Hasil Pencarian - Arif B Ekici

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  1. 1
    Novel loci for non-syndromic coarctation of the aorta in sporadic and familial cases.

    Novel loci for non-syndromic coarctation of the aorta in sporadic and familial cases. oleh Julia Moosmann, Steffen Uebe, Sven Dittrich, André Rüffer, Arif B Ekici, Okan Toka

    Diterbitkan 2015-01-01
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  2. 2
    Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice

    Th2 single-cell heterogeneity and clonal distribution at distant sites in helminth-infected mice oleh Daniel Radtke, Natalie Thuma, Christine Schülein, Philipp Kirchner, Arif B Ekici, Kilian Schober, David Voehringer

    Diterbitkan 2022-08-01
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  3. 3
    Differential Effects of Very-Low-Volume Exercise Modalities on Telomere Length, Inflammation, and Cardiometabolic Health in Obese Metabolic Syndrome Patients: A Subanalysis from Two Randomized Controlled Trials

    Differential Effects of Very-Low-Volume Exercise Modalities on Telomere Length, Inflammation, and Cardiometabolic Health in Obese Metabolic Syndrome Patients: A Subanalysis from Tw... oleh Dejan Reljic, Adriana Koller, Hans J. Herrmann, Arif B. Ekici, Markus F. Neurath, Yurdagül Zopf

    Diterbitkan 2023-10-01
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  4. 4
    Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability

    Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability oleh Ute Scheller, Kathrin Pfisterer, Steffen Uebe, Arif B. Ekici, André Reis, Rami Jamra, Fulvia Ferrazzi

    Diterbitkan 2018-04-01
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  5. 5
    Experimental Epileptogenesis in a Cell Culture Model of Primary Neurons from Rat Brain: A Temporal Multi-Scale Study

    Experimental Epileptogenesis in a Cell Culture Model of Primary Neurons from Rat Brain: A Temporal Multi-Scale Study oleh Janos Jablonski, Lucas Hoffmann, Ingmar Blümcke, Anna Fejtová, Steffen Uebe, Arif B. Ekici, Vadym Gnatkovsky, Katja Kobow

    Diterbitkan 2021-11-01
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  6. 6
    Impaired ATF3 signaling involves SNAP25 in SOD1 mutant ALS patients

    Impaired ATF3 signaling involves SNAP25 in SOD1 mutant ALS patients oleh Volkan Yazar, Julia K. Kühlwein, Antje Knehr, Veselin Grozdanov, Arif B. Ekici, Albert C. Ludolph, Karin M. Danzer

    Diterbitkan 2023-07-01
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  7. 7
    High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder

    High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder oleh Edna Grünblatt, Beatrice Oneda, Arif B. Ekici, Juliane Ball, Julia Geissler, Steffen Uebe, Marcel Romanos, Anita Rauch, Susanne Walitza

    Diterbitkan 2017-11-01
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  8. 8
    Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability

    Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability oleh Bernt Popp, Abbas Agaimy, Cornelia Kraus, Karl X. Knaup, Arif B. Ekici, Steffen Uebe, André Reis, Michael Wiesener, Christiane Zweier

    Diterbitkan 2019-05-01
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  9. 9
    Interspecies Single‐Cell RNA‐Seq Analysis Reveals the Novel Trajectory of Osteoclast Differentiation and Therapeutic Targets

    Interspecies Single‐Cell RNA‐Seq Analysis Reveals the Novel Trajectory of Osteoclast Differentiation and Therapeutic Targets oleh Yasunori Omata, Hiroyuki Okada, Steffen Uebe, Naohiro Izawa, Arif B. Ekici, Kerstin Sarter, Taku Saito, Georg Schett, Sakae Tanaka, Mario M. Zaiss

    Diterbitkan 2022-07-01
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  10. 10
    The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy

    The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy oleh Moritz Hebebrand, Ulrike Hüffmeier, Regina Trollmann, Ute Hehr, Steffen Uebe, Arif B. Ekici, Cornelia Kraus, Mandy Krumbiegel, André Reis, Christian T. Thiel, Bernt Popp

    Diterbitkan 2019-02-01
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  11. 11
    Rare copy number variants are a common cause of short stature.

    Rare copy number variants are a common cause of short stature. oleh Diana Zahnleiter, Steffen Uebe, Arif B Ekici, Juliane Hoyer, Antje Wiesener, Dagmar Wieczorek, Erdmute Kunstmann, André Reis, Helmuth-Guenther Doerr, Anita Rauch, Christian T Thiel

    Diterbitkan 2013-01-01
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  12. 12
    Reduced syncytin-1 expression levels in placental syndromes correlates with epigenetic hypermethylation of the ERVW-1 promoter region.

    Reduced syncytin-1 expression levels in placental syndromes correlates with epigenetic hypermethylation of the ERVW-1 promoter region. oleh Matthias Ruebner, Pamela L Strissel, Arif B Ekici, Elisabeth Stiegler, Ulf Dammer, Tamme W Goecke, Florian Faschingbauer, Fabian B Fahlbusch, Matthias W Beckmann, Reiner Strick

    Diterbitkan 2013-01-01
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  13. 13
    Improved Bladder Tumor RNA Isolation from Archived Tissues Using Methylene Blue for Normalization, Multiplex RNA Hybridization, Sequencing and Subtyping

    Improved Bladder Tumor RNA Isolation from Archived Tissues Using Methylene Blue for Normalization, Multiplex RNA Hybridization, Sequencing and Subtyping oleh Stefanie A. Köhler, Lisa Brandl, Pamela L. Strissel, Laura Gloßner, Arif B. Ekici, Miriam Angeloni, Fulvia Ferrazzi, Veronika Bahlinger, Arndt Hartmann, Matthias W. Beckmann, Markus Eckstein, Reiner Strick

    Diterbitkan 2022-09-01
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  14. 14
    In Vivo Protein Complementation Demonstrates Presynaptic α-Synuclein Oligomerization and Age-Dependent Accumulation of 8–16-mer Oligomer Species

    In Vivo Protein Complementation Demonstrates Presynaptic α-Synuclein Oligomerization and Age-Dependent Accumulation of 8–16-mer Oligomer Species oleh Martin Kiechle, Bjoern von Einem, Lennart Höfs, Patrizia Voehringer, Veselin Grozdanov, Daniel Markx, Rosanna Parlato, Diana Wiesner, Benjamin Mayer, Olena Sakk, Bernd Baumann, Soeren Lukassen, Birgit Liss, Arif B. Ekici, Albert C. Ludolph, Paul Walther, Boris Ferger, Pamela J. McLean, Björn H. Falkenburger, Jochen H. Weishaupt, Karin M. Danzer

    Diterbitkan 2019-11-01
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  15. 15
    TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)

    TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23) oleh Louise A Stephen, Hasan Tawamie, Gemma M Davis, Lars Tebbe, Peter Nürnberg, Gudrun Nürnberg, Holger Thiele, Michaela Thoenes, Eugen Boltshauser, Steffen Uebe, Oliver Rompel, André Reis, Arif B Ekici, Lynn McTeir, Amy M Fraser, Emma A Hall, Pleasantine Mill, Nicolas Daudet, Courtney Cross, Uwe Wolfrum, Rami Abou Jamra, Megan G Davey, Hanno J Bolz

    Diterbitkan 2015-09-01
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  16. 16
    Roflumilast inhibits tumor growth and migration in STK11/LKB1 deficient pancreatic cancer

    Roflumilast inhibits tumor growth and migration in STK11/LKB1 deficient pancreatic cancer oleh Shuman Zhang, Duo Yun, Hao Yang, Markus Eckstein, Gihan Daw Elbait, Yaxing Zhou, Yanxi Lu, Hai Yang, Jinping Zhang, Isabella Dörflein, Nathalie Britzen-Laurent, Susanne Pfeffer, Marc P. Stemmler, Andreas Dahl, Debabrata Mukhopadhyay, David Chang, Hang He, Siyuan Zeng, Bin Lan, Benjamin Frey, Chuanpit Hampel, Eva Lentsch, Paradesi Naidu Gollavilli, Christian Büttner, Arif B. Ekici, Andrew Biankin, Regine Schneider-Stock, Paolo Ceppi, Robert Grützmann, Christian Pilarsky

    Diterbitkan 2024-03-01
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  17. 17
    Susceptibility gene mutations in germline and tumors of patients with HER2-negative advanced breast cancer

    Susceptibility gene mutations in germline and tumors of patients with HER2-negative advanced breast cancer oleh Peter A. Fasching, Chunling Hu, Steven N. Hart, Matthias Ruebner, Eric C. Polley, Rohan D. Gnanaolivu, Andreas D. Hartkopf, Hanna Huebner, Wolfgang Janni, Peyman Hadji, Hans Tesch, Sabrina Uhrig, Johannes Ettl, Michael P. Lux, Diana Lüftner, Markus Wallwiener, Lena A. Wurmthaler, Chloë Goossens, Volkmar Müller, Matthias W. Beckmann, Alexander Hein, Daniel Anetsberger, Erik Belleville, Pauline Wimberger, Michael Untch, Arif B. Ekici, Hans-Christian Kolberg, Arndt Hartmann, Florin-Andrei Taran, Tanja N. Fehm, Diethelm Wallwiener, Sara Y. Brucker, Andreas Schneeweiss, Lothar Häberle, Fergus J. Couch

    Diterbitkan 2024-07-01
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  18. 18
    The UGT1A6_19_GG genotype is a breast cancer risk factor

    The UGT1A6_19_GG genotype is a breast cancer risk factor oleh Christina eJustenhoven, Ofure eObazee, Stefan eWinter, Sylvia eRabstein, Anne eLotz, Volker eHarth, Beate ePesch, Thomas eBruening, Christian eBaisch, Jaana M Hartikainen, Arto eMannermaa, Veli-Matti eKosma, Vesa eKataja, Robert eWinqvist, Katri ePylkaes, Arja eJukkola-Vuorinen, Mervi eGrip, Peter eFasching, Matthias eBeckmann, Arif B Ekici, Alexander eHein, Per eHall, Jingmei eLi, Jenny eChang-Claude, Dieter eFlesch-Janys, Petra eSeibold, Anja eRudolph, Ute eHamann, Yon-Dschun eKo, Hiltrud eBrauch

    Diterbitkan 2013-06-01
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  19. 19
    Estrogen receptor beta rs1271572 polymorphism and invasive ovarian carcinoma risk: pooled analysis within the Ovarian Cancer Association Consortium.

    Estrogen receptor beta rs1271572 polymorphism and invasive ovarian carcinoma risk: pooled analysis within the Ovarian Cancer Association Consortium. oleh Galina Lurie, Lynne R Wilkens, Pamela J Thompson, Yurii B Shvetsov, Rayna K Matsuno, Michael E Carney, Rachel T Palmieri, Anna H Wu, Malcolm C Pike, Celeste L Pearce, Usha Menon, Aleksandra Gentry-Maharaj, Simon A Gayther, Susan J Ramus, Alice S Whittemore, Valerie McGuire, Weiva Sieh, Paul D P Pharoah, Honglin Song, Jacek Gronwald, Anna Jakubowska, Cezary Cybulski, Jan Lubinski, Joellen M Schildkraut, Andrew Berchuck, Susanne Krüger Kjær, Estrid Høgdall, Peter A Fasching, Matthias W Beckmann, Arif B Ekici, Alexander Hein, Georgia Chenevix-Trench, Penelope M Webb, Jonathan Beesley, Australian Ovarian Cancer Study Group, Australian Cancer Study Group, Marc T Goodman, Ovarian Cancer Association Consortium

    Diterbitkan 2011-01-01
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  20. 20
    Copeptin, Natriuretic Peptides, and Cardiovascular Outcomes in Patients With CKD: The German Chronic Kidney Disease (GCKD) Study

    Copeptin, Natriuretic Peptides, and Cardiovascular Outcomes in Patients With CKD: The German Chronic Kidney Disease (GCKD) Study oleh Markus P. Schneider, Matthias Schmid, Jennifer Nadal, Vera Krane, Turgay Saritas, Martin Busch, Ulla T. Schultheiss, Heike Meiselbach, Nele Friedrich, Matthias Nauck, Jürgen Floege, Florian Kronenberg, Christoph Wanner, Kai-Uwe Eckardt, Kai-Uwe Eckardt, Heike Meiselbach, Mario Schiffer, Hans-Ulrich Prokosch, Barbara Bärthlein, Andreas Beck, André Reis, Arif B. Ekici, Susanne Becker, Dinah Becker-Grosspitsch, Ulrike Alberth-Schmidt, Birgit Hausknecht, Anke Weigel, Gerd Walz, Anna Köttgen, Ulla T. Schultheiß, Fruzsina Kotsis, Simone Meder, Erna Mitsch, Ursula Reinhard, Jürgen Floege, Turgay Saritas, Elke Schaeffner, Seema Baid-Agrawal, Kerstin Theisen, Hermann Haller, Jan Menne, Martin Zeier, Claudia Sommerer, Johanna Theilinger, Gunter Wolf, Martin Busch, Rainer Paul, Thomas Sitter, Christoph Wanner, Vera Krane, Antje Börner-Klein, Britta Bauer, Florian Kronenberg, Julia Raschenberger, Barbara Kollerits, Lukas Forer, Sebastian Schönherr, Hansi Weissensteiner, Peter Oefner, Wolfram Gronwald, Matthias Schmid, Jennifer Nadal

    Diterbitkan 2023-11-01
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