Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Fuchs, Helmut  [Clear All Filters]
2024
Tollot-Wegner M, Jessen M, Kim KM, Sanz-Moreno A, Spielmann N, Gailus-Durner V, Fuchs H, de Angelis MHrabĕ, von Eyss B. TRPS1 maintains luminal progenitors in the mammary gland by repressing SRF/MRTF activity. Breast Cancer Res. 2024;26(1):74.
2018
Jensen LR, Garrett L, Hölter SM, Rathkolb B, Racz I, Adler T, Prehn C, Hans W, Rozman J, Becker L, et al. A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 gene. Biochim Biophys Acta Mol Basis Dis. 2018.
2016
Diener S, Bayer S, Sabrautzki S, Wieland T, Mentrup B, Przemeck GKH, Rathkolb B, Graf E, Hans W, Fuchs H, et al. Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia. Mamm Genome. 2016.
2015
de Angelis MHrabě, Nicholson G, Selloum M, White JK, Morgan H, Ramirez-Solis R, Sorg T, Wells S, Fuchs H, Fray M, et al. Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nat Genet. 2015.
2014
Blanco S, Dietmann S, Flores JV, Hussain S, Kutter C, Humphreys P, Lukk M, Lombard P, Treps L, Popis M, et al. Aberrant methylation of tRNAs links cellular stress to neuro-developmental disorders. EMBO J. 2014.
Kraus P, V S, Yu HBing, Xing X, Lim SLan, Adler T, Pimentel JAntonio Ag, Becker L, Bohla A, Garrett L, et al. Pleiotropic Functions for Transcription Factor Zscan10. PLoS One. 2014;9(8):e104568.