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Peter Lohse

Showing results (31-40 of 121) with videos related to

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British Journal of Haematology|August 22, 2003
T-cell receptor excision circles: a novel prognostic parameter for the outcome of transplantation in multiple myeloma patientsMirija Svaldi, Andrea Judith Lanthaler, Martin Dugas, et al.
Arthritis and Rheumatism|August 1, 2007
Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutationTania Kümpfel, Lisa-Ann Hoffmann, Heike Rübsamen, et al.
Human Pathology|April 30, 2002
Microsatellite instability, loss of heterozygosity, and loss of hMLH1 and hMSH2 protein expression in endometrial carcinomaGloria Peiró, Joachim Diebold, Peter Lohse, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 8, 2009
Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German childrenMartin Lacher, Sebastian Schroepf, Antje Ballauff, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|January 15, 2010
Leptin gene (TTTC)(n) microsatellite polymorphism as well as leptin receptor R223Q and PPARgamma2 P12A substitutions are not associated with hypertensive disorders in pregnancyAnnette Wiedemann, Franziska Vocke, Justine S Fitzgerald, et al.
Atherosclerosis|February 18, 2014
Homozygosity for a partial deletion of apoprotein A-V signal peptide results in intracellular missorting of the protein and chylomicronemia in a breast-fed infantKirstin Albers, Christian Schlein, Kirsten Wenner, et al.
Plos One|March 3, 2010
The cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's diseaseMartin Storr, Dominik Emmerdinger, Julia Diegelmann, et al.
Gastroenterology|January 13, 2006
Severe TNF receptor-associated periodic syndrome due to 2 TNFRSF1A mutations including a new F60V substitutionStephan L Haas, Peter Lohse, Wilhelm H Schmitt, et al.
ISRN Pediatrics|March 6, 2012
GCK-MODY (MODY 2) Caused by a Novel p.Phe330Ser MutationWalter Bonfig, Sandra Hermanns, Katharina Warncke, et al.
Platelets|October 25, 2007
Gender-specific and menstrual cycle dependent differences in circulating microparticlesBettina Toth, Katharina Nikolajek, Andreas Rank, et al.
Pageof 13

Showing results (31-40 of 121) with videos related to

Sort By:
Pageof 13
British Journal of Haematology|August 22, 2003
T-cell receptor excision circles: a novel prognostic parameter for the outcome of transplantation in multiple myeloma patientsMirija Svaldi, Andrea Judith Lanthaler, Martin Dugas, et al.
Arthritis and Rheumatism|August 1, 2007
Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutationTania Kümpfel, Lisa-Ann Hoffmann, Heike Rübsamen, et al.
Human Pathology|April 30, 2002
Microsatellite instability, loss of heterozygosity, and loss of hMLH1 and hMSH2 protein expression in endometrial carcinomaGloria Peiró, Joachim Diebold, Peter Lohse, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 8, 2009
Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German childrenMartin Lacher, Sebastian Schroepf, Antje Ballauff, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|January 15, 2010
Leptin gene (TTTC)(n) microsatellite polymorphism as well as leptin receptor R223Q and PPARgamma2 P12A substitutions are not associated with hypertensive disorders in pregnancyAnnette Wiedemann, Franziska Vocke, Justine S Fitzgerald, et al.
Atherosclerosis|February 18, 2014
Homozygosity for a partial deletion of apoprotein A-V signal peptide results in intracellular missorting of the protein and chylomicronemia in a breast-fed infantKirstin Albers, Christian Schlein, Kirsten Wenner, et al.
Plos One|March 3, 2010
The cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's diseaseMartin Storr, Dominik Emmerdinger, Julia Diegelmann, et al.
Gastroenterology|January 13, 2006
Severe TNF receptor-associated periodic syndrome due to 2 TNFRSF1A mutations including a new F60V substitutionStephan L Haas, Peter Lohse, Wilhelm H Schmitt, et al.
ISRN Pediatrics|March 6, 2012
GCK-MODY (MODY 2) Caused by a Novel p.Phe330Ser MutationWalter Bonfig, Sandra Hermanns, Katharina Warncke, et al.
Platelets|October 25, 2007
Gender-specific and menstrual cycle dependent differences in circulating microparticlesBettina Toth, Katharina Nikolajek, Andreas Rank, et al.
Pageof 13