نتایج جستجو برای: relative mutation dosage

تعداد نتایج: 763656  

Fatemeh Fahmi Mohsen Musaviun Saeid Reza Khatami Seyed Reza Kazemi Nezhad,

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common hereditary enzymatic disorders in human, increases the vulnerability of erythrocytes to oxidative stress. It is also characterized by remarkable molecular and biochemical heterogeneity. According to previous investigations, G6PD Cosenza (G1376C) is a common G6PD mutation in some parts of Iran. Therefore in the present...

Journal: :iranian journal of pharmaceutical research 0
maryam kazemipour department of chemistry, faculty of sciences, kerman branch, islamic azad university, ir iran. iman fakhari department of chemistry, faculty of sciences, kerman branch, islamic azad university, ir iran. mehdi ansari herbal and traditional medicines research center, kerman university of medical sciences, kerman, iran.

gabapentin is an anticonvulsant widely used in the treatment of epilepsy. no peculiar chromophore is available on the gabapentin moiety for direct analysis by absorption spectrophotometry. a sensitive spectrophotometric method for the determination of gabapentin in bulk, pharmaceutical formulations and human plasma has been developed. in this method, gabapentin directly derivatized with vanilli...

Journal: :Mathematical biosciences 2008
Robert F Stengel

We examine the dynamics of infection by the human immunodeficiency virus (HIV), as well as therapies that minimize viral load, restore adaptive immunity, and use minimal dosage of anti-HIV drugs. Virtual therapies for wild-type infections are demonstrated; however, the HIV infection is never cured, requiring continued treatment to keep the condition in remission. With high viral turnover and mu...

Journal: :iranian journal of medical sciences 0
seyed reza kazemi nezhad department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran fatemeh fahmi department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran saeid reza khatami department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran mohsen musaviun department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran

glucose-6-phosphate dehydrogenase (g6pd) deficiency is one of the most common hereditary enzymatic disorders in human, increases the vulnerability of erythrocytes to oxidative stress. it is also characterized by remarkable molecular and biochemical heterogeneity. according to previous investigations, g6pd cosenza (g1376c) is a common g6pd mutation in some parts of iran. therefore in the present...

2014
Michael R. Eccles Cherie A. Stayner

Gene dosage effects have emerged as playing a central role in the pathogenesis of polycystic kidney disease. Yet, how gene dosage can ultimately have an impact on the formation of kidney cysts remains unknown. In this commentary we review the evidence for the role of gene dosage effects versus the "2-hit" mutation model in polycystic kidney disease (PKD), and also discuss how gene networks may ...

In this paper, a new version of multi-objective differential evolution with dynamically adaptable mutation factor is used for Pareto optimization of a 5-degree of freedom vehicle vibration model excited by non-stationary random road profile. In this way, non-dominated sorting algorithm and crowding distance criterion have been combined to differential evolution with fuzzified mutation in order ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Fiona M F Lun Nancy B Y Tsui K C Allen Chan Tak Y Leung Tze K Lau Pimlak Charoenkwan Katherine C K Chow Wyatt Y W Lo Chanane Wanapirak Torpong Sanguansermsri Charles R Cantor Rossa W K Chiu Y M Dennis Lo

Prenatal diagnosis of monogenic diseases, such as cystic fibrosis and beta-thalassemia, is currently offered as part of public health programs. However, current methods based on chorionic villus sampling and amniocentesis for obtaining fetal genetic material pose a risk to the fetus. Since the discovery of cell-free fetal DNA in maternal plasma, the noninvasive prenatal assessment of paternally...

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