Genetic basis for increased intestinal permeability in families with Crohn’s disease: role of CARD15 3020insC mutation?
Buhner, S, Buning, C, Genschel, J, Kling, K, Herrmann, D, Dignass, A, Kuechler, I, Krueger, S, Schmidt, H H-J, Lochs, H
Published in Gut (01.03.2006)
Published in Gut (01.03.2006)
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Journal Article
Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease
Gromadzka, G., Schmidt, H.H.-J., Genschel, J., Bochow, B., Rodo, M., Tarnacka, B., Litwin, T., Chabik, G., Członkowska, A.
Published in Clinical genetics (01.12.2005)
Published in Clinical genetics (01.12.2005)
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Journal Article
Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation
Büning, C., Genschel, J., Bühner, S., Krüger, S., Kling, K., Dignass, A., Baier, P., Bochow, B., Ockenga, J., Schmidt, H. H.‐J., Lochs, H.
Published in Alimentary pharmacology & therapeutics (15.05.2004)
Published in Alimentary pharmacology & therapeutics (15.05.2004)
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Journal Article
In Vitro and in Vivo Function of the C-Terminus of Escherichia Coli Single-Stranded DNA Binding Protein
Curth, Ute, Genschel, Jochen, Urbanke, Claus, Greipel, Joachim
Published in Nucleic acids research (15.07.1996)
Published in Nucleic acids research (15.07.1996)
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Journal Article
Wilson Disease: High Prevalence in a Mountaineous Area of Crete
Dedoussis, G. V. Z., Genschel, J., Sialvera, T‐E., Bochow, B., Manolaki, N., Manios, Y., Tsafantakis, E., Schmidt, H.
Published in Annals of human genetics (01.05.2005)
Published in Annals of human genetics (01.05.2005)
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Journal Article
The C/C_₁₃₉₁₀ and G/G_₂₂₀₁₈ Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel Disease
Büning, C, Ockenga, J, Krüger, S, Jurga, J, Baier, P, Dignass, A, Vogel, A, Strassburg, C, Weltrich, R, Genschel, J, Lochs, H, Schmidt, H
Published in Scandinavian journal of gastroenterology (2003)
Published in Scandinavian journal of gastroenterology (2003)
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Journal Article
A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy
Genschel, Janine, Bochow, Bettina, Kuepferling, Susanne, Ewert, Ralf, Hetzer, Roland, Lochs, Herbert, Schmidt, Hartmut H-J.
Published in Human mutation (01.02.2001)
Published in Human mutation (01.02.2001)
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Journal Article
Keratin 8 Y54H and G62C mutations are not associated with inflammatory bowel disease
Büning, C., Halangk, J., Dignass, A., Ockenga, J., Deindl, P., Nickel, R., Genschel, J., Landt, O., Lochs, H., Schmidt, H., Witt, H.
Published in Digestive and liver disease (01.06.2004)
Published in Digestive and liver disease (01.06.2004)
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Journal Article
A new LMNA mutation causing limb girdle muscular dystrophy 1B
Spuler, Simone, Geier, Christian, Osterziel, Karl Josef, Gutberlet, Matthias, Genschel, Janine, Lehmann, Thomas-Nicolas, Zinn-Justin, Sophie, Gilquin, Bernard, Schmidt, Hartmut
Published in Journal of neurology (01.05.2005)
Published in Journal of neurology (01.05.2005)
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Journal Article
A sensitive noninvasive method for monitoring successful liver-directed gene transfer of the low-density lipoprotein receptor in Watanabe hyperlipidemic rabbits in vivo
TIETGE, U. J. F, CICHON, G, LOCHS, H, BURCHERT, W, SCHMIDT, Hh-J, BÜTTNER, C, GENSCHEL, J, HEEREN, J, GIELOW, P, GREWE, N, DOGAR, M, BEISIEGEL, U, MANNS, M. P
Published in Gene therapy (01.04.2004)
Published in Gene therapy (01.04.2004)
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Journal Article
A new frameshift mutation at codon 466 (1397delA) within the LMNA gene
Genschel, Janine, Baier, Peter, Kuepferling, Susanne, Proepsting, Marcus J., Buettner, Carsten, Ewert, Ralf, Hetzer, Roland, Lochs, Herbert, Schmidt, Hartmut H.-J.
Published in Human mutation (01.09.2000)
Published in Human mutation (01.09.2000)
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Journal Article
Three novel mutations (P760L, L1305P, Q1351Stop) causing Wilson disease
Genschel, Janine, Czlonkowska, Anna, Sommer, Grit, Buettner, Carsten, Bochow, Bettina, Lochs, Herbert, Schmidt, Hartmut H-J.
Published in Human mutation (01.02.2001)
Published in Human mutation (01.02.2001)
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Journal Article