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Results: 1-25/33
Authors:
Voet, T
Vermeesch, J
Carens, A
Durr, J
Labaere, C
Duhamel, H
David, G
Marynen, P
Citation: T. Voet et al., Efficient male and female germline transmission of a human chromosomal vector in mice, GENOME RES, 11(1), 2001, pp. 124-136
Authors:
Van Limbergen, H
Beverloo, HB
van Drunen, E
Janssens, A
Hahlen, K
Poppe, B
Van Roy, N
Marynen, P
De Paepe, A
Slater, R
Speleman, F
Citation: H. Van Limbergen et al., Molecular cytogenetic and clinical findings in ETV6/ABL1-positive leukemia, GENE CHROM, 30(3), 2001, pp. 274-282
Authors:
Lopez-Correa, C
Dorschner, M
Brems, H
Lazaro, C
Clementi, M
Upadhyaya, M
Dooijes, D
Moog, U
Kehrer-Sawatzki, H
Rutkowski, JL
Fryns, JP
Marynen, P
Stephens, K
Legius, E
Citation: C. Lopez-correa et al., Recombination hotspot in NF1 microdeletion patients, HUM MOL GEN, 10(13), 2001, pp. 1387-1392
Authors:
Jun, L
Frints, S
Duhamel, H
Herold, A
Abad-Rodrigues, J
Dotti, C
Izaurralde, E
Marynen, P
Froyen, G
Citation: L. Jun et al., NXF5, a novel member of the nuclear RNA export factor family, is lost in amale patient with a syndromic form of mental retardation, CURR BIOL, 11(18), 2001, pp. 1381-1391
Authors:
Veugelers, M
De Cat, B
Delande, N
Esselens, C
Bonk, I
Vermeesch, J
Marynen, P
Fryns, JP
David, G
Citation: M. Veugelers et al., A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 genecluster on chromosome 13q32, MATRIX BIOL, 20(5-6), 2001, pp. 375-385
Authors:
Cools, J
Mentens, N
Marynen, P
Citation: J. Cools et al., A new family of small, palmitoylated, membrane-associated proteins, characterized by the presence of a cysteine-rich hydrophobic motif, FEBS LETTER, 492(3), 2001, pp. 204-209
Authors:
Frints, SGM
Fryns, JP
Lagae, L
Syrrou, M
Marynen, P
Devriendt, K
Citation: Sgm. Frints et al., Xp22.3;Yq11.2 chromosome translocation and its clinical manifestations, ANN GENET, 44(2), 2001, pp. 71-76
Authors:
Maes, B
Vanhentenrijk, V
Wlodarska, I
Cools, J
Peeters, B
Marynen, P
De Wolf-Peeters, C
Citation: B. Maes et al., The NPM-ALK and the ATIC-ALK fusion genes can be detected in non-neoplastic cells, AM J PATH, 158(6), 2001, pp. 2185-2193
Authors:
Baens, M
Steyls, A
Dierlamm, J
De Wolf-Peeters, C
Marynen, P
Citation: M. Baens et al., Structure of the MLT gene and molecular characterization of the genomic breakpoint junctions in the t(11;18)(q21;q21) of marginal zone B-cell lymphomas of MALT type, GENE CHROM, 29(4), 2000, pp. 281-291
Authors:
Maes, B
Baens, M
Marynen, P
De Wolf-Peeters, C
Citation: B. Maes et al., The product of the t(11;18), an API2-MLT fusion, is an almost exclusive finding in marginal zone cell lymphoma of extranodal MALT-type, ANN ONCOL, 11(5), 2000, pp. 521-526
Authors:
van de Loosdrecht, AA
Kok, K
de Vries, B
van der Veen, AY
van den Berg, E
Esselink, MT
Marynen, P
Vellenga, E
van Imhoff, GW
Citation: Aa. Van De Loosdrecht et al., Breakpoint analysis by fluorescence in situ hybridization in myelodysplastic syndromes with t(3;12)(q26;p13) and expression of EVI1, LEUKEMIA, 14(10), 2000, pp. 1857-1858
Authors:
Hernandez, JM
Gonzalez, MB
Garcia, JL
Ferro, MT
Gutierrez, NC
Marynen, P
San Miguel, JF
Citation: Jm. Hernandez et al., Two cases of myeloid disorders and a t(8;12)(q12;p13), HAEMATOLOG, 85(1), 2000, pp. 31-34
Authors:
Falzetti, D
Vermeesch, JR
Matteucci, C
Ciolli, S
Martelli, MF
Marynen, P
Mecucci, C
Citation: D. Falzetti et al., Microdissection and FISH investigations in acute myeloid leukemia: A step forward to full identification of complex karyotypic changes, CANC GENET, 118(1), 2000, pp. 28-34
Genomic imbalances including amplification of the tyrosine kinase gene JAK2 in CD30(+) Hodgkin cells
Authors:
Joos, S
Kupper, M
Ohl, S
von Bonin, F
Mechtersheimer, G
Bentz, M
Marynen, P
Moller, P
Pfreundschuh, M
Trumper, L
Lichter, P
Citation: S. Joos et al., Genomic imbalances including amplification of the tyrosine kinase gene JAK2 in CD30(+) Hodgkin cells, CANCER RES, 60(3), 2000, pp. 549-552
Authors:
Dierlamm, J
Baens, M
Stefanova-Ouzounova, M
Hinz, K
Wlodarska, I
Maes, B
Steyls, A
Driessen, A
Verhoef, G
Gaulard, P
Hagemeijer, A
Hossfeld, DK
De Wof-Peeters, C
Marynen, P
Citation: J. Dierlamm et al., Detection of t(11;18)(q21;q21) by interphase fluorescence in situ hybridization using API2 and MLT specific probes, BLOOD, 96(6), 2000, pp. 2215-2218
Authors:
Ma, ZG
Cools, J
Marynen, P
Cui, XL
Siebert, R
Gesk, S
Schlegelberger, B
Peeters, B
De Wolf-Peeters, C
Wlodarska, I
Morris, SW
Citation: Zg. Ma et al., Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive anaplastic lymphoma kinase (ALK) tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesis, BLOOD, 95(6), 2000, pp. 2144-2149
Authors:
Alpen, B
Neubauer, A
Dierlamm, J
Marynen, P
Thiede, C
Bayerdorffer, E
Stolte, M
Citation: B. Alpen et al., Translocation t(11;18) absent in early gastric marginal zone B-cell lymphoma of MALT type responding to eradication of Helicobacter pylori infection, BLOOD, 95(12), 2000, pp. 4014-4015
Authors:
Vogels, A
Devriendt, K
Vermeesch, JR
Van Dael, R
Marynen, P
Dewaele, P
Hageman, J
Holvoet, M
Fryns, JP
Citation: A. Vogels et al., Cryptic translocation t(5;18) in familial mental retardation, ANN GENET, 43(3-4), 2000, pp. 117-123
Authors:
Baens, M
Steyls, A
Geboes, K
Marynen, P
De Wolf-Peeters, C
Citation: M. Baens et al., The product of the t(11;18), an API2-MLT fusion, marks nearly half of gastric MALT type lymphomas without large cell proliferation, AM J PATH, 156(4), 2000, pp. 1433-1439
Authors:
Correa, CL
Brems, H
Lazaro, C
Marynen, P
Legius, E
Citation: Cl. Correa et al., Unequal meiotic crossover: A frequent cause of NF1 microdeletions, AM J HU GEN, 66(6), 2000, pp. 1969-1974
Authors:
Carrie, A
Jun, L
Bienvenu, T
Vinet, MC
McDonell, N
Couvert, P
Zemni, R
Cardona, A
Van Buggenhout, G
Frints, S
Hamel, B
Moraine, C
Ropers, HH
Strom, T
Howell, GR
Whittaker, A
Ross, MT
Kahn, A
Fryns, JP
Beldjord, C
Marynen, P
Chelly, J
Citation: A. Carrie et al., A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation, NAT GENET, 23(1), 1999, pp. 25-31
Authors:
Correa, CL
Brems, H
Lazaro, C
Estivill, X
Clementi, M
Mason, S
Rutkowski, JL
Marynen, P
Legius, E
Citation: Cl. Correa et al., Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions, HUM MUTAT, 14(5), 1999, pp. 387-393
Authors:
Baens, M
Wlodarska, I
Corveleyn, A
Hoornaert, I
Hagemeijer, A
Marynen, P
Citation: M. Baens et al., A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKN1B: Hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p), GENOMICS, 56(1), 1999, pp. 40-50
Authors:
Vermeesch, JR
Duhamel, H
Petit, P
Falzetti, D
Fryns, JP
Marynen, P
Citation: Jr. Vermeesch et al., Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male, HUM GENET, 105(6), 1999, pp. 611-618
Authors:
Cools, J
Peeters, P
Voet, T
Aventin, A
Meeucci, C
Grandchamp, B
Marynen, P
Citation: J. Cools et al., Genomic organization of human JAK2 and mutation analysis of its JH2-domainin leukemia, CYTOG C GEN, 85(3-4), 1999, pp. 260-266