Johan Staaf
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- 2012
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Mark
Amplification and overexpression of the ABCC3 (MRP3) gene in primary breast cancer
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- Contribution to journal › Article
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Mark
The retinoblastoma gene undergoes rearrangements in BRCA1-deficient basal-like breast cancer.
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- Contribution to journal › Article
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Mark
Characterisation of amplification patterns and target genes at chromosome 11q13 in CCND1-amplified sporadic and familial breast tumours.
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- Contribution to journal › Article
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Mark
Molecular profiling reveals low- and high-grade forms of primary melanoma
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- Contribution to journal › Article
- 2011
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Mark
High-resolution genomic profiling of male breast cancer reveals differences hidden behind the similarities with female breast cancer
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- Contribution to journal › Article
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Mark
Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer
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- Contribution to journal › Article
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Mark
GOBO: Gene Expression-Based Outcome for Breast Cancer Online.
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- Contribution to journal › Article
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Mark
Identification of new microRNAs in paired normal and tumor breast tissue suggests a dual role for the ERBB2/Her2 gene.
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- Contribution to journal › Article
- 2010
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Mark
Genomic profiling of breast cancer by microarray-based technology and bioinformatics
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- Thesis › Doctoral thesis (compilation)
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Mark
Genetic profiles of gastroesophageal cancer: combined analysis using expression array and tiling array-comparative genomic hybridization
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- Contribution to journal › Article
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Mark
Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics
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- Contribution to journal › Article
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Mark
Molecular subtypes of breast cancer are associated with characteristic DNA methylation patterns
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- Contribution to journal › Article
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Mark
High-resolution genomic and expression analyses of copy number alterations in HER2-amplified breast cancer
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- Contribution to journal › Article
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Mark
Zoom-in array comparative genomic hybridization (aCGH) to detect germline rearrangements in cancer susceptibility genes.
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- Contribution to journal › Article
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Mark
Genetic profiles distinguish different types of hereditary ovarian cancer.
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- Contribution to journal › Article
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Mark
Identification of Subtypes in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer Reveals a Gene Signature Prognostic of Outcome.
(
- Contribution to journal › Article
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Mark
Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: a high-resolution genomic screening of newly diagnosed patients.
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- Contribution to journal › Article
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Mark
Multiple metastases from cutaneous malignant melanoma patients may display heterogeneous genomic and epigenomic patterns.
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- Contribution to journal › Article
- 2009
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Mark
High-Resolution Genomic Profiling of Carboplatin Resistance in Early-Stage Epithelial Ovarian Carcinoma
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- Contribution to journal › Article
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Mark
Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: A high-resolution genomic screening in newly diagnosed patients
2009) 14th Annual Meeting of the European-Hematology-Association In Haematologica-The Hematology Journal 94. p.0354-0354(
- Contribution to journal › Published meeting abstract
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Mark
MiRNA expression in urothelial carcinomas: Important roles of miR-10a, miR-222, miR-125b, miR-7 and miR-452 for tumor stage and metastasis, and frequent homozygous losses of miR-31.
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- Contribution to journal › Article
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Mark
Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.
(
- Contribution to journal › Article
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Mark
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.
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- Contribution to journal › Article
- 2008
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Mark
Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays
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- Contribution to journal › Article
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Mark
Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia-A comparative study of four differently designed, high resolution microarray platforms.
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- Contribution to journal › Article
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Mark
Effect of polyamine deficiency on proteins involved in Okazaki fragment maturation.
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- Contribution to journal › Article
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Mark
Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-banding
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- Contribution to journal › Article
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Mark
Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms
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- Contribution to journal › Article
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Mark
Genomic alterations in coleorectal cencer in relationship to stage and survival assesed by tiling BAC array CGH
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- Contribution to journal › Published meeting abstract
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Mark
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
(
- Contribution to journal › Article
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Mark
Heterogeneous genetic profiles in soft tissue myoepitheliomas
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- Contribution to journal › Article
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Mark
Array-CGH identifies cyclin D1 and UBCH10 amplicons in anaplastic thyroid carcinoma.
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- Contribution to journal › Article
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Mark
Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).
(
- Contribution to journal › Article
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Mark
Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios.
(
- Contribution to journal › Article
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Mark
Different cell cycle kinetic effects of N1,N11-diethylnorspermine-induced polyamine depletion in four human breast cancer cell lines.
(
- Contribution to journal › Article
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Mark
Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair
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- Contribution to journal › Article
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Mark
Molecular mechanisms underlying N1, N11-diethylnorspermine-induced apoptosis in a human breast cancer cell line.
(
- Contribution to journal › Article
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Mark
Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation.
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- Contribution to journal › Article
- 2007
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Mark
Continuous-index hidden Markov modelling of array CGH copy number data.
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- Contribution to journal › Article
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Mark
Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida
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- Contribution to journal › Article
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Mark
Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients
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- Contribution to journal › Article
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Mark
Robust smooth segmentation approach for array CGH data analysis
(
- Contribution to journal › Article
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Mark
Genomic profiling of malignant melanoma using tiling-resolution arrayCGH.
(
- Contribution to journal › Article
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Mark
Non-coding antisense transcription detected by conventional and single-stranded cDNA microarray
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- Contribution to journal › Article
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Mark
Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and breakage/fusion/breakage cycles?
(
- Contribution to journal › Letter
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Mark
Cytogenetic characterization and gene expression profiling of the trastuzumab-resistant breast cancer cell line JIMT-1.
(
- Contribution to journal › Article
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Mark
Normalization of array-CGH data: influence of copy number imbalances
(
- Contribution to journal › Article
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Mark
Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities
(
- Contribution to journal › Article
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Mark
High-resolution genomic profiles of breast cancer cell lines assessed by tiling BAC array comparative genomic hybridization.
(
- Contribution to journal › Article
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Mark
Isolated 46,XY gonadal dysgenesis in two sisters caused by a Xp21.2 interstitial duplication containing the DAX1 gene.
(
- Contribution to journal › Article
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Mark
Tumor genome wide DNA alterations assessed by array CGH in patients with poor and excellent survival following operation for colorectal cancer
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- Contribution to journal › Article
- 2006
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Mark
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities
(
- Contribution to journal › Letter
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Mark
High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
(
- Contribution to journal › Article
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Mark
Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2
(
- Contribution to journal › Article
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Mark
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
(
- Contribution to journal › Article
- 2005
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Mark
Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to similar to 650 kb
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- Contribution to journal › Article
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Mark
Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridization.
(
- Contribution to journal › Article
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Mark
Mapping of a novel ocular and cutaneous malignant melanoma susceptibility locus to chromosome 9q21.32.
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- Contribution to journal › Article
- 2004
-
Mark
ACID: a database for microarray clone information
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- Contribution to journal › Article
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Mark
Flexible geniom® one Microarrays im Vergleich mit etablierten Technologien
(
- Contribution to journal › Article
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