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pro vyhledávání: '"Silke Rickert-Sperling"'
This 2nd edition has been extensively updated and provides comprehensive and current insight into congenital heart diseases, from embryonic development through to clinical features, including human genetics and our current knowledge of the underlying
Publikováno v:
Oxford Medicine
A large quantity of molecular information on heart development, function, and disease has been generated over recent decades. However, most recent studies have been dominated by reductionistic approaches, and thus many aspects remain unclear, particu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eaa16c5adfa3a40f70cc5f3903d08d4
https://doi.org/10.1093/med/9780198757269.003.0033
https://doi.org/10.1093/med/9780198757269.003.0033
This book provides comprehensive insights into congenital heart disease from embryonic development through to clinical features, including human genetics and our current knowledge of the underlying molecular pathways. It is divided into three parts:
Publikováno v:
Congenital Heart Diseases: The Broken Heart ISBN: 9783709118825
Tetralogy of Fallot (TOF) and double outlet right ventricle (DORV) are conotruncal defects resulting from disturbances of the second heart field and the neural crest, which can occur as isolated malformations or as part of multiorgan syndromes. Their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3710394b2b2689364bd9a382dc374cb8
https://doi.org/10.1007/978-3-7091-1883-2_32
https://doi.org/10.1007/978-3-7091-1883-2_32
Autor:
Ana Dopazo, Alberto Gatto, Marcel Grunert, Enrique Lara-Pezzi, Cornelia Dorn, Silke Rickert-Sperling, Jesús Vázquez, Fátima Sánchez-Cabo
Publikováno v:
Congenital Heart Diseases: The Broken Heart ISBN: 9783709118825
Over the last decades, the study of congenital heart disease (CHD) has benefited from various model systems and the development of molecular biological techniques enabling the analysis of single gene as well as global effects. In this chapter, we fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09b5e817e7c78505b0bbc7ca9a40862f
https://doi.org/10.1007/978-3-7091-1883-2_18
https://doi.org/10.1007/978-3-7091-1883-2_18
Publikováno v:
Congenital Heart Diseases: The Broken Heart ISBN: 9783709118825
Ventricular septal defects (VSDs) are recognized as one of the commonest congenital heart diseases (CHD), accounting for up to 40 % of all cardiac malformations, and occur as isolated CHDs as well as together with other cardiac and extracardiac conge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03dbc08a89438b060a8955acc468d11d
https://doi.org/10.1007/978-3-7091-1883-2_23
https://doi.org/10.1007/978-3-7091-1883-2_23
Publikováno v:
Congenital Heart Diseases: The Broken Heart
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42f25cc30436bc9e3e94036d7b820c74
https://doi.org/10.1007/978-3-7091-1883-2
https://doi.org/10.1007/978-3-7091-1883-2
Autor:
Andreas Perrot, Silke Rickert-Sperling
Publikováno v:
Congenital Heart Diseases: The Broken Heart ISBN: 9783709118825
Defects of situs are associated with complex sets of congenital heart defects in which the normal concordance of asymmetric thoracic and abdominal organs is disturbed. The cellular and molecular mechanisms underlying the formation of the embryonic le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ea8aedbc3ab51b850a527e43a15798b
https://doi.org/10.1007/978-3-7091-1883-2_38
https://doi.org/10.1007/978-3-7091-1883-2_38
Publikováno v:
Congenital Heart Diseases: The Broken Heart ISBN: 9783709118825
Cardiac development is a fine-tuned process governed by complex transcriptional networks, in which transcription factors (TFs) interact with other regulatory layers. In this chapter, we first introduce the core cardiac TFs including Gata, Hand, Nkx2,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f0f66e77d9719ae69713d6417d7ce33
https://doi.org/10.1007/978-3-7091-1883-2_12
https://doi.org/10.1007/978-3-7091-1883-2_12