نتایج جستجو برای: X-linked diseases

تعداد نتایج: 1596385  

Journal: :iranian journal of basic medical sciences 0
amir abbas rahimi molecular medicine department, pasteur institute of iran, tehran, iran mohammad hassan shahhosseiny department of microbiology, islamic azad university, shahr-e- qods branch, tehran, iran ghasem ahangari medical biotechnology department, national institute of genetic engineering and biotechnology, tehran, iran jalal izadi mobarakeh department of pharmacology, tehran medical science branch, islamic azad university, tehran, iran

objective(s):to determine the fetal discernment in suspected cases of sex linked recessive disease in the first trimester of pregnancy. materials and methods: after collection of 100 chorionic villi samples, the dnas were extracted and baby gender was determined. meanwhile, after increasing the sensitivity, the system was able to detect the sex of each cell which was obtained by biopsy. results...

Journal: :Genetics in Medicine 2020

Journal: :jentashapir journal of health research 0
sahar baheri physiology research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran ghasem saki physiology research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; physiology research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran. tel/fax: +98-6113332036 javad mohammadi asl department of genetics, faculty of medicine, ahvaz jundishapur university of medical sciences, ahvaz, ir iran ali khodadadi department of immunology, faculty of medicine, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

conclusions albumin gradient method is the enrichment of y-bearing chromosome sperms. separation of spermatozoa by albumin gradient method, introduced by ericsson, is a suitable method for sex selection of male offspring. this technique is safe, because it neither requires toxic materials during sperm separation, nor involves embryo manipulation. objectives the study aimed to assess the separat...

Journal: :Clinical & Experimental Immunology 2008

Journal: :genetics in the 3rd millennium 0
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Objective(s):To determine the fetal discernment in suspected cases of sex linked recessive disease in the first trimester of pregnancy. Materials and Methods: After collection of 100 Chorionic Villi samples, the DNAs were extracted and baby gender was determined. Meanwhile, after increasing the sensitivity, the system was able to detect the sex of each cell which was obtained by biopsy. Resul...

Journal: :international clinical neurosciences journal 0
mahdi taherian food and drug administration, reference laboratory for food and drug control, tehran, iran. hossein maghsoudi department of biology, payame noor university, tehran, iran. kazem bidaki department of biology, payame noor university, tehran, iran. reza taherian students' research committee, school of medicine, shahid beheshti university of medical sciences, tehran, iran.

x-chromosome inactivation (xci) is a process by which one of the copies of the x chromosome in mammalian female cells is inactivated. the xci causes a balanced x-linked gene quantity between male and females; moreover, it results mosaic females which have paternal active x in some cells and maternal active x in others. cellular mosaicism is a noteworthy phenomenon and lowers the risk of x-linke...

Journal: :iranian journal of allergy, asthma and immunology 0
bahram mir saeid ghazi asghar aghamohammadi ali kouhi abolhassan farhoudi mostafa moin nima rezaei

primary immunodeficiencies (pid) are a group of disorders, characterized by an unusual susceptibility to infections. delay in diagnosis results in increased morbidity and mortality in affected patients. the purpose of this study was to determine the mortality rate of iranian immunodeficient patients referred to children medical center hospital affiliated to tehran university of medical sciences...

Journal: :Endocrines 2022

Since phosphate is indispensable for skeletal mineralization, chronic hypophosphatemia causes rickets and osteomalacia. Fibroblast growth factor 23 (FGF23), which mainly produced by osteocytes in bone, functions as the central regulator of metabolism increasing renal excretion suppressing production 1,25-dihydroxyvitamin D. The excessive action FGF23 results hypophosphatemic diseases, include a...

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