David Gisselsson Nord
Titel
docent, ST-läkare
Organisation
046-173418
0733-914036
David [dot] Gisselsson_Nord [at] med [dot] lu [dot] se
Publikationer (hämtat ur Lunds universitets publikationsdatabas)
författare
- 2013
- 2012
- Biphasic, Hyperdiploid Breast Tumors in Children: A Distinct Entity?
- Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney
- Copy Number Defects of G1-Cell Cycle Genes in Neuroblastoma are Frequent and Correlate with High Expression of E2F Target Genes and a Poor Prognosis
- Oncogenic activation of FOXR1 by 11q23 intrachromosomal deletion-fusions in neuroblastoma
- Prevalence of germline TP53 mutations and history of Li-Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: A population-based survey.
- SIX1 protein expression selectively identifies blastemal elements in Wilms tumor.
- Tumor-initiating cells in childhood neuroblastoma--letter.
- 2011
- Alternative lengthening of telomeres-An enhanced chromosomal instability in aggressive non-MYCN amplified and telomere elongated neuroblastomas.
- Aneuploidy in cancer: Sudden or sequential?
- High-resolution genomic profiling of an adult Wilms' tumor: evidence for a pathogenesis distinct from corresponding pediatric tumors.
- Intratumor diversity and clonal evolution in cancer-a skeptical standpoint.
- Mechanisms of Whole Chromosome Gains in Tumors - Many Answers to a Simple Question.
- Mutations in CEP57 cause mosaic variegated aneuploidy syndrome
- 2010
- Deletions of 16q in Wilms Tumors Localize to Blastemal-Anaplastic Cells and Are Associatedwith Reduced Expression of the IRXB Renal Tubulogenesis Gene Cluster.
- Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis.
- Genetic bottlenecks and the hazardous game of population reduction in cell line based research.
- Modeling the human 8p11-myeloproliferative syndrome in immuno-deficient mice.
- Modeling the human 8p11-myeloproliferative syndrome in immunodeficient mice
- 2009
- Bone Marrow Multipotent Mesenchymal Stroma Cells Act as Pericyte-like Migratory Vehicles in Experimental Gliomas.
- HIF-2 alpha maintains an undifferentiated state in neural crest-like human neuroblastoma tumor-initiating cells
- High-resolution imaging of mitotic instability
- High-resolution imaging of mitotic instability
- Low frequency of EWSR1 rearrangements in neoplasms classified as high-risk wilms tumors.
- Telomere length in neuroblastoma: a prognostic factor?
- 2008
- Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12
- Binomial mitotic segregation of MYCN-carrying double minutes in neuroblastoma illustrates the role of randomness in oncogene amplification.
- Classification of chromosome segregation errors in cancer.
- Glial Progenitor-Like Phenotype in Low-Grade Glioma and Enhanced CD133-Expression and Neuronal Lineage Differentiation Potential in High-Grade Glioma
- Glial progenitor-like phenotype in low-grade glioma and enhanced CD133-expression and neuronal lineage differentiation potential in high-grade glioma.
- High levels of HIF-2alpha highlight an immature neural crest-like neuroblastoma cell cohort located in a perivascular niche.
- High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.
- Tumor Specific Migration Of Bone-Marrow Derived Rat Mesenchymal Stem Cells In The Invasive N29 Rat Brain Tumor Model
- When the genome plays dice: circumvention of the spindle assembly checkpoint and near-random chromosome segregation in multipolar cancer cell mitoses.
- 2007
- A case of Cornelia de Lange syndrome from Sudan
- Cancer stem cells: Differentiation block or developmental back-tracking?
- Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma
- Defective chromosome segregation and telomere dysfunction in aggressive Wilms' tumors
- Distinct Mitotic Segregation Errors Mediate Chromosomal Instability in Aggressive Urothelial Cancers
- Distinct evolutionary mechanisms for genomic imbalances in high-risk and low-risk neuroblastomas
- Distinct mitotic segregation errors mediate chromosomal instability in aggressive urothelial cancers.
- Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability.
- Telomere dysfunction and telomerase activation in cancer - a pathological paradox?
- 2006
- A del(X)(p11) carrying SRY sequences in an infant with ambiguous genitalia
- Cryptic terminal chromosome rearrangements in colorectal carcinoma cell lines detected by subtelomeric FISH analysis.
- Female genital mutilation of a karyotypic male presenting as a female with delayed puberty
- Molecular cytogenetic characterization of the 11q13 amplicon in head and neck squamous cell carcinoma.
- 2005
- Connecting mitotic instability and chromosome aberrations in cancer-can telomeres bridge the gap?
- Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
- Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells
- Mitotic instability in cancer - Is there method in the madness?
- Statistical behavior of complex cancer karyotypes.
- Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
- Telomere-mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma
- 2004
- A model for karyotypic evolution in testicular germ cell tumors.
- Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
- Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
- Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
- Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
- Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
- Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
- Sudanesiska cytogenetiker - vision om en ny form av bistånd
- Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas.
- Wilms tumors develop through two distinct karyotypic pathways.
- 2003
- A novel fusion gene, SS18L1/SSX1, in synovial sarcoma.
- Chromosome instability in cancer: how, when, and why?
- Ovarian Carcinoma Develops through Multiple Modes of Chromosomal Evolution.
- Power law distribution of chromosome aberrations in cancer.
- Ring Y chromosome in an azoospermic male with short stature: additional evidence for a distinct ring Y syndrome in non-mosaic patients?
- 2002
- Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
- Coping with complexity. multivariate analysis of tumor karyotypes.
- Cytogenetic aberrations and their prognostic impact in chondrosarcoma.
- Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
- Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition.
- Multivariate analysis of chromosomal imbalances in breast cancer delineates cytogenetic pathways and reveals complex relationships among imbalances.
- Tumour morphology--interplay between chromosome aberrations and founder cell differentiation.
- 2001
- Abnormal nuclear shape in solid tumors reflects mitotic instability
- Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH
- ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization
- Limitations of chromosome classification by multicolor karyotyping
- Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution
- PLAG1 alterations in lipoblastoma: involvement in varied mesenchymal cell types and evidence for alternative oncogenic mechanisms
- Refined characterisation of chromosome aberrations in tumours by multicolour banding and electronic mapping resources
- Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
- 2000
- Chromosomal Instability and Genomic Amplification in Bone and Soft Tissue Tumours
- Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
- Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study
- Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia
- Putting chromosome aberrations on the map
- Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p
- 1999
- Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics
- The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
- Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics
- Variable stability of chromosomes containing amplified alpha-satellite sequences in human mesenchymal tumours
- 1998
- A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences
- Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma
- Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization
