نتایج جستجو برای: پروتوپورفیرین ix
تعداد نتایج: 18979 فیلتر نتایج به سال:
A series of non-cyclic polyethers with different end groups and chain length were used for the extraction of lithium salt from aqueous into various organic phases viz. Chloroform, Carbon tetrachloride, 1,2-dichloroethane, to study the influence of structural variations within the extractant molecule upon the extraction selectivity and efficiency. The ionophores used were viz. DEG (I), DEGDME (I...
Background: Bernard-Soulier syndrome is a rare inherited bleeding disease caused by quantitative or qualitative defect of GPIb/IX/V, a platelet complex that binds the Von Willebrand factor. The expression of GPIb-IX-V complex can be evaluated by flow cytometry and confirmed by the absence of ristocetin-induced platelet aggregation in platelet-rich plasma. The main aim of the present study was t...
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بررسی تنوع ژنتیکی مارکر rs438601در جمعیت اصفهان: یک مارکر آگاهیدهنده در تشخیصهای مولکولی هموفیلی B
Introduction: Hemophilia B is an X-linked recessive genetic disease caused by mutations in the coagulation Factor IX gene. Mutations in the Factor IX gene result in dysfunction or deficiency of coagulation factor of IX. Direct mutation analysis involves the ideal method for molecular diagnosis of the disease. However, due to the high number of identified mutations in the gen, the lack of a comm...
To determine the functional role of the metal-dependent conformational changes in Factor IX, two populations of conformation-specific anti-Factor IX antibodies were prepared. Anti-Factor IX X Mg(II) antibodies bind to Factor IX in the presence of Mg(II) and other metal ions, but not in the absence of metal ions. Anti-Factor IX X Ca(II)-specific antibodies bind to Factor IX in the presence of Ca...
Previous genetic and biochemical studies led to the identification of two large RNase T1-resistant oligonucleotides, designated the G(IX) (+) and G(IX) (-) oligonucleotides, whose presence in the genomes of closely related murine leukemia viruses is mutually exclusive and predictive of two properties of the viral envelope glycoprotein gp70. Viruses harboring the G(IX) (+) oligonucleotide induce...
چکید ه سابقه و هدف هموفیلی B یک بیماری وابسته به جنس مغلوب است که در اثر کاهش مقدار و یا نقص عملکرد فاکتور IX انعقادی رخ میدهد. ژن فاکتور IX انعقادی به طول 34 کیلو باز، دارای 8 اگزون است. جهش در نواحی مختلف ژن فاکتور IX انعقادی سبب نقص در پروتئین IX انعقادی و بیماری هموفیلی B میگردد. هدف از این مطالعه تعیین جهش در ژن فاکتور IX انعقادی بیماران مبتلا به هموفیلی B در استان اصفهان و یافتن...
چکید ه سابقه و هدف هموفیلی B لیدن یک بیماری خونریزی دهنده ارثی است که با بیان تغییر یافته فاکتور IX شرح داده می شود. این شکل از هموفیلی در ارتباط با موتاسیونهای نقطهای متنوع در محدودهای 40 نوکلئوتیدی از ناحیه پروموتوری ژن فاکتور IX رخ میدهد. بیماران کلاسیک هموفیلی B لیدن دارای سطح فاکتور IX پلاسمایی Units/ml 1/0(کمتر از 15%) در دوران قبل از بلوغ هستند اما متعاقب بلوغ، سطح فاکتور IX در...
background: hemophilia b is a bleeding disorder with a recessive x-linked inheritance pattern, in which the infected individuals have low levels of factor ix in their plasma. affected individuals may have bleeding episodes after trauma or spontaneously considering the plasma level of factor ix. in order to prevent these episodes and to control bleeding, they should use coagulation factor concen...
This report concerns a cell surface antigen (G(IX); G = Gross) which exhibits mendelian inheritance but which also appears de novo in cells that become productively infected with MuLV (Gross), the wild-type leukemia virus of the mouse. In normal mice, G(IX) is a cell surface allo-antigen confined to lymphoid cells and found in highest amount on thymocytes. Four categories of inbred mouse strain...
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