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Human Genetics|August 29, 2013
The missing "link": an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutationJulia Schreml, Burak Durmaz, Ozgur Cogulu, et al.Human Molecular Genetics|January 7, 2015
CRIM1 haploinsufficiency causes defects in eye development in human and mouseFilippo Beleggia, Yun Li, Jieqing Fan, et al.Scientific Reports|November 16, 2017
Targeting a non-oncogene addiction to the ATR/CHK1 axis for the treatment of small cell lung cancerFabian Doerr, Julie George, Anna Schmitt, et al.Cancer Research|August 14, 2019
Dual Inhibition of GLUT1 and the ATR/CHK1 Kinase Axis Displays Synergistic Cytotoxicity in KRAS-Mutant Cancer CellsJohanna Erber, Joachim D Steiner, Jörg Isensee, et al.BMC Research Notes|September 8, 2025
Imaging mass cytometry dataset of small-cell lung cancer tumors and tumor microenvironmentsFrance Rose, Olta Ibruli, Luca Lichius, et al.Cell|April 17, 2026
Cancer neuroscience: The past, the present, and the road aheadFrank Winkler, Sophie Heuer, Ferdinand Althammer, et al.Communications Biology|May 13, 2025
TAT-CRE inhalation enables tumor induction corresponding to adenoviral Cre-recombinase in a lung cancer mouse modelTabea Gewalt, Anna M Dmitrieva, Felix Elsner, et al.American Journal of Human Genetics|February 17, 2015
Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfectaLutz Garbes, Kyungho Kim, Angelika Rieß, et al.Blood Advances|December 7, 2023
An inducible Cd79b mutation confers ibrutinib sensitivity in mouse models of Myd88-driven diffuse large B-cell lymphomaRuth Flümann, Julia Hansen, Jörn Meinel, et al.Nature Communications|April 7, 2021
Ferroptosis response segregates small cell lung cancer (SCLC) neuroendocrine subtypesChristina M Bebber, Emily S Thomas, Jenny Stroh, et al.Pageof 4