Pages that link to "Q28589104"
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The following pages link to Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1 (Q28589104):
Displayed 50 items.
- The notch ligand JAGGED1 as a target for anti-tumor therapy (Q21129294) (← links)
- Jagged 1 (Q21985075) (← links)
- A non-transmembrane form of Jagged-1 regulates the formation of matrix-dependent chord-like structures (Q22253207) (← links)
- Soluble Jagged 1 represses the function of its transmembrane form to induce the formation of the Src-dependent chord-like phenotype (Q24291369) (← links)
- Notch receptors and hematopoiesis (Q24291629) (← links)
- Members of the Jagged/Notch gene families are expressed in injured arteries and regulate cell phenotype via alterations in cell matrix and cell-cell interaction (Q24291667) (← links)
- NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway (Q24293498) (← links)
- Segmental expression of Notch and Hairy genes in nephrogenesis (Q24299797) (← links)
- Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice (Q24310111) (← links)
- Regulation of Notch1 and Dll4 by vascular endothelial growth factor in arterial endothelial cells: implications for modulating arteriogenesis and angiogenesis (Q24540581) (← links)
- Binding of Delta1, Jagged1, and Jagged2 to Notch2 rapidly induces cleavage, nuclear translocation, and hyperphosphorylation of Notch2 (Q24550771) (← links)
- CADASIL: Notch signaling defect or protein accumulation problem? (Q24630181) (← links)
- Alagille syndrome: pathogenesis, diagnosis and management (Q24631094) (← links)
- Protein O -fucosyltransferase 1 is an essential component of Notch signaling pathways (Q24677654) (← links)
- JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype (Q24680927) (← links)
- Delta-like ligand 4 (Dll4) is induced by VEGF as a negative regulator of angiogenic sprouting (Q24685542) (← links)
- The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear (Q25256767) (← links)
- Endothelial Transdifferentiation of Tumor Cells Triggered by the Twist1-Jagged1-KLF4 Axis: Relationship between Cancer Stemness and Angiogenesis (Q26773015) (← links)
- Genetics of the ovarian reserve (Q26777164) (← links)
- Notch: a key regulator of tumor angiogenesis and metastasis (Q26858778) (← links)
- Genetics of congenital heart disease: the glass half empty (Q26862793) (← links)
- Of mice and men: molecular genetics of congenital heart disease (Q26995476) (← links)
- Signaling pathways in the development of infantile hemangioma (Q26996608) (← links)
- The molecular regulation of arteriovenous specification and maintenance (Q28088632) (← links)
- The expression of Jagged1 in the developing mammalian heart correlates with cardiovascular disease in Alagille syndrome (Q28137728) (← links)
- Cranial neural crest ablation of Jagged1 recapitulates the craniofacial phenotype of Alagille syndrome patients (Q28255041) (← links)
- Notch signaling in human development and disease (Q28258962) (← links)
- Endothelial expression of the Notch ligand Jagged1 is required for vascular smooth muscle development (Q28267098) (← links)
- Endothelial deletion of murine Jag1 leads to valve calcification and congenital heart defects associated with Alagille syndrome (Q28277874) (← links)
- Jagged1 in the portal vein mesenchyme regulates intrahepatic bile duct development: insights into Alagille syndrome (Q28297967) (← links)
- Mouse hesr1 and hesr2 genes are redundantly required to mediate Notch signaling in the developing cardiovascular system (Q28304868) (← links)
- Biochemical characterization and cellular effects of CADASIL mutants of NOTCH3 (Q28483874) (← links)
- Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse development (Q28504465) (← links)
- Haploinsufficient lethality and formation of arteriovenous malformations in Notch pathway mutants (Q28505269) (← links)
- Defective smooth muscle development in qkI-deficient mice (Q28506549) (← links)
- Vascular patterning defects associated with expression of activated Notch4 in embryonic endothelium (Q28506571) (← links)
- Regulation of mammalian Notch signaling and embryonic development by the protein O-glucosyltransferase Rumi (Q28507731) (← links)
- The association of Notch2 and NF-kappaB accelerates RANKL-induced osteoclastogenesis (Q28508398) (← links)
- A mutant receptor tyrosine phosphatase, CD148, causes defects in vascular development (Q28508534) (← links)
- Suppression of Notch signalling by the COUP-TFII transcription factor regulates vein identity (Q28509237) (← links)
- Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes (Q28510729) (← links)
- Segmentation defects of Notch pathway mutants and absence of a synergistic phenotype in lunatic fringe/radical fringe double mutant mice (Q28512351) (← links)
- Notch1 and 2 cooperate in limb ectoderm to receive an early Jagged2 signal regulating interdigital apoptosis (Q28512806) (← links)
- The murine ortholog of notchless, a direct regulator of the notch pathway in Drosophila melanogaster, is essential for survival of inner cell mass cells (Q28586313) (← links)
- The extracellular matrix protein MAGP-2 interacts with Jagged1 and induces its shedding from the cell surface (Q28586405) (← links)
- Mind bomb-2 is an E3 ligase for Notch ligand (Q28586483) (← links)
- The Notch target genes Hey1 and Hey2 are required for embryonic vascular development (Q28586854) (← links)
- Quaking is essential for blood vessel development (Q28587833) (← links)
- Presenilin 1 is essential for cardiac morphogenesis (Q28592290) (← links)
- Jagged1 (JAG1): Structure, expression, and disease associations (Q28606584) (← links)