نتایج جستجو برای: chromosome 5q21

تعداد نتایج: 119353  

Abstract A karyotypic study was performed on 12 Iranian local onion (Allium cepa L.) populations. A number of mitotic cells at metaphase stage for each population were prepared. Chromosomes of suitable mitotic cells were counted and various parameters, including long arm (L), short arm (S), total length of chromosome (TL), relative length of chromosome (RL), arm ratio (AR), r-value, total chro...

امین بخش, محمد, جبارپور بنیادی, مرتضی, حیدزاده, محمد, عمرانی, امید, نصیری, محبوبه, هاشمی, فضیله,

Background & Objective: Down syndrome is one of the most common chromosome aneuploidies causing mental retardation which occurs in approximately 1/230 pregnancies. It is usually caused by the presence of an extra chromosome 21. The aim of this study was to evaluate the simple PCR based DNA diagnostic method and also to determine the parental origin of the extra chromosome 21 in trisomal Down sy...

Background and Aims: Azoospermia factor (AZF) region of the Y-chromosome has several genes which are responsible for normal spermatogenesis. Microdeletions of these genes are associated with azoospermia and oligospermia. These microdeletions are too small to be detected by karyotyping. They can be easily identified using polymerase chain reaction. The aim of this study is to determine the frequ...

Journal: :international journal of reproductive biomedicine 0
mohammadreza dehghani elena rossi annalisa vetro gianni russo zahra hashemian orsetta zuffardi

background: in most mammals, sex is determined at the beginning of gestation by the constitution of the sex chromosomes, xy in males and xx in females. case: here we report an interesting case characterized by ambiguous genitalia and ovotestis in a newborn carrying an apparently female karyotype (46 xx). array comparative genomic hybridization (array-cgh) revealed an unbalanced rearrangement re...

Journal: :journal of cell and molecular research 0
masoud ranjbar roya karamian fatemeh hajmoradi

the genus onobrychis belongs to family fabaceae and has about 130 species throughout the world. onobrychis sect. hymenobrychis with nearly 14 species in iran is one of the important sections of the genus. the chromosome number and meiotic behaviour were studied in two populations of onobrychis chorassanica belonging to this section native to iran. this report is the first cytogenetic analysis o...

ژورنال: علمی شیلات ایران 2013
خسروانی زاده, علی, نوروزفشخامی, محمدرضا, پورکاظمی, محمد,

The chromosomal spread and karyotype of Spirlin (Alburnoides bipunctatus) from Zabol region were identified using tissue squashing techniques with injection of 0.5ml/100g body weight of 0.01% Colchicines solution in fish fingerlings. Kidney and gill tissues were extracted and chopped in KCl 0.075M for 30 min and fixed in Carnoy solution in 3 stages. The chromosomal spreads were stained in 20% G...

Journal: :molecular biology research communications 2013
mozhgan sedigh-ardekani iraj saadat mostafa saadat

propranolol (pl), a non-selective beta-blocker, is a cardiovascular drug widely used to treat hypertension. the present study was concerned with assessing the cytogenetic effects of this drug on chinese hamster ovary (cho) cell line. mtt assay was then carried out to determine the cytotoxicity index (ic50) of the drug. the ic50 value of pl was 0.43±0.02 mm. to investigate the clastogenic effect...

ژورنال: :مجله گیاهشناسی ایران 1999
سید رضا صفوی

مشاهدات کروموزومی 16 نمونه متعلق به 12 گونه گزارش می شود. شش گونه از گونه های مذکور برای این اولین بار شمارش کروموزومی شده اند. همچنین رفتار کروموزومی در تقسیم میتوز گونه ها مورد توجه قرار گرفته است.

E. Rezvannejad M. Rashki M. Yaghoobi

Body weight (BW) and carcass traits are complex and important economic traits that may benefit from the implementation of MAS. The objective of the current study was to identify QTL associated with BW and carcass traits in an experimental half-sib cross of Japanese quails selected for BW at 4 weeks of age. Body weight and carcass traits were measured in the F2 population. Total F2 individuals a...

Asadi F, Ghaheri A, Reihani-Sabet F Roodgar Saffari J Sadighi Gilani MA Zamanian MR,

Background: Microdeletions of the long arm of the chromosome Y are the most common molecular genetic cause of severe infertility in men which affect three regions of AZFa, AZFb and AZFc (Azoospermia factor). These regions contain various genes involved in spermatogenesis. The effect of ethnicity on the patterns of Y chromosome microdeletions has not been extensively studied, particulary in Iran...

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