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BMC Medical Genomics|March 6, 2022
Association of CATSPER1, SPATA16 and TEX11 genes polymorphism with idiopathic azoospermia and oligospermia risk in Iranian populationMohammadreza Behvarz, Seyyed Ali Rahmani, Elham Siasi Torbati, et al.
BMC Medical Genomics|March 29, 2022
Findings from precision oncology in the clinic: rare, novel variants are a significant contributor to scaling molecular diagnosticsKenneth D Doig, Christopher G Love, Thomas Conway, et al.
BMC Medical Genomics|April 2, 2022
The landscape of GWAS validation; systematic review identifying 309 validated non-coding variants across 130 human diseasesAmmar J Alsheikh, Sabrina Wollenhaupt, Emily A King, et al.
BMC Medical Genomics|June 5, 2019
Hepatic transcriptomic signatures of statin treatment are associated with impaired glucose homeostasis in severely obese patientsDaniel Margerie, Philippe Lefebvre, Violeta Raverdy, et al.
BMC Medical Genomics|October 18, 2019
The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington's disease brainFilisia Agus, Diego Crespo, Richard H Myers, et al.
BMC Medical Genomics|October 18, 2019
Genome-wide discovery and characterization of long noncoding RNAs in patients with multiple myelomaMinqiu Lu, Ying Hu, Yin Wu, et al.
BMC Medical Genomics|June 2, 2019
Single-cell RNA sequencing reveals the impact of chromosomal instability on glioblastoma cancer stem cellsYanding Zhao, Robert Carter, Sivaraman Natarajan, et al.
BMC Medical Genomics|October 19, 2019
Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencingDebora Mancini-DiNardo, Thaddeus Judkins, John Kidd, et al.
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