Showing results (31-40 of 46) with videos related to
Sort By:
Pageof 5
Molecular Carcinogenesis|February 24, 2006
Dephosphorylation of p-ERK1/2 in relation to tumor remission after HER-2 and Raf1 blocking therapy in a conditional mouse tumor modelCarolin K Hausherr, Ilka B Schiffer, Susanne Gebhard, et al.Oncotarget|April 13, 2018
Calcium-sensing receptor (CaSR) promotes development of bone metastasis in renal cell carcinomaSebastian Frees, Ines Breuksch, Tobias Haber, et al.Proceedings of the National Academy of Sciences of the United States of America|March 4, 2005
Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumorDirk Prawitt, Thorsten Enklaar, Barbara Gärtner-Rupprecht, et al.EXCLI Journal|February 28, 2022
Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformationDanuta Galetzka, Julia Böck, Lukas Wagner, et al.Oncotarget|September 15, 2017
Overriding TKI resistance of renal cell carcinoma by combination therapy with IL-6 receptor blockadeKei Ishibashi, Tobias Haber, Ines Breuksch, et al.Human Molecular Genetics|November 3, 2012
The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sitesJasmin Beygo, Valentina Citro, Angela Sparago, et al.Journal of Molecular Medicine (Berlin, Germany)|September 26, 2020
Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patientsDanuta Galetzka, Tobias Müller, Marcus Dittrich, et al.Cancer Research|February 12, 2005
Premature senescence is a primary fail-safe mechanism of ERBB2-driven tumorigenesis in breast carcinoma cellsTatjana M Trost, Ekkehart U Lausch, Stephan A Fees, et al.British Journal of Cancer|May 27, 2020
Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort studySümeyye Cöktü, Claudia Spix, Melanie Kaiser, et al.Epigenomics|June 21, 2016
Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbancesSusanne Bens, Julia Kolarova, Jasmin Beygo, et al.Pageof 5