Division of Clinical Genetics
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- 2008
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Mark
A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1.
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- Contribution to journal › Article
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Mark
When the genome plays dice: circumvention of the spindle assembly checkpoint and near-random chromosome segregation in multipolar cancer cell mitoses.
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- 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.
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- Contribution to journal › Article
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Mark
Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors.
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- Contribution to journal › Article
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Mark
The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1.
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- Contribution to journal › Article
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Mark
BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias.
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- Contribution to journal › Article
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Mark
Cytogenetic and molecular cytogenetic findings in lipoblastoma.
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- Contribution to journal › Article
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Regulatory Issues for Genetic Testing in Clinical Practice.
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- Contribution to journal › Article
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Increased sensitivity to bleomycin in upper aerodigestive tract mucosa of head and neck squamous cell carcinoma patients.
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- Contribution to journal › Article
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Mark
FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.
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- Contribution to journal › Article
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Mark
Recurrent and multiple bladder tumors show conserved expression profiles.
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- Contribution to journal › Article
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Mark
Binomial mitotic segregation of MYCN-carrying double minutes in neuroblastoma illustrates the role of randomness in oncogene amplification.
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- Contribution to journal › Article
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Mark
An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera
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- Contribution to journal › Article
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Mark
Exit of pediatric pre-B acute lymphoblastic leukaemia cells from the bone marrow to the peripheral blood is not associated with cell maturation or alterations in gene expression.
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- Contribution to journal › Article
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Mark
Classification of chromosome segregation errors in cancer.
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- Contribution to journal › Article
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Mark
Delection of the SCN gene cluster on 2q24.4 is associated with severe epilepsy an array-based genotype-phenotype correlation and a comprehensive review of previously published area
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- Contribution to journal › Article
- 2007
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Mark
Reduced high-frequency QRS components in electrocardiogram leads facing an area of the heart with intraventricular conduction delay due to bundle branch block.
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- Contribution to journal › Article
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Mark
Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).
(
- Contribution to journal › Article
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Mark
High-frequency electrocardiogram analysis in the ability to predict reversible perfusion defects during adenosine myocardial perfusion imaging.
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- Contribution to journal › Article
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Mark
Successful treatment of a child with t(15;19)-positive tumor.
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- Contribution to journal › Article
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Mark
Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations
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- Contribution to journal › Article
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Mark
Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome.
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- Contribution to journal › Article
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Mark
Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma
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- Contribution to journal › Article
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Mark
The molecular signature of MDS stem cells supports a stem-cell origin of 5q - myelodysplastic syndromes
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- Contribution to journal › Article
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Mark
Cytogenetic evolution patterns in CML post-SCT.
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- Contribution to journal › Article
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Mark
Distinct mitotic segregation errors mediate chromosomal instability in aggressive urothelial cancers.
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- Contribution to journal › Article
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Mark
Threshold-free high-power methods for the ontological analysis of genome-wide gene expression studies
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- Contribution to journal › Article
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Mark
A hypothesis-generating search for new genetic breast cancer syndromes - a national study in 803 Swedish families
(
- Contribution to journal › Article
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Mark
Defective chromosome segregation and telomere dysfunction in aggressive Wilms' tumors
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- Contribution to journal › Article
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Mark
Generation of human cortical neurons from a new immortal fetal neural stem cell line.
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- Contribution to journal › Article
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Mark
Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias.
(
- Contribution to journal › Article
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Mark
Discrepancies between estimated and perceived risk of cancer among individuals with hereditary nonpolyposis colorectal cancer
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- Contribution to journal › Article
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Mark
Telomere dysfunction and telomerase activation in cancer - a pathological paradox?
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- Contribution to journal › Article
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Mark
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype
(
- Contribution to journal › Article
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Mark
Proposals for standardized Protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes
(
- Contribution to journal › Article
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Mark
Tiling resolution array CGH of dic(7;9)(p11 approximately 13;p11 approximately 13) in B-cell precursor acute lymphoblastic leukemia reveals clustered breakpoints at 7p11.2 approximately 12.1 and 9p13.1.
(
- Contribution to journal › Article
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Mark
Response to letter by the ISCN standing committee
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- Contribution to journal › Letter
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Mark
Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3
(
- 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
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature
(
- Contribution to journal › Scientific review
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Mark
Report of an international survey of molecular genetic testing laboratories
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- Contribution to journal › Article
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Mark
Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera
(
- Contribution to journal › Article
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Mark
Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status.
(
- Contribution to journal › Article
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Mark
Bladder cancer, a two phased disease?
(
- Contribution to journal › Scientific review
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Mark
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
(
- Contribution to journal › Article
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Mark
On the Origin of Syn- and Metachronous Urothelial Carcinomas.
(
- Contribution to journal › Scientific review
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Mark
Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies
(
- Contribution to journal › Article
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Mark
Establishment of a cell line from a chemotherapy resistant diffuse large B-cell lymphoma
(
- Contribution to journal › Letter
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Mark
Comparison of the proximal promoter regions of the PAX3 and PAX7 genes
(
- Contribution to journal › Article
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Mark
Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.
(
- Contribution to journal › Scientific review
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Mark
Cytogenetic findings in pediatric renal cell carcinoma
(
- Contribution to journal › Article
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Mark
Fusion genes in angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
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Mark
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma
(
- Contribution to journal › Letter
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Mark
Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability.
(
- Contribution to journal › Article
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Mark
Germline E-cadherin mutations in familial lobular breast cancer
(
- Contribution to journal › Article
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Mark
Study of ATP-release from acoustically levitated eryhrocytes
(
- Contribution to journal › Published meeting abstract
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Mark
Brister i genetisk kunskap i vården?
2007) p.109-109(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Study of ATP-release from acoustically levitated eryhrocytes
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
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Mark
THE ANDROGEN RECEPTOR GGN POLYMORPHISM. Genetic and functional analyses.
(
- Thesis › Doctoral thesis (compilation)
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Mark
Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region
(
- Contribution to journal › Article
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Mark
Microarray analysis of gliomas reveals chromosomal position-associated gene expression patterns and identifies potential immunotherapy targets.
(
- Contribution to journal › Article
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Mark
Cancer stem cells: Differentiation block or developmental back-tracking?
(
- Contribution to journal › Letter
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Mark
Etisk argumentation och klinisk verklighet kan med fördel förenas.
(
- Contribution to journal › Article
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Mark
Papillomavirus type 16 E6/E7 and human telomerase reverse transcriptase in esophageal cell immortalization and early transformation
(
- Contribution to journal › Article
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Mark
Genetic variant of the human homologous recombination-associated gene RMI1 (S455N) impacts the risk of AML/MDS and malignant melanoma.
(
- Contribution to journal › Article
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Mark
Distinct evolutionary mechanisms for genomic imbalances in high-risk and low-risk neuroblastomas
(
- Contribution to journal › Article
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Mark
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
(
- Contribution to journal › Article
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Mark
Deregulation of the Wilms' tumour gene 1 protein (WT1) by BCR/ABL1 mediates resistance to imatinib in human leukaemia cells
(
- Contribution to journal › Article
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Mark
A case of Cornelia de Lange syndrome from Sudan
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- Contribution to journal › Article
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Mark
The impact of translocations and gene fusions on cancer causation.
(
- Contribution to journal › Scientific review
- 2006
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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
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Mark
Cross-platform classification in microarray-based leukemia diagnostics
(
- Contribution to journal › Article
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Mark
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
(
- Contribution to journal › Article
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Mark
Human short-term repopulating cells have enhanced telomerase reverse transcriptase expression.
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- Contribution to journal › Article
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Mark
Education in medical genetics for non-genetic health care providers in sweden.
(
- Contribution to journal › Article
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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
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Mark
High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.
(
- Contribution to journal › Article
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Mark
Handy book on cancer genetics risk assessment
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
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Mark
Expression profiling of Wilms tumors reveals new candidate genes for different clinical parameters
(
- Contribution to journal › Article
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Mark
Serial changes in the high-frequency ECG during the first year following acute myocardial infarction.
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- Contribution to journal › Article
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Mark
A gene fusion network in human neoplasia.
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- Contribution to journal › Article
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Mark
The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
(
- Contribution to journal › Article
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Mark
Fine-needle aspiration of neurilemoma (schwannoma). A clinicocytopathologic study of 116 patients
(
- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of the 11q13 amplicon in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
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Mark
Fusion of the Tumor-Suppressor Gene CHEK2 and the Gene for the Regulatory Subunit B of Protein Phosphatase 2 PPP2R2A in Childhood Teratoma.
(
- Contribution to journal › Article
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Mark
Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias
(
- Contribution to journal › Letter
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Mark
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.
(
- Contribution to journal › Article
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Mark
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2 : implications for formation and pathogenetic outcome of the idic(7)(p11.2)
(
- Contribution to journal › Article
-
Mark
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22)
(
- Contribution to journal › Article
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Mark
Detection of cell cycle- and differentiation stage-dependent human telomerase reverse transcriptase expression in single living cancer cells.
(
- Contribution to journal › Article
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Mark
Trisomy 19 as the sole chromosomal abnormality in proliferative chronic myelomonocytic leukemia
2006) In Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis 30(8). p.1043-1047(
- Contribution to journal › Article
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Mark
Cryptic terminal chromosome rearrangements in colorectal carcinoma cell lines detected by subtelomeric FISH analysis.
(
- Contribution to journal › Article
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Mark
Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer.
(
- Contribution to journal › Letter
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Mark
Deregulation of cyclin D2 by juxtaposition with T-cell receptor alpha/delta locus in t(12;14)(p13;q11)-positive childhood T-cell acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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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
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Mark
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene
(
- Contribution to journal › Article
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Mark
Genetic education for non-geneticist health professionals
(
- Contribution to journal › Article
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Mark
Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours
(
- Contribution to journal › Article
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Mark
Comparison of EASI-derived 12-lead electrocardiograms versus paramedic-acquired 12-lead electrocardiograms using Mason-Likar limb lead configuration in patients with chest pain
(
- Contribution to journal › Article
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Mark
C2028T polymorphism in exon 12 and dinucleotide repeat polymorphism in intron 13 of the HIF-1 alpha gene define HIF-1 alpha protein expression in non-small cell lung cancer
(
- Contribution to journal › Article