Showing results (441-450 of 2,754) with videos related to

Sort By:
Pageof 276
BMC Medical Genomics|January 29, 2010
Association of adipocyte genes with ASP expression: a microarray analysis of subcutaneous and omental adipose tissue in morbidly obese subjectsRobin E MacLaren, Wei Cui, HuiLing Lu, et al.
BMC Medical Genomics|April 5, 2018
Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case reportLiuh Ling Goh, Yingshan Lee, Ee Shien Tan, et al.
BMC Medical Genomics|April 5, 2023
Test development, optimization and validation of a WGS pipeline for genetic disordersZiying Yang, Xu Yang, Yan Sun, et al.
BMC Medical Genomics|April 20, 2023
Basement membrane-related regulators for prediction of prognoses and responses to diverse therapies in hepatocellular carcinomaRuili Ding, Chuanbing Zhao, Yixin Jing, et al.
BMC Medical Genomics|March 29, 2023
Outcomes of two different unbalanced segregations from a maternal t(4;10)(q33;p15.1) translocationJudith Fan, T Niroshini Senaratne, Jason Y Liu, et al.
BMC Medical Genomics|March 29, 2023
Bioinformatics screening of colorectal-cancer causing molecular signatures through gene expression profiles to discover therapeutic targets and candidate agentsMd Abu Horaira, Md Ariful Islam, Md Kaderi Kibria, et al.
BMC Medical Genomics|April 4, 2023
Xp22.31 copy number variations in 87 fetuses: refined genotype-phenotype correlations by prenatal and postnatal follow-upHuamei Hu, Yulin Huang, Renke Hou, et al.
BMC Medical Genomics|April 4, 2023
Confounding factors in profiling of locus-specific human endogenous retrovirus (HERV) transcript signatures in primary T cells using multi-study-derived datasetsMartin V Hamann, Maisha Adiba, Ulrike C Lange
BMC Medical Genomics|April 4, 2023
Expression signature and molecular basis of CDH11 in OSCC detected by a combination of multiple methodsYuxing Wei, Xujie Cheng, Limei Deng, et al.
BMC Medical Genomics|March 30, 2021
Genetic investigation of 211 Chinese families expands the mutational and phenotypical spectra of hereditary retinopathy genes through targeted sequencing technologyZhouxian Bai, Yanchuan Xie, Lina Liu, et al.
Pageof 276