نتایج جستجو برای: chromosomal sensitivity

تعداد نتایج: 380653  

Journal: :Asian Pacific journal of cancer prevention : APJCP 2008
M Ayati V Najjaran Tousi T Sabokba H Vaziri-Nasab F Mehrkhani H Jamshidian J Dastan A R Mosavi-Jarrahi S R Ghaffari

Urinary cells obtained from voided urine specimens of 46 patients with urothelial carcinomas (UCs) and 10 normal individuals were analyzed with 3 different centromeric fluorescence in situ hybridization (FISH) probes. The overall sensitivity of cytology was 48.9% compared to 95.7%with the FISH technique. The minimum values were found for stage Ta and grade 1 (90.5 and 89.4) and sensitivity of F...

Journal: :Indian Scientific Journal Of Research In Engineering And Management 2023

Natural genetic material may help identify abnormalities and provide insight into the workings of gene expression systems. Disorders associated with chromosomal include single nucleotide polymorphisms (SNPs), minor insertions deletions, significant aberrations. In order to analyse DNA sequences, one most important components biological study, various techniques have been used. Thus, analysis co...

Journal: :iranian journal of pathology 2006
iran rashidi javad mohammadi asl

objective: approximately 15-20% of clinically recognizable pregnancies end in spontaneous abortion. the incidence of chromosomal abnormalities in those abortions is as high as 50%.a modest but clinically important proportion of spontaneous abortions is caused by a balanced chromosomal aberration in one of the parents. this results from the production of gametes and embryos with unbalanced chrom...

Journal: :iranian journal of pathology 2013
akbar safaei mohamad reza farzaneh sadat noori

background and objective: failure to thrive (ftt) is a sign that describes a particular problem rather than a diagnosis and explain growth failure or more advanced failure to gain weight appropriately. the aim of this study was to determine the prevalence and type of chromosomal abnormalities in patients presented with ftt. materials and method: one hundred ftt cases with clinical impression o...

Journal: :Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2014
Thanawan Ratanasiri Thawalwong Ratanasiri Ratana Komwilaisak Piyamas Saksiriwuttho

OBJECTIVE To assess the value of second trimester genetic ultrasound for screening of Down syndrome conducted at Srinagarind Hospital, Khon Kaen, Thailand. MATERIAL AND METHOD The present study sample comprised of 4,033 pregnant women at high risk forfetal chromosomal abnormality, from 17th to 23th week, who had performed second trimester genetic ultrasound before genetic amniocentesis betwee...

Journal: :مجله دانشگاه علوم پزشکی شهرکرد 0
داریوش فاتحی daryoush fatehi

due to importance of combination therapies in cancer treatment, this study was performed to find the effects of hyperthermia and neutron irradiation and heir combination on the human lymphocytes. blood samples were treated separately with 41.5 °c for 30 and 60 minutes, 43 °c for 15 and 30 minutes, as well as 10 cgy neutron irradiation. they also treated with hyperthermia followed by irradiation...

A AMINI, MH . BADAKHSH, SH DADGAR, SR DADGAR,

Early identification of fetuses with chromosomal abnormalities enables health care providers to form an appropriate management plan for each patient. The main objective of this study was to determine the role of ultrasonography in screening and identifying fetuses at risk for chromosomal abnormalities. A retrospective review of 6480 patients from the Obstetrics and Gynecology ward of Firou...

One of the major causes of spontaneous abortion before the fourth month of pregnancy is chromosomal abnormalities. We report an unusual case of a familial balanced chromosomal translocation in a consanguineous couple who experienced 4 spontaneous abortions. Chromosomal studies were performed on the basis of G-banding technique at high resolution and revealed 46, XX, t (16 6) (p12 q26) and 46, X...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 1995
J K Wiencke S Pemble B Ketterer K T Kelsey

Genetic traits that confer increased susceptibility to DNA and chromosomal damage from reactive epoxide and peroxides could be important individual risk factors in the development of human cancers. To provide an index of individual sensitivity to expoxides, we previously studied sister chromatid exchange (SCE) induction in peripheral blood lymphocytes and identified a trait involving sensitivit...

Journal: :Haematologica 2013
Terry J Gaymes Azim M Mohamedali Miranda Patterson Nazia Matto Alexander Smith Austin Kulasekararaj Rajani Chelliah Nicola Curtin Farzin Farzaneh Sydney Shall Ghulam J Mufti

Inactivation of the DNA mismatch repair pathway manifests as microsatellite instability, an accumulation of mutations that drives carcinogenesis. Here, we determined whether microsatellite instability in acute myeloid leukemia and myelodysplastic syndrome correlated with chromosomal instability and poly (ADP-ribose) polymerase (PARP) inhibitor sensitivity through disruption of DNA repair functi...

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