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Genetic variants of Adam17 differentially regulate TGFβ signaling to modify vascular pathology in mice and humans

Proceedings of the National Academy of Sciences - PNAS, 2014-05, Vol.111 (21), p.7723-7728

2014

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A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)

The Lancet (British edition), 2004-03, Vol.363 (9412), p.852-859

2004

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Endoglin has a crucial role in blood cell-mediated vascular repair

Circulation (New York, N.Y.), 2006-11, Vol.114 (21), p.2288-2297

2006

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Vascular defects associated with hereditary hemorrhagic telangiectasia revealed in patient-derived isogenic iPSCs in 3D vessels on chip

Stem cell reports, 2022-07, Vol.17 (7), p.1536-1545

2022

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A Pulmonary Right-to-Left Shunt in Patients With Hereditary Hemorrhagic Telangiectasia Is Associated With an Increased Prevalence of Migraine

Chest, 2005-10, Vol.128 (4), p.2485-2489

2005

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Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

Nature communications, 2012-01, Vol.3 (1), p.616-616, Article 616

2012

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Interaction Between ALK1 Signaling and Connexin40 in the Development of Arteriovenous Malformations

Arteriosclerosis, thrombosis, and vascular biology, 2016-04, Vol.36 (4), p.707-717

2016

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Hereditary hemorrhagic telangiectasia: an update on transforming growth factor β signaling in vasculogenesis and angiogenesis

Cardiovascular research, 2003-04, Vol.58 (1), p.20-31

2003

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Embolotherapy of pulmonary arteriovenous malformations: long-term results in 112 patients

Journal of vascular and interventional radiology, 2004-05, Vol.15 (5), p.451-456

2004

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The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands Antilles: A family screening

American journal of medical genetics. Part A, 2003-02, Vol.116A (4), p.324-328

2003

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Unusual Complications After Embolization of a Pulmonary Arteriovenous Malformation

Chest, 1996-05, Vol.109 (5), p.1401-1404

1996

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Quantification of right-to-left shunt with 99mTc-labelled albumin macroaggregates and 100% oxygen in patients with hereditary haemorrhagic telangiectasia

Clinical science (1979), 2002-02, Vol.102 (2), p.127

2002

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Genetic variants of Adam17 differentially regulate TGF[Beta] signaling to modify vascular pathology in mice and humans

Proceedings of the National Academy of Sciences - PNAS, 2014-05, Vol.111 (21), p.7723

2014

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Bleeding risk of cerebral vascular malformations in hereditary hemorrhagic telangiectasia

Journal of neurosurgery, 2000-05, Vol.92 (5), p.779-784

2000

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Quantification of right-to-left shunt with (99m)Tc-labelled albumin macroaggregates and 100% oxygen in patients with hereditary haemorrhagic telangiectasia

Clinical science (1979), 2002-02, Vol.102 (2), p.127

2002

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Value of capillary microscopy in the diagnosis of hereditary hemorrhagic telangiectasia

Archives of dermatology (1960), 2000-06, Vol.136 (6), p.732

2000

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Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and Hereditary Hemorrhagic Telangiectasia

Nature communications, 2012-01, Vol.3, p.616-616

2012

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The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands antilles: A family screening

American journal of medical genetics, 2003, Vol.116A (4), p.324-328

2003

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Pulmonary Arteriovenous Malformations and Hereditary Hemorrhagic Telangiectasia: Embolotherapy Using Balloons and Coils-Reply

Archives of internal medicine (1960), 1996-12, Vol.156 (22), p.2628

Haitjema, Tjeerd

1996

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Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease): new insights in pathogenesis, complications, and treatment

Archives of internal medicine (1960), 1996-04, Vol.156 (7), p.714

1996

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Bleeding risk of cerebrovascular malformations in hereditary hemorrhagic telangiectasia

Journal of neurosurgery, 2000-05, Vol.92 (5), p.779

2000

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Erratum: Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

Nature communications, 2012-10, Vol.3 (1), p.1148, Article 1148

2012

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Sequence-specific Binding of prePhoD to Soluble TatAd Indicates Protein-mediated Targeting of the Tat Export in Bacillus subtilis

The Journal of biological chemistry, 2003-10, Vol.278 (40), p.38428-38436

2003

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Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles : evidence for a founder effect

Human genetics, 2000-07, Vol.107 (1), p.40-44

2000

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Genetic variants of Adam17 differentially regulate TGFβ signaling to modify vascular pathology in mice and humans

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)

Endoglin has a crucial role in blood cell-mediated vascular repair

Vascular defects associated with hereditary hemorrhagic telangiectasia revealed in patient-derived isogenic iPSCs in 3D vessels on chip

A Pulmonary Right-to-Left Shunt in Patients With Hereditary Hemorrhagic Telangiectasia Is Associated With an Increased Prevalence of Migraine

Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

Interaction Between ALK1 Signaling and Connexin40 in the Development of Arteriovenous Malformations

Hereditary hemorrhagic telangiectasia: an update on transforming growth factor β signaling in vasculogenesis and angiogenesis

Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14

Embolotherapy of pulmonary arteriovenous malformations: long-term results in 112 patients

The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands Antilles: A family screening

Unusual Complications After Embolization of a Pulmonary Arteriovenous Malformation

Quantification of right-to-left shunt with 99mTc-labelled albumin macroaggregates and 100% oxygen in patients with hereditary haemorrhagic telangiectasia

Genetic variants of Adam17 differentially regulate TGF[Beta] signaling to modify vascular pathology in mice and humans

Bleeding risk of cerebral vascular malformations in hereditary hemorrhagic telangiectasia

Quantification of right-to-left shunt with (99m)Tc-labelled albumin macroaggregates and 100% oxygen in patients with hereditary haemorrhagic telangiectasia

Value of capillary microscopy in the diagnosis of hereditary hemorrhagic telangiectasia

Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and Hereditary Hemorrhagic Telangiectasia

The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands antilles: A family screening

Pulmonary Arteriovenous Malformations and Hereditary Hemorrhagic Telangiectasia: Embolotherapy Using Balloons and Coils-Reply

Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease): new insights in pathogenesis, complications, and treatment

Bleeding risk of cerebrovascular malformations in hereditary hemorrhagic telangiectasia

Erratum: Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

Sequence-specific Binding of prePhoD to Soluble TatAd Indicates Protein-mediated Targeting of the Tat Export in Bacillus subtilis

Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles : evidence for a founder effect

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