Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sara E. Rasmussen"'
Autor:
Ashira Blazer, Yingzhi Qian, Martin Paul Schlegel, Huda Algasas, Jill P. Buyon, Ken Cadwell, Michael Cammer, Sean P. Heffron, Feng-Xia Liang, Shilpi Mehta-Lee, Timothy Niewold, Sara E. Rasmussen, Robert M. Clancy
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Polymorphisms in the Apolipoprotein L1 (APOL1) gene are common in ancestrally African populations, and associate with kidney injury and cardiovascular disease. These risk variants (RV) provide an advantage in resisting Trypanosoma brucei, the causal
Externí odkaz:
https://doaj.org/article/6b5cd445de0c400eaa76643f1f731b7c
Autor:
Androo J. Markham, Sara E. Rasmussen, Jane E. Salmon, Wilnelly Martinez‐Ortiz, Timothy J. Cardozo, Robert M. Clancy, Jill P. Buyon
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 4, Iss 5, Pp n/a-n/a (2015)
Background Only 2% of mothers positive for anti‐SSA/Ro (Ro) antibodies have children with congenital heart block (CHB). This study aimed to determine whether reactivity with p305, an epitope within the α1G T‐type calcium channel, confers added r
Externí odkaz:
https://doaj.org/article/7cc44dd31b0e4e189b55be6d161c3270
Autor:
Sara E. Rasmussen, Jill P. Buyon, Harmony R. Reynolds, Rebecca Dann, Nicole Bornkamp, Hanane El Bannoudi, Robert R. Clancy, Jeffrey S. Berger, Nicole Allen
Publikováno v:
Journal of Thrombosis and Haemostasis. 17:532-537
Essentials Systemic lupus erythematosus (SLE) patients are at increased risk for premature CVD. Platelet activity, vascular dysfunction and carotid artery plaque are associated with FcγRIIA genotype in SLE. FcγRIIA genotype was not associated with
Autor:
Ashira D Blazer, Michael Cammer, Shilpi S. Mehta-Lee, Jill P. Buyon, Sara E. Rasmussen, Timothy B. Niewold, Feng-Xia Liang, Sean P. Heffron, Martin Schlegel, Yingzhi Qian, Robert R. Clancy, Ken Cadwell
Apolipoprotein L1 (APOL1) gene risk variants (RV) associate with renal and cardiovascular disease particularly in SLE. We hypothesized that in RV-carrying human umbilical vein endothelial cells (HUVECs) cytokine-induced APOL1 expression compromises m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e555ee3f869928d78aa39fe2d885013
https://doi.org/10.1101/2020.03.18.996702
https://doi.org/10.1101/2020.03.18.996702
Autor:
Marc K. Halushka, Sara E. Rasmussen, Sean Whelton, Jill P. Buyon, Peter M. Izmirly, Hilary Parton, Amit Saxena, Dilip S. Nath, Robert R. Clancy, Avi Z. Rosenberg, K. Rais-Bahrami
Publikováno v:
Autoimmunity Reviews. 16:980-983
While the relationship between maternal connective tissue diseases and neonatal rashes was described in the 1960s and congenital heart block in the 1970s, the "culprit" antibody reactivity to the SSA/Ro-SSB/La ribonucleoprotein complex was not identi
Autor:
Nicole Allen, Jill P. Buyon, Tessa J. Barrett, Jonathan D. Newman, Sara E. Rasmussen, Janet Nwaukoni, Sokha Nhek, Jeffrey S. Berger, Emanuela Marcantoni, Robert R. Clancy, Kristen A. Lee, Maya Rubin
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 37:707-716
Objective— Systemic lupus erythematosus (SLE) is associated with the premature development of cardiovascular disease. The platelet–endothelium interaction is important in the pathogenesis of cardiovascular disease. In this study, we investigated
Autor:
Miao Chang, Sara E. Rasmussen, Marc K. Halushka, Jill P. Buyon, Robert R. Clancy, Tenzin Lhakhang
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 202(1)
Given that diseases associated with anti-SSA/Ro autoantibodies, such as systemic lupus erythematosus and Sjögren syndrome, are linked with an upregulation of IFN and type I IFN–stimulated genes, including sialic acid–binding Ig-like lectin 1 (Si
Autor:
Jill P. Buyon, Robert R. Clancy, Miroslav Blumenberg, Tanisha Jackson, Androo J. Markham, Sara E. Rasmussen
Publikováno v:
American journal of physiology. Heart and circulatory physiology. 313(3)
The signature lesion of SSA/Ro autoantibody-associated congenital heart block (CHB) is fibrosis and a macrophage infiltrate, supporting an experimental focus on cues influencing the fibroblast component. The transcriptomes of human fetal cardiac fibr
Autor:
Robert R. Clancy, Timothy Cardozo, Sara E. Rasmussen, Jane E. Salmon, Wilnelly Martinez-Ortiz, Androo J. Markham, Jill P. Buyon
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Only 2% of mothers positive for anti‐ SSA /Ro (Ro) antibodies have children with congenital heart block ( CHB ). This study aimed to determine whether reactivity with p305, an epitope within the α 1G T‐type calcium channel, confers ad