المؤلفون: Fabian Muehlberg, Edyta Blaszczyk, Kerstin Will, Stefan Wilczek, Joerg Brederlau, Jeanette Schulz‐Menger

المصدر: ESC Heart Failure, Vol 9, Iss 4, Pp 2147-2156 (2022)

مصطلحات موضوعية: Sepsis, Septic cardiomyopathy, Non‐ischaemic cardiomyopathy, Inflammation, Septic shock, Cardiac MR, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2055-5822

URL الوصول: https://doaj.org/article/66851ac39c684b729f4ae2cac46085be

المؤلفون: Gerard Tobin, Ulf Thunberg, Karin Karlsson, Fiona Murray, Anna Laurell, Kerstin Will, Richard Rosenquist, Gunnar Juliusson, Christer Sundström, Ola Söderberg, Göran Roos

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://bloodjournal.hematologylibrary.org/content/104/9/2879.full.pdf.

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.334.427; http://bloodjournal.hematologylibrary.org/content/104/9/2879.full.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.334.427
http://bloodjournal.hematologylibrary.org/content/104/9/2879.full.pdf

المؤلفون: Tobias Obser, Ulrich Budde, Florian Oyen, Barbara Zieger, Jan Jacques Michiels, Reinhard Schneppenheim, Antje Pieconka, Kerstin Will, Sonja Schneppenheim

المصدر: Blood

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Genotype, Von Willebrand factor type A domain, Disintegrins, Amino Acid Motifs, Immunology, Mutation, Missense, ADAMTS13 Protein, Gene Expression, von Willebrand Disease, Type 2, medicine.disease_cause, Biochemistry, Von Willebrand factor, hemic and lymphatic diseases, von Willebrand Factor, Von Willebrand disease, medicine, Humans, Missense mutation, Family, Genetics, Mutation, biology, Cell Biology, Hematology, medicine.disease, Phenotype, Recombinant Proteins, ADAMTS13, Protein Structure, Tertiary, ADAM Proteins, Case-Control Studies, biology.protein, Female, Human medicine, Protein Multimerization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::128ebbfaaf8350a994555fa6219bb3f3
https://doi.org/10.1182/blood-2009-07-226324

المؤلفون: Andrea Sieberer, Georg Golderer, Kerstin Will, Michael Spannagl, Andrea Griesmacher, Helmut W. Ott, Susanne Perkhofer, Mirjam Schnapka-Koepf, Ulrich Budde, Burghardt Scheibe

المصدر: American Journal of Clinical Pathology. 133:322-330

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Fluorescence, chemistry.chemical_compound, Von Willebrand factor, hemic and lymphatic diseases, von Willebrand Factor, Von Willebrand disease, medicine, Humans, Platelet, Sodium dodecyl sulfate, Electrophoresis, Agar Gel, Gel electrophoresis, biology, Sodium Dodecyl Sulfate, General Medicine, Carbocyanines, medicine.disease, Molecular biology, Electrophoresis, chemistry, Agarose gel electrophoresis, biology.protein, Agarose, Densitometry, circulatory and respiratory physiology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47fab8bc5ae8b37df769f02f1dd15a3c
https://doi.org/10.1309/ajcpzsbtd2bwomvl

المؤلفون: Emilio Avallone, Heike Schmitt, Giorgio Lilli, Athanasia Warnecke, Anke Lesinski-Schiedat, Thomas Lenarz, Kerstin Willenborg

المصدر: Acta Otorhinolaryngologica Italica, Vol 42, Iss 4, Pp 364-371 (2022)

مصطلحات موضوعية: Otorhinolaryngology, RF1-547

وصف الملف: electronic resource

Relation: https://www.actaitalica.it/article/view/2074; https://doaj.org/toc/1827-675X

URL الوصول: https://doaj.org/article/1c46a687d3c449d49ac5edc72a9b6fe9

المؤلفون: Kerstin Will, Ulrich Budde, Harald Lenk, Reinhard Schneppenheim, Tobias Obser, Rainer Schwaab, Sonja Schneppenheim, Florian Oyen, Johannes Oldenburg

المصدر: Thrombosis and haemostasis. 92(1)

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Heterozygote, Mutant, DNA Mutational Analysis, Gene Expression, In Vitro Techniques, Compound heterozygosity, medicine.disease_cause, Hemophilia A, Von Willebrand factor, hemic and lymphatic diseases, von Willebrand Factor, Von Willebrand disease, medicine, Humans, Binding site, Protein Structure, Quaternary, Genetics, Mutation, Binding Sites, Factor VIII, biology, business.industry, Heterozygote advantage, Hematology, medicine.disease, Phenotype, Recombinant Proteins, Pedigree, von Willebrand Diseases, Amino Acid Substitution, biology.protein, Female, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6260bcad3370db8809a43d050756a4c3
https://pubmed.ncbi.nlm.nih.gov/15213838

المؤلفون: Kerstin Will, Ravi Kumar Dutta, Jonas Ungerbäck, Rebeqa Gunnarsson, Mats Fredrikson, Mats Linderholm, Peter Söderkvist, Gunnar Juliusson

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://liu.diva-portal.org/smash/get/diva2:642902/FULLTEXT01.pdf.

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.428.5584; http://liu.diva-portal.org/smash/get/diva2:642902/FULLTEXT01.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.428.5584
http://liu.diva-portal.org/smash/get/diva2:642902/FULLTEXT01.pdf

المؤلفون: Tom A. Mendum, Aneesh Chandran, Kerstin Williams, H. Martin Vordermeier, Bernardo Villarreal-Ramos, H. Wu, Albel Singh, Alex A. Smith, Rachel E. Butler, Aravind Prasad, Neeraj Bharti, Ruma Banerjee, Sunitha M. Kasibhatla, Apoorva Bhatt, Graham R. Stewart, Johnjoe McFadden

المصدر: BMC Genomics, Vol 20, Iss 1, Pp 1-13 (2019)

مصطلحات موضوعية: Mycobacterium bovis BCG, Transposon library, Cattle, Mycobacterium tuberculosis, Pyruvate carboxylase, Cyclopropane-fatty-acyl-phospholipid synthase, Biotechnology, TP248.13-248.65, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12864-019-5791-1; https://doaj.org/toc/1471-2164

URL الوصول: https://doaj.org/article/faa5bbfd9bdf4147b30d7a1e6daf6243

المؤلفون: Florian Oyen, Ulrich Budde, Heike Eckert, Reinhard Schneppenheim, Antje Pieconka, Sonja Schneppenheim, Tobias Obser, Kerstin Will, Olivier Marggraf

المصدر: Blood. 110:2711-2711

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, biology, Von Willebrand factor type A domain, Chemistry, Immunology, Mutant, Wild type, Cell Biology, Hematology, medicine.disease, Biochemistry, Phenotype, Molecular biology, law.invention, Genotype-phenotype distinction, Von Willebrand factor, law, hemic and lymphatic diseases, Von Willebrand disease, medicine, biology.protein, Recombinant DNA, circulatory and respiratory physiology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d812a4c8dcbc764a310a951664a45e11
https://doi.org/10.1182/blood.v110.11.2711.2711

المؤلفون: Axel Benner, Larry Mansouri, Davide Rossi, Aneela Majid, Kerstin Willander, Anton Parker, Gareth Bond, Sarka Pavlova, Holger Nückel, Olaf Merkel, Paolo Ghia, Emili Montserrat, Mohd Arifin Kaderi, Richard Rosenquist, Gianluca Gaidano, Martin J.S. Dyer, Peter Söderkvist, Mats Linderholm, David Oscier, Zuzana Tvaruzkova, Sarka Pospisilova, Ulrich Dührsen, Richard Greil, Hartmut Döhner, Stephan Stilgenbauer, Thorsten Zenz

المصدر: Haematologica, Vol 99, Iss 8 (2014)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: https://haematologica.org/article/view/7107; https://doaj.org/toc/0390-6078; https://doaj.org/toc/1592-8721

URL الوصول: https://doaj.org/article/4c66616d07e24363aff3f1ae2d78014c