Authors:
Scheel, C
Schaefer, KL
Jauch, A
Keller, M
Wai, D
Brinkschmidt, C
van Valen, F
Boecker, W
Dockhorn-Dworniczak, B
Poremba, C
Citation: C. Scheel et al., Alternative lengthening of telomeres is associated with chromosomal instability in osteosarcomas, ONCOGENE, 20(29), 2001, pp. 3835-3844
Authors:
Granzow, M
Popp, S
Weber, S
Schoell, B
Holtgreve-Grez, H
Senf, L
Hager, D
Boschert, J
Scheurlen, W
Jauch, A
Citation: M. Granzow et al., Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics, CANC GENET, 130(1), 2001, pp. 79-83
Authors:
Sharma, P
Jarvis, A
Jauch, A
St Heaps, L
Shaw, P
Smith, A
Citation: P. Sharma et al., Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia, CANC GENET, 127(2), 2001, pp. 177-180
Authors:
Scholz, I
Popp, S
Granzow, M
Schoell, B
Holtgreve-Grez, H
Takeuchi, S
Schrappe, M
Harbott, J
Teigler-Schlegel, A
Zimmermann, M
Fischer, C
Koeffler, HP
Bartram, CR
Jauch, A
Citation: I. Scholz et al., Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis, CANC GENET, 124(2), 2001, pp. 89-97
Authors:
Tsukasaki, K
Krebs, J
Nagai, K
Tomonaga, M
Koeffler, HP
Bartram, CR
Jauch, A
Citation: K. Tsukasaki et al., Comparative genomic hybridization analysis in adult T-cell leukemia/lymphoma: correlation with clinical course, BLOOD, 97(12), 2001, pp. 3875-3881
Authors:
Brown, J
Horsley, SW
Jung, C
Saracoglu, K
Janssen, B
Brough, M
Daschner, M
Beedgen, B
Kerkhoffs, G
Eils, R
Harris, PC
Jauch, A
Kearney, L
Citation: J. Brown et al., Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay,M-TEL, EUR J HUM G, 8(12), 2000, pp. 903-910
Authors:
Sperandio, M
Weber, L
Jauch, A
Janssen, B
Mehls, O
Schaefer, F
Citation: M. Sperandio et al., Cutaneous white spots in a child with polycystic kidneys: a clue to TSC2/PKD1 gene mutation, NEPH DIAL T, 15(6), 2000, pp. 909-912
Authors:
Granzow, M
Popp, S
Keller, M
Holtgreve-Grez, H
Brough, M
Schoell, B
Rauterberg-Ruland, I
Hager, HD
Tariverdian, G
Jauch, A
Citation: M. Granzow et al., Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5) (q27;p15.3) in a family with three mentally retarded individuals, HUM GENET, 107(1), 2000, pp. 51-57
Authors:
Speleman, F
Callens, B
Logghe, K
Van Roy, N
Horsley, SW
Jauch, A
Verschraegen-Spae, MR
Leroy, JG
Citation: F. Speleman et al., Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35 -> qter: Molecular cytogenetic analysis and clinical phenotype intwo generations, AM J MED G, 93(5), 2000, pp. 349-354
Authors:
Oner, G
Jauch, A
Eggermann, T
Hardwick, R
Kirsch, S
Schiebel, K
Rappold, G
Robson, L
Smith, A
Citation: G. Oner et al., Mosaic rearrangement of chromosome 18: Characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin, AM J MED G, 92(2), 2000, pp. 101-106
Authors:
von Knobloch, R
Bugert, P
Jauch, A
Kalble, T
Kovacs, G
Citation: R. Von Knobloch et al., Allelic changes at multiple regions of chromosome 5 are associated with progression of urinary bladder cancer, J PATHOLOGY, 190(2), 2000, pp. 163-168
Authors:
Popp, S
Waltering, S
Holtgreve-Grez, H
Jauch, A
Proby, C
Leigh, IM
Boukamp, P
Citation: S. Popp et al., Genetic characterization of a human skin carcinoma progression model: fromprimary tumor to metastasis, J INVES DER, 115(6), 2000, pp. 1095-1103
Authors:
Klugbauer, S
Jauch, A
Lengfelder, E
Demidchik, E
Rabes, HM
Citation: S. Klugbauer et al., A novel type of RET rearrangement (PTC8) in childhood papillary thyroid carcinomas and characterization of the involved gene (RFG8), CANCER RES, 60(24), 2000, pp. 7028-7032
Authors:
Janssen, JWG
Vaandrager, JW
Heuser, T
Jauch, A
Kluin, PM
Geelen, E
Bergsagel, PL
Kuehl, WM
Drexler, HG
Otsuki, T
Bartram, CR
Schuuring, E
Citation: Jwg. Janssen et al., Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32), BLOOD, 95(8), 2000, pp. 2691-2698
Authors:
Williamson, C
Cavaco, BM
Jauch, A
Dixon, PH
Forbes, S
Harding, B
Holtgreve-Grez, H
Schoell, B
Pereira, MC
Font, AP
Loureiro, MM
Sobrinho, LG
Santos, MA
Thakker, RV
Citation: C. Williamson et al., Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999), J BONE MIN, 14(8), 1999, pp. 1472-1472
Citation: A. Jauch et al., Meta-analysis of six clinical phase III studies comparing lomefloxacin 0.3% eye drops twice daily to five standard antibiotics in patients with acutebacterial conjunctivitis, GR ARCH CL, 237(9), 1999, pp. 705-713