Auflistung 4 Medizinische Fakultät nach Titel

DSpace Repositorium (Manakin basiert)

Auflistung 4 Medizinische Fakultät nach Titel

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  • Genomic features of exceptional response in vemurafenib +/- cobimetinib-treated patients with BRAF(V600)-mutated metastatic melanoma
    Yan, Yibing; Wongchenko, Matthew J.; Robert, Caroline; Larkin, James; Ascierto, Paolo A.; Dreno, Brigitte; Maio, Michele; Garbe, Claus; Chapman, Paul B.; Sosman, Jeffrey A.; Shi, Zhen; Koeppen, Hartmut; Hsu, Jessie J.; Chang, Ilsung; Caro, Ivor; Rooney, Isabelle; McArthur, Grant A.; Ribas, Antoni (2019)
  • Genomic insights into specialized metabolism in the marine actinomycete Salinispora
    Letzel, Anne-Catrin; Li, Jing; Amos, Gregory C. A.; Millan-Aguinaga, Natalie; Ginigini, Joape; Abdelmohsen, Usama R.; Gaudencio, Susana P.; Ziemert, Nadine; Moore, Bradley S.; Jensen, Paul R. (2017)
  • Genomic profiling for clinical decision making in lymphoid neoplasms
    de Leval, Laurence; Alizadeh, Ash A.; Bergsagel, P. Leif; Campo, Elias; Davies, Andrew; Dogan, Ahmet; Fitzgibbon, Jude; Horwitz, Steven M.; Melnick, Ari M.; Morice, William G.; Morin, Ryan D.; Nadel, Bertrand; Pileri, Stefano A.; Rosenquist, Richard; Rossi, Davide; Salaverria, Itziar; Steidl, Christian; Treon, Steven P.; Zelenetz, Andrew D.; Advani, Ranjana H.; Allen, Carl E.; Ansell, Stephen M.; Chan, Wing C.; Cook, James R.; Cook, Lucy B.; D'Amore, Francesco; Dirnhofer, Stefan; Dreyling, Martin; Dunleavy, Kieron; Feldman, Andrew L.; Fend, Falko; Gaulard, Philippe; Ghia, Paolo; Gribben, John G.; Hermine, Olivier; Hodson, Daniel J.; Hsi, Eric D.; Inghirami, Giorgio; Jaffe, Elaine S.; Karube, Kennosuke; Kataoka, Keisuke; Klapper, Wolfram; Kim, Won Seog; King, Rebecca L.; Ko, Young H.; LaCasce, Ann S.; Lenz, Georg; Martin-Subero, Jose, I; Piris, Miguel A.; Pittaluga, Stefania; Pasqualucci, Laura; Quintanilla-Martinez, Leticia; Rodig, Scott J.; Rosenwald, Andreas; Salles, Gilles A.; San-Miguel, Jesus; Savage, Kerry J.; Sehn, Laurie H.; Semenzato, Gianpietro; Staudt, Louis M.; Swerdlow, Steven H.; Tam, Constantine S.; Trotman, Judith; Vose, Julie M.; Weigert, Oliver; Wilson, Wyndham H.; Winter, Jane N.; Wu, Catherine J.; Zinzani, Pier L.; Zucca, Emanuele; Bagg, Adam; Scott, David W. (2022)
  • Genomic resources for wild populations of the house mouse, Mus musculus and its close relative Mus spretus
    Harr, Bettina; Karakoc, Emre; Neme, Rafik; Teschke, Meike; Pfeifle, Christine; Pezer, Zeljka; Babiker, Hiba; Linnenbrink, Miriam; Montero, Inka; Scavetta, Rick; Abai, Mohammad Reza; Puente Molins, Marta; Schlegel, Mathias; Ulrich, Rainer G.; Altmueller, Janine; Franitza, Marek; Buentge, Anna; Kuenzel, Sven; Tautz, Diethard (2016)
  • Genomic stratification by expression of HLA-DRB4 alleles identifies differential innate and adaptive immune transcriptional patterns - A strategy to detect predictors of methotrexate response in early rheumatoid arthritis
    Mans, Karsten; Tandon, Neeraj; Bonin, Marc O.; Smiljanovic, Biljana; Schendel, Pascal; Martus, Peter; Listing, Joachim; Detert, Jacqueline; Backhaus, Marina; Neumann, Thomas; Winchester, Robert J.; Burmester, Gerd-R.; Stuhlmüller, Bruno; Sörensen, Till A.; Häupl, Thomas (2016)
  • Genomic surveillance of SARS-CoV-2 in the Republic of Congo
    Ntoumi, Francine; Mapanguy, Claujens Chastel Mfoutou; Tomazatos, Alexandru; Pallerla, Srinivas Reddy; Le Thi Kieu Linh; Casadei, Nicolas; Angelov, Angel; Sonnabend, Michael; Peter, Silke; Kremsner, Peter G.; Velavan, Thirumalaisamy P. (2021)
  • Genomics of ADME gene expression: mapping expression quantitative trait loci relevant for absorption, distribution, metabolism and excretion of drugs in human liver
    Schroeder, A.; Klein, K.; Winter, S.; Schwab, M.; Bonin, M.; Zell, A.; Zanger, U. M. (2013)
  • Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): A study protocol
    Borges, Jessica Bassani; de Oliveira, Victor Fernandes; Ferreira, Glaucio Monteiro; Los, Bruna; Almendros Afonso Barbosa, Thais Kristini; Rodrigues Marcal, Elisangela da Silva; Dagli-Hernandez, Carolina; Costa de Freitas, Renata Caroline; Bortolin, Raul Hernandes; Mori, Augusto Akira; Crespo Hirata, Thiago Dominguez; Imoto Nakaya, Helder Takashi; Bastos, Gisele Medeiros; Thurow, Helena Strelow; Goncalves, Rodrigo Marques; de Araujo, Daniel Branco; Zatz, Henry Paulo; Bertolami, Adriana; Faludi, Andre Arpad; Bertolami, Marcelo Chiara; de Moraes Rego Sousa, Amanda Guerra; Franca, Joao Italo Dias; Jannes, Cinthia Elim; Pereira, Alexandre da Costa; Nakazone, Marcelo Arruda; Silva Souza, Doroteia Rossi; Carmo, Tayanne Silva; Sampaio, Marcelo Ferraz; Gorjao, Renata; Pithon-Curi, Tania Cristina; Moriel, Patricia; Silbiger, Vivian Nogueira; Luchessi, Andre Ducati; Goes de Araujo, Jessica Nayara; Naslavsky, Michel Satya; Wang, Jaqueline Yu Ting; Kronenberger, Thales; Cerda, Alvaro; Lin-Wang, Hui Tzu; Garofalo, Adriana Regina; Fajardo, Cristina Moreno; Crespo Hirata, Rosario Dominguez; Hirata, Mario Hiroyuki (2021)
  • Genotyp-Phänotyp-Korrelation bei Schwerhörigkeit: Genetische Varianten im peripheren Hörsystem und die Hörleistung mit Cochlea-Implantat
    Dofek, Saskia Jasmin (2019)
  • Genotyp-Phänotyp-Korrelationen bei Kindern und Jugendlichen mit nichtklassischem adrenogenitalen Syndrom mit 21-Hydroxylase-Defekt
    Doerr, H. G.; Schulze, N.; Bettendorf, M.; Binder, G.; Bonfig, W.; Denzer, C.; Dunstheimer, D.; Salzgeber, K.; Schmidt, H.; Schwab, K. O.; Voss, E.; Wabitsch, M.; Woelfle, J. (2020)
  • Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
    Kouz, Karim; Lissewski, Christina; Spranger, Stephanie; Mitter, Diana; Riess, Angelika; Lopez-Gonzalez, Vanesa; Luettgen, Sabine; Aydin, Hatip; von Deimling, Florian; Evers, Christina; Hahn, Andreas; Hempel, Maja; Issa, Ulrike; Kahlert, Anne-Karin; Lieb, Adrian; Villavicencio-Lorini, Pablo; Juliana Ballesta-Martinez, Maria; Nampoothiri, Sheela; Ovens-Raeder, Angela; Puchmajerova, Alena; Satanovskij, Robin; Seidel, Heide; Unkelbach, Stephan; Zabel, Bernhard; Kutsche, Kerstin; Zenker, Martin (2016)
  • Genotype correlates with the natural history of severe bile salt export pump deficiency
    van Wessel, Daan B. E.; Thompson, Richard J.; Gonzales, Emmanuel; Jankowska, Irena; Sokal, Etienne; Grammatikopoulos, Tassos; Kadaristiana, Agustina; Jacquemin, Emmanuel; Spraul, Anne; Lipinski, Patryk; Czubkowski, Piotr; Rock, Nathalie; Shagrani, Mohammad; Broering, Dieter; Algoufi, Talal; Mazhar, Nejat; Nicastro, Emanuele; Kelly, Deirdre A.; Nebbia, Gabriella; Arnell, Henrik; Fischler, Bjoern; Hulscher, Jan B. F.; Serranti, Daniele; Arikan, Cigdem; Polat, Esra; Debray, Dominique; Lacaille, Florence; Goncalves, Cristina; Hierro, Loreto; Bartolo, Gema Munoz; Mozer-Glassberg, Yael; Azaz, Amer; Brecelj, Jernej; Dezsofi, Antal; Calvo, Pier Luigi; Grabhorn, Enke; Sturm, Ekkehard; van der Woerd, Wendy J.; Kamath, Binita M.; Wang, Jian-She; Li, Liting; Durmaz, Oezlem; Onal, Zerrin; Bunt, Ton M. G.; Hansen, Bettina E.; Verkade, Henkjan J. (2020)
  • Genotype-Phenotype Association and Impact on Outcomes following Guided De-Escalation of Anti-Platelet Treatment in Acute Coronary Syndrome Patients : The TROPICAL-ACS Genotyping Substudy
    Gross, Lisa; Trenk, Dietmar; Jacobshagen, Claudius; Krieg, Anne; Gawaz, Meinrad; Massberg, Steffen; Baylacher, Monika; Aradi, Daniel; Stimpfle, Fabian; Hromek, Julia; Vogelgesang, Anja; Hadamitzky, Martin; Sibbing, Dirk; Geisler, Tobias (2018)
  • Genotype-phenotype correlation in PRKN-associated Parkinson's disease
    Menon, Poornima Jayadev; Sambin, Sara; Criniere-Boizet, Baptiste; Courtin, Thomas; Tesson, Christelle; Casse, Fanny; Ferrien, Melanie; Mariani, Louise-Laure; Carvalho, Stephanie; Lejeune, Francois-Xavier; Rebbah, Sana; Martet, Gaspard; Houot, Marion; Lanore, Aymeric; Mangone, Graziella; Roze, Emmanuel; Vidailhet, Marie; Aasly, Jan; Gan Or, Ziv; Yu, Eric; Dauvilliers, Yves; Zimprich, Alexander; Tomantschger, Volker; Pirker, Walter; Alvarez, Ignacio; Pastor, Pau; Di Fonzo, Alessio; Bhatia, Kailash P.; Magrinelli, Francesca; Houlden, Henry; Real, Raquel; Quattrone, Andrea; Limousin, Patricia; Korlipara, Prasad; Foltynie, Thomas; Grosset, Donald; Williams, Nigel; Narendra, Derek; Lin, Hsin-Pin; Jovanovic, Carna; Svetel, Marina; Lynch, Timothy; Gallagher, Amy; Vandenberghe, Wim; Gasser, Thomas; Brockmann, Kathrin; Morris, Huw R.; Borsche, Max; Klein, Christine; Corti, Olga; Brice, Alexis; Lesage, Suzanne; Corvol, Jean Christophe (2024)
  • Genotype-phenotype correlations in RHOBTB2- associated neurodevelopmental disorders
    Langhammer, Franziska; Maroofian, Reza; Badar, Rueda; Gregor, Anne; Rochman, Michelle; Ratliff, Jeffrey B.; Koopmans, Marije; Herget, Theresia; Hempel, Maja; Kortuem, Fanny; Heron, Delphine; Mignot, Cyril; Keren, Boris; Brooks, Susan; Botti, Christina; Ben-Zeev, Bruria; Argilli, Emanuela; Sherr, Elliot H.; Gowda, Vykuntaraju K.; Srinivasan, Varunvenkat M.; Bakhtiari, Somayeh; Kruer, Michael C.; Salih, Mustafa A.; Kuechler, Alma; Muller, Eric A.; Blocker, Karli; Kuismin, Outi; Park, Kristen L.; Kochhar, Aaina; Brown, Kathleen; Ramanathan, Subhadra; Clark, Robin D.; Elgizouli, Magdeldin; Melikishvili, Gia; Tabatadze, Nazhi; Stark, Zornitza; Mirzaa, Ghayda M.; Ong, Jinfon; Grasshoff, Ute; Bevot, Andrea; von Wintzingerode, Lydia; Jamra, Rami A.; Hennig, Yvonne; Goldenberg, Paula; Al Alam, Chadi; Charif, Majida; Boulouiz, Redouane; Bellaoui, Mohammed; Amrani, Rim; Al Mutairi, Fuad; Tamim, Abdullah M.; Abdulwahab, Firdous; Alkuraya, Fowzan S.; Khouj, Ebtissal M.; Alvi, Javeria R.; Sultan, Tipu; Hashemi, Narges; Karimiani, Ehsan G.; Ashrafzadeh, Farah; Imannezhad, Shima; Efthymiou, Stephanie; Houlden, Henry; Sticht, Heinrich; Zweier, Christiane (2023)
  • Genotype-phenotype correlations in syndromic forms of hereditary retinal diseases
    Nasser, Fadi (2021)
  • Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review
    Atasu, Burcu; Acarli, Ayse Nur Ozdag; Bilgic, Basar; Baykan, Betul; Demir, Erol; Ozluk, Yasemin; Turkmen, Aydin; Hauser, Ann-Kathrin; Guven, Gamze; Hanagasi, Hasmet; Gurvit, Hakan; Emre, Murat; Gasser, Thomas; Lohmann, Ebba (2022)
  • Genotype-Phenotype Correlations, Dystonia and Disease Progression in Spinocerebellar Ataxia Type 14
    Chelban, Viorica; Wiethoff, Sarah; Fabian-Jessing, Bjorn K.; Haridy, Nourelhoda A.; Khan, Alaa; Efthymiou, Stephanie; Becker, Esther B. E.; O'Connor, Emer; Hersheson, Joshua; Newland, Katrina; Hojland, Allan Thomas; Gregersen, Pernille A.; Lindquist, Suzanne G.; Petersen, Michael B.; Nielsen, Jorgen E.; Nielsen, Michael; Wood, Nicholas W.; Giunti, Paola; Houlden, Henry (2018)
  • Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency
    Felzen, Antonia; van Wessel, Daan B. E.; Gonzales, Emmanuel; Thompson, Richard J.; Jankowska, Irena; Shneider, Benjamin L.; Sokal, Etienne; Grammatikopoulos, Tassos; Kadaristiana, Agustina; Jacquemin, Emmanuel; Spraul, Anne; Lipinski, Patryk; Czubkowski, Piotr; Rock, Nathalie; Shagrani, Mohammad; Broering, Dieter; Nicastro, Emanuele; Kelly, Deirdre; Nebbia, Gabriella; Arnell, Henrik; Fischler, Bjoern; Hulscher, Jan B. F.; Serranti, Daniele; Arikan, Cigdem; Polat, Esra; Debray, Dominique; Lacaille, Florence; Goncalves, Cristina; Hierro, Loreto; Bartolo, Gema Munoz; Mozer-Glassberg, Yael; Azaz, Amer; Brecelj, Jernej; Dezsofi, Antal; Calvo, Pier Luigi; Grabhorn, Enke; Hartleif, Steffen; van der Woerd, Wendy J.; Kamath, Binita M.; Wang, Jian-She; Li, Liting; Durmaz, Ozlem; Kerkar, Nanda; Jorgensen, Marianne Horby; Fischer, Ryan; Jimenez-Rivera, Carolina; Alam, Seema; Cananzi, Mara; Laverdure, Noemie; Ferreira, Cristina Targa; Guerrero, Felipe Ordonez; Wang, Heng; Sency, Valerie; Kim, Kyung Mo; Chen, Huey-Ling; de Carvalho, Elisa; Fabre, Alexandre; Bernabeu, Jesus Quintero; Zellos, Aglaia; Alonso, Estella M.; Sokol, Ronald J.; Suchy, Frederick J.; Loomes, Kathleen M.; McKiernan, Patrick J.; Rosenthal, Philip; Turmelle, Yumirle; Horslen, Simon; Schwarz, Kathleen; Bezerra, Jorge A.; Wang, Kasper; Hansen, Bettina E.; Verkade, Henkjan J. (2023)
  • Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6
    Reetz, Kathrin; Costa, Ana S.; Mirzazade, Shahram; Lehmann, Anna; Juzek, Agnes; Rakowicz, Maria; Boguslawska, Romana; Schoels, Ludger; Linnemann, Christoph; Mariotti, Caterina; Grisoli, Marina; Duerr, Alexandra; van de Warrenburg, Bart P.; Timmann, Dagmar; Pandolfo, Massimo; Bauer, Peter; Jacobi, Heike; Hauser, Till-Karsten; Klockgether, Thomas; Schulz, Joerg B. (2013)