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BMC Medical Genomics|June 16, 2021
A method for cryopreservation and single nucleus RNA-sequencing of normal adult human interventricular septum heart tissue reveals cellular diversity and functionAmy Larson, Michael T ChinBMC Medical Genomics|December 1, 2020
Utility of a custom designed next generation DNA sequencing gene panel to molecularly classify endometrial cancers according to The Cancer Genome Atlas subgroupsEirwen M Miller, Nicole E Patterson, Gregory M Gressel, et al.BMC Medical Genomics|May 27, 2021
In-vivo design feedback and perceived utility of a genetically-informed smoking risk tool among current smokers in the communityJessica L Bourdon, Amelia Dorsey, Maia Zalik, et al.BMC Medical Genomics|March 11, 2020
Transcriptome analysis of HPV-induced warts and healthy skin in humansLaith N Al-Eitan, Amneh H Tarkhan, Mansour A Alghamdi, et al.BMC Medical Genomics|July 8, 2022
Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected familyJing Chen, Qinqin Xiang, Xiao Xiao, et al.BMC Medical Genomics|July 8, 2022
Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutationXue Gong, Yunru He, Guoyan Lu, et al.BMC Medical Genomics|June 15, 2022
FTO rs62033406 A>G associated with the risk of osteonecrosis of the femoral head among the Chinese Han populationYuan Wang, Wei Zhong, Shaofeng Wang, et al.BMC Medical Genomics|December 25, 2022
Novel compound heterozygous mutations of MTHFR Gene in a Chinese family with homocystinuria due to MTHFR deficiencyYitong Lu, Shaozhi Zhao, Xiaohui He, et al.BMC Medical Genomics|June 20, 2021
Screening the genome for HCC-specific CpG methylation signatures as biomarkers for diagnosis and prognosis evaluationRui-Kun Zhang, Jia-Lin LiuBMC Medical Genomics|June 23, 2021
Frequent POLE-driven hypermutation in ovarian endometrioid cancer revealed by mutational signatures in RNA sequencingJaime I Davila, Pritha Chanana, Vivekananda Sarangi, et al.Pageof 276