Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Andreas, Kindmark"'
Autor:
Alexander Moumtsidis, Rebecka Steffen Johansson, MD, Hui Xue, PhD, Peter Kellman, PhD, Andreas Kindmark, MD, PhD, Jannike Nickander, MD, PhD
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 26, Iss , Pp 100186- (2024)
Externí odkaz:
https://doaj.org/article/d6e19ef06e034f74bb2783c836deb546
Autor:
Janet L. Cunningham, Gunnel Nordmark, David Fällmar, Simon Cervenka, Maike Gallwitz, Roland Säll, Peter T. Schmidt, Johan Rönnelid, Barbro Persson, Andreas Kindmark, Joachim Burman
Publikováno v:
Journal of Affective Disorders Reports, Vol 13, Iss , Pp 100597- (2023)
Immunological mechanisms, both alone and in combination, are associated with a broad range of psychiatric disorders encompassing autoimmune, autoinflammatory disorders but also genetic, metabolic, or other immunological disorders. Early treatment imp
Externí odkaz:
https://doaj.org/article/0f642af304b643f49e7b07a8f774e76c
Autor:
Martin Johnsson, Helena Wall, Fernando A Lopes Pinto, Robert H Fleming, Heather A McCormack, Cristina Benavides-Reyes, Nazaret Dominguez-Gasca, Estefania Sanchez-Rodriguez, Ian C Dunn, Alejandro B Rodriguez-Navarro, Andreas Kindmark, Dirk-Jan de Koning
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 13, Iss 2 (2022)
AbstractOsteoporosis and bone fractures are a severe problem for the welfare of laying hens, with genetics and environment, such as housing system, each making substantial contributions to bone strength. In this work, we performed genetic analyses of
Externí odkaz:
https://doaj.org/article/0972b530f7bb4a2d8cc55d652959c66f
Autor:
Pantelis Clewemar, Nils P. Hailer, Yasmin Hailer, Joakim Klar, Andreas Kindmark, Östen Ljunggren, Eva‐Lena Stattin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Abstract Background Osteogenesis imperfecta (OI) is a clinical and genetic heterogeneous group of connective tissue disorders, characterized by bone fragility and a propensity to fracture. Methods In this report we describe the clinical phenotype of
Externí odkaz:
https://doaj.org/article/6a36ed3a6eec4e16b918d8628693c73d
Autor:
Anne Björk, Dan Mellström, Claes Ohlsson, Magnus Karlsson, Hans Mallmin, Gunnar Johansson, Östen Ljunggren, Andreas Kindmark
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0209268 (2018)
ObjectivePolymorphisms in the CYP2R1 gene encoding Vitamin D 25-hydroxylase have been reported to correlate with circulating levels of 25-OH vitamin D3 (25(OH)D). It is unknown whether these variations also affect overall bone metabolism. In order to
Externí odkaz:
https://doaj.org/article/cbce40e690144f50a367614fbdad622f
Autor:
Kristofer Andersson, Göran Dahllöf, Katarina Lindahl, Andreas Kindmark, Giedre Grigelioniene, Eva Åström, Barbro Malmgren
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176466 (2017)
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused mainly by mutations in the collagen I genes (COL1A1 and COL1A2). Dentinogenesis imperfecta (DGI) and other dental aberrations are common features of OI. W
Externí odkaz:
https://doaj.org/article/00a0e237b4d34705b538f4610e27dbf4
Autor:
Bengt Fellström, Claes Ohlsson, Per Anton Westerberg, Torbjörn Linde, Östen Ljunggren, Andreas Kindmark, Ping-Hsun Wu, Dan Mellström, Åsa Tivesten, Magnus Karlsson
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
Scientific Reports
Scientific Reports
The Klotho (KL) gene is involved in phosphate homeostasis. Polymorphisms in this gene have been reported to be associated with the risk of cardiovascular disease. Here we used computational tools to predict the damage-associated single nucleotide pol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::145a387f87b2d4948f5e375bafa346c9
http://link.springer.com/article/10.1038/s41598-020-66517-5
http://link.springer.com/article/10.1038/s41598-020-66517-5
Publikováno v:
International Journal of Medical Sciences, Vol 5, Iss 6, Pp 361-365 (2008)
Osteogenesis imperfecta (OI) is generally caused by a dominant mutation in Collagen I, encoded by the genes COL1A1 and COL1A2. To date there is no satisfactory therapy for OI, but inactivation of the mutant allele through small interfering RNAs (siRN
Externí odkaz:
https://doaj.org/article/ff979d3f76f14a529d22e6e19113f1d3
Autor:
Bo Freyschuss, Maria K. Svensson, Thomas Cars, Lars Lindhagen, Helena Johansson, Andreas Kindmark
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 37(4)
Results from real-world evidence (RWE) from the largest healthcare region in Sweden show low uptake of antiresorptive (AR) treatment, but beneficial effect in those receiving treatment, especially for the composite outcome of hip fracture or death. F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::477f70015c2597aa1b327a36c8762bab
https://pubmed.ncbi.nlm.nih.gov/34984745
https://pubmed.ncbi.nlm.nih.gov/34984745
