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Molecular Genetics & Genomic Medicine|March 26, 2019
Functional analysis of haplotypes and promoter activity at the 5' region of the human GABRB3 gene and associations with schizophreniaYi Liu, Mei Ding, Yong-Ping Liu, et al.Molecular Genetics & Genomic Medicine|March 28, 2019
Uniparental isodisomy of chromosome 1 results in glycogen storage disease type III with profound growth retardationEmanuela Ponzi, Viola Alesi, Francesca R Lepri, et al.Molecular Genetics & Genomic Medicine|February 22, 2019
Targeted next generation sequencing identified novel loss-of-function mutations in MERTK gene in Chinese patients with retinitis pigmentosaSong Liu, Jian Gang Bi, Yunlong Hu, et al.Molecular Genetics & Genomic Medicine|February 23, 2019
Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencingSamantha N Hartin, Waheeda A Hossain, David Francis, et al.Molecular Genetics & Genomic Medicine|February 23, 2019
The promising novel biomarkers and candidate small molecule drugs in kidney renal clear cell carcinoma: Evidence from bioinformatics analysis of high-throughput dataBo Zhang, Qiong Wu, Ziheng Wang, et al.Molecular Genetics & Genomic Medicine|August 28, 2019
The role of AGG interruptions in the FMR1 gene stability: A survey in ethnic groups with low and high rate of consanguinityEsther Manor, Raphael Gonen, Benjamin Sarussi, et al.Molecular Genetics & Genomic Medicine|August 29, 2019
SOD3 overexpression alleviates cerebral ischemia-reperfusion injury in ratsShuaiqi Sun, Ning Gao, Xiqi Hu, et al.Molecular Genetics & Genomic Medicine|August 21, 2019
miR-1249-3p accelerates the malignancy phenotype of hepatocellular carcinoma by directly targeting HNRNPKHongchun Shu, Jia Hu, Huiqiu DengMolecular Genetics & Genomic Medicine|September 8, 2019
Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variationsVincent Gatinois, Nicole Bigi, Eve Mousty, et al.Molecular Genetics & Genomic Medicine|September 7, 2019
Docking-based approach for identification of mutations that disrupt binding between Bcl-2 and Bax proteins: Inducing apoptosis in cancer cellsPawan Kumar Raghav, Rajesh Kumar, Vinod Kumar, et al.Pageof 252