Zobrazeno 1 - 10
of 8 839
pro vyhledávání: '"Willecke, K."'
Autor:
Dermietzel, R., Traub, O., Hwang, T. K., Beyer, E., Bennett, M. V. L., Spray, D. C., Willecke, K.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1989 Dec . 86(24), 10148-10152.
Externí odkaz:
https://www.jstor.org/stable/34818
Autor:
Eckardt, D., Theis, M., Degen, J., Ott, T., van Rijen, H.V.M., Kirchhoff, S., Kim, J.-S., de Bakker, J.M.T., Willecke, K. *
Publikováno v:
In Journal of Molecular and Cellular Cardiology 2004 36(1):101-110
Autor:
Rabionet M; Lipid Pathobiochemistry Group, German Cancer Research Center, Heidelberg, Germany., Bernard P; Infinity, Université Toulouse, CNRS, Inserm, UPS, Toulouse, France., Pichery M; Infinity, Université Toulouse, CNRS, Inserm, UPS, Toulouse, France., Marsching C; Lipid Pathobiochemistry Group, German Cancer Research Center, Heidelberg, Germany.; Center for Applied Research in Biomedical Mass Spectrometry (ABIMAS), Mannheim, Germany.; Center for Mass Spectrometry and Optical Spectroscopy (CeMOS), Mannheim University of Applied Sciences, Mannheim, Germany.; Instrumental Analytics and Bioanalytics, Mannheim University of Applied Sciences, Mannheim, Germany., Bayerle A; Lipid Pathobiochemistry Group, German Cancer Research Center, Heidelberg, Germany., Dworski S; Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada., Kamani MA; University Health Network, Toronto, Ontario, Canada., Chitraju C; Department of Genetics and Complex Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.; Department of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA., Gluchowski NL; Department of Genetics and Complex Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.; Department of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.; Division of Gastroenterology and Nutrition, Boston Children's Hospital, Boston, Massachusetts, USA., Gabriel KR; Department of Genetics and Complex Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.; Department of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.; Howard Hughes Medical Institute, Boston, Massachusetts, USA., Asadi A; Department of Molecular Biosciences, The Wenner-Gren Institute, The Arrhenius Laboratories, Stockholm University, Stockholm, Sweden., Ebel P; Molecular Genetics, Life and Medical Sciences Institute (LIMES), University of Bonn, Bonn, Germany., Hoekstra M; Leiden Academic Centre for Drug Research, Division of BioTherapeutics, Leiden University, Leiden, Netherlands., Dumas S; Department of Nutritional sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA., Ntambi JM; Department of Nutritional sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA.; Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA., Jacobsson A; Department of Molecular Biosciences, The Wenner-Gren Institute, The Arrhenius Laboratories, Stockholm University, Stockholm, Sweden., Willecke K; Molecular Genetics, Life and Medical Sciences Institute (LIMES), University of Bonn, Bonn, Germany., Medin JA; Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada.; University Health Network, Toronto, Ontario, Canada.; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.; Medical College of Wisconsin, Milwaukee, Wisconsin, USA., Jonca N; Infinity, Université Toulouse, CNRS, Inserm, UPS, Toulouse, France.; CHU Toulouse, Hôpital Purpan, Laboratoire de Biologie Cellulaire et Cytologie, Institut Fédératif de Biologie, Toulouse, France., Sandhoff R; Lipid Pathobiochemistry Group, German Cancer Research Center, Heidelberg, Germany.; Center for Applied Research in Biomedical Mass Spectrometry (ABIMAS), Mannheim, Germany.
Publikováno v:
Lipids [Lipids] 2022 May; Vol. 57 (3), pp. 183-195. Date of Electronic Publication: 2022 Mar 23.
Publikováno v:
European Journal of Biochemistry. 1969, Vol. 8 Issue 4, p503-509. 7p.
Autor:
Kovács-Öller, Tamás1,2,3,4 (AUTHOR) kovacs-oller.tamas@pte.hu, Szarka, Gergely1,2,3,4 (AUTHOR) jerjely@gamma.ttk.pte.hu, Hoffmann, Gyula1,2,3,4 (AUTHOR) hgyula@gamma.ttk.pte.hu, Péntek, Loretta1,2 (AUTHOR) pentekloretta00@gmail.com, Valentin, Gréta1,2 (AUTHOR) g.vtin83@gmail.com, Ross, Liliana5 (AUTHOR) liliana.ross@ucalgary.ca, Völgyi, Béla1,2,3,4 (AUTHOR) volgyi01@gamma.ttk.pte.hu
Publikováno v:
Biomolecules (2218-273X). Jul2023, Vol. 13 Issue 7, p1119. 15p.
Autor:
Lall, VK, Bruce, G, Voytenko, L, Drinkhill, M, Wellershaus, K, Willecke, K, Deuchars, J, Deuchars, SA
Chronically elevated sympathetic nervous activity underlies many cardiovascular diseases. Elucidating the mechanisms contributing to sympathetic nervous system output may reveal new avenues of treatment. The contribution of the gap junctional protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::fa4a97863483e025f61b015845d7064c
https://eprints.whiterose.ac.uk/116053/9/3966.full.pdf
https://eprints.whiterose.ac.uk/116053/9/3966.full.pdf
Autor:
Abrams, Charles K.1 (AUTHOR) cabrams1@uic.edu
Publikováno v:
Biomolecules (2218-273X). Apr2023, Vol. 13 Issue 4, p712. 18p.
Autor:
Trovato-Salinaro, A., Belluardo, N., Frinchi, M., von Maltzahn, J., Willecke, K., Condorelli, D. F., Mudò, G.
Publikováno v:
American Journal of Physiology: Cell Physiology; Mar2009, Vol. 296 Issue 3, pC593-C606, 14p, 3 Color Photographs, 7 Black and White Photographs, 1 Diagram
Autor:
Cea, LA, Puebla, C, Cisterna, BA, Escamilla, R, Vargas, AA, Frank, M, Martinez-Montero, P, Prior, C, Molano, J, Esteban-Rodriguez, I, Pascual, I, Gallano, P, Lorenzo, G, Pian, H, Barrio, LC, Willecke, K, Saez, JC
Publikováno v:
CELLULAR AND MOLECULAR LIFE SCIENCES
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Skeletal muscles of patients with Duchenne muscular dystrophy (DMD) show numerous alterations including inflammation, apoptosis, and necrosis of myofibers. However, the molecular mechanism that explains these changes remains largely unknown. Here, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::2d9cda8669cd714b288fcbb74ff2eedb
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=7226
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=7226
Autor:
Foo, Brian1,2 (AUTHOR) brian.foo@med.uni-goettingen.de, Amedei, Hugo3 (AUTHOR), Kaur, Surmeet3 (AUTHOR), Jaawan, Samir1,2 (AUTHOR), Boshnakovska, Angela4 (AUTHOR), Gall, Tanja4 (AUTHOR), de Boer, Rudolf A.5,6 (AUTHOR), Silljé, Herman H. W.5 (AUTHOR), Urlaub, Henning2,3,7 (AUTHOR), Rehling, Peter4 (AUTHOR), Lenz, Christof2,3,7 (AUTHOR) christof.lenz@med.uni-goettingen.de, Lehnart, Stephan E.1,2 (AUTHOR) brian.foo@med.uni-goettingen.de
Publikováno v:
PLoS ONE. 10/24/2024, Vol. 19 Issue 10, p1-45. 45p.