نتایج جستجو برای: پروتوپورفیرین ix

تعداد نتایج: 18979  

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...

Amirizadeh N, Faranoush M, Farsinejad A, Gharehbaghian A, Hadjati S, Toogeh Gh,

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...

Journal: :medical journal of islamic republic of iran 0
hassan mansouri torghabeh experimental hematology group. medical sciencesschool. tarbiat modares university (t.m. u.). tehran, iran. allakbar pourfathollah experimental hematology group. medical sciencesschool. tarbiat modares university (t.m. u.). tehran, iran. mahmood mahmood ian shooshtari the iranian ~blood transfusion organization research center, tehran. zahra rezaie-yazd the internal ward, ghaem hospital. mashhad, iran. habffiollahe smaili mashhad medical sciences university, mashhad, iran.

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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...

Journal: :The Journal of biological chemistry 1987
H A Liebman B C Furie B Furie

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...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1980
H Donis-Keller J Rommelaere R W Ellis N Hopkins

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...

زینلی, سیروس, سمیعی, شهرام, نفیسی, نفیسه, هورفر, حمیدرضا, کریمی‌پور, مرتضی, کمالی دولت‌آبادی, عصمت, کوکبی, لیلا,

  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...

اله‌بخشیان, عاطفه, اله‌بخشیان, مهدی, رستگار لاری, قاسم, روانبد, شیرین, علا, فریدون, محمدی, محمدحسین, کاظمی, احمد,

  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...

Journal: :iranian journal of blood and cancer 0
hassan mansouri torghabeh aliakbar pourfathollah mahmoud mahmoudian shoushtari

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...

Journal: :The Journal of Experimental Medicine 1971
Elisabeth Stockert Lloyd J. Old Edward A. Boyse

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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