Autophagy Genes for Wet Age-Related Macular Degeneration in a Finnish Case-Control Study.
Genes
Paterno, Jussi J JJ; Koskela, Ali A; Hyttinen, Juha M T JMT; Vattulainen, Elina E; Synowiec, Ewelina E; Tuuminen, Raimo R; Watala, Cezary C; Blasiak, Janusz J; Kaarniranta, Kai K
Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.
Communications Biology
Perrino, Peter A PA; Talbot, Lidiya L; Kirkland, Rose R; Hill, Amanda A; Rendall, Amanda R AR; Mountford, Hayley S HS; Taylor, Jenny J; , ; Buscarello, Alexzandrea N AN; Lahiri, Nayana N; Saggar, Anand A; Fitch, R Holly RH; Newbury, Dianne F DF
A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma.
Scientific Reports
Stringer, Brett W BW; Day, Bryan W BW; D'Souza, Rochelle C J RCJ; Jamieson, Paul R PR; Ensbey, Kathleen S KS; Bruce, Zara C ZC; Lim, Yi Chieh YC; Goasdoué, Kate K; Offenhäuser, Carolin C; Akgül, Seçkin S; Allan, Suzanne S; Robertson, Thomas T; Lucas, Peter P; Tollesson, Gert G; Campbell, Scott S; Winter, Craig C; Do, Hongdo H; Dobrovic, Alexander A; Inglis, Po-Ling PL; Jeffree, Rosalind L RL; Johns, Terrance G TG; Boyd, Andrew W AW
Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.
Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort.
Frontiers In Genetics
Klein, Kathrin K; Tremmel, Roman R; Winter, Stefan S; Fehr, Sarah S; Battke, Florian F; Scheurenbrand, Tim T; Schaeffeler, Elke E; Biskup, Saskia S; Schwab, Matthias M; Zanger, Ulrich M UM
Myopathy With SQSTM1 and TIA1 Variants: Clinical and Pathological Features.
Frontiers In Neurology
Niu, Zhiyv Z; Pontifex, Carly Sabine CS; Berini, Sarah S; Hamilton, Leslie E LE; Naddaf, Elie E; Wieben, Eric E; Aleff, Ross A RA; Martens, Kristina K; Gruber, Angela A; Engel, Andrew G AG; Pfeffer, Gerald G; Milone, Margherita M
Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.
Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Genomics of ADME gene expression: mapping expression quantitative trait loci relevant for absorption, distribution, metabolism and excretion of drugs in human liver.
The Pharmacogenomics Journal
Schröder, A A; Klein, K K; Winter, S S; Schwab, M M; Bonin, M M; Zell, A A; Zanger, U M UM
High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.
Bmc Genetics
Daelemans, Caroline C; Ritchie, Matthew E ME; Smits, Guillaume G; Abu-Amero, Sayeda S; Sudbery, Ian M IM; Forrest, Matthew S MS; Campino, Susana S; Clark, Taane G TG; Stanier, Philip P; Kwiatkowski, Dominic D; Deloukas, Panos P; Dermitzakis, Emmanouil T ET; Tavaré, Simon S; Moore, Gudrun E GE; Dunham, Ian I