Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Thrombosis and KLKB1[original query] |
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| Gene variants associated with deep vein thrombosis. JAMA 2008 Mar 299 (11): 1306-14. Bezemer Irene D, Bare Lance A, Doggen Carine J M, Arellano Andre R, Tong Carmen, Rowland Charles M, Catanese Joseph, Young Bradford A, Reitsma Pieter H, Devlin James J, Rosendaal Frits |
| Genetic variants associated with deep vein thrombosis: the F11 locus. Journal of thrombosis and haemostasis : JTH 2009 Jul . Li Y, Bezemer I, Rowland CM, Tong CH, Arellano AR, Catanese JJ, Devlin JJ, Reitsma PH, Bare LA, Rosendaal FR |
| Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism. Journal of thrombosis and haemostasis : JTH 2011 Jun 9 (6): 1133-42. Heit J A, Cunningham J M, Petterson T M, Armasu S M, Rider D N, DE Andrade |
| New gene variants associated with venous thrombosis: a replication study in White and Black Americans. Journal of thrombosis and haemostasis : JTH 2011 Mar 9 (3): 489-95. Austin H, De Staercke C, Lally C, Bezemer I D, Rosendaal F R, Hooper W |
| Genetic predisposition to bevacizumab-induced hypertension. Gynecologic oncology 2017 Sep . Frey Melissa K, Dao Fanny, Olvera Narciso, Konner Jason A, Dickler Maura N, Levine Douglas |
| Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes. Journal of thrombosis and haemostasis : JTH 2018 Aug . de Haan H G, van Hylckama Vlieg A, Lotta L A, Gorski M M, Bucciarelli P, Martinelli I, Baglin T P, Peyvandi F, Rosendaal F R, |
| Genetic determinants of activity and antigen levels of contact system factors. Journal of thrombosis and haemostasis : JTH 2018 Oct . Rohmann J L, de Haan H G, Algra A, Vossen C Y, Rosendaal F R, Siegerink |
| Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population. Thrombosis research 2019 5 179 37-44. Fiatal Szilvia, Pikó Péter, Kósa Zsigmond, Sándor János, Ádány Ró |
| COVID-19-Related Coagulopathy-Is Transferrin a Missing Link? Diagnostics (Basel, Switzerland) 2020 8 10 (8): . McLaughlin Katie-May, Bechtel Marco, Bojkova Denisa, Münch Christian, Ciesek Sandra, Wass Mark N, Michaelis Martin, Cinatl Jindri |
| Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence. Journal of thrombosis and haemostasis : JTH 2020 3 18 (7): 1598-1617. Barco Stefano, Sollfrank Stefanie, Trinchero Alice, Adenaeuer Anke, Abolghasemi Hassan, Conti Laura, Häuser Friederike, Kremer Hovinga Johanna A, Lackner Karl J, Loewecke Felicia, Miloni Erwin, Vazifeh Shiran Nader, Tomao Luigi, Wuillemin Walter A, Zieger Barbara, Lämmle Bernhard, Rossmann Hei |
| c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans. Journal of thrombosis and haemostasis : JTH 2020 10 19 (1): 147-152. Adenaeuer Anke, Ezigbo Eyiuche D, Fawzy Nazir Hanan, Barco Stefano, Trinchero Alice, Laubert-Reh Dagmar, Strauch Konstantin, Wild Philipp S, Lackner Karl J, Lämmle Bernhard, Rossmann Hei |
Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.
Journal of thrombosis and haemostasis : JTH 2021 9 . Wan Jun, Vadaq Nadira, Konings Joke, Jaeger Martin, Kumar Vinod, de Laat Bas, Joosten Leo, Netea Mihai G, van der Ven Andre J, de Groot Philip G, de Mast Quirijn, Roest Ma |
| Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
| Genetics of osteopontin in patients with chronic kidney disease: The German Chronic Kidney Disease study. PLoS genetics 2022 4 18 (4): e1010139. Cheng Yurong, Li Yong, Scherer Nora, Grundner-Culemann Franziska, Lehtimäki Terho, Mishra Binisha H, Raitakari Olli T, Nauck Matthias, Eckardt Kai-Uwe, Sekula Peggy, Schultheiss Ulla T, |
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