Australia (AU)

ISCEV extended protocol for the photopic negative response (PhNR) of the full-field electroretinogram (2018) Frishman L, Sustar M, Kremers J, Mcanany JJ, Sarossy M, Tzekov R, Viswanathan S Journal article De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation (2018) Basilicata MF, Bruel AL, Semplicio G, Valsecchi CIK, Aktas T, Duffourd Y, Rumpf T, et al. Journal article MiR-205-5p and miR-342-3p cooperate in the repression of the E2F1 transcription factor in the context of anticancer chemotherapy resistance (2018) Lai X, Gupta SK, Schmitz U, Marquardt S, Knoll S, Spitschak A, Wolkenhauer O, et al. Journal article, Original article Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation (2018) Teumer A, Chaker L, Groeneweg S, Li Y, Di Munno C, Barbieri C, Schultheiss UT, et al. Journal article De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder (2018) Gregor A, Sadleir LG, Asadollahi R, Azzarello-Burri S, Battaglia A, Ousager LB, Boonsawat P, et al. Journal article Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses (2018) Painter JN, O'Mara TA, Morris AP, Cheng THT, Gorman M, Martin L, Hodson S, et al. Journal article Identification of nine new susceptibility loci for endometrial cancer (2018) O'Mara TA, Glubb DM, Amant F, Annibali D, Ashton K, Attia J, Auer PL, et al. Journal article Effective Priming of Herpes Simplex Virus-Specific CD8+T CellsIn VivoDoes Not Require Infected Dendritic Cells (2018) Whitney PG, Makhlouf C, Macleod B, Ma JZ, Gressier E, Greyer M, Hochheiser K, et al. Journal article Biallelic Expression of Mucin-1 in Autosomal Dominant Tubulointerstitial Kidney Disease: Implications for Nongenetic Disease Recognition (2018) Knaup K, Hackenbeck T, Popp B, Stoeckert J, Wenzel A, Büttner-Herold M, Pfister F, et al. Journal article Biphasic papillary renal cell carcinoma is a rare morphological variant with frequent multifocality: a study of 28 cases (2018) Trpkov K, Athanazio D, Magi-Galluzzi C, Yilmaz H, Clouston D, Agaimy A, Williamson SR, et al. Journal article