Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Ingrid Braenne"'
Autor:
Ingrid Brænne, Suna Onengut-Gumuscu, Ruoxi Chen, Ani W. Manichaikul, Stephen S. Rich, Wei-Min Chen, Charles R. Farber, the TEDDY Study Group
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Significant progress has been made in elucidating genetic risk factors influencing Type 1 diabetes (T1D); however, features other than genetic variants that initiate and/or accelerate islet autoimmunity that lead to the development of clinic
Externí odkaz:
https://doaj.org/article/9421c0710b934d629143b663772e71fc
Autor:
Ingrid Brænne, Lingyao Zeng, Christina Willenborg, Vinicius Tragante, Thorsten Kessler, CARDIoGRAM Consortium, CARDIoGRAMplusC4D Consortium, Cristen J Willer, Markku Laakso, Lars Wallentin, Paul W Franks, Veikko Salomaa, Abbas Dehghan, Thomas Meitinger, Nilesh J Samani, Folkert W Asselbergs, Jeanette Erdmann, Heribert Schunkert
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0182999 (2017)
Glatiramer acetate is used therapeutically in multiple sclerosis but also known for adverse effects including elevated coronary artery disease (CAD) risk. The mechanisms underlying the cardiovascular side effects of the medication are unclear. Here,
Externí odkaz:
https://doaj.org/article/73eeb4fe985946ec82b07e430312a6f3
Autor:
Patrick Linsel-Nitschke, Anika Götz, Jeanette Erdmann, Ingrid Braenne, Peter Braund, Christian Hengstenberg, Klaus Stark, Marcus Fischer, Stefan Schreiber, Nour Eddine El Mokhtari, Arne Schaefer, Jürgen Schrezenmeir, Diana Rubin, Anke Hinney, Thomas Reinehr, Christian Roth, Jan Ortlepp, Peter Hanrath, Alistair S Hall, Massimo Mangino, Wolfgang Lieb, Claudia Lamina, Iris M Heid, Angela Doering, Christian Gieger, Annette Peters, Thomas Meitinger, H-Erich Wichmann, Inke R König, Andreas Ziegler, Florian Kronenberg, Nilesh J Samani, Heribert Schunkert, Wellcome Trust Case Control Consortium (WTCCC), Cardiogenics Consortium
Publikováno v:
PLoS ONE, Vol 3, Iss 8, p e2986 (2008)
Rare mutations of the low-density lipoprotein receptor gene (LDLR) cause familial hypercholesterolemia, which increases the risk for coronary artery disease (CAD). Less is known about the implications of common genetic variation in the LDLR gene rega
Externí odkaz:
https://doaj.org/article/5721ef7b49874c65bb1475a6eb9de291
Autor:
Patrick Linsel-Nitschke, Anika Götz, Jeanette Erdmann, Ingrid Braenne, Peter Braund, Christian Hengstenberg, Klaus Stark, Marcus Fischer, Stefan Schreiber, Nour Eddine El Mokhtari, Arne Schaefer, Jürgen Schrezenmeir, Diana Rubin, Anke Hinney, Thomas Reinehr, Christian Roth, Jan Ortlepp, Peter Hanrath, Alistair S. Hall, Massimo Mangino, Wolfgang Lieb, Claudia Lamina, Iris M. Heid, Angela Doering, Christian Gieger, Annette Peters, Thomas Meitinger, H.-Erich Wichmann, Inke R. König, Andreas Ziegler, Florian Kronenberg, Nilesh J. Samani, Heribert Schunkert
Publikováno v:
PLoS ONE, Vol 3, Iss 9 (2008)
Externí odkaz:
https://doaj.org/article/f3ca093aff2e471481e40480b42087f0
Autor:
Heribert Schunkert, Jeanette Erdmann, Stephanie Tennstedt, Jana Wobst, Thomas Meitinger, Tim M. Strom, Hendrik B. Sager, Tan An Dang, Michael Wierer, Ingrid Braenne, Thorsten Kessler
Publikováno v:
Circulation 144, 662-665 (2021)
Autor:
Ingrid Braenne, Christopher J Chermside-Scabbo, Matthew J. Silva, Michael D. Brodt, Taylor L Harris, Charles R. Farber, Bo Zhang
Publikováno v:
J Bone Miner Res
Mechanical loading is a potent strategy to induce bone formation, but with aging, the bone formation response to the same mechanical stimulus diminishes. Our main objectives were to (i) discover the potential transcriptional differences and (ii) comp
Autor:
null Christopher J Chermside‐Scabbo, null Taylor L Harris, null Michael D Brodt, null Ingrid Braenne, null Bo Zhang, null Charles R Farber, null Matthew J Silva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3096244c77fe2dbb52d8aa97d3d53677
https://doi.org/10.1002/jbmr.4031/v3/response1
https://doi.org/10.1002/jbmr.4031/v3/response1
Autor:
Charles R. Farber, Ingrid Braenne, Michael D. Brodt, Bo Zhang, Christopher J Chermside-Scabbo, Matthew J. Silva, Taylor L Harris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc2df19dd527701ce892d28db8f8c4e3
https://doi.org/10.1002/jbmr.4031/v2/response1
https://doi.org/10.1002/jbmr.4031/v2/response1
Autor:
Karin Wulff, Konrad Bork, Lars Steinmüller-Magin, Jochen Hardt, Ingrid Braenne, Günther Witzke, Heidi Rossmann
Publikováno v:
Allergy. 74:2479-2481
Autor:
Ingrid Braenne, Günther Witzke, Lars Steinmüller-Magin, Petra Staubach-Renz, Karin Wulff, Jochen Hardt, Konrad Bork
Publikováno v:
Allergy. 73:442-450
Background Hereditary angioedema (HAE) with normal C1-INH (HAEnCI) may be linked to specific mutations in the coagulation factor 12 (FXII) gene (HAE-FXII) or functional mutations in other genes that are still unknown. We sought to identify and charac