نتایج جستجو برای: Tandem

تعداد نتایج: 54806  

Journal: :مجله دانشکده پزشکی دانشگاه علوم پزشکی تهران 0
حسن توفیقی tofighi h حسین حسنیان مقدم hassanian moghaddam h معصومه ناجی naji m افروز نیکبخت دهکردی nikbakht dehkordi a هادی نمازی namazi h

dna typing is a new method with important applications in forensic medicine. in the present study, we evaluated application of dna typing in iran. loci hum lpl, hum tpox, hum f13, hum vw 31a, hum th01 and hum fes/fps of dna short tandem repeats were studied. to determine sensitivity of the test, 85 mother-child couples (1020 chromosomes) that were referred to dna section of legal medicine organ...

Journal: :journal of industrial engineering, international 2009
e miandoabchi r zanjirani farahani

a tandem agv configuration connects all cells of a manufacturing area by means of non-overlapping, sin-gle-vehicle closed loops. each loop has at least one additional p/d station, provided as an interface between adjacent loops. this study describes the development of three tabu search algorithms for the design of tandem agv systems. the first algorithm was developed based on the basic definiti...

Journal: :iranian journal of child neurology 0
shadab salehpour assistant professor of pediatric endocrinology and fellowship of bone and inherited metabolic disorders, shahid beheshti university of medical sciences, tehan, iran

a clinical presentation of a metabolic disorder, often first seen in infants who present with poor feeding, vomiting, tachypnea, acidosis, hyperammonemia, ketosis, ketonuria, irritability, and convulsions or hypotonia and lethargy, findings that are otherwise suggestive of neonatal sepsis diseases with oa isovaleric and propionic acidemias, maple syrup urine disease, medium chain acyl dehydroge...

Journal: :iranian biomedical journal 0
morteza bagheri isa abdi rad nima hosseini jazani rasou zarrin ahad ghazavi

background: the variable numbers of tandem-repeat (vntr) alleles at the phenylalanine hydroxylase (pah) gene have been used in carrier detection and prenatal diagnosis in phenylketonuria families. this study was carried out to analyze vntr alleles at the pah gene in iranian azeri turkish population. methods: in this study, 200 alleles from general population were studied by pcr. results: the fr...

Journal: :journal of family and reproductive health 0
habib nasiri department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i jila dastan iranian fetal medicine foundation, tehran, iran mohammad hasan seifi school of medicine, iran university of medical sciences, tehran, iran noori dalooi department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i saeed reza ghaffari department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i

objective: classic cell culture and karyotyping is routinely used for prenatal detection of different chromosomal abnormalities. molecular cytogenetic techniques have also recently been developed and used for this purpose. quantitative florescence pcr using short tandem repeat (str) markers has more potential for high throughput diagnosis. marker heterozygosity in short tandem repeats (str) is ...

Journal: :international journal of hematology-oncology and stem cell research 0
marjan yaghmaie medical genetics department, faculty of medical sciences, tarbiat modares university, tehran, iran hossein mozdarani medical genetics department, faculty of medical sciences, tarbiat modares university, tehran, iran kamran alimoghaddam hematology, oncology and stem cell transplantation research center, shariati hospital, tehran university, tehran, iran ardeshir ghavamzadeh hematology, oncology and stem cell transplantation research center, shariati hospital, tehran university, tehran, iran seyed hamiollah ghaffari hematology, oncology and stem cell transplantation research center, shariati hospital, tehran university, tehran, iran

introduction: the secondary genetic changes other than the pml-rara fusion gene may contribute to the acute promyelocytic leukemogenesis. chromosomal alterations and mutation of flt3 tyrosine kinase receptor are the frequent genetic alterations in acute myeloid leukemia (aml). however, the prognostic significance of flt3 mutations in acute promyelocytic leukemia (apl) is not firmly established....

Journal: :international journal of advanced design and manufacturing technology 0
ahmad haghani department of mechanics, faculty of engineering, shahrekord branch, islamic azad university, shahrekord, iran

strip tearing during cold rolling process has always been considered among the main concerns for steel companies. several works have been done so far regarding the examination of the issue. in this paper, experimental data from cold rolling tandem mill is used for detecting strip tearing. sensors are placed across the cold rolling tandem mill. they receive information on parameters (such as ang...

Journal: :middle east journal of cancer 0
hind dehbi genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco yaya kassogue genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco sanaa nasserddine genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco asma quessar department of onco-hematology, ibn rochd university hospital, casablanca, morocco sellama nadifi genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco

background :according to numerous studies, fms-like tyrosine kinase 3, internal tandem duplication, and the d835 mutation are associated with a poor prognostic clinical outcome in acute myeloid leukemia patients. detection of the fms-like tyrosine kinase 3 mutation in patients who present with normal karyotype acute myeloid leukemia helps in both the understanding of the disease and the treatme...

Journal: :avicenna journal of medical biotechnology 0

background: classification of molar gestation into complete hydatidiform mole (chm) and partial hydatidiform mole (phm) is done according to clinical, ultrasonographic, histologic and genetic criteria. however, making a distinction between chm and phm using histologic criteria alone may be difficult and several studies have shown that misclassifications are frequent, even for experienced pathol...

E Miandoabchi R Zanjirani Farahani

A tandem AGV configuration connects all cells of a manufacturing area by means of non-overlapping, sin-gle-vehicle closed loops. Each loop has at least one additional P/D station, provided as an interface between adjacent loops. This study describes the development of three tabu search algorithms for the design of tandem AGV systems. The first algorithm was developed based on the basic definiti...

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