Bruce Poppe

Polymorphisms in nonhomologous end-joining genes associated with breast cancer risk and chromosomal radiosensitivity (2009)

Willems, Petra, Claes, Kathleen, Baeyens, Ans, Vandersickel, Veerle, Werbrouck, Joke, Deruyck, Kim, ...

Genome profiling of acute myelomonocytic leukemia: alteration of the MYB locus in MYST3-linked cases (2009)

Murati, A, Gervais, C, Carbuccia, N, Finetti, P, Cervera, N, Adelaide, J, ...

The t(8; 16)(p11; p13) is a rare translocation involved in de novo and therapy-related myelomonocytic and monocytic acute leukemia. It fuses two genes encoding histone acetyltransferases (HATs),...

EVI1activation in blast crisis CML due to juxtaposition to the rare 17q22 partner region as part of a 4-way variant translocation t(9;22) (2008)

De Weer, An, Poppe, Bruce, Cauwelier, Barbara, Carlier, Andre, Dierick, Jan, Verhasselt, Bruno, ...

Abstract Background Variant translocations t(9;22) occur in 5 to 10% of newly diagnosed CMLs and additional genetic changes are present in 60–80% of patients in blast crisis (BC). Here, we report...

Polymorphisms in nonhomologous end-joining genes associated with breast cancer risk and chromosomal radiosensitivity (2008)

Willems, Petra, Claes, Kathleen, Baeyens, Ans, Vandersickel, Veerle, Werbrouck, Joke, De Ruyck, Kim, ...

Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis population (2008)

TERRYN, W, Poppe, Bruce, WUYTS, B, Claes, Kathleen, MAES, B, VERBEELEN, D, ...

Rapid and sensitive detection of BRCA1/2 mutations in a diagnostic setting: Comparison of two high-resolution melting platforms (2008)

De Leeneer, Kim, COENE, ILSE, Poppe, Bruce, De Paepe, Anne, Claes, Kathleen

EVII activation in blast crisis CML due to juxtaposition to the rare 17q22 partner region as part of a 4-way variant translocation t(9;22) (2008)

De Weer, An, Poppe, Bruce, Cauwelier, Barbara, CARLIER, A, DIERICK, J, Verhasselt, Bruno, ...

Background: Variant translocations t( 9; 22) occur in 5 to 10% of newly diagnosed CMLs and additional genetic changes are present in 60 - 80% of patients in blast crisis ( BC). Here, we report on a...

Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogenetique de hematologique (2008)

GERVAIS, C, MURATI, A, HELIAS, C, STRUSKI, S, EISCHEN, A, LIPPERT, E, ...

EVI1 overexpression in t(3;17) positive myeloid malignancies results from juxtaposition of EVI1 to the MSI2 locus at 17q22 (2008)

De Weer, An, Speleman, Franki, Cauwelier, Barbara, Van Roy, Nadine, Yigit, Nurten, Verhasselt, Bruno, ...

Chromosomal translocations involving the EVI1 locus are a recurrent finding in myeloid leukemia and are associated with poor prognosis. In this study, we performed a detailed molecular...

MICRORNA PROFILING OF EVI1 DEREGULATED MYELOID LEUKEMIA (2008)

De Weer, An, Poppe, Bruce, Mestdagh, Pieter, Van Vlierberghe, Pieter, Van Roy, Nadine, De Paepe, Anne, ...

Two-tier approach for the detection of alpha-galactosidase A deficiency in kidney transplant recipients (2008)

De Schoenmakere, Gert, Poppe, Bruce, Wuyts, Birgitte, Claes, Kathleen, Cassiman, David, Maes, Bart, ...

Background. Anderson-Fabry disease (AFD) is an X-linked condition originating from a deficiency in alpha-galactosidase, a lysosomal enzyme. Multi-organ involvement ensues in early adulthood and vital...

EVII activation in blast crisis CML due to juxtaposition to the rare 17q22 partner region as part of a 4-way variant translocation t(9;22) (2008)

De Weer, An, Poppe, Bruce, Cauwelier, Barbara, Carlier, Andre, Dierick, Jan, Verhasselt, Bruno, ...

Background: Variant translocations t( 9; 22) occur in 5 to 10% of newly diagnosed CMLs and additional genetic changes are present in 60 - 80% of patients in blast crisis ( BC). Here, we report on a...

EVI1 overexpression in t(3;17) positive myeloid malignancies results from juxtaposition of EVI1 to the MSI2 locus at 17q22 (2008)

De Weer, An, Speleman, Franki, Cauwelier, Barbara, Van Roy, Nadine, Yigit, Nurten, Verhasselt, Bruno, ...

Chromosomal translocations involving the EVI1 locus are a recurrent finding in myeloid leukemia and are associated with poor prognosis. In this study, we performed a detailed molecular...

MicroRNA signatures in genetic subtypes of T-cell acute lymphoblastic leukemia. (2008)

Van Vlierberghe, Pieter, Poppe, Bruce, Van Roy, Nadine, Taghon, Tom, Plum, Jean, Cauwelier, B, ...

Copy number alterations and copy number variation in cancer: close encounters of the bad kind (2008)

Speleman, Franki, Kumps, Candy, Buysse, Karen, Poppe, Bruce, Menten, Björn, De Preter, Katleen

Recent studies have unveiled copy number variants (CNVs) as an important source of genetic variation. Many of these CNVs contain coding sequences, which have been shown to be dosage sensitive....

Slow progression of chronic renal failure in a woman of short stature and leg deformities: what is the link? (2008)

Vanacker, An, Segaert, Marc, Verbanck, Johan, Van Dorpe, Jo, Poppe, Bruce, Maes, Bart

Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis population (2008)

Terryn, Wim, Poppe, Bruce, Wuyts, Birgitte, Claes, Kathleen, Maes, Bart, Verbeelen, Dierik, ...

Introduction. Fabry's disease (AFD) is an X-linked lysosomal storage disease, resulting from a deficiency in alpha-galactosidase A (AGALA). Untreated, this leads to precocious failure of vital organ...

Two-tier approach for the detection of alpha-galactosidase A deficiency in kidney transplant recipients (2008)

Schoenmakere, Gert De, Poppe, Bruce, Wuyts, Birgitte, Claes, Kathleen, Cassiman, David, Maes, Bart, ...

Background. Anderson–Fabry disease (AFD) is an X-linked condition originating from a deficiency in alpha-galactosidase, a lysosomal enzyme. Multi-organ involvement ensues in early adulthood and...

Borstkanker en erfelijkheid (2007)

Poppe, Bruce, De Wilde, Philippe, De Paepe, Anne

Acquired chromosomal rearrangements targeting selected transcription factors: contribution of molecular cytogenetic and expression analyses to the identification of clinically and biologically relevant subgroups in hematological malignancies (2007)

Poppe, Bruce, De Paepe, Anne, Speleman, Franki

A detailed inventory of DNA copy number alterations in four commonly used Hodgkin's lymphoma cell lines (2007)

Feys, Tom, Poppe, Bruce, De Preter, Katleen, Van Roy, Nadine, Verhasselt, Bruno, DE PAEPE, P, ...

Identification of EVI1 transcriptional target genes using RNAI (2007)

De Weer, An, Poppe, Bruce, CAUWEUER, B, Van Roy, Nadine, Verhasselt, Bruno, Speleman, Franki

A detailed inventory of DNA copy number alterations in four commonly used Hodgkin lymphoma cell lines (2007)

Feys, Tom, Poppe, Bruce, De Preter, Katleen, Van Roy, Nadine, Verhasselt, Bruno, De Paepe, Pascale, ...

De bijdrage van M-FISH aan de moleculaire diagnostiek in de hemato-oncologie (2007)

Poppe, Bruce, Van Roy, Nadine, Yigit, Nurten, De Paepe, Anne, Speleman, Franki

MicroRNA profiling of EVI1 deregulated myeloid leukemia (2007)

De Weer, An, Poppe, Bruce, Mestdagh, Pieter, Van Roy, Nadine, De Paepe, Anne, Verhasselt, Bruno, ...

Report of an unusual translocation t(3;14)(q26;q32) involving both EVI1 and IGH in an unclassified acute myeloid leukaemia (AML) (2007)

HAVELANGE, V, AMEYE, G, DEWEER, A, BAHLOULA, K, MULLIER, C, LIBOUTON, JM, ...

Borstkanker en erfelijkheid (2007)

Poppe, Bruce, De Wilde, Philippe, De Paepe, Anne

Acquired chromosomal rearrangements targeting selected transcription factors : contribution of molecular cytogenetic and expression analyses to the identification of clinically and biologically relevant subgroups in hematological malignancies (2007)

Poppe, Bruce, De Paepe, Anne, Speleman, Franki

Array CGH analysis of subnanogram quantities of DNA using whole genome amplification: Opportunities for detection of copy number alterations in Hodgkin's lymphoma (2007)

Feys, Tom, Poppe, Bruce, Verhasselt, Bruno, DE PAEPE, P, Menten, Björn, Vandesompele, Jo, ...

Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCR beta-HOXA rearrangement: a study of the Groupe Francophone de Cytogenetique Hematologique (2007)

Cauwelier, Barbara, CAVÉ, H, GERVAIS, C, LESSARD, M, BARIN, C, PEROT, C, ...

Preliminary screening results for fabry disease in young stroke patients reveals a new mutation (2007)

Hemelsoet, Dimitri, Poppe, Bruce, SIEBEN, ANNE, VANHEE, FREDERIK, PROOT, PASCAL, DE CLERCK, M, ...

Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRb-HOXA rearrangement : a study of the Groupe Francophone de Cytogénétique Hématologique (GFCH). (2007)

Cauwelier, B, Cavé, H, Gervais, C, Lessard, M, Barin, C, Perot, C, ...

Recently, we and others described a new chromosomal rearrangement, that is, inv( 7)( p15q34) and t( 7; 7)( p15; q34) involving the T-cell receptor beta ( TCR beta) ( 7q34) and the HOXA gene locus (...

GAB2 is a novel target of 11q amplification in AML/MDS (2006)

ZATKOVA, A, SCHOCH, C, Speleman, Franki, Poppe, Bruce, MANNHALTER, C, FONATSCH, C, ...

Molecular cytogenetic study of 126 unselected T-ALL cases reveals high incidence of TCR beta locus rearrangements and putative new T-cell oncogenes (2006)

Cauwelier, Barbara, DASTUGUE, N, COOLS, J, Poppe, Bruce, HERENS, C, De Paepe, Anne, ...

EVII is consistently expressed as principal transcript in common and rare recurrent 3q26 rearrangements (2006)

Poppe, Bruce, DASTUGUE, N, Vandesompele, Jo, Cauwelier, Barbara, DE SMET, B, Yigit, Nurten, ...

Recurrent T(3;17)translocations in AML with EVI1 rearrangement (2006)

De Weer, An, Poppe, Bruce, Cauwelier, Barbara, Van Roy, Nadine, DASTUGUE, N, De Moerloose, Barbara, ...

Screening for EVII: ectopic expression absent in T-cell acute lymphoblastic leukemia patients and cell lines (2006)

De Weer, An, Poppe, Bruce, Cauwelier, Barbara, Van Roy, Nadine, DASTUGUE, N, HAGEMEIJER, A, ...

Recurrent t(3;17) translocations in AML with EVII rearrangement. (2006)

De Weer, A, Poppe, Bruce, Cauwelier, B, Van Roy, Nadine, Dastugue, N, De Moerloose, Barbara, ...

Rapid detection of VHL exon deletions using real-time quantitative PCR (2005)

Hoebeeck, Jasmien, Poppe, Bruce, De Smet, Els, Yigit, Nurten, Claes, Kathleen, ...

A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias (2005)

Speleman, Franki, Cauwelier, Barbara, DASTUGUE, N, COOLS, J, Verhasselt, Bruno, Poppe, Bruce, ...

Novel cryptic chromosomal rearrangements in childhood acute lymphoblastic leukemia detected by multiple color fluorescent in situ hybridization (2005)

Poppe, Bruce, Cauwelier, Barbara, VAN LIMBERGEN, H, Yigit, Nurten, Philippe, Jan, Verhasselt, Bruno, ...

HOYA gene cluster rearrangement in a t(7;9)(p15;q34) in a child with MDS (2005)

Poppe, Bruce, Yigit, Nurten, De Moerloose, Barbara, De Paepe, Anne, Benoit, Yves, Speleman, Franki

PAX5/IGH rearrangement is a recurrent finding in a subset of aggressive B-NHL with complex chromosomal rearrangements (2005)

Poppe, Bruce, DE PAEPE, P, MICHAUX, L, DASTUGUE, N, BASTARD, C, HERENS, C, ...

Recente moleculaire inzichten in erfelijke borst- en ovariumkanker in België (2005)

Claes, Kathleen, Poppe, Bruce, COENE, ILSE, MESSIAEN, L, De Paepe, Anne

Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignancies (2004)

Poppe, Bruce, Vandesompele, Jo, SCHOCH, C, LINDVALL, C, MROZEK, K, BLOOMFIELD, CD, ...

Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951 (2004)

CAVÉ, H, SUCIU, S, PREUDHOMME, C, Poppe, Bruce, ROBERT, A, UYTTEBROECK, A, ...

Routine microsatellite instability testing in sporadic colorectal tumours (2004)

VAN DAMME, NANCY, Demetter, Pieter, Claes, Kathleen, Poppe, Bruce, BAERT, F, ROELENS, J, ...

The impact of proband mediated information dissemination in families with a BRCA1/2 gene mutation (2004)

SERMIJN, E, GOELEN, G, TEUGELS, E, KAUFMAN, L, BONDUELLE, M, NEYNS, B, ...

BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families (2004)

Claes, Kathleen, Poppe, Bruce, COENE, ILSE, De Paepe, Anne, Messiaen, Ludwine

Translocation t(2;3)(p15-23;q26-27) in myeloid malignancies: report of 21 new cases, clinical, cytogenetic and molecular genetic features (2004)

STEVENS-KROEF, M, Poppe, Bruce, VAN KESSEL, AG, ...

Recommendations for the cytogenetic management of myelodysplastic syndromes proposed by the Groupe Francais de Cytogenetique Hematologique (GFCH) (2004)

BASTARD, C, LUCQUET, I, MOZZICONACCI, MJ, Poppe, Bruce, RAYNAUD, S, Speleman, Franki

Recommendations for the cytogenetic management of acute myeloblastic leukemia (AML) proposed by the Groupe Francais de Cytogenetique Hematologique (GFCH) (2004)

BASTARD, C, BARANGER, L, BILHOU-NABERA, C, CHARRIN, C, DASTUGUE, N, ECLACHE, V, ...

Recommendations for the cytogenetic management of adult and chidhoodacute lymphoblastic leukemia (ALL) proposed by the Groupe Francais de Cytogenetique Hematologique (GFCH) (2004)

BARANGER, L, BARI, C, CHARRIN, C, CORNILLET-LEFEBVRE, P, DASTUGUE, N, LAFAGE-POCHITALOFF, M, ...

Chromosomal radiosensitivity in BRCA1 and BRCA2 mutation carriers (2004)

Baeyens, Ans, Thierens, Hubert, Claes, Kathleen, Poppe, Bruce, De Ridder, Leo, Vral, Anne

ALK activation by the CLTC-ALK fusion is a recurrent event in large B-cell lymphoma (2003)

Van Krieken, Han, Verhasselt, Bruno, Simons, Annet, ...

We present 3 cases of large B-cell lymphoma (LBCL) with a granular cytoplasmic staining for anaplastic lymphoma kinase (ALK). All of the cases showed striking similarities in morphology and...

BRCA1/2 mutation spectrum and frequencies in Belgian breast/ovarian cancer families (2003)

Claes, Kathleen, Poppe, Bruce, COENE, ILSE, De Paepe, Anne, Messiaen, Ludwine

Differentiating pathogenic mutations from polymorphic alterations in the splice sites of BRCA1 and BRCA2 (2003)

Claes, Kathleen, Poppe, Bruce, MACHACKOVA, E, COENE, ILSE, FORETOVA, L, De Paepe, Anne, ...

Therapie van het colorectaal carcinoom : kunnen biologische merkers het beleid beïnvloeden? (2003)

SIERENS, B, Peeters, Marc, Poppe, Bruce, DEMETTER, C, CUVELIER, C, DE VOS, M

BRCA genmutaties bij borstkanker (2003)

Poppe, Bruce, Van Den Broecke, Rudy, De Paepe, Anne

t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Francais de Cytogenetique Hematologique (GFCH) (2003)

BERGER, R, DASTUGUE, N, BUSSON, M, PEROT, C, BALLERINI, P, ...

ALK activation by the CLTC-ALK fusion is a recurrent event in large B-cell lymphoma (2003)

DE PAEPE, P, BAENS, M, VAN KRIEKEN, H, Verhasselt, Bruno, STUL, M, SIMONS, ANN, ...

Therapie van het colorectaal carcinoom: kunnen biologische merkers het beleid beïnvloeden? (2003)

SIERENS, B, Peeters, Marc, Poppe, Bruce, De Paepe, Anne, Demetter, Pieter, Cuvelier, Claude, ...

BRCA-genmutaties bij borstkanker (2003)

Poppe, Bruce, Van Den Broecke, Rudy, De Paepe, Anne

3q rearrangements in myeloid malignancies (2003)

Poppe, Bruce, DASTUGUE, N, Speleman, Franki

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes (2002)

Vandesompele, Jo, De Preter, Katleen, Pattyn, Filip, Poppe, Bruce, Van Roy, Nadine, De Paepe, Anne, ...

Abstract Background Gene-expression analysis is increasingly important in biological research, with real-time reverse transcription PCR (RT-PCR) becoming the method of choice for high-throughput and...

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. (2002)

Claes, Kathleen, Vandesompele, Jo, Poppe, Bruce, DAHAN, K, COENE, I, De Paepe, Anne, ...

t(9;14)(p13;q32). (2002)

Poppe, Bruce, DE PAEPE, P, Speleman, Franki

Clear cell sarcoma. (2002)

Poppe, Bruce, FORSYTH, R, DHAENE, K, Speleman, Franki

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. (2002)

Vandesompele, Jo, De Preter, Katleen, Pattyn, Filip, Poppe, Bruce, Van Roy, Nadine, De Paepe, Anne, ...

Molecular cytogenetic analysis of 10;11 rearrangements in acute myeloid leukemia. (2002)

Van Limbergen, Heidi, Poppe, Bruce, JANSSENS, A, DE BOCK, R, De Paepe, Anne, NOENS, L, ...

Meerkleuren fluorescentie in situ hybridisatie : methodologie en toepassingen in diagnostiek en onderzoek. (2002)

Van Limbergen, Heidi, Poppe, Bruce, Vermeulen, Stefan, Van Roy, Nadine, De Paepe, Anne, Speleman, Franki

Wanneer speelt erfelijkheid een rol (2002)

De Paepe, Anne, Poppe, Bruce

Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predisposition. (2002)

Baeyens, Ans, Thierens, Hubert, Claes, Kathleen, Poppe, Bruce, Messiaen, Ludwine, De Ridder, Leo, ...

Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH. (2002)

Van Limbergen, Heidi, Poppe, Bruce, MICHAUX, L, HERENS, C, BROWN, J, Noens, Lucien, ...

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes (2002)

De Paepe, Anne, De Preter, Katleen, Pattyn, Filip, Poppe, Bruce, Speleman, Franki, Van Roy, Nadine, ...

HOX11L2 expression linked to t(5;14)(q35;q32) is not associated with poor prognosis in childhood T-ALL treated in EORTC trials 58 881 and 58 951 (2002)

CAVÉ, H, SUCIU, S, PREUDHOMME, C, Poppe, Bruce, ROBERT, A, UYTTEBROEK, A, ...

Chromosomal aberrations in Bloom syndrome patients with myeloid malignancies. (2001)

Poppe, Bruce, Van Limbergen, Heidi, Van Roy, Nadine, VANDECRUYS, E, De Paepe, Anne, Benoit, Yves, ...

Molecular cytogenetic and clinical findings in ETV6/ABL1-positive leukemia. (2001)

Van Limbergen, Heidi, BEVERLOO, HB, VAN DRUNEN, E, Janssens, Ann, HAHLEN, K, Poppe, Bruce, ...

Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines. (2001)

Van Roy, Nadine, Van Limbergen, Heidi, Vandesompele, Jo, Van Gele, Mireille, Poppe, Bruce, SALWEN, H, ...

Genetisch advies bij het familiaal voorkomen van borstkanker (2001)

Poppe, Bruce, MEIRE, I, DELVAUX, I, Claes, Kathleen, MESSIAEN, L, De Paepe, Anne

Molecular characterization of a t(2;3)(p23;q26): A recurrent translocation involving the EVI1 gene (2001)

Poppe, Bruce, Yigit, Nurten, MARYNEN, P, HAGEMEIJER, A, VAN LIMBERGEN, H, DE SMET, B, ...

Familiale borst- en/of ovariumkanker : diagnostisch en predictief genetisch onderzoek. (2000)

Delvaux, Isabelle, DE VOS, M, Poppe, Bruce, Mortier, Geert, De Paepe, Anne

Genetica en kanker : perspectieven voor diagnose en behandeling. (2000)

Speleman, Franki, Poppe, Bruce

Chromosome 2 short arm translocations revealed by M-FISH analysis of neuroblastoma cell lines. (2000)

Van Roy, Nadine, Van Limbergen, Heidi, Vandesompele, Jo, Van Gele, Mireille, Poppe, Bruce, Laureys, Genevieve, ...

Repetitive analyses of P-glycoprotein in chornic myeloid leukaemia. (2000)

De Moerloose, Barbara, MUYLAERT, A, GEMMEL, F, JANSSENS, A, Poppe, Bruce, Dhooge, Catharina, ...

Identification and characterisation of a founder mutation in the Belgian breast/ovarian cancer population (2000)

Claes, Kathleen, Poppe, Bruce, SCHEIR, PETRA, DE VOS, M, DELVEAUX, I, COENE, ILSE, ...

Genetic counselling and testing for hereditary breast and ovarian cancer: The gent(le) approach. (1999)

DE VOS, M, Poppe, Bruce, Delvaux, Isabelle, Mortier, Geert, Claes, Kathleen, Messiaen, Ludwine, ...

Cytogenetic findings in bloom syndrome patients with myeloid malignancies (1999)

Poppe, Bruce, Benoit, Yves, VAN LIMBERGEN, H, Van Roy, Nadine, VANDECRUYS, ELS, JAUCH, A, ...

Unusual chromosome 16 rearrangement with absence of classical CBFB/MYH11 fusion transcripts (1999)

VAN LIMBERGEN, H, VAN DER REIJDEN, BA, Poppe, Bruce, Van Roy, Nadine, DAUWERSE, H, De Paepe, Anne, ...

Chromosome 7 short arm deletions and disease progression in CML (1999)

Poppe, Bruce, VAN LIMBERGEN, H, JANSSENS, ANN, Van Roy, Nadine, De Moerloose, Barbara, PHILLIPE, J, ...

A single step real-time quantitative RT-PCR reaction for detection of the BCR/ABL fusion product (1999)

VAN LIMBEREN, H, Poppe, Bruce, De Paepe, Anne, Offner, Fritz, MENSINK, E, ...

Identification of a novel CBFB/MYH11 fusion in a patient with AML-M1 and a t(16;16)(p13;q22) (1999)

VAN LIMBERGEN, H, Poppe, Bruce, Offner, Fritz, Van Roy, Nadine, DAUWERSE, H, ...

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

Vandesompele, Jo, De Preter, Katleen, Pattyn, Filip, Poppe, Bruce, Van Roy, Nadine, De Paepe, Anne, ...

Using real-time reverse transcription PCR ten housekeeping genes from different abundance and functional classes in various human tissues were evaluated. The conventional use of a single gene for...

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

Vandesompele, Jo, De Preter, Katleen, Pattyn, Filip, Poppe, Bruce, Van Roy, Nadine, De Paepe, Anne, ...

Using real-time reverse transcription PCR ten housekeeping genes from different abundance and functional classes in various human tissues were evaluated. The conventional use of a single gene for...

EVI1 activation in blast crisis CML due to juxtaposition to the rare 17q22 partner region as part of a 4-way variant translocation t(9;22)

De Weer, An, Poppe, Bruce, Cauwelier, Barbara, Carlier, Andre, Dierick, Jan, Verhasselt, Bruno, ...

Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian Patient Population and Identification of a Belgian Founder Mutation BRCA1 IVS5+3A>G. Disease markers, 15, 1999, 69-73.

Claes, Kathleen, MACHACKOVA, E, DE VOS, M, Poppe, Bruce, De Paepe, Anne, Messiaen, Ludwine