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Roscovitine is a proteostasis regulator that corrects the trafficking defect of F508del‐CFTR by a CDK‐independent mechanism

British journal of pharmacology, 2014-11, Vol.171 (21), p.4831-4849

2014

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Maintaining Low Ca2+ Level in the Endoplasmic Reticulum Restores Abnormal Endogenous F508del‐CFTR Trafficking in Airway Epithelial Cells

Traffic (Copenhagen, Denmark), 2006-05, Vol.7 (5), p.562-573

2006

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Endothelial-to-Mesenchymal Transition in Pulmonary Hypertension

Circulation (New York, N.Y.), 2015-03, Vol.131 (11), p.1006-1018

2015

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(252) Pressure Controlled Hypothermic Lung Perfusion is not Better Than Cold Storage for Lung Preservation

The Journal of heart and lung transplantation, 2023-04, Vol.42 (4), p.S122-S122

2023

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Characteristics and outcomes of patients developing pulmonary hypertension associated with proteasome inhibitors

The European respiratory journal, 2024-06, Vol.63 (6), p.2302158

2024

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Left Ventricular Diastolic Dysfunction in Chronic Thromboembolic Pulmonary Hypertension

The Journal of heart and lung transplantation, 2022-04, Vol.41 (4), p.S26-S27

2022

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Identification of TRPC6 as a novel potential target to activate CaCC in human CF airway epithelial cells

Journal of cystic fibrosis, 2010, Vol.9, p.S16-S16

2010

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Calcium homeostasis is abnormal in cystic fibrosis airway epithelial cells but is normalized after rescue of F508del-CFTR

Cell calcium (Edinburgh), 2008-02, Vol.43 (2), p.175-183

2008

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Leflunomide, an immunomodulator, inhibits vascular tone ex vivo

Archives of Cardiovascular Diseases Supplements, 2021-05, Vol.13 (2), p.189-189

2021

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SUR1/Kir6.2 potassium channel a new actor involved in pulmonary arterial hypertension

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.214-214

2020

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B53 PHOUND IN TRANSLATION: Heterozygote Bmpr2 Mutation In Rat: A New Strategy To Understand Pah Pathobiology

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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A107 ETIOLOGY OF PAH: GO YOUR OWN WAY: Vascular Olfactory Receptors: New Suspects In Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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D107 DIAMONDS AND PEARLS: PULMONARY HYPERTENSION PHENOTYPES: Patterns Of Pulmonary Vascular Remodeling And Expression Of Serine-Threonine Kinase Gcn2 In Pulmonary Veno-Occlusive Disease: a Comparative Analysis

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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Electrical cardiometry: ICON (contractility index) and detection of left ventricular failure

Archives of Cardiovascular Diseases Supplements, 2020-01, Vol.12 (1), p.171-172

2020

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Early detection of left ventricular failure in right ventricular congenital heart diseases

Archives of Cardiovascular Diseases Supplements, 2020-01, Vol.12 (1), p.165-165

2020

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Orai1 channel inhibition preserves left ventricular systolic function and normal Ca2+ handling after pressure overload

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.241-242

2020

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Roscovitine is a proteostasis regulator that corrects the trafficking defect of F 508del‐ CFTR by a CDK ‐independent mechanism

British journal of pharmacology, 2014-11, Vol.171 (21), p.4831-4849

2014

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A18 BLINDED BY THE LIGHT: INSIGHT FROM GENETICS IN PAH: Potassium Channel Subfamily K Member 3 (kcnk3) Contributes To The Development Of Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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CN2 regulates BMP signaling: Consequence for PVOD pathobiology and therapeutic management

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.217-217

2020

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D25 ETIOLOGY AND DETERMINANTS OF PROGNOSIS IN PULMONARY HYPERTENSION: Chemotherapy-Induced Pulmonary Hypertension: Role Of Alkylating Agents

American journal of respiratory and critical care medicine, 2015-01, Vol.191, p.1

2015

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B95 NOVEL THERAPEUTIC TARGETS IN PULMONARY HYPERTENSION: INSIGHTS FROM TRANSLATIONAL AND PRECLINICAL STUDIES: Evidence For The Involvement Of Interferon In The Pathogenesis Of Pulmonary Arterial Hypertension; Role Of Endothelin-1 And Ip10

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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Sheehan's syndrome: a recurrent obstetrical complication

Annales françaises d'anesthésie et de réanimation, 1999-04, Vol.18 (4), p.430-435

1999

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Unraveling the Impact of miR-146a in Pulmonary Arterial Hypertension Pathophysiology and Right Ventricular Function

International journal of molecular sciences, 2024-08, Vol.25 (15), p.8054

2024

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Orai1 Channel Inhibition Preserves Left Ventricular Systolic Function and Normal Ca2+ Handling After Pressure Overload

Circulation (New York, N.Y.), 2020-01, Vol.141 (3), p.199-216

2020

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Serine 165 phosphorylation of SHARPIN regulates the activation of NF-κB

iScience, 2021-01, Vol.24 (1), p.101939-101939, Article 101939

2021

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Roscovitine is a proteostasis regulator that corrects the trafficking defect of F508del‐CFTR by a CDK‐independent mechanism

Maintaining Low Ca2+ Level in the Endoplasmic Reticulum Restores Abnormal Endogenous F508del‐CFTR Trafficking in Airway Epithelial Cells

Endothelial-to-Mesenchymal Transition in Pulmonary Hypertension

(252) Pressure Controlled Hypothermic Lung Perfusion is not Better Than Cold Storage for Lung Preservation

Characteristics and outcomes of patients developing pulmonary hypertension associated with proteasome inhibitors

Left Ventricular Diastolic Dysfunction in Chronic Thromboembolic Pulmonary Hypertension

Identification of TRPC6 as a novel potential target to activate CaCC in human CF airway epithelial cells

Calcium homeostasis is abnormal in cystic fibrosis airway epithelial cells but is normalized after rescue of F508del-CFTR

Leflunomide, an immunomodulator, inhibits vascular tone ex vivo

SUR1/Kir6.2 potassium channel a new actor involved in pulmonary arterial hypertension

B53 PHOUND IN TRANSLATION: Heterozygote Bmpr2 Mutation In Rat: A New Strategy To Understand Pah Pathobiology

A107 ETIOLOGY OF PAH: GO YOUR OWN WAY: Vascular Olfactory Receptors: New Suspects In Pulmonary Arterial Hypertension

D107 DIAMONDS AND PEARLS: PULMONARY HYPERTENSION PHENOTYPES: Patterns Of Pulmonary Vascular Remodeling And Expression Of Serine-Threonine Kinase Gcn2 In Pulmonary Veno-Occlusive Disease: a Comparative Analysis

Electrical cardiometry: ICON (contractility index) and detection of left ventricular failure

Early detection of left ventricular failure in right ventricular congenital heart diseases

Orai1 channel inhibition preserves left ventricular systolic function and normal Ca2+ handling after pressure overload

Roscovitine is a proteostasis regulator that corrects the trafficking defect of F 508del‐ CFTR by a CDK ‐independent mechanism

A18 BLINDED BY THE LIGHT: INSIGHT FROM GENETICS IN PAH: Potassium Channel Subfamily K Member 3 (kcnk3) Contributes To The Development Of Pulmonary Arterial Hypertension

CN2 regulates BMP signaling: Consequence for PVOD pathobiology and therapeutic management

D25 ETIOLOGY AND DETERMINANTS OF PROGNOSIS IN PULMONARY HYPERTENSION: Chemotherapy-Induced Pulmonary Hypertension: Role Of Alkylating Agents

B95 NOVEL THERAPEUTIC TARGETS IN PULMONARY HYPERTENSION: INSIGHTS FROM TRANSLATIONAL AND PRECLINICAL STUDIES: Evidence For The Involvement Of Interferon In The Pathogenesis Of Pulmonary Arterial Hypertension; Role Of Endothelin-1 And Ip10

Sheehan's syndrome: a recurrent obstetrical complication

Unraveling the Impact of miR-146a in Pulmonary Arterial Hypertension Pathophysiology and Right Ventricular Function

Orai1 Channel Inhibition Preserves Left Ventricular Systolic Function and Normal Ca2+ Handling After Pressure Overload

Serine 165 phosphorylation of SHARPIN regulates the activation of NF-κB

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