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Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali 01. Januar 2001 / J Physiol Selective activation of nociceptors by P2X receptor agonists in normal and inflamed rat skin S.G. Hamilton S.B. McMahon G.R. Lewin 20. Dezember 2001 / Neuron The DRASIC cation channel contributes to the detection of cutaneous touch and acid stimuli in mice M.P. Price S.L. McIlwrath J.H. Xie C. Cheng J. Qiao D.E. Tarr K.A. Sluka T.J. Brennan G.R. Lewin M.J. Welsh 01. Mai 2001 / J Neurosci Lack of neurotrophin-4 causes selective structural and chemical deficits in sympathetic ganglia and their preganglionic innervation A. Roosen A. Schober J. Strelau M. Boettner J. Faulhaber G. Bendner S.L. McIlwrath H. Seller H. Ehmke G.R. Lewin K. Unsicker 03. Juli 2001 / Proc Natl Acad Sci U S A BDNF but not NT-4 is required for normal flexion reflex plasticity and function P.A. Heppenstall G.R. Lewin 09. Juli 2009 / Physiol Genomics Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1 H. Vogel M. Nestler F. Rueschendorf M.D. Block S. Tischer R. Kluge A. Schurmann H.G. Joost S. Scherneck 23. November 2001 / Circ Res The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system M.L. Bang T. Centner F. Fornoff A.J. Geach M. Gotthardt M. McNabb C.C. Witt D. Labeit C.C. Gregorio H. Granzier S. Labeit 23. Januar 2009 / PLoS Genet A systematic approach to mapping recessive disease genes in individuals from outbred populations F. Hildebrandt S.F. Heeringa F. Rueschendorf M. Attanasio G. Nuernberg C. Becker D. Seelow N. Huebner G. Chernin C.N. Vlangos W. Zhou J.F. O'Toole B.E. Hoskins M.T. Wolf B.G. Hinkes H. Chaib S. Ashraf S.J. Allen V. Vega-Warner E. Wise H.M. Harville R.H. Lyons J. Washburn J. Macdonald P. Nuernberg E.A. Otto 01. Mai 2009 / Pediatr Allergy Immunol ICOS-gene variants are not associated with atopic disease susceptibility in European children K.C. Beier S. Humberdros H. Witt S. Illi F. Rueschendorf R. Nickel Y.A. Lee S. Lau U. Wahn E. Hamelmann 01. September 2009 / Pediatr Allergy Immunol IL13 variants are associated with total serum IgE and early sensitization to food allergens in children with atopic dermatitis S.E. Zitnik F. Rueschendorf S. Mueller C. Sengler Y.A. Lee R.W. Griffioen P. Meglio U. Wahn H. Witt R. Nickel Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali
01. Januar 2001 / J Physiol Selective activation of nociceptors by P2X receptor agonists in normal and inflamed rat skin S.G. Hamilton S.B. McMahon G.R. Lewin
20. Dezember 2001 / Neuron The DRASIC cation channel contributes to the detection of cutaneous touch and acid stimuli in mice M.P. Price S.L. McIlwrath J.H. Xie C. Cheng J. Qiao D.E. Tarr K.A. Sluka T.J. Brennan G.R. Lewin M.J. Welsh
01. Mai 2001 / J Neurosci Lack of neurotrophin-4 causes selective structural and chemical deficits in sympathetic ganglia and their preganglionic innervation A. Roosen A. Schober J. Strelau M. Boettner J. Faulhaber G. Bendner S.L. McIlwrath H. Seller H. Ehmke G.R. Lewin K. Unsicker
03. Juli 2001 / Proc Natl Acad Sci U S A BDNF but not NT-4 is required for normal flexion reflex plasticity and function P.A. Heppenstall G.R. Lewin
09. Juli 2009 / Physiol Genomics Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1 H. Vogel M. Nestler F. Rueschendorf M.D. Block S. Tischer R. Kluge A. Schurmann H.G. Joost S. Scherneck
23. November 2001 / Circ Res The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system M.L. Bang T. Centner F. Fornoff A.J. Geach M. Gotthardt M. McNabb C.C. Witt D. Labeit C.C. Gregorio H. Granzier S. Labeit
23. Januar 2009 / PLoS Genet A systematic approach to mapping recessive disease genes in individuals from outbred populations F. Hildebrandt S.F. Heeringa F. Rueschendorf M. Attanasio G. Nuernberg C. Becker D. Seelow N. Huebner G. Chernin C.N. Vlangos W. Zhou J.F. O'Toole B.E. Hoskins M.T. Wolf B.G. Hinkes H. Chaib S. Ashraf S.J. Allen V. Vega-Warner E. Wise H.M. Harville R.H. Lyons J. Washburn J. Macdonald P. Nuernberg E.A. Otto
01. Mai 2009 / Pediatr Allergy Immunol ICOS-gene variants are not associated with atopic disease susceptibility in European children K.C. Beier S. Humberdros H. Witt S. Illi F. Rueschendorf R. Nickel Y.A. Lee S. Lau U. Wahn E. Hamelmann
01. September 2009 / Pediatr Allergy Immunol IL13 variants are associated with total serum IgE and early sensitization to food allergens in children with atopic dermatitis S.E. Zitnik F. Rueschendorf S. Mueller C. Sengler Y.A. Lee R.W. Griffioen P. Meglio U. Wahn H. Witt R. Nickel