Microenvironmental regulation of epithelial-mesenchymal transitions in cancer - Wikidata - wikimedia - TriplyDB

Microenvironmental regulation of epithelial-mesenchymal transitions in cancer

Microenvironmental regulation of epithelial-mesenchymal transitions in cancer

http://www.wikidata.org/entity/Q36831337

about

Update in lung cancer and mesothelioma 2012 Intratumoral heterogeneity: Clonal cooperation in epithelial-to-mesenchymal transition and metastasis Regulation of tumor metastasis by myeloid-derived suppressor cells Impact of laminitis on the canonical Wnt signaling pathway in basal epithelial cells of the equine digital laminae Versican and the regulation of cell phenotype in disease Pathophysiological Functions of Rnd3/RhoE Cellular Plasticity in Prostate Cancer Bone Metastasis Krüppel-like factor 4 acts as an oncogene in colon cancer stem cell-enriched spheroid cells Epithelial-mesenchymal transition and tumor suppression are controlled by a reciprocal feedback loop between ZEB1 and Grainyhead-like-2 NF-κB regulates mesenchymal transition for the induction of non-small cell lung cancer initiating cells.Stemness in Cancer: Stem Cells, Cancer Stem Cells, and Their Microenvironment.STAT3 and epithelial-mesenchymal transitions in carcinomas Versican and the control of inflammation.TPL2 kinase regulates the inflammatory milieu of the myeloma niche Pellino-1 promotes lung carcinogenesis via the stabilization of Slug and Snail through K63-mediated polyubiquitination.Cell state plasticity, stem cells, EMT, and the generation of intra-tumoral heterogeneity.HiJAK'd Signaling; the STAT3 Paradox in Senescence and Cancer Progression.The motile breast cancer phenotype roles of proteoglycans/glycosaminoglycans.miR-27a regulates cisplatin resistance and metastasis by targeting RKIP in human lung adenocarcinoma cells Research on the efficacy of Celastrus Orbiculatus in suppressing TGF-β1-induced epithelial-mesenchymal transition by inhibiting HSP27 and TNF-α-induced NF-κ B/Snail signaling pathway in human gastric adenocarcinoma.A role for versican in the development of leiomyosarcoma Chemokine ligand 20 enhances progression of hepatocellular carcinoma via epithelial-mesenchymal transition Hepatic stellate cells secreted hepatocyte growth factor contributes to the chemoresistance of hepatocellular carcinoma A pilot study of FDG PET/CT detects a link between brown adipose tissue and breast cancer Downregulation of BRAF activated non-coding RNA is associated with poor prognosis for non-small cell lung cancer and promotes metastasis by affecting epithelial-mesenchymal transition.MiRNA 17 family regulates cisplatin-resistant and metastasis by targeting TGFbetaR2 in NSCLC.Changes in protein expression in two cholangiocarcinoma cell lines undergoing formation of multicellular tumor spheroids in vitro Wilms' tumor protein induces an epithelial-mesenchymal hybrid differentiation state in clear cell renal cell carcinoma Tumor microenvironment: a new treatment target for cancer Alternative RNA splicing and cancer HGF and TGFβ1 differently influenced Wwox regulatory function on Twist program for mesenchymal-epithelial transition in bone metastatic versus parental breast carcinoma cells Inhibition of Hedgehog signalling by NVP-LDE225 (Erismodegib) interferes with growth and invasion of human renal cell carcinoma cells dbEMT: an epithelial-mesenchymal transition associated gene resource.53BP1 suppresses epithelial-mesenchymal transition by downregulating ZEB1 through microRNA-200b/429 in breast cancer.Risk prediction for late-stage ovarian cancer by meta-analysis of 1525 patient samples.An evidence-based knowledgebase of metastasis suppressors to identify key pathways relevant to cancer metastasis.Low expression of KLF17 is associated with tumor invasion in esophageal carcinoma.LincHOTAIR epigenetically silences miR34a by binding to PRC2 to promote the epithelial-to-mesenchymal transition in human gastric cancer The long non-coding RNA TUG1 indicates a poor prognosis for colorectal cancer and promotes metastasis by affecting epithelial-mesenchymal transition AEG-1 activates Wnt/PCP signaling to promote metastasis in tongue squamous cell carcinoma

P2860

Q24619675-55DA8CF8-0406-42DA-A2FA-98B0354E6711 Q26991480-D8B1F043-FB5D-46C3-86E8-E03BC4F5953E Q27022125-438D9E37-A59F-44AC-8F9A-1FC1D17BEC36 Q27315213-9F92184A-AC81-4684-8316-2AD75C816E8D Q27690926-503AB4E4-F014-430D-93D8-A88965E0DFED Q28078292-666FC55B-BCA6-4430-B99F-834953DE671B Q28085013-C1773049-6F0D-49E7-8B77-C9422F502E36 Q28486138-0980DC58-ACFB-47D9-96AD-B1686E2D5C72 Q28662207-593FF4FC-9823-41A0-A22F-3760D2DBC3F2 Q30417710-9BC91DA9-F55E-4D99-BF53-F86D53580EB6 Q33572252-7F7C7004-F1C4-43B8-AE94-3FBC8F00DE76 Q33623947-BE79398E-1C83-4EF4-AC88-D31CE359B6A9 Q33690423-CE8001FA-7AA1-4648-8517-8A62387515E5 Q33714724-088592C3-D195-4752-AD25-DCDF83A37978 Q33759917-5D7D0BFC-A20C-4781-9D7C-FEDB88252A4D Q33767473-9B9BB2CE-59D3-46A9-9A2B-C07680BDDC03 Q33820241-2A672D9F-F25B-454F-B895-1466AA7E3A64 Q34031745-08978FAD-D0B3-4529-A7D3-C155CE52AD57 Q34151444-2AE620B6-B3D8-4890-A45B-62EC6B68C5DD Q34515164-F000E92F-418A-4780-9E35-40C65E44EEE1 Q34634226-D1FA553F-38F5-4ECF-B1C8-8A15E060C38F Q34932446-7A4C1BA9-2676-424A-A77C-2A07C29ADAD9 Q34984377-893C5E8B-3763-4A55-A9A9-DEA352232AFD Q35101196-547C7618-1EE2-4DB9-8562-DB2B2DA04C7D Q35127340-27E59A23-18ED-49B8-85B0-B95110911656 Q35145398-BA9F08E6-8B29-40CF-9F65-4A6A4DCFCFA5 Q35164379-2AE73426-695E-4725-898E-E4FF61AADE97 Q35206917-45C8099D-D202-4A36-9EB3-35D40F11FA79 Q35361431-8EBBCDBA-0D76-4659-BABE-3B2DFED1CFC2 Q35589667-7557C880-B57C-422E-8AFD-F621E0D4CB7A Q35676582-1D56E5E1-C6CC-4DB7-AF9E-D612A40F2D3A Q35678417-CA6B816D-DFCF-4B3A-8378-057C480B22DC Q35769090-8F386D5A-B2F4-4DA2-811F-5231822C4580 Q36016208-558D23C8-4DBA-41A7-83AD-A00F31F088C1 Q36087199-51D52DDC-38A5-4901-BF2D-58E617A7808F Q36187490-C83A1AC1-22AC-4261-BC7C-5E570D81B365 Q36261674-E817B0F3-9B0D-44AD-B78F-F3B2515CCA5F Q36293805-4C5B5FE8-D8EB-4884-ADCA-835294FFC3F0 Q36555840-2ABFE0C2-0D59-47F7-A340-580B678EB57D Q36739042-3F104E91-47A6-49BC-9BDD-F1C9CCC7FDD5

P2860

Microenvironmental regulation of epithelial-mesenchymal transitions in cancer

http://www.wikidata.org/entity/Q36831337

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

Microenvironmental regulation of epithelial-mesenchymal transitions in cancer

@en

type

label

Microenvironmental regulation of epithelial-mesenchymal transitions in cancer

@en

prefLabel

Microenvironmental regulation of epithelial-mesenchymal transitions in cancer

@en

P1433

Q36831337-08DD425C-8E97-4943-A006-F6CED5077EB0

P1476

Q36831337-6EAB33BE-57D4-464C-9F1D-D870EC1F892B

P2093

Q36831337-2247BB63-22C1-4373-9FF7-FD85B2C3408B

Q36831337-5D7C8FB4-3FDC-48AD-8F3D-88DF252280E1

Q36831337-785B38E1-B42C-4C35-87A0-0BD1140FA007

Q36831337-9EAB9F2C-BA5D-4DB4-873C-978DEE588884

Q36831337-FF35DBA8-1443-46A3-88D6-1A8CC37390A0

P2860

Q36831337-04FBD342-E3E3-4176-9DAC-8222B61E1335

Q36831337-113915A4-C427-4181-8F9A-638E95D6C909

Q36831337-1A156E14-5AAC-4D67-B186-EA1FDB39B7D8

Q36831337-1A49D2E8-F0F8-478B-AE31-54B2B7AB9EA6

Q36831337-1B3F8198-6E2B-48BD-A2AB-98CEAE7FF1DA

Q36831337-1F93DFAB-C791-4B7A-BB54-C4A501B7F127

Q36831337-29A505D6-AC9E-484D-B5B1-71292A7FE0F4

Q36831337-29FA038C-022A-4A48-B553-68163C700AAE

Q36831337-30507432-9AE8-431F-90CD-1C9C20C1CE8E

Q36831337-32D04691-10D9-4269-ACC6-A8C21CF931C4

P304

Q36831337-111AF4D7-F1CB-4E92-9741-DBB5A68E257C

P31

Q36831337-37A00136-B68F-47A3-A134-195BCB17E510

P356

Q36831337-D897C933-C223-44BA-BB66-4A62E730DF60

P407

Q36831337-A04B0FA7-A01A-4A46-BABB-3184C261E1FA

P433

Q36831337-3040F357-8292-4025-A2F4-883787DC7DDC

P478

Q36831337-C0623A00-F9F8-4555-8BB1-7C630A71E2D6

P577

Q36831337-35726CA5-A1C5-4AE1-BE0B-33F2BB0F2FCA

P5875

Q36831337-954049DF-04F5-4540-AF8E-0E0B63CF2D07

P698

Q36831337-CC057B57-C262-41F8-AA7E-BA1A5CEEA296

P932

Q36831337-37CE8481-1584-49EE-95CC-B3C78763276F

P356

0008-5472.CAN-12-1223

P1433

Cancer Research

P1476

Microenvironmental regulation of epithelial-mesenchymal transitions in cancer

@en

P2093

Dingcheng Gao

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

Jenny C Chang

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

Linda T Vahdat

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

Stephen Wong

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

Vivek Mittal

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

P2860

The miR-200 family inhibits epithelial-mesenchymal transition and cancer cell migration by direct targeting of E-cadherin transcriptional repressors ZEB1 and ZEB2

The ZEB/miR-200 feedback loop--a motor of cellular plasticity in development and cancer?

A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells

The basics of epithelial-mesenchymal transition

Mesenchymal transition and dissemination of cancer cells is driven by myeloid-derived suppressor cells infiltrating the primary tumor

Epithelial-mesenchymal transitions in development and disease

Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing

The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1

Transitions between epithelial and mesenchymal states: acquisition of malignant and stem cell traits

Localized and reversible TGFbeta signalling switches breast cancer cells from cohesive to single cell motility

P304

4883-4889

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

P31

scholarly article

P356

10.1158/0008-5472.CAN-12-1223

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

P407

P433

19

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

P478

72

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

P577

2012-09-20T00:00:00Z

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

P5875

236847693

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

P698

23002209

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

P932

3649848

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