Pages that link to "Q47597072"

The following pages link to UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosis (Q47597072):

Displaying 48 items.

• The ubiquilin gene family: evolutionary patterns and functional insights (Q21283993) (← links)
• Ubiquilin-2 (UBQLN2) binds with high affinity to the C-terminal region of TDP-43 and modulates TDP-43 levels in H4 cells: characterization of inhibition by nucleic acids and 4-aminoquinolines (Q24337496) (← links)
• Ultrastructural studies of ALS mitochondria connect altered function and permeability with defects of mitophagy and mitochondriogenesis (Q26782995) (← links)
• Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis (Q26863439) (← links)
• Frontotemporal dementia: a bridge between dementia and neuromuscular disease (Q28081198) (← links)
• Ubiquilin-2 drives NF-κB activity and cytosolic TDP-43 aggregation in neuronal cells. (Q30671325) (← links)
• Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Continuum (Q33653996) (← links)
• UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration (Q33930908) (← links)
• Application of next-generation sequencing technologies in Neurology (Q34658348) (← links)
• Signature changes in ubiquilin expression in the R6/2 mouse model of Huntington's disease (Q35122320) (← links)
• Pathogenic Ubqln2 gains toxic properties to induce neuron death (Q36649076) (← links)
• Emerging evidence of coding mutations in the ubiquitin-proteasome system associated with cerebellar ataxias (Q36671121) (← links)
• CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia (Q36809438) (← links)
• UBQLN2 Mediates Autophagy-Independent Protein Aggregate Clearance by the Proteasome (Q37214887) (← links)
• Clinical neurogenetics: amyotrophic lateral sclerosis (Q37274526) (← links)
• Next-generation sequencing in understanding complex neurological disease (Q37331388) (← links)
• Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS-FTD-linked UBQLN2 mutations (Q37451158) (← links)
• The changing scene of amyotrophic lateral sclerosis (Q38086771) (← links)
• Protein aggregation in amyotrophic lateral sclerosis. (Q38106862) (← links)
• Amyotrophic lateral sclerosis: an update on recent genetic insights (Q38148471) (← links)
• SQSTM1 mutations--bridging Paget disease of bone and ALS/FTLD. (Q38184230) (← links)
• Stress granules at the intersection of autophagy and ALS. (Q38835008) (← links)
• TDP-43/FUS in motor neuron disease: Complexity and challenges. (Q38969736) (← links)
• Autophagy Dysregulation in ALS: When Protein Aggregates Get Out of Hand (Q41525479) (← links)
• Impaired Mitophagy Plays a Role in Denervation of Neuromuscular Junctions in ALS Mice (Q41549091) (← links)
• Increased Ubqln2 expression causes neuron death in transgenic rats (Q41649780) (← links)
• The Genetics of Monogenic Frontotemporal Dementia (Q46958756) (← links)
• Evaluation of Skin Fibroblasts from Amyotrophic Lateral Sclerosis Patients for the Rapid Study of Pathological Features. (Q48158855) (← links)
• Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration. (Q48265316) (← links)
• Traumatic injury induces Stress Granule Formation and enhances Motor Dysfunctions in ALS/FTD Models (Q50047147) (← links)
• The distinct genetic pattern of ALS in Turkey and novel mutations. (Q52967015) (← links)
• Complement components are upregulated and correlate with disease progression in the TDP-43Q331K mouse model of amyotrophic lateral sclerosis. (Q54958681) (← links)
• The Emerging Role of DNA Damage in the Pathogenesis of the C9orf72 Repeat Expansion in Amyotrophic Lateral Sclerosis (Q57471221) (← links)
• Mutant UBQLN2 promotes toxicity by modulating intrinsic self-assembly (Q58863611) (← links)
• Personalized Medicine and Molecular Interaction Networks in Amyotrophic Lateral Sclerosis (ALS): Current Knowledge (Q60957022) (← links)
• A Variant Identified in a Sporadic Amyotrophic Lateral Sclerosis Patient Impairs Microtubule Stability and Axonal Mitochondria Distribution (Q60958104) (← links)
• Structure of hRpn10 Bound to UBQLN2 UBL Illustrates Basis for Complementarity between Shuttle Factors and Substrates at the Proteasome (Q61727849) (← links)
• Chronic optogenetic induction of stress granules is cytotoxic and reveals the evolution of ALS-FTD pathology (Q64069641) (← links)
• The debated toxic role of aggregated TDP-43 in amyotrophic lateral sclerosis: a resolution in sight? (Q64089818) (← links)
• Non-Proteasomal UbL-UbA Family of Proteins in Neurodegeneration (Q64249414) (← links)
• Implications of Selective Autophagy Dysfunction for ALS Pathology (Q89658236) (← links)
• The genetics of amyotrophic lateral sclerosis: current insights (Q90530653) (← links)
• RNA Granules and Their Role in Neurodegenerative Diseases (Q91771264) (← links)
• Motor Neuron Susceptibility in ALS/FTD (Q91970420) (← links)
• Key role of UBQLN2 in pathogenesis of amyotrophic lateral sclerosis and frontotemporal dementia (Q91997239) (← links)
• Multifaceted Genes in Amyotrophic Lateral Sclerosis-Frontotemporal Dementia (Q98177370) (← links)
• Structure, dynamics and functions of UBQLNs: at the crossroads of protein quality control machinery (Q99612550) (← links)
• Aggresome formation and liquid-liquid phase separation independently induce cytoplasmic aggregation of TAR DNA-binding protein 43 (Q100958408) (← links)