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UBQLN2
Machine Learning Models for Predicting Protein Condensate Formation from Sequence Determinants and Embeddings
The Ubiquitin Proteasome System in Neuromuscular Disorders: Moving Beyond Movement
Aggresomal Sequestration and STUB1-Mediated Ubiquitylation During Mammalian Proteaphagy of Inhibited Proteasomes
RTL8 Promotes Nuclear Localization of UBQLN2 to Subnuclear Compartments Associated with Protein Quality Control
Deciphering the Molecular Profile of Plaques, Memory Decline And
Mutant Uromodulin Expression Leads to Altered Homeostasis of the Endoplasmic Reticulum and Activates the Unfolded Protein Response
Differential Effects of STCH and Stress-Inducible Hsp70 on the Stability and Maturation of NKCC2
UBQLN2/Ubiquilin 2 Mutation and Pathology in Familial Amyotrophic Lateral Sclerosis Kelly L
Characterisation of Human and Mouse SOD1-ALS Proteins in Vivo and in Vitro
Phenotype Informatics
Structure of Hrpn10 Bound to UBQLN2 UBL Illustrates Basis for Complementarity Between Shuttle Factors and Substrates at the Proteasome
Anti-UBQLN2 Antibody
C9ORF72 and UBQLN2 Are Genetic Causes of ALS in New Zealand: a Genetic and Pathological Study Using Banked Human Brain Tissue
Mutant UBQLN2 Promotes Toxicity by Modulating Intrinsic Self-Assembly
1 a Novel ALS-Associated Variant in UBQLN4 Regulates Motor Axon Morphogenesis
An Emerging Role for the Ubiquitin-Proteasome System in the Breakdown of Transient Protein Inclusions
UBE3A Antibody (C-Term) Purified Rabbit Polyclonal Antibody (Pab) Catalog # AP2154B
Gene Expression Changes in the Ventral Tegmental Area of Male Mice with Alternative Social Behavior Experience in Chronic Agonistic Interactions
Top View
Polyclonal Antibody to Ubiquilin-2 (UBQLN2) (C-Term) - Purified
Structure, Dynamics and Functions of Ubqlns: at the Crossroads of Protein Quality Control Machinery
Learning the Molecular Grammar of Protein Condensates from Sequence
Mutations in UBQLN2 Cause Dominant X-Linked Juvenile and Adult-Onset ALS and ALS/Dementia
Ubqln2 (NM 018798) Mouse Tagged ORF Clone Product Data
Mutations in UBQLN2 Cause Dominant X-Linked Juvenile and Adult-Onset ALS and ALS/Dementia
Striking Phenotypic Variation in a Family with the P506S UBQLN2 Mutation Including Amyotrophic Lateral Sclerosis, Spastic Paraplegia, and Frontotemporal Dementia
ALS-Linked Mutations Impair UBQLN2 Stress-Induced Biomolecular Condensate Assembly in Cells
Novel UBQLN2 Mutations Linked to Amyotrophic
A Pipeline for the Analysis and Interpretation of DNA NGS Data of ALS Patients
Anti-Ubiquilin 2 Antibody [6H9] (ARG10728)
UBQLN1 : a Multi-Domain Protein with Multiple Functions
Striking Phenotypic Variation in a Family with the P506S UBQLN2 Mutation Including Amyotrophic Lateral Sclerosis, Spastic Paraplegia and Frontotemporal Dementia
Protein Content and Lipid Profiling of Isolated Native Autophagosomes
Global Survey of Escape from X Inactivation by RNA-Sequencing in Mouse
Key Role of UBQLN2 in Pathogenesis of Amyotrophic Lateral Sclerosis And
Mutant UBQLN2P497H in Motor Neurons Leads to ALS-Like
Novel UBQLN2 Mutations Linked to Amyotrophic Lateral Sclerosis and Atypical Hereditary Spastic Paraplegia Phenotype Through Defective HSP70-Mediated Proteolysis