Division of Clinical Genetics
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- 2005
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Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
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- Contribution to journal › Article
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Mark
Mitotic instability in cancer - Is there method in the madness?
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- Contribution to journal › Article
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Mark
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.
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- Contribution to journal › Article
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Mark
Trisomies in Hematologic Malignancies
2005) In Lund University Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
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- Contribution to journal › Article
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Mark
Genetic Characterization of Bone and Soft Tissue Tumors
2005)(
- Thesis › Doctoral thesis (compilation)
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Mark
Ny kunskap om arv och ärftlighet ger nya aspekter på hjärtsjukdom
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- Contribution to journal › Article
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Mark
Immortalization of human extravillous cytotrophoblasts by human papilloma virus gene E6E7: sequential cytogenetic and molecular genetic characterization.
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- Contribution to journal › Article
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Mark
Karyotypic evolution and tumor progression in head and neck squamous cell carcinomas.
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- Contribution to journal › Article
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Mark
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
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- Contribution to journal › Article
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Mark
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations
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- Contribution to journal › Article
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Mark
Gene Expression Studies of Hematologic Malignacies
2005)(
- Thesis › Doctoral thesis (compilation)
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Mark
Connecting mitotic instability and chromosome aberrations in cancer-can telomeres bridge the gap?
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- Contribution to journal › Scientific review
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Mark
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
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- Contribution to journal › Article
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Mark
Book review: Genetic predisposition of cancer, 2nd ed.
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- Contribution to journal › Review (Book/Film/Exhibition/etc.)
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Mark
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells
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- Contribution to journal › Article
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Mark
Euploidy in somatic cells from R6/2 transgenic Huntington's disease mice
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- Contribution to journal › Article
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Mark
Nya rön om fragil X-syndromet komplicerar genetisk vägledning. Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt
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- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of chromosome aberrations in soft tissue and bone tumors
2005)(
- Thesis › Doctoral thesis (compilation)
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Mark
Fusion of the HMGA2 and NFIB genes in lipoma
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- Contribution to journal › Article
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Mark
Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia.
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- Contribution to journal › Article
- 2004
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Mark
Hoxb4-deficient mice undergo normal hematopoietic development but exhibit a mild proliferation defect in hematopoietic stem cells
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- Contribution to journal › Article
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Mark
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
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- Contribution to journal › Article
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Mark
Activation of the GLI Oncogene through Fusion with the beta-Actin Gene (ACTB) in a Group of Distinctive Pericytic Neoplasms: Pericytoma with t(7;12).
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- Contribution to journal › Article
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Mark
Identification of genes differentially regulated by the P210 BCR/ABL1 fusion oncogene using cDNA microarrays.
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- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion).
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- Contribution to journal › Article
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Mark
Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.
(
- Contribution to journal › Article
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Mark
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
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- Contribution to journal › Article
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Mark
Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
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- Contribution to journal › Article
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Mark
Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo
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- Contribution to journal › Article
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Mark
Pearson correlation analysis of micro-array data allows for the identification of genetic targets for early B-cell factor.
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- Contribution to journal › Article
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Mark
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
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- Contribution to journal › Article
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Mark
Approximate geodesic distances reveal biologically relevant structures in microarray data
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- Contribution to journal › Article
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Mark
Vascular endothelial growth factor gene polymorphisms and pre-eclampsia
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- Contribution to journal › Article
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Mark
Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells
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- Contribution to journal › Article
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Mark
Abstracts from the Ninth Annual Meeting of the Society for Neuro-Oncology
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- Contribution to journal › Article
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Mark
Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
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- Contribution to journal › Article
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Mark
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma
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- Contribution to journal › Article
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Mark
An excess of chromosome 1 breakpoints in male infertility.
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- Contribution to journal › Article
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Mark
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
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- Contribution to journal › Article
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Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
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- Contribution to journal › Article
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Mark
Cytogenetic and molecular genetic characterization of immortalized human ovarian surface epithelial cell lines: consistent loss of chromosome 13 and amplification of chromosome 20
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- Contribution to journal › Article
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Mark
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
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- Contribution to journal › Scientific review
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Mark
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
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- Contribution to journal › Article
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Mark
Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.
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- Contribution to journal › Article
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Mark
Tumor karyotype predicts clinical outcome in colorectal cancer patients
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- Contribution to journal › Article
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Mark
A model for karyotypic evolution in testicular germ cell tumors.
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- Contribution to journal › Article
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Mark
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.
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- Contribution to journal › Article
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Mark
MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
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- Contribution to journal › Article
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Mark
Sudanesiska cytogenetiker - vision om en ny form av bistånd
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- Contribution to journal › Article