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Dorothee Wernet

Showing results (1-10 of 29) with videos related to

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Deutsche Medizinische Wochenschrift (1946)|December 17, 2009
[AB0-incompatible kidney transplantation--case 13/2009]Martina Guthoff, Dorothee Wernet, Wolfgang Steurer, et al.
Rheumatology International|July 20, 2007
Is there a predisposition for the development of autoimmune diseases in patients with fibromyalgia? Retrospective analysis with long term follow-upIna Kötter, Daniela Neuscheler, Ilhan Günaydin, et al.
Transfusion|September 27, 2005
A noninvasive strategy for screening prospective blood donors for anemiaRamin Lotfi, Dorothee Wernet, Uwe Starke, et al.
Transplantation|August 27, 2011
HLA antibody specification using single-antigen beads--a technical solution for the prozone effectMartina Schnaidt, Christof Weinstock, Marija Jurisic, et al.
The Journal of General Virology|August 30, 2008
Identification of HLA-A*01- and HLA-A*02-restricted CD8+ T-cell epitopes shared among group B enterovirusesAndreas O Weinzierl, Despina Rudolf, Dominik Maurer, et al.
European Journal of Immunology|January 27, 2010
Involvement of CD91 and scavenger receptors in Hsp70-facilitated activation of human antigen-specific CD4+ memory T cellsNadja Fischer, Markus Haug, William W Kwok, et al.
Experimental and Molecular Pathology|March 11, 2004
Cytotoxic activity of natural killer cells lacking killer-inhibitory receptors for self-HLA class I molecules against autologous hematopoietic stem cells in healthy individualsRoger Grau, Karl S Lang, Dorothee Wernet, et al.
Pharmacogenetics|July 1, 2004
Comprehensive analysis of thiopurine S-methyltransferase phenotype-genotype correlation in a large population of German-Caucasians and identification of novel TPMT variantsElke Schaeffeler, Christine Fischer, Dierk Brockmeier, et al.
Biochemical Pharmacology|May 7, 2003
Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and EgyptiansChristoph Köhle, Bernd Möhrle, Peter A Münzel, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 11, 2003
Cutting edge: predetermined avidity of human CD8 T cells expanded on calibrated MHC/anti-CD28-coated microspheresSteffen Walter, Leah Herrgen, Oliver Schoor, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

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Pageof 3
Deutsche Medizinische Wochenschrift (1946)|December 17, 2009
[AB0-incompatible kidney transplantation--case 13/2009]Martina Guthoff, Dorothee Wernet, Wolfgang Steurer, et al.
Rheumatology International|July 20, 2007
Is there a predisposition for the development of autoimmune diseases in patients with fibromyalgia? Retrospective analysis with long term follow-upIna Kötter, Daniela Neuscheler, Ilhan Günaydin, et al.
Transfusion|September 27, 2005
A noninvasive strategy for screening prospective blood donors for anemiaRamin Lotfi, Dorothee Wernet, Uwe Starke, et al.
Transplantation|August 27, 2011
HLA antibody specification using single-antigen beads--a technical solution for the prozone effectMartina Schnaidt, Christof Weinstock, Marija Jurisic, et al.
The Journal of General Virology|August 30, 2008
Identification of HLA-A*01- and HLA-A*02-restricted CD8+ T-cell epitopes shared among group B enterovirusesAndreas O Weinzierl, Despina Rudolf, Dominik Maurer, et al.
European Journal of Immunology|January 27, 2010
Involvement of CD91 and scavenger receptors in Hsp70-facilitated activation of human antigen-specific CD4+ memory T cellsNadja Fischer, Markus Haug, William W Kwok, et al.
Experimental and Molecular Pathology|March 11, 2004
Cytotoxic activity of natural killer cells lacking killer-inhibitory receptors for self-HLA class I molecules against autologous hematopoietic stem cells in healthy individualsRoger Grau, Karl S Lang, Dorothee Wernet, et al.
Pharmacogenetics|July 1, 2004
Comprehensive analysis of thiopurine S-methyltransferase phenotype-genotype correlation in a large population of German-Caucasians and identification of novel TPMT variantsElke Schaeffeler, Christine Fischer, Dierk Brockmeier, et al.
Biochemical Pharmacology|May 7, 2003
Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and EgyptiansChristoph Köhle, Bernd Möhrle, Peter A Münzel, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 11, 2003
Cutting edge: predetermined avidity of human CD8 T cells expanded on calibrated MHC/anti-CD28-coated microspheresSteffen Walter, Leah Herrgen, Oliver Schoor, et al.
Pageof 3