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1181
Identification of the CaCRT gene family and function of CaCRT1 under low-temperature stress in pepper (Capsicum annuum L.)
Published 2025-01-01“…The genes were found to be located on different chromosomes, and phylogenetic tree and collinearity analyses were performed. …”
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1182
A genome-wide association study identified candidate regions and genes for commercial traits in a Landrace population
Published 2025-01-01“…Our analysis revealed a total of 118 genome-wide significant signals located on chromosomes SSC1, SSC2, SSC7, SSC12, and SSC13, respectively. …”
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1183
Cytosolic DNA composition is determined by genomic instability mechanism and regulates dendritic cell-mediated anti-tumor immunity
Published 2025-02-01“…Summary: Patients with colorectal cancers (CRCs) that have microsatellite instability (MSI) (MSI CRCs) face a better prognosis than those with the more common chromosomal instability (CIN) subtype (CIN CRCs) due to improved T cell-mediated anti-tumor immune responses. …”
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1184
A near-complete genome assembly of Cinchona calisaya
Published 2025-01-01“…Notably, 99.75% of the sequences have been successfully anchored to 17 chromosomes, with only 12 gaps remaining. BUSCO assessment indicates that 97.40% of complete core genes are present in the assembly. …”
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1185
Unique Genotypic Differences Discovered among Indigenous Bangladeshi Rice Landraces
Published 2014-01-01“…An identity map for these genotypes was constructed with all the 12 chromosomes of the rice genome. Polymorphism information content (PIC) scores of the 34 SSR markers were 0.098 to 0.89 where on average 7.5 alleles were observed. …”
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1186
MAPPING OF QTLS DETERMINING THE EXPRESSION OF AGRONOMICALLY AND ECONOMICALLY VALUABLE FEATURES IN SPRING WHEAT (TRITICUM AESTIVUM L.) GROWN IN ENVIRONMENTALLY DIFFERENT RUSSIA REGI...
Published 2014-12-01“…QTLs for traits studied, mapped on 21 chromosomes, manifested themselves under contrasting environmental conditions with varying degrees of reliability. …”
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1187
Identification and Characterization of the <i>LecRLKs</i> Gene Family in Maize, and Its Role Under Biotic and Abiotic Stress
Published 2024-12-01“…It analyzes the gene structure, chromosomal locations, phylogenetic classification, promoter homoeotropic elements, and expression patterns under both biotic and abiotic stresses. …”
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1188
Pseudohypoparathyroidism type 1A presenting as short stature and congenital hypothyroidism
Published 2025-01-01“…However, reduced growth velocity can also occur as the first sign of chronic anemia, malnutrition, deprivation (psychosocial dwarfism), chromosomal abnormalities, genetic syndromes and inflammatory bowel diseases. …”
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1189
Epichloë scottii sp. nov., a new endophyte isolated from Melica uniflora is the missing ancestor of Epichloë disjuncta
Published 2022-02-01“…We further release a telomere-to-telomere de novo assembly of all seven chromosomes and the mitogenome of E. scottii sp. nov.…”
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1190
Diphenhydramine as a Cause of Drug-Induced Liver Injury
Published 2017-01-01“…A 28-year-old man with history of 13/14-chromosomal translocation presented with fevers, vomiting, and jaundice. …”
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1191
A Review: CRISPR Cas System and the Mechanism With an Inhibition of Binding of CRISPR Cas‐9
Published 2025-01-01“…This review emphasizes the effect of DNA structure and chromosomal protein on Cas 9 binding with a distinct classification of Cas types. …”
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1192
Genotypic and Phenotypic Assessment of Hyaluronidase among Type Strains of a Select Group of Staphylococcal Species
Published 2009-01-01“…The purpose of the present study was to determine the prevalence of hyaluronidase among clinical strains of Staphylococcus aureus and among other Staphylococcus species. Spent media and chromosomal DNA were assessed for hyaluronidase activity and the absence or presence of a hyaluronidase gene (hysA) by Southern analysis, respectively. …”
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1193
Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T
Published 2020-01-01“…Left ventricular hypertrabeculation/noncompaction is a myocardial abnormality of unknown etiology/pathogenesis, which is frequently associated with neuromuscular disorders or chromosomal defects. LVHT in association with a MYOT mutation has not been reported. …”
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1194
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1195
Stably Integrated for Assessment of Invasion Kinetics
Published 2008-09-01“…Thus, a nondestructive real-time assay was developed to report eukaryotic cell invasion kinetics using lux+ Salmonella that contain chromosomally integrated luxCDABE genes. Bioluminescence-based invasion assays using lux+ Salmonella exhibited inoculum dose-response correlation, distinguished invasion-competent from invasion-incompetent Salmonella , and discriminated relative Salmonella invasiveness in accordance with environmental conditions that induce invasion gene expression. …”
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1196
Genetic Basis of Sjögren's Syndrome. How Strong is the Evidence?
Published 2006-01-01“…The observed aggregation of AIDs in families of patients with primary SS is nevertheless supportive for a genetic component in its etiology. In the absence of chromosomal regions identified by linkage studies, research has focused on candidate gene approaches (by biological plausibility) rather than on positional approaches. …”
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1197
Transformation of Follicular Lymphoma to Double Hit B-Cell Lymphoma Causing Hypercalcemia in a 69-Year-Old Female: A Case Report and Review of the Literature
Published 2014-01-01“…Double hit B-cell lymphomas are rare tumors that are defined by a chromosomal breakpoint affecting the MYC/8q24 locus in combination with another recurrent breakpoint, mainly a t(14;18)(q32;q21) involving BCL2. …”
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1198
Models for Natural Killer Cell Repertoire Formation
Published 2003-01-01“…Since inhibitory receptor genes and MHC class I genes are located on different chromosomes, and are hence not automatically co-inherited, NK cells apparently adapt to the MHC environment during their development. …”
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1199
Identification of homozygosity-rich regions in the Holstein genome
Published 2023-09-01“…The length of the ROH segments varied from 1 Mb to over 16 Mb, with the largest number of ROH having a length of 1–2 Mb. Of the 29 chromosomes, BTA 14, BTA 16, and BTA 7 were the most covered by ROH. …”
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1200
The Impact of the Metabolic Syndrome Severity on the Appearance of Primary and Permanent DNA Damage
Published 2024-12-01“…Unrepaired damage can lead to DNA base changes, chromosomal mutations, genomic loss and instability, and disrupted gene and protein expression. …”
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