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CHMP2B
Mutations in CHMP2B in Lower Motor Neuron Predominant Amyotrophic Lateral Sclerosis (ALS)
Genetic Screen Identifies Serpin5 As a Regulator of the Toll Pathway and CHMP2B Toxicity Associated with Frontotemporal Dementia
Progranulin Mutations in Dutch Familial Frontotemporal Lobar Degeneration
CHMP2B Regulates TDP-43 Phosphorylation and Proteotoxicity Via Modulating
Association of Imputed Prostate Cancer Transcriptome with Disease Risk Reveals Novel Mechanisms
Frontotemporal Dementia Caused by CHMP2B Mutation Is Characterised by Neuronal Lysosomal Storage Pathology
CHMP2B (NM 001244644) Human Tagged ORF Clone Product Data
76173 CHMP2B (D4G3K) Rabbit Mab
Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family
Ik2/TBK1 and Hook/Dynein, an Adaptor Complex for Early
A Neurodegenerative Disease Mutation That Accelerates the Clearance of Apoptotic Cells
Renoprotective Effect of Combined Inhibition of Angiotensin-Converting Enzyme and Histone Deacetylase
Variation in Protein Coding Genes Identifies Information Flow
CHMP2B Gene Charged Multivesicular Body Protein 2B
The ESCRT-III Proteins IST1 and CHMP1B Assemble Around Nucleic Acids
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Frontotemporal Dementia Causative CHMP2B Impairs Neuronal
Molecular Genetics of Neurodegenerative Dementias
Top View
CSF Neurofilament Light Concentration Is Increased in Presymptomatic CHMP2B Mutation Carriers Nina Rostgaard, Peter Roos, Erik Portelius, Et Al
Mutations in Bassoon in Individuals with Familial and Sporadic
ACE2 Interaction Networks in COVID-19
Mechanical Properties and Function of CHMP2B in the ESCRT Membrane Remodelling and Scission Pathway Maryam Alqabandi
Single-Cell RNA-Seq of Mouse Dopaminergic Neurons Informs Candidate Gene Selection For
Zhang Et Al. Stem Cell Res. 2016 (CRISPR)
Generation of a Human Induced Pluripotent Stem Cell Line Via CRISPR-Cas9 Mediated Integration of a Site-Specific Heterozygous Mutation in CHMP2B
Mining the Dark Matter of the Cancer Proteome for Novel Biomarkers
Frontotemporal Dementia Caused by CHMP2B Mutation Is Characterised by Neuronal Lysosomal Storage Pathology
CHMP2B-Related Frontotemporal Dementia
Investigation of RNA Binding Protein Pumilio As a Genetic Modifier of Mutant CHMP2B in Rf Ontotemporal Dementia (FTD): a Masters Thesis
Frontotemporal Dementia Caused by CHMP2B Mutations
Frontotemporal Dementia Caused by CHMP2B Mutation Is Characterised by Neuronal Lysosomal Storage Pathology
CHMP2B (1-213, His-Tag) Human Protein – AR39055PU-L | Origene
Mutations in CHMP2B in Lower Motor Neuron Predominant Amyotrophic Lateral Sclerosis (ALS)
What Can Machine Learning Approaches in Genomics Tell Us About the Molecular Basis of Amyotrophic Lateral Sclerosis?
Lessons Learned from CHMP2B, Implications for Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
Generating and Characterising Knockout and Transgenic Mouse Models of Frontotemporal Dementia Caused by CHMP2B Mutation
TMEM106B and Apoe Polymorphisms in CHMP2B Mediated Frontotemporal
In Vivo Quantitative Phosphoproteomic Profiling Identifies Novel Regulators
A NOVEL Cerna ANALYSIS for LMNA and ZMPSTE24 RELATED to MECHANISMS of PROGEROID LAMINOPATHIES