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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 5, 2019
Mice with a Brd4 Mutation Represent a New Model of NephrocalcinosisCaroline M Gorvin, Nellie Y Loh, Michael J Stechman, et al.Pharmacogenomics|April 21, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association studyStefan Wolking, Herbert Schulz, Anne T Nies, et al.Epilepsia|February 6, 2019
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsyHerbert Schulz, Ann-Kathrin Ruppert, Federico Zara, et al.Plos One|September 4, 2009
The FunGenES database: a genomics resource for mouse embryonic stem cell differentiationHerbert Schulz, Raivo Kolde, Priit Adler, et al.Plos Genetics|May 8, 2015
Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsiesDennis Lal, Ann-Kathrin Ruppert, Holger Trucks, et al.Nature|September 10, 2010
A trans-acting locus regulates an anti-viral expression network and type 1 diabetes riskMatthias Heinig, Enrico Petretto, Chris Wallace, et al.Nature Genetics|April 30, 2008
SNP and haplotype mapping for genetic analysis in the rat, Kathrin Saar, Alfred Beck, et al.Nature Genetics|May 12, 2015
PDE3A mutations cause autosomal dominant hypertension with brachydactylyPhilipp G Maass, Atakan Aydin, Friedrich C Luft, et al.Epilepsia|January 17, 2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies, Costin Leu, Carolien G F de Kovel, et al.Nature Genetics|May 28, 2013
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats, Amelie Baud, Roel Hermsen, et al.Pageof 13