About: A murine model of hereditary hemorrhagic telangiectasia

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description	наукова стаття, опублікована в листопаді 1999 (uk) artículu científicu espublizáu en 1999 (ast) 1999 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy) vedecký článok (publikovaný 1999/11/01) (sk) vědecký článek publikovaný v roce 1999 (cs) 1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت في نوفمبر 1999) (ar) wetenschappelijk artikel (gepubliceerd op 1999/11/01) (nl) im November 1999 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28592376-B05A14E0-570B-44A1-8730-19F13CC483AF
publication date	1999-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28592376-6B8F9329-BDD7-43DE-8E64-DDA6C83A6927
language of work or name	English
cites work	wds:Q28592376-00D6B2B1-1B9B-4252-850B-A195DB163B3D wds:Q28592376-0A73287C-7E29-42EC-A6E7-FE44F2317D1B wds:Q28592376-0C037775-D004-4888-9C16-35F00FA2F50E wds:Q28592376-16B3F9F2-690F-4D2F-BC50-5841B1BADC22 wds:Q28592376-29E8620B-3E65-427C-9ADA-9A8359039AE2 wds:Q28592376-30907233-A9F2-45A6-88B2-C2D29B4DB9B7 wds:Q28592376-4E05B001-9F7D-4FB1-91B9-CA2895661919 wds:Q28592376-4E525233-22F2-4F5D-8DFF-841FD5C70A60 wds:Q28592376-51318D13-E3EA-4BC6-BFEB-FFA8DE8AC2D4 wds:Q28592376-5B220314-274D-4DBB-BF0D-4B1F7F16E594 wds:Q28592376-60B29A3B-97CF-4414-918F-3CC855B9B433 wds:Q28592376-60CDC0EF-2885-40B3-AFE4-2FBEFA7EC95C wds:Q28592376-66F3B5B4-F13A-4748-9393-C76A4D9CBDA0 wds:Q28592376-6706796B-B251-4E2E-82C9-CBA5D7F05948 wds:Q28592376-6B96C754-E999-4A15-8614-2B44BB5A47E9 wds:Q28592376-7969FF41-5DBA-4E80-A9E0-696328B717DB wds:Q28592376-7C966909-96DF-4367-8EF8-C71700900195 wds:Q28592376-816E97D5-DB1C-4F02-A225-005476BAD12C wds:Q28592376-8223F94B-6AE3-4435-9061-B9E3D8A061F2 wds:Q28592376-82962BEA-4E41-4542-9EE9-B706C5FFBB4E wds:Q28592376-8BC810C2-D562-4148-A64D-B8D8B0EA6AEE wds:Q28592376-94597ADC-064C-4AB0-9C70-711B653C9A4E wds:Q28592376-9DC56D1F-7801-4A96-8AF9-96E5CDC99616 wds:Q28592376-9E7F547B-38A3-4D9D-B4B4-407B1A17C3E2 wds:Q28592376-B32FA2CF-4CA6-4885-B3B6-570DFA9706A2 wds:Q28592376-B4D98B21-3E9E-4BC9-8E6F-6ED508E98A1E wds:Q28592376-C32BA266-3D50-4C49-9708-6222F203826F wds:Q28592376-C74C00F7-7962-49C3-A2AE-2020644359E3 wds:Q28592376-D12388D8-8B2D-4764-B6E5-03C088ED7A51 wds:Q28592376-D6B4845A-DA49-4B2F-80E8-01086B8BDDB2 wds:Q28592376-DB7C5FAA-6056-404E-9C13-78A10D23A5B8 wds:Q28592376-DFB538FA-7382-48B4-82DF-6AB3740B6D73 wds:Q28592376-E2EB7D90-D12A-4080-A77A-B1920F44429B wds:Q28592376-E3129776-2AE5-4220-B15F-353AD5A46354 wds:Q28592376-EB5C47C6-F50F-4A88-9840-00638EEB5FFC wds:Q28592376-F31D6D07-D6D3-4C97-9739-7D7AA38EB6CA wds:Q28592376-F70B350D-F501-4701-AF8B-4EEAC15D20E6 wds:Q28592376-F945D0AA-2E24-47FF-B5EB-2EBA534B6202 wds:Q28592376-FE4185BB-5892-4115-A0E6-31F7B258B05C wds:Q28592376-FF8A520A-6435-4CC8-8D51-DEFE0DD90938
cites work	Maternal rescue of transforming growth factor-beta 1 null mice Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1 Defective angiogenesis in mice lacking endoglin Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. Role of endoglin in cellular responses to transforming growth factor-beta. A comparative study with betaglycan. Endoglin regulates trophoblast differentiation along the invasive pathway in human placental villous explants TGF-beta 3-mediated tissue interaction during embryonic heart development TGF-beta receptor type II deficiency results in defects of yolk sac hematopoiesis and vasculogenesis Role of PDGF-B and PDGFR-beta in recruitment of vascular smooth muscle cells and pericytes during embryonic blood vessel formation in the mouse Pericyte loss and microaneurysm formation in PDGF-B-deficient mice Mechanisms of angiogenesis Requirement of type III TGF-beta receptor for endocardial cell transformation in the heart Molecular characterization and in situ localization of murine endoglin reveal that it is a transforming growth factor-beta binding protein of endothelial and stromal cells Endoglin is a component of the transforming growth factor-beta receptor system in human endothelial cells Endoglin modulates cellular responses to TGF-beta 1. Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2 Defective haematopoiesis and vasculogenesis in transforming growth factor-beta 1 knock out mice Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia Hereditary hemorrhagic telangiectasia Blood vessel formation: what is its molecular basis? Distinct roles of the receptor tyrosine kinases Tie-1 and Tie-2 in blood vessel formation Requisite role of angiopoietin-1, a ligand for the TIE2 receptor, during embryonic angiogenesis Dominant-negative and targeted null mutations in the endothelial receptor tyrosine kinase, tek, reveal a critical role in vasculogenesis of the embryo Epithelial-mesenchymal transformation of embryonic cardiac endothelial cells is inhibited by a modified antisense oligodeoxynucleotide to transforming growth factor beta 3. The receptor tyrosine kinase TIE is required for integrity and survival of vascular endothelial cells. Endoglin is an accessory protein that interacts with the signaling receptor complex of multiple members of the transforming growth factor-beta superfamily Antibodies to the Type II TGFbeta receptor block cell activation and migration during atrioventricular cushion transformation in the heart Genetic heterogeneity in hereditary haemorrhagic telangiectasia Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin? Ultrastructure and three-dimensional organization of the telangiectases of hereditary hemorrhagic telangiectasia Production of the transforming growth factor-beta binding protein endoglin is regulated during chick heart development Identification of a human endothelial cell antigen with monoclonal antibody 44G4 produced against a pre-B leukemic cell line Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms Mutant endoglin in hereditary hemorrhagic telangiectasia type 1 is transiently expressed intracellularly and is not a dominant negative Portal shunting and resistance to Schistosoma mansoni in 129 strain mice Schistosoma mansoni: evidence that vascular abnormalities correlate with the 'non-permissive' trait in 129/Ola mice Distribution of endoglin in early human development reveals high levels on endocardial cushion tissue mesenchyme during valve formation Visualizing human embryos
author name string	wds:Q28592376-04A1A909-6B67-4623-9623-4C4F4F427EC2 wds:Q28592376-0D956837-D7D8-4C1E-88AD-9B7B078F7824 wds:Q28592376-767771FB-2F24-4617-B138-0035D496C220
OpenCitations bibliographic resource ID	wds:Q28592376-9E63EEE2-3DEE-4D58-ABA5-80692CFCA5E5
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/4424473

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