Seizure and Hepatosplenomegaly—Rare Manifestation of Parvovirus B-19: A Case Report and Review of the Literature by Yadav Kamlesh, Gupta Pallav, Murari Manjula, Malik Rohan

“…PCR showed amplification of parvovirus genomic sequences. Present case highlights an atypical presentation of Parvovirus B19 infection as fever, rash and hepatosplenomegaly.…”
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Palaeogenetic study of human migrations around the Caspian Sea during protohistory by Perle Guarino-Vignon

“…Our analyses based on modern and ancient DNA genomic data show that the present-day Indo-Iranian-speaking populations, the Tajiks and the Yaghnobis, display a strong genetic continuity with the Iron Age populations of southern Central Asia. …”
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Sekwencjonowanie genomu/eksomu człowieka - aspekt bioetyczny by Andrzej Kochański

“…Thus, at present geneticists have access to the whole genome instead of separate/selected genes. Clinical genetics in the era of genomic sequencing has to cope with new challenges concerning the confidentiality of genetic data, genetic discrimination, genetic and clinical determinism, or incidental findings detected in genome analysis. …”
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Nuclear Reprogramming in Mouse Primordial Germ Cells: Epigenetic Contribution by Massimo De Felici

“…The unique capability of germ cells to give rise to a new organism, allowing the transmission of primary genetic information from generation to generation, depends on their epigenetic reprogramming ability and underlying genomic totipotency. Recent studies have shown that genome-wide epigenetic modifications, referred to as “epigenetic reprogramming”, occur during the development of the gamete precursors termed primordial germ cells (PGCs) in the embryo. …”
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A genetically confirmed hybrid between Natrix astreptophora and N. maura, two deeply divergent and ancient snake species by Andrea Criado-Flórez, Juan Pablo González de la Vega, Gabriel Martínez del Marmol, Uwe Fritz

“…In the face of previously published genomic signatures for ancient gene flow between N. astreptophora and N. maura, our finding raises the question of whether occasional hybridization still contributes to a continued exchange of genetic information between these two deeply divergent and old taxa.…”
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Chorioamnionitis and Lung Injury in Preterm Newborns by Gustavo Rocha

“…Genetic susceptibility to BPD is an evolving area of research and several studies have directly related the risk of BPD to genomic variants. There is a substantial heterogeneity across the studies in the magnitude of the association between chorioamnionitis and BPD, and whether or not the association is statistically significant. …”
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Species-Specific Gene, spt5, in the Qualitative and Quantitative Detection of Boletus reticulatus by Zhan Lei, Chen Zhang, Yinjiao Li, Lunzhao Yi, Ying Shang

“…Meanwhile, SYBR Green I based quantitative PCR results were highly sensitive, and the limit of detection was 0.04 ng of genomic DNA. These experiments illustrated that spt5 is an ideal species-specific gene for the quantitative and qualitative detection of B. reticulatus. …”
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African Orphan Crops under Abiotic Stresses: Challenges and Opportunities by Zerihun Tadele

“…The application of modern genetic and genomic tools to the breeding of these crops can provide enormous opportunities for ensuring world food security but is only in its infancy. …”
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New data on the distribution of six morphologically cryptic species of Niphargus stygius species complex (Amphipoda: Niphargidae) by Janko Šet, Špela Borko

“… Subterranean amphipods, morphologically resembling Niphargus stygius species complex, were molecularly analysed. We isolated genomic DNA and amplified the subunit I of mitochondrial cytochrome oxidase gene (COI) for 94 specimens from 37 localities. …”
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Exploring the Impact of Large Language Models on Disease Diagnosis by Ibrahim Almubark

“…This review shows that LLMs have utilized a variety of medical data sources, including general medical databases, specialized documents, medical images, and genomic data. Moreover, the focus of these LLMs spans a broad spectrum of healthcare fields, addressing chronic conditions, respiratory diseases, cancer, and rare diseases. …”
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Template switching during DNA replication is a prevalent source of adaptive gene amplification by Julie N Chuong, Nadav Ben Nun, Ina Suresh, Julia Cano Matthews, Titir De, Grace Avecilla, Farah Abdul-Rahman, Nathan Brandt, Yoav Ram, David Gresham

“…Copy number variants (CNVs) are an important source of genetic variation underlying rapid adaptation and genome evolution. Whereas point mutation rates vary with genomic location and local DNA features, the role of genome architecture in the formation and evolutionary dynamics of CNVs is poorly understood. …”
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The application of Vavilov’s approaches to the phylogeny and evolution of cultivated species of the genus <i>Avena</i> L. by I. G. Loskutov, A. A. Gnutikov, E. V. Blinova, A. V. Rodionov

“…The methods and approaches that use DNA markers and genomic technologies, and are promising for the study of oat polymorphism and phylogeny have been actively researched recently. …”
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Annotation and characterization of immunoglobulin loci and CDR3 polymorphism in water buffalo (Bubalus bubalis) by Yunlan Deng, Fengli Wu, Fengli Wu, Qianqian Li, Lidie Yao, Chengzhi Yang, Long Ma, Xinsheng Yao, Jun Li

“…The CDR3 repertoires were constructed using genomic DNA extracted from spleen samples of five healthy buffaloes. …”
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Implementation of Accurate and Fast DNA Cytometry by Confocal Microscopy in 3D by Lennert S. Ploeger, André Huisman, Jurryt van der Gugten, Dionne M. van der Giezen, Jeroen A. M. Beliën, Abdelhadi Y. Abbaker, Hub F. J. Dullens, William Grizzle, Neal M. Poulin, Gerrit A. Meijer, Paul J. van Diest

“…Background: DNA cytometry is a powerful method for measuring genomic instability. Standard approaches that measure DNA content of isolated cells may induce selection bias and do not allow interpretation of genomic instability in the context of the tissue. …”
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Set of 15 SNP-SNP Markers for Detection of Unbalanced Degraded DNA Mixtures and Noninvasive Prenatal Paternity Testing by Ranran Zhang, Yu Tan, Li Wang, Hui Jian, Jing Zhu, Yuanyuan Xiao, Mengyu Tan, Jiaming Xue, Fan Yang, Fan Yang, Weibo Liang

“…Besides, all fetal alleles in maternal plasma were confirmed by genotyping fetal genomic DNA from amniocentesis and paternal genomic DNA from peripheral blood. …”
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The miR-146a SNP Rs2910164 and miR-155 SNP rs767649 Are Risk Factors for Non-Small Cell Lung Cancer in the Iranian Population by Neda K. Dezfuli, Ian M. Adcock, Shamila D. Alipoor, Sharareh Seyfi, Babak Salimi, Maryam Mafi Golchin, Neda Dalil Roofchayee, Mohammad Varhram, Esmaeil Mortaz

“…Allele frequencies from the genomic DNA of blood cells were studied using PCR-RFLP and their association with the risk of lung cancer was evaluated. …”
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Syringocystadenocarcinoma Papilliferum in a Fifteen-Year-Old Girl: A Case Report and Review of the Literature by Jordan N. Halsey, Esteban Fernandez Faith, Suzanna J. Logan, Archana Shenoy, Kathleen M. Schieffer, Catherine E. Cottrell, Anna P. Lillis, Jennifer H. Aldrink, Bhuvana A. Setty, Gregory D. Pearson

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Molecular characterization of the TUBG1 meshwork's influence on Cytoskeletal organization by Darina Malycheva, Maria Alvarado-Kristensson

“…The γ-tubulin (TUBG) meshwork is a central regulator of cellular architecture, orchestrating processes such as microtubule nucleation, mitochondrial organization, and genomic integrity. This study investigates the molecular impact of TUBG depletion on the cytoskeleton. …”
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ASGCL: Adaptive Sparse Mapping-based graph contrastive learning network for cancer drug response prediction. by Yunyun Dong, Yuanrong Zhang, Yuhua Qian, Yiming Zhao, Ziting Yang, Xiufang Feng

“…Personalized cancer drug treatment is emerging as a frontier issue in modern medical research. Considering the genomic differences among cancer patients, determining the most effective drug treatment plan is a complex and crucial task. …”
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