نتائج البحث - "VWF propeptide"

1

دورية أكاديمية

Elevated von Willebrand factor levels in multiple myeloma: dysregulated mechanisms of both secretion and clearance

المؤلفون: Claire Comerford, Sukhraj Pal Singh Dhami, Philip Murphy, Sean Patmore, Soracha Ward, Nadiya Pushkar, Ulrich Budde, Ellie Karampini, James O'Donnell, Siobhan Glavey, John Quinn, Jamie O'Sullivan

مصطلحات موضوعية: Cardiovascular medicine and haematology, Oncology and carcinogenesis, Clinical pharmacology and therapeutics, Von Willebrand Factor, FVIII, multiple myeloma, VWF propeptide, ADAMTS13, von Willebrand disease, Bleeding disorders, MM, VWF, monoclonal gammopathy, MGUS, smouldering MM (SM), endothelial damage

العلاقة: 10779/rcsi.24936729.v1; https://figshare.com/articles/journal_contribution/Elevated_von_Willebrand_factor_levels_in_multiple_myeloma_dysregulated_mechanisms_of_both_secretion_and_clearance/24936729Test

الإتاحة: https://figshare.com/articles/journal_contribution/Elevated_von_Willebrand_factor_levels_in_multiple_myeloma_dysregulated_mechanisms_of_both_secretion_and_clearance/24936729Test

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2

دورية أكاديمية

Importance of Genotyping in von Willebrand Disease to Elucidate Pathogenic Mechanisms and Variability in Phenotype

المؤلفون: Atiq, Ferdows, Boender, Johan, van Heerde, Waander L., Tellez Garcia, Juan M., Schoormans, Selene C., Krouwel, Sandy, Cnossen, Marjon H., Laros-van Gorkom, Britta A. P., de Meris, Joke, Fijnvandraat, Karin, van der Bom, Johanna G., Meijer, Karina, van Galen, Karin P. M., Eikenboom, Jeroen, Leebeek, Frank W. G.

المصدر: WiN Study Grp , Atiq , F , Boender , J , van Heerde , W L , Tellez Garcia , J M , Schoormans , S C , Krouwel , S , Cnossen , M H , Laros-van Gorkom , B A P , de Meris , J , Fijnvandraat , K , van der Bom , J G , Meijer , K , van Galen , K P M , Eikenboom , J & Leebeek , F W G 2022 , ' Importance of Genotyping in von Willebrand Disease to Elucidate Pathogenic Mechanisms and Variability in Phenotype ....

مصطلحات موضوعية: CLINICAL MARKERS, FACTOR SURVIVAL, VWF PROPEPTIDE, MANAGEMENT, DIAGNOSIS, FAMILIES

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/458c5292-11c8-42f0-8101-3e2474f66e02Test

الإتاحة: https://doi.org/10.1097/HS9.0000000000000718Test
https://hdl.handle.net/11370/458c5292-11c8-42f0-8101-3e2474f66e02Test
https://research.rug.nl/en/publications/458c5292-11c8-42f0-8101-3e2474f66e02Test
https://pure.rug.nl/ws/files/220730816/Importance_of_Genotyping_in_von_Willebrand_Disease.4.pdfTest

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3

Importance of Genotyping in von Willebrand Disease to Elucidate Pathogenic Mechanisms and Variability in Phenotype

المؤلفون: Atiq, F., Boender, J., Heerde, W.L. van, Garcia, J.M.T., Schoormans, S.C., Krouwel, S., Cnossen, M.H., Laros-van Gorkom, B.A.P., Meris, J. de, Fijnvandraat, K., Bom, J.G. van der, Meijer, K., Galen, K.P.M. van, Eikenboom, J., Leebeek, F.W.G., WIN Study Grp

المساهمون: Paediatric Haematology, ARD - Amsterdam Reproduction and Development, Hematology, Pediatrics, Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET)

المصدر: Hemasphere, 6
HemaSphere, 6(6). Wolters Kluwer Health
HemaSphere, 6(6):E718. Wolters Kluwer Health
HemaSphere, 6(6):718. LIPPINCOTT WILLIAMS & WILKINS
HemaSphere, 6(6). LIPPINCOTT WILLIAMS & WILKINS
Hemasphere, 6, 6

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, All institutes and research themes of the Radboud University Medical Center, CLINICAL MARKERS, hemic and lymphatic diseases, Vascular damage Radboud Institute for Health Sciences [Radboudumc 16], VWF PROPEPTIDE, MANAGEMENT, Hematology, FACTOR SURVIVAL, DIAGNOSIS, FAMILIES, circulatory and respiratory physiology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e440d0fc40434b724c7de88f6a6693eTest
https://doi.org/10.1097/hs9.0000000000000718Test

4

دورية أكاديمية

Von Willebrand factor propeptide in severe coronavirus disease 2019 (COVID-19): evidence of acute and sustained endothelial cell activation.

المصدر: British journal of haematology ; 192 ; 4 ; 714 ; 719 ; United Kingdom ; Ireland ; England

مصطلحات موضوعية: COVID-19, SARS-CoV-2, VWF propeptide, coagulopathy, endothelium

العلاقة: http://hdl.handle.net/10147/630748Test; British journal of haematology

الإتاحة: https://doi.org/10.1111/bjh.17273Test
http://hdl.handle.net/10147/630748Test

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5

N-linked glycans within the A2 domain of von Willebrand factor modulate macrophage-mediated clearance

المؤلفون: Clive Drakeford, James S. O’Donnell, Lauren Brady, Padraic G. Fallon, Jamie M. O’Sullivan, Alain Chion, Orla Sheils, Thomas A. J. McKinnon, Sonia Aguila, Roger J. S. Preston, Michael Laffan, Niall Dalton, Teresa M. Brophy, Gudmundur Bergsson, Soracha E. Ward

المساهمون: British Heart Foundation

المصدر: Europe PubMed Central

مصطلحات موضوعية: 030204 cardiovascular system & hematology, Biochemistry, Mice, chemistry.chemical_compound, 0302 clinical medicine, HUMAN VONWILLEBRAND-FACTOR, hemic and lymphatic diseases, 1114 Paediatrics And Reproductive Medicine, Macrophage, IN-VIVO, Mice, Knockout, SHEAR-STRESS, biology, medicine.diagnostic_test, MOUSE MODEL, Hematology, ADAMTS13, Cell biology, VWF PROPEPTIDE, cardiovascular system, Life Sciences & Biomedicine, HUMAN FACTOR-VIII, circulatory and respiratory physiology, congenital, hereditary, and neonatal diseases and abnormalities, Glycan, Proteolysis, Immunology, Protein domain, Mutation, Missense, 1102 Cardiovascular Medicine And Haematology, DOMINANT MODIFIER, 03 medical and health sciences, Protein Domains, Von Willebrand factor, Polysaccharides, Cell Line, Tumor, von Willebrand Factor, Von Willebrand disease, medicine, Animals, Humans, PLASMA-LEVELS, Ristocetin, Science & Technology, Macrophages, ABO BLOOD-GROUP, 1103 Clinical Sciences, Cell Biology, medicine.disease, Amino Acid Substitution, chemistry, biology.protein, FACTOR SURVIVAL, 030215 immunology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a0edef87f40fc1cecc5eea23f4f1b6fTest
https://doi.org/10.1182/blood-2016-04-709436Test

6

أخبار

Mutations in the D1 domain of von Willebrand factor impair their propeptide-dependent multimerization, intracellular trafficking and secretion

المؤلفون: Yin, Jie, Ma, Zhenni, Su, Jian, Wang, Jiong-Wei, Zhao, Xiaojuan, Ling, Jing, Bai, Xia, Ouyang, Wanyan, Wang, Zhaoyue, Yu, Ziqiang, Ruan, Changgeng

مصطلحات موضوعية: von Willebrand disease, VWF propeptide, VWF gene mutation, VWF multimerization, ER retention

العلاقة: http://www.jhoonline.org/content/8/1/73Test

الإتاحة: http://www.jhoonline.org/content/8/1/73Test

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7

von Willebrand factor propeptide and the phenotypic classification of von Willebrand disease

المساهمون: RS: GROW - Developmental Biology, RS: GROW - R4 - Reproductive and Perinatal Medicine, Hematology, Pediatrics, CCA - Disease profiling, CCA - Innovative therapy, CCA - Quality of life, Anatomy and neurosciences, NCA - Neuroinflamation, Vascular Ageing Programme (VAP), Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET), ACS - Amsterdam Cardiovascular Sciences, AII - Amsterdam institute for Infection and Immunity, Paediatric Infectious Diseases / Rheumatology / Immunology, Vascular Medicine, Other departments

المصدر: Blood, 125(19), 3006-3013
Blood, 125(19), 3006-3013. The American Society of Hematology
Blood, 125(19), 3006-3013. American Society of Hematology
Sanders, Y V, Groeneveld, D, Meijer, K, Fijnvandraat, K, Cnossen, M H, Van Der Bom, J G, Coppens, M, De Meris, J, Laros-Van Gorkom, B A P, Mauser-Bunschoten, E P, Leebeek, F W G, Eikenboom, J, Fijnvandraat, K, Coppens, M, Kors, A, Zweegman, S, De Meris, J, Goverde, G J, Jonkers, M H, Dors, N, Nijziel, M R, Meijer, K, Tamminga, R Y J, Van Der Linden, P W, Ypma, P F, Van Der Bom, J G, Eikenboom, J, Smiers, F J W, Granzen, B, Hamulyák, K, Brons, P, Laros-Van Gorkom, B A P, Cnossen, M H & Sanders, Y V 2015, ' von Willebrand factor propeptide and the phenotypic classification of von Willebrand disease ', Blood, vol. 125, no. 19, pp. 3006-3013 . https://doi.org/10.1182/blood-2014-09-603241Test
Blood, 125, 3006-13
Blood, 125(19), 3006-3013. AMER SOC HEMATOLOGY
Blood, 125, 19, pp. 3006-13

مصطلحات موضوعية: Male, VONWILLEBRAND-FACTOR, CLEARANCE, Vascular damage Radboud Institute for Health Sciences [Radboudumc 16], Biochemistry, hemic and lymphatic diseases, Missense mutation, ASSAY, ADULT PATIENTS, Child, Netherlands, Aged, 80 and over, biology, FACTOR-VIII, Hematology, Middle Aged, Prognosis, QUANTITATIVE-ANALYSIS, Null allele, Pathophysiology, von Willebrand Diseases, Phenotype, Child, Preschool, cardiovascular system, VWF PROPEPTIDE, Female, circulatory and respiratory physiology, Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Immunology, Hemorrhage, Rare cancers Radboud Institute for Molecular Life Sciences [Radboudumc 9], DIAGNOSIS, Young Adult, Von Willebrand factor, Antigen, Internal medicine, von Willebrand Factor, Von Willebrand disease, medicine, Humans, Clinical significance, Protein Precursors, Protein precursor, Aged, MULTIMERIZATION, business.industry, Infant, Cell Biology, medicine.disease, Cross-Sectional Studies, Endocrinology, Mutation, biology.protein, business, FACTOR SURVIVAL, Follow-Up Studies