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Results:
1-19
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Results: 19
Authors:
Pusch, CM
Maurer, J
Ramser, J
Tomiuk, J
Achatz, H
Pesch, K
Lichtner, P
Apfelstedt-Sylla, E
Jacobi, FK
Berger, W
Meindl, A
Wissinger, B
Citation: Cm. Pusch et al., Complete form of X-linked congenital stationary night blindness: Refined mapping and evidence of genetic homogeneity, INT J MOL M, 7(2), 2001, pp. 155-161
Authors:
Brandau, O
Meindl, A
Fassler, R
Aszodi, A
Citation: O. Brandau et al., A novel gene, tendin, is strongly expressed in tendons and ligaments and shows high homology with chondromodulin-I, DEV DYNAM, 221(1), 2001, pp. 72-80
Authors:
Ladanyi, M
Lui, MY
Antonescu, CR
Krause-Boehm, A
Meindl, A
Argani, P
Healey, JH
Ueda, T
Yoshikawa, H
Meloni-Ehrig, A
Sorensen, PHB
Mertens, F
Mandahl, N
van den Berghe, H
Sciot, R
Dal Cin, P
Bridge, J
Citation: M. Ladanyi et al., The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25, ONCOGENE, 20(1), 2001, pp. 48-57
Authors:
Rudolph, G
Meindl, A
Bechmann, M
Schworm, HD
Achatz, H
Boergen, KP
Kampik, A
Berninger, T
Meitinger, T
Citation: G. Rudolph et al., X-linked ocular albinism (Nettleship-falls): a novel 29-bp deletion in exon 1. Carrier detection by ophthalmic examination and DNA analysis, GR ARCH CL, 239(3), 2001, pp. 167-172
Authors:
Atanassova, V
Meindl, A
Ring, C
Citation: V. Atanassova et al., Prevalence of Staphylococcus aureus and staphylococcal enterotoxins in rawpork and uncooked smoked ham - a comparison of classical culturing detection and RFLP-PCR, INT J F MIC, 68(1-2), 2001, pp. 105-113
Authors:
Matzdorff, A
Meindl, A
Pralle, H
Citation: A. Matzdorff et al., Wiskott-Aldrich syndrome in an adult, DEUT MED WO, 125(6), 2000, pp. 147-150
Authors:
Pusch, CM
Zeitz, C
Brandau, O
Pesch, K
Achatz, H
Feil, S
Scharfe, C
Maurer, J
Jacobi, FK
Pinckers, A
Andreasson, S
Hardcastle, A
Wissinger, B
Berger, W
Meindl, A
Citation: Cm. Pusch et al., The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein, NAT GENET, 26(3), 2000, pp. 324-327
Authors:
Vervoort, R
Lennon, A
Bird, AC
Tulloch, B
Axton, R
Miano, MG
Meindl, A
Meitinger, T
Ciccodicola, A
Wright, AF
Citation: R. Vervoort et al., Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa, NAT GENET, 25(4), 2000, pp. 462-466
Authors:
Zemni, R
Bienvenu, T
Vinet, MC
Sefiani, A
Carrie, A
Billuart, P
McDonell, N
Couvert, P
Francis, F
Chafey, P
Fauchereau, F
Friocourt, G
des Portes, V
Cardona, A
Frints, S
Meindl, A
Brandau, O
Ronce, N
Moraine, C
van Bokhoven, H
Ropers, HH
Sudbrak, R
Kahn, A
Fryns, JP
Beldjord, R
Chelly, J
Citation: R. Zemni et al., A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation, NAT GENET, 24(2), 2000, pp. 167-170
Authors:
Jacobi, FK
Broghammer, M
Pesch, K
Zrenner, E
Berger, W
Meindl, A
Pusch, CM
Citation: Fk. Jacobi et al., Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1, HUM GENET, 107(1), 2000, pp. 89-91
Authors:
Strahm, B
Rittweiler, K
Duffner, U
Brandau, O
Orlowska-Volk, M
Karajannis, MA
zur Stadt, U
Tiemann, M
Reiter, A
Brandis, M
Meindl, A
Niemeyer, CM
Citation: B. Strahm et al., Recurrent B-cell non-Hodgkin's lymphoma in two brothers with X-linked lymphoproliferative disease without evidence for Epstein-Barr virus infection, BR J HAEM, 108(2), 2000, pp. 377-382
Authors:
Derry, JMJ
Gormally, E
Means, GD
Zhao, W
Meindl, A
Kelley, RI
Boyd, Y
Herman, GE
Citation: Jmj. Derry et al., Mutations in a Delta(8)-Delta(7) sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata, NAT GENET, 22(3), 1999, pp. 286-290
Authors:
Brandau, O
Schuster, V
Weiss, M
Hellebrand, H
Fink, FM
Kreczy, A
Friedrich, W
Strahm, B
Niemeyer, C
Belohradsky, BH
Meindl, A
Citation: O. Brandau et al., Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP), HUM MOL GEN, 8(13), 1999, pp. 2407-2413
Low incidence of germline and somatic alterations in the E-cadherin gene in lobular breast carcinoma
Authors:
Schmutzler, RK
Derakhshandeh-Peykar, P
Freihoff, D
Brandau, O
Meindl, A
Citation: Rk. Schmutzler et al., Low incidence of germline and somatic alterations in the E-cadherin gene in lobular breast carcinoma, DIS MARKER, 15(1-3), 1999, pp. 123-123
Authors:
Backe, J
Hofferbert, S
Skawran, B
Dork, T
Stuhrmann, M
Karstens, JH
Untch, M
Meindl, A
Burgemeister, R
Chang-Claude, J
Weber, BHF
Citation: J. Backe et al., Frequency of BRCA1 mutation 5382insC in German breast cancer patients, GYNECOL ONC, 72(3), 1999, pp. 402-406
Authors:
Meindl, A
Osterrieder, N
Citation: A. Meindl et N. Osterrieder, The equine herpesvirus 1 U(S)2 homolog encodes a nonessential membrane-associated virion component, J VIROLOGY, 73(4), 1999, pp. 3430-3437
Authors:
Freihoff, D
Kempe, A
Beste, B
Wappenschmidt, B
Kreyer, E
Hayashi, Y
Meindl, A
Krebs, D
Wiestler, OD
von Deimling, A
Schmutzler, RK
Citation: D. Freihoff et al., Exclusion of a major role for the PTEN tumour-suppressor gene in breast carcinomas, BR J CANC, 79(5-6), 1999, pp. 754-758
Authors:
Neubauer, A
Meindl, A
Osterrieder, N
Citation: A. Neubauer et al., Mutations within the US2 and glycoprotein B genes of the equine herpesvirus 1 vaccine strain RacH do not account for its attenuation, BERL MUN TI, 112(9), 1999, pp. 351-354
Authors:
Klopstock, T
Chahrokh-Zadeh, S
Holinski-Feder, E
Meindl, A
Gasser, T
Pongratz, D
Muller-Felber, W
Citation: T. Klopstock et al., Markedly different course of Friedreich's ataxia in sib pairs with similarGAA repeat expansions in the frataxin gene, ACT NEUROP, 97(2), 1999, pp. 139-142
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1-19
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