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Effect of selection for growth on reproductive traits in Nellore females: Genetic parameters and genome-wide association studies
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MicroRNA bioinformatics in precision oncology: an integrated pipeline from NGS to AI-based target discovery
Despite the growing recognition of microRNAs (miRNAs) as critical biomarkers in cancer, current approaches to their analys...
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Association of polymorphisms of antioxidants (GSTM1/T1) and inflammation-related genes (CXCL8, IL-33, and IL-6) with chronic obstructive pulmonary disease (COPD)
Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality globally. COPD, within its cont...
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Extricating the allelic variation, population structure and genetic potential in buckwheat genotypes and substantiation of high yielding and stable genotypes with superior biochemical quality
Buckwheat is an underutilized crop with high nutritional values and antioxidant properties. The study was conducted with a...
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Genetic variations in NFKB1 signaling molecules: implications for acute lymphoblastic leukemia in Saudi Arabia
Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signaling regulates immune responses and tumor...
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The role of the gene in porcine adipogenesis: a study using CRISPR/Cas9-edited mesenchymal stem cells
Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 is a powerful tool for gene editing and the regula...
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Rare co-existence of 15q26 deletion syndrome and lymphangioleiomyomatosis: diagnostic and therapeutic challenge
15q26 deletion syndrome is a rare genetic condition caused by the deletion of terminal end of the long arm of chromosome 1...
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Further evidence for a wide phenotypic and mutational spectrum of Cohen syndrome: case report and literature review
Cohen syndrome (CS) is a rare autosomal recessive disorder caused by biallelic pathogenic variants in the VPS13B gene. It ...
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Exploring the pathogenic mechanism of RNH1 in colorectal cancer based on eQTL, Multi-omics and deep learning
Background: Colorectal cancer (CRC) is a major global health concern with increasing incidence. Current treatments, though...
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Clinicopathological and genomic profiling in undifferentiated pleomorphic sarcoma: Small series, clear message
Undifferentiated pleomorphic sarcoma (UPS) is a diagnosis of exclusion; given limited effective treatments and marked hete...
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Computational analysis of Non-synonymous SNP effects on human PLVAP gene structure and function
Plasmalemma vesicle-associated protein (PLVAP) plays a pivotal role in regulating endothelial permeability and maintaining...
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Polymorphism of the gene in Polish children and adolescents with short stature and diverse growth hormone secretion
HMGA2 is one of the common genes strongly associated with adult and childhood height. Some studies have also linked this g...
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Characterization of spelt wheat ( L.) genotypes using DArTseq technology
The aim of this study was to apply DArTseq technology to analyze T. spelta L. (spelt wheat) genotypes in order to eliminat...
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Accelerating genetic gain through integrated genomic selection in crop plants
Meeting the projected 70% rise in agricultural output by 2050 to sustain a global population of 9.6 billion poses a formid...
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When genetics meets immunology: the assessment of genetic and immunological backgrounds in advanced NSCLC patients treated with immunotherapy – preliminary study
Non-small-cell lung cancer treatment relies greatly on immunotherapy, especially in individuals without targetable mutatio...
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Updated sequence of ramoplanin biosynthetic gene cluster from ATCC 33,076
Actinoplanes ramoplaninifer ATCC 33,076 is the only known producer of the glycolipodepsipeptide antibiotic ramoplanin. Ram...
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Epstein–barr virus and multiple sclerosis: from pathogenesis and diagnosis to EBV-specific T cell therapy and gene-targeted therapeutics
Multiple sclerosis (MS) is a central nervous system (CNS) disorder defined by inflammation, demyelination, and neuronal da...
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Genetic architecture of the sieve element occlusion (SEO) family underlying potential regulatory mechanisms in citrus stress response
The Sieve Element Occlusion (SEO) proteins are subunits that assemble into structural filamentous phloem proteins, commonl...
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Fibrodysplasia ossificans progressiva: genetic and clinical characterization in a cohort of Polish patients and review of potential therapies
Fibrodysplasia ossificans progressiva (FOP; OMIM #135100) is a rare genetic disorder characterized by congenital malformat...
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In silico approach on structural and functional characterization of heat shock protein from
The 70 kDa heat shock proteins (Hsp70 s) are highly conserved and ubiquitous molecular chaperones. Hsp70 proteins are inti...
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Spinocerebellar ataxia 27B (SCA27B)—a systematic review and a case report of a Polish family
Dominantly inherited GAA repeat expansions in the FGF14 gene have recently been identified as the cause of spinocerebellar...
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Melatonin in crop plants: from biosynthesis through pleiotropic effects to enhanced stress resilience
Melatonin plays a crucial role in enhancing plant resilience to environmental stresses by regulating physiological and bio...
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Transcriptomic analysis of inhibitory effects of isothiazolone antimicrobial agents on ZR
The preservation of marine specimens requires effective methods to ensure research accuracy and ecological sustainability....
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Identification of non-synonymous SNPs affecting structure and function of MLH1 and NBN proteins: a computational approach
The genes NBN and MLH1 are critical for DNA repair, and this study aimed to detect and predict the effects of pathogenic s...
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Genome-wide identification and characterization of NAC transcription factor–derived microsatellites in wheat ( L.)
Bread wheat (Triticum aestivum L.) is one of the widely consumed staple foods, providing 20% of the total protein and calo...
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Elucidating the transcriptomic response of adult-derived mHypoA-2/12 mouse hypothalamic neuron cell line to cannabidiol (CBD) exposure
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Genetic mapping of the head blight resistance gene in wheat Guixie 3
Fusarium head blight (FHB) is a global detrimental disease affecting wheat production. While Guixie 3 shows strong resista...
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Riboflavin treatment in L-2-hydroxyglutaric aciduria: report on a pediatric patient and literature review
L-2-hydroxyglutaric aciduria (L-2-HGA, #236,792) is an autosomal recessive neurodegenerative disorder caused by the defici...
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Identification of a migracytosis and angiogenesis-associated lncRNAs signature in immunotherapy in breast cancer
Migracytosis and angiogenesis were crucial in breast cancer (BRCA) progression. This study aimed to develop a prognostic s...
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