edoc

Items where Author is "Burger, Bettina"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item Type | Refereed
Jump to: 2020 | 2019 | 2017 | 2015 | 2014 | 2013 | 2011 | 2010 | 2009 | 2008
Number of items: 21.

2020

Imahorn, Elias and Aushev, Magomet and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Reichelt, Julia and Itin, Peter H. and Burger, Bettina. (2020) Gene expression is stable in a complete CIB1 knockout keratinocyte model. Scientific reports, 10 (1). p. 14952.

2019

Renz, Patricia and Imahorn, Elias and Spoerri, Iris and Aushev, Magomet and March, Oliver P. and Wariwoda, Hedwig and Von Arb, Sarah and Volz, Andreas and Itin, Peter H. and Reichelt, Julia and Burger, Bettina. (2019) Arginine- but not alanine-rich carboxy-termini trigger nuclear translocation of mutant keratin 10 in ichthyosis with confetti. Journal of cellular and molecular medicine, 23 (12). pp. 8442-8452.

Burgener, Anne-Valérie and Bantug, Glenn R. and Meyer, Benedikt J. and Higgins, Rebecca and Ghosh, Adhideb and Bignucolo, Olivier and Ma, Eric H. and Loeliger, Jordan and Unterstab, Gunhild and Geigges, Marco and Steiner, Rebekah and Enamorado, Michel and Ivanek, Robert and Hunziker, Danielle and Schmidt, Alexander and Müller-Durovic, Bojana and Grählert, Jasmin and Epple, Raja and Dimeloe, Sarah and Lötscher, Jonas and Sauder, Ursula and Ebnöther, Monika and Burger, Bettina and Heijnen, Ingmar and Martínez-Cano, Sarai and Cantoni, Nathan and Brücker, Rolf and Kahlert, Christian R. and Sancho, David and Jones, Russell G. and Navarini, Alexander and Recher, Mike and Hess, Christoph. (2019) SDHA gain-of-function engages inflammatory mitochondrial retrograde signaling via KEAP1-Nrf2. Nature Immunology, 20 (10). pp. 1311-1321.

2017

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.

2015

Burger, Bettina and Spörri, Iris and Stegmann, Danielle A. and De Mesmaker, Julie and Schaub, Stefan and Itin, Peter H. and Steiger, Jürg and Arnold, Andreas W.. (2015) Risk of Cutaneous Squamous Cell Carcinoma Development in Renal Transplant Recipients Is Independent of TMC/EVER Alterations. Dermatology, 231 (3). pp. 245-252.

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.

2014

Eytan, O. and Qiaoli, L. and Nousbeck, Janna and van Steensel, Maurice and Burger, Bettina and Hohl, Daniel and Taieb, A. and Prey, S. and Bachmann, Daniel and Avitan-Hersh, Emily and Jin Chung, H. and Shemer, Avner and Trau, Henri and Bergman, R. and Fuchs-Telem, D. and Warshauer, E. and Israeli, S. and Itin, Peter H. and Sarig, Ofer and Uitto, Jouni and Sprecher, E.. (2014) Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris. British Journal of Dermatology, 170 (5). pp. 1196-1198.

2013

Bruegger, Christelle and Kempf, Werner and Spoerri, Iris and Arnold, Andreas W. and Itin, Peter H. and Burger, Bettina. (2013) MicroRNA expression differs in cutaneous squamous cell carcinomas and healthy skin of immunocompetent individuals. Experimental dermatology, 22 (6). pp. 426-428.

2011

Nousbeck, Janna and Burger, Bettina and Fuchs-Telem, Dana and Pavlovsky, Mor and Fenig, Shlomit and Sarig, Ofer and Itin, Peter and Sprecher, Eli. (2011) A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia. American journal of human genetics, Vol. 89, H. 2. pp. 302-307.

Arnold, Andreas W. and Burger, Bettina and Kump, Erwin and Rufle, Alexander and Tyring, Stephen K. and Kempf, Werner and Häusermann, Peter and Itin, Peter H.. (2011) Homozygosity for the c.917A--<T (p.N306l) polymorphism in the EVER2/TMC8 gene of two sisters with epidermodysplasia verruciformis Lewandowsky-Lutz originally described by Wilhelm Lutz. Dermatology, 222 (1). pp. 81-86.

Burger, Bettina and Fuchs, Dana and Sprecher, Eli and Itin, Peter. (2011) The immigration delay disease : adermatoglyphia-inherited absence of epidermal ridges. Journal of the American Academy of Dermatology, Vol. 64, H. 5. pp. 974-980.

2010

Burger, Bettina and Hershkovitz, Dov and Indelman, Margarita and Kovac, Michal and Galambos, Jörg and Haeusermann, Peter and Sprecher, Eli and Itin, Peter H.. (2010) Buschke-Ollendorff syndrome in a three-generation family: influence of a novel LEMD3 mutation to tropoelastin expression. European journal of dermatology : EJD, 20 (6). pp. 693-697.

Burger, Bettina and Kind, Fabiola and Spoerri, Iris and Rütten, Arno and Battegay, Manuel and Häusermann, Peter and Itin, Peter H. and Arnold, Andreas W.. (2010) HIV-positive child with epidermodysplasia verruciformis-like lesions and homozygous mutation in TMC6. AIDS, 24 (17). pp. 2758-2760.

Has, Cristina and Burger, Bettina and Volz, A. and Kohlhase, Jürgen and Bruckner-Tuderman, Leena and Itin, Peter. (2010) Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancer. Dermatology (Basel, Switzerland), 221 (4). pp. 309-312.

Itin, Peter H. and Heinimann, Karl and Attenhofer, Michèle and Boesch, Nemya and De Lorenzo, Rosaria and Trüb, Swantje and Burger, Bettina. (2010) Precalcaneal congenital fibrolipomatous hamartomas : is there a pathogenetic relationship with Gardner Syndrome? EJD : European journal of dermatology, Vol. 20, no. 2. pp. 246-247.

Itin, Peter H. and Heinimann, Karl and Attenhofer, Michèle and Boesch, Nemya and De Lorenzo, Rosaria and Trüb, Swantje and Burger, Bettina. (2010) Precalcaneal congenital fibrolipomatous hamartomas: is there a pathogenetic relationship with Gardner Syndrome? European journal of dermatology : EJD, 20 (2). pp. 246-247.

Itin, Peter H. and Burger, Bettina. (2010) Spontaneous fading of reticular pigmentation in Naegeli-Franceschetti-Jadassohn syndrome. Dermatology, 221 (2). pp. 135-136.

Itin, Peter H. and Burger, Bettina. (2010) [Genodermatoses for practitioners--principles and concepts]. Therapeutische Umschau. Revue thérapeutique, 67 (9). pp. 483-485.

2009

Itin, Peter and Burger, Bettina. (2009) Mosaic manifestations of monogenic skin diseases. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 7 (9). pp. 744-748.

2008

Burger, Bettina and Itin, Peter. (2008) Hereditäre Hauttumoren speziell der Frau. Schweizer Zeitschrift für Onkologie, 2. pp. 20-24.

Burger, Bettina and Itin, Peter. (2008) Muir-Torre syndrome. Dermatology, 217 (1). pp. 56-57.

This list was generated on Mon Sep 28 05:03:21 2020 CEST.