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1361
Elucidating genetic variability between randomly bred domestic cats and Persian domestic cats from different geographical locations using microsatellite markers
Published 2024-11-01“…We selected eight STR markers with different chromosomal locations based on polymorphism and observed allele numbers in the next step. …”
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1362
Lake Baikal amphipods and their genomes, great and small
Published 2024-05-01“…For about onetenth of the Baikal amphipod species, nuclear genome sizes and chromosome numbers are known. While genome sizes vary within one order of magnitude, the karyotypes are relatively stable (2n = 52 for most species studied). …”
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1363
Pseudodominant Nanophthalmos in a Roma Family Caused by a Novel PRSS56 Variant
Published 2020-01-01“…Analysis of single nucleotide polymorphisms in linkage disequilibrium with the c.1509G>C in PRSS56 suggested a shared chromosomal segment. The nanophthalmos phenotype, characterized in detail in the younger individual, encompassed bilateral corneal steepening, retinal folds, buried optic head drusen, and restricted visual fields, but no signs of retinal dystrophy. …”
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1364
Emerging Challenges in Methicillin Resistance of Coagulase-Negative Staphylococci
Published 2025-01-01“…Staphylococcal cassette chromosome <i>mec</i> (SCC<i>mec</i>) typing was performed. …”
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1365
Optimization, characterization and biosafety of oregano, rosemary and mint oil mixture against Penicillium digitatum in citrus using L-optimal mixture design
Published 2025-01-01“…However, the optimized mixture did not induce significant chromosomal aberrations compared to the control, suggesting minimal genotoxic effects. …”
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1366
Using artificial intelligence methods for the optimal synthesis of reversible networks
Published 2024-11-01“…A genetic algorithm was developed, featuring multi-component mutation and a matrix approach to chromosome encoding combined with Tabu search to avoid local optima. …”
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1367
Familial Mediterranean Gene (MEFV) Mutation in Parents of Children with Familial Mediterranean Fever: What Are the Exceptions?
Published 2018-01-01“…Familial Mediterranean Fever (FMF) is one of the most prevalent periodic fever syndromes; MEFV, the responsible gene for the disease, is in the short arm of chromosome16. In the considerable count of the FMF patients, only one mutation is found in the MEFV and parents, who were the obligatory carriers for that mutation, were asymptomatic. …”
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1368
The extremely halotolerant black yeast Hortaea werneckii - a model for intraspecific hybridization in clonal fungi
Published 2019-07-01“…Due to the limited number of phylogenetically informative characters in the ribosomal DNA dataset, the partial genes encoding for β-tubulin (BTB) and mini-chromosome maintenance protein (MCM7) were also sequenced. …”
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1369
Energy-Saving Metro Train Timetable Optimization Method Based on a Dynamic Passenger Flow Distribution
Published 2022-01-01“…The PSO-GA structure has PSO as the main body and integrates the chromosome crossover and mutation operations of the GA into the iterative process to improve the search efficiency of the algorithm. …”
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1370
The Characteristic of Biofilm Formation in ESBL-Producing K. pneumoniae Isolates
Published 2024-01-01“…Thirty ESBL-producing K. pneumoniae isolates from 25 inpatients at Ruijin Hospital, Shanghai, were subjected to pulsed-field gel electrophoresis (PFGE) to estimate genomic relatedness. Based on the chromosomal DNA patterns we obtained, we identified 21 PFGE profiles from the 30 isolates, eight of which had high homology indicating that they may have genetic relationships and/or potential clonal advantages within the hospital. …”
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1371
Comparative assessment of the copy number of satellite repeats in the genome of Triticeae species
Published 2023-12-01“…Our assessment of the copy number of new satellite repeats in the St-genome and the analysis of their amplification specificity between species can contribute to the molecular-genetic and chromosome markers used for evolutionary, phylogenetic, and population studies of Triticeae species.…”
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1372
Virulence-associated variants in Cryptococcus neoformans sequence type 93 are less likely to be associated with population structure compared to independent rare mutations
Published 2025-01-01“…We investigated the karyotype of ST93A and ST93B using contour-clamped gel electrophoresis and long-read sequencing and found that the extensive long-range linkage was not due to chromosomal rearrangements. Overall, we found that the two subpopulations in ST93 are driven by SNPs in LD. …”
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1373
TERT de novo mutation-associated dyskeratosis congenita and porto-sinusoidal vascular disease: a case report
Published 2025-01-01“…Conclusion When discovering reticular rash and unknown portal hypertension, it is necessary to perform whole exome sequencing and chromosome length testing to clarify the possibility of dyskeratosis congenita/telomere biology disorder with porto-sinusoidal vascular disease.…”
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1374
THE DEVELOPMENT OF SCIENCE AND THE FATE OF A SCIENTIST (FOLLOWING GENETICS)
Published 1997-01-01“…Morgan, 1911, "The Chromosome–The Feature"; 3) O. T. Avery et al., 1944, "The DNA Molecule–The Feature"; and 4) V. …”
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1375
Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep.
Published 2013-04-01“…In both populations, an X chromosome region, close to the BMP15 gene, harbored clusters of markers with suggestive evidence of association at significance levels between 1E(-05) and 1E(-07). …”
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1376
Genome-wide identification and characterization of the bZIP family in the Mangrove Plant Kandelia obovata and its role in response to stress
Published 2025-02-01“…Results In the K. obovata genome, 66 bZIP genes were identified and named KobZIP1 to KobZIP66, categorized based on their chromosomal locations. These KobZIP genes exhibited diversity in physicochemical properties, such as protein length, molecular weight, and isoelectric point, and were all predicted to localize to the nucleus. …”
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1377
HnRNPM modulates alternative splicing in germ cells by recruiting PTBP1
Published 2025-01-01“…Methods The expression of hnRNPM in germ cells at different stages was detected by polymerase chain reaction, western blotting, a single-cell database, and chromosome spreading assays. Conditional hnRNPM knockout mice were generated to observe the development of testes and germ cells in male mice. …”
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1378
Preimplantation genetic testing for aneuploidy in severe male factor infertility: protocol for a multicenter randomised controlled trial
Published 2022-07-01“…Secondary outcomes will be embryo implantation rate, biochemical pregnancy rate, clinical pregnancy rate, spontaneous abortion rate, ongoing pregnancy rate, preterm birth rate, fetal chromosomal abnormality rate, birth defect rate and treatment complications. …”
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1379
Prenatal ultrasound diagnosis, associated anomalies and pregnancy outcomes of fetal right aortic arch
Published 2025-01-01“…In terms of typing, 78 cases (49.7%) of right aortic arch-aberrant left subclavian artery (RAA-ALSA) and 75 cases (47.8%) of right aortic arch-mirror branch (RAA-MB), 3 cases (1.9%) of right aortic arch-isolated left subclavian artery (RAA-ILSA) and 1 case (0.6%) of right aortic arch-isolated left innominate artery (RAA-ILINA) were identified, and the incidence of combined cardiac anomalies and chromosomal anomalies was significantly greater in the RAA-MB group than the RAA-ALSA group. …”
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1380
Dynamics and regulatory roles of RNA m6A methylation in unbalanced genomes
Published 2025-01-01“…RNA m6A modification in Drosophila has proven to be involved in sex determination regulated by Sxl and may affect X chromosome expression through the MSL complex. The dosage-related effects under the condition of genomic imbalance (i.e. aneuploidy) are related to various epigenetic regulatory mechanisms. …”
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