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Results: 1-14 |
Results: 14
Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes
Authors: Immervoll, T Loesgen, S Dutsch, G Gohlke, H Herbon, N Klugbauer, S Dempfle, A Bickeboller, H Becker-Follmann, J Ruschendorf, F Saar, K Reis, A Wichmann, HE Wjst, M
Citation: T. Immervoll et al., Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes, HUM MUTAT, 18(4), 2001, pp. 327-336
Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region
Authors: Fuchshuber, A Kroiss, S Karle, S Berthold, S Huck, K Burton, C Rahman, N Koptides, M Deltas, C Otto, E Ruschendorf, F Feest, T Hildebrandt, F
Citation: A. Fuchshuber et al., Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region, GENOMICS, 72(3), 2001, pp. 278-284
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma
Authors: Niemann, S Becker-Follmann, J Nurnberg, G Ruschendorf, F Sieweke, N Hugens-Penzel, M Traupe, H Wienker, TF Reis, A Muller, U
Citation: S. Niemann et al., Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma, AM J MED G, 98(1), 2001, pp. 32-36
A major susceptibility locus for atopic dermatitis maps to chromosome 3q21
Authors: Lee, YA Wahn, U Kehrt, R Tarani, L Businco, L Gustafsson, D Andersson, F Oranje, AP Wolkertstorfer, A von Berg, A Hoffmann, U Kuster, W Wienker, T Ruschendorf, F Reis, A
Citation: Ya. Lee et al., A major susceptibility locus for atopic dermatitis maps to chromosome 3q21, NAT GENET, 26(4), 2000, pp. 470-473
Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease
Authors: Kroiss, S Huck, K Berthold, S Ruschendorf, F Scolari, F Caridi, G Ghiggeri, GM Hildebrant, F Fuchshuber, A
Citation: S. Kroiss et al., Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease, NEPH DIAL T, 15(6), 2000, pp. 818-821
Genetics of atopy in a mouse model: polymorphism of the IL-5 receptor alpha chain
Authors: Daser, A Koetz, K Batjer, N Jung, M Ruschendorf, F Goltz, M Ellerbrok, H Renz, H Walter, J Paulsen, M
Citation: A. Daser et al., Genetics of atopy in a mouse model: polymorphism of the IL-5 receptor alpha chain, IMMUNOGENET, 51(8-9), 2000, pp. 632-638
A European study on the genetics of mite sensitization
Authors: Kurz, T Strauch, K Heinzmann, A Braun, S Jung, M Ruschendorf, F Moffatt, MF Cookson, WOCM Inacio, F Ruffilli, A Nordskov-Hansen, G Peltre, G Forster, J Kuehr, J Reis, A Wienker, TF Deichmann, KA
Citation: T. Kurz et al., A European study on the genetics of mite sensitization, J ALLERG CL, 106(5), 2000, pp. 925-932
Splitting schizophrenia: Periodic catatonia-susceptibility locus on chromosome 15q15
Authors: Stober, G Saar, K Ruschendorf, F Meyer, J Nurnberg, G Jatzke, S Franzek, E Reis, A Lesch, KP Wienker, TF Beckmann, H
Citation: G. Stober et al., Splitting schizophrenia: Periodic catatonia-susceptibility locus on chromosome 15q15, AM J HU GEN, 67(5), 2000, pp. 1201-1207
Genomewide scan in German families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13
Authors: Lee, YA Ruschendorf, F Windemuth, C Schmitt-Egenolf, M Stadelmann, A Nurnberg, G Stander, M Wienker, TF Reis, A Traupe, H
Citation: Ya. Lee et al., Genomewide scan in German families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13, AM J HU GEN, 67(4), 2000, pp. 1020-1024
Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree
Authors: Omran, H Fernandez, C Jung, M Haffner, K Fargier, B Villaquiran, A Waldherr, R Gretz, N Brandis, M Ruschendorf, F Reis, A Hildebrandt, F
Citation: H. Omran et al., Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree, AM J HU GEN, 66(1), 2000, pp. 118-127
Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium test
Authors: Jacob, N Ruschendorf, F Schmitt-Egenolf, M Hennies, HC Friedl, G Stander, M Wienker, TF Reis, A Traupe, H
Citation: N. Jacob et al., Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium test, J INVES DER, 112(4), 1999, pp. 514-515
Genetic dissection of X-linked interspecific hybrid placental dysplasia incongenic mouse strains
Authors: Hemberger, MC Pearsall, RS Zechner, U Orth, A Otto, S Ruschendorf, F Fundele, R Elliott, R
Citation: Mc. Hemberger et al., Genetic dissection of X-linked interspecific hybrid placental dysplasia incongenic mouse strains, GENETICS, 153(1), 1999, pp. 383-390
Limb mammary syndrome: A new genetic disorder with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies maps to human chromosome 3q27
Authors: van Bokhoven, H Jung, M Smits, APT van Beersum, S Ruschendorf, F van Steensel, M Veenstra, M Tuerlings, JHAM Mariman, ECM Brunner, HG Wienker, TF Reis, A Ropers, HH Hamel, BCJ
Citation: H. Van Bokhoven et al., Limb mammary syndrome: A new genetic disorder with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies maps to human chromosome 3q27, AM J HU GEN, 64(2), 1999, pp. 538-546
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster
Authors: Vollmer, M Jung, M Ruschendorf, F Ruf, R Wienker, T Reis, A Krapf, R Hildebrandt, F
Citation: M. Vollmer et al., The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster, AM J HU GEN, 63(6), 1998, pp. 1724-1731
Risultati: 1-14 |