نتایج جستجو برای: structural mutation

تعداد نتایج: 669694  

Voet Th

The nature and pace of genome mutation is largely unknown. Standard methods to investigate DNA-mutation rely on arraying or sequencing DNA from a population of cells, hence the genetic composition of individual cells is lost and de novo mutation in cell(s) is concealed within the bulk signal. We developed methods based on (SNP-) arraying and next-generation sequencing of single-cell whole-genom...

A. Jayant Kulkarni, S. Kazemzadeh Azad ,

The present study is an attempt to propose a mutation-based real-coded genetic algorithm (MBRCGA) for sizing and layout optimization of planar and spatial truss structures. The Gaussian mutation operator is used to create the reproduction operators. An adaptive tournament selection mechanism in combination with adaptive Gaussian mutation operators are proposed to achieve an effective search in ...

Journal: :journal of family and reproductive health 0
ebrahim dastgerdy neonatology center of semnan university of medical sciences, emam khomeini hospital of garmsar gholamali mamori neonatology center of mashhad university of medical sciences, ghaem hospital of mashhad jalil afshari neonatology center of mashhad university of medical sciences, ghaem hospital of mashhad reza saeedi neonatology center of mashhad university of medical sciences, ghaem hospital of mashhad fatemeh shahbazi biology department, payame noor university, karaj unit, karaj, iran mahboobeh shirazi department of obstetrics and gynecology, tehran university of medical sciences, tehran, iran.

objective: jaundice with indirect hyperbilirubinemia is one of the most common neonatal problems that occur in 60% of term and 80% of preterm neonates but the causes are mostly unknown. it is suggested that race plays an important role in the prevalence of hyperbilirubinemia. it is a common problem in iran that worries both parents and pediatricians. it has been found that a mutation in the ugt...

مروتی, سعید, ناصری, فرنوش,

Dentinogenesis imperfecta (DI) is an inherited disorder affecting dentin. Defective dentin formation results in discolored teeth that are prone to attrition and fracture. Mutation in dentin and the main gene in this disease is DSPP. Heterozygous mutations in this gene cause tooth sialophosphoprotein (DSPP) causes dentin disorders DI I and II. Imperfecta is a dominant autosomal trait that affec...

Introduction: Mutations in the BRCA1 gene are major risk factors for breast and ovarian cancers. However, the relationship between some BRCA1 mutations and cancer risk remains largely unknown. Cancer risk predictions could be improved by evaluation of the impairment degree in the BRCA1 functions due to a specific mutation. This study aimed to assess the functional effect of a novel variant (Glu...

Introduction: Mutations in the BRCA1 gene are major risk factors for breast and ovarian cancers. However, the relationship between some BRCA1 mutations and cancer risk remains largely unknown. Cancer risk predictions could be improved by evaluation of the impairment degree in the BRCA1 functions due to a specific mutation. This study aimed to assess the functional effect of a novel variant (Glu...

Journal: :applied biotechnology reports 0
maryam zare faranak hadi zarrin minuchehr jafar amani ali hatef salmanian

mammalian ∆-(1)-pyrroline-5-carboxylate synthase (p5cs) enzyme catalyzes the coupled phosphorylation and reduction-conversion of glutamate to ∆-(1)-pyrroline-5-carboxylate (p5c), a critical step in the proline, ornithine, citrulline and arginine biosynthesis. in plants and mammals, p5cs consists of two separate enzymatic domains: n-terminal γ-glutamyl kinase (γ-gk) and c-terminal γ-glutamyl pho...

Journal: :iranian journal of allergy, asthma and immunology 0
zahra alizadeh immunology, asthma & allergy research institute, tehran university of medical sciences, tehran, iran mohammad reza fazlollahi immunology, asthma & allergy research institute, tehran university of medical sciences, tehran, iran payman eshghi department of pediatrics department, mofid children hospital, shaheed beheshti medical university, tehran, iran amir ali hamidieh hematology-oncology & sct research centre, shariati hospital, tehran university of medical sciences, tehran, iran zahra pourpak immunology, asthma & allergy research institute, tehran university of medical sciences, tehran, iran mohsen ghadami immunology, asthma & allergy research institute, tehran university of medical sciences, tehran, iran

severe congenital neutropenia (scn) is a rare primary immunodeficiency. different genes are found to be associated with scn, including ela2, hax1, was, gfi1, g-csfr. also, recently g6pc3 as a rare gene in scn has been reported. patients with g6pc3 often have cardiac and/or urogenital malformations. two patients with   persistent   severe   neutropenia,   recurrent   infections   and   maturatio...

Density functional theory methods(DFT) and natural bond orbital (NBO) analysis were used to investigate the effects of isomerism and side chain mutation at a microscopic level on the stability, binding energy and NMR/NQR tensors of structural isomers, L- methionylasparagine (Met-Asn) and L- asparagylmethionine (Asn-Met) in the gas phase. The results represented that the isomerism and side chain...

Journal: :Journal of molecular biology 1999
T C Wood W R Pearson

The relationship between sequence similarity and structural similarity has been examined in 36 protein families with five or more diverse members whose structures are known. The structural similarity within a family (as determined with the DALI structure comparison program) is linearly related to sequence similarity (as determined by a Smith-Waterman search of the protein sequences in the struc...

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