegeneration in Mice with Huntington’S Disease
F-Actin Binding Regions on the Androgen Receptor and Huntingtin
Lentiviral-Mediated Delivery of Mutant Huntingtin in the Striatum of Rats
GAPDH Controls Extracellular Vesicle Biogenesis and Enhances Therapeutic Potential Of
Huntington's Disease
Dnaj/Hsc70 Chaperone Complexes Control the Extracellular Release of Neurodegenerative‐Associated Proteins
Mutant Huntingtin Impairs PNKP and ATXN3, Disrupting DNA Repair And
Huntingtin and Its Role in Mechanisms of RNA-Mediated Toxicity
HIP2 (H-6): Sc-390339
Huntingtin Modulates Transcription, Occupies Gene Promoters in Vivo, and Binds Directly to DNA in a Polyglutamine-Dependent Manner
P53 Tumor Suppressor Protein Regulates the Levels of Huntingtin Gene Expression
Brain Glyceraldehyde-3-Phosphate Dehydrogenase Activity in Human Trinucleotide Repeat Disorders
Anti-KMT3A / SETD2 Antibody (ARG54749)
SETD2 Rabbit Pab
HIP2 (Q-16): Sc-50736
How Do Post-Translational Modifications Influence The
Evidence for Cholinergic Dysfunction in Autosomal Dominant Kufs Disease
Brain-Derived Neurotrophic Factor in Cerebrospinal Fluid and Plasma Is Not a Biomarker for Huntington’S Disease
Emerging New Roles of the Lysosome and Neuronal Ceroid Lipofuscinoses Anil B
Early Striatal Dendrite Deficits Followed by Neuron Loss with Advanced Age in the Absence of Anterograde Cortical Brain- Derived Neurotrophic Factor
Phosphorylation of Huntingtin by Cyclin-Dependent Kinase 5 Is Induced by DNA Damage and Regulates Wild-Type and Mutant Huntingtin Toxicity in Neurons
Real-Time Imaging of Huntingtin Aggregates Diverting Target Search