Latest papers

Transformation of the 5q- syndrome to acute lymphoblastic leukemia: a report of two cases and review of the literature.

Systemic mastocytosis in a child with t(8;21) acute myeloid leukemia.

Cytogenetic and molecular characterization of a hepatosplenic T-cell lymphoma: report of a novel chromosomal aberration.

Comment concerning: Intraoperative 5-aminolevulinic-acid-induced fluorescence in meningiomas, Acta Neurochir DOl 1O.1007/s00701-010-0708-4, Intratumoral heterogeneity and fluorescence intensity in meningioma after 5-ALA pretreatment. FAU - Hefti, Martin AU - Hefti M LA - eng PT - Letter DEP - 20110130 PL - Austria TA - Acta Neurochir (Wien) JT - Acta neurochirurgica JID - 0151000 RN - 0 (Photosensitizing Agents) RN - 106-60-5 (Aminolevulinic Acid) SB - IM MHDA- 2011/07/21 06:00 PHST- 2010/11/11 [received] PHST- 2011/01/13 [accepted] PHST- 2011/01/30 [aheadofprint] AID - 10.1007/s00701-011-0950-4 [doi] PST - ppublish SO - Acta Neurochir (Wien). 2011 Apr;153(4):959-60. Epub 2011 Jan 30.

EZH2 promotes expansion of breast tumor initiating cells through activation of RAF1-β-catenin signaling.

Massive genomic rearrangement acquired in a single catastrophic event during cancer development.

Evaluation of Kras gene mutation and copy number gain in non-small cell lung cancer.

Association between genetic subgroups of pancreatic ductal adenocarcinoma defined by high density 500 K SNP-arrays and tumor histopathology.

Digital karyotyping reveals probable target genes at 7q21.3 locus in hepatocellular carcinoma.

Cytogenetic instability in childhood acute lymphoblastic leukemia survivors.

Baller-Gerold syndrome associated with dextrocardia.

Genetics and molecular biology of mesothelioma.

Exploring the molecular mechanisms of nickel-induced genotoxicity and carcinogenicity: a literature review.

First trimester screening--new directions for antenatal care?

Atypical cytogenetics in therapy-related myelodysplastic syndrome secondary to indolent B-cell lymphoma.

Familial occurrence of Turner syndrome: casual event or increased risk?

Concurrent occurrence of chronic lymphocytic thyroiditis with hypothyroidism and growth hormone deficiency in a Turner's syndrome patient.

[Ion channel dysfunction in pathogenesis of idiopathic epilepsies].

A review of the genotoxicity of 1,2-dichloroethane (EDC).

19p13.3 aberrations are associated with dysmorphic features and deviant psychomotor development.