D Gisselsson
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Explore the profile of D Gisselsson including associated specialties, affiliations and a list of published articles.
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36
Citations
713
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Recent Articles
1.
Santo E, Ebus M, Koster J, Schulte J, Lakeman A, van Sluis P, et al.
Oncogene
. 2011 Aug;
31(12):1571-81.
PMID: 21860421
Neuroblastoma tumors frequently show loss of heterozygosity of chromosome 11q with a shortest region of overlap in the 11q23 region. These deletions are thought to cause inactivation of tumor suppressor...
2.
Gisselsson D
Cytogenet Genome Res
. 2010 Dec;
133(2-4):190-201.
PMID: 21124017
Whole chromosome gain is the most common type of gross genomic abnormality observed in human tumors. It is particularly frequent in lympho-haematopoietic and embryonic neoplasms, where trisomies and tetrasomies are...
3.
Gebre-Medhin S, Broberg K, Jonson T, Gorunova L, Vult von Steyern F, Brosjo O, et al.
Cytogenet Genome Res
. 2009 May;
124(2):121-7.
PMID: 19420923
Giant cell tumor of bone (GCTB) is characterized cytogenetically by frequent telomeric associations (tas). To explore the mechanisms behind the formation of tas in GCTB and to investigate their karyotypic...
4.
Pietras A, Gisselsson D, Ora I, Noguera R, Beckman S, Navarro S, et al.
J Pathol
. 2008 Jan;
214(4):482-8.
PMID: 18189331
High HIF-2alpha protein levels in the sympathetic nervous system-derived childhood tumour neuroblastoma as well as immature phenotype correlate to unfavourable outcome. Here we show that a small subset of perivascularly...
5.
Davidsson J, Collin A, Oreberg M, Gisselsson D
Clin Genet
. 2007 Nov;
73(1):44-9.
PMID: 18005181
Supernumerary ring chromosomes (SRC) account for approximately 10% of prenatal marker chromosomes and 60% of these SRCs are associated with an abnormal phenotype of the patient carrying them. SRCs have,...
6.
Calcagnile O, Gisselsson D
Cytogenet Genome Res
. 2007 Nov;
118(2-4):270-6.
PMID: 18000380
Telomerase is expressed in more than 90% of human cancers. Telomere maintenance by this enzyme is believed to safeguard genomic integrity in neoplastic cells. Nevertheless, many telomerase-expressing tumours exhibit chromosomal...
7.
Glanz C, Rebetz J, Stewenius Y, Persson A, Englund E, Mandahl N, et al.
Neuropathol Appl Neurobiol
. 2007 Jul;
33(4):440-54.
PMID: 17617873
Glioblastoma multiforme (GBM) and other high-grade brain tumours are typically characterized by complex chromosome abnormalities and extensive intratumour cytogenetic heterogeneity. The mechanisms behind this diversity have been little explored. In...
8.
Jin C, Jin Y, Gisselsson D, Wennerberg J, Wah T, Stromback B, et al.
Cytogenet Genome Res
. 2006 Oct;
115(2):99-106.
PMID: 17065789
Amplification of 11q13 DNA sequences and overexpression of CCND1 are common findings in head and neck squamous cell carcinoma (HNSCC), identified in about 30% of the cases. However, little is...
9.
Stewenius Y, Tanke H, Wiegant J, Gisselsson D
Cytogenet Genome Res
. 2006 Sep;
114(3-4):257-62.
PMID: 16954663
Epithelial tumour karyotypes are often difficult to study by standard cytogenetic methods because of poor chromosome preparation quality and the high complexity of their genomic rearrangements. Subtelomeric fluorescence in situ...
10.
Ellaithi M, Gisselsson D, Nilsson T, Abd El-Fatah S, Ali T, Elagib A, et al.
BMC Pediatr
. 2006 Apr;
6:11.
PMID: 16594994
Background: SRY (sex-determining region, Y) is the gene responsible of gonadal differentiation in the male and it is essential for the regular development of male genitalia. Translocations involving the human...