A Multifunctional LNA Oligonucleotide-Based Strategy Blocks AR Expression and Transactivation Activity in PCa Cells von Castanotto, Daniela, Zhang, Xiaowei, Rüger, Jacqueline, Alluin, Jessica, Sharma, Ritin, Pirrotte, Patrick, Joenson, Lars, Ioannou, Silvia, Nelson, Michael S., Vikeså, Jonas, Hansen, Bo Rode, Koch, Troels, Jensen, Mads Aaboe, Rossi, John J., Stein, Cy A.

Volltext

Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature von Ostergaard, Elsebet, Weraarpachai, Woranontee, Ravn, Kirstine, Born, Alfred Peter, Jønson, Lars, Duno, Morten, Wibrand, Flemming, Shoubridge, Eric A, Vissing, John

Volltext

Germline Chromothripsis Driven by L1-Mediated Retrotransposition and Alu/Alu Homologous Recombination von Nazaryan-Petersen, Lusine, Bertelsen, Birgitte, Bak, Mads, Jønson, Lars, Tommerup, Niels, Hancks, Dustin C, Tümer, Zeynep

Volltext

Functional characterization of BRCA1 gene variants by mini-gene splicing assay von Steffensen, Ane Y, Dandanell, Mette, Jønson, Lars, Ejlertsen, Bent, Gerdes, Anne-Marie, Nielsen, Finn C, Hansen, Thomas vO

Volltext

Molecular Composition of IMP1 Ribonucleoprotein Granules von J⊘nson, Lars, Vikesaa, Jonas, Krogh, Anders, Nielsen, Lars K., Hansen, Thomas vO, Borup, Rehannah, Johnsen, Anders H., Christiansen, Jan, Nielsen, Finn C.

Volltext

RNA-binding IMPs promote cell adhesion and invadopodia formation von Vikesaa, Jonas, Hansen, Thomas VO, Jønson, Lars, Borup, Rehannah, Wewer, Ulla M, Christiansen, Jan, Nielsen, Finn C

Volltext

Next-generation sequencing: proof of concept for antenatal prediction of the fetal Kell blood group phenotype from cell-free fetal DNA in maternal plasma von Rieneck, Klaus, Bak, Mads, Jønson, Lars, Clausen, Frederik Banch, Krog, Grethe Risum, Tommerup, Niels, Nielsen, Leif Kofoed, Hedegaard, Morten, Dziegiel, Morten Hanefeld

Volltext

Identification of six pathogenic RAD51C mutations via mutational screening of 1228 Danish individuals with increased risk of hereditary breast and/or ovarian cancer von Jønson, Lars, Ahlborn, Lise B., Steffensen, Ane Y., Djursby, Malene, Ejlertsen, Bent, Timshel, Susanne, Nielsen, Finn C., Gerdes, Anne-Marie, Hansen, Thomas V. O.

Volltext

Personalized oncology: genomic screening in phase 1 von Tuxen, Ida Viller, Jønson, Lars, Santoni-Rugiu, Eric, Hasselby, Jane Preuss, Nielsen, Finn Cilius, Lassen, Ulrik

Volltext

Abstract 3140: Differential clonal selection in tumor tissue and cell-free DNA from a neratinib-treated refractory breast cancer patient harboring an activating ERBB2 (HER2) mutati... von Joenson, Lars, Yde, Christina W., Østrup, Olga, Mau-Sørensen, Morten, Nielsen, Finn C., Lassen, Ulrik

Volltext

Dynamics of mutant BRAF V600E in free circulating DNA (fcDNA) of non-melanoma cancer patients (pts) in response to treatment with BRAF and MEK/EGFR inhibitors von Mau-Soerensen, Morten, Ahlborn, Lise Barlebo, Joenson, Lars, Oestrup, Olga, Hasselby, Jane Preuss, Santoni-Rugiu, Eric, Nielsen, Finn Cilius, Lassen, Ulrik Niels, Yde, Christina Westmose

Volltext

Actionable targets in recurrent bile duct and pancreatic cancer in a prospective cohort of patients evaluated by whole exome sequencing and SNP array analysis von Tuxen, Ida Elisabeth Viller, Mau-Soerensen, Morten, Yde, Christina Westmose, Joenson, Lars, Oestrup, Olga, Hasselby, Jane Preuss, Santoni-Rugiu, Eric, Lassen, Ulrik Niels, Nielsen, Finn Cilius

Volltext

Characterization of BRCA1 and BRCA2 splicing variants: a collaborative report by ENIGMA consortium members von Thomassen, Mads, Blanco, Ana, Montagna, Marco, Hansen, Thomas V. O., Pedersen, Inge S., Gutiérrez-Enríquez, Sara, Menéndez, Mireia, Fachal, Laura, Santamariña, Marta, Steffensen, Ane Y., Jønson, Lars, Agata, Simona, Whiley, Phillip, Tognazzo, Silvia, Tornero, Eva, Jensen, Uffe B., Balmaña, Judith, Kruse, Torben A., Goldgar, David E., Lázaro, Conxi, Diez, Orland, Spurdle, Amanda B., Vega, Ana

Volltext

Copenhagen prospective personalized oncology (CoPPO): Sequencing and array-based pipeline for selection of patients to phase 1 studies von Tuxen, Ida Elisabeth Viller, Santoni-Rugiu, Eric, Joenson, Lars, Vikesaa, Jonas, Mau-Soerensen, Morten, Nielsen, Finn Cilius, Lassen, Ulrik Niels

Volltext

Molecular profiling of tumour budding to implicate TGF-β mediated epithelial-mesenchymal transition as a therapeutic target von Jensen, David Hebbelstrup, Dabelsteen, Erik, Specht, Lena, Fiehn, anne-Marie Kanstrup, Therkildsen, Marianne Hamilton, Nielsen, Finn Cilius, Joenson, Lars, Vikesaa, Jonas, von Buchwald, Christian

Volltext

Genome‐wide identification of genes required for growth of Saccharomyces cerevisiae under ethanol stress von van Voorst, Frank, Houghton‐Larsen, Jens, Jønson, Lars, Kielland‐Brandt, Morten C., Brandt, Anders

Volltext

Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families von Hansen, Thomas v. O, Jønson, Lars, Albrechtsen, Anders, Andersen, Mette K, Ejlertsen, Bent, Nielsen, Finn C

Volltext

Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations von Ahlborn, Lise B., Steffensen, Ane Y., Jønson, Lars, Djursby, Malene, Nielsen, Finn C., Gerdes, Anne-Marie, Hansen, Thomas V. O.

Volltext

IMP3 RNP Safe Houses Prevent miRNA-Directed HMGA2 mRNA Decay in Cancer and Development von Jønson, Lars, Christiansen, Jan, Hansen, Thomas V.O., Vikeså, Jonas, Yamamoto, Yohei, Nielsen, Finn C.

Volltext

Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a nucleotide 249T>A/c.130T>A (p.Cys44Ser) mutation in two Greenlandic Inuit families: implications for... von Hansen, Thomas v. O, Jønson, Lars, Albrechtsen, Anders, Steffensen, Ane Y, Bergsten, Eva, Myrhøj, Torben, Ejlertsen, Bent, Nielsen, Finn C

Volltext