Resultados de procura - Weinhold, Nils

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

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

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Local Function Conservation in Sequence and Structure Space por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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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