Auflistung 4 Medizinische Fakultät nach Titel

DSpace Repositorium (Manakin basiert)

Auflistung 4 Medizinische Fakultät nach Titel

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  • Heterogeneity of Host TLR2 Stimulation by Staphylocoocus aureus Isolates
    Hilmi, Dina; Parcina, Marijo; Stollewerk, Daniel; Ostrop, Jenny; Josten, Michaele; Meilaender, Alina; Zaehringer, Ulrich; Wichelhaus, Thomas A.; Bierbaum, Gabriele; Heeg, Klaus; Wolz, Christiane; Bekeredjian-Ding, Isabelle (2014)
  • Heterogeneity of the Stearoyl-CoA desaturase-1 (SCD1) Gene and Metabolic Risk Factors in the EPIC-Potsdam Study
    Arregui, Maria; Buijsse, Brian; Stefan, Norbert; Corella, Dolores; Fisher, Eva; di Giuseppe, Romina; Coltell, Oscar; Knueppel, Sven; Aleksandrova, Krasimira; Joost, Hans-Georg; Boeing, Heiner; Weikert, Cornelia (2012)
  • Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies
    Perez-Palma, Eduardo; Helbig, Ingo; Klein, Karl Martin; Anttila, Verneri; Horn, Heiko; Reinthaler, Eva Maria; Gormley, Padhraig; Ganna, Andrea; Byrnes, Andrea; Pernhorst, Katharina; Toliat, Mohammad R.; Saarentaus, Elmo; Howrigan, Daniel P.; Hoffman, Per; Miquel, Juan Francisco; De Ferrari, Giancarlo V.; Nuernberg, Peter; Lerche, Holger; Zimprich, Fritz; Neubauer, Bern A.; Becker, Albert J.; Rosenow, Felix; Perucca, Emilio; Zara, Federico; Weber, Yvonne G.; Lal, Dennis (2017)
  • Heterogeneous impact of hypoxia on cellular radiation sensitivity of three squamous cell carcinoma lines
    Hauth, Franziska Dorothea (2018)
  • Heterogeneous pathway activation and drug response modelled in colorectal-tumor-derived 3D cultures
    Schumacher, Dirk; Andrieux, Geoffroy; Boehnke, Karsten; Keil, Marlen; Silvestri, Alessandra; Silvestrov, Maxine; Keilholz, Ulrich; Haybaeck, Johannes; Erdmann, Gerrit; Sachse, Christoph; Templin, Markus; Hoffmann, Jens; Boerries, Melanie; Schaefer, Reinhold; Regenbrecht, Christian R. A. (2019)
  • Heterogenität des multifokalen Prostatakarzinoms - Differentielle Darstellung von RANK und RANKL in Knochenmark, Serum sowie in den unterschiedlichen Tumorarealen multifokaler Prostatakarzinome mittels der Tissue microarray Technik
    Kromer, Daniel Martin (2023)
  • Heterologous microProtein expression identifies LITTLE NINJA, a dominant regulator of jasmonic acid signaling
    Hong, Shin-Young; Sun, Bin; Straub, Daniel; Blaakmeer, Anko; Mineri, Lorenzo; Koch, Jonas; Brinch-Pedersen, Henrik; Holme, Inger B.; Burow, Meike; Jorgensen, Hans Jorgen Lyngs; Mar Alba, M.; Wenkel, Stephan (2020)
  • Heterologous protection against malaria by a simple chemoattenuated PfSPZ vaccine regimen in a randomized trial
    Sulyok, Zita; Fendel, Rolf; Eder, Bianca; Lorenz, Freia-Raphaella; Natasha, K. C.; Karnahl, Matthias; Lalremruata, Albert; Nguyen, The T.; Held, Jana; Adjadi, Folashade Almeine Cyntiche; Klockenbring, Torsten; Flugge, Judith; Woldearegai, Tamirat Gebru; Calle, Carlos Lamsfus; Ibanez, Javier; Rodi, Miriam; Egger-Adam, Diane; Kreidenweiss, Andrea; Kohler, Carsten; Esen, Meral; Sulyok, Mihaly; Manoj, Anita; Richie, Thomas L.; Sim, B. Kim Lee; Hoffman, Stephen L.; Mordmuller, Benjamin; Kremsner, Peter G. (2021)
  • Heterotrimeric G Stimulatory Protein alpha Subunit Is Required for Intestinal Smooth Muscle Contraction in Mice
    Qin, Xiaoteng; Liu, Shangming; Lu, Qiulun; Zhang, Meng; Jiang, Xiuxin; Hu, Sanyuan; Li, Jingxin; Zhang, Cheng; Gao, Jiangang; Zhu, Min-Sheng; Feil, Robert; Li, Huashun; Chen, Min; Weinstein, Lee S.; Zhang, Yun; Zhang, Wencheng (2017)
  • Heterotrimeric G-protein subunit Gαi2 contributes to agonist-sensitive apoptosis and degranulation in murine platelets
    Cao, Hang; Qadri, Syed M.; Lang, Elisabeth; Pelzl, Lisann; Umbach, Anja Tasneem; Leiss, Veronika; Birnbaumer, Lutz; Nürnberg, Bernd; Pieske, Burkert; Völkl, Jakob Georg Jonathan; Gawaz, Meinrad Paul; Bissinger, Rosi; Lang, Florian (2018)
  • Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease
    Huttenlocher, Johanna; Stefansson, Hreinn; Steinberg, Stacy; Helgadottir, Hafdis T.; Sveinbjornsdottir, Sigurlaug; Riess, Olaf; Bauer, Peter; Stefansson, Kari (2015)
  • Heterozygous Carriage of a Dysfunctional Toll-like Receptor 9 Allele Affects CpG Oligonucleotide Responses in B Cells
    Knezevic, Jelena; Pavlinic, Dinko; Rose, William A., II; Leifer, Cynthia A.; Bendelja, Kreso; Gabrilovac, Jelka; Parcina, Marijo; Lauc, Gordan; Kubarenko, Andriy V.; Petricevic, Branka; Vrbanec, Damir; Bulat-Kardum, Ljiljana; Bekeredjian-Ding, Isabelle; Pavelic, Jasminka; Dembic, Zlatko; Weber, Alexander N. R. (2012)
  • Heterozygous carriage of the alpha1-antitrypsin Pi*Z variant increases the risk to develop liver cirrhosis
    Strnad, Pavel; Buch, Stephan; Hamesch, Karim; Fischer, Janett; Rosendahl, Jonas; Schmelz, Renate; Brueckner, Stefan; Brosch, Mario; Heimes, Carolin V.; Woditsch, Vivien; Scholten, David; Nischalke, Hans Dieter; Janciauskiene, Sabina; Mandorfer, Mattias; Trauner, Michael; Way, Michael J.; McQuillin, Andrew; Reichert, Matthias C.; Krawczyk, Marcin; Casper, Markus; Lammert, Frank; von Schoenfels, Witigo; Hinz, Sebastian; Burmeister, Greta; Hellerbrand, Claus; Teufel, Andreas; Feldman, Alexandra; Schattenberg, Joern M.; Bantel, Heike; Pathil, Anita; Demir, Muenevver; Kluwe, Johannes; Boettler, Tobias; Ridinger, Monika; Wodarz, Norbert; Soyka, Michael; Rietschel, Marcella; Kiefer, Falk; Weber, Thomas; Marhenke, Silke; Vogel, Arndt; Hinrichsen, Holger; Canbay, Ali; Schlattjan, Martin; Sosnowsky, Katharina; Sarrazin, Christoph; von Felden, Johann; Geier, Andreas; Deltenre, Pierre; Sipos, Bence; Schafmayer, Clemens; Nothnagel, Michael; Aigner, Elmar; Datz, Christian; Stickel, Felix; Morgan, Marsha Yvonne; Hampe, Jochen; Berg, Thomas; Trautwein, Christian (2019)
  • Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy
    Kim, Hong Joo; Mohassel, Payam; Donkervoort, Sandra; Guo, Lin; O'Donovan, Kevin; Coughlin, Maura; Lornage, Xaviere; Foulds, Nicola; Hammans, Simon R.; Foley, A. Reghan; Fare, Charlotte M.; Ford, Alice F.; Ogasawara, Masashi; Sato, Aki; Iida, Aritoshi; Munot, Pinki; Ambegaonkar, Gautam; Phadke, Rahul; O'Donovan, Dominic G.; Buchert, Rebecca; Grimmel, Mona; Topf, Ana; Zaharieva, Irina T.; Brady, Lauren; Hu, Ying; Lloyd, Thomas E.; Klein, Andrea; Steinlin, Maja; Kuster, Alice; Mercier, Sandra; Marcorelles, Pascale; Pereon, Yann; Fleurence, Emmanuelle; Manzur, Adnan; Ennis, Sarah; Upstill-Goddard, Rosanna; Bello, Luca; Bertolin, Cinzia; Pegoraro, Elena; Salviati, Leonardo; French, Courtney E.; Shatillo, Andriy; Raymond, F. Lucy; Haack, Tobias; Quijano-Roy, Susana; Bohm, Johann; Nelson, Isabelle; Stojkovic, Tanya; Evangelista, Teresinha; Straub, Volker; Romero, Norma B.; Laporte, Jocelyn; Muntoni, Francesco; Nishino, Ichizo; Tarnopolsky, Mark A.; Shorter, James; Bonnemann, Carsten G.; Taylor, J. Paul (2022)
  • Heterozygous pathogenic variants involving CBFB cause a new skeletal disorder resembling cleidocranial dysplasia
    Beyltjens, Tessi; Boudin, Eveline; Revencu, Nicole; Boeckx, Nele; Bertrand, Miriam; Schuetz, Leon; Haack, Tobias B.; Weber, Axel; Biliouri, Eleni; Vinksel, Mateja; Zagozen, Anja; Peterlin, Borut; Pai, Shashidhar; Telegrafi, Aida; Henderson, Lindsay B.; Ells, Courtney; Turner, Lesley; Wuyts, Wim; Van Hul, Wim; Hendrickx, Gretl; Mortier, Geert R. (2023)
  • Heterozygous truncating variants inSUFUcause congenital ocular motor apraxia
    Schroeder, Simone; Li, Yun; Yigit, Gokhan; Altmueller, Janine; Bader, Ingrid; Bevot, Andrea; Biskup, Saskia; Dreha-Kulaczewski, Steffi; Korenke, G. Christoph; Kottke, Raimund; Mayr, Johannes A.; Preisel, Martin; Toelle, Sandra P.; Wente-Schulz, Sarah; Wortmann, Saskia B.; Hahn, Heidi; Boltshauser, Eugen; Uhmann, Anja; Wollnik, Bernd; Brockmann, Knut (2021)
  • Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy
    Park, Joohyun; Tucci, Arianna; Cipriani, Valentina; Demidov, German; Rocca, Clarissa; Senderek, Jan; Butryn, Michaela; Velic, Ana; Lam, Tanya; Galanaki, Evangelia; Cali, Elisa; Vestito, Letizia; Maroofian, Reza; Deininger, Natalie; Rautenberg, Maren; Admard, Jakob; Hahn, Gesa-Astrid; Bartels, Claudius; van Os, Nienke J. H.; Horvath, Rita; Chinnery, Patrick F.; Tiet, May Yung; Hewamadduma, Channa; Hadjivassiliou, Marios; Tofaris, George K.; Wood, Nicholas W.; Hayer, Stefanie N.; Bender, Friedemann; Menden, Benita; Cordts, Isabell; Klein, Katrin; Huu Phuc Nguyen; Krauss, Joachim K.; Blahak, Christian; Strom, Tim M.; Sturm, Marc; van de Warrenburg, Bart; Lerche, Holger; Macek, Boris; Synofzik, Matthis; Ossowski, Stephan; Timmann, Dagmar; Wolf, Marc E.; Smedley, Damian; Riess, Olaf; Schoels, Ludger; Houlden, Henry; Haack, Tobias B.; Hengel, Holger (2022)
  • Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
    O'Donnell-Luria, Anne H.; Pais, Lynn S.; Faundes, Victor; Wood, Jordan C.; Sveden, Abigail; Luria, Victor; Abou Jamra, Rami; Accogli, Andrea; Amburgey, Kimberly; Anderlid, Britt Marie; Azzarello-Burri, Silvia; Basinger, Alice A.; Bianchini, Claudia; Bird, Lynne M.; Buchert, Rebecca; Carre, Wilfrid; Ceulemans, Sophia; Charles, Perrine; Cox, Helen; Culliton, Lisa; Curro, Aurora; Demurger, Florence; Dowling, James J.; Duban-Bedu, Benedicte; Dubourg, Christele; Eiset, Saga Elise; Escobar, Luis F.; Ferrarini, Alessandra; Haack, Tobias B.; Hashim, Mona; Heide, Solveig; Helbig, Katherine L.; Helbig, Ingo; Heredia, Raul; Heron, Delphine; Isidor, Bertrand; Jonasson, Amy R.; Joset, Pascal; Keren, Boris; Kok, Fernando; Kroes, Hester Y.; Lavillaureix, Alinoe; Lu, Xin; Maas, Saskia M.; Maegawa, Gustavo H. B.; Marcelis, Carlo L. M.; Mark, Paul R.; Masruha, Marcelo R.; McLaughlin, Heather M.; McWalter, Kirsty; Melchinger, Esther U.; Mercimek-Andrews, Saadet; Nava, Caroline; Pendziwiat, Manuela; Person, Richard; Ramelli, Gian Paolo; Ramos, Luiza L. P.; Rauch, Anita; Reavey, Caitlin; Renieri, Alessandra; Riess, Angelika; Sanchez-Valle, Amarilis; Sattar, Shifteh; Saunders, Carol; Schwarz, Niklas; Smol, Thomas; Srour, Myriam; Steindl, Katharina; Syrbe, Steffen; Taylor, Jenny C.; Telegrafi, Aida; Thiffault, Isabelle; Trauner, Doris A.; van der Linden, Helio, Jr.; van Koningsbruggen, Silvana; Villard, Laurent; Vogel, Ida; Vogt, Julie; Weber, Yvonne G.; Wentzensen, Ingrid M.; Widjaja, Elysa; Zak, Jaroslav; Baxter, Samantha; Banka, Siddharth; Rodan, Lance H.; Mcrae, Jeremy F.; Clayton, Stephen; Fitzgerald, Tomas W.; Kaplanis, Joanna; Prigmore, Elena; Rajan, Diana; Sifrim, Alejandro; Aitken, Stuart; Akawi, Nadia; Alvi, Mohsan; Ambridge, Kirsty; Barrett, Daniel M.; Bayzetinova, Tanya; Jones, Philip; Jones, Wendy D.; King, Daniel (2019)
  • Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2
    Christians, Anne; Kesdiren, Esra; Hennies, Imke; Hofmann, Alejandro; Trowe, Mark-Oliver; Brand, Frank; Martens, Helge; Gjerstad, Ann Christin; Gucev, Zoran; Zirngibl, Matthias; Geffers, Robert; Seeman, Tomas; Billing, Heiko; Bjerre, Anna; Tasic, Velibor; Kispert, Andreas; Ure, Benno; Haffner, Dieter; Dingemann, Jens; Weber, Ruthild G. (2023)
  • Hexagonal arrays of plasmonic gold nanopyramids on flexible substrates for surface-enhanced Raman scattering
    Simo, P. Christian; Laible, Florian; Horneber, Anke; Burkhardt, Claus J.; Fleischer, Monika (2022)