Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
about
Suppression of the novel ER protein Maxer by mutant ataxin-1 in Bergman glia contributes to non-cell-autonomous toxicityBergmann glial S100B activates myo-inositol monophosphatase 1 and Co-localizes to purkinje cell vacuoles in SCA1 transgenic miceThe ducky(2J) mutation in Cacna2d2 results in reduced spontaneous Purkinje cell activity and altered gene expressionCell-autonomous death of cerebellar purkinje neurons with autophagy in Niemann-Pick type C diseaseDevelopmental delay in motor skill acquisition in Niemann-Pick C1 mice reveals abnormal cerebellar morphogenesis.β-Catenin is critical for cerebellar foliation and laminationHypoxic preconditioning differentially affects GABAergic and glutamatergic neuronal cells in the injured cerebellum of the neonatal ratERBB3-mediated regulation of Bergmann glia proliferation in cerebellar lamination.Radial glia: progenitor, pathway, and partnerShp2-dependent ERK signaling is essential for induction of Bergmann glia and foliation of the cerebellumExpression of LPP3 in Bergmann glia is required for proper cerebellar sphingosine-1-phosphate metabolism/signaling and developmentCorticotropin-releasing factor and urocortin differentially modulate rat Purkinje cell dendritic outgrowth and differentiation in vitroEvidence for oxidative stress in the developing cerebellum of the rat after chronic mild carbon monoxide exposure (0.0025% in air)Delta-like 1 regulates Bergmann glial monolayer formation during cerebellar developmentAnti-glial nuclear antibody: marker of lung cancer-related paraneoplastic neurological syndromesExpression of S100B during embryonic development of the mouse cerebellum.P2Y1 receptor switches to neurons from glia in juvenile versus neonatal rat cerebellar cortex.Distinct modes of neuritic growth in purkinje neurons at different developmental stages: axonal morphogenesis and cellular regulatory mechanismsIdentification of novel glial genes by single-cell transcriptional profiling of Bergmann glial cells from mouse cerebellum.Analogous mechanism regulating formation of neocortical basal radial glia and cerebellar Bergmann glia.Huwe1 ubiquitin ligase is essential to synchronize neuronal and glial differentiation in the developing cerebellumFGF/FGFR2 signaling regulates the generation and correct positioning of Bergmann glia cells in the developing mouse cerebellumWnt/β-catenin signalling is active in a highly dynamic pattern during development of the mouse cerebellum.Antibodies to Delta/notch-like epidermal growth factor-related receptor in patients with anti-Tr, paraneoplastic cerebellar degeneration, and Hodgkin lymphoma.Activation of Wnt/β-catenin signalling affects differentiation of cells arising from the cerebellar ventricular zoneCellular commitment in the developing cerebellumSmall-cell lung cancer-associated autoantibodies: potential applications to cancer diagnosis, early detection, and therapy.Glial S100B protein modulates mutant ataxin-1 aggregation and toxicity: TRTK12 peptide, a potential candidate for SCA1 therapyGrowth and differentiation factor 10 (Gdf10) is involved in Bergmann glial cell development under Shh regulation.Neuron-derived FGF9 is essential for scaffold formation of Bergmann radial fibers and migration of granule neurons in the cerebellum.Calcitonin gene-related peptide (CGRP) triggers Ca2+ responses in cultured astrocytes and in Bergmann glial cells from cerebellar slices.SOX3 expression in the glial system of the developing and adult mouse cerebellum.Primary Cilia in the Murine Cerebellum and in Mutant Models of Medulloblastoma.Glial S100B Positive Vacuoles In Purkinje Cells: Earliest Morphological Abnormality In SCA1 Transgenic Mice.AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival.Olig2/Plp-positive progenitor cells give rise to Bergmann glia in the cerebellumConsensus Paper: Cerebellar Development.D-serine signalling as a prominent determinant of neuronal-glial dialogue in the healthy and diseased brainThe Purkinje neuron acts as a central regulator of spatially and functionally distinct cerebellar precursors.Connexin43 and bergmann glial gap junctions in cerebellar function.
P2860
Q24317850-91CBDA7B-FEFB-4D47-9ABB-D1EEBF7E3328Q24622447-178D383E-76EC-4751-89C6-18A104F536E7Q24676262-7C6EA8B0-7D9C-48E5-98D7-73D726A4871CQ24811579-7CEDA02D-9401-4841-8C5F-9AFFA71BD784Q27316686-FC1F0AD0-3B63-4C67-B2DA-4D88C915F7CDQ27318680-52720F6A-2AFE-490C-87E1-F8DBA11B2789Q27319945-78DA5325-931F-48E0-A5EC-B484747B43DDQ27345740-8F4517B2-84B0-492D-B77E-DB4BA273824DQ28237232-F966814D-3F1F-4B3E-AD3F-5722F7DC4452Q28506451-E3EA726C-E5A4-4B9D-9941-F641693C0412Q28508004-8AB63296-4959-46B4-8C73-28CADD17CEBCQ28571592-C8F8F72C-38DF-4853-819B-9D5B5CD0EF3DQ28580983-17DE04AE-FE98-4F01-80C1-2B2DD5EA3E65Q28587949-61C2545C-20E0-4392-901B-1A826DADCBE3Q33216878-2DA8FD5B-C717-40B7-AD15-F424D2C50650Q33278810-CC801460-44C7-4A83-9886-4B18810D1D85Q33289232-2FCC5499-DBCC-45B7-B2DA-83D6C351C905Q33498498-920F3C65-8497-4DD0-BCFB-BC03CA258434Q33532620-3FD9AB29-82CB-478A-A379-740C459B48C4Q33758337-2D027BA3-8C0E-4E7D-B258-0C0F2F458F87Q33778488-4E40E451-8FE1-4826-B104-E2C23C6DAC44Q33830856-DBF28A37-4374-456F-94ED-A6548B2A5CBDQ33999110-F8EC79C0-2FF7-4F2B-A8F9-2A0758834D72Q34036378-FD395D92-4290-49D8-9472-42347C4096EFQ34374349-27670293-ECF6-4591-AD01-4C313FE991B3Q34460069-4D554470-BFD8-4C28-BF67-AFE9A65F2530Q34826137-61BC5D2E-23BD-4F52-96C3-79B308D7E142Q35126073-BE9F0C51-65B8-406E-8F52-1F88FC21613AQ35194659-AB148EE9-95E3-4C8F-81A1-6ACD23C4E68EQ35685824-D01EE3B9-80F5-4E77-BDEF-C18E729DAFFFQ35704162-944867D5-2D8D-4A51-A990-F034A8AB1609Q35925349-A098CE01-BAE7-4267-8BCA-A2447E6377B3Q35943359-DB54525A-70DB-46BD-A45E-0BF2E74EFC66Q36327420-17BA362E-FC38-4664-A7C2-9766886737E2Q36357926-88C2A04F-A9EB-4E1A-AC71-861BAC779E97Q36738094-D9BC053B-3575-4A70-8D85-65EB126A305CQ36840256-D4C5184A-E569-4ABF-BA38-AF1C01252A13Q37118079-6FBD0750-C6BF-48DA-A62E-C8E77FE08FB5Q37387175-349F25FF-A9A8-4422-BFB5-577348F85EE7Q37395801-23B9D39C-5CAA-400B-A1B7-629F26CD06FC
P2860
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@ast
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@en
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@nl
type
label
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@ast
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@en
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@nl
prefLabel
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@ast
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@en
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@nl
P2860
P1476
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells.
@en
P2093
Keiko Yamada
Masahiko Watanabe
P2860
P304
P356
10.1046/J.0022-7722.2002.00021.X
P577
2002-06-01T00:00:00Z
P5875
P6179
1003840612