Identification of genetic characteristics in pediatric epilepsy with focal cortical dysplasia type 2 using deep whole‐exome sequencing
Sign Up to like & getrecommendations! Published in 2022 at "Molecular Genetics & Genomic Medicine"
DOI: 10.1002/mgg3.2086
Abstract: Focal cortical dysplasia type 2 (FCD2) is a malformation of cortical development that constitutes a common cause of pediatric focal epilepsy. Germline or somatic variants in the mammalian target of rapamycin (mTOR) signaling pathway genes… read more here.
Keywords: focal cortical; identification genetic; dysplasia type; cortical dysplasia ... See more keywords
PCR: Identification of Genetic Polymorphisms.
Sign Up to like & getrecommendations! Published in 2017 at "Methods in molecular biology"
DOI: 10.1007/978-1-4939-6990-6_13
Abstract: Polymerase chain reaction (PCR) enables the amplification of a specific sequence of deoxyribonucleic acid (DNA) through the process of three main steps: template DNA denaturation, annealing of the primers to complementary sequences, and primer extension… read more here.
Keywords: identification genetic; dna; genetic polymorphisms; biology ... See more keywords
Identification and genetic characterization of porcine circovirus 3 on pig farms in Serbia
Sign Up to like & getrecommendations! Published in 2019 at "Archives of Virology"
DOI: 10.1007/s00705-019-04455-y
Abstract: Backgroud The presence of PCV3 genome has been detected in pigs affected by different clinical and pathological conditions as well as in healthy animals. Its presence has been reported in many countries of North and… read more here.
Keywords: pig; identification genetic; presence; pcv ... See more keywords
Molecular identification and genetic analysis of cherry cultivars using capillary electrophoresis with fluorescence-labeled SSR markers
Sign Up to like & getrecommendations! Published in 2017 at "3 Biotech"
DOI: 10.1007/s13205-017-1036-7
Abstract: Molecular identification and genetic analysis of cherry are necessary for solving the problem of synonyms and homonyms that occur in cherry production. In this study, capillary electrophoresis with fluorescent-labeled simple sequence repeat (SSR) primers was… read more here.
Keywords: cherry; identification genetic; analysis; cherry cultivars ... See more keywords
Identification of genetic biomarkers in urine for early detection of prostate cancer.
Sign Up to like & getrecommendations! Published in 2020 at "Current problems in cancer"
DOI: 10.1016/j.currproblcancer.2020.100616
Abstract: Prostate cancer screening is a challenging and vital issue in the aspects of the current tests and risk assessments. Prostate cancer risk assessments are currently carried out by using blood, urine and tissue biomarkers with… read more here.
Keywords: identification genetic; genetic biomarkers; cancer identification; prostate cancer ... See more keywords
Molecular identification and genetic divergence of new-world Callithrichinae marmosets based on the mitochondrial COI gene
Sign Up to like & getrecommendations! Published in 2019 at "Forensic Science International: Genetics Supplement Series"
DOI: 10.1016/j.fsigss.2019.09.107
Abstract: Abstract The New World marmosets of the sub-family Callitrichinae includes genera of marmosets, tamarins, and lion tamarins. They are small, arboreal, diurnal, insectivore/frugivores inhabiting forested, rural, and urban areas of tropical Central and South America.… read more here.
Keywords: identification genetic; new world; marmosets based; molecular identification ... See more keywords
Identification of genetic basis of obesity and mechanistic link of genes and lipids in Pakistani population
Sign Up to like & getrecommendations! Published in 2018 at "Bioscience Reports"
DOI: 10.1042/bsr20180281
Abstract: We aimed to identify the genetic causes of common forms of obesity in the Pakistani people and find out the mechanistic link by observing the relationship of genes and serum lipid traits. Four hundred and… read more here.
Keywords: identification genetic; showed association; genetic basis; association ... See more keywords
Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent
Sign Up to like & getrecommendations! Published in 2018 at "Ophthalmic Genetics"
DOI: 10.1080/13816810.2017.1373830
Abstract: ABSTRACT Purpose: To investigate the clinical characteristics and genetic basis of inherited retinal degeneration (IRD) in six unrelated pedigrees from Mexico. Methods: A complete ophthalmic evaluation including measurement of visual acuities, Goldman kinetic or Humphrey… read more here.
Keywords: identification genetic; ush2a rpe65; degeneration; fam161a genes ... See more keywords
Identification of genetic targets in acute myeloid leukaemia for designing targeted therapy
Sign Up to like & getrecommendations! Published in 2020 at "British Journal of Haematology"
DOI: 10.1111/bjh.17129
Abstract: Few effective therapies exist for acute myeloid leukaemia (AML), in part due to the molecular heterogeneity of this disease. We sought to identify genes crucial to deregulated AML signal transduction pathways which, if inhibited, could… read more here.
Keywords: nox family; identification genetic; myeloid leukaemia; acute myeloid ... See more keywords
Identification and genetic characterization of Saprolegnia parasitica, isolated from farmed and wild fish in Finland.
Sign Up to like & getrecommendations! Published in 2023 at "Journal of fish diseases"
DOI: 10.1111/jfd.13795
Abstract: Oomycete infections in farmed fish are one of the most significant disease issues in salmonid aquaculture worldwide. In the present study, Saprolegnia spp. in different farmed fish species in Finland were identified, and the molecular… read more here.
Keywords: fish finland; parasitica; identification genetic; saprolegnia parasitica ... See more keywords
Modern genomic techniques in the identification of genetic causes of cardiomyopathy
Sign Up to like & getrecommendations! Published in 2022 at "Heart"
DOI: 10.1136/heartjnl-2021-320424
Abstract: Over the past three decades numerous disease-causing genes have been linked to the pathogenesis of heritable cardiomyopathies, but many causal genes are yet to be identified. Next-generation sequencing (NGS) platforms have revolutionised clinical testing capacity… read more here.
Keywords: techniques identification; disease; identification genetic; cardiomyopathy ... See more keywords