Abrogation of E-cadherin-mediated cell-cell contact in mouse embryonic stem cells results in reversible LIF-independent self-renewal.
about
Soft substrates promote homogeneous self-renewal of embryonic stem cells via downregulating cell-matrix tractionsDrosophila E-cadherin functions in hematopoietic progenitors to maintain multipotency and block differentiationBrachyury cooperates with Wnt/β-catenin signalling to elicit primitive-streak-like behaviour in differentiating mouse embryonic stem cellsDifferentiation of embryonic stem cells 1 (Dies1) is a component of bone morphogenetic protein 4 (BMP4) signaling pathway required for proper differentiation of mouse embryonic stem cellsAbrogation of E-cadherin-mediated cellular aggregation allows proliferation of pluripotent mouse embryonic stem cells in shake flask bioreactorsTransdifferentiation of pancreatic cells by loss of contact-mediated signalingCulture of human pluripotent stem cells using completely defined conditions on a recombinant E-cadherin substratum3D niche microarrays for systems-level analyses of cell fate.E-cadherin acts as a regulator of transcripts associated with a wide range of cellular processes in mouse embryonic stem cellsDivergent reprogramming routes lead to alternative stem-cell states.E-cadherin is transcriptionally activated via suppression of ZEB1 transcriptional repressor by small RNA-mediated gene silencing.p120-catenin regulates REST and CoREST, and modulates mouse embryonic stem cell differentiationE-cadherin is crucial for embryonic stem cell pluripotency and can replace OCT4 during somatic cell reprogramming.Pleiotropy of glycogen synthase kinase-3 inhibition by CHIR99021 promotes self-renewal of embryonic stem cells from refractory mouse strainsThe self-renewal of mouse embryonic stem cells is regulated by cell-substratum adhesion and cell spreadingLoss of function of e-cadherin in embryonic stem cells and the relevance to models of tumorigenesisPhysiological β-catenin signaling controls self-renewal networks and generation of stem-like cells from nasopharyngeal carcinoma.Mapping the networks for pluripotency.Antioxidants maintain E-cadherin levels to limit Drosophila prohemocyte differentiation.microRNA-103/107 Family Regulates Multiple Epithelial Stem Cell CharacteristicsNuclear signaling from cadherin adhesion complexesWnt/β-catenin signaling promotes differentiation, not self-renewal, of human embryonic stem cells and is repressed by Oct4Regulation of stem cell plasticity: mechanisms and relevance to tissue biology and cancer.p120 Catenin-Mediated Stabilization of E-Cadherin Is Essential for Primitive Endoderm SpecificationEstablishment of leukemia inhibitory factor (LIF)-independent iPS cells with potentiated Oct4Efficient derivation of lateral plate and paraxial mesoderm subtypes from human embryonic stem cells through GSKi-mediated differentiation.Development and application of neural stem cells for treating various human neurological diseases in animal models.Microfluidic-based patterning of embryonic stem cells for in vitro development studies.Cell adhesion molecules and their relation to (cancer) cell stemness.Inhibition of glycogen synthase kinase-3 alleviates Tcf3 repression of the pluripotency network and increases embryonic stem cell resistance to differentiation.E-cadherin's role in development, tissue homeostasis and disease: Insights from mouse models: Tissue-specific inactivation of the adhesion protein E-cadherin in mice reveals its functions in health and disease.Molecular targets of luteolin in cancerDifferential requirement for the dual functions of β-catenin in embryonic stem cell self-renewal and germ layer formation.Isolation and characterization of string-forming female germline stem cells from ovaries of neonatal mice.LIF signal in mouse embryonic stem cells.Sulfated glycosaminoglycans: their distinct roles in stem cell biology.Beta-catenin is vital for the integrity of mouse embryonic stem cells.Decellularized feeders: an optimized method for culturing pluripotent cellsPatterned three-dimensional encapsulation of embryonic stem cells using dielectrophoresis and stereolithography.Jarid2 Coordinates Nanog Expression and PCP/Wnt Signaling Required for Efficient ESC Differentiation and Early Embryo Development.
P2860
Q21091073-2D9081C2-A1AA-4F12-991B-D64662B52A09Q27306691-9E229478-C6DD-45F7-A755-C7B9D7800648Q28245798-F1B24B7F-671C-40B4-836D-9F0DB1F89689Q28591978-790416A8-7DFB-4396-9BCC-95CDC44262D2Q28749175-60574225-67C5-4232-8C47-03360B1EEB24Q30543433-B4AFED00-A460-4A26-838C-5BC955466121Q33594940-D34F2A95-CE90-4EEC-A4D2-B362268E24D8Q33924052-69F26B19-85D1-4839-AA0A-FCDDE6FDCAE5Q33968068-F26B2545-DAB6-4044-99F9-4B29C6D9FDC5Q34042718-0308CAA3-B4EB-45B7-9556-BEDC1FEC48D2Q34113601-2232FA41-7DCE-48D3-9039-BAA1E7B0788AQ34178708-3B7A9770-80E3-4ACA-AA42-CAF963194EEAQ34187775-B177D418-254C-464A-A110-C03F7F16DDB8Q34249409-216DB3E3-ADB6-4F54-BE4B-2C5D556BBC4FQ34358735-52F60749-CF61-4EB1-8E6B-C55ADDEF1A2AQ34423998-5FDD7951-F850-4D5C-919C-F8E7E08DC1A3Q35001181-2174F342-7458-4DAB-BE32-58F65157A920Q35088510-D9005C7E-1DAB-44FF-8606-5CF286B266D0Q35255096-93BEC71B-83EE-4F7D-86EC-9CBE935DA9A6Q35537098-53634E4C-5A3B-4171-A683-C009885610A6Q35539061-01F71DF8-7CBB-4255-AA64-146A85F07E86Q35849667-836B5BBB-7B78-4897-B2BF-00A5E9ECE47AQ35939439-285B860F-872A-4AFD-B51C-CAFF8FF84457Q36111209-BD5C70F6-AE6D-4728-9CA4-3AB28F7550D3Q36421360-7EB0429F-2A3B-403B-954B-D97D5B16A906Q36936889-548F5C39-60C8-4266-8838-77FDCA7EBCFEQ37217325-4F690D2F-FD9B-4A45-A900-1C28ADB34C72Q37351419-4272B47D-64FA-4BA5-AE50-BD86FECB85E5Q38188463-96AFF4B5-E92A-400B-A548-F657AC31FA4CQ38256000-DC081535-2E7C-433A-A5F6-4167B163F307Q38275614-E9C161BC-17FB-45A0-BA4C-28D46663A806Q38365120-275003A9-D731-4900-8A1C-14773E5D87BFQ38473082-0C9AE18A-8F06-4D5F-9344-AB5A681E8E0AQ38639206-F27D1F08-FCE6-4F88-84D7-01CE9112BCE3Q38820725-65BAA395-461A-46F1-838E-F392D769D585Q38973334-6FF8A13F-DBFB-4F21-9F82-CD2AF7DA1DDFQ39030226-ADF20B81-D66B-4B87-ABAB-2C7A35161B43Q39069222-E0BF1289-11CE-4240-8006-B26CC00ADB3BQ39184884-DD6CC2AC-0074-4E8C-8578-802BBD5351CFQ40720099-A069C95D-3ECC-49E2-9EA7-E3BF2A56464F
P2860
Abrogation of E-cadherin-mediated cell-cell contact in mouse embryonic stem cells results in reversible LIF-independent self-renewal.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Abrogation of E-cadherin-media ...... LIF-independent self-renewal.
@en
Abrogation of E-cadherin-media ...... LIF-independent self-renewal.
@nl
type
label
Abrogation of E-cadherin-media ...... LIF-independent self-renewal.
@en
Abrogation of E-cadherin-media ...... LIF-independent self-renewal.
@nl
prefLabel
Abrogation of E-cadherin-media ...... LIF-independent self-renewal.
@en
Abrogation of E-cadherin-media ...... LIF-independent self-renewal.
@nl
P2093
P2860
P50
P356
P1433
P1476
Abrogation of E-cadherin-media ...... e LIF-independent self-renewal
@en
P2093
Angela M Eastham
Angela Russell
Dominik Eckardt
Francesca Soncin
Lisa Mohamet
Nicoletta Bobola
Sarah Ritson
Steve Davies
P2860
P304
P356
10.1002/STEM.134
P577
2009-09-01T00:00:00Z