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Kreutz N. Hübner M.R. James M.T. Bihoreau D. Gauguier G.M. Lathrop D. Ganten K. Lindpaintner January 01, 1995 / Hypertension Altered angiotensinogen amino acid sequence and plasma angiotensin II levels in genetically hypertensive rats: a study on cause and effects N. Huebner R. Kreutz S. Takahashi D. Ganten K. Lindpaintner January 01, 1995 / Mamm Genome The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4 N. Hübner R. Kreutz S. Rubattu Y.A. Lee D. Ganten P.D. Allen K. Lindpaintner November 01, 1995 / Circulation Genetic linkage of the ACE gene to plasma angiotensin-converting enzyme activity but not to blood pressure: a quantitative trait locus confers identical complex phenotypes in human and rat hypertension R. Kreutz N. Hübner D. Ganten K. Lindpaintner January 01, 1995 / Herz Genetics in arterial hypertension - clinical and experimental aspects N. Hübner D. Ganten January 01, 1995 Genetische Analyse des Bluthochdrucks Y.A. Lee N. Hübner D. Ganten January 05, 2007 / Am J Med Genet B Neuropsychiatr Genet Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy S. Lorenz A. Heils J.M. Kasper T. Sander January 01, 2007 / Bioinformatics Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE J. Dietter M. Mattheisen R. Fuerst F. Rueschendorf T.F. Wienker K. Strauch March 01, 2007 / Hum Genet Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci H. Najmabadi M.M. Motazacker M. Garshasbi K. Kahrizi A. Tzschach W. Chen F. Behjati V. Hadavi S.E. Nieh S.S. Abedini R. Vazifehmand S.G. Firouzabadi P. Jamali M. Falah S.M. Seifati A. Grueters S. Lenzner L.R. Jensen F. Rueschendorf A.W. Kuss H.H. Ropers April 01, 2007 / Epilepsy Res Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy A. Hempelmann J. Cobilanschi A. Heils H. Muhle U. Stephani Y. Weber H. Lerche T. Sander Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
September 12, 1995 / Proc Natl Acad Sci U S A Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10 R. Kreutz N. Hübner M.R. James M.T. Bihoreau D. Gauguier G.M. Lathrop D. Ganten K. Lindpaintner
January 01, 1995 / Hypertension Altered angiotensinogen amino acid sequence and plasma angiotensin II levels in genetically hypertensive rats: a study on cause and effects N. Huebner R. Kreutz S. Takahashi D. Ganten K. Lindpaintner
January 01, 1995 / Mamm Genome The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4 N. Hübner R. Kreutz S. Rubattu Y.A. Lee D. Ganten P.D. Allen K. Lindpaintner
November 01, 1995 / Circulation Genetic linkage of the ACE gene to plasma angiotensin-converting enzyme activity but not to blood pressure: a quantitative trait locus confers identical complex phenotypes in human and rat hypertension R. Kreutz N. Hübner D. Ganten K. Lindpaintner
January 01, 1995 / Herz Genetics in arterial hypertension - clinical and experimental aspects N. Hübner D. Ganten
January 05, 2007 / Am J Med Genet B Neuropsychiatr Genet Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy S. Lorenz A. Heils J.M. Kasper T. Sander
January 01, 2007 / Bioinformatics Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE J. Dietter M. Mattheisen R. Fuerst F. Rueschendorf T.F. Wienker K. Strauch
March 01, 2007 / Hum Genet Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci H. Najmabadi M.M. Motazacker M. Garshasbi K. Kahrizi A. Tzschach W. Chen F. Behjati V. Hadavi S.E. Nieh S.S. Abedini R. Vazifehmand S.G. Firouzabadi P. Jamali M. Falah S.M. Seifati A. Grueters S. Lenzner L.R. Jensen F. Rueschendorf A.W. Kuss H.H. Ropers
April 01, 2007 / Epilepsy Res Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy A. Hempelmann J. Cobilanschi A. Heils H. Muhle U. Stephani Y. Weber H. Lerche T. Sander