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Results: 1-25 | 26-29
Results: 1-25/29
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance
Authors: Pesch, UEA Leo-Kottler, B Mayor, S Jurklies, B Kellner, U Apfelstedt-Sylla, E Zrenner, E Alexander, C Wissinger, B
Citation: Uea. Pesch et al., OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance, HUM MOL GEN, 10(13), 2001, pp. 1359-1368
Expression of a glypican-related 62-kDa antigen is decreased in hepatocellular carcinoma in correspondence to the grade of tumor differentiation
Authors: Lage, H Kellner, U Tannapfel, A Dietel, M
Citation: H. Lage et al., Expression of a glypican-related 62-kDa antigen is decreased in hepatocellular carcinoma in correspondence to the grade of tumor differentiation, VIRCHOWS AR, 438(6), 2001, pp. 567-573
Vitrectomy in advanced Coats disease
Authors: Krause, L Kreusel, KM Jandeck, C Kellner, U Foerster, MH
Citation: L. Krause et al., Vitrectomy in advanced Coats disease, OPHTHALMOLO, 98(4), 2001, pp. 387-390
Clinical findings in autosomal recessive enhanced S-cone sensitivity syndrome
Authors: Jurklies, B Weismann, M Kellner, U Zrenner, E Bornfeld, N
Citation: B. Jurklies et al., Clinical findings in autosomal recessive enhanced S-cone sensitivity syndrome, OPHTHALMOLO, 98(3), 2001, pp. 285-293
Multifocal electroretinography (mfERG)
Authors: Seeliger, MW Jurklies, B Kellner, U Palmowski, A Bach, M Kretschmann, U
Citation: Mw. Seeliger et al., Multifocal electroretinography (mfERG), OPHTHALMOLO, 98(11), 2001, pp. 1112-1127
Cathepsin L antisense oligonucleotides in a human osteosarcoma cell line: Effects on the invasive phenotype
Authors: Krueger, S Kellner, U Buehling, F Roessner, A
Citation: S. Krueger et al., Cathepsin L antisense oligonucleotides in a human osteosarcoma cell line: Effects on the invasive phenotype, CANC GENE T, 8(7), 2001, pp. 522-528
CNGA3 mutations in hereditary cone photoreceptor disorders
Authors: Wissinger, B Gamer, D Jagle, H Giorda, R Marx, T Mayer, S Tippmann, S Broghammer, M Jurklies, B Rosenberg, T Jacobson, SG Sener, EC Tatlipinar, S Hoyng, CB Castellan, C Bitoun, P Andreasson, S Rudolph, G Kellner, U Lorenz, B Wolff, G Verellen-Dumoulin, C Schwartz, M Cremers, FPM Apfelstedt-ylla, E Zrenner, E Salati, R Sharpe, LT Kohl, S
Citation: B. Wissinger et al., CNGA3 mutations in hereditary cone photoreceptor disorders, AM J HU GEN, 69(4), 2001, pp. 722-737
Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene
Authors: den Hollander, AI Heckenlively, JR van den Born, LI de Kok, YJM van der Velde-Visser, SD Kellner, U Jurklies, B van Schooneveld, MJ Blankenagel, A Rohrschneider, K Wissinger, B Cruysberg, JRM Deutman, AF Brunner, HG Apfeldstedt-Sylla, E Hoyng, CB Cremers, FPM
Citation: Ai. Den Hollander et al., Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene, AM J HU GEN, 69(1), 2001, pp. 198-203
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
Authors: Alexander, C Votruba, M Pesch, UEA Thiselton, DL Mayer, S Moore, A Rodriguez, M Kellner, U Leo-Kottler, B Auburger, G Bhattacharya, SS Wissinger, B
Citation: C. Alexander et al., OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28, NAT GENET, 26(2), 2000, pp. 211-215
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration
Authors: Kramer, F White, K Pauleikhoff, D Gehrig, A Passmore, L Rivera, A Rudolph, G Kellner, U Andrassi, M Lorenz, B Rohrschneider, K Blankenagel, A Jurklies, B Schilling, H Schutt, F Holz, FG Weber, BHF
Citation: F. Kramer et al., Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration, EUR J HUM G, 8(4), 2000, pp. 286-292
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21
Authors: Kohl, S Baumann, B Broghammer, M Jagle, H Sieving, P Kellner, U Spegal, R Anastasi, M Zrenner, E Sharpe, LT Wissinger, B
Citation: S. Kohl et al., Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21, HUM MOL GEN, 9(14), 2000, pp. 2107-2116
Electrophysiological diagnosis in ophthalmology
Authors: Bach, M Kellner, U
Citation: M. Bach et U. Kellner, Electrophysiological diagnosis in ophthalmology, OPHTHALMOLO, 97(12), 2000, pp. 898-920
Ocular changes in prenatures
Authors: Jandeck, C Kellner, U Foerster, MH
Citation: C. Jandeck et al., Ocular changes in prenatures, OPHTHALMOLO, 97(11), 2000, pp. 799-818
Open globe injuries in children
Authors: Jandeck, C Kellner, U Bornfeld, N Foerster, MH
Citation: C. Jandeck et al., Open globe injuries in children, GR ARCH CL, 238(5), 2000, pp. 420-426
Multifocal ERG in chloroquine retinopathy: regional variance of retinal dysfunction
Authors: Kellner, U Kraus, H Foerster, MH
Citation: U. Kellner et al., Multifocal ERG in chloroquine retinopathy: regional variance of retinal dysfunction, GR ARCH CL, 238(1), 2000, pp. 94-97
Human DNA-topoisomerases - Diagnostic and therapeutic implications for cancer
Authors: Kellner, U Rudolph, P Parwaresch, R
Citation: U. Kellner et al., Human DNA-topoisomerases - Diagnostic and therapeutic implications for cancer, ONKOLOGIE, 23(5), 2000, pp. 424-430
Detection of four new single-stranded telomeric DNA binding proteins by means of an optimized protein blotting procedure
Authors: Kellner, U Haenssle, HA Rudolph, P Parwaresch, R
Citation: U. Kellner et al., Detection of four new single-stranded telomeric DNA binding proteins by means of an optimized protein blotting procedure, PATH RES PR, 196(12), 2000, pp. 801-806
High topoisomerase II alpha expression associates with high proliferation rate and and poor prognosis in oligodendrogliomas
Authors: Miettinen, HE Jarvinen, TAH Kellner, U Kauraniemi, P Parwaresch, R Rantala, I Kalimo, H Paljarvi, L Isola, J Haapasalo, H
Citation: He. Miettinen et al., High topoisomerase II alpha expression associates with high proliferation rate and and poor prognosis in oligodendrogliomas, NEUROP AP N, 26(6), 2000, pp. 504-512
Expression of DNA topoisomerases in chronic proliferative kidney disease
Authors: Ivanova, LV Rudolph, P Kellner, U Jurgensen, A Tareeva, IE Alm, P Proppe, D
Citation: Lv. Ivanova et al., Expression of DNA topoisomerases in chronic proliferative kidney disease, KIDNEY INT, 58(4), 2000, pp. 1603-1612
Vasoproliferative tumours of the retina
Authors: Heimann, H Bornfeld, N Vij, O Coupland, SE Bechrakis, NE Kellner, U Foerster, MH
Citation: H. Heimann et al., Vasoproliferative tumours of the retina, BR J OPHTH, 84(10), 2000, pp. 1162-1169
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
Authors: den Hollander, AI ten Brink, JB de Kok, YJM van Soest, S van den Born, LI van Driel, MA van de Pol, DJR Payne, AM Bhattacharya, SS Kellner, U Hoyng, CB Westerveld, A Brunner, HG Bleeker-Wagemakers, EM Deutman, AF Heckenlively, JR Cremers, FPM Bergen, AAB
Citation: Ai. Den Hollander et al., Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12), NAT GENET, 23(2), 1999, pp. 217-221
Ophthalmologic screening in preterm infants
Authors: Clemens, S Eckardt, C Gerding, H Grote, A Jandeck, C Kellner, U Lorenz, B Petersen, J Seiberth, V Stark, N Ulbig, MW Zubcov, A Jorch, G Pohlandt, F
Citation: S. Clemens et al., Ophthalmologic screening in preterm infants, OPHTHALMOLO, 96(4), 1999, pp. 257-263
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls
Authors: Thieme, H Wissinger, B Jandeck, C Christ-Adler, M Kraus, H Kellner, U Foerster, MH
Citation: H. Thieme et al., A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girls, GR ARCH CL, 237(9), 1999, pp. 714-719
Mapping and genomic characterization of the gene encoding diacylglycerol kinase gamma (DAGK3): assessment of its role in dominant optic atrophy (OPA1)
Authors: Stohr, H Klein, J Gehrig, A Koehler, MR Jurklies, B Kellner, U Leo-Kottler, B Schmid, M Weber, BHF
Citation: H. Stohr et al., Mapping and genomic characterization of the gene encoding diacylglycerol kinase gamma (DAGK3): assessment of its role in dominant optic atrophy (OPA1), HUM GENET, 104(1), 1999, pp. 99-105
Opthalmological screening-examination of newborns
Authors: Clemens, S Eckardt, C Gerding, H Grote, A Jandeck, C Kellner, U Lorenz, B Seiberth, V Stark, N Ulbig, MW Zubcov, A Jorch, G Pohlandt, F
Citation: S. Clemens et al., Opthalmological screening-examination of newborns, MONATS KIND, 147(9), 1999, pp. 848-854
Risultati: 1-25 | 26-29