CYP2R1 (vitamin D 25-hydroxylase) gene is associated with susceptibility to type 1 diabetes and vitamin D levels in Germans
Ramos-Lopez, Elizabeth, Brück, Patrick, Jansen, Thomas, Herwig, Jürgen, Badenhoop, Klaus
Published in Diabetes/metabolism research and reviews (01.11.2007)
Published in Diabetes/metabolism research and reviews (01.11.2007)
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A promoter polymorphism of the CYP27B1 gene is associated with Addison's disease, Hashimoto's thyroiditis, Graves' disease and type 1 diabetes mellitus in Germans
Lopez, ER, Zwermann, O, Segni, M, Meyer, G, Reincke, M, Seissler, J, Herwig, J, Usadel, KH, Badenhoop, K
Published in European journal of endocrinology (01.08.2004)
Published in European journal of endocrinology (01.08.2004)
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3-methylcrotonyl-CoA carboxylase deficiency: clinical, biochemical, enzymatic and molecular studies in 88 individuals
Grünert, Sarah C, Stucki, Martin, Morscher, Raphael J, Suormala, Terttu, Bürer, Celine, Burda, Patricie, Christensen, Ernst, Ficicioglu, Can, Herwig, Jürgen, Kölker, Stefan, Möslinger, Dorothea, Pasquini, Elisabetta, Santer, René, Schwab, K Otfried, Wilcken, Bridget, Fowler, Brian, Yue, Wyatt W, Baumgartner, Matthias R
Published in Orphanet journal of rare diseases (29.05.2012)
Published in Orphanet journal of rare diseases (29.05.2012)
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IDDM patients neither show humoral reactivities against endogenous retroviral envelope protein nor do they differ in retroviral mRNA expression from healthy relatives or normal individuals
BADENHOOP, K, DONNER, H, NEUMANN, J, HERWIG, J, KURTH, R, USADEL, K. H, TÖNJES, R. R
Published in Diabetes (New York, N.Y.) (01.01.1999)
Published in Diabetes (New York, N.Y.) (01.01.1999)
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CTLA4 gene haplotypes cannot protect from iddm in the presence of high-risk HLA DQ8 or DQ2 alleles in German families
DONNER, H, SEIDL, C, BRAUN, J, SIEGMUND, T, HERWIG, J, SEIFRIED, E, USADEL, K. H, BADENHOOP, K
Published in Diabetes (New York, N.Y.) (01.07.1998)
Published in Diabetes (New York, N.Y.) (01.07.1998)
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Vitamin D binding protein alleles and susceptibility for type 1 diabetes in Germans
Pani, M A, Donner, H, Herwig, J, Usadel, K H, Badenhoop, K
Published in Autoimmunity (Chur, Switzerland) (01.01.1999)
Published in Autoimmunity (Chur, Switzerland) (01.01.1999)
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Detection of mutations in the apolipoprotein CII gene by denaturing gradient gel electrophoresis. Identification of the splice site variant apolipoprotein CII-Hamburg in a patient with severe hypertriglyceridemia
Nauck, Markus S, Nissen, Henrik, Hoffmann, Michael M, Herwig, Jurgen, Pullinger, Clive R, Averna, Maurizio, Geisel, Jurgen, Wieland, Heinrich, Marz, Winfried
Published in Clinical chemistry (Baltimore, Md.) (01.07.1998)
Published in Clinical chemistry (Baltimore, Md.) (01.07.1998)
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The Presence or Absence of a Retroviral Long Terminal Repeat Influences the Genetic Risk for Type 1 Diabetes Conferred by Human Leukocyte Antigen DQ Haplotypes
Donner, Horst, Tönjes, Ralf R., Van der Auwera, Bart, Siegmund, Thorsten, Braun, Jens, Weets, Ilse, Herwig, Jürgen, Kurth, Reinhard, Usadel, Klaus Henning, Badenhoop, Klaus
Published in The journal of clinical endocrinology and metabolism (01.04.1999)
Published in The journal of clinical endocrinology and metabolism (01.04.1999)
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CTLA4 Alanine-17 Confers Genetic Susceptibility to Graves’ Disease and to Type 1 Diabetes Mellitus1
Donner, Horst, Rau, Harald, Walfish, Paul G, Braun, Jens, Siegmund, Thorsten, Finke, Reinhard, Herwig, Jürgen, Usadel, Klaus H, Badenhoop, Klaus
Published in The journal of clinical endocrinology and metabolism (01.01.1997)
Published in The journal of clinical endocrinology and metabolism (01.01.1997)
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COMPOSITIONS AND THEIR USE AS SEAMING COMPONENTS
BERLINEANU ANDREAS, HERWIG JURGEN, BUKOHL, MARGIT, GITTENMAIER STEFAN, KRANNIG KAI-STEFFEN, BOERS GEERT, LOOS KATRIN
Year of Publication 30.08.2024
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Year of Publication 30.08.2024
Patent
CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus
DONNER, H, RAU, H, WALFISH, P. G, BRAUN, J, SIEGMUND, T, FINKE, R, HERWIG, J, USADEL, K. H, BADENHOOP, K
Published in The journal of clinical endocrinology and metabolism (1997)
Published in The journal of clinical endocrinology and metabolism (1997)
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The cblD Defect Causes Either Isolated or Combined Deficiency of Methylcobalamin and Adenosylcobalamin Synthesis
Suormala, Terttu, Baumgartner, Matthias R, Coelho, David, Zavadakova, Petra, Kozich, Viktor, Koch, Hans Georg, Berghaüser, Martin, Wraith, James E, Burlina, Alberto, Sewell, Adrian, Herwig, Jürgen, Fowler, Brian
Published in The Journal of biological chemistry (08.10.2004)
Published in The Journal of biological chemistry (08.10.2004)
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Vitamin D 1alpha-hydroxylase (CYP1alpha) polymorphism in Graves' disease, Hashimoto's thyroiditis and type 1 diabetes mellitus
Pani, MA, Regulla, K, Segni, M, Krause, M, Hofmann, S, Hufner, M, Herwig, J, Pasquino, AM, Usadel, KH, Badenhoop, K
Published in European journal of endocrinology (01.06.2002)
Published in European journal of endocrinology (01.06.2002)
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Phenoxaphosphino-Modified Xantphos-Type Ligands in the Rhodium-Catalysed Hydroformylation of Internal and Terminal Alkenes
Bronger, Raymond P. J., Bermon, Jochem P., Herwig, Jürgen, Kamer, Paul C. J., van Leeuwen, Piet W. N. M.
Published in Advanced synthesis & catalysis (01.06.2004)
Published in Advanced synthesis & catalysis (01.06.2004)
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Argininosuccinate lyase deficiency (ASL) and carbohydrate-deficient transferrin (CDT): Experience with four independent CDT analysis methods — misleading results given by the %CDT TIA assay
Arndt, Torsten, Gressner, Axel, Herwig, Jürgen, Meier, Ursula, Sewell, Adrian C.
Published in Clinica chimica acta (01.11.2006)
Published in Clinica chimica acta (01.11.2006)
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