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Cousin, M.A.* et al.: RINT1 Bi-allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities. Am. J. Hum. Genet. 105, 108-121 (2019)
Yang, Y.* et al.: Acylcarnitine profiles in serum and muscle of dairy cows receiving conjugated linoleic acids or a control fat supplement during early lactation. J. Dairy Sci. 102, 754-767 (2019)
Shashi, V.* et al.: Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegeneration. EMBO J., accepted (2018)
Yang, Y.* et al.: Molecular genetic overlap between migraine and major depressive disorder. Eur. J. Hum. Genet. 26, 1202-1216 (2018)
Cooper, H.M.* et al.: ATPase-deficient mitochondrial inner membrane protein ATAD3a disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia. Hum. Mol. Genet. 26, 1432-1443 (2017)
Lessel, D.* et al.: De novo missense mutations in DHX30 impair global translation and cause a neurodevelopmental disorder. Am. J. Hum. Genet. 101, 716-724 (2017)
Wahl, S. et al.: Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity. Nature 541, 81-86 (2017)
Yin, R.* et al.: Dispersal and transmission of avian paramyxovirus serotype 4 among wild birds and domestic poultry. Front. Cell. Infect. Microbiol. 7:212 (2017)
He, X.* et al.: Analysis of titanium and other metals in human jawbones with dental implants - a case series study. Dent. Mater. 32, 1042-1051 (2016)
Xie, Q.* et al.: Pax6 Interactions with chromatin and identification of its novel direct target genes in lens and forebrain. PLoS ONE 8:e54507 (2013)
Lu, X.* et al.: Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. Nat. Genet. 44, 890-894 (2012)
Hemme, C.L.* et al.: Sequencing of multiple clostridial genomes related to biomass conversion and biofuel production. J. Bacteriol. 192, 6494-6496 (2010)
Sarwar, N.* et al.: Triglyceride-mediated pathways and coronary disease: Collaborative analysis of 101 studies. Lancet 375, 1634-1639 (2010)