Poppe B - Search Results

1

Prevalence of BRCA1/2 mutations in sporadic breast/ovarian cancer patients and identification of a novel de novo BRCA1 mutation in a patient diagnosed with late onset breast and ovarian cancer: implications for genetic testing.

De Leeneer K, Coene I, Crombez B, Simkens J, Van den Broecke R, Bols A, Stragier B, Vanhoutte I, De Paepe A, Poppe B, Claes K. De Leeneer K, et al. Among authors: poppe b. Breast Cancer Res Treat. 2012 Feb;132(1):87-95. doi: 10.1007/s10549-011-1544-9. Epub 2011 May 7. Breast Cancer Res Treat. 2012. PMID: 21553119

2

Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > G.

Claes K, Machackova E, De Vos M, Poppe B, De Paepe A, Messiaen L. Claes K, et al. Among authors: poppe b. Dis Markers. 1999 Oct;15(1-3):69-73. doi: 10.1155/1999/241046. Dis Markers. 1999. PMID: 10595255 Free PMC article.

3

Genetic counselling and testing for hereditary breast and ovarian cancer: the gent(le) approach.

De Vos M, Poppe B, Delvaux I, Mortier G, Claes K, Messiaen L, De Paepe A. De Vos M, et al. Among authors: poppe b. Dis Markers. 1999 Oct;15(1-3):191-5. doi: 10.1155/1999/809125. Dis Markers. 1999. PMID: 10595277 Free PMC article.

4

Chromosome 2 short arm translocations revealed by M-FISH analysis of neuroblastoma cell lines.

Van Roy N, Van Limbergen H, Vandesompele J, Van Gele M, Poppe B, Laureys G, De Paepe A, Speleman F. Van Roy N, et al. Among authors: poppe b. Med Pediatr Oncol. 2000 Dec;35(6):538-40. doi: 10.1002/1096-911x(20001201)35:6<538::aid-mpo8>3.0.co;2-c. Med Pediatr Oncol. 2000. PMID: 11107111

5

Molecular cytogenetic and clinical findings in ETV6/ABL1-positive leukemia.

Van Limbergen H, Beverloo HB, van Drunen E, Janssens A, Hählen K, Poppe B, Van Roy N, Marynen P, De Paepe A, Slater R, Speleman F. Van Limbergen H, et al. Among authors: poppe b. Genes Chromosomes Cancer. 2001 Mar;30(3):274-82. Genes Chromosomes Cancer. 2001. PMID: 11170285

6

Chromosomal aberrations in Bloom syndrome patients with myeloid malignancies.

Poppe B, Van Limbergen H, Van Roy N, Vandecruys E, De Paepe A, Benoit Y, Speleman F. Poppe B, et al. Cancer Genet Cytogenet. 2001 Jul 1;128(1):39-42. doi: 10.1016/s0165-4608(01)00392-2. Cancer Genet Cytogenet. 2001. PMID: 11454428

7

Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines.

Van Roy N, Van Limbergen H, Vandesompele J, Van Gele M, Poppe B, Salwen H, Laureys G, Manoel N, De Paepe A, Speleman F. Van Roy N, et al. Among authors: poppe b. Genes Chromosomes Cancer. 2001 Oct;32(2):126-35. doi: 10.1002/gcc.1174. Genes Chromosomes Cancer. 2001. PMID: 11550280

8

Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH.

Van Limbergen H, Poppe B, Michaux L, Herens C, Brown J, Noens L, Berneman Z, De Bock R, De Paepe A, Speleman F. Van Limbergen H, et al. Among authors: poppe b. Genes Chromosomes Cancer. 2002 Jan;33(1):60-72. doi: 10.1002/gcc.1212. Genes Chromosomes Cancer. 2002. PMID: 11746988

9

Molecular cytogenetic analysis of 10;11 rearrangements in acute myeloid leukemia.

Van Limbergen H, Poppe B, Janssens A, De Bock R, De Paepe A, Noens L, Speleman F. Van Limbergen H, et al. Among authors: poppe b. Leukemia. 2002 Mar;16(3):344-51. doi: 10.1038/sj.leu.2402397. Leukemia. 2002. PMID: 11896537 Review.

10

Pathological splice mutations outside the invariant AG/GT splice sites of BRCA1 exon 5 increase alternative transcript levels in the 5' end of the BRCA1 gene.

Claes K, Vandesompele J, Poppe B, Dahan K, Coene I, De Paepe A, Messiaen L. Claes K, et al. Among authors: poppe b. Oncogene. 2002 Jun 13;21(26):4171-5. doi: 10.1038/sj.onc.1205520. Oncogene. 2002. PMID: 12037674

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