Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del-CFTR Homozygous Patient Populations

por Stanke, Frauke, Becker, Tim, Ismer, Haide Susanne, Dunsche, Inga, Hedtfeld, Silke, Kontsendorn, Julia, Dittrich, Anna-Maria, Tümmler, Burkhard
Publicado 2021

Analysis of CF patient survival confirms STAT3 as a CF-modifying gene with changing impact over time

por Dunsche, Inga, Raddatz, Ellen L, Ismer, Haide, Hedtfeld, Silke, Tamm, Stephanie, Moser, Saskia, Kontsendorn, Julia, Tümmler, Burkhard, Janciauskiene, Sabina, Dittrich, Anna-Maria, Stanke, Frauke
Publicado 2022