Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Meredith J Ventura"'
Publikováno v:
Lupus. 31:1163-1174
Objectives We conducted a systematic review with metanalysis to investigate the utility of erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and procalcitonin (PCT) in diagnosing infections in hospitalized patients with SLE. Methods We
Autor:
Kelly M. Gawron, Marcus J. Miller, Adam D. Kennedy, V. Reid Sutton, Mousumi Bose, William B. Rizzo, Ann B. Moser, Qin Sun, Richard Jones, Leroy Hubert, Meredith J. Ventura, Nancy Braverman, Taraka R. Donti, Sarah H. Elsea, Michael F. Wangler
Publikováno v:
Genet Med
PURPOSE: Peroxisome biogenesis disorders–Zellweger spectrum disorders (PBD-ZSD) are metabolic diseases with multisystem manifestations. Individuals with PBD-ZSD exhibit impaired peroxisomal biochemical functions and have abnormal levels of peroxiso
Autor:
Wendell A. Fleming, Kim L. Gonzalez, Jaeseok Park, Meredith J. Ventura, Mauro A. Rinaldi, Ashish B. Patel, Bonnie Bartel
Publikováno v:
Plant Physiology. 174:2231-2247
A variety of metabolic pathways are sequestered in peroxisomes, conserved organelles that are essential for human and plant survival. Peroxin (PEX) proteins generate and maintain peroxisomes. The PEX1 ATPase facilitates recycling of the peroxisome ma
Autor:
Lori S. Sullivan, Ann B. Moser, Rui Chen, Richard Jones, Meredith J. Ventura, Michael F. Wangler, Mingchu Xu, Annette E. Whitney, Sara J. Bowne, Stephen P. Daiger, Dianna K H Wheaton, David G. Birch
Publikováno v:
Molecular Genetics and Metabolism Reports
Peroxisomal biogenesis disorders (PBD) are caused by mutations in PEX genes, and are typically diagnosed with biochemical testing in plasma followed by confirmatory testing. Here we report the unusual diagnostic path of a child homozygous for PEX1 p.
Publikováno v:
Plant Physiology. 172:1643-1656
Most eukaryotic cells require peroxisomes, organelles housing fatty acid β-oxidation and other critical metabolic reactions. Peroxisomal matrix proteins carry peroxisome-targeting signals that are recognized by one of two receptors, PEX5 or PEX7, in
Autor:
Andrew R. DiNardo, Kalpana Bhairavarasu, Emmanuel Guajardo, Robert L. Atmar, Riyad Y. Kherallah, Xunyan Ye, Eva H. Clark, Meredith J. Ventura, Sandeep K. Agarwal, Pedro A. Piedra
Publikováno v:
Annals of the Rheumatic Diseases
We read with great interest the article by Pouletty et al reporting 16 paediatric patients presenting with Kawa-COVID-19, an inflammatory syndrome similar to Kawasaki disease (KD) associated with SARS-CoV-2 infection.1 All 16 patients met criteria fo