Pages that link to "Q28585397"
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The following pages link to Endoglin, an ancillary TGFbeta receptor, is required for extraembryonic angiogenesis and plays a key role in heart development (Q28585397):
Displayed 50 items.
- Endoglin (Q21423349) (← links)
- Early endosomal regulation of Smad-dependent signaling in endothelial cells (Q24292399) (← links)
- Interaction and functional interplay between endoglin and ALK-1, two components of the endothelial transforming growth factor-beta receptor complex (Q24294521) (← links)
- Extracellular and cytoplasmic domains of endoglin interact with the transforming growth factor-beta receptors I and II (Q24297609) (← links)
- Endoglin mediates fibronectin/α5β1 integrin and TGF-β pathway crosstalk in endothelial cells (Q24297899) (← links)
- Regulation of ALK-1 signaling by the nuclear receptor LXRbeta (Q24312839) (← links)
- Casein kinase 2beta as a novel enhancer of activin-like receptor-1 signaling (Q24313348) (← links)
- Endoglin phosphorylation by ALK2 contributes to the regulation of prostate cancer cell migration (Q24314139) (← links)
- Cellular response to hypoxia involves signaling via Smad proteins (Q24314797) (← links)
- Human retroviral gag- and gag-pol-like proteins interact with the transforming growth factor-beta receptor activin receptor-like kinase 1 (Q24324369) (← links)
- Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease (Q24645017) (← links)
- Targeting BMP signalling in cardiovascular disease and anaemia (Q26783734) (← links)
- Role of endoglin in fibrosis and scleroderma (Q26821836) (← links)
- BMPs and their clinical potentials (Q26824827) (← links)
- Adhesion molecule expression and function of primary endothelial cells in benign and malignant tissues correlates with proliferation (Q27315862) (← links)
- Endoglin regulates mural cell adhesion in the circulatory system (Q27326704) (← links)
- Mononuclear cells and vascular repair in HHT (Q28084374) (← links)
- TGFbeta signaling in growth control, cancer, and heritable disorders (Q28142605) (← links)
- Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis (Q28236856) (← links)
- Loss of distinct arterial and venous boundaries in mice lacking endoglin, a vascular-specific TGFbeta coreceptor (Q28506951) (← links)
- Endoglin is required for myogenic differentiation potential of neural crest stem cells (Q28510584) (← links)
- Endoglin haploinsufficiency promotes fibroblast accumulation during wound healing through Akt activation (Q28511364) (← links)
- Identification of endoglin in rat hepatic stellate cells: new insights into transforming growth factor beta receptor signaling (Q28575076) (← links)
- Endoglin is dispensable for angiogenesis, but required for endocardial cushion formation in the midgestation mouse embryo (Q28588583) (← links)
- The TGFβ type II receptor plays a critical role in the endothelial cells during cardiac development (Q28588875) (← links)
- VE-cadherin is a critical endothelial regulator of TGF-beta signalling (Q28594650) (← links)
- TGF-beta signaling in tumor suppression and cancer progression (Q29615427) (← links)
- Endoglin and Alk5 regulate epithelial-mesenchymal transformation during cardiac valve formation. (Q30480194) (← links)
- Vascular endothelial growth factor receptor signaling is required for cardiac valve formation in zebrafish. (Q30492901) (← links)
- ALK1 signalling analysis identifies angiogenesis related genes and reveals disparity between TGF-beta and constitutively active receptor induced gene expression (Q30811602) (← links)
- Infantile Hemangioma Originates From A Dysregulated But Not Fully Transformed Multipotent Stem Cell. (Q30826592) (← links)
- Correlation between CD105 expression and postoperative recurrence and metastasis of hepatocellular carcinoma (Q33241639) (← links)
- Endoglin and activin receptor-like-kinase 1 are co-expressed in the distal vessels of the lung: implications for two familial vascular dysplasias, HHT and PAH. (Q33385083) (← links)
- Loss of Notch signalling induced by Dll4 causes arterial calibre reduction by increasing endothelial cell response to angiogenic stimuli (Q33393502) (← links)
- Mutation analysis of "Endoglin" and "Activin receptor-like kinase" genes in German patients with hereditary hemorrhagic telangiectasia and the value of rapid genotyping using an allele-specific PCR-technique (Q33464720) (← links)
- Physical exercise, fitness and dietary pattern and their relationship with circadian blood pressure pattern, augmentation index and endothelial dysfunction biological markers: EVIDENT study protocol (Q33575065) (← links)
- Characterization of the human Activin-A receptor type II-like kinase 1 (ACVRL1) promoter and its regulation by Sp1 (Q33619784) (← links)
- Endoglin: a novel target for therapeutic intervention in acute leukemias revealed in xenograft mouse models (Q33640207) (← links)
- Endoglin in liver fibrogenesis: Bridging basic science and clinical practice (Q33728841) (← links)
- Endothelial follistatin-like-1 regulates the postnatal development of the pulmonary vasculature by modulating BMP/Smad signaling. (Q33738647) (← links)
- Supermodels and disease: insights from the HHT mice. (Q33773949) (← links)
- Patterning and gastrulation defects caused by the tw18 lethal are due to loss of Ppp2r1a (Q33830549) (← links)
- Brain arteriovenous malformation modeling, pathogenesis, and novel therapeutic targets (Q33843008) (← links)
- Hereditary hemorrhagic telangiectasia: A model for blood vessel growth and enlargement (Q33854081) (← links)
- Molecular pathways: can activin-like kinase pathway inhibition enhance the limited efficacy of VEGF inhibitors? (Q33957962) (← links)
- Investigation of endoglin wild-type and missense mutant protein heterodimerisation using fluorescence microscopy based IF, BiFC and FRET analyses (Q33981941) (← links)
- Endoglin deficiency impairs stroke recovery (Q33988427) (← links)
- Circulating endoglin concentration is not elevated in chronic kidney disease (Q34008908) (← links)
- Thalidomide stimulates vessel maturation and reduces epistaxis in individuals with hereditary hemorrhagic telangiectasia (Q34021937) (← links)
- Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatment (Q34024081) (← links)