A novel t(6;14)(q25∼q27;q32) in acute myelocytic leukemia involves the BCL11B gene

Autor: Antoinette A. T. P. Brink, Shama L. van Zelderen-Bhola, G. C. Beverstock, Carla Rosenberg, Renee M.Y. Barge, Karoly Szuhai, Anton K. Raap, Vladimir Bezrookove

Publikováno v: Bezrookove, V, Van Zelderen-Bhola, S L, Brink, A, Szuhai, K, Raap, A K, Barge, R, Beverstock, G C & Rosenberg, C 2004, ' A novel t(6;14)(q25∼q27;q32) in acute myelocytic leukemia involves the BCL11B gene ', Cancer Genetics and Cytogenetics, vol. 149, no. 1, pp. 72-76 . https://doi.org/10.1016/S0165-4608(03)00302-9
Cancer Genetics and Cytogenetics, 149(1), 72-76. Elsevier Inc.

Cytogenetic studies in a patient with acute myelocytic leukemia (AML) revealed as the sole karyotypic alteration a half-cryptic rearrangement, identified with 48-color combined binary ratio-labeled fluorescence in situ hybridization (pq-COBRA-FISH) a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5b4d19d0665235847548a2206ba9be1
https://doi.org/10.1016/s0165-4608(03)00302-9

Effect of mast cell growth factor (c-kit ligand) on clonogenic leukemic precursor cells

Autor: H M, Goselink, D E, Williams, W E, Fibbe, H W, Wessels, G C, Beverstock, R, Willemze, J H, Falkenburg

Publikováno v: Blood. 80:750-757

Mast cell growth factor (MGF), the ligand for the c-kit receptor, has been shown to be a hematopoietic growth factor that preferentially stimulates the proliferation of immature hematopoietic progenitor cells (HPC). We studied the effect of MGF on th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e585922a64e41f660381596e29933d3
https://doi.org/10.1182/blood.v80.3.750.bloodjournal803750

46,XY del(18) (q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome

Autor: G. C. Beverstock, P. de Jong, P. D. Maaswinkel-Mooij

Publikováno v: Clinical Genetics. 43:76-78

A mosaic karyotype: 46, XY, del(18) (q21.3q22.2)/47, XY, del(18) (q21.3q22.2) + marker, was found in a mentally retarded male with a mild form of the 18q— syndrome and aplasia of the right thumb. By fluorescent in situ hybridisation, the marker chr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::310af554a59f6b4581053cef13dedf09
https://doi.org/10.1111/j.1399-0004.1993.tb04431.x

Prenatal diagnosis of trisomy 13 on fetal cells obtained from maternal blood after minor enrichment

Autor: J C, Oosterwijk, W E, Mesker, M C, Ouwerkerk-Van Velzen, C F, Knepflé, K C, Wiesmeijer, G C, Beverstock, G J, Van Ommen, H J, Tanke, H H, Kanhai

Publikováno v: Prenatal diagnosis. 18(10)

In a pilot study to establish fetal nucleated red blood cell (NRBC) detection in maternal blood, trisomy 13 was diagnosed by FISH analysis at 11 weeks' gestation. The NRBCs were detected after a single-step ficoll density gradient enrichment. In bloo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::69b529a0b9f6b18270e8af78fa6e1056
https://pubmed.ncbi.nlm.nih.gov/9826902

Fetal cell detection in maternal blood: a study in 236 samples using erythroblast morphology, DAB and HbF staining, and FISH analysis

Autor: J C, Oosterwijk, W E, Mesker, M C, Ouwerkerk-van Velzen, C F, Knepflé, K C, Wiesmeijer, G C, Beverstock, G J, van Ommen, H H, Kanhai, H J, Tanke

Publikováno v: Cytometry. 32(3)

A protocol to detect fetal nucleated red blood cells (NRBCs) was tested in 217 pregnant women and in 19 nonpregnant controls. All the pregnant women were sampled after chorionic villus sampling (CVS); 20 were also sampled pre-CVS. NRBC recognition wa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::192114fd32afd1bfa134bd645baefce2
https://pubmed.ncbi.nlm.nih.gov/9667506