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Published in 2019 at "Molecular Genetics & Genomic Medicine"
DOI: 10.1002/mgg3.737
Abstract: Aneurysmal subarachnoid hemorrhage (aSAH) has high fatality and permanent disability rates due to the severe damage to brain cells and inflammation. The SERPINE1 gene that encodes PAI‐1 for the regulation of tissue plasminogen activator is… read more here.
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Published in 2018 at "Hemoglobin"
DOI: 10.1080/03630269.2018.1553789
Abstract: Abstract β-Globin haplotypes were used to investigate the origin of three common β-globin mutations, IVS-I-110 (G>A); HBB: c.93-21G>A, IVS-I-1 (G>A); HBB: c.92 + 1G>A and codon 39 (C>T); HBB: c.118C > T in Syrian patients. Haplotype analysis was… read more here.
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Published in 2020 at "Journal of Cosmetic Dermatology"
DOI: 10.1111/jocd.13730
Abstract: Chronic spontaneous urticaria (CSU) is a distressing skin disease. Family clustering and heterogeneity in the onset and progression indicate that susceptibility to CSU is a complex trait. In this study, we performed haplotype analysis for… read more here.
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Published in 2018 at "BMC Neuroscience"
DOI: 10.1186/s12868-018-0413-4
Abstract: BackgroundAPOE ε4 allele is most common genetic risk factor for Alzheimer’s disease (AD) and cognitive decline. However, it remains poorly understood why only some carriers of APOE ε4 develop AD and how ethnic variabilities in APOE locus… read more here.
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Published in 2019 at "BMC Medical Genomics"
DOI: 10.1186/s12920-019-0600-x
Abstract: BackgroundPreimplantation genetic testing for monogenic defects (PGT-M) has been available in clinical practice. This study aimed to validate the applicability of targeted capture sequencing in developing personalized PGT-M assay.MethodsOne couple at risk of transmitting Usher… read more here.
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Published in 2023 at "Life Science Alliance"
DOI: 10.26508/lsa.202201761
Abstract: cbNIPT by WGS and haplotype analysis predict the inherited genotypes for families with monogenic diseases and provide a potentially better solution for prenatal diagnosis of monogenic diseases. Monogenic inherited diseases are common causes of congenital… read more here.
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Published in 2022 at "Frontiers in Plant Science"
DOI: 10.3389/fpls.2022.841767
Abstract: Jujube (family Rhamnaceae) is an important economic fruit tree in China. In this study, we reported 26 chloroplast (cp) sequences of jujube using Illumina paired-end sequencing. The sequence length of cp genome was 161, 367–161,… read more here.
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Published in 2022 at "Frontiers in Plant Science"
DOI: 10.3389/fpls.2022.897772
Abstract: Glume hairiness or pubescence is an important morphological trait with high heritability to distinguish/characterize wheat and is related to the resistance to biotic and abiotic stresses. Hg1 (formerly named Hg) on chromosome arm 1AS controlled… read more here.
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Published in 2021 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms222312723
Abstract: The aim of the presented study is a genetic characterization of the hexaploid wheat Triticum aestivum L. Two approaches were used for the genealogical study of hexaploid wheats—the complete sequencing of chloroplast DNA and PCR-based… read more here.
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Published in 2022 at "Pathogens"
DOI: 10.3390/pathogens11050519
Abstract: Echinococcus granulosus sensu lato (s.l.) causes cystic echinococcosis in ungulates and humans. The current study was designed to find the genetic diversity and haplotypic profiles of hydatid cysts from the lungs of cattle in three… read more here.