BACKGROUND Breast cancer and skin cancer rates among patients with Parkinson's disease are higher than in non-Parkinson's disease cases, and Jewish-Ashkenazi LRRK2*G2019S mutation carriers have higher breast cancer rates than noncarriers. Because additional Parkinson's disease predisposition genes are implicated in the malignant transformation process, we hypothesized that the association betwe...

A t(5;12)(q33;p13) translocation is a recurrent chromosome abnormality in a subgroup of myeloid malignancies with features of both myeloproliferative disorders and myelodysplastic syndromes (MDSs). The molecular consequence of a t(5;12) is a fusion between the platelet-derived growth factor receptor-B gene on chromosome 5 and a novel ETS-like gene, TEL, on chromosome 12. We report on three pati...

pericentric inversions of chromosome 9 are among the most frequent chromosomal rearrangement in human. a few cytogeneticists consider inversions of chromosome 9 as a normal variant. however, many reports in the recent literature link pericentric inversions of chromosome 9 with infertility, recurrent abortions, and a number of other abnormal conditions. we report a case of homozygosity pericentr...

A prospective study was performed to investigate changes in metal levels and chromosome aberrations in patients within 2 years of receiving metal-on-metal hip arthroplasties. There was a statistically significant increase of cobalt and chromium concentrations, with a small increase in molybdenum, in whole blood at 6, 12, and 24 months after surgery. There was also a statistically significant in...

The technique of chromosome-in-situ suppression (CISS)-hybridization (chromosome painting) has now been well established. However, all standard protocols so far require long renaturation times (typically 12 hours and more). Here, we describe a new, extremely fast protocol for chromosome painting using a commercially available, directly fluorescence labelled probe for chromosome 8. The hybridiza...

To refine the chromosomal localization of a putative tumor suppressor gene, we analyzed the loss of heterozygosity (LOH) of chromosome 12 in 36 primary non-small cell lung cancer (NSCLC) samples with matched normal DNA using 22 highly informative polymorphic markers. Twelve cases showed LOH at one or more loci on chromosome 12. LOH of chromosome arm 12p was more frequent in large cell carcinoma...

Writ/i the technical assistance of Miss Lila Fliegelnian O CCASIONAL REPORTS have presemited cytogenetic data from cases of megaloblastic anemia.ii,uul Although no consistemit cytogenetic abnormalities have yet beeii found, a variety of changes have been described in some cases of pernicious anemia.m’ ’m” The significance of these findings is not clear. This report describes cytogenetic observa...

Caryological studies were carried out on ten species of the genus Suaeda belonging to 27 samples of different populations in Iran. Important chromosome features including numbers, lengths, centromere locations and caryotypes were studied. All the species have basic chromosome numbers of x=9. Chromosome counts of S. acuminata (C.A.Mey.) Moq. (2n=18), S. aegyptiaca (Hasselq.) Zoh., (2n=l8)...

This paper reports on the karyotyping of mullet fish species, Liza klunzingeri, endemic of the Persian Gulf. The metaphase chromosome spreads, obtained from kidney cells of 13 specimens were examined. The diploid chromosome number was found to be 2n=48. The karyotype was discovered to be consisted of 48 acrocentric chromosome pairs. The arm number was determined to be NF=48. The chromosome numb...