Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Lisa M, Rice"'
Autor:
Lisa M. Rice, Julio C. Mantero, Eric A. Stratton, Rod Warburton, Kari Roberts, Nicholas Hill, Robert W. Simms, Robyn Domsic, Harrison W. Farber, Robert Lafyatis
Publikováno v:
Arthritis Research & Therapy, Vol 24, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/9ab18744497a46f1a0b519a10722ce0e
Autor:
Lisa M. Rice, Julio C. Mantero, Eric A. Stratton, Rod Warburton, Kari Roberts, Nicholas Hill, Robert W. Simms, Robyn Domsic, Harrison W. Farber, Robert Layfatis
Publikováno v:
Arthritis Research & Therapy, Vol 20, Iss 1, Pp 1-10 (2018)
Abstract Background Systemic sclerosis-associated pulmonary arterial hypertension (SSc-PAH) is one of the leading causes of death in SSc. Identification of a serum-based proteomic diagnostic biomarker for SSc-PAH would allow for rapid non-invasive sc
Externí odkaz:
https://doaj.org/article/c88a7f4ebc044f3e831d2bbd36eaef54
Autor:
Xue-Jun Zhao, Ai-Walid Mohsen, Stephanie Mihalik, Keaton Solo, Shakuntala Basu, Ermal Aliu, Huifang Shi, Catherine Kochersberger, Anuradha Karunanidhi, Clinton Van’t Land, Kimberly A Coughlan, Summar Siddiqui, Lisa M Rice, Shawn Hillier, Eleonora Guadagnin, Christine DeAntonis, Paloma H Giangrande, Paolo G V Martini, Jerry Vockley
Publikováno v:
Human Molecular Genetics.
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common inherited disorder of mitochondrial fatty acid β-oxidation (FAO) in humans. Patients exhibit clinical episodes often associated with fasting. Symptoms include hypoketotic hypog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04ee4ce800a0b2e58a7d5a0c14f253df
https://doi.org/10.1093/hmg/ddad076
https://doi.org/10.1093/hmg/ddad076
Autor:
Xue-Jun Zhao, AI-Walid Mohsen, Stephanie Mihalik, Keaton Solo, Ermal Aliu, Huifang Shi, Shakuntala Basu, Catherine Kochersperger, Clinton Van’t Land, Anuradha Karunanidhi, Kimberly A. Coughlan, Summar Siddiqui, Lisa M. Rice, Shawn Hillier, Eleonora Guadagnin, Paloma H. Giangrande, Paolo G.V. Martini, Jerry Vockley
Publikováno v:
Molecular genetics and metabolism. 138(1)
Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is an inborn error of long chain fatty acid β-oxidation (FAO) with limited treatment options. Patients present with heterogeneous clinical phenotypes affecting predominantly heart, liver, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::228970ae4fa01c2c912de4580f8de16f
https://pubmed.ncbi.nlm.nih.gov/36580829
https://pubmed.ncbi.nlm.nih.gov/36580829
Autor:
Sokratis A. Apostolidis, Giuseppina Stifano, Tracy Tabib, Lisa M. Rice, Christina M. Morse, Bashar Kahaleh, Robert Lafyatis
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Objective: The mechanisms that lead to endothelial cell (EC) injury and propagate the vasculopathy in Systemic Sclerosis (SSc) are not well understood. Using single cell RNA sequencing (scRNA-seq), our goal was to identify EC markers and signature pa
Externí odkaz:
https://doaj.org/article/cae8b99b309c494c887a574f013ca6ee
Autor:
Christopher Tunkey, Minjung Choi, Wei Zheng, Gilles Besin, Lisa M. Rice, Andrea Frassetto, Athanasios Dousis, Edward J. Miracco, Uma Rajarajacholan, Erik Owen, Patrick Finn, Fabienne Rajas, Eleonora Guadagnin, Kristin E. Burke, Mike Zimmer, Vincent Verzieux, Christopher Pepin, Cosmin Mihai, meredith##Wolfrom, Maud Soty, Becca Levy, Joe Sarkis, Zach Zalinger, Barbara Tran, Marine Silva, Arianna Markel, Ling Yin, Paloma H. Giangrande, Vi Nguyen, Jingsong Cao, Marjie Hard, Paolo Martini, Gilles Mithieux, Jenny Zhuo, Shi Liang, Edward Weisser, Vladimir Presnyak, Anne-Renee##Graham, Tatiana Ketova, Lei Ci
Publikováno v:
Nature Communications
Nature Communications, Nature Publishing Group, 2021, 12 (1), pp.3090. ⟨10.1038/s41467-021-23318-2⟩
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
Nature Communications, Nature Publishing Group, 2021, 12 (1), pp.3090. ⟨10.1038/s41467-021-23318-2⟩
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
Glycogen Storage Disease 1a (GSD1a) is a rare, inherited metabolic disorder caused by deficiency of glucose 6-phosphatase (G6Pase-α). G6Pase-α is critical for maintaining interprandial euglycemia. GSD1a patients exhibit life-threatening hypoglycemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fdb1236707c2ddf86e727dfcbc9b5e5
http://europepmc.org/articles/PMC8149455
http://europepmc.org/articles/PMC8149455
Autor:
Greg Nowak, Xuling Zhu, Marianne Eybye, Lisa M. Rice, Ahmad Karadagi, Andrea Frassetto, Ewa Ellis, Paolo Martini, Alex G. Cavedon, Helen Zemack, Stephen C. Strom, Rebecca A. White, Eleonora Guadagnin, Carl Jorns
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Alpha 1-antitrypsin (AAT) deficiency arises from an inherited mutation in the SERPINA1 gene. The disease causes damage in the liver where the majority of the AAT protein is produced. Lack of functioning circulating AAT protein also causes uninhibited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09833b0cee585a1db2cfbeaad7ac9403
https://doi.org/10.1038/s41598-020-64017-0
https://doi.org/10.1038/s41598-020-64017-0
Publikováno v:
Journal of Pathogens, Vol 2012 (2012)
Aims. The goal of this study was to construct a single tube molecular diagnostic multiplex assay for the detection of microbial pathogens commonly associated with septicemia, using LATE-PCR and Lights-On/Lights-Off probe technology. Methods and Resul
Externí odkaz:
https://doaj.org/article/599034d7fee847a1bceb96ca3440d49a
Autor:
Lisa M. Rice, Robert Lafyatis, David Montani, Julio C. Mantero, Guillemette Marot, Eric Hachulla, Marc Humbert, D. Launay, Jean-Luc Cracowski, Sébastien Sanges, Ly Tu, Christophe Guignabert, Camille Ternynck
Publikováno v:
La Revue de Médecine Interne. 41:A32-A33
Introduction L’objectif de ce travail est d’etudier les alterations du proteome serique des patients atteints d’hypertension arterielle pulmonaire (HTAP) associee a la clerodermie systemique (SSc), d’identifier les proteines correlees a la se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e714c3201866518ca430fd3ec5c69df8
https://doi.org/10.1016/j.revmed.2020.10.059
https://doi.org/10.1016/j.revmed.2020.10.059
Autor:
Robert W. Simms, Julio C. Mantero, Jessica Ziemek, Jessica K. Gordon, Giuseppina Stifano, Robert Lafyatis, Robyn T. Domsic, Lisa M. Rice
Publikováno v:
Journal of Investigative Dermatology. 137:62-70
In this study we systematically investigated alterations in the serum proteome of patients with diffuse cutaneous systemic sclerosis and identified differentially expressed proteins that correlated with disease severity. Our goal was to identify a co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30b3ab00c6964e81c7beb8dc9a10597f
https://doi.org/10.1016/j.jid.2016.08.027
https://doi.org/10.1016/j.jid.2016.08.027