Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells. - Wikidata - awgldk - TriplyDB

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

http://www.wikidata.org/entity/Q33519181

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NEK1 mutations cause short-rib polydactyly syndrome type majewski Human basal body basics Cell cycle progression by the repression of primary cilia formation in proliferating cells The role of the cilium in normal and abnormal cell cycles: emphasis on renal cystic pathologies The IN/OUT assay: a new tool to study ciliogenesis The ciliary membrane.The roles of evolutionarily conserved functional modules in cilia-related trafficking.Proteomic analysis of intact flagella of procyclic Trypanosoma brucei cells identifies novel flagellar proteins with unique sub-localization and dynamics Primary Cilia in Tumor Biology: The Primary Cilium as a Therapeutic Target in Cholangiocarcinoma.Repression of GW/P body components and the RNAi microprocessor impacts primary ciliogenesis in human astrocytes HDAC6 inhibition restores ciliary expression and decreases tumor growth Primary cilia are decreased in breast cancer: analysis of a collection of human breast cancer cell lines and tissues Expression and prognostic significance of TCTN1 in human glioblastoma CUSP9* treatment protocol for recurrent glioblastoma: aprepitant, artesunate, auranofin, captopril, celecoxib, disulfiram, itraconazole, ritonavir, sertraline augmenting continuous low dose temozolomide.Ultrastructural characterization of primary cilia in pathologically characterized human glioblastoma multiforme (GBM) tumors.The primary cilium as a biomarker in the hypoxic adaptation of bone marrow-derived mesenchymal stromal cells: a role for the secreted frizzled-related proteins Coevolution reveals a network of human proteins originating with multicellularity.Primary cilia and aberrant cell signaling in epithelial ovarian cancer.PCM1 Depletion Inhibits Glioblastoma Cell Ciliogenesis and Increases Cell Death and Sensitivity to Temozolomide.Normal mammary development and function in mice with Ift88 deleted in MMTV- and K14-Cre expressing cells Primary cilia are present on human blood and bone marrow cells and mediate Hedgehog signaling.FREQUENT SUBGRAPH MINING OF PERSONALIZED SIGNALING PATHWAY NETWORKS GROUPS PATIENTS WITH FREQUENTLY DYSREGULATED DISEASE PATHWAYS AND PREDICTS PROGNOSIS.Disruption of KIF3A in patient-derived glioblastoma cells: effects on ciliogenesis, hedgehog sensitivity, and tumorigenesis.Detection of primary cilia in human glioblastoma.CCRK depletion inhibits glioblastoma cell proliferation in a cilium-dependent manner.The Fungal Metabolite Brefeldin A Inhibits Dvl2-Plk1-Dependent Primary Cilium Disassembly Primary cilia as a novel horizon between neuron and environment.Primary cilia in gastric gastrointestinal stromal tumours (GISTs): an ultrastructural study.Primary cilia attenuate hedgehog signalling in neoplastic chondrocytes.Neoexpression of a functional primary cilium in colorectal cancer cells.Maintaining centrosomes and cilia.LPA signaling is regulated through the primary cilium: a novel target in glioblastoma.Signaling through the Primary Cilium.Neural network detected in a presumed vestigial trait: ultrastructure of the salmonid adipose fin.Primary Cilia Mediate Diverse Kinase Inhibitor Resistance Mechanisms in Cancer.Primary cilium and glioblastoma Oncometabolite induced primary cilia loss in pheochromocytoma Glioma cell proliferation is enhanced in the presence of tumor-derived cilia vesicles Hedgehog Signaling in Lung Cancer: From Oncogenesis to Cancer Treatment Resistance

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P2860

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

http://www.wikidata.org/entity/Q33519181

description

2009 nî lūn-bûn

@nan

2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@ast

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@en

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@nl

type

label

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@ast

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@en

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@nl

prefLabel

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@ast

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@en

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@nl

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1471-2407-9-448

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P1476

Primary ciliogenesis defects are associated with human astrocytoma/glioblastoma cells.

@en

P2093

Jerome B Rattner

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

P2860

A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence

Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function

The Ciliopathies: An Emerging Class of Human Genetic Disorders

Cep164, a novel centriole appendage protein required for primary cilium formation

Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes

Pericentrin forms a complex with intraflagellar transport proteins and polycystin-2 and is required for primary cilia assembly

CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

Functional dissection of Rab GTPases involved in primary cilium formation

CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease

CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290

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1471-2407-9-448

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448

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scholarly article

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10.1186/1471-2407-9-448

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9

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Marvin J Fritzler

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2009-12-17T00:00:00Z

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40695303

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1036892796

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20017937

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cilium morphogenesis

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2806408

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