Zobrazeno 1 - 10
of 358
pro vyhledávání: '"BRADLEY A. YODER"'
Autor:
Mehtab K. Sekhon, Bradley A. Yoder
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-7 (2018)
Abstract Background Necrotizing enterocolitis (NEC) is a serious complication of prematurity. Our objective was to evaluate the impact of an umbilical cord milking protocol (UCM) and pasteurized donor human milk (PDHM) on NEC rates in infants less th
Externí odkaz:
https://doaj.org/article/e6a28ef66f14409996d250fb31bd1786
Publikováno v:
American Journal of Perinatology Reports, Vol 06, Iss 01, Pp e148-e154 (2016)
Abstract Objective This study aims to examine the relationship between antenatal magnesium sulfate (MgSO4) and neonatal death and/or severe necrotizing enterocolitis (NEC) among infants
Externí odkaz:
https://doaj.org/article/a000dc9eff744d9fa07cde37e597a83f
Autor:
Elizabeth J. Wilk, Timothy C. Howton, Jennifer L. Fisher, Vishal H. Oza, Ryan T. Brownlee, Kasi C. McPherson, Hannah L. Cleary, Bradley K. Yoder, James F. George, Michal Mrug, Brittany N. Lasseigne
Publikováno v:
Molecular Medicine, Vol 29, Iss 1, Pp 1-21 (2023)
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is one of the most prevalent monogenic human diseases. It is mostly caused by pathogenic variants in PKD1 or PKD2 genes that encode interacting transmembrane proteins polycystin
Externí odkaz:
https://doaj.org/article/a29d831d0f624c96a1f2239ed4a5233e
Autor:
Zhang Li, Kurt A. Zimmerman, Sreelakshmi Cherakara, Phillip H. Chumley, James F. Collawn, Jun Wang, Courtney J. Haycraft, Cheng J. Song, Teresa Chacana, Reagan S. Andersen, Mandy J. Croyle, Ernald J. Aloria, Raksha P. Hombal, Isis N. Thomas, Hanan Chweih, Kristin L. Simanyi, James F. George, John M. Parant, Michal Mrug, Bradley K. Yoder
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 1 (2023)
Externí odkaz:
https://doaj.org/article/d33111929bb3477fae3f2ddadac69a61
Autor:
Jun Wang, Holly R. Thomas, Robert G. Thompson, Stephanie C. Waldrep, Joseph Fogerty, Ping Song, Zhang Li, Yongjie Ma, Peu Santra, Jonathan D. Hoover, Nan Cher Yeo, Iain A. Drummond, Bradley K. Yoder, Jeffrey D. Amack, Brian Perkins, John M. Parant
Publikováno v:
Disease Models & Mechanisms, Vol 15, Iss 12 (2022)
Externí odkaz:
https://doaj.org/article/5728cfeb2b524af68015cb523dbf9266
Autor:
Matthew D. Cheung, Elise N. Erman, Kyle H. Moore, Jeremie M.P. Lever, Zhang Li, Jennifer R. LaFontaine, Gelare Ghajar-Rahimi, Shanrun Liu, Zhengqin Yang, Rafay Karim, Bradley K. Yoder, Anupam Agarwal, James F. George
Publikováno v:
JCI Insight, Vol 7, Iss 20 (2022)
The kidney contains a population of resident macrophages from birth that expands as it grows and forms a contiguous network throughout the tissue. Kidney-resident macrophages (KRMs) are important in homeostasis and the response to acute kidney injury
Externí odkaz:
https://doaj.org/article/b97df05f74f3447c9bc4cd10ffa3410d
Autor:
Mary Claire Doss, Sean Mullen, Ronald Roye, Juling Zhou, Phillip Chumley, Elias Mrug, Darren P. Wallace, Feng Qian, Peter C. Harris, Bradley K. Yoder, Harrison Kim, Michal Mrug
Publikováno v:
American Journal of Physiology-Renal Physiology. 324:F423-F430
Total kidney volume (TKV) is a valuable readout in preclinical studies for autosomal dominant and autosomal recessive polycystic kidney diseases (ADPKD and ARPKD). Since conventional TKV assessment by manual contouring of kidney areas in all images i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbb4aca665b03f77422297186a9e127f
https://doi.org/10.1152/ajprenal.00295.2022
https://doi.org/10.1152/ajprenal.00295.2022
Autor:
Ariel Tarrell, Matthew Grinsell, Mary Murray, Kimberlee Weaver Lewis, Bradley A. Yoder, Sabrina Malone Jenkins
Publikováno v:
Journal of Perinatology. 43:642-646
The gold standard for diagnosing metabolic bone disease in pediatrics is dual-energy x-ray absorptiometry (DXA). Bone quantitative ultrasound (QUS) has increasing applications. This study compared the relationship of DXA to QUS in preterm infants.Pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be045de6d8e3550332548572c341f65d
https://doi.org/10.1038/s41372-022-01588-y
https://doi.org/10.1038/s41372-022-01588-y
Autor:
Cheng J. Song, Zhang Li, Ummey Khalecha Bintha Ahmed, Sarah J. Bland, Alex Yashchenko, Shanrun Liu, Ernald J. Aloria, Jeremie M. Lever, Nancy M. Gonzalez, Marisa A. Bickel, Cory B. Giles, Constantin Georgescu, Jonathan D. Wren, Mark L. Lang, Etty N. Benveniste, Laurie E. Harrington, Leo Tsiokas, James F. George, Kenneth L. Jones, David K. Crossman, Anupam Agarwal, Michal Mrug, Bradley K. Yoder, Katharina Hopp, Kurt A. Zimmerman
Publikováno v:
J Am Soc Nephrol
BACKGROUND: Inducible disruption of cilia-related genes in adult mice results in slowly progressive cystic disease, which can be greatly accelerated by renal injury. METHODS: To identify in an unbiased manner modifier cells that may be influencing th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b68546a95ed560353a481fa4245dbfd
https://doi.org/10.1681/asn.2021030278
https://doi.org/10.1681/asn.2021030278
Autor:
Michal Mrug, Cheng Jack Song, Bradley K. Yoder, Sarah J. Bland, Zhang Li, Alex Yashchenko, Kurt A. Zimmerman, David K. Crossman, Juling Zhou, Ernald Jules G. Aloria
Publikováno v:
Lab Invest
Hepatorenal fibrocystic disease (HRFCD) is a genetically inherited disorder related to primary cilia dysfunction in which patients display varying levels of fibrosis, bile duct expansion, and inflammation. In mouse models of HRFCD, the phenotype is g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79e204a107cde0ea82b86c45c338cf69
https://doi.org/10.1038/s41374-021-00627-0
https://doi.org/10.1038/s41374-021-00627-0