HMGA2 and Smads co-regulate SNAIL1 expression during induction of epithelial-to-mesenchymal transition - Wikidata - wikimedia - TriplyDB

HMGA2 and Smads co-regulate SNAIL1 expression during induction of epithelial-to-mesenchymal transition

HMGA2 and Smads co-regulate SNAIL1 expression during induction of epithelial-to-mesenchymal transition

http://www.wikidata.org/entity/Q24318681

about

Microphthalmia-associated transcription factor (MITF) promotes differentiation of human retinal pigment epithelium (RPE) by regulating microRNAs-204/211 expression Suppression of nonhomologous end joining repair by overexpression of HMGA2 Let-7 and miR-200 microRNAs: guardians against pluripotency and cancer progression Mechanisms of TGFβ-Induced Epithelial-Mesenchymal Transition Effect of Cigarette Smoking on Epithelial to Mesenchymal Transition (EMT) in Lung Cancer Signal Transduction Pathways of EMT Induced by TGF-β, SHH, and WNT and Their Crosstalks The role of the oncofetal H19 lncRNA in tumor metastasis: orchestrating the EMT-MET decision Glioblastoma Circulating Cells: Reality, Trap or Illusion?Central role of Snail1 in the regulation of EMT and resistance in cancer: a target for therapeutic intervention Molecular mechanisms of epithelial-mesenchymal transition ΔNp63α and microRNAs: leveraging the epithelial-mesenchymal transition Let-7a inhibits migration, invasion and epithelial-mesenchymal transition by targeting HMGA2 in nasopharyngeal carcinoma TGFβ signalling in context Coupled reversible and irreversible bistable switches underlying TGFβ-induced epithelial to mesenchymal transition The code of non-coding RNAs in lung fibrosis Let-7 Sensitizes KRAS Mutant Tumor Cells to Chemotherapy The transcription factors Snail and Slug activate the transforming growth factor-beta signaling pathway in breast cancer The RhoA activator GEF-H1/Lfc is a transforming growth factor-beta target gene and effector that regulates alpha-smooth muscle actin expression and cell migration Hyperoxic treatment induces mesenchymal-to-epithelial transition in a rat adenocarcinoma model.Complete reversal of epithelial to mesenchymal transition requires inhibition of both ZEB expression and the Rho pathway The importance of the retinoid X receptor alpha in modulating inflammatory signaling in acute murine colitis.Specific microRNA-mRNA Regulatory Network of Colon Cancer Invasion Mediated by Tissue Kallikrein-Related Peptidase 6.Tenascin-X promotes epithelial-to-mesenchymal transition by activating latent TGF-β Role of androgens and the androgen receptor in epithelial-mesenchymal transition and invasion of prostate cancer cells Integrated analyses identify the involvement of microRNA-26a in epithelial-mesenchymal transition during idiopathic pulmonary fibrosis.The Effect of Snail1 Gene Silencing by siRNA in Metastatic Breast Cancer Cell Lines.ASK-ing EMT not to spread cancer.Epithelial-mesenchymal transition in prostate cancer: an overview.Analysis of gene expression in PTHrP-/- mammary buds supports a role for BMP signaling and MMP2 in the initiation of ductal morphogenesis.Yap1 is required for endothelial to mesenchymal transition of the atrioventricular cushion.OVOL2 antagonizes TGF-β signaling to regulate epithelial to mesenchymal transition during mammary tumor metastasis.Transforming growth factor beta promotes complexes between Smad proteins and the CCCTC-binding factor on the H19 imprinting control region chromatin.TGFβ-induced invasion of prostate cancer cells is promoted by c-Jun-dependent transcriptional activation of Snail1 Key signalling nodes in mammary gland development and cancer. The Snail1-Twist1 conspiracy in malignant breast cancer progression.Snail family regulation and epithelial mesenchymal transitions in breast cancer progression Crosstalk between transcription factors and microRNAs in human protein interaction network A novel network integrating a miRNA-203/SNAI1 feedback loop which regulates epithelial to mesenchymal transition.MiR-182 overexpression in tumourigenesis of high-grade serous ovarian carcinoma.Multilayer control of the EMT master regulators.The tumor microenvironment in colorectal carcinogenesis.

P2860

074db5b0d4b800055d2322fe366b0a57469a2fcc 12252d99bdae09671a47ec27d6b4c739430c8cad 55eea0e1de9dcd1bff6c32e6fa6430d3ab11c278 5a92e3ad52ba6fdd042238dbe0dbef6919af352c 69d24631bdbea500bdd2ba07a9c142c27b4c44d0 7d66f6eb0af9247d33c7ffb52e5584b41ba042f7 810d374abe800062c321f5fadb59eaa1ddac0f3f 9ca8295b95f1e4ac2560e7296c4afd948f4fb6bc c5398b5dc166754988f7bd9699e8f03919b98c60 d35001872b28fed3b67a2236754d157162de3624 f2532a15c22270ce9da37084284fc895dd57bbf1 f4b419017fc1739e4b6e40557680d23ec6b64626

P248

Q24316369-C5D9A5AD-880F-43AA-BDBE-0823A4519D10 Q24338991-8BBC046E-9EF3-479E-B521-B9D0A59DEAAD Q24653755-A92FC8FF-DFAB-488C-BD8C-79D2329A6A3E Q26745545-38E0237E-59DF-47BE-B1E6-9E4FEBD9384F Q26748357-8C0908A0-47E9-40FB-8C21-3918C317D9E2 Q26752554-885FD41E-A4A1-4955-8B27-2A7A24444BDB Q26775618-2D2F740B-1D4C-410C-8B81-FCF1927E156E Q26823823-A2597935-87FE-4498-BD68-7E8F42ADC52A Q26864839-004852D0-3A79-4807-A3D9-C85439190B16 Q27013743-AB0D2B56-E205-484A-AF2F-37E69B2B72D3 Q28077508-0AFA2799-9228-42CB-AFEB-5A14740E6083 Q28260661-B3B3D20A-AC5A-4D29-BD19-C6B2DD3AEB26 Q28275410-E722AD1C-C69E-4D42-82F9-6E9F188D0A94 Q28297232-715EF4AF-DAA4-450D-A181-D22D93FFD85D Q28386827-8A49CDAA-6DF9-4E21-8A03-1BC16A747FDA Q28547017-0D9D59D6-6E8D-4BB0-BB40-E7CFEFA837E4 Q28743642-3B66EFE9-C680-4D8B-BA5D-F786F2578E21 Q30436035-654EC053-F1F5-4E3C-891E-66C0869A5B79 Q33487733-3CEBB91B-FD3B-495A-B853-066BD64BB1C0 Q33520113-F4DA44C1-3F7E-418A-BADB-C87A8E51CD30 Q33565057-01E9A27D-9168-4D94-98DA-8217EE53A70F Q33581581-6E289C83-7A47-4332-B250-8621DCACD08B Q33601451-4EA0A13A-07A5-45DE-BA3D-07931C54C098 Q33694557-28BE5E33-FD93-4792-8ACE-FC4DC52CEDFD Q33720132-7E9DC805-4773-4639-9D3E-3AF21D262B58 Q33720686-0A04053C-030E-4F69-A7B6-1B2AAA7C83BC Q33733916-E940E8C7-D180-4B7C-91A1-CE7C598C3AE1 Q33798864-1E821192-222B-43AF-9D14-7D4DB4C61524 Q33822636-B0DCDD54-6A2A-4882-9603-20105ACB82DE Q33846400-7A4E28A1-E547-48B9-8A27-20DF702D9616 Q33889211-3DF58182-C44B-434F-9194-8D230F882EE5 Q33924215-3B446041-4807-4EC6-8B57-34ED5BE54461 Q34028544-35C0B9B5-6AB3-488B-A51E-C22EEF4CAEE0 Q34048090-2176BCF5-20D6-4E9E-8822-411D34A3109A Q34095480-CAB50F61-59E1-415B-8763-60A85366D1A9 Q34194215-217C38DC-7330-4D49-AAC6-1919486926A9 Q34239006-34C07E9C-5EEF-4EC5-953E-9AF01BBEDE93 Q34253391-4455D8C1-B965-4B16-BA9C-BC3CBA8ECDAB Q34340552-E5A9FF1B-98BE-4DC5-A01C-D7FB0757E5BB Q34343645-48448595-43CA-4474-9A98-5873AFE74876

P2860

HMGA2 and Smads co-regulate SNAIL1 expression during induction of epithelial-to-mesenchymal transition

http://www.wikidata.org/entity/Q24318681

description

2008 nî lūn-bûn

@nan

2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@ast

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@en

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@en-gb

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@nl

type

label

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@ast

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@en

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@en-gb

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@nl

prefLabel

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@ast

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@en

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@en-gb

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@nl

P1433

Q24318681-58B8D7B8-5E12-4985-BF0A-9DCD1E4849A1

P1476

Q24318681-C5A6B837-9C25-4D4C-A3C3-92C565B2AA11

P2093

Q24318681-1ECE1C54-9F37-429E-BEC3-1540B11B72B3

Q24318681-22567D76-A0A6-4A85-AFD2-4CBCB30D51FF

Q24318681-729ACDE1-45F1-433F-90D8-87E482EEC23B

Q24318681-742A8021-5E5F-4E85-810E-362F695CB06D

Q24318681-E44AC1A4-0948-4CBD-B46A-2714C70EBC97

Q24318681-F91E9CCF-8789-4BE0-8BEF-F4E0A731CAD8

P2860

Q24318681-091C98CA-881E-4450-B2CA-850D7FB24030

Q24318681-2A0128E3-2E81-444C-87AA-0EE88CB9BFB0

Q24318681-2BCA9E0F-4C44-45B8-A6BB-6602A5FA3F34

Q24318681-2D2569EA-8FA4-41B6-9D89-1CAAA166170E

Q24318681-2D98DBDF-02FA-4908-95A2-05F3F0DDA873

Q24318681-33356924-E869-44E7-88B5-B27FA845D421

Q24318681-3880F0C3-308D-469D-8D13-D261234E1759

Q24318681-805E89F1-16D3-4FAB-819C-7DBB1A91E724

Q24318681-85F2094C-439B-4A8E-8902-EE1565399B95

Q24318681-8F9E6EC8-0F15-47C1-8F48-F283FC6A9716

P304

Q24318681-F7BF41A9-7868-4964-8E32-B9C33E9A0037

P31

Q24318681-B8741D1A-26EF-4294-A823-8C9045502214

P3181

Q24318681-50BFB647-A4CE-4127-9032-BDD612A8EFD8

P356

Q24318681-2EFA086D-45C1-4295-BD7D-724519B0558E

P407

Q24318681-00ECB55D-716F-46B7-BD2A-C52861BFE7AE

P433

Q24318681-55ED06A1-676B-44F0-AA23-CC425C3A3F04

P478

Q24318681-1F1DA2B2-D418-417A-9023-12D6EFF9E9C6

P577

Q24318681-4650EF78-7CC2-4A12-9523-71B4696DF99F

P698

Q24318681-8AFE0E3F-90B2-4722-80E8-B5375C3F2C2B

P921

Q24318681-21AFE11C-E539-4536-B395-B4F5E319B0A1

Q24318681-389EB0EB-A9FF-4C92-B1D5-E59FCDD69A93

Q24318681-4F3BA04C-D4BD-4351-AEB7-07A1DC41D842

Q24318681-616A84E4-2049-4097-91FB-500CAB178A0C

Q24318681-683577C5-04B3-4FF9-A233-51DA95ECCC8B

Q24318681-CC6CEAB0-6448-4D5E-A85A-A09393A4ADCB

Q24318681-EA6F8658-E5A6-4606-9938-6D82044EF9F8

P932

Q24318681-065EE2A3-DA90-456B-BC3F-5453AC8347A4

P3181

P356

P1433

Journal of Biological Chemistry

P1476

HMGA2 and Smads co-regulate SN ...... lial-to-mesenchymal transition

@en

P2093

Amparo Cano

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

Aristidis Moustakas

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

Carl-Henrik Heldin

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

E-Jean Tan

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

Hector Peinado

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

Sylvie Thuault

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

P2860

The second AT-hook of the architectural transcription factor HMGA2 is determinant for nuclear localization and function

Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis

Molecular dissection of the architectural transcription factor HMGA2

A role for Id in the regulation of TGF-beta-induced epithelial-mesenchymal transdifferentiation

Complex networks orchestrate epithelial-mesenchymal transitions

Snail, Zeb and bHLH factors in tumour progression: an alliance against the epithelial phenotype?

TGF-beta and epithelial-to-mesenchymal transitions

TGF-beta and the Smad signaling pathway support transcriptomic reprogramming during epithelial-mesenchymal cell transition

Non-Smad TGF-beta signals.

The logic of TGFbeta signaling.

P304

33437-46

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

P31

scholarly article

P3181

2379644

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

P356

10.1074/JBC.M802016200

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

P407

P433

48

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

P478

283

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

P577

2008-11-28T00:00:00Z

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

P698

18832382

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

P921

Transforming growth factor beta 1

Snail family zinc finger 1

SMAD family member 4

High mobility group AT-hook 2

SMAD family member 2

SMAD family member 3

P932

2662269

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