Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Maike Ziegler"'
1
Immunohistochemical analysis of the gingiva with periodontitis of type I plasminogen deficiency compared to gingiva with gingivitis and periodontitis and healthy gingiva
Autor: Nina M. Christiansen, Volker Schuster, Idil Kurtulus Waschulewski, Aslan Gökbuget, Maike Ziegler, Werner Götz, Gerhard Wahl
Publikováno v: Archives of Oral Biology. 72:75-86
Objective Type I plasminogen deficiency (Plgdef) is an uncommon chronic inflammation of mucous membranes. Gingival enlargements usually proceed with progressive periodontal destruction and tooth-loss. Plasmin(ogen)-independent enzymatic mechanisms fo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::134866db6f4c55402d27f8a94cecaff5
https://doi.org/10.1016/j.archoralbio.2016.07.013
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2
Treatment of plasminogen deficiency patients with fresh frozen plasma
Autor: Maike Ziegler, Ayse Ayzit Atabek, Haluk Cokugras, Tiraje Celkan, Buket Dönmez-Demir, Guzin Iskeleli, Hilal Özdağ, Nina M. Christiansen, Volker Schuster, Gürcan Dikme, Hande Kizilocak, Nihal Özdemir, Begum Sirin Koc
Publikováno v: Pediatric bloodcancer. 65(2)
Congenital plasminogen (Plg) deficiency leads to the development of ligneous membranes on mucosal surfaces. Here, we report our experience with local and intravenous fresh frozen plasma (FFP). We retrospectively reviewed medical files of 17 patients
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244cca7ad303ead29f013b6d4536e571
https://pubmed.ncbi.nlm.nih.gov/29271612
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3
A K19E missense mutation in the plasminogen gene is a common cause of familial hypoplasminogenaemia
Autor: Volker Schuster, Isobel D. Walker, Maike Ziegler, Katrin Tefs, Nicole Pietzsch, Campbell R Tait
Publikováno v: Blood Coagulation & Fibrinolysis. 14:411-416
The prevalence of familial plasminogen deficiency in Scotland has recently been calculated at 2.9/1000. However, little is known of the molecular genetic background and the frequency of plasminogen gene mutations in most cases of inherited plasminoge
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::716781a4f279199300e6adc38c0872d5
https://doi.org/10.1097/00001721-200306000-00014
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4
Isoelectric focusing pattern of plasminogen mutants of patients with hypoplasminogenemia: correlation of in-vitro data with computer-predicted isoelectric points (pI)
Autor: Boris Hügle, Maria Ott-Gueorguieva, Maike Ziegler, Louise Kobelt, Volker Schuster, Christian Hintze, Katrin Tefs
Publikováno v: Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 22(6)
Plasminogen (plg), the circulating proenzyme of plasmin in blood, is a polymorphic protein and most of these natural variants have been identified using isoelectric focusing (IEF) gel electrophoresis. Here, we show that a rare plg gene polymorphism 5
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1547a0375f81e21e59b8d13800b7e16
https://pubmed.ncbi.nlm.nih.gov/21537161
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7
Characterization of plasminogen variants in healthy subjects and plasminogen mutants in patients with inherited plasminogen deficiency by isoelectric focusing gel electrophoresis
Autor: Volker Schuster, Maike Ziegler, Katrin Tefs, Stefan Seregard, Maria Georgieva, Boris Hügle, Campbell R Tait, Lori Luchtman-Jones
Publikováno v: Thrombosis and haemostasis. 92(2)
SummaryPlasmin(ogen) plays an important role in fibrinolysis and wound healing. Severe hypoplasminogenemia has recently been linked to ligneous conjunctivitis. Plasminogen (plg) is known as a polymorphic protein and most of these variants have been i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8df353e6800fc76087f28169dae67d0e
https://pubmed.ncbi.nlm.nih.gov/15269832
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8
A nucleic acid exchange in Intron F (Intron F-14T>G) in the human plasminogen gene is only a common polymorphism and not a true mutation
Autor: Volker Schuster, Maike Ziegler, Boris Hügle, Katrin Tefs, Maria Georgieva
Publikováno v: Thrombosis and Haemostasis. 91:830-831
Reply to: A nucleic acid exchange in Intron F (Intron F-14T>G) in the human plasminogen gene is only a common polymorphism and not a true mutation
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0f744ebdd83eca4997ce80233c1b0a54
https://doi.org/10.1055/s-0037-1614275
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