Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.
Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss.
American Journal Of Human Genetics
Trpchevska, Natalia N; Freidin, Maxim B MB; Broer, Linda L; Oosterloo, Berthe C BC; Yao, Shuyang S; Zhou, Yitian Y; Vona, Barbara B; Bishop, Charles C; Bizaki-Vallaskangas, Argyro A; Canlon, Barbara B; Castellana, Fabio F; Chasman, Daniel I DI; Cherny, Stacey S; Christensen, Kaare K; Concas, Maria Pina MP; Correa, Adolfo A; Elkon, Ran R; , ; Mengel-From, Jonas J; Gao, Yan Y; Giersch, Anne B S ABS; Girotto, Giorgia G; Gudjonsson, Alexander A; Gudnason, Vilmundur V; Heard-Costa, Nancy L NL; Hertzano, Ronna R; Hjelmborg, Jacob V B JVB; Hjerling-Leffler, Jens J; Hoffman, Howard J HJ; Kaprio, Jaakko J; Kettunen, Johannes J; Krebs, Kristi K; Kähler, Anna K AK; Lallemend, Francois F; Launer, Lenore J LJ; Lee, I-Min IM; Leonard, Hampton H; Li, Chuan-Ming CM; Lowenheim, Hubert H; Magnusson, Patrik K E PKE; van Meurs, Joyce J; Milani, Lili L; Morton, Cynthia C CC; Mäkitie, Antti A; Nalls, Mike A MA; Nardone, Giuseppe Giovanni GG; Nygaard, Marianne M; Palviainen, Teemu T; Pratt, Sheila S; Quaranta, Nicola N; Rämö, Joel J; Saarentaus, Elmo E; Sardone, Rodolfo R; Satizabal, Claudia L CL; Schweinfurth, John M JM; Seshadri, Sudha S; Shiroma, Eric E; Shulman, Eldad E; Simonsick, Eleanor E; Spankovich, Christopher C; Tropitzsch, Anke A; Lauschke, Volker M VM; Sullivan, Patrick F PF; Goedegebure, Andre A; Cederroth, Christopher R CR; Williams, Frances M K FMK; Nagtegaal, Andries Paul AP
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
Bruse, Shannon S; Moreau, Michael M; Bromberg, Yana Y; Jang, Jun-Ho JH; Wang, Nan N; Ha, Hongseok H; Picchi, Maria M; Lin, Yong Y; Langley, Raymond J RJ; Qualls, Clifford C; Klensney-Tait, Julia J; Zabner, Joseph J; Leng, Shuguang S; Mao, Jenny J; Belinsky, Steven A SA; Xing, Jinchuan J; Nyunoya, Toru T
Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.
Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC