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Wyszukujesz frazę ""PULMONARY hypertension"" wg kryterium: Temat


Starter badań:

Tytuł :
Inhibiting miR‑1 attenuates pulmonary arterial hypertension in rats.
Autorzy :
Liu Y; Department of Intensive Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
Li Y; Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
Li J; Department of Intensive Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
Zuo X; Department of Intensive Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
Cao Q; Department of Intensive Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
Xie W; Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
Wang H; Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
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Źródło :
Molecular medicine reports [Mol Med Rep] 2021 Apr; Vol. 23 (4). Date of Electronic Publication: 2021 Feb 19.
Typ publikacji :
Journal Article
MeSH Terms :
Connective Tissue Growth Factor/*genetics
Familial Primary Pulmonary Hypertension/*therapy
MicroRNAs/*genetics
Pulmonary Arterial Hypertension/*therapy
Animals ; Antagomirs/pharmacology ; Disease Models, Animal ; Familial Primary Pulmonary Hypertension/genetics ; Familial Primary Pulmonary Hypertension/pathology ; Gene Expression Regulation/genetics ; Heart Ventricles/drug effects ; Heart Ventricles/pathology ; Humans ; MicroRNAs/antagonists & inhibitors ; Pulmonary Arterial Hypertension/genetics ; Pulmonary Arterial Hypertension/pathology ; Rats ; Rats, Sprague-Dawley ; Ventricular Remodeling/genetics
Czasopismo naukowe
Tytuł :
Prognostic Significance of Systemic Arterial Stiffness Evaluated by Cardio-Ankle Vascular Index in Patients with Idiopathic Pulmonary Hypertension.
Autorzy :
Radchenko GD; Department of Symptomatic Hypertension, 'National Scientific Center 'The M.D. Strazhesko Institute of Cardiology'' of National Academy of Medical Science, Kyiv, Ukraine.
Sirenko YM; Department of Symptomatic Hypertension, 'National Scientific Center 'The M.D. Strazhesko Institute of Cardiology'' of National Academy of Medical Science, Kyiv, Ukraine.
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Źródło :
Vascular health and risk management [Vasc Health Risk Manag] 2021 Mar 09; Vol. 17, pp. 77-93. Date of Electronic Publication: 2021 Mar 09 (Print Publication: 2021).
Typ publikacji :
Comparative Study; Journal Article
MeSH Terms :
Cardio Ankle Vascular Index*
Hemodynamics*
Vascular Stiffness*
Familial Primary Pulmonary Hypertension/*diagnosis
Adult ; Familial Primary Pulmonary Hypertension/mortality ; Familial Primary Pulmonary Hypertension/physiopathology ; Female ; Humans ; Male ; Middle Aged ; Predictive Value of Tests ; Prognosis ; Retrospective Studies ; Risk Assessment ; Risk Factors
Czasopismo naukowe
Tytuł :
BLTx Combined With Cardiac Correction in Treatment of PAH in Puerpera: Is It a Feasible Strategy?
Autorzy :
Huang J; Department of Lung Transplant Center, Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, China.
Pan J; Department of Thoracic Surgery, Affiliated Nanjing Drum Tower Hospital of Nanjing University, Nanjing, China.
Wang Z; Department of Lung Transplant Center, Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, China.
Wang D; Department of Thoracic Surgery, Affiliated Nanjing Drum Tower Hospital of Nanjing University, Nanjing, China.
Chen J; Department of Lung Transplant Center, Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, China. Electronic address: .
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Źródło :
The Annals of thoracic surgery [Ann Thorac Surg] 2021 Apr; Vol. 111 (4), pp. e249-e251. Date of Electronic Publication: 2020 Sep 17.
Typ publikacji :
Case Reports
MeSH Terms :
Pregnancy Complications, Cardiovascular*
Cardiac Surgical Procedures/*methods
Familial Primary Pulmonary Hypertension/*surgery
Heart Septal Defects, Atrial/*surgery
Lung Transplantation/*methods
Adult ; Echocardiography ; Familial Primary Pulmonary Hypertension/diagnosis ; Female ; Heart Septal Defects, Atrial/complications ; Heart Septal Defects, Atrial/diagnosis ; Humans ; Pregnancy ; Radiography, Thoracic
Raport
Tytuł :
Peripheral microangiopathy in precapillary pulmonary hypertension: a nailfold video capillaroscopy prospective study.
Autorzy :
Arvanitaki A; Department of Cardiology III - Adult Congenital and Valvular Heart Disease, University Hospital Muenster, Albert-Schweitzer-Campus 1, 48149, Muenster, Germany.; Department of Cardiology, AHEPA University Hospital, Medical School, Aristotle University of Thessaloniki, 1 St. Kyriakidi Street, 54636, Thessaloniki, Greece.; Fourth Department of Internal Medicine, Hippokration University Hospital, Medical School, Aristotle University of Thessaloniki, 49 Konstantinoupoleos Street, 54642, Thessaloniki, Greece.
Giannakoulas G; Department of Cardiology, AHEPA University Hospital, Medical School, Aristotle University of Thessaloniki, 1 St. Kyriakidi Street, 54636, Thessaloniki, Greece.
Triantafyllidou E; Fourth Department of Internal Medicine, Hippokration University Hospital, Medical School, Aristotle University of Thessaloniki, 49 Konstantinoupoleos Street, 54642, Thessaloniki, Greece.
Feloukidis C; Department of Cardiology, AHEPA University Hospital, Medical School, Aristotle University of Thessaloniki, 1 St. Kyriakidi Street, 54636, Thessaloniki, Greece.
Boutou AK; Department of Respiratory Medicine, G. Papanikolaou Hospital, Thessaloniki, Greece.
Garyfallos A; Fourth Department of Internal Medicine, Hippokration University Hospital, Medical School, Aristotle University of Thessaloniki, 49 Konstantinoupoleos Street, 54642, Thessaloniki, Greece.
Karvounis H; Department of Cardiology, AHEPA University Hospital, Medical School, Aristotle University of Thessaloniki, 1 St. Kyriakidi Street, 54636, Thessaloniki, Greece.
Dimitroulas T; Fourth Department of Internal Medicine, Hippokration University Hospital, Medical School, Aristotle University of Thessaloniki, 49 Konstantinoupoleos Street, 54642, Thessaloniki, Greece. .
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Źródło :
Respiratory research [Respir Res] 2021 Jan 21; Vol. 22 (1), pp. 27. Date of Electronic Publication: 2021 Jan 21.
Typ publikacji :
Journal Article; Observational Study
MeSH Terms :
Capillaries/*diagnostic imaging
Capillaries/*physiology
Familial Primary Pulmonary Hypertension/*diagnostic imaging
Microcirculation/*physiology
Microscopic Angioscopy/*methods
Pulmonary Embolism/*diagnostic imaging
Adult ; Aged ; Case-Control Studies ; Familial Primary Pulmonary Hypertension/physiopathology ; Female ; Humans ; Hypertension, Pulmonary/diagnostic imaging ; Hypertension, Pulmonary/physiopathology ; Male ; Middle Aged ; Prospective Studies ; Pulmonary Embolism/physiopathology
Czasopismo naukowe
Tytuł :
Central Role of Dendritic Cells in Pulmonary Arterial Hypertension in Human and Mice.
Autorzy :
van Uden D; Department of Pulmonary Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Koudstaal T; Department of Pulmonary Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
van Hulst JAC; Department of Pulmonary Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Bergen IM; Department of Pulmonary Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Gootjes C; Department of Pulmonary Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Morrell NW; Department of Medicine, University of Cambridge & NIHR BioResource for Translational Research & Addenbrooke's Hospital NHS Foundation Trust & Royal Papworth Hospital NHS Foundation Trust, Cambridge CB2 0QQ, UK.
van Loo G; VIB Center for Inflammation Research, 9052 Ghent, Belgium.; Department of Biomedical Molecular Biology, Ghent University, 9052 Ghent, Belgium.
von der Thüsen JH; Department of Pathology, Erasmus MC, University Medical Center Rotterdam, 3015 GE Rotterdam, The Netherlands.
van den Bosch TPP; Department of Pathology, Erasmus MC, University Medical Center Rotterdam, 3015 GE Rotterdam, The Netherlands.
Ghigna MR; School of Medicine, Université Paris-Saclay, 94270 Le Kremlin-Bicêtre, France.; INSERM UMR_S 999, Pulmonary Hypertension: Pathology and Novel Therapies, Hôpital Marie Lannelongue, 92350 Le Plessis Robinson, France.; Division of Pathology, Marie Lannelongue Hospital, 92350 Le Plessis Robinson, France.
Perros F; School of Medicine, Université Paris-Saclay, 94270 Le Kremlin-Bicêtre, France.; INSERM UMR_S 999, Pulmonary Hypertension: Pathology and Novel Therapies, Hôpital Marie Lannelongue, 92350 Le Plessis Robinson, France.
Montani D; School of Medicine, Université Paris-Saclay, 94270 Le Kremlin-Bicêtre, France.; INSERM UMR_S 999, Pulmonary Hypertension: Pathology and Novel Therapies, Hôpital Marie Lannelongue, 92350 Le Plessis Robinson, France.; Department of Respiratory and Intensive Care Medicine, Pulmonary Hypertension National Referral Center, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Bicêtre, 94270 Le Kremlin-Bicêtre, France.
Kool M; Department of Pulmonary Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Boomars KA; Department of Pulmonary Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Hendriks RW; Department of Pulmonary Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2021 Feb 10; Vol. 22 (4). Date of Electronic Publication: 2021 Feb 10.
Typ publikacji :
Journal Article
MeSH Terms :
Dendritic Cells/*immunology
Familial Primary Pulmonary Hypertension/*immunology
Animals ; Bone Morphogenetic Protein Receptors, Type II/genetics ; Dendritic Cells/pathology ; Familial Primary Pulmonary Hypertension/genetics ; Familial Primary Pulmonary Hypertension/pathology ; Gene Deletion ; Heart Ventricles/immunology ; Heart Ventricles/pathology ; Humans ; Immunity, Innate ; Mice ; Mutation ; Toll-Like Receptor 4/immunology ; Tumor Necrosis Factor alpha-Induced Protein 3/genetics
Czasopismo naukowe
Tytuł :
The Rho kinase 2 (ROCK2)-specific inhibitor KD025 ameliorates the development of pulmonary arterial hypertension.
Autorzy :
Yamamura A; Department of Physiology, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan. Electronic address: .
Nayeem MJ; Department of Physiology, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Sato M; Department of Physiology, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan. Electronic address: .
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Źródło :
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2021 Jan 01; Vol. 534, pp. 795-801. Date of Electronic Publication: 2020 Nov 05.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Familial Primary Pulmonary Hypertension/*pathology
Heterocyclic Compounds, 4 or More Rings/*pharmacology
Pulmonary Arterial Hypertension/*drug therapy
rho-Associated Kinases/*genetics
Animals ; Cell Line ; Cell Proliferation/drug effects ; Familial Primary Pulmonary Hypertension/enzymology ; Humans ; Male ; Monocrotaline/toxicity ; Muscle, Smooth, Vascular/cytology ; Muscle, Smooth, Vascular/drug effects ; Pulmonary Arterial Hypertension/chemically induced ; Pulmonary Arterial Hypertension/physiopathology ; Pulmonary Artery/physiopathology ; Rats, Sprague-Dawley ; Up-Regulation ; Vascular Remodeling ; rho-Associated Kinases/antagonists & inhibitors ; rho-Associated Kinases/metabolism
Czasopismo naukowe
Tytuł :
Protein biomarkers and risk scores in pulmonary arterial hypertension associated with ventricular septal defect: integration of multi-omics and validation.
Autorzy :
Yuan C; Center for Basic Medical Research and Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences, Tianjin, China.; School of Medicine, Nankai University, Tianjin, China.
Chen HX; Center for Basic Medical Research and Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences, Tianjin, China.
Hou HT; Center for Basic Medical Research and Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences, Tianjin, China.
Wang J; Center for Basic Medical Research and Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences, Tianjin, China.
Yang Q; Center for Basic Medical Research and Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences, Tianjin, China.
He GW; Center for Basic Medical Research and Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences, Tianjin, China.; Department of Cardiovascular Surgery, The First Affiliated Hospital, Zhejiang University, Hangzhou, Zhejiang, China.; Drug Research and Development Center, Wannan Medical College, Wuhu, Anhui, China.; Department of Surgery, Oregon Health and Science University, Portland, Oregon.
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Źródło :
American journal of physiology. Lung cellular and molecular physiology [Am J Physiol Lung Cell Mol Physiol] 2020 Nov 01; Vol. 319 (5), pp. L810-L822. Date of Electronic Publication: 2020 Sep 02.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Familial Primary Pulmonary Hypertension/*metabolism
Heart Septal Defects, Ventricular/*complications
Hypertension, Pulmonary/*metabolism
Pulmonary Arterial Hypertension/*metabolism
Biomarkers/blood ; Child ; Child, Preschool ; Familial Primary Pulmonary Hypertension/physiopathology ; Female ; Genomics ; Heart Septal Defects, Ventricular/metabolism ; Humans ; Hypertension, Pulmonary/physiopathology ; Male ; Phosphatidylinositol 3-Kinases/metabolism ; Pulmonary Arterial Hypertension/physiopathology ; Risk Factors
Czasopismo naukowe
Tytuł :
Distinct patterns of soluble leukocyte activation markers are associated with etiology and outcomes in precapillary pulmonary hypertension.
Autorzy :
Lekva T; Research Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, 0027, Oslo, Norway. .
Gullestad L; Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.; Faculty of Medicine, University of Oslo, Oslo, Norway.; Center for Heart Failure Research, K.G. Jebsen Cardiac Research Center and Center for Heart Failure, University of Oslo, Oslo, Norway.
Broch K; Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Aukrust P; Research Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, 0027, Oslo, Norway.; Faculty of Medicine, University of Oslo, Oslo, Norway.; Section of Clinical Immunology and Infectious Diseases, Oslo University Hospital, Rikshospitalet, Oslo, Norway.; K.G. Jebsen Thrombosis Research and Expertise Center, University of Tromsø, Tromsö, Norway.
Andreassen AK; Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Ueland T; Research Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Sognsvannsveien 20, 0027, Oslo, Norway.; Faculty of Medicine, University of Oslo, Oslo, Norway.; K.G. Jebsen Thrombosis Research and Expertise Center, University of Tromsø, Tromsö, Norway.
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Źródło :
Scientific reports [Sci Rep] 2020 Oct 29; Vol. 10 (1), pp. 18540. Date of Electronic Publication: 2020 Oct 29.
Typ publikacji :
Journal Article
MeSH Terms :
Biomarkers/*blood
Familial Primary Pulmonary Hypertension/*blood
Familial Primary Pulmonary Hypertension/*etiology
Leukocytes/*metabolism
Adult ; Antigens, CD/metabolism ; Antigens, Differentiation, Myelomonocytic/metabolism ; Familial Primary Pulmonary Hypertension/metabolism ; Female ; Humans ; Lipocalin-2/metabolism ; Macrophages/metabolism ; Male ; Middle Aged ; Monocytes/metabolism ; Neutrophils/metabolism ; Peroxidase/metabolism ; Prognosis ; Receptors, Cell Surface/metabolism
Czasopismo naukowe
Tytuł :
Extracorporeal Membrane Oxygenation as a Postoperative Left Ventricle Conditioning Tool After Lung Transplantation in Patients With Primary Pulmonary Artery Hypertension: First Polish Experience.
Autorzy :
Stącel T; Silesian Center for Heart Diseases, Zabrze, Poland.
Antończyk R; Silesian Center for Heart Diseases, Zabrze, Poland; Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, Medical University of Silesia, Katowice, Poland.
Latos M; Silesian Center for Heart Diseases, Zabrze, Poland; Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, Medical University of Silesia, Katowice, Poland. Electronic address: .
Nęcki M; Silesian Center for Heart Diseases, Zabrze, Poland.
Przybyłowski P; Silesian Center for Heart Diseases, Zabrze, Poland; First Chair of General Surgery Jagiellonian University, Medical College, Kraków, Poland.
Zembala M; Silesian Center for Heart Diseases, Zabrze, Poland; Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, Medical University of Silesia, Katowice, Poland.
Ochman M; Silesian Center for Heart Diseases, Zabrze, Poland; Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, Medical University of Silesia, Katowice, Poland.
Urlik M; Silesian Center for Heart Diseases, Zabrze, Poland.
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Źródło :
Transplantation proceedings [Transplant Proc] 2020 Sep; Vol. 52 (7), pp. 2113-2117. Date of Electronic Publication: 2020 Apr 02.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Lung Transplantation*
Extracorporeal Membrane Oxygenation/*methods
Familial Primary Pulmonary Hypertension/*complications
Heart Diseases/*etiology
Heart Diseases/*therapy
Adult ; Familial Primary Pulmonary Hypertension/surgery ; Female ; Heart Ventricles/physiopathology ; Humans ; Male ; Middle Aged ; Poland ; Pulmonary Artery/physiopathology ; Young Adult
Czasopismo naukowe
Tytuł :
Heart-lung transplantation for idiopathic pulmonary arterial hypertension and giant pulmonary artery aneurysm - case report.
Autorzy :
Eadington T; Department of Heart and Lung Transplantation, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK. .
Santhanakrishnan K; Department of Heart and Lung Transplantation, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK.
Venkateswaran R; Department of Heart and Lung Transplantation, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK.; Honorary Senior Lecturer, Division of Cardiovascular Science, University of Manchester, Manchester, UK.
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Źródło :
Journal of cardiothoracic surgery [J Cardiothorac Surg] 2020 Jul 13; Vol. 15 (1), pp. 169. Date of Electronic Publication: 2020 Jul 13.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Heart-Lung Transplantation*
Aneurysm/*surgery
Familial Primary Pulmonary Hypertension/*surgery
Pulmonary Artery/*surgery
Aneurysm/etiology ; Familial Primary Pulmonary Hypertension/complications ; Female ; Heart Failure/complications ; Humans ; Middle Aged
Czasopismo naukowe
Tytuł :
Right ventricular fibrosis in idiopathic pulmonary arterial hypertension.
Autorzy :
Yoshihara S; Department of Diagnostic Radiology, Iwata City Hospital, Iwata, Japan.
Suzuki S; Department of Pathology, Iwata City Hospital, Iwata, Japan.
Matsunaga M; Department of Cardiology, Iwata City Hospital, Iwata, Japan.
Ohnishi I; Department of Pathology, Iwata City Hospital, Iwata, Japan.
Naito M; Department of Diagnostic Radiology, Iwata City Hospital, Iwata, Japan.
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Źródło :
Acta cardiologica [Acta Cardiol] 2020 Jun; Vol. 75 (3), pp. 263-264. Date of Electronic Publication: 2019 Feb 08.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Cardiomyopathies*/etiology
Cardiomyopathies*/pathology
Cardiomyopathies*/physiopathology
Familial Primary Pulmonary Hypertension*/complications
Familial Primary Pulmonary Hypertension*/diagnosis
Familial Primary Pulmonary Hypertension*/physiopathology
Heart Ventricles*/diagnostic imaging
Heart Ventricles*/pathology
Heart Ventricles*/physiopathology
Hypertrophy, Right Ventricular*/diagnostic imaging
Hypertrophy, Right Ventricular*/etiology
Hypertrophy, Right Ventricular*/pathology
Hypertrophy, Right Ventricular*/physiopathology
Ventricular Septum*/diagnostic imaging
Ventricular Septum*/pathology
Biopsy/*methods
Computed Tomography Angiography/*methods
Aged ; Autopsy ; Echocardiography/methods ; Fatal Outcome ; Female ; Fibrosis/diagnostic imaging ; Fibrosis/etiology ; Fibrosis/pathology ; Humans
Czasopismo naukowe
Tytuł :
Pediatric lung transplantation in the largest lung transplantation center of China: embarking on a long road.
Autorzy :
Yue B; Wuxi Lung Transplant Center, Department of Thoracic Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, China.
Wu B; Wuxi Lung Transplant Center, Department of Thoracic Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, China.
Zhang J; Wuxi Lung Transplant Center, Department of Thoracic Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, China.
Xu H; Wuxi Lung Transplant Center, Department of Thoracic Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, China.
Wei D; Wuxi Lung Transplant Center, Department of Thoracic Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, China.
Hu C; Wuxi Lung Transplant Center, Department of Thoracic Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, China.
Chen J; Wuxi Lung Transplant Center, Department of Thoracic Surgery, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, China. .
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Źródło :
Scientific reports [Sci Rep] 2020 Jul 27; Vol. 10 (1), pp. 12471. Date of Electronic Publication: 2020 Jul 27.
Typ publikacji :
Journal Article
MeSH Terms :
Familial Primary Pulmonary Hypertension/*surgery
Adolescent ; Child ; China ; Extracorporeal Membrane Oxygenation ; Familial Primary Pulmonary Hypertension/physiopathology ; Female ; Follow-Up Studies ; Humans ; Lung/physiopathology ; Lung/surgery ; Lung Transplantation ; Male ; Retrospective Studies ; Treatment Outcome
Czasopismo naukowe
Tytuł :
Basement Membrane Remodeling Controls Endothelial Function in Idiopathic Pulmonary Arterial Hypertension.
Autorzy :
Jandl K; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.; Division of Pharmacology and.
Marsh LM; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.
Hoffmann J; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.
Mutgan AC; Division of Physiology, Otto Loewi Research Center.
Baum O; Institute of Physiology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Bloch W; German Sports University Cologne, Cologne, Germany; and.
Thekkekara-Puthenparampil H; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.
Kolb D; Gottfried Schatz Research Center.
Sinn K; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.; Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, Vienna, Austria.
Klepetko W; Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, Vienna, Austria.
Heinemann A; Division of Pharmacology and.
Olschewski A; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.; Experimental Anaesthesiology, Department of Anaesthesiology and Intensive Care Medicine, and.
Olschewski H; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Kwapiszewska G; Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Austria.; Division of Physiology, Otto Loewi Research Center.
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Źródło :
American journal of respiratory cell and molecular biology [Am J Respir Cell Mol Biol] 2020 Jul; Vol. 63 (1), pp. 104-117.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Basement Membrane/*physiopathology
Endothelial Cells/*physiology
Familial Primary Pulmonary Hypertension/*physiopathology
Pulmonary Artery/*physiopathology
Adult ; Basement Membrane/metabolism ; Collagen Type IV/metabolism ; Endothelial Cells/metabolism ; Extracellular Matrix/metabolism ; Extracellular Matrix/physiology ; Extracellular Matrix Proteins/metabolism ; Familial Primary Pulmonary Hypertension/metabolism ; Female ; Humans ; Laminin/metabolism ; Male ; Proteoglycans/metabolism ; Pulmonary Artery/metabolism
Czasopismo naukowe
Tytuł :
Association of Rare PTGIS Variants With Susceptibility and Pulmonary Vascular Response in Patients With Idiopathic Pulmonary Arterial Hypertension.
Autorzy :
Wang XJ; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Xu XQ; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.; Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Hospital, Beijing, China.
Sun K; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.; Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Hospital, Beijing, China.
Liu KQ; McKusick-Zhang Center for Genetic Medicine, State Key Laboratory of Medical Molecular Biology, Peking Union Medical College, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Beijing, China.
Li SQ; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Jiang X; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.; Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Hospital, Beijing, China.
Zhao QH; Department of Cardiopulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Wang L; Department of Cardiopulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Peng FH; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Ye J; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Wu Y; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Jiang R; Ministry of Education (MOE) Key Laboratory of Bioinformatics, Bioinformatics Division, Beijing National Research Center for Information Science and Technology, Department of Automation, Tsinghua University, Beijing, China.
Zhang J; Cardiovascular Research Center, Xi'an Jiaotong University School of Basic Medical Sciences, Xi'an, China.
Huang W; Department of Cardiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing Medical University, Chongqing, China.
Wei WB; Cardiovascular Center, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Yan Y; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Li JH; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Liu QQ; State Key Laboratory of Cardiovascular Disease, FuWai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Li S; Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Wang Y; Department of Respiratory Medicine, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Zhang SY; Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Hospital, Beijing, China.
Zhang X; McKusick-Zhang Center for Genetic Medicine, State Key Laboratory of Medical Molecular Biology, Peking Union Medical College, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Beijing, China.
Jing ZC; Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Hospital, Beijing, China.
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Źródło :
JAMA cardiology [JAMA Cardiol] 2020 Jun 01; Vol. 5 (6), pp. 677-684.
Typ publikacji :
Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
MeSH Terms :
Genetic Predisposition to Disease*
Cytochrome P-450 Enzyme System/*genetics
Familial Primary Pulmonary Hypertension/*genetics
Pulmonary Wedge Pressure/*physiology
Vascular Resistance/*physiology
Adult ; Case-Control Studies ; Cytochrome P-450 Enzyme System/metabolism ; Familial Primary Pulmonary Hypertension/physiopathology ; Female ; Humans ; Male ; Phenotype ; Whole Genome Sequencing/methods ; Young Adult
Czasopismo naukowe
Tytuł :
Comprehensive identification of signaling pathways for idiopathic pulmonary arterial hypertension.
Autorzy :
Liu B; Department of Pathophysiology, School of Basic Medicine, and Key Laboratory of Pulmonary Diseases of Ministry of Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zhu L; Department of Pathophysiology, School of Basic Medicine, and Key Laboratory of Pulmonary Diseases of Ministry of Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yuan P; Department of Cardiopulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Marsboom G; Department of Pharmacology, University of Illinois College of Medicine, Chicago, Illinois.
Hong Z; Department of Pharmacology, University of Illinois College of Medicine, Chicago, Illinois.
Liu J; Department of Cardiopulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Zhang P; Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Hu Q; Department of Pathophysiology, School of Basic Medicine, and Key Laboratory of Pulmonary Diseases of Ministry of Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
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Źródło :
American journal of physiology. Cell physiology [Am J Physiol Cell Physiol] 2020 May 01; Vol. 318 (5), pp. C913-C930. Date of Electronic Publication: 2020 Mar 11.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Familial Primary Pulmonary Hypertension/*genetics
Heart Failure/*genetics
Receptors, CCR5/*genetics
Receptors, Complement/*genetics
Adult ; Calcium Channel Blockers/adverse effects ; Calcium Channel Blockers/therapeutic use ; Calcium Signaling/genetics ; Caveolin 1/genetics ; Cell Proliferation/drug effects ; Familial Primary Pulmonary Hypertension/drug therapy ; Familial Primary Pulmonary Hypertension/pathology ; Female ; HEK293 Cells ; Heart Failure/drug therapy ; Heart Failure/pathology ; Humans ; Male ; Middle Aged ; Myocytes, Smooth Muscle/metabolism ; Myocytes, Smooth Muscle/pathology ; Nerve Tissue Proteins/genetics ; Potassium Channels, Tandem Pore Domain/genetics ; Pulmonary Artery/metabolism ; Pulmonary Artery/pathology ; Signal Transduction/genetics ; Whole Exome Sequencing
Czasopismo naukowe
Tytuł :
Plasma markers in pulmonary hypertension subgroups correlate with patient survival.
Autorzy :
Koudstaal, T. (AUTHOR)
van Uden, D. (AUTHOR)
van Hulst, J. A. C. (AUTHOR)
Heukels, P. (AUTHOR)
Bergen, I. M. (AUTHOR)
Geenen, L. W. (AUTHOR)
Baggen, V. J. M. (AUTHOR)
van den Bosch, A. E. (AUTHOR)
van den Toorn, L. M. (AUTHOR)
Chandoesing, P. P. (AUTHOR)
Kool, M. (AUTHOR)
Boersma, E. (AUTHOR)
Hendriks, R. W. (AUTHOR)
Boomars, K. A. (AUTHOR)
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Źródło :
Respiratory Research. 5/4/2021, Vol. 22 Issue 1, p1-13. 13p.
Czasopismo naukowe
Tytuł :
The alveolar epithelial cells are involved in pulmonary vascular remodeling and constriction of hypoxic pulmonary hypertension.
Autorzy :
Wang, Yanxia (AUTHOR)
Li, Xiaoming (AUTHOR)
Niu, Wen (AUTHOR)
Chen, Jian (AUTHOR)
Zhang, Bo (AUTHOR)
Zhang, Xiumin (AUTHOR)
Wang, Yingmei (AUTHOR)
Dang, Shaokang (AUTHOR)
Li, Zhichao (AUTHOR)
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Źródło :
Respiratory Research. 5/4/2021, Vol. 22 Issue 1, p1-16. 16p.
Czasopismo naukowe
Tytuł :
Studies on metal–organic framework (MOF) nanomedicine preparations of sildenafil for the future treatment of pulmonary arterial hypertension.
Autorzy :
Mohamed, Nura A.
Abou-Saleh, Haissam
Kameno, Yu
Marei, Isra
de Nucci, Gilberto
Ahmetaj-Shala, Blerina
Shala, Fisnik
Kirkby, Nicholas S.
Jennings, Lewis
Al-Ansari, Dana E.
Davies, Robert P.
Lickiss, Paul D.
Mitchell, Jane A.
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Źródło :
Scientific Reports. 4/19/2021, Vol. 11 Issue 1, p1-8. 8p.
Czasopismo naukowe

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