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pro vyhledávání: '"Amir Mashayekhi"'
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 1, Iss 1, Pp 1145-1150 (2017)
Background: Coagulation factor 7 (FVII) is a vitamin-k-dependent serine protease with an essential role in initiation of extrinsic pathway of coagulation cascade. Extrinsic pathway is the major mechanism of clot formation in physiologic conditions. C
Externí odkaz:
https://doaj.org/article/9432672456d945bf98e7641095883c26
Autor:
Amir Mashayekhi, Ezatollah Ghasemi
Publikováno v:
Trends in Medical Sciences. 2
Coagulation factor VII (FVII) is a vitamin K-dependent serine protease that plays a pivotal role in normal hemostasis. Mature FVII is a glycoprotein comprised γ-carboxyglutamic acid-rich (Gla) domain, two epidermal growth factor (EGF)-like domains,
Publikováno v:
Operations Research Forum. 3
Publikováno v:
Iranian Journal of Biotechnology
Background: Coagulation Factor VII is a vitamin K-dependent serine protease which has a pivotal role in the initiation of the coagulation cascade. The congenital Factor VII deficiency is a recessive hemorrhagic disorder that occurs due to mutations o
Publikováno v:
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics, Vol 20, Iss 2, Pp 19-25 (2017)
Balkan Journal of Medical Genetics, Vol 20, Iss 2, Pp 19-25 (2017)
Coagulation factor VII (FVII) is a key enzyme of the extrinsic coagulation cascade that is predominantly produced by hepatocytes. The F7 gene mutations cause FVII deficiency with considerable molecular and phenotypic heterogeneity. We characterized t
Autor:
Fariborz Soheili, Amir Mashayekhi, Zahed Khatooni, Hossein Jafari, Zahra Jalili, Mahtab Rahbar
Publikováno v:
Congenital heart disease. 13(2)
Background The mutations in GATA4 gene induce inherited atrial and ventricular septation defects, which is the most frequent forms of congenital heart defects (CHDs) constituting about half of all cases. Method We have performed High resolution melti
Publikováno v:
Molecular medicine reports. 17(2)
Factor VII (FVII) serves an essential role in the initiation of blood coagulation. Mutations in conserved residues within its serine protease domain may lead to dysregulated coagulation activity. The objective of the present study was to elucidate th
Publikováno v:
Medicine
Hematological parameters are appraised routinely to determine overall human health and to diagnose and monitor certain diseases. In GWASs, more than 30 loci carrying common deoxyribonucleic acid (DNA) polymorphisms have been identified related to hem
Autor:
Seyed Reza Kazemi Nezhad, Saeid Reza Khatami, Amir Mashayekhi, Maryam Ghaderi Gandomani, Setareh Daneshmand
Publikováno v:
Journal of genetics. 90(1)
C untilfurther use. Genomic DNA was extracted from whole bloodof the G6PD deficient subjects using DNA extraction kit(Roche Molecular Biochemicals, Switzerland). All sampleswere analysed by PCR-RFLP method for the G1003A muta-tion in exon 9 which is
Autor:
Kazemi Nezhad, S. R., amir mashayekhi, Khatami, S. R., Daneshmand, S., Fahmi, F., Ghaderigandmani, M., Jalali-Far, M. A.
Publikováno v:
Iranian Journal of Public Health, Vol 38, Iss 3 (2009)
Scopus-Elsevier
Iranian Journal of Public Health, Vol 38, Iss 3, Pp 127-131 (2009)
Scopus-Elsevier
Iranian Journal of Public Health, Vol 38, Iss 3, Pp 127-131 (2009)
"nBackground: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most frequent genetic enzymatic disorder in human, which is inherited as an X-linked gene. It encodes a housekeeping enzyme, which is vital for cell survival. According to p