1,660 results on '"Ried, Thomas"'
Search Results
202. Molecular patterns in the evolution of serrated lesion of the colorectum
203. Concurrent V(D)J recombination and DNA end instability increase interchromosomal trans-rearrangements in ATM-deficient thymocytes
204. Macrophage migration inhibitory factor induces epithelial to mesenchymal transition, enhances tumor aggressiveness and predicts clinical outcome in resected pancreatic ductal adenocarcinoma
205. Genomic instability in mouse Burkitt lymphoma is dominated by illegitimate genetic recombinations, not point mutations
206. Mammary tumors in mice conditionally mutant for Brca1 exhibit gross genomic instability and centrosome amplification yet display a recurring distribution of genomic imbalances that is similar to human breast cancer
207. MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site
208. Characterization of Chromosomal Translocations in Mouse Models of Hematological Malignancies Using Spectral Karyotyping, FISH, and Immunocytochemistry
209. Centrosome abnormalities, recurring deletions of chromosome 4, and genomic amplification of HER2/neu define mouse mammary gland adenocarcinomas induced by mutant HER2/neu
210. AID is required to initiate Nbs1/γ-H2AX focus formation and mutations at sites of class switching
211. Linking the human cytogenetic map with nucleotide sequence: the CCAP clone set
212. Complex rearrangements involving der(8)t(8;20) and der(14)t(8;14)t(11;14), CCND1, and duplication of IgH constant region in acute plasmablastic leukemia
213. Comparative genome hybridization reveals specific genomic imbalances during the genesis from benign through borderline to malignant ovarian tumors
214. Horizontal transmission and retention of malignancy, as well as functional human genes, after spontaneous fusion of human glioblastoma and hamster host cells in vivo
215. All-trans-retinoic acid and cetuximab: Effects on colon adenocarcinoma cell viability
216. Serum mesothelin and megakaryocyte potentiating factor in pancreatic and biliary cancers
217. Effects of granulocyte–colony-stimulating factor on Monosomy 7 aneuploidy in healthy hematopoietic stem cell and granulocyte donors
218. Molekulare Genetik des Pankreaskarzinoms
219. Ataxia telangiectasia mutated is essential during adult neurogenesis
220. Silencing of the Wnt transcription factor TCF4 sensitizes colorectal cancer cells to (chemo-) radiotherapy
221. Decreased microRNA-214 levels in breast cancer cells coincides with increased cell proliferation, invasion and accumulation of the Polycomb Ezh2 methyltransferase
222. A genomic strategy for the functional validation of colorectal cancer genes identifies potential therapeutic targets
223. Genome Instability Profiles Predict Disease Outcome in a Cohort of 4,003 Patients with Breast Cancer
224. Abstract 2498: miFISH single cell analysis as a potential tool to stratify the progression risk in patients with Atypical Ductal Hyperplasia (ADH)
225. Single-Cell–Derived Primary Rectal Carcinoma Cell Lines Reflect Intratumor Heterogeneity Associated with Treatment Response
226. NO•/RUNX3/kynurenine metabolic signaling enhances disease aggressiveness in pancreatic cancer
227. TCF7L2 Silencing Reprograms the 4D Nucleome of Colorectal Cancer Cells
228. Tetraploidy-Associated Genetic Heterogeneity Confers Chemo-Radiotherapy Resistance to Colorectal Cancer Cells
229. Experimental Validation of a Multidimensional Model for an Indirect Temperature Swing Adsorption Unit
230. Novel renal medullary carcinoma cell lines, UOK353 and UOK360 , provide preclinical tools to identify new therapeutic treatments
231. Tumor heterogeneity assessed by sequencing and fluorescencein situhybridization (FISH) data
232. Suppressing proteasome mediated processing of topoisomerase II DNA-protein complexes preserves genome integrity
233. Author response: Suppressing proteasome mediated processing of topoisomerase II DNA-protein complexes preserves genome integrity
234. A targeted disruption of the murine Brca1 gene causes γ-irradiation hypersensitivity and genetic instability
235. Amplification of Ki-ras and elevation of MAP kinase activity during mammary tumor progression in C3(1)/SV40 Tag transgenic mice
236. Identification of de novo chromosomal markers and derivatives by spectral karyotyping
237. DNA repair protein Ku80 suppresses chromosomal aberrations and malignant transformation
238. A 12-gene genomic instability signature predicts clinical outcomes in multiple cancer types
239. The landscape of genomic copy number alterations in colorectal cancer and their consequences on gene expression levels and disease outcome
240. Myc/p53 interactions in transgenic mouse mammary development, tumorigenesis and chromosomal instability
241. Nucleation Capacity and Presence of Centrioles Define a Distinct Category of Centrosome Abnormalities that Induces Multipolar Mitoses in Cancer Cells
242. Homage to Theodor Boveri (1862–1915): Boveriʼs Theory of Cancer as a Disease of the Chromosomes, and the Landscape of Genomic Imbalances in Human Carcinomas
243. The extent of chromosomal aberrations induced by chemotherapy in non-human primates depends on the schedule of administration
244. The gene expression signature of genomic instability in breast cancer is an independent predictor of clinical outcome
245. Characterization of ABCG2 gene amplification manifesting as extrachromosomal DNA in mitoxantrone-selected SF295 human glioblastoma cells
246. Pediatric pancreatoblastoma: histopathologic and cytogenetic characterization of tumor and derived cell line
247. Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities
248. Investigation of cell populations in an in vitro intratumoral heterogeneity model of solid tumors
249. Characterization of double minute chromosomes’ DNA content in a human high grade astrocytoma cell line by using comparative genomic hybridization and fluorescence in situ hybridization
250. Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation: A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGH
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