Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis. - Wikidata - awgldk - TriplyDB

Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis.

Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q31143351

about

Pathways and genes differentially expressed in the motor cortex of patients with sporadic amyotrophic lateral sclerosis SOD1 Transcriptional and Posttranscriptional Regulation and Its Potential Implications in ALS Opposite Interplay between PPAR Gamma and Canonical Wnt/Beta-Catenin Pathway in Amyotrophic Lateral Sclerosis Cytoplasmic sequestration of FUS/TLS associated with ALS alters histone marks through loss of nuclear protein arginine methyltransferase 1.A Case for Microtubule Vulnerability in Amyotrophic Lateral Sclerosis: Altered Dynamics During Disease The potential of GPNMB as novel neuroprotective factor in amyotrophic lateral sclerosis The complex molecular biology of amyotrophic lateral sclerosis (ALS)Gene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration.Ubiquilin-2 drives NF-κB activity and cytosolic TDP-43 aggregation in neuronal cells.c-Abl inhibition delays motor neuron degeneration in the G93A mouse, an animal model of amyotrophic lateral sclerosis.No widespread induction of cell death genes occurs in pure motoneurons in an amyotrophic lateral sclerosis mouse model.Microarrays and the microscope: balancing throughput with resolution.Axonal involvement in the Wlds neuroprotective effect: analysis of pure motoneurons in a mouse model protected from motor neuron disease at a pre-symptomatic age.New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients Sporadic ALS has compartment-specific aberrant exon splicing and altered cell-matrix adhesion biology.Amyotrophic lateral sclerosis, gene deregulation in the anterior horn of the spinal cord and frontal cortex area 8: implications in frontotemporal lobar degeneration Deregulated expression of cytoskeleton related genes in the spinal cord and sciatic nerve of presymptomatic SOD1(G93A) Amyotrophic Lateral Sclerosis mouse model.Global gene expression profiling of somatic motor neuron populations with different vulnerability identify molecules and pathways of degeneration and protection Neuroprotective function of cellular prion protein in a mouse model of amyotrophic lateral sclerosis.Transcriptional profile of primary astrocytes expressing ALS-linked mutant SOD1.Phosphatase and tensin homologue/protein kinase B pathway linked to motor neuron survival in human superoxide dismutase 1-related amyotrophic lateral sclerosis.Diagnosis and management of motor neurone disease.Physical activity as an exogenous risk factor in motor neuron disease (MND): a review of the evidence.Single molecule transcription profiling with AFM.Differential gene expression in patients with amyotrophic lateral sclerosis.Identification of epigenetically altered genes in sporadic amyotrophic lateral sclerosis.Absence of disturbed axonal transport in spinal and bulbar muscular atrophy.Early gene expression changes in spinal cord from SOD1(G93A) Amyotrophic Lateral Sclerosis animal model.Expression profiling of drug response--from genes to pathways.Aging--RNA in development and disease.Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.Identification of pharmacological targets in amyotrophic lateral sclerosis through genomic analysis of deregulated genes and pathways.A Pilot Trial of Pioglitazone HCl and Tretinoin in ALS: Cerebrospinal Fluid Biomarkers to Monitor Drug Efficacy and Predict Rate of Disease Progression.The Regulatory Machinery of Neurodegeneration in In Vitro Models of Amyotrophic Lateral Sclerosis.Cargo distributions differentiate pathological axonal transport impairments.Current and future directions in genomics of amyotrophic lateral sclerosis.Biomarkers for amyotrophic lateral sclerosis.Microarrays in Parkinson's disease: a systematic approach.Retinoid signaling alterations in amyotrophic lateral sclerosis.

P2860

Q21266563-F9FFB8E0-C642-464C-A661-BB1FABBFF551 Q21296781-FF8EFACE-8B2E-4798-A4D9-435A9E73B5C3 Q26742196-2A2417C9-7E36-45BA-882D-B3429EE48FDA Q27301265-933B9436-F3B7-4BC5-8876-D01835E11B69 Q28079299-F824FDA8-947A-42C8-BB66-2B83772B932A Q28117892-AC68D41F-72C3-4BCD-ADAB-28C752665FBF Q28263899-97BD9716-6817-495E-9F38-3B123138E19E Q30659873-36D74203-C593-4C53-B3C9-45A16ADCB763 Q30671325-5F6A5DBE-9372-4333-9002-1E159A04CDE6 Q31104448-945C7DDA-617C-4555-B25E-2127ACD70F28 Q33224176-C6F5C40D-382C-4F0F-9F44-5AAC953B504B Q33248412-57D37416-2E9B-44E6-8F15-2818B3F76EE4 Q33280825-EAC502B1-BF5F-4415-B6D1-5B419C987F4D Q33338981-13855D96-6296-424E-867A-03DE1ECA47CD Q33497640-F24B1242-3751-4EF0-A524-5EB30CF4158A Q33552181-04691640-23F4-48BE-A02D-3E619321D159 Q33563621-18B88A22-099A-4460-A19D-2A1502F5F418 Q33659976-A320EB07-5558-44B9-A8BA-AF0D8E4BCDF5 Q33687971-ECC55233-8F81-4BD3-AAA4-46383D4399B7 Q33703773-1102C331-D6D7-443E-9D6D-3D0DE7C0A5F3 Q33723622-B27FCBE8-A290-4907-BF5B-5B4C65A48CAE Q33791649-2EF8193B-CB01-4FAE-A836-03E53F9F6C07 Q34010576-835C1BB4-1C86-4E6C-8FF5-C906B348236F Q34016411-172C9C2A-BE6B-4780-871A-305F786D2E1D Q34070222-CD489DEC-2ADB-4125-B844-453137408B86 Q34168574-ABA6CEE7-AB8B-4018-B4BF-C5B5D09AC7CE Q34541013-00929041-FC46-4237-BE49-DBA6524A0583 Q34766996-597CCFBC-23BE-476E-A83E-0284CBFFE11A Q35058419-42B30E50-4912-4C4B-80EC-613D3C6570EC Q35236866-3FEA0F99-5418-452E-815D-A8102810990F Q35605882-0D30E982-4A90-41AC-8CB2-6C440543005A Q35906336-42DB7F55-5367-4D07-9A8E-FF6A2F140743 Q36087937-1349607E-229A-4434-8839-A9C304E51535 Q36090794-27121002-A41B-4FF7-BBBE-F16F8740A787 Q36284525-7A087A54-6D05-4C73-AC70-791618D97385 Q36407372-A4F5823C-A848-40C7-8978-170F7CDCDE83 Q36473151-490B2460-BF8F-4653-80F3-764CAC6ABF70 Q36481118-6896312D-B3CF-4FDB-BD61-345807E47A1D Q36525157-772F7191-9CAB-4DCF-B050-D284B8724DA8 Q36576439-69050B25-7079-4E7E-A08D-5AC377CCAEC3

P2860

Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q31143351

description

2005 nî lūn-bûn

@nan

2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2005年の論文

@ja

2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

Gene expression profile of spi ...... amyotrophic lateral sclerosis.

@ast

Gene expression profile of spi ...... amyotrophic lateral sclerosis.

@en

type

label

Gene expression profile of spi ...... amyotrophic lateral sclerosis.

@ast

Gene expression profile of spi ...... amyotrophic lateral sclerosis.

@en

prefLabel

Gene expression profile of spi ...... amyotrophic lateral sclerosis.

@ast

Gene expression profile of spi ...... amyotrophic lateral sclerosis.

@en

P1433

Q31143351-D2E8B83E-4428-4586-925D-E47C23F36701

P1476

Q31143351-3E262EB1-B91C-4DF5-B353-2D8E9F4FC21D

P2093

Q31143351-0D95BC02-5865-4463-9AF4-106E6A50371C

Q31143351-48497A35-6F48-49A6-9EB8-4B8DB73FB907

Q31143351-49F0A52F-6458-46A4-A674-4BCEAE1001B2

Q31143351-49FA237E-EDD0-4DDE-89F3-B53D4844EC23

Q31143351-52C7640A-486D-4C1B-9F70-BDE410EF13F9

Q31143351-6B84D442-AFA8-48D8-B445-60105DE7AE9D

Q31143351-6FB91359-ABEC-4087-9DEA-E298EF7CB1E2

Q31143351-81CC17FD-ABA2-44EB-B349-DA1F716C4164

Q31143351-8831FA81-4A25-4607-97F6-797508076CC9

Q31143351-B1FA13B9-6BBD-4899-A64B-9FE7B86AD76A

P2860

Q31143351-54A3779A-1E35-48AE-BC64-7C827403DF2F

Q31143351-892069EF-42C2-4BA9-BAEF-39890BD12A95

Q31143351-DF8CD3CA-99D9-4027-9497-0614FC2F535C

P304

Q31143351-9A8D5FE6-F4D9-430F-8F47-1E6ED7A578DA

P31

Q31143351-331977FC-EF4C-4722-9383-8E14A5CA825D

P356

Q31143351-5115211B-AAD2-470E-A23A-EF71AA68C5D9

P433

Q31143351-2E6641B2-2438-4A1A-ABEF-DD96E80F039F

P478

Q31143351-C93E132A-07AE-4944-94C4-6A2A316D192E

P50

Q31143351-34DDFEBB-81C4-49ED-97B1-72ABFCA6C6F1

P577

Q31143351-D3D6F188-B77C-479E-BFFA-A97A153740AE

P698

Q31143351-1B2CD201-D766-42AB-945F-646C3F9DAC07

P921

Q31143351-9C11C2A0-9D6A-461C-99B2-79EC906B0917

P356

P1433

Annals of Neurology

P1476

Gene expression profile of spi ...... amyotrophic lateral sclerosis.

@en

P2093

Fumiaki Tanaka

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

Hideyuki Takeuchi

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

Hiroaki Adachi

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

Jun-ichi Niwa

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

Manabu Doyu

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

Mari Yoshida

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

Masahiko Yamamoto

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

Masahisa Katsuno

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

Shinichi Terao

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

Shinsuke Ishigaki

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

P2860

Dorfin localizes to the ubiquitylated inclusions in Parkinson's disease, dementia with Lewy bodies, multiple system atrophy, and amyotrophic lateral sclerosis

Alterations in G(1) to S phase cell-cycle regulators during amyotrophic lateral sclerosis.

Retinoid signaling and the generation of regional and cellular diversity in the embryonic mouse spinal cord.

P304

236-251

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

P31

scholarly article

P356

10.1002/ANA.20379

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

P433

2

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

P478

57

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

P50

P577

2005-02-01T00:00:00Z

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

P698

15668976

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

P921

amyotrophic lateral sclerosis