Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fiona E A, McGuigan"'
Autor:
Ines Foessl, J. H. Duncan Bassett, Åshild Bjørnerem, Björn Busse, Ângelo Calado, Pascale Chavassieux, Maria Christou, Eleni Douni, Imke A. K. Fiedler, João Eurico Fonseca, Eva Hassler, Wolfgang Högler, Erika Kague, David Karasik, Patricia Khashayar, Bente L. Langdahl, Victoria D. Leitch, Philippe Lopes, Georgios Markozannes, Fiona E. A. McGuigan, Carolina Medina-Gomez, Evangelia Ntzani, Ling Oei, Claes Ohlsson, Pawel Szulc, Jonathan H. Tobias, Katerina Trajanoska, Şansın Tuzun, Amina Valjevac, Bert van Rietbergen, Graham R. Williams, Tatjana Zekic, Fernando Rivadeneira, Barbara Obermayer-Pietsch
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
A synoptic overview of scientific methods applied in bone and associated research fields across species has yet to be published. Experts from the EU Cost Action GEMSTONE (“GEnomics of MusculoSkeletal Traits translational Network”) Working Group 2
Externí odkaz:
https://doaj.org/article/f56aa12424184b2093ef7db929b89a6f
Publikováno v:
Archives of Osteoporosis. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::786d6ae43a91c1b4a119a832032084d5
https://doi.org/10.1007/s11657-022-01164-z
https://doi.org/10.1007/s11657-022-01164-z
Publikováno v:
Archives of osteoporosis. 17(1)
This study describes that low bone density is prevalent in premenopausal Saudi women, especially women of normal weight and vitamin D deficiency. Although BMD is higher in obese young women, this may not be beneficial later in life in conjunction wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::55246a47c28649bb44dfced9bbd540d5
https://pubmed.ncbi.nlm.nih.gov/36107272
https://pubmed.ncbi.nlm.nih.gov/36107272
Autor:
Stuart H Ralston, André G Uitterlinden, Maria Luisa Brandi, Susana Balcells, Bente L Langdahl, Paul Lips, Roman Lorenc, Barbara Obermayer-Pietsch, Serena Scollen, Mariona Bustamante, Lise Bjerre Husted, Alisoun H Carey, Adolfo Diez-Perez, Alison M Dunning, Alberto Falchetti, Elzbieta Karczmarewicz, Marcin Kruk, Johannes P. T. M van Leeuwen, Joyce B. J van Meurs, Jon Mangion, Fiona E. A McGuigan, Leonardo Mellibovsky, Francesca del Monte, Huibert A. P Pols, Jonathan Reeve, David M Reid, Wilfried Renner, Fernando Rivadeneira, Natasja M van Schoor, Rachael E Sherlock, John P. A Ioannidis
Publikováno v:
PLoS Medicine, Vol 3, Iss 5 (2006)
Externí odkaz:
https://doaj.org/article/d533184ce5314ba9985c7ffd9b2c1be5
Autor:
Stuart H Ralston, André G Uitterlinden, Maria Luisa Brandi, Susana Balcells, Bente L Langdahl, Paul Lips, Roman Lorenc, Barbara Obermayer-Pietsch, Serena Scollen, Mariona Bustamante, Lise Bjerre Husted, Alisoun H Carey, Adolfo Diez-Perez, Alison M Dunning, Alberto Falchetti, Elzbieta Karczmarewicz, Marcin Kruk, Johannes P T M van Leeuwen, Joyce B J van Meurs, Jon Mangion, Fiona E A McGuigan, Leonardo Mellibovsky, Francesca del Monte, Huibert A P Pols, Jonathan Reeve, David M Reid, Wilfried Renner, Fernando Rivadeneira, Natasja M van Schoor, Rachael E Sherlock, John P A Ioannidis, GENOMOS Investigators
Publikováno v:
PLoS Medicine, Vol 3, Iss 4, p e90 (2006)
BackgroundOsteoporosis and fracture risk are considered to be under genetic control. Extensive work is being performed to identify the exact genetic variants that determine this risk. Previous work has suggested that a G/T polymorphism affecting an S
Externí odkaz:
https://doaj.org/article/d104a86c6a92461b932122e123dbc392
Autor:
Bente L, Langdahl, André G, Uitterlinden, Stuart H, Ralston, Thomas A, Trikalinos, Susanne, Balcells, Maria Luisa, Brandi, Serena, Scollen, Paul, Lips, Roman, Lorenc, Barbara, Obermayer-Pietsch, David M, Reid, Jácome Bruges, Armas, Pascal P, Arp, Amelia, Bassiti, Mariona, Bustamante, Lise Bjerre, Husted, Alison H, Carey, Ramon, Pérez Cano, Harald, Dobnig, Alison M, Dunning, Astrid, Fahrleitner-Pammer, Alberto, Falchetti, Elzbieta, Karczmarewicz, Marcin, Kruk, Johannes P T M, van Leeuwen, Laura, Masi, Joyce B J, van Meurs, Jon, Mangion, Fiona E A, McGuigan, Leonardo, Mellibovsky, Leif, Mosekilde, Xavier, Nogués, Huibert A P, Pols, Jonathan, Reeve, Wilfried, Renner, Fernando, Rivadeneira, Natasja M, van Schoor, John P A, Ioannidis, Jacqueline C, Witteman
Publikováno v:
Langdahl, B L, Uitterlinden, A G, Ralston, S H, Trikalinos, T A, Balcells, S, Brandi, M L, Scollen, S, Lips, P T A M, Lorenc, R, Obermayer-Pietsch, B, Reid, D M, Armas, J B, Arp, P P, Bassiti, A, Bustamante, M, Husted, L B, Carey, A H, Perez, C R, Dobnig, H, Dunning, A M, Fahrleitner-Pammer, A, Falchetti, A, Karczmarewicz, E, Kruk, M, van Leeuwen, J P T M, Masi, L, van Meurs, J B, Mangion, J, McGuigan, F E, Mellibovsky, L, Mosekilde, L, Nogues, X, Pols, H A P, Reeve, J, Renner, W, Rivadeneira, F, van Schoor, N M & Loannidis, J P 2008, ' Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study ', Bone, vol. 42, no. 5, pp. 969-981 . https://doi.org/10.1016/j.bone.2007.11.007
Bone
Bone, 42(5), 969-981. Elsevier Inc.
Langdahl, B L, Uitterlinden, A G, Ralston, S H, Trikalinos, T A, Balcells, S, Brandi, M L, Scollen, S, Lips, P, Lorenc, R, Obermayer-Pietsch, B, Reid, D M, Armas, J B, Arp, P P, Bassiti, A, Bustamante, M, Husted, L B, Carey, A H, Pérez Cano, R, Dobnig, H, Dunning, A M, Fahrleitner-Pammer, A, Falchetti, A, Karczmarewicz, E, Kruk, M, van Leeuwen, J P T M, Masi, L, van Meurs, J B J, Mangion, J, McGuigan, F E A, Mellibovsky, L, Mosekilde, L, Nogués, X, Pols, H A P, Reeve, J, Renner, W, Rivadeneira, F, van Schoor, N M, Ioannidis, J P A, APOSS investigators, DOPS investigators, EPOS investigators, EPOLOS investigators, FAMOS investigators, LASA investigators, ERGO investigators & GENOMOS Study 2008, ' Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study. ', Bone, vol. 42, no. 5, pp. 969-81 . https://doi.org/10.1016/j.bone.2007.11.007
Bone
Bone, 42(5), 969-981. Elsevier Inc.
Langdahl, B L, Uitterlinden, A G, Ralston, S H, Trikalinos, T A, Balcells, S, Brandi, M L, Scollen, S, Lips, P, Lorenc, R, Obermayer-Pietsch, B, Reid, D M, Armas, J B, Arp, P P, Bassiti, A, Bustamante, M, Husted, L B, Carey, A H, Pérez Cano, R, Dobnig, H, Dunning, A M, Fahrleitner-Pammer, A, Falchetti, A, Karczmarewicz, E, Kruk, M, van Leeuwen, J P T M, Masi, L, van Meurs, J B J, Mangion, J, McGuigan, F E A, Mellibovsky, L, Mosekilde, L, Nogués, X, Pols, H A P, Reeve, J, Renner, W, Rivadeneira, F, van Schoor, N M, Ioannidis, J P A, APOSS investigators, DOPS investigators, EPOS investigators, EPOLOS investigators, FAMOS investigators, LASA investigators, ERGO investigators & GENOMOS Study 2008, ' Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study. ', Bone, vol. 42, no. 5, pp. 969-81 . https://doi.org/10.1016/j.bone.2007.11.007
Introduction: The TGFB1 gene which encodes transforming growth factor beta 1, is a strong candidate for susceptibility to osteoporosis and several studies have reported associations between bone mineral density (BMD), osteoporotic fractures and polym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8574ac3095c19688bd42efb1899cecb
https://doi.org/10.1016/j.bone.2007.11.007
https://doi.org/10.1016/j.bone.2007.11.007
Autor:
Joyce B J, van Meurs, Thomas A, Trikalinos, Stuart H, Ralston, Susana, Balcells, Maria Luisa, Brandi, Kim, Brixen, Douglas P, Kiel, Bente L, Langdahl, Paul, Lips, Osten, Ljunggren, Roman, Lorenc, Barbara, Obermayer-Pietsch, Claes, Ohlsson, Ulrika, Pettersson, David M, Reid, Francois, Rousseau, Serena, Scollen, Wim, Van Hul, Lidia, Agueda, Kristina, Akesson, Lidia I, Benevolenskaya, Serge L, Ferrari, Göran, Hallmans, Albert, Hofman, Lise Bjerre, Husted, Marcin, Kruk, Stephen, Kaptoge, David, Karasik, Magnus K, Karlsson, Mattias, Lorentzon, Laura, Masi, Fiona E A, McGuigan, Dan, Mellström, Leif, Mosekilde, Xavier, Nogues, Huibert A P, Pols, Jonathan, Reeve, Wilfried, Renner, Fernando, Rivadeneira, Natasja M, van Schoor, Kurt, Weber, John P A, Ioannidis, André G, Uitterlinden, Ulrica, Bergström
Publikováno v:
JAMA (Journal of the American Medical Association), Vol. 299, No 11 (2008) pp. 1277-90
CONTEXT: Mutations in the low-density lipoprotein receptor-related protein 5 (LRP5) gene cause rare syndromes characterized by altered bone mineral density (BMD). More common LRP5 variants may affect osteoporosis risk in the general population. OBJEC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3e582b68c30924a09a3087e72b53bd64
https://archive-ouverte.unige.ch/unige:2039
https://archive-ouverte.unige.ch/unige:2039
