Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Valerie K. Salato"'
Autor:
Sujith Rajan, Paula E. North, Wenquan Hu, Joyce Bischoff, Zhi Fang, Suresh Kumar, Qing R Miao, Zhong Liu, M. Mahmood Hussain, Valerie K. Salato
Publikováno v:
JCI Insight, Vol 6, Iss 3 (2021)
JCI Insight
JCI Insight
Infantile hemangioma is a vascular tumor characterized by the rapid growth of disorganized blood vessels followed by slow spontaneous involution. The underlying molecular mechanisms that regulate hemangioma proliferation and involution still are not
Autor:
Natalya S. Zinkevich, Paula E. North, Matthew J. Durand, Michael Riedel, Valerie K. Salato, David D. Gutterman, Charles F. Reuben, Victoria Nasci, John B. Hijjawi, Andreas M. Beyer
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 36:1254-1262
Objective— This study examined vascular actions of angiotensin 1–7 (ANG 1–7) in human atrial and adipose arterioles. Approach and Results— The endothelium-derived hyperpolarizing factor of flow-mediated dilation (FMD) switches from antiprolif
Autor:
Jing Ma, Valerie K. Salato, Juan M. Pascual, Nam X. Nguyen, Anastasia Sacharidou, Marcel Mettlen, Richard C. Wang, Eunice E. Lee, Wentao Mi, Youxing Jiang, Philip W. Shaul, Paula E. North
Publikováno v:
Molecular Cell. 58(5):845-853
Protein kinase C has been implicated in the phosphorylation of the erythrocyte/brain glucose transporter, GLUT1, without a clear understanding of the site(s) of phosphorylation and the possible effects on glucose transport. Through in vitro kinase as
Autor:
Paula E. North, Patricia E. Burrows, Philip E. Lapinski, Philip D. King, Valerie K. Salato, Abbas Doosti
Capillary malformation-arteriovenous malformation (CM-AVM) is an autosomal dominant vascular disorder that is associated with inherited inactivating mutations of the RASA1 gene in the majority of cases. Characteristically, patients exhibit one or mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6d4a06b3b1e21ed9f1b5f61ef08a049
https://europepmc.org/articles/PMC5766414/
https://europepmc.org/articles/PMC5766414/
Publikováno v:
RNA Biology. 7:179-190
The discovery of increasing numbers of genes with overlapping sequences highlights the problem of expression in the context of constraining regulatory elements from more than one gene. This study identifies regulatory sequences encompassed within two
Autor:
Kim B. Yancey, Christoph M. Lanschuetzer, Marleen M. Janson, Janet A. Fairley, Zelmira Lazarova, Valerie K. Salato
Publikováno v:
Journal of the American Academy of Dermatology. 58:951-958
Background Antiepiligrin cicatricial pemphigoid is a mucosal-predominant subepidermal blistering disease associated with an increased relative risk of cancer. In contrast to prior reports showing that anti-laminin (L)-332 autoantibodies are a reliabl
Autor:
Zhong Liu, Mary L. Holtz, Paula E. North, Ujala Rana, Hartmut Weiler, Magdalena Chrzanowska-Wodnicka, Sara Szabo, Michelle Bordas, Qing Robert Miao, Ravindra P. Misra, Valerie K. Salato, Stephanie M. Cossette, Baofeng Zhao, Jamie Foeckler, Wenquan Hu, Ramani Ramchandran, Suresh Kumar
Publikováno v:
Developmental biology. 410(2)
Nogo-B receptor (NgBR) was identified as a receptor specific for Nogo-B. Our previous work has shown that Nogo-B and its receptor (NgBR) are essential for chemotaxis and morphogenesis of endothelial cells in vitro and intersomitic vessel formation vi
Publikováno v:
Clinical Immunology. 116:54-64
Pemphigus vulgaris (PV) is an acquired immunobullous disorder. At the early stage of the disease (mucosal PV), patients display only autoimmunity to desmoglein (Dsg) 3 and develop mucosal blisters; while at the later stage of the disease (mucocutaneo