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Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease

Journal of Medical Genetics, 2006-02, Vol.43 (2), p.97-110

2006

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Review: The enigmatic role of endoglin in the placenta

Placenta (Eastbourne), 2014-02, Vol.35, p.S93-S99

2014

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Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms

Thorax, 1999-08, Vol.54 (8), p.714-729

1999

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Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations

Journal of medical genetics, 2006-09, Vol.43 (9), p.722-728

2006

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Endoglin regulates transforming growth factor-beta signaling and chondrocyte function

Osteoarthritis and cartilage, 2014-04, Vol.22, p.S159-S159

2014

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Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia

The European respiratory journal, 2009-10, Vol.34 (4), p.875-881

2009

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Organization and Expression Strategy of the Ambisense Genome of Densonucleosis Virus of Galleria mellonella

Journal of Virology, 2003-10, Vol.77 (19), p.10357-10365

2003

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Age-dependent endothelial nitric oxide synthase uncoupling in pulmonary arteries of endoglin heterozygous mice

American journal of physiology. Lung cellular and molecular physiology, 2009-12, Vol.297 (6), p.L1170-L1178

2009

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Structural Basis of the Human Endoglin-BMP9 Interaction: Insights into BMP Signaling and HHT1

Cell reports (Cambridge), 2017-05, Vol.19 (9), p.1917-1928

2017

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Evaluation of some proximal sensing methods for mapping soils in urbanized terrain, Detroit, Michigan, USA

Catena (Giessen), 2016-08, Vol.143, p.145-158

2016

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Nonascites-forming advanced-stage serous ovarian cancer is related to a superior epithelial antigen presentation and enhanced infiltrating T-cell response

Gynecologic oncology, 2013-07, Vol.130 (1), p.e132-e132

2013

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Contrast-enhanced molecular ultrasound differentiates endoglin genotypes in mouse embryos

Angiogenesis (London), 2015-01, Vol.18 (1), p.69-81

2015

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Le rôle de l'endogline dans le système vasculaire et cardiovasculaire

M.S. Médecine sciences, 2000, Vol.16 (8-9), p.968

2000

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Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasia

The European respiratory journal, 2004-03, Vol.23 (3), p.373-377

2004

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Endoglin is a component of the transforming growth factor-beta receptor system in human endothelial cells

The Journal of biological chemistry, 1992-09, Vol.267 (27), p.19027-19030

1992

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Primary structure of endoglin, an RGD-containing glycoprotein of human endothelial cells

The Journal of biological chemistry, 1990-05, Vol.265 (15), p.8361-8364

1990

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Visceral manifestations in hereditary haemorrhagic telangiectasia type 2

Journal of medical genetics, 2003-07, Vol.40 (7), p.494-502

2003

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Differentially androgen-modulated genes in ovarian epithelial cells from BRCA mutation carriers and control patients predict ovarian cancer survival and disease progression

Oncogene, 2007-01, Vol.26 (2), p.198-214

2007

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IFPA Meeting 2013 Workshop Report III: Maternal placental immunological interactions, novel determinants of trophoblast cell fate, dual ex vivo perfusion of the human placenta

Placenta, 2014-02, Vol.35 (SUPPL), p.S15-S19

2014

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Endoglin modulates cellular responses to TGF-beta 1

The Journal of cell biology, 1996-06, Vol.133 (5), p.1109-1121

1996

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No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia

Journal of medical genetics, 2004-11, Vol.41 (11), p.e119-e119

2004

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Up-regulation of endoglin on vascular endothelial cells in human solid tumors: implications for diagnosis and therapy

Clinical cancer research, 1995-12, Vol.1 (12), p.1623-1634

1995

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Expression Analysis of Four Endoglin Missense Mutations Suggests That Haploinsufficiency Is the Predominant Mechanism for Hereditary Hemorrhagic Telangiectasia Type 1

Human molecular genetics, 1999-11, Vol.8 (12), p.2171-2181

1999

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A Role for Endoglin in Coupling eNOS Activity and Regulating Vascular Tone Revealed in Hereditary Hemorrhagic Telangiectasia

Circulation research, 2005-04, Vol.96 (6), p.684-692

2005

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Conducting Authentic Moth Research with Students to Encourage Scientific Inquiry

Science scope (Washington, D.C.), 2024-07, Vol.47 (4), p.56-62

2024

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Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease

Review: The enigmatic role of endoglin in the placenta

Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms

Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations

Endoglin regulates transforming growth factor-beta signaling and chondrocyte function

Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia

Organization and Expression Strategy of the Ambisense Genome of Densonucleosis Virus of Galleria mellonella

Age-dependent endothelial nitric oxide synthase uncoupling in pulmonary arteries of endoglin heterozygous mice

Structural Basis of the Human Endoglin-BMP9 Interaction: Insights into BMP Signaling and HHT1

Evaluation of some proximal sensing methods for mapping soils in urbanized terrain, Detroit, Michigan, USA

Nonascites-forming advanced-stage serous ovarian cancer is related to a superior epithelial antigen presentation and enhanced infiltrating T-cell response

Contrast-enhanced molecular ultrasound differentiates endoglin genotypes in mouse embryos

Le rôle de l'endogline dans le système vasculaire et cardiovasculaire

Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasia

Endoglin is a component of the transforming growth factor-beta receptor system in human endothelial cells

Primary structure of endoglin, an RGD-containing glycoprotein of human endothelial cells

Visceral manifestations in hereditary haemorrhagic telangiectasia type 2

Differentially androgen-modulated genes in ovarian epithelial cells from BRCA mutation carriers and control patients predict ovarian cancer survival and disease progression

IFPA Meeting 2013 Workshop Report III: Maternal placental immunological interactions, novel determinants of trophoblast cell fate, dual ex vivo perfusion of the human placenta

Endoglin modulates cellular responses to TGF-beta 1

No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia

Up-regulation of endoglin on vascular endothelial cells in human solid tumors: implications for diagnosis and therapy

Expression Analysis of Four Endoglin Missense Mutations Suggests That Haploinsufficiency Is the Predominant Mechanism for Hereditary Hemorrhagic Telangiectasia Type 1

A Role for Endoglin in Coupling eNOS Activity and Regulating Vascular Tone Revealed in Hereditary Hemorrhagic Telangiectasia

Conducting Authentic Moth Research with Students to Encourage Scientific Inquiry

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