Items where Division is "03 Faculty of Medicine > Departement Biomedizin > Department of Biomedicine, University Hospital Basel"

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Number of items at this level: 32.


Spoerri, Iris and Bircher, Andreas J. and Link, Susanne and Heijnen, Ingmar A. F. M. and Scherer Hofmeier, Kathrin. (2018) Delayed-type allergy to cobalt - comparison of a flow cytometric lymphocyte proliferation test with patch testing. Contact Dermatitis, 79 (1). pp. 31-33.


Bircher, Andreas J. and Hofmeier, Kathrin Scherer and Link, Susanne and Heijnen, Ingmar. (2017) Food allergy to the carbohydrate galactose-alpha-1,3-galactose (alpha-gal): four case reports and a review. European Journal of Dermatology, 27 (1). pp. 3-9.

Calabrese, Diego and Wieland, Stefan F.. (2017) Highly Sensitive Detection of HBV RNA in Liver Tissue by In Situ Hybridization. Methods in Molecular Biology, 1540. pp. 119-134.

Moreau, Adrien and Mercier, Aurélie and Thériault, Olivier and Boutjdir, Mohamed and Burger, Bettina and Keller, Dagmar I. and Chahine, Mohamed. (2017) Biophysical, Molecular, and Pharmacological Characterization of Voltage-Dependent Sodium Channels From Induced Pluripotent Stem Cell-Derived Cardiomyocytes. Canadian Journal of Cardiology, 33 (2). pp. 269-278.


Johansen, Stephan and Treves, Susan and Müller, Clemens R. and Mögele, Susanne and Schneiderbanger, Daniel and Roewer, Norbert and Schuster, Frank. (2016) Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia. Neuromuscular Disorders, 26 (1). pp. 21-25.

Jungbluth, Heinz and Ochala, Julien and Treves, Susan and Gautel, Mathias. (2016) Current and future therapeutic approaches to the congenital myopathies. Seminars in Cell and Developmental Biology, 64. pp. 191-200.

Lopez, Rubén J. and Byrne, Susan and Vukcevic, Mirko and Sekulic-Jablanovic, Marijana and Xu, Lifen and Brink, Marijke and Alamelu, Jay and Voermans, Nicol and Snoeck, Marc and Clement, Emma and Muntoni, Francesco and Zhou, Haiyan and Radunovic, Aleksandar and Mohammed, Shehla and Wraige, Elizabeth and Zorzato, Francesco and Treves, Susan and Jungbluth, Heinz. (2016) An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities. Science Signaling, 9 (435). ra68.

Mosca, Barbara and Eckhardt, Jan and Bergamelli, Leda and Treves, Susan and Bongianino, Rossana and De Negri, Marco and Priori, Silvia G. and Protasi, Feliciano and Zorzato, Francesco. (2016) Role of the JP45-Calsequestrin Complex on Calcium Entry in Slow Twitch Skeletal Muscles. Journal of Biological Chemistry, 291 (28). pp. 14555-14565.

Saxer, Franziska and Scherberich, Arnaud and Todorov, Atanas and Studer, Patrick and Miot, Sylvie and Schreiner, Simone and Güven, Sinan and Tchang, Laurent A. H. and Haug, Martin and Heberer, Michael and Schaefer, Dirk J. and Rikli, Daniel and Martin, Ivan and Jakob, Marcel. (2016) Implantation of Stromal Vascular Fraction Progenitors at Bone Fracture Sites: From a Rat Model to a First-in-Man Study. Stem Cells, 34 (12). pp. 2956-2966.

Sekulic-Jablanovic, Marijana and Ullrich, Nina D. and Goldblum, David and Palmowski-Wolfe, Anja and Zorzato, Francesco and Treves, Susan. (2016) Functional characterization of orbicularis oculi and extraocular muscles. Journal of General Physiology, 147 (5). pp. 395-406.

Treves, Susan and Jungbluth, Heinz and Voermans, Nicol and Muntoni, Francesco and Zorzato, Francesco. (2016) Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives. Seminars in Cell and Developmental Biology, 64. pp. 201-212.

Wang, Min and Keogh, Adrian and Treves, Susan and Idle, Jeffrey R. and Beyoğlu, Diren. (2016) The metabolomic profile of gamma-irradiated human hepatoma and muscle cells reveals metabolic changes consistent with the Warburg effect. PeerJ, 4. e1624.


Kraeva, N. and Heytens, L. and Jungbluth, H. and Treves, S. and Voermans, N. and Kamsteeg, C. and Ceuterick-de Groote, C. and Baets, J. and Riaz, S.. (2015) Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy. Neuromuscular Disorders, 25 (7). pp. 567-576.

Rokach, Ori and Sekulic-Jablanovic, Marijana and Voermans, Nicol and Wilmshurst, Jo and Pillay, Komala and Heytens, Luc and Zhou, Haiyan and Muntoni, Francesco and Gautel, Mathias and Nevo, Yoram and Mitrani-Rosenbaum, Stella and Attali, Ruben and Finotti, Alessia and Gambari, Roberto and Mosca, Barbara and Jungbluth, Heinz and Zorzato, Francesco and Treves, Susan. (2015) Epigenetic changes as a common trigger of muscle weakness in congenital myopathies. Human Molecular Genetics, 24 (16). pp. 4636-4647.

Sekulic, M. and Palmowski-Wolfe, A. and Zorzato, F. and Treves, S.. (2015) Characterization of excitation-contraction coupling components in human extraocular muscles. Biochemical Journal, 466 (1). pp. 29-36.

Snoek, M. and van Engelen, B. G. M. and Küsters, B. and Lammens, M. and Meijer, R. and Molenaar, J. P. F. and Raaphorst, J. and Verschuuren-Bemelmans, C. C. and Straathof, C. S. M. and Sie, L. T. L. and de Coo, I. F. and van der Pol, W. L. and de Visser, M. and Scheffer, H. and Treves, S. and Jungbluth, H. and Voermans, N. and Kamsteef, E.-J.. (2015) RYR1‐related myopathies: a wide spectrum of phenotypes throughout life. European Journal of Neurology, 22 (7). pp. 1094-1112.

Spoerri, I. and Scherer, K. and Michel, S. and Link, S. and Bircher, A. J. and Heijnen, I. A. F. M.. (2015) Detection of nickel and palladium contact hypersensitivity by a flow cytometric lymphocyte proliferation test. Allergy, 70 (3). pp. 323-327.

Spoerri, Iris and Brena, Michela and De Mesmaeker, Julie and Schlipf, Nina and Fischer, Judith and Tadini, Gianluca and Itin, Peter H. and Burger, Bettina. (2015) The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndrome. JAMA dermatology, 151 (1). pp. 64-69.


Burger, B. and Itin, P. H.. (2014) Epidermodysplasia verruciformis. Current problems in dermatology, 45. pp. 123-131.

Nousbeck, J. and Sarig, O. and Magal, L. and Warshauer, E. and Burger, B. and Itin, P. and Sprecher, E.. (2014) Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes. British Journal of Dermatology, 171 (6). pp. 1521-1524.


Eberle, Alex N. and Bapst, Jean-Philippe and Calame, Martine and Tanner, Heidi and Froidevaux, Sylvie. (2010) MSH Radiopeptides for Targeting Melanoma Metastases. Advances in experimental medicine and biology, Vol. 681,. pp. 133-142.

Eberle, Alex N. and Mild, Gabriele and Zumsteg, Urs. (2010) Cellular models for the study of the pharmacology and signaling of melanin-concentrating hormone receptors. Journal Of Receptors And Signal Transduction, Vol. 30, H. 6. pp. 385-402.

Lindinger, Andrea and Peterli, Ralph and Peters, Thomas and Kern, Beatrice and von Flüe, Markus and Calame, Martine and Hoch, Matthias and Eberle, Alex N. and Lindinger, Peter W.. (2010) Mitochondrial DNA content in human omental adipose tissue. Obesity surgery, Vol. 20, H. 1. pp. 84-92.

Mastrofrancesco, Arianna and Kokot, Agatha and Eberle, Alex and Gibbons, Nicholas C. J. and Schallreuter, Karin U. and Strozyk, Elwira and Picardo, Mauro and Zouboulis, Christos C. and Luger, Thomas A. and Böhm, Markus. (2010) KdPT, a tripeptide derivative of alpha-melanocyte-stimulating hormone, suppresses IL-1 beta-mediated cytokine expression and signaling in human sebocytes. Journal of immunology, Vol. 185, H. 3. pp. 1903-1911.


Dantas, Maria Fernanda. Molecular basis and functional characterization of human 3-methylcrotonyl-CoA carboxylase deficiency. 2009, Doctoral Thesis, University of Basel, Faculty of Science.

Eberle, Alex N. and Mild, Gabriele. (2009) Receptor-mediated tumor targeting with radiopeptides. Part 1. General principles and methods. Journal of receptors and signal transduction, Vol. 29, H. 1. pp. 1-37.

Knecht, Steven and Ricklin, Daniel and Eberle, A. N. and Ernst Beat, . (2009) Oligohis-tags : mechanisms of binding to Ni2+-NTA surfaces. Journal of Molecular Recognition, Vol. 22. pp. 270-279.

Langenkamp, Ulrich and Siegler, Uwe and Jörger, Simon and Diermayr, Stefan and Gratwohl, Alois and Kalberer, Christian P. and Wodnar-Filipowicz, Aleksandra. (2009) Human acute myeloid leukemia CD34+CD38- stem cells are susceptible to allorecognition and lysis by single KIR-expressing natural killer cells. Haematologica : journal of hematology, Vol. 94. pp. 1590-1594.


Hoch, M. and Eberle, A. N. and Peterli, R. and Peters, T. and Seboek, D. and Keller, U. and Muller, B. and Linscheid, P.. (2008) LPS induces interleukin-6 and interleukin-8 but not tumor necrosis factor-alpha in human adipocytes. Cytokine, 41 (1). pp. 29-37.

Hoch, M. and Hirzel, E. and Lindinger, P. and Eberle, A. N. and Linscheid, P. and Martin, I. and Peters, T. and Peterli, R.. (2008) Weak functional coupling of the melanocortin-1 receptor expressed in human adipocytes. Journal of receptors and signal transduction, Vol. 28. pp. 485-504.

Kenins, L. and Gill, J. W. and Boyd, R. L. and Holländer, G. A. and Wodnar-Filipowicz, A.. (2008) Intrathymic expression of Flt3 ligand enhances thymic recovery after irradiation. Journal of experimental medicine, Vol. 205, H. 3. pp. 523-531.


Bracci, L. and Vukcevic, M. and Spagnoli, G. and Ducreux, S. and Zorzato, F. and Treves, S.. (2007) Ca2+ signaling through ryanodine receptor 1 enhances maturation and activation of human dendritic cells. Journal of Cell Science, 120 (13). pp. 2232-2240.

This list was generated on Fri Jun 5 03:53:49 2020 CEST.