نتایج جستجو برای: chromosome 9

تعداد نتایج: 593632  

2006
Irene Orlow Pilar Lianes Louis Lacombe Guido Dalbagni Victor E. Reuter Carlos Cordon-Cardo

Chromosome 9 allelic losses have been reported as a frequent and early eventoccurringin bladdercancer.It hasbeenpostulatedthata candidate tumor suppressor gene may reside on this chromosome, alterations of which may lead to the development of a subset of superficial bladder tumors.Morerecently,theinvolvementoftwo differentregionsharboring suppressor loci, one on each of both chromosome 9 arms, ...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان کرمانشاه 1370

cml in breif cml is characterized by the proliferation of large numbers of immature wbc in the blood and bone marrow. in most of the patients , it is a clonal disorder in which all cell lines, express the philadelphia chromosome)q/22 translocation(it accounts for 20 of all leukemias and most cases occur over 25 yrs of age. the disease usually begins insidiously,but symptoms referable to anemia ...

2001
Bor-Yaw Lin S.-J. Chang H.-M. Lin

The centromere of chromosomes 1, 6 and 9 are physically mapped by the hypoploids of the six most proximal B-A translocations. The hypoploids are deficient for a paternal chromosome arm and, as a result, lose the paternal signal of those RFLP markers located on the missing chromosome arm. Of those markers missing from the hypoploids, the two most proximal ones on each arm of a chromosome define ...

Journal: :Blood 1984
R Bernstein M R Pinto J Rosendorff S Kramer B Mendelow

Two patients with chronic myeloid leukemia (CML) showed previously undescribed variants of a "masked" Ph1 abnormality. The first patient had the karyotype 46,XY, + 21, -9, -22, +mar9,mar18 at presentation in the chronic phase. The dicentric marker 9 was interpreted as representing the usual translocation of 22q11 to 9q34, followed by translocation of the Ph1 chromosome (the deleted 22) to 9p an...

Journal: :Blood 1990
C M Morris N Heisterkamp M A Kennedy P H Fitzgerald J Groffen

Leukemic cells from a patient with Ph-negative chronic myeloid leukemia (CML) had a normal karyotype. M-BCR was rearranged and chromosome in situ hybridization showed an ABL insertion between 5' and 3' M-BCR on an apparently normal chromosome 22. The association of 5' BCR and 3' ABL at the 5' junction of the chromosome 9 insert was typical of that found for the BCR-ABL fusion gene in other pati...

Journal: :Genetics 2000
O Riera-Lizarazu M I Vales E V Ananiev H W Rines R L Phillips

In maize (Zea mays L., 2n = 2x = 20), map-based cloning and genome organization studies are often complicated because of the complexity of the genome. Maize chromosome addition lines of hexaploid cultivated oat (Avena sativa L., 2n = 6x = 42), where maize chromosomes can be individually manipulated, represent unique materials for maize genome analysis. Maize chromosome addition lines are partic...

Journal: :Genetics 1997
T Foote M Roberts N Kurata T Sasaki G Moore

Detailed physical mapping of markers from rice chromosome 9, and from syntenous (at the genetic level) regions of other cereal genomes, has resulted in rice yeast artificial chromosome (YAC) contigs spanning parts of rice 9. This physical mapping, together with comparative genetic mapping, has demonstrated that synteny has been largely maintained between the genomes of several cereals at the le...

Journal: :Anticancer research 2012
Tamas Beothe Anetta Nagy Laszlo Farkas Gyula Kovacs

BACKGROUND Mutation of the p53 gene has been implicated in the development of carcinoma in situ (CIS) to invasive solid urothelial carcinomas (UC) whereas loss of heterozygosity (LOH) at chromosome 9 has been suggested to plag part in the development of papillary UCs. PATIENTS AND METHODS The p53 mutation and LOH at chromosomes 17p13.1 and 9 were analysed in 120 UCs. Tumor and matched normal ...

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