AAAAAA

   
Results: 1-9 |
Results: 9

Authors: Zipp, F Windemuth, C Dichgans, J Wienker, T Martin, R Muller, C
Citation: F. Zipp et al., Peripheral blood cell bulk cultures are not suitable for the analysis of the genetic control of T-cell cytokine function, IMMUNOL LET, 78(1), 2001, pp. 21-27

Authors: Schmitt-Egenolf, M Windemuth, C Hennies, HC Albis-Camps, M von Engelhardt, B Wienker, T Reis, A Traupe, H Blasczyk, R
Citation: M. Schmitt-egenolf et al., Comparative association analysis reveals that corneodesmosin is more closely associated with psoriasis than HLA-Cw0602-B*5701 in German families, TISSUE ANTI, 57(5), 2001, pp. 440-446

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

Authors: Omran, H Haffner, K Volkel, A Kuehr, J Ketelsen, UP Ross, UH Konietzko, N Wienker, T Brandis, M Hildebrandt, F
Citation: H. Omran et al., Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene, AM J RESP C, 23(5), 2000, pp. 696-702

Authors: Zipp, F Windemuth, C Pankow, H Dichgans, J Wienker, T Martin, R Muller, C
Citation: F. Zipp et al., Multiple sclerosis associated amino acids of polymorphic regions relevant for the HLA antigen binding are confined to HLA-DR2, HUMAN IMMUN, 61(10), 2000, pp. 1021-1030

Authors: Hampe, J Wienker, T Nurnberg, P Schreiber, S
Citation: J. Hampe et al., Mapping genes for polygenic disorders: Considerations for study design in the complex trait of inflammatory bowel disease, HUMAN HERED, 50(2), 2000, pp. 91-101

Authors: Erdmann, J Riedel, K Rohde, K Folgmann, I Wienker, T Fleck, E Regitz-Zagrosek, V
Citation: J. Erdmann et al., Characterization of polymorphisms in the promoter of the human angiotensinII subtype 1 (AT1) receptor gene, ANN HUM GEN, 63, 1999, pp. 369-374

Authors: Wirth, B Herz, M Wetter, A Moskau, S Hahnen, E Rudnik-Schoneborn, S Wienker, T Zerres, K
Citation: B. Wirth et al., Quantitative analysis of survival motor neuron copies: Identification of subtle SMN1 mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implications for genetic counseling, AM J HU GEN, 64(5), 1999, pp. 1340-1356

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: 1-9 |