Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Martina S. Burczyk"'
Autor:
Arthi Sridhar, Melanie Philipp, Susana S. Lopes, Stephanie M. Ware, Petra Pennekamp, Pedro Sampaio, Max Angenendt, Raquel Jacinto, Heymut Omran, Maja Hempel, Martina S. Burczyk, Paul Walther, Martin D. Burkhalter, Cornelia Donow
Publikováno v:
Journal of Clinical Investigation
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
J Clin Invest
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
J Clin Invest
About 1% of all newborns are affected by congenital heart disease (CHD). Recent findings identify aberrantly functioning cilia as a possible source for CHD. Faulty cilia also prevent the development of proper left-right asymmetry and cause heterotaxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b75444e3a6c07c1d7ca8d70bac0539e3
https://doi.org/10.1172/jci98890
https://doi.org/10.1172/jci98890
Autor:
Thilo Diehl, Teresa Casar Tena, Maja Hempel, Davor Lessel, Melanie Philipp, Martina S. Burczyk, Tim M. Strom, Christian Kubisch
Publikováno v:
Human Genetics. 136:339-346
GATA5 belongs to the GATA family of transcription factors characterized by highly evolutionarily conserved zinc-finger DNA-binding domains. Mouse models have implicated a role of GATA5 during mammalian embryogenesis, including proper heart developmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::177c97bde6262eeb8b914d6454f92891
https://doi.org/10.1007/s00439-017-1762-2
https://doi.org/10.1007/s00439-017-1762-2
Autor:
Monika Kustermann, Svenja Laue, Yinghong Cui, Douglas G. Tilley, Laurel A. Grisanti, Melanie Rothe, Michael Kauk, Carsten Hoffmann, Melanie Philipp, WH Zimmermann, Teresa Casar Tena, Allessandra Moretti, Farah Raad, Michael Kühl, Martina S. Burczyk, Sabrina Matysik, Martin D. Burkhalter, Cornelia Donow, Jürgen Wess
Publikováno v:
JCI Insight
Deterioration or inborn malformations of the cardiac conduction system (CCS) interfere with proper impulse propagation in the heart and may lead to sudden cardiac death or heart failure. Patients afflicted with arrhythmia depend on antiarrhythmic med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d95a3d11c2efe67a92a1fc8c1ec423a
https://doi.org/10.1172/jci.insight.121971
https://doi.org/10.1172/jci.insight.121971