Division of Clinical Genetics
901 – 1000 of 1270
- show: 100
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2006
-
Mark
Molecular characterization of early-stage bladder carcinomas by expression profiles, FGFR3 mutation status, and loss of 9q.
(
- Contribution to journal › Article
-
Mark
Comparison of ST-Segment Deviation to Scintigraphically Quantified Myocardial Ischemia During Acute Coronary Occlusion Induced by Percutaneous Transluminal Coronary Angioplasty.
(
- Contribution to journal › Article
-
Mark
Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre-B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement.
(
- Contribution to journal › Article
-
Mark
Determination of the ability of high-frequency ECG to estimate left ventricular mass in humans, determined by magnetic resonance imaging.
(
- Contribution to journal › Article
-
Mark
Education in medical genetics for non-genetic health care providers in sweden.
(
- Contribution to journal › Article
-
Mark
Re: Wilting et al. Increased gene copy numbers at chromosome 20q are frequent in both squamous cell carcinomas and adenocarcinomas of the cervix. J Pathol 2006; 209:220-230.
(
- Contribution to journal › Letter
-
Mark
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
(
- Contribution to journal › Article
-
Mark
Human short-term repopulating cells have enhanced telomerase reverse transcriptase expression.
(
- Contribution to journal › Article
-
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
-
Mark
Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma
(
- Contribution to journal › Article
- 2005
-
Mark
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
-
Mark
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
(
- Contribution to journal › Article
-
Mark
Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene
(
- Contribution to journal › Article
-
Mark
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
(
- Contribution to journal › Article
-
Mark
Mitotic instability in cancer - Is there method in the madness?
(
- Contribution to journal › Article
-
Mark
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.
(
- Contribution to journal › Article
-
Mark
Genetic education and nongenetic health professionals: Educational providers and curricula in Europe.
(
- Contribution to journal › Article
-
Mark
Trisomies in Hematologic Malignancies
2005) In Lund University Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
(
- Contribution to journal › Article
-
Mark
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
(
- Contribution to journal › Article
-
Mark
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells
(
- Contribution to journal › Article
-
Mark
Fusion of the HMGA2 and NFIB genes in lipoma
(
- Contribution to journal › Article
-
Mark
Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Connecting mitotic instability and chromosome aberrations in cancer-can telomeres bridge the gap?
(
- Contribution to journal › Scientific review
-
Mark
Euploidy in somatic cells from R6/2 transgenic Huntington's disease mice
(
- Contribution to journal › Article
-
Mark
Book review: Genetic predisposition of cancer, 2nd ed.
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
Karyotypic evolution and tumor progression in head and neck squamous cell carcinomas.
(
- Contribution to journal › Article
-
Mark
Immortalization of human extravillous cytotrophoblasts by human papilloma virus gene E6E7: sequential cytogenetic and molecular genetic characterization.
(
- Contribution to journal › Article
-
Mark
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations
(
- Contribution to journal › Article
-
Mark
Gene Expression Studies of Hematologic Malignacies
2005)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Ny kunskap om arv och ärftlighet ger nya aspekter på hjärtsjukdom
(
- Contribution to journal › Article
-
Mark
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
(
- Contribution to journal › Article
-
Mark
Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses)
(
- Contribution to journal › Article
-
Mark
Molecular cytogenetic characterization of chromosome aberrations in soft tissue and bone tumors
2005)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic Characterization of Bone and Soft Tissue Tumors
2005)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer.
(
- Contribution to journal › Article
-
Mark
Amplification and overexpression of Aurora kinase A (AURKA) in immortalized human ovarian epithelial (HOSE) cells
(
- Contribution to journal › Article
-
Mark
Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma
(
- Contribution to journal › Article
-
Mark
The parental origin of trisomy 14 in hyperdiploid childhood ALL
(
- Contribution to journal › Letter
-
Mark
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Clear cell hidradenoma of the skin - a third tumor type with a t(11;19)-associated TORC1-MAML2 gene fusion
(
- Contribution to journal › Article
-
Mark
Prevalence of Stroke and Vascular Risk Factors among First-Degree Relatives of Stroke Patients and Control Subjects.
(
- Contribution to journal › Article
-
Mark
Core-needle biopsy performed by the cytopathologist : a technique to complement fine-needle aspiration of soft tissue and bone lesions
(
- Contribution to journal › Article
-
Mark
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.
(
- Contribution to journal › Article
-
Mark
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
(
- Contribution to journal › Article
-
Mark
Culturing of human tumor cells for use in immune gene tumor therapy
2005) World Federation of Neuro-Oncology Second Quadrennial Meeting and the Sixth Meeting of the European Association for Neuro-Oncology In Neuro-Oncology 7(3). p.371-371(
- Contribution to journal › Published meeting abstract
-
Mark
Statistical behavior of complex cancer karyotypes.
(
- Contribution to journal › Scientific review
-
Mark
Telomere-mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma
(
- Contribution to journal › Article
-
Mark
Nya rön om fragil X-syndromet komplicerar genetisk vägledning. Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt
(
- Contribution to journal › Article
- 2004
-
Mark
Pearson correlation analysis of micro-array data allows for the identification of genetic targets for early B-cell factor.
(
- Contribution to journal › Article
-
Mark
Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo
(
- Contribution to journal › Article
-
Mark
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
(
- Contribution to journal › Article
-
Mark
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
(
- Contribution to journal › Article
-
Mark
Abstracts from the Ninth Annual Meeting of the Society for Neuro-Oncology
(
- Contribution to journal › Article
-
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.
(
- Contribution to journal › Article
-
Mark
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
(
- Contribution to journal › Article
-
Mark
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas.
(
- Contribution to journal › Article
-
Mark
Reduced high-frequency QRS components in patients with ischemic heart disease compared to normal subjects
(
- Contribution to journal › Article
-
Mark
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
(
- Contribution to journal › Article
-
Mark
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
(
- Contribution to journal › Article
-
Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
(
- Contribution to journal › Article
-
Mark
Cytogenetic and molecular genetic characterization of immortalized human ovarian surface epithelial cell lines: consistent loss of chromosome 13 and amplification of chromosome 20
(
- Contribution to journal › Article
-
Mark
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
-
Mark
Comparison of signal quality between EASI and Mason-Likar 12-lead electrocardiograms during physical activity.
(
- Contribution to journal › Article
-
Mark
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer
(
- Contribution to journal › Article
-
Mark
The need for oncogenetic counselling - Ten years' experience of a regional oncogenetic clinic
(
- Contribution to journal › Article
-
Mark
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
(
- Contribution to journal › Article
-
Mark
Wilms tumors develop through two distinct karyotypic pathways.
(
- Contribution to journal › Article
-
Mark
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
-
Mark
Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients
(
- Contribution to journal › Article
-
Mark
Establishment and phenotypic characterization of human U937 cells with inducible P210 BCR/ABL expression reveals upregulation of CEACAM1 (CD66a).
(
- Contribution to journal › Article
-
Mark
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
(
- Contribution to journal › Article
-
Mark
Sequential cytogenetic and molecular cytogenetic characterization of an SV40T-immortalized nasopharyngeal cell line transformed by Epstein-Barr virus latent membrane protein-1 gene
(
- Contribution to journal › Article
-
Mark
External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 years
(
- Contribution to journal › Article
-
Mark
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma
(
- Contribution to journal › Article
-
Mark
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
(
- Contribution to journal › Article
-
Mark
Cytogenetic and fluorescence in situ hybridization characterization of clonal chromosomal aberrations and CCND1 amplification in esophageal carcinomas
(
- Contribution to journal › Article
-
Mark
Sudanesiska cytogenetiker - vision om en ny form av bistånd
(
- Contribution to journal › Article
-
Mark
Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
(
- Contribution to journal › Article
-
Mark
Genetic analyses of multiple myeloma and related plasma cell dyscrasias
2004)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetisk rådgivning och fosterdiagnostik.
2004) p.56-56(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Molecular Characterization of Genomic Amplifications in Pancreatic Cancer
2004)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Regulation of genetic testing in clinical practice
(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Studies on Molecular Genetics of B cell Development
2004)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Characterization of Genetic Abnormalities at Disease Progression of Chronic Myeloid Leukemia
2004)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic characterization of bone and soft tissue tumors
(
- Contribution to journal › Article
-
Mark
Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas.1
(
- Contribution to journal › Article
-
Mark
A model for karyotypic evolution in testicular germ cell tumors.
(
- Contribution to journal › Article
-
Mark
Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.
(
- Contribution to journal › Article
-
Mark
Approximate geodesic distances reveal biologically relevant structures in microarray data
(
- Contribution to journal › Article
-
Mark
Vascular endothelial growth factor gene polymorphisms and pre-eclampsia
(
- Contribution to journal › Article
-
Mark
Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells
(
- Contribution to journal › Article
-
Mark
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
(
- Contribution to journal › Article
-
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.
(
- Contribution to journal › Article
-
Mark
Tumor karyotype predicts clinical outcome in colorectal cancer patients
(
- Contribution to journal › Article
-
Mark
Hoxb4-deficient mice undergo normal hematopoietic development but exhibit a mild proliferation defect in hematopoietic stem cells
(
- Contribution to journal › Article
-
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).
(
- Contribution to journal › Article