Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Jayme D. Allen"'
Publikováno v:
Palliative Medicine Reports, Vol 2, Iss 1, Pp 93-100 (2021)
Objective: The primary objective was to evaluate the efficacy of a weekly palliative care-guided, case-based discussion of high-risk infants on Neonatal Intensive Care Unit (NICU) physician (MD) and Advanced Practice Provider (APP) perceptions of ped
Externí odkaz:
https://doaj.org/article/082f9e33cebf4d2b8d394a93396527ee
Publikováno v:
Palliative Medicine Reports
Objective: The primary objective was to evaluate the efficacy of a weekly palliative care-guided, case-based discussion of high-risk infants on Neonatal Intensive Care Unit (NICU) physician (MD) and Advanced Practice Provider (APP) perceptions of ped
Publikováno v:
Journal of Pain and Symptom Management. 57:394-395
Autor:
Acrista J Hole, Jayme D. Allen, Elizabeth Summitt, Colin M. Rogerson, Kevin Valentine, Samer Abu-Sultaneh
Publikováno v:
Critical Care Medicine. 48:609-609
Autor:
David A. Ingram, Jonathan Chernoff, D. Wade Clapp, Waylan K. Bessler, Andrew S. McDaniel, Clemens Hofmann, Zahara M. Jaffer, Elizabeth G. Michels, Jayme D. Allen, Shi Chen, Su Jung Park, Sarah J. Burgin
Publikováno v:
Blood. 112:4646-4654
Neurofibromatosis type 1 (NF1) is a common genetic disorder caused by mutations in the NF1 locus, which encodes neurofibromin, a negative regulator of Ras. Patients with NF1 develop numerous neurofibromas, which contain many inflammatory mast cells t
Autor:
Linda C. Walker, Jayme D Allen, Heather N. Yeowell, Sheau-Fung Thai, Mayra A. Overstreet, Saood Murad
Publikováno v:
Matrix Biology. 19:37-46
This study describes the relative contribution of the 10 cysteine residues in lysyl hydroxylase 1 (LH1) to enzyme activity. We have identified a novel mutation of a 15-bp deletion in exon 11 in one LH1 allele, that codes for amino acids 367-371 (DLCR
Autor:
Michael Silverman, Jayme D. Allen, Peter N. LeSouëf, Howard B. Panitch, Janet Stocks, Robert S. Tepper, Peter D. Sly, M. Henschen, MG Morris, Robert G. Castile, Monika Gappa, J. McNamara, Wayne J. Morgan
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 161:1760-1762
Autor:
Andrew S. McDaniel, Shi Chen, Waylan K. Bessler, Jeffrey B. Travers, Ethel Derr-Yellin, Su Jung Park, Sarah J. Burgin, Jayme D. Allen, Clemens Hofmann, Zahara M. Jaffer, Mary Ann Sells, Simon J. Atkinson, Elizabeth G. Michels, David A. Ingram, Jonathan Chernoff, D. Wade Clapp
Mast cells are key participants in allergic diseases via activation of high-affinity IgE receptors (FcϵRI) resulting in release of proinflammatory mediators. The biochemical pathways linking IgE activation to calcium influx and cytoskeletal changes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9be012ae42cb0ab872caa92fb35724db
https://europepmc.org/articles/PMC2661857/
https://europepmc.org/articles/PMC2661857/
Autor:
Yan Li, Shi Chen, D. Wade Clapp, Jin Yuan, Feng Chun Yang, David A. Ingram, Jayme D. Allen, Waylan K. Bessler
Publikováno v:
Blood. 108:3612-3612
Neurofibromin, the protein encoded by the NF1 tumor-suppressor gene, negatively regulates the output of p21 ras proteins by accelerating the hydrolysis of active Ras-guanosine triphosphate to inactive Ras-guanosine diphosphate. Children with neurofib
Publikováno v:
Pediatric Research. 60:490-490
Pak 1 (p21-activated kinase) is involved in the regulation of airway smooth muscle (ASM) contraction in vitro. We hypothesized that the genetic disruption of Pak1 would attenuate in vivo airway responsiveness to acetylcholine (ACh) in non-sensitized