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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 8, 1999
Hypochromic red cells and reticulocyte haemglobin content as markers of iron-deficient erythropoiesis in patients undergoing chronic haemodialysisP Cullen, J Söffker, M Höpfl, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 24, 1998
Plasminogen activator inhibitor-1 4G/5G-polymorphism and factor V Q506 mutation are not associated with myocardial infarction in young menR Junker, J Heinrich, H Schulte, et al.
Nanotechnology|January 9, 2020
Highly dispersed Co deposited on Al2O3 particles via CoCp2 + H2 ALDJacob M Clary, Staci A Van Norman, Hans H Funke, et al.
Nature Protocols|April 27, 2021
Creating custom synthetic genomes in Escherichia coli with REXER and GENESISWesley E Robertson, Louise F H Funke, Daniel de la Torre, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutationAudra L Bettinelli, Theodorus J Mulder, Birgit H Funke, et al.
Journal of Pharmaceutical Sciences|February 13, 2023
A Single Dose, Thermostable, Trivalent Human Papillomavirus Vaccine Formulated Using Atomic Layer DepositionAlyssa E Witeof, Natalie M Meinerz, Kathryne D Walker, et al.
Clinical and Experimental Immunology|October 2, 2008
Single cell analysis of B lymphocytes from Wegener's granulomatosis: B cell receptors display affinity maturation within the granulomatous lesionsJ Voswinkel, G Assmann, G Held, et al.
Stroke|December 4, 1998
Factor V Leiden mutation is a risk factor for cerebral venous thrombosis: a case-control study of 55 patientsP Lüdemann, D G Nabavi, R Junker, et al.
Annals of the Rheumatic Diseases|September 4, 2004
Interleukin 10 promoter microsatellite polymorphisms are associated with response to long term treatment with etanercept in patients with rheumatoid arthritisH Schotte, B Schlüter, S Drynda, et al.
Clinical and Experimental Rheumatology|September 24, 2009
Association of rheumatoid arthritis with Mdm2 SNP309 and genetic evidence for an allele-specific interaction between MDM2 and p53 P72R variants: a case control studyG Assmann, J Voswinkel, M Mueller, et al.
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