A systematic evaluation of hybridization-based mouse exome capture system

por Gao, Qingsong, Sun, Wei, You, Xintian, Froehler, Sebastian, Chen, Wei
Publicado 2013

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation

por Farag, Heba Gamal, Froehler, Sebastian, Oexle, Konrad, Ravindran, Ethiraj, Schindler, Detlev, Staab, Timo, Huebner, Angela, Kraemer, Nadine, Chen, Wei, Kaindl, Angela M
Publicado 2013

HDAC4 mutations cause diabetes and induce β‐cell FoxO1 nuclear exclusion

por Gong, Maolian, Yu, Yong, Liang, Lei, Vuralli, Dogus, Froehler, Sebastian, Kuehnen, Peter, Du Bois, Philipp, Zhang, Jingjing, Cao, Aidi, Liu, Yuantao, Hussain, Khalid, Fielitz, Jens, Jia, Shiqi, Chen, Wei, Raile, Klemens
Publicado 2019

Plasma-based longitudinal mutation monitoring as a potential predictor of disease progression in subjects with adenocarcinoma in advanced non-small cell lung cancer

por Jiang, John, Adams, Hans-Peter, Lange, Maria, Siemann, Sandra, Feldkamp, Mirjam, McNamara, Sylvie, Froehler, Sebastian, Yaung, Stephanie J., Yao, Lijing, Balasubramanyam, Aarthi, Tikoo, Nalin, Ju, Christine, Achenbach, H. Jost, Krügel, Rainer, Palma, John F.
Publicado 2020