Showing results (1361-1370 of 2,771) with videos related to
Sort By:
Pageof 278
BMC Medical Genomics|June 13, 2026
Genetic diversity of the Plasmodium falciparum msp2 gene in children from the Eastern Democratic Republic of Congo: a comparative study of clinical and subclinical infectionsMoski Morisho Nasibu, Lambert Morisho Mulakwa, Serge Muganda Chirimwami, et al.BMC Medical Genomics|July 4, 2026
Elective genomic sequencing for adults in research, clinical and commercial contextsMichael D Linderman, Sophia M Adelson, Tala M Berro, et al.BMC Medical Genomics|June 19, 2026
Genomic determinants of fluoroquinolone resistance in Escherichia coli in Nigeria: dominance of QRDR mutations and limited contribution of PMQR in a cross-sectional studyNubwa Medugu, Mabel Kamweli Aworh, Khadija Abdulraheem, et al.BMC Medical Genomics|July 9, 2026
Identification and growth features of developmental delay with macrocephaly caused by a novel TRIO variant affecting the second SH3 domainSi-Yuan Zhang, Jie-Yuan Jin, Lei Zeng, et al.BMC Medical Genomics|July 7, 2026
Integrated transcriptomic and metabolomic analysis identifies a core gene-metabolite network linking lysine degradation and propanoate metabolism to psoriasis pathogenesisHongkai Zheng, Rujun Xue, Wei Li, et al.BMC Medical Genomics|July 14, 2026
Gender-wise distribution of metabolic risk factors and their relationship with fibroblast growth factor 1 and gene polymorphism (rs152524)Saima Naz Mohsin, Faiza Saleem, Natasha Waheed, et al.BMC Medical Genomics|July 21, 2026
Breakpoint-level characterization of a novel CEP290 tandem duplication in trans with a pathogenic splice-site variant in a patient with Leber congenital amaurosisShumei Xu, Jia Geng, Wenyu Xiong, et al.BMC Medical Genomics|July 16, 2026
The infero-apical left ventricular aneurysm and long QT syndrome caused by mutation delKKP 1504-1506 in SCN5A geneZhijuan Lu, Jiadong Lin, Yi Chen, et al.BMC Medical Genomics|July 25, 2015
Expression analysis of human adipose-derived stem cells during in vitro differentiation to an adipocyte lineageLatha Satish, J Michael Krill-Burger, Phillip H Gallo, et al.BMC Medical Genomics|May 27, 2025
Comprehensive analysis of a novel LYST mutation in a Tunisian patient with Chediak-Higashi syndromeYessine Amri, Saoussen Chouchene, Hajer Foddha, et al.Pageof 278