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Regulation of transcription factor E2F3a and its clinical relevance in ovarian cancer

Oncogene, 2011-09, Vol.30 (38), p.4038-4049

2011

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Clinical outcome of pretreated B-cell chronic lymphocytic leukemia following alemtuzumab therapy: a retrospective study on various cytogenetic risk categories

Annals of oncology, 2010-12, Vol.21 (12), p.2410-2419

2010

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Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia

Clinical genetics, 2007-01, Vol.71 (1), p.67-75

2007

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Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system

British Journal of Cancer, 1999-09, Vol.81 (2), p.242-251

1999

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Whole Genome Amplification from Microdissected Chromosomes

Cytogenetic and genome research, 2009-01, Vol.125 (2), p.98-102

2009

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Parental Origin of de novo Cytogenetically Balanced Reciprocal Non-Robertsonian Translocations

Cytogenetic and genome research, 2012-06, Vol.136 (4), p.242-245

2012

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Switch of the mutation type of the NPM1 gene in acute myeloid leukemia (AML): relapse or secondary AML?

Blood cancer journal (New York), 2014-06, Vol.4 (6), p.e221-e221

2014

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IgM myeloma: more on a rare entity

British journal of haematology, 2008-10, Vol.143 (1), p.146-148

2008

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Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis

Clinical genetics, 2010-12, Vol.78 (6), p.548-553

2010

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LIM-domain protein cysteine- and glycine-rich protein 2 (CRP2) is a novel marker of hepatic stellate cells and binding partner of the protein inhibitor of activated STAT1

Biochemical journal, 2001-11, Vol.359 (Pt 3), p.485-496

2001

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Unfavourable prognosis of patients with trisomy 18q21 detected by fluorescence in situ hybridisation in t(11;18) negative, surgically resected, gastrointestinal B cell lymphomas

Journal of clinical pathology, 2004-04, Vol.57 (4), p.360-364

2004

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Both Donor and Recipient Origins of Smooth Muscle Cells in Vein Graft Atherosclerotic Lesions

Circulation research, 2002-10, Vol.91 (7), p.e13-e20

2002

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Smooth muscle cells in transplant atherosclerotic lesions are originated from recipients, but not bone marrow progenitor cells

Circulation (New York, N.Y.), 2002-10, Vol.106 (14), p.1834-1839

2002

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Mutations in the Δ 7-sterol Reductase Gene in Patients with the Smith--Lemli--Opitz Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1998-07, Vol.95 (14), p.8181-8186

1998

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Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH

Nature genetics, 1999-04, Vol.21 (4), p.357-358

1999

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Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations

Cytogenetics and cell genetics, 1998, Vol.80 (1-4), p.188

1998

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Cyclin E dysregulation and chromosomal instability in endometrial cancer

Oncogene, 2004-05, Vol.23 (23), p.4187-4192

2004

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616 - Early Lymph Node Metastasis: Altered Microrna Expression in Colon Cancer

Annals of oncology, 2012-09, Vol.23, p.ix209-ix209

2012

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Early Lymph Node Metastasis: Altered Microrna Expression in Colon Cancer

Annals of oncology, 2012-09, Vol.23, p.ix209

2012

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High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization

Immunogenetics (New York), 2001-09, Vol.53 (7), p.611-615

2001

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Myelodysplastic/myeloproliferative disease with erythropoietic hyperplasia (erythroid preleukemia) and the unique translocation (8;9)(p23;p24): first description of a case

Human pathology, 2005-10, Vol.36 (10), p.1148-1151

2005

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Combined study of prostatic carcinoma by classical cytogenetic analysis and comparative genomic hybridization

International journal of oncology, 2001-12, Vol.19 (6), p.1263

2001

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6p22-Genamplifikation und Methylierung des miR-34a Promoters, zwei EGF-R unabhängige Mechanismen der E2F3a-Regulation beim Ovarialkarzinom

Geburtshilfe und Frauenheilkunde, 2011, Vol.71 (4)

2011

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Hypermetaphase and interphase fluorescence in situ hybridisation for monitoring of remission status in Philadelphia chromosome positive chronic myeloid leukaemia

International journal of oncology, 2000-12, Vol.17 (6), p.1245

2000

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Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations : delineation of the phenotype

Human genetics, 1997-05, Vol.99 (5), p.596-601

1997

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Regulation of transcription factor E2F3a and its clinical relevance in ovarian cancer

Clinical outcome of pretreated B-cell chronic lymphocytic leukemia following alemtuzumab therapy: a retrospective study on various cytogenetic risk categories

Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia

Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system

Whole Genome Amplification from Microdissected Chromosomes

Parental Origin of de novo Cytogenetically Balanced Reciprocal Non-Robertsonian Translocations

Switch of the mutation type of the NPM1 gene in acute myeloid leukemia (AML): relapse or secondary AML?

IgM myeloma: more on a rare entity

Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis

LIM-domain protein cysteine- and glycine-rich protein 2 (CRP2) is a novel marker of hepatic stellate cells and binding partner of the protein inhibitor of activated STAT1

Unfavourable prognosis of patients with trisomy 18q21 detected by fluorescence in situ hybridisation in t(11;18) negative, surgically resected, gastrointestinal B cell lymphomas

Both Donor and Recipient Origins of Smooth Muscle Cells in Vein Graft Atherosclerotic Lesions

Smooth muscle cells in transplant atherosclerotic lesions are originated from recipients, but not bone marrow progenitor cells

Mutations in the Δ 7-sterol Reductase Gene in Patients with the Smith--Lemli--Opitz Syndrome

Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH

Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations

Cyclin E dysregulation and chromosomal instability in endometrial cancer

616 - Early Lymph Node Metastasis: Altered Microrna Expression in Colon Cancer

Early Lymph Node Metastasis: Altered Microrna Expression in Colon Cancer

High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization

Myelodysplastic/myeloproliferative disease with erythropoietic hyperplasia (erythroid preleukemia) and the unique translocation (8;9)(p23;p24): first description of a case

Combined study of prostatic carcinoma by classical cytogenetic analysis and comparative genomic hybridization

6p22-Genamplifikation und Methylierung des miR-34a Promoters, zwei EGF-R unabhängige Mechanismen der E2F3a-Regulation beim Ovarialkarzinom

Hypermetaphase and interphase fluorescence in situ hybridisation for monitoring of remission status in Philadelphia chromosome positive chronic myeloid leukaemia

Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations : delineation of the phenotype

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