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781
Nanopore-based random genomic sampling for intraoperative molecular diagnosis
Published 2025-01-01“…Results In our retrospective cohort of 26 malignant brain tumors, iSCORED demonstrated 100% concordance in CNV detection, including chromosomal alterations and oncogene amplifications, when compared to clinically validated assays such as Next-Generation Sequencing and Chromosomal Microarray. …”
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782
Assessment of diversity of Indian aromatic rice germplasm collections for morphological, agronomical, quality traits and molecular characters to identify a core set for crop improv...
Published 2020-10-01“…The markers are informative in analyzing the diversity as the PIC values estimated varied from 0.17 (RM577 on chromosome 1) to 0.72 (RM276 on chromosome 6) with an average of 0.54 per locus. …”
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783
11p15.4 Microdeletion Associates with Hemihypertrophy
Published 2018-01-01“…The results of whole genome SNP microarray analysis showed approximately 77 Kb interstitial deletion of the short arm of chromosome 11 (11p15.4). We report novel clinical findings of this rare genetic condition.…”
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784
A Triad of Congenital Diaphragmatic Hernia, Meckel’s Diverticulum, and Heterotopic Pancreas
Published 2014-01-01“…It is known to be associated with extradiaphragmatic malformations, which include cardiac, renal, genital, and chromosomal abnormalities. Herein, we report a newborn born with concurrent congenital diaphragmatic hernia, Meckel’s diverticulum, and heterotopic pancreatic tissue. …”
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785
PHOTOPROBER® Biotin: An Alternative Method for Labeling Archival DNA for Comparative Genomic Hybridization
Published 2004-01-01“…Comparative genomic hybridization (CGH) represents a powerful method for screening the entire genome of solid tumors for chromosomal imbalances. Particularly it enabled the molecular cytogenetic analysis of archival, formalin‐fixed, paraffin‐embedded (FFPE) tissue. …”
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786
Systemic lupus erythematosus in a patient with 22q11.2 deletion syndrome: A case report and review of the literature
Published 2024-11-01“…22q11.2 deletion syndrome (MIM: 192430/188400, ORPHA: 567) is the most common chromosomal microdeletion disorder, caused by a hemizygous microdeletion of 2.5 million base pairs on chromosome 22. …”
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787
Raise of short-stemmed vaviloid branched spike lines and their cytogenetics
Published 2015-07-01“…Chromosomal identification of such lines will allow their use in genetic studies concerning specified traits, in particular, the vaviloid branched spike.…”
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788
Assessment of Cytogenotoxicity of Plastic Industrial Effluent Using Allium cepa Root Tip Cells
Published 2023-01-01“…With rising effluent concentrations, the mitotic index (M.I.) rapidly dropped. Chromosomal abnormalities were caused by the plastic effluent in the root cells of Allium cepa, especially sticky chromosome and binucleated cells being the most frequently seen at lower concentrations of 15%. …”
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789
Recent Advances in DNA Systems for In Situ Telomerase Activity Detection and Imaging
Published 2025-01-01“…Telomeres play a key role in maintaining chromosome stability and cellular aging. They consist of repetitive DNA sequences that protect chromosome ends and regulate cell division. …”
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790
Evolution of CpG-islands by means of tandem duplications
Published 2017-02-01“…One of the most pronounced tandems are located in chromosome 19, known for its abundance of segment duplications and gene expansion. …”
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791
Determination the site of antibiotic resistance genes in Escherichia coli isolated From Urinary Tract Infection
Published 2018-10-01“…The results showed that the antibiotic resistance genes of Amikacin, Erythromycin, Tetracyclin, and Trimethoprim were located on a plasmid, whereas Amoxicillin, Ampicillin, Chloramphenicol, Ciprofloxacin, Nalidixic acid and Penicillin were located on chromosomal DNA. The results also demonstrated an inability to produce alpha or beta-hemolysin indicating that the genes which are responsible for hemolysin production were also located on chromosomal DNA. …”
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792
Tuber Cinereum Diverticula in a 28-Month-Old with Xq21 Deletion Syndrome
Published 2014-01-01“…Imaging revealed corpus callosum dysgenesis, forniceal hypoplasia, vermian hypoplasia, and hypothalamic dysmorphism characterized by tuber cinereum diverticula. Subsequent chromosomal microarray showed an Xq21 deletion. We present a case of Xq21 deletion syndrome with midline brain anomalies and a novel hypothalamic malformation.…”
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793
Solving degree-constrained multicast routing problem by a heuristic genetic algorithm
Published 2007-01-01“…With the purpose to solve the degree constrained multicast routing model efficiently,the evolutionary strategy was introduced into heuristic search methods by employing the chromosome as the heuristic information for global searching,and then a hybrid genetic algorithm was proposed.The algorithm not only avoids the difficulty of coding for multicast trees,but also possesses fast convergency and global optimizing capability.Meanwhile,the efficiency of the method is supported by a great number of numerical experiments.…”
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794
Annotation and characterization of immunoglobulin loci and CDR3 polymorphism in water buffalo (Bubalus bubalis)
Published 2025-01-01“…The Igκ locus, located on chromosome 12, encompasses 24 Vκ genes, 5 Jκ genes, and 1 Cκ gene, while the Igλ locus on chromosome 17 includes 71 Vλ genes, 3 Jλ genes, and 3 Cλ genes. …”
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795
Clastogenic Effects of Glyphosate in Bone Marrow Cells of Swiss Albino Mice
Published 2009-01-01“…Therefore, in the present study, genotoxic effects of the herbicide glyphosate were analyzed by measuring chromosomal aberrations (CAs) and micronuclei (MN) in bone marrow cells of Swiss albino mice. …”
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796
INLUENCE OF ALIEN GENETIC MATERIAL ON THE MANIFESTATION OF AGRONOMICALLY IMPORTANT TRAITS OF COMMON WHEAT (T. aestivum L.)
Published 2018-05-01“…Additionally, alien gene introgression from wild relatives occurs through whole chromosome or chromosome arm substitutions, or long translocated fragments that, together with target loci, may contain genetic material that afects other agronomically important traits. …”
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797
Regulatory logic of endogenous RNAi in silencing de novo genomic conflicts.
Published 2023-06-01“…These data suggest that endo-RNAi are especially critical during incipient stages of intrinsic sex chromosome conflicts, and that continual cycles of distortion and resolution may contribute to speciation.…”
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798
Comparative Studies on Cellular Behaviour of Carnation (Dianthus caryophyllus Linn. cv. Grenadin) Grown In Vivo and In Vitro for Early Detection of Somaclonal Variation
Published 2013-01-01“…Cellular parameters including the mitotic index (MI), chromosome count, ploidy level (nuclear DNA content), mean cell and nuclear areas, and cell doubling time (Cdt) were determined from the 2 mm root tip segments of this species. …”
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799
MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing
Published 2024-01-01“…Its robust capability to effectively detect a wide range of complex chromosomal aberrations, including rare and subtle variations, positions it as a promising and valuable addition to prenatal diagnostic technologies. …”
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800
Genetic profiling of multidrug-resistant Acinetobacter baumannii from a tertiary care center in Malaysia
Published 2025-02-01“…The antibiotic resistance genes, blaOXA-23, blaOXA-24, blaADC, blaVIM, and blaIMP, were detected in chromosomal and plasmid DNA using PCR. Insertion sequence ISAba1/blaOXA-23 gene was detected on chromosomal DNA only. …”
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