Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Graham Rykiel"'
Autor:
Graham Rykiel, Claudia S López, Jessica L Riesterer, Ian Fries, Sanika Deosthali, Katherine Courchaine, Alina Maloyan, Kent Thornburg, Sandra Rugonyi
Publikováno v:
eLife, Vol 9 (2020)
Cardiac pumping depends on the morphological structure of the heart, but also on its subcellular (ultrastructural) architecture, which enables cardiac contraction. In cases of congenital heart defects, localized ultrastructural disruptions that incre
Externí odkaz:
https://doaj.org/article/fc24e5a5d945488fb19bae519e84c0af
Autor:
Mark R. Helmers, Caitlin J. Bowen, Kelly S. Benke, Elena Gallo MacFarlane, Zachary Burger, Graham Rykiel, Juan Francisco Calderón Giadrosic, Elaine C. Davis, Harry C. Dietz
Publikováno v:
J Clin Invest
Vascular Ehlers-Danlos syndrome (vEDS) is an autosomal-dominant connective tissue disorder caused by heterozygous mutations in the COL3A1 gene, which encodes the pro-α 1 chain of collagen III. Loss of structural integrity of the extracellular matrix
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::450ccfb10cf2a10cd73a85fba7765606
https://doi.org/10.1172/jci130730
https://doi.org/10.1172/jci130730
Publikováno v:
Anatomical record (Hoboken, N.J. : 2007)REFERENCES. 304(12)
Vascular endothelial growth factor (VEGF) plays a critical role during early heart development. Clinical evidence shows that conditions associated with changes in VEGF signaling in utero are correlated with an increased risk of congenital heart defec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8099532e5ec643a7d2c0175072fb2577
https://pubmed.ncbi.nlm.nih.gov/33620155
https://pubmed.ncbi.nlm.nih.gov/33620155
Autor:
Jessica L. Riesterer, Claudia S. López, Katherine Courchaine, Sandra Rugonyi, Sanika Deosthali, Kent L. Thornburg, Ian Fries, Graham Rykiel, Alina Maloyan
Publikováno v:
eLife, Vol 9 (2020)
eLife
eLife
Cardiac pumping depends on the morphological structure of the heart, but also on its subcellular (ultrastructural) architecture, which enables cardiac contraction. In cases of congenital heart defects, localized ultrastructural disruptions that incre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9b1d1606aba447d87f417786e446968
https://doi.org/10.7554/elife.58138
https://doi.org/10.7554/elife.58138
Autor:
Claudia S. López, Ian Fries, Graham Rykiel, Kent L. Thornburg, Sanika Deosthali, Alina Maloyan, Sandra Rugonyi, Jessica L. Riesterer, Katherine Courchaine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3b2beabd534a6faa32c5cdea54c4699
https://doi.org/10.7554/elife.58138.sa2
https://doi.org/10.7554/elife.58138.sa2
Autor:
Jessica McQuiston, Kent L. Thornburg, Sandra Rugonyi, Katherine Courchaine, Alina Maloyan, Claudia S. López, Sanika Deosthali, Ian Fries, Graham Rykiel
Efficient cardiac pumping depends on the morphological structure of the heart, but also on its sub-cellular (ultrastructural) architecture, which enables cardiac contraction. In cases of congenital heart defects, localized sub-cellular disruptions in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de7a7cdb6cbd4e1ad97578e845a01df0
Publikováno v:
Progress in Biophysics and Molecular Biology. 137:95-110
The role of hemodynamics in cardiovascular development is not well understood. Indeed, it would be remarkable if it were, given the dauntingly complex array of intricately synchronized genetic, molecular, mechanical, and environmental factors at play
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7487a28104674bc59867753f9986c56
https://doi.org/10.1016/j.pbiomolbio.2018.05.005
https://doi.org/10.1016/j.pbiomolbio.2018.05.005
Autor:
Elena Gallo MacFarlane, Graham Rykiel, Mark R. Helmers, Caitlin J. Bowen, Elaine C. Davis, Zachary Burger, Juan Francisco Calderón Giadrosic, Harry C. Dietz
Vascular Ehlers-Danlos Syndrome (vEDS) is an autosomal-dominant connective tissue disorder caused by heterozygous mutations in the COL3A1 gene[1][1]. Currently, loss of structural integrity of the extracellular matrix is believed to drive the signs a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f3fc0d7b392cacc0c177c72316f88cc
https://doi.org/10.1101/627653
https://doi.org/10.1101/627653
Publikováno v:
The FASEB Journal. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f92b96133b396e8504220814bf871293
https://doi.org/10.1096/fasebj.2019.33.1_supplement.18.1
https://doi.org/10.1096/fasebj.2019.33.1_supplement.18.1
Autor:
Michael B. Filla, Anastasiia Aleksandrova, Andras Czirok, Edina Kosa, Sandra Rugonyi, Charles D. Little, Rusty Lansford, Graham Rykiel, Alan Petersen, Brenda J. Rongish
Publikováno v:
The FASEB Journal. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4365a0d9af4242094c276b66b0772574
https://doi.org/10.1096/fasebj.2018.32.1_supplement.94.1
https://doi.org/10.1096/fasebj.2018.32.1_supplement.94.1