Pages that link to "Q42250384"
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The following pages link to Mutations in 2 distinct genetic pathways result in cerebral cavernous malformations in mice. (Q42250384):
Displaying 50 items.
- Loss of CCM3 impairs DLL4-Notch signalling: implication in endothelial angiogenesis and in inherited cerebral cavernous malformations (Q24314844) (← links)
- Structural mechanism of CCM3 heterodimerization with GCKIII kinases (Q24337504) (← links)
- Cerebral cavernous malformation is a vascular disease associated with activated RhoA signaling (Q26849566) (← links)
- Molecular mechanisms controlling vascular lumen formation in three-dimensional extracellular matrices (Q26996223) (← links)
- Endothelial cell-cell adhesion during zebrafish vascular development (Q27005949) (← links)
- Vascular anomalies: from genetics toward models for therapeutic trials (Q27025402) (← links)
- Lack of CCM1 induces hypersprouting and impairs response to flow (Q27301327) (← links)
- Micro-CT Imaging Reveals Mekk3 Heterozygosity Prevents Cerebral Cavernous Malformations in Ccm2-Deficient Mice (Q27329910) (← links)
- KLF4 is a key determinant in the development and progression of cerebral cavernous malformations (Q30278010) (← links)
- Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations (Q30389638) (← links)
- CCM1-ICAP-1 complex controls β1 integrin-dependent endothelial contractility and fibronectin remodeling (Q30542261) (← links)
- Developmental timing of CCM2 loss influences cerebral cavernous malformations in mice (Q34209951) (← links)
- PDCD10 gene mutations in multiple cerebral cavernous malformations (Q34420456) (← links)
- The pathobiology of vascular malformations: insights from human and model organism genetics (Q34544980) (← links)
- KRIT1 protein depletion modifies endothelial cell behavior via increased vascular endothelial growth factor (VEGF) signaling (Q34552843) (← links)
- Strategy for identifying repurposed drugs for the treatment of cerebral cavernous malformation. (Q35167117) (← links)
- Downregulation of programmed cell death 10 is associated with tumor cell proliferation, hyperangiogenesis and peritumoral edema in human glioblastoma (Q35816668) (← links)
- ANKS1B Interacts with the Cerebral Cavernous Malformation Protein-1 and Controls Endothelial Permeability but Not Sprouting Angiogenesis (Q35876785) (← links)
- The cerebral cavernous malformation pathway controls cardiac development via regulation of endocardial MEKK3 signaling and KLF expression. (Q36109992) (← links)
- Apicobasal polarity of brain endothelial cells (Q36595837) (← links)
- Minimal homozygous endothelial deletion of Eng with VEGF stimulation is sufficient to cause cerebrovascular dysplasia in the adult mouse (Q36600362) (← links)
- Nogo-B receptor deficiency causes cerebral vasculature defects during embryonic development in mice (Q36619170) (← links)
- Loss of endothelial programmed cell death 10 activates glioblastoma cells and promotes tumor growth (Q36705891) (← links)
- Endothelial exocytosis of angiopoietin-2 resulting from CCM3 deficiency contributes to cerebral cavernous malformation (Q37239068) (← links)
- A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation (Q37270784) (← links)
- Introduction to cerebral cavernous malformation: a brief review (Q37351147) (← links)
- Cerebral cavernous malformation proteins at a glance. (Q37583343) (← links)
- STRIPAK complexes: structure, biological function, and involvement in human diseases (Q37590616) (← links)
- Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration (Q37618688) (← links)
- Signaling pathways and the cerebral cavernous malformations proteins: lessons from structural biology. (Q37722299) (← links)
- Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management (Q38003193) (← links)
- SOcK, MiSTs, MASK and STicKs: the GCKIII (germinal centre kinase III) kinases and their heterologous protein-protein interactions (Q38124367) (← links)
- A murine toolbox for imaging the neurovascular unit (Q38263461) (← links)
- PTEN/PI3K/Akt/VEGF signaling and the cross talk to KRIT1, CCM2, and PDCD10 proteins in cerebral cavernous malformations (Q38268858) (← links)
- Up-regulation of NADPH oxidase-mediated redox signaling contributes to the loss of barrier function in KRIT1 deficient endothelium. (Q38622980) (← links)
- Oxidative stress and inflammation in cerebral cavernous malformation disease pathogenesis: Two sides of the same coin. (Q38957623) (← links)
- Cerebral cavernous malformations arise independent of the heart of glass receptor (Q39113906) (← links)
- Focal defects in single-celled tubes mutant for Cerebral cavernous malformation 3, GCKIII, or NSF2. (Q41517629) (← links)
- Decreased Krev interaction-trapped 1 expression leads to increased vascular permeability and modifies inflammatory responses in vivo (Q42414313) (← links)
- EndMT contributes to the onset and progression of cerebral cavernous malformations (Q45333641) (← links)
- CCM-3/STRIPAK promotes seamless tube extension through endocytic recycling (Q47035963) (← links)
- Ccm3 functions in a manner distinct from Ccm1 and Ccm2 in a zebrafish model of CCM vascular disease (Q47073658) (← links)
- KRIT1 loss-of-function induces a chronic Nrf2-mediated adaptive homeostasis that sensitizes cells to oxidative stress: Implication for Cerebral Cavernous Malformation disease (Q47369895) (← links)
- Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model. (Q48118976) (← links)
- Heg1 and Ccm1/2 proteins control endocardial mechanosensitivity during zebrafish valvulogenesis. (Q48175918) (← links)
- Dysregulated exocytosis of angiopoietin-2 drives cerebral cavernous malformation (Q48526422) (← links)
- Cerebrovascular disorders associated with genetic lesions (Q57456322) (← links)
- Cerebral Cavernous Malformations Develop Through Clonal Expansion of Mutant Endothelial Cells (Q57784186) (← links)
- The STRIPAK complex components FAM40A and FAM40B regulate endothelial cell contractility via ROCKs (Q60482387) (← links)
- Phenotypic characterization of murine models of cerebral cavernous malformations (Q89267281) (← links)