نتایج جستجو برای: molecular diagnostic
تعداد نتایج: 904784 فیلتر نتایج به سال:
leptospirosis is a zoonotic disease with global distribution that caused by pathogenic spirochetes of the genus leptospira. accurate diagnosis for differentiation of leptospirosis from other pyrogenic infections prevailing in the same locality and is imperative for proper treatment. therefore a molecular diagnostic test with high specificity and sensitivity such as pcr is essential. gene encodi...
the genus entamoeba contains many species, six of which (entamoeba histolytica, entamoeba dispar, entamoeba moshkovskii, entamoeba polecki, entamoeba coli, and entamoeba hartmanni) reside in the human intestinal lumen. entamoeba histolytica is the causative agent of amebiasis in humans with a worldwide distribution. correct detection of e.histolytica is frequently a major concern in diagnostic ...
The genus Entamoeba contains many species, six of which (Entamoeba histolytica, Entamoeba dispar, Entamoeba moshkovskii, Entamoeba polecki, Entamoeba coli, and Entamoeba hartmanni) reside in the human intestinal lumen. Entamoeba histolytica is the causative agent of amebiasis in humans with a worldwide distribution. Correct detection of E.histolytica is frequently a major concern in diagnostic ...
به دلیل عوارض غیر قابل جبران توکسوپلاسموزیس در افراد دچار نقص سیستم ایمنی و نوزادان متولد شده از مادران آلوده، نیاز مبرم به تکنیک های سریع، حساس و دقیق برای شناسایی توکسوپلاسما گوندی احساس می شود. روش های مولکولی به عنوان روش های حساس تر و اختصاصی-تر از رو ش های سرولوژیک در تشخیص توکسوپلاسموزیس مطرح هستند. در این مطالعه، استفاده از روش real-time nasba برای سنجش کمی بار انگلی در خون ر ت های آلو...
Objective(s): Mutations in the UGT1A1 gene are responsible for hyperbilirubinemia syndromes including Crigler-Najjar type 1 and 2 and Gilbert syndrome. In view of the genetic heterogeneity and involvement of large numbers of the disease causing mutations, the application of polymorphic markers in the UGTA1 gene could be useful in molecular diagnosis of the disease. Materials and Methods: In the...
Down syndrome is one of the most common causes of mental retardation observed in approximately 1/700 live birth. The use of two or more STR markers related to chromosome 21 facilitates the diagnosis of Down syndrome within about six hours from the collection of the samples. This is the first study has been performed in Iranian population to assess the diagnostic value of using small tandem repe...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید