𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Deletion of a common region on the long arm of chromosome 6 in acute lymphoblastic leukaemia

✍ Scribed by Dr. Lia P. Menasce; Vassilis Orphanos; Mauro Santibanez-Koref; John M. Boyle; Christine J. Harrison


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
340 KB
Volume
10
Category
Article
ISSN
1045-2257

No coin nor oath required. For personal study only.

✦ Synopsis


We have characterised a region of deletion on the long arm of chromosome 6 (6q) in six cases of acute lymphobiastic leukaemia, by fluorescence in situ hybridisation, using a series of YAC clones which map to 6q. Conventional cytogenetic analysis of four of these cases had been interpreted as showing terminal deletions of 6q. We demonstrated by FISH that in all cases the deletions were interstitial. D6S246 (6q16.3) was the only marker which was missing in all six cases, indicating a common region of deletion between the markers M6P I at 6q 14-1 5 and FYN at 6q2I. Our results suggest the presence of a tumour suppressor gene within this interval. Genes Chrom Cancer 10:26-29 (1994).


πŸ“œ SIMILAR VOLUMES


Common region of deletion on the long ar
✍ Lia P. Menasce; Vassilis Orphanos; Mauro Santibanez-Koref; John M. Boyle; Dr. Ch πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 253 KB

## Abstract We have used fluorescence in situ hybridisation (FISH) with a series of yeast artificial chromosome (YAC) clones that map to the long arm of chromosome 6 (6__q__) to define the region(s) of deletion in seven cases of non‐Hodgkin's lymphoma (NHL), in which a deletion of 6q had been detec

Deletion of a portion of the long arm of
✍ Goldberg, Rosalie ;Fish, Bernard ;Ship, Arthur ;Shprintzen, Robert J. πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 English βš– 333 KB πŸ‘ 3 views

## Abstract We describe a 3‐year‐old male with deletion of part of 6q. The karyotype was 46,XY,del(6q) in both lymphocytes and skin fibroblasts. The patient had: frontal bossing, epicanthal folds, broad nasal bridge, apparently low‐set and posteriorly angulated ears, micrognathia, cardiac defects,

Fine mapping of a region of common delet
✍ Annet M. J. Voesten; Engelien H. Bijleveld; Andries Westerveld; Theo J. M. Hulse πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 214 KB πŸ‘ 2 views

Allelic loss on chromosome 10 is a frequent event in high grade gliomas. Earlier studies have shown that in most cases a complete copy of chromosome 10 is lost in the tumor. To define more accurately and specifically the region of common deletion on chromosome arm 10p, we have screened a large serie

Commonly deleted regions on the long arm
✍ Ken Sakata; Gen Tamura; Satoshi Nishizuka; Chihaya Maesawa; Yasushi Suzuki; Take πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 93 KB πŸ‘ 2 views

During an allelotype analysis of differentiated adenocarcinoma of the stomach, we observed frequent loss of heterozygosity (LOH) on several chromosomes including the long arm of chromosome 21 (21q). Therefore, we analyzed DNA isolated from 45 tumors for LOH at 10 loci on 21q by using polymorphic mic

Genetic alterations in localized prostat
✍ Alain Latil; Jean-Christophe Baron; Olivier Cussenot; Georges Fournier; Thierry πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 964 KB

Accumulation of mutations in oncogenes and tumor suppressor genes transforms a normal cell into a malignant cell by allowing it to escape from normal control of growth. In prostate tumorigenesis, the current model envisages specific mutations of the TP53 tumor suppressor gene and loss of loci, detec