Výsledky vyhledávání - Weinhold, Nils

The impact of the protein interactome on the syntenic structure of mammalian genomes Autor Kirk, Isa Kristina, Weinhold, Nils, Brunak, Søren, Belling, Kirstine

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Protein-Protein interactions uncover candidate ‘core genes’ within omnigenic disease networks Autor Ratnakumar, Abhirami, Weinhold, Nils, Mar, Jessica C., Riaz, Nadeem

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Local Function Conservation in Sequence and Structure Space Autor Weinhold, Nils, Sander, Oliver, Domingues, Francisco S., Lengauer, Thomas, Sommer, Ingolf

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Genome-wide analysis of non-coding regulatory mutations in cancer Autor Weinhold, Nils, Jacobsen, Anders, Schultz, Nikolaus, Sander, Chris, Lee, William

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Systematic Characterisation of Cellular Localisation and Expression Profiles of Proteins Containing MHC Ligands Autor Juncker, Agnieszka S., Larsen, Mette V., Weinhold, Nils, Nielsen, Morten, Brunak, Søren, Lund, Ole

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p53-intact cancers escape tumor suppression through loss of long noncoding RNA Dino Autor Marney, Christina B., Anderson, Erik S., Adnan, Mutayyaba, Peng, Kai-Lin, Hu, Ya, Weinhold, Nils, Schmitt, Adam M.

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Recurrent SERPINB3 and SERPINB4 Mutations in Patients that Respond to Anti-CTLA4 Immunotherapy Autor Riaz, Nadeem, Havel, Jonathan J., Kendall, Sviatoslav M., Makarov, Vladimir, Walsh, Logan A., Desrichard, Alexis, Weinhold, Nils, Chan, Timothy A.

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Deciphering Diseases and Biological Targets for Environmental Chemicals using Toxicogenomics Networks Autor Audouze, Karine, Juncker, Agnieszka Sierakowska, Roque, Francisco J. S. S. A., Krysiak-Baltyn, Konrad, Weinhold, Nils, Taboureau, Olivier, Jensen, Thomas Skøt, Brunak, Søren

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Pan-cancer analysis of bi-allelic alterations in homologous recombination DNA repair genes Autor Riaz, Nadeem, Blecua, Pedro, Lim, Raymond S., Shen, Ronglai, Higginson, Daniel S., Weinhold, Nils, Norton, Larry, Weigelt, Britta, Powell, Simon N., Reis-Filho, Jorge S.

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ChemProt: a disease chemical biology database Autor Taboureau, Olivier, Nielsen, Sonny Kim, Audouze, Karine, Weinhold, Nils, Edsgärd, Daniel, Roque, Francisco S., Kouskoumvekaki, Irene, Bora, Alina, Curpan, Ramona, Jensen, Thomas Skøt, Brunak, Søren, Oprea, Tudor I.

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Relating genomic variation to drug response in childhood acute lymphoblastic leukemia by multiplexed targeted sequencing Autor Wesolowska, Agata, Dalgaard, Marlene D, Borst, Louise, Gautier, Laurent, Bak, Mads, Weinhold, Nils, Nielsen, Betina F, Nersting, Jacob, Tommerup, Niels, Brunak, Søren, Ponten, Thomas Sicheritz, Leffers, Henrik, Schmiegelow, Kjeld, Gupta, Ramneek

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Genome-Wide Assessment of the Association of Rare and Common Copy Number Variations to Testicular Germ Cell Cancer Autor Edsgärd, Daniel, Dalgaard, Marlene D., Weinhold, Nils, Wesolowska-Andersen, Agata, Rajpert-De Meyts, Ewa, Ottesen, Anne Marie, Juul, Anders, Skakkebæk, Niels E., Skøt Jensen, Thomas, Gupta, Ramneek, Leffers, Henrik, Brunak, Søren

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Exonuclease mutations in DNA polymerase epsilon reveal replication strand specific mutation patterns and human origins of replication Autor Shinbrot, Eve, Henninger, Erin E., Weinhold, Nils, Covington, Kyle R., Göksenin, A. Yasemin, Schultz, Nikolaus, Chao, Hsu, Doddapaneni, HarshaVardhan, Muzny, Donna M., Gibbs, Richard A., Sander, Chris, Pursell, Zachary F., Wheeler, David A.

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DNA methyltransferase 1 and DNA methylation patterning contribute to germinal center B-cell differentiation Autor Shaknovich, Rita, Cerchietti, Leandro, Tsikitas, Lucas, Kormaksson, Matthias, De, Subhajyoti, Figueroa, Maria E., Ballon, Gianna, Yang, Shao Ning, Weinhold, Nils, Reimers, Mark, Clozel, Thomas, Luttrop, Karin, Ekstrom, Tomas J., Frank, Jared, Vasanthakumar, Aparna, Godley, Lucy A., Michor, Franziska, Elemento, Olivier, Melnick, Ari

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A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation Autor Dalgaard, Marlene D, Weinhold, Nils, Edsgärd, Daniel, Silver, Jeremy D, Pers, Tune H, Nielsen, John E, Jørgensen, Niels, Juul, Anders, Gerds, Thomas A, Giwercman, Aleksander, Giwercman, Yvonne L, Cohn-Cedermark, Gabriella, Virtanen, Helena E, Toppari, Jorma, Daugaard, Gedske, Jensen, Thomas S, Brunak, Søren, Rajpert-De Meyts, Ewa, Skakkebæk, Niels E, Leffers, Henrik, Gupta, Ramneek

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Prevalence and Co-Occurrence of Actionable Genomic Alterations in High-Grade Bladder Cancer Autor Iyer, Gopa, Al-Ahmadie, Hikmat, Schultz, Nikolaus, Hanrahan, Aphrothiti J., Ostrovnaya, Irina, Balar, Arjun V., Kim, Philip H., Lin, Oscar, Weinhold, Nils, Sander, Chris, Zabor, Emily C., Janakiraman, Manickam, Garcia-Grossman, Ilana R., Heguy, Adriana, Viale, Agnes, Bochner, Bernard H., Reuter, Victor E., Bajorin, Dean F., Milowsky, Matthew I., Taylor, Barry S., Solit, David B.

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Genetic diversity of tumors with mismatch repair deficiency influences anti–PD-1 immunotherapy response Autor Mandal, Rajarsi, Samstein, Robert M., Lee, Ken-Wing, Havel, Jonathan J., Wang, Hao, Krishna, Chirag, Sabio, Erich Y., Makarov, Vladimir, Kuo, Fengshen, Blecua, Pedro, Ramaswamy, Apoorva T., Durham, Jennifer N., Bartlett, Bjarne, Ma, Xiaoxiao, Srivastava, Raghvendra, Middha, Sumit, Zehir, Ahmet, Hechtman, Jaclyn F., Morris, Luc GT, Weinhold, Nils, Riaz, Nadeem, Le, Dung T., Diaz, Luis A., Chan, Timothy A.

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The SWI/SNF Protein PBRM1 Restrains VHL Loss-Driven Clear Cell Renal Cell Carcinoma Autor Nargund, Amrita M., Pham, Can G., Dong, Yiyu, Wang, Patricia I., Osmangeyoglu, Hatice U., Xie, Yuchen, Aras, Omer, Han, Song, Oyama, Toshinao, Takeda, Shugaku, Ray, Chelsea E., Dong, Zhenghong, Berge, Mathieu, Hakimi, A Ari, Monette, Sebastien, Lekaye, Carl L., Koutcher, Jason A., Leslie, Christina S., Creighton, Chad J., Weinhold, Nils, Lee, William, Tickoo, Satish K., Wang, Zhong, Cheng, Emily H., Hsieh, James J.

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Genomic Biomarkers of a Randomized Trial Comparing First-line Everolimus and Sunitinib in Patients with Metastatic Renal Cell Carcinoma Autor Hsieh, James J., Chen, David, Wang, Patricia I., Marker, Mahtab, Redzematovic, Almedina, Chen, Ying-Bei, Selcuklu, S. Duygu, Weinhold, Nils, Bouvier, Nancy, Huberman, Kety H., Bhanot, Umesh, Chevinsky, Michael S., Patel, Parul, Pinciroli, Patrizia, Won, Helen H., You, Daoqi, Viale, Agnes, Lee, William, Hakimi, A. Ari, Berger, Michael F., Socci, Nicholas D., Cheng, Emily H., Knox, Jennifer, Voss, Martin H., Voi, Maurizio, Motzer, Robert J.

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Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis Autor Erson-Omay, E. Zeynep, Çağlayan, Ahmet Okay, Schultz, Nikolaus, Weinhold, Nils, Omay, S. Bülent, Özduman, Koray, Köksal, Yavuz, Li, Jie, Serin Harmancı, Akdes, Clark, Victoria, Carrión-Grant, Geneive, Baranoski, Jacob, Çağlar, Caner, Barak, Tanyeri, Coşkun, Süleyman, Baran, Burçin, Köse, Doğan, Sun, Jia, Bakırcıoğlu, Mehmet, Moliterno Günel, Jennifer, Pamir, M. Necmettin, Mishra-Gorur, Ketu, Bilguvar, Kaya, Yasuno, Katsuhito, Vortmeyer, Alexander, Huttner, Anita J., Sander, Chris, Günel, Murat

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