Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key? - Test2 - elhamkhani - TriplyDB

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

http://www.wikidata.org/entity/Q28087798

about

Confocal Spectroscopy to Study Dimerization, Oligomerization and Aggregation of Proteins: A Practical Guide Paradoxical Roles of Antioxidant Enzymes: Basic Mechanisms and Health Implications Differential effects of phytotherapic preparations in the hSOD1 Drosophila melanogaster model of ALS.The Role of Proteases in Hippocampal Synaptic Plasticity: Putting Together Small Pieces of a Complex Puzzle.Spread of pathology in amyotrophic lateral sclerosis: assessment of phosphorylated TDP-43 along axonal pathways.Disease-related gene module detection based on a multi-label propagation clustering algorithm.Nucleocytoplasmic transport in C9orf72-mediated ALS/FTD.Pathological TDP-43 changes in Betz cells differ from those in bulbar and spinal α-motoneurons in sporadic amyotrophic lateral sclerosis.Old versus New Mechanisms in the Pathogenesis of ALS.Non-neuronal Cells in ALS: Role of Glial, Immune cells and Blood-CNS Barriers.Physiological functions and pathobiology of TDP-43 and FUS/TLS proteins.Oligomeropathies and pathogenesis of Alzheimer and Parkinson's diseases.Neuron-to-Neuron Transfer of FUS in Drosophila Primary Neuronal Culture Is Enhanced by ALS-Associated Mutations.Pathogenic mechanisms of prion protein, amyloid-β and α-synuclein misfolding: the prion concept and neurotoxicity of protein oligomers.Involvement of Cellular Prion Protein in α-Synuclein Transport in Neurons.Identify Huntington's disease associated genes based on restricted Boltzmann machine with RNA-seq data.Let's make microglia great again in neurodegenerative disorders.Amyotrophic lateral sclerosis as a protein level, non-genomic disease: Therapy with S2RM exosome released molecules.Amyotrophic lateral sclerosis as a protein level, non-genomic disease: Therapy with S2RM exosome released molecules.Anterior Cingulate Cortex TDP-43 Pathology in Sporadic Amyotrophic Lateral Sclerosis.A computational combinatorial approach identifies a protein inhibitor of superoxide dismutase 1 misfolding, aggregation, and cytotoxicity.A Pathogenic Mechanism Potentially Operative in Multiple Progressive Diseases and Its Therapeutic Implications.Amyotrophic lateral sclerosis Minimotifs dysfunction is pervasive in neurodegenerative disorders Aggregated SOD1 causes selective death of cultured human motor neurons Amyloid assembly and disassembly

P2860

Q26752808-E2AAFE55-C9F1-4D32-9992-5AE5DA12FD51 Q28392715-9FBB7240-38E9-419F-AB64-907D9D06613F Q30835468-DE229A97-7AE4-4E61-B13A-2B8F5A1C8E0B Q33361879-C370A4A1-DC95-489B-9EFC-E1274985B3AF Q35896504-1E05CE93-E255-4582-A072-B94E7A4B7370 Q36380503-96E85D4D-08E4-49CF-9CBB-0062C0E1C986 Q37028365-44AE2A61-3D14-4E53-AFDC-C53BC269E872 Q37553471-7887ED6C-6C70-4C6C-BB73-481EF55E8D18 Q38700722-F29E06E4-F8F7-4428-8722-4FCF09B0A71E Q38701186-BF5D1445-07FB-4C79-9E43-1860EDABE8B9 Q38789192-98EC1162-B947-4539-9EAB-EA8C95ADC25F Q38794219-2DC69175-818B-40D9-910B-15A259E8385B Q38827430-55BBC79A-3F5D-4150-B959-F36D564EE453 Q38928728-066EBF84-A3A1-4D16-9C93-42D331DCA88C Q40321151-B9A455ED-76AE-46F3-8E44-04C243491F20 Q42375276-78CEC6E5-DC7A-4F07-83B1-08EBD2483124 Q46926746-D1698644-F752-4F78-B2C7-EBBCC9464950 Q47169869-6E69353E-07B4-4D2B-B976-59FF2A0B8B13 Q47193821-A7C39A16-572C-4752-AAD6-CD57A64388B6 Q47351963-173FD532-A1B0-4380-BB31-160851E4A052 Q47741777-5509BB62-B255-42D1-B0A1-59F55C5C1976 Q47835909-11A53D85-614C-4B65-8DA6-06FB1C193454 Q56531747-F5E98A7A-AEFA-4E6E-9ABB-1B3880AB9D02 Q57174649-60E56497-4FAC-4332-97C2-874D45BEFC91 Q58608836-5D6B1C5E-5E6F-44CF-ABE9-D3C9C8CBE8EE Q58621641-DD491567-C5F2-422E-A095-076C84B63FEF

P2860

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

http://www.wikidata.org/entity/Q28087798

description

2015 nî lūn-bûn

@nan

2015 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի մարտին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@ast

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@en

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@nl

type

label

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@ast

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@en

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@nl

prefLabel

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@ast

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@en

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@nl

P1433

Q28087798-C1BB44FD-8797-43C6-86A4-54D8C29CEB4B

P1476

Q28087798-46FF5929-186A-4F53-92D4-CAE203DA1DD8

P2093

Q28087798-430EF4D2-6B99-4DF8-8E82-8681FA51A447

Q28087798-B593C90A-834B-4A38-92F6-37D38EAECC52

P2860

Q28087798-0B41F406-73C9-40FB-88E4-93D4CB3D0D98

Q28087798-2547EE9A-D590-4157-B0E9-611C87B03FF0

Q28087798-2641AB32-6A34-4ABD-8C97-E30D0F42B5A4

Q28087798-3D1BE8AF-0D65-427C-A4CD-809B5BC4ABC8

Q28087798-3F9F0E0D-F91B-4A4C-AAE7-F2E286E0C5F8

Q28087798-4C76BC5C-F957-4D7D-B8E0-E99A579D9BF6

Q28087798-5DF02684-CE0F-47B1-9CC0-C02B8BE2DEC7

Q28087798-5E205CDF-785D-456B-A42E-C2DE2A8CB37D

Q28087798-62FFC7CC-4FB4-4C1E-B6FA-6E1BAB9151FF

Q28087798-65CC74F3-1425-4D22-85A9-AA6BAA362D20

P304

Q28087798-9C578EF4-5869-42AC-B06A-943598ECDCF7

P31

Q28087798-3E823BD3-AEB3-4226-A4BE-DA9AAEFB2D9F

P3181

Q28087798-6649E796-1FA2-405E-BD56-CA78A6B7F2DF

P356

Q28087798-A56B5F96-3074-4C38-91AA-7F7FDBAFA72C

P407

Q28087798-4DD8F5CE-F7B2-4ED1-99F6-7DDD98ECCC22

P433

Q28087798-5577F990-EC25-4FC2-8644-7CB67FD5EA6C

P478

Q28087798-44916C86-2C96-4763-B32D-6624CB5EF591

P577

Q28087798-1C5D1BC5-2DAA-4B20-9995-429245BE04A5

P5875

Q28087798-76709CBC-75F9-4C01-8D5F-4DD2DD147247

P698

Q28087798-7153291B-9558-4D41-9AEC-683027F0EE97

P921

Q28087798-472B5F51-F5B0-4C55-B874-B3A5FA032DC6

Q28087798-B75A47FB-5A33-4F5A-835C-564C79A8CED3

P932

Q28087798-5BB40346-B30B-4677-8BB0-C60FF35976F8

P3181

P356

P1433

Experimental neurobiology

P1476

Prion-like Mechanism in Amyotrophic Lateral Sclerosis: are Protein Aggregates the Key?

@en

P2093

Hyung-Jun Kim

http://www.w3.org/2001/XMLSchema#string

Shynrye Lee

http://www.w3.org/2001/XMLSchema#string

P2860

Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

Sustained translational repression by eIF2α-P mediates prion neurodegeneration

Prion-like propagation of mutant superoxide dismutase-1 misfolding in neuronal cells

A seeding reaction recapitulates intracellular formation of Sarkosyl-insoluble transactivation response element (TAR) DNA-binding protein-43 inclusions

Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders

State of play in amyotrophic lateral sclerosis genetics

The past, present and future of stem cell clinical trials for ALS

Protein aggregates and regional disease spread in ALS is reminiscent of prion-like pathogenesis

Oral treatment targeting the unfolded protein response prevents neurodegeneration and clinical disease in prion-infected mice

P304

1-7

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

1968068

http://www.w3.org/2001/XMLSchema#string

P356

10.5607/EN.2015.24.1.1

http://www.w3.org/2001/XMLSchema#string

P407

P433

1

http://www.w3.org/2001/XMLSchema#string

P478

24

http://www.w3.org/2001/XMLSchema#string

P577

2015-03-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

273778545

http://www.w3.org/2001/XMLSchema#string

P698

25792864

http://www.w3.org/2001/XMLSchema#string

P921

amyotrophic lateral sclerosis

Prion protein family

P932

4363329

http://www.w3.org/2001/XMLSchema#string