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Peter Lohse

Showing results (51-60 of 121) with videos related to

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Virchows Archiv : an International Journal of Pathology|April 9, 2010
Amyloid in endomyocardial biopsiesBarbara Kieninger, Magdalena Eriksson, Reinhard Kandolf, et al.
Proteomics|January 15, 2002
Generating addressable protein microarrays with PROfusion covalent mRNA-protein fusion technologyShawn Weng, Ke Gu, Philip W Hammond, et al.
Immunogenetics|February 18, 2006
Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel diseaseFabian Schnitzler, Stephan Brand, Tanja Staudinger, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|May 29, 2015
Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutationsElisabeth Schuh, Peter Lohse, Birgit Ertl-Wagner, et al.
Blood|September 28, 2006
Eosinophils are a major intravascular location for tissue factor storage and exposureChristine Moosbauer, Eberhard Morgenstern, Susan L Cuvelier, et al.
Geburtshilfe Und Frauenheilkunde|October 3, 2022
Reduced Steroid Synthesis in the Follicular Fluid of MTHFR 677TT Mutation Carriers: Effects of Increased Folic Acid AdministrationRoman Pavlik, Stephanie Hecht, Ulrich Noss, et al.
Hormone Research in Paediatrics|January 31, 2012
A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiencySusanne Bechtold-Dalla Pozza, Stefan Hiedl, Julia Roeb, et al.
Cardiovascular Diabetology|May 17, 2006
Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndromeUli C Broedl, Michael Lehrke, Elisabeth Fleischer-Brielmaier, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2017
TNFRSF1A and MEFV mutations in childhood onset multiple sclerosisAstrid Blaschek, Rüdiger V Kries, Peter Lohse, et al.
The Journal of Molecular Diagnostics : JMD|March 28, 2009
Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens: identification of three novel mutations in the APOA1 geneMagdalena Eriksson, Stefan Schönland, Saniye Yumlu, et al.
Pageof 13

Showing results (51-60 of 121) with videos related to

Sort By:
Pageof 13
Virchows Archiv : an International Journal of Pathology|April 9, 2010
Amyloid in endomyocardial biopsiesBarbara Kieninger, Magdalena Eriksson, Reinhard Kandolf, et al.
Proteomics|January 15, 2002
Generating addressable protein microarrays with PROfusion covalent mRNA-protein fusion technologyShawn Weng, Ke Gu, Philip W Hammond, et al.
Immunogenetics|February 18, 2006
Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel diseaseFabian Schnitzler, Stephan Brand, Tanja Staudinger, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|May 29, 2015
Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutationsElisabeth Schuh, Peter Lohse, Birgit Ertl-Wagner, et al.
Blood|September 28, 2006
Eosinophils are a major intravascular location for tissue factor storage and exposureChristine Moosbauer, Eberhard Morgenstern, Susan L Cuvelier, et al.
Geburtshilfe Und Frauenheilkunde|October 3, 2022
Reduced Steroid Synthesis in the Follicular Fluid of MTHFR 677TT Mutation Carriers: Effects of Increased Folic Acid AdministrationRoman Pavlik, Stephanie Hecht, Ulrich Noss, et al.
Hormone Research in Paediatrics|January 31, 2012
A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiencySusanne Bechtold-Dalla Pozza, Stefan Hiedl, Julia Roeb, et al.
Cardiovascular Diabetology|May 17, 2006
Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndromeUli C Broedl, Michael Lehrke, Elisabeth Fleischer-Brielmaier, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2017
TNFRSF1A and MEFV mutations in childhood onset multiple sclerosisAstrid Blaschek, Rüdiger V Kries, Peter Lohse, et al.
The Journal of Molecular Diagnostics : JMD|March 28, 2009
Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens: identification of three novel mutations in the APOA1 geneMagdalena Eriksson, Stefan Schönland, Saniye Yumlu, et al.
Pageof 13