Publications
Found 10 results
Filters: Keyword is Mutation [Clear All Filters]
Low-frequency somatic mutations are heritable in tropical trees and . Proc Natl Acad Sci U S A. 2024;121(10):e2313312121. doi:10.1073/pnas.2313312121.
. Re-evaluating the driving force behind mutations. Elife. 2023;12. doi:10.7554/eLife.89706.
Anti-Müllerian hormone regulation by the bone morphogenetic proteins in the sheep ovary: deciphering a direct regulatory pathway. Endocrinology. 2015;156(1):301-13. doi:10.1210/en.2014-1551.
. Does heterozygosity at the DMRT3 gene make French trotters better racers?. Genet Sel Evol. 2015;47:10. doi:10.1186/s12711-015-0095-7.
Genetic variants within the second intron of the KCNQ1 gene affect CTCF binding and confer a risk of Beckwith-Wiedemann syndrome upon maternal transmission. J Med Genet. 2014;51(8):502-11. doi:10.1136/jmedgenet-2014-102368.
. Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes. Clin Genet. 2012;81(4):350-61. doi:10.1111/j.1399-0004.2011.01822.x.
Molecular characterization of the porcine TEAD3 (TEF-5) gene: examination of a promoter mutation as the causal mutation of a quantitative trait loci affecting the androstenone level in boar fat. J Anim Breed Genet. 2012;129(4):325-35. doi:10.1111/j.1439-0388.2011.00979.x.
Epilepsy caused by an abnormal alternative splicing with dosage effect of the SV2A gene in a chicken model. PloS one. 2011;6:e26932. doi:10.1371/journal.pone.0026932.
Epilepsy caused by an abnormal alternative splicing with dosage effect of the SV2A gene in a chicken model. PLoS One. 2011;6(10):e26932. doi:10.1371/journal.pone.0026932.