Showing results (941-950 of 1,113) with videos related to
Sort By:
Pageof 112
Human Genomics|September 24, 2015
Eyeing the Cyr61/CTGF/NOV (CCN) group of genes in development and diseases: highlights of their structural likenesses and functional dissimilaritiesIzabela Krupska, Elspeth A Bruford, Brahim ChaqourHuman Genomics|October 15, 2015
Integrative DNA methylation and gene expression analysis to assess the universality of the CpG island methylator phenotypeMatahi Moarii, Fabien Reyal, Jean-Philippe VertHuman Genomics|December 16, 2014
Whole exome sequencing of a single osteosarcoma case--integrative analysis with whole transcriptome RNA-seq dataEne Reimann, Sulev Kõks, Xuan Dung Ho, et al.Human Genomics|December 16, 2014
Molecular signatures that correlate with induction of lens regeneration in newts: lessons from proteomic analysisKonstantinos Sousounis, Rital Bhavsar, Mario Looso, et al.Human Genomics|September 10, 2020
Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese populationMandy H Y Tsang, Anna K Y Kwong, Kate L S Chan, et al.Human Genomics|September 12, 2020
Analysis of ACE2 genetic variants in 131 Italian SARS-CoV-2-positive patientsAntonio Novelli, Michela Biancolella, Paola Borgiani, et al.Human Genomics|February 20, 2020
TRPM3_miR-204: a complex locus for eye development and diseaseAlan ShielsHuman Genomics|March 8, 2020
Hyperinsulinism associated with GLUD1 mutation: allosteric regulation and functional characterization of p.G446V glutamate dehydrogenaseKarolina Luczkowska, Caroline Stekelenburg, Frédérique Sloan-Béna, et al.Human Genomics|February 1, 2018
Meeting report of the 2017 KidGen Renal Genetics SymposiumKushani Jayasinghe, Cathy Quinlan, Zornitza Stark, et al.Human Genomics|February 4, 2018
The genetic structure of the Belgian populationJimmy Van den Eynden, Tine Descamps, Els Delporte, et al.Pageof 112