Neurobiology and cellular pathogenesis of glycolipid storage diseases. - Test2 - elhamkhani - TriplyDB

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

http://www.wikidata.org/entity/Q35153227

about

Cell-cell signaling drives the evolution of complex traits: introduction-lung evo-devo Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in α-mannosidosis.Future perspectives for glycolipid research in medicine.Endosomal/lysosomal processing of gangliosides affects neuronal cholesterol sequestration in Niemann-Pick disease type C.A historical perspective of the glycosphingolipids and sphingolipidoses.Secondary lipid accumulation in lysosomal disease.Elevation of GM2 ganglioside during ethanol-induced apoptotic neurodegeneration in the developing mouse brain.Lipid rafts and Alzheimer's disease: protein-lipid interactions and perturbation of signaling.Pathogenic cascades in lysosomal disease-Why so complex?Mucopolysaccharidosis type I: current knowledge on its pathophysiological mechanisms.Gangliosides of the Vertebrate Nervous System Enzyme replacement improves ataxic gait and central nervous system histopathology in a mouse model of metachromatic leukodystrophy.

P2860

Q28750658-952137CF-A27B-45C8-8058-C1DF67B09500 Q30499614-C2AAD280-4521-4C42-9064-568012809D5D Q35153243-D8BDC66B-54C7-41C3-923A-04CE090A5F5C Q35167848-82036C49-9E3B-42AD-870F-CA796BD59E97 Q35213537-45123994-5352-422C-A8D7-177A4DA2B2F1 Q35240940-BBA5D8D4-C803-4147-89B6-A80A6FDC9BCB Q35886150-F179ED4B-BA26-4E65-8A33-A1C84909700A Q36052691-03C28DFD-2DE2-46BD-963E-A57E997C05AE Q37364596-EC3D693B-A2AF-416D-A997-EAD0D1E4EDCC Q38004963-D35EED9F-F613-4201-8C2E-C56918BBE202 Q38853822-A67DA2C1-C552-474B-85D7-47CAC65FCB49 Q39505508-60C6B777-16D7-4130-B9B4-70BF21EB9699

P2860

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

http://www.wikidata.org/entity/Q35153227

description

2003 nî lūn-bûn

@nan

2003 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի մայիսին հրատարակված գիտական հոդված

@hy

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

@ast

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

@en

type

label

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

@ast

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

@en

prefLabel

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

@ast

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

@en

P1433

Q35153227-55BB8659-6EB4-43F8-AEC1-8A3DF35FF59E

P1476

Q35153227-D50F62A3-D679-4E2C-A80B-101E51501F8B

P2093

Q35153227-5463FDF4-F724-4488-9622-26B885A53E59

P2860

Q35153227-059EA591-6B5B-41EB-8FBD-57E17C97B848

Q35153227-076E8D53-EC6B-4DF6-8A53-B7DFBBB02772

Q35153227-07E15968-7A3E-4961-A717-1417A5A6FD43

Q35153227-092F4879-F363-41B4-9079-2836A537E4EB

Q35153227-0940A2C9-B2C0-400B-8818-DDEB583A6FB9

Q35153227-0FA12EC2-C81C-49ED-BDD4-C14E7DB451DF

Q35153227-1229249F-5615-459B-A4FD-E517EE2677B4

Q35153227-13513B53-96DD-41D5-8E68-179A1B7CAE3A

Q35153227-161CC252-D59F-4C79-9FB1-1C5AAA46D045

Q35153227-162296F7-6DF2-4151-9811-917CC62A0471

P304

Q35153227-AB21981D-CFDE-45DC-BD29-5D4EFC3D2428

P31

Q35153227-8D79286C-AD53-4DD0-9F52-DEE66F127B13

P356

Q35153227-075A3521-2013-48DE-897D-E564F762823C

P407

Q35153227-F6934BD2-36B2-4655-8658-F6E0D2F6DCD5

P433

Q35153227-8ED7DD9C-E99E-4C23-9768-DB49271CEB7C

P478

Q35153227-96F79BC2-7FA1-4027-BA6A-55F596545A8F

P577

Q35153227-D72B55AD-E5E2-40BF-89B6-F79A4FA8244A

P5875

Q35153227-F2924483-BC50-41A5-B9CC-BBE1105D89C5

P698

Q35153227-EBADF431-8FD3-49B3-91D5-E403A2317730

P932

Q35153227-74AF4DB5-4383-49A9-8B99-B43E53F5178D

P356

P1433

Philosophical Transactions of the Royal Society B

P1476

Neurobiology and cellular pathogenesis of glycolipid storage diseases.

@en

P2093

Steven U Walkley

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

P2860

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis

AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2

CaM-kinases: modulators of synaptic plasticity

Transmembrane molecular pump activity of Niemann-Pick C1 protein

Interaction between two adapter proteins, PAG and EBP50: a possible link between membrane rafts and actin cytoskeleton

The molecular basis of CaMKII function in synaptic and behavioural memory

Functions of lipid rafts in biological membranes

Synaptic activity and the construction of cortical circuits

The role of alpha-CaMKII autophosphorylation in neocortical experience-dependent plasticity.

Neurons in Niemann-Pick disease type C accumulate gangliosides as well as unesterified cholesterol and undergo dendritic and axonal alterations.

P304

893-904

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

P31

scholarly article

P356

10.1098/RSTB.2003.1276

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

P407

P433

1433

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

P478

358

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

P577

2003-05-01T00:00:00Z

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

P5875

10710583

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

P698

12803923

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

P932

1693176

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