Authors:
Betz, RC
Schoser, BGH
Kasper, D
Ricker, K
Ramirez, A
Stein, V
Torbergsen, T
Lee, YA
Nothen, MM
Wienker, TF
Malin, JP
Propping, P
Reis, A
Mortier, W
Jentsch, TJ
Vorgerd, M
Kubisch, C
Citation: Rc. Betz et al., Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle inrippling muscle disease, NAT GENET, 28(3), 2001, pp. 218-219
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
Authors:
Vafiadaki, E
Reis, A
Keers, S
Harrison, R
Anderson, LVB
Raffelsberger, T
Ivanova, S
Hoger, H
Bittner, RE
Bushby, K
Bashir, R
Citation: E. Vafiadaki et al., Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation, NEUROREPORT, 12(3), 2001, pp. 625-629
Authors:
Niero, R
Moser, R
Busato, ACB
Yunes, RA
Reis, A
Cechinel, V
Citation: R. Niero et al., A comparative chemical study of Maytenus ilicifolia Mart. Reiss and Maytenus robusta Reiss (Celastraceae), Z NATURFO C, 56(1-2), 2001, pp. 158-161
Authors:
Pickard, B
Dean, W
Engemann, S
Bergmann, K
Fuermann, M
Jung, M
Reis, A
Allen, N
Reik, W
Walter, J
Citation: B. Pickard et al., Epigenetic targeting in the mouse zygote marks DNA for later methylation: a mechanism for maternal effects in development, MECH DEVEL, 103(1-2), 2001, pp. 35-47
Authors:
Appel, S
Reichwald, K
Zimmermann, WG
Reis, A
Rosenthal, A
Hennies, HC
Citation: S. Appel et al., Identification and localization of a new human myotubularin-related protein gene, MTMR8, on 8p22-p23, GENOMICS, 75(1-3), 2001, pp. 6-8
Authors:
Reinhard, T
Reis, A
Bohringer, D
Malinowski, M
Voiculescu, A
Heering, P
Godehardt, E
Sundmacher, R
Citation: T. Reinhard et al., Systemic mycophenolate mofetil in comparison with systemic cyclosporin A in high-risk keratoplasty patients: 3 years' results of a randomized prospective clinical trial, GR ARCH CL, 239(5), 2001, pp. 367-372
Authors:
Rauch, A
Schellmoser, S
Kraus, C
Dorr, HG
Trautmann, U
Altherr, MR
Pfeiffer, RA
Reis, A
Citation: A. Rauch et al., First known microdeletion within the Wolf-Hirschhorn-syndrome critical region refines genotype-phenotype correlation, AM J MED G, 99(4), 2001, pp. 338-342
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
Authors:
Graw, J
Loster, J
Soewarto, D
Fuchs, H
Meyer, B
Reis, A
Wolf, E
Balling, R
de Angelis, MH
Citation: J. Graw et al., Characterization of a new, dominant V124E mutation in the mouse alpha A-crystallin-encoding gene, INV OPHTH V, 42(12), 2001, pp. 2909-2915
Citation: Km. Petersson et al., Cognitive processing in literate and illiterate subjects: A review of somerecent behavioral and functional neuroimaging data, SC J PSYCHO, 42(3), 2001, pp. 251-267
Authors:
Mafra, I
Lanza, B
Reis, A
Marsilio, V
Campestre, C
De Angelis, M
Coimbra, MA
Citation: I. Mafra et al., Effect of ripening on texture, microstructure and cell wall polysaccharidecomposition of olive fruit (Olea europaea), PHYSL PLANT, 111(4), 2001, pp. 439-447
Authors:
Reis, A
Reinhard, T
Voiculescu, A
Mayer, K
Sundmacher, R
Citation: A. Reis et al., Highly active antiviral and immunosuppressive therapy following keratoplasty in patients with herpetic eye disease, KLIN MONATS, 218(3), 2001, pp. 183-186
Authors:
Mayer, K
Reinhard, T
Reis, A
Bohringer, D
Sundmacher, R
Citation: K. Mayer et al., FK 506 ointment 0.1% - A new therapeutic option for atopic blepharitis. Clinical trial with 14 patients, KLIN MONATS, 218(11), 2001, pp. 733-736
Authors:
Bayoumi, R
Saar, K
Lee, YA
Nurnberg, G
Reis, A
Nur-E-Kamal, M
Al-Gazali, LI
Citation: R. Bayoumi et al., Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26, J MED GENET, 38(6), 2001, pp. 369-373
Authors:
Vanita,"Sarhadi, V
Reis, A
Jung, M
Singh, D
Sperling, K
Singh, JR
Burger, J
Citation: V. Vanita,"sarhadi et al., A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its pseudogene, J MED GENET, 38(6), 2001, pp. 392-396