نتایج جستجو برای: tetra arms
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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...
سابقه و هدف: ژن FGFR3 نقش مهمی در تنظیم رشد، تمایز و رگ زایی دارد. تغییرات ژنتیکی ژن FGFR3 یکی از عوامل موثر در ابتلا به سرطان مثانه می باشد. جهش های فعال FGFR3 در حدود 70% از تومورهای مثانه غیرمهاجم به عضله مشاهده شده است. هدف از این مطالعه بررسی ارتباط جهشT375C ژن FGFR3 درDNA ژنومی استخراجی از اپی تلیال ادرار و خطر سرطان مثانه می باشد. مواد و روشها: در این مطالعه مورد-شاهدی، تعداد 100 فرد...
Background: Type 2 diabetes is a metabolic disorder characterized by high blood sugar levels that can damage nerves. Many organs are affected ،especially the foot that leading to loss of sensation. These factors make favorable conditions for the development of diabetic foot ulcers. Polymorphisms (Thr399Ile) of Toll Like Receptor4 (TLR4) gene due to malfunction of TLR4 protein which plays an imp...
Introduction: Multiple sclerosis (MS) is an acute disease of the central nervous system (CNS) associated with the degradation of myelin sheet around the nerve cells. It is assumed to be a multifactorial disorder that is to say numerous environmental and genetic factors are involved in the disease. Therefore, this study aimed to investigate the association between rs1800624 single nucleotide pol...
Introduction: Nephrotic syndrome (NS) is a genetic disease belonging to a heterogeneous group of glomerular disorders, which mainly occurs within the children. Linkage analysis using single nucleotide polymorphisms (SNP) is used as an indirect method in molecular diagnosis of the disease. A large number of SNP markers have been introduced in NPHS2gene in the available electronic databases. M...
The receptor and the receptor axis CXCL12 / CXCR4 are the two pairs studied in the metastasis of breast cancer. The purpose of this study was to investigate the relationship between the occurrence of CXCR4 / CXCL12 genes polymorphism and the clinical and pathological characteristics of patients with metastatic breast cancer under chemotherapy. Material and methods: Genomic DNA was extracted f...
In the title compound, [Cu(C(6)H(5)O(3))(C(18)H(15)P)(2)]·C(18)H(15)P·CH(3)OH, the pyran-4-one ring is appromimately planar (r.m.s deviation = 0.0138 Å), with the Cu(I) atom 0.451 (5) Å out of the plane. The Cu(I) atom has a distorted tetra-hedral coordination. The O-Cu-O angle is 80.07 (8)° and the P-Cu-P angle is 123.49 (3)°. The crystal packing is stablized by intra-molecular C-H⋯O inter-act...
In the title compound, C(32)H(19)BN(6)O(2), the B atom adopts a BON(3) tetra-hedral coordination geometry. In the crystal, pairs of mol-ecules are associated through aromatic π-π stacking inter-actions between the concave faces of the boronsubphthalocyanine fragments at a centroid-centroid distance of 3.4951 (19) Å and a weaker inter-action of the same type between the convex faces of the same ...
چکیده سابقه و هدف سقط مکرر خودبه‌خودی، به ختم بارداری قبل از هفته 20 حاملگی اطلاق میشود. در برخی از زنان با سابقه سقط مکرر، جهشهای ژن ترومبوفیلیک منجر به ایجاد لختههای خونی در عروق جفت، کاهش اکسیژنرسانی و مرگ جنین میشود. هدف از این مطالعه، بررسی ارتباط پلیمورفیسمهای 807C/T (ژن GPIa) و pLA1/pLA2 (ژن GPIIIa) با سقط مکرر خودبه‌خودی بود. مواد و روشها در این مطالعه مورد - شاهدی، 50 خانم...
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