Point Mutation
Mostrando 1-12 de 2265 artigos, teses e dissertações.
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1. Bibliometric analysis of global sickle cell disease research from 1997 to 2017
Abstract Introduction Sickle cell disease is an autosomal recessive genetic disease caused by a single point mutation in the β-globin chain of the hemoglobin. It has been recognized by the World Health Organization as a public health priority since 2006. Methods The Scopus database was used in this study with the search descriptors: “sickle cell” and
Hematology, Transfusion and Cell Therapy. Publicado em: 2022
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2. Heterologous expression and mutagenesis of recombinant Vespa affinis hyaluronidase protein (rVesA2)
Abstract Background: Crude venom of the banded tiger waspVespa affinis contains a variety of enzymes including hyaluronidases, commonly known as spreading factors. Methods: The cDNA cloning, sequence analysis and structural modelling of V. affinis venom hyaluronidase (VesA2) were herein described. Moreover, heterologous expression and mutagenesis of rVesA2
J. Venom. Anim. Toxins incl. Trop. Dis. Publicado em: 05/12/2019
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3. Description of a human Bocavirus recombinant strain in the Americas
Human bocaviruses (HBoV) are mainly associated with respiratory and gastroenteric infections. These viruses belong to the family Parvoviridae, genus Bocaparvovirus and are classified in four subtypes (HBoV1-4). Recombination and point mutation have been described as basis of parvovirus evolution. In this study three viral sequences were obtained from positiv
Mem. Inst. Oswaldo Cruz. Publicado em: 21/10/2019
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4. Galium spurium and G. aparine Resistance to ALS-Inhibiting Herbicides in Northern Greece
RESUMO: O conhecimento do nível de resistência das populações de plantas daninhas e dos herbicidas aos quais eles sobrevivem é importante para recomendar conselhos adequados aos agricultores e permitir a seleção de estratégias de gestão apropriadas. Experimentos de resposta de plantas inteiras foram realizados para estudar os níveis de resistência
Planta daninha. Publicado em: 17/10/2019
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5. Molecular profile of non-small cell lung cancer in northeastern Brazil
RESUMO Objetivo: Investigar os subtipos histológicos e perfis de mutação do carcinoma pulmonar de células não pequenas no Brasil, bem como as correlações entre os subtipos histológicos, a expressão do gene anaplastic lymphoma kinase (ALK, quinase do linfoma anaplásico), o estado de mutação do gene EGFR e a expressão de programmed death-ligand 1
J. bras. pneumol.. Publicado em: 03/06/2019
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6. Lack of quadruple and quintuple mutant alleles associated with sulfadoxine-pyrimethamine resistance in Plasmodium vivax isolates from Brazilian endemic areas
BACKGROUND AND OBJECTIVE Brazil is responsible for a large number of Plasmodium vivax cases in America. Given the emergence of P. vivax parasites resistant to chloroquine and the effectiveness of antifolates in vivax malaria treatment together with a correlation between mutations in P. vivax dhfr and dhps genes and SP treatment failure, the point mutations
Mem. Inst. Oswaldo Cruz. Publicado em: 04/02/2019
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7. Multi-Objective Cooperative Paths Planning for Multiple Parafoils System Using a Genetic Algorithm
ABSTRACT In large-scale natural disasters and military supplies, multiple parafoils are more capable of performing actual tasks. The cooperative paths planning for multiple parafoils with different initial positions and headings is an important step in multiple parafoils airdrop, which has to satisfy multiple objectives, namely, parafoils can’t collide wit
J. Aerosp. Technol. Manag.. Publicado em: 07/01/2019
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8. Importance of the putative furin recognition site 742RNRR745 for antiangiogenic Sema3C activity in vitro
Angiogenesis is one of the key processes in the growth and development of tumors. Class-3 semaphorins (Sema3) are characterized as axon guidance factors involved in tumor angiogenesis by interacting with the vascular endothelial growth factor signaling pathway. Sema3 proteins convey their regulatory signals by binding to neuropilins and plexins receptors, wh
Braz J Med Biol Res. Publicado em: 08/10/2018
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9. Analysis of radioprotection and antimutagenic effects of Ilex paraguariensis infusion and its component rutin
DNA repair pathways, cell cycle checkpoints, and redox protection systems are essential factors for securing genomic stability. The aim of the present study was to analyze the effect of Ilex paraguariensis (Ip) infusion and one of its polyphenolic components rutin on cellular and molecular damage induced by ionizing radiation. Ip is a beverage drank by most
Braz J Med Biol Res. Publicado em: 16/07/2018
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10. The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori
ABSTRACT In this study, we evaluated the mutations of Helicobacter pylori associated with resistance to clarithromycin and levofloxacin. Furthermore, based on the proposed interaction between antimicrobial resistance and pathogenicity, we correlated the mutation profiles of the strains with the presence of the pathogenicity gene cagA. We analyzed 80 gastric
Rev. Inst. Med. trop. S. Paulo. Publicado em: 28/06/2018
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11. Lack of association between rrl and erm(41) mutations and clarithromycin resistance in Mycobacterium abscessus complex
BACKGROUND Mycobacterium abscessus complex (MABC) includes species with high resistance rates among mycobacterial pathogens. In fact, MABC infections may not respond to clarithromycin treatment, which has historically been very effective against MABC infection. Molecular markers have been proposed to detect both acquired (rrl polymorphisms) and inducible (e
Mem. Inst. Oswaldo Cruz. Publicado em: 2017-11
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12. Familial Dysautonomia: Mechanisms and Models
Abstract Hereditary Sensory and Autonomic Neuropathies (HSANs) compose a heterogeneous group of genetic disorders characterized by sensory and autonomic dysfunctions. Familial Dysautonomia (FD), also known as HSAN III, is an autosomal recessive disorder that affects 1/3,600 live births in the Ashkenazi Jewish population. The major features of the disease are
Genet. Mol. Biol.. Publicado em: 04/08/2016