Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alex Yashchenko"'
Autor:
Alex Yashchenko, Sarah J. Bland, Cheng J. Song, Ummey Khalecha Bintha Ahmed, Rachel Sharp, Isabella G. Darby, Audrey M. Cordova, Morgan E. Smith, Jeremie M. Lever, Zhang Li, Ernald J. Aloria, Shuja Khan, Bibi Maryam, Shanrun Liu, Michael R. Crowley, Kenneth L. Jones, Lauren A. Zenewicz, James F. George, Michal Mrug, David K. Crossman, Katharina Hopp, Stavros Stavrakis, Mary B. Humphrey, Florent Ginhoux, Kurt A. Zimmerman
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Kidney macrophages are comprised of both monocyte-derived and tissue resident populations; however, the heterogeneity of kidney macrophages and factors that regulate their heterogeneity are poorly understood. Herein, we performed single cell RNA sequ
Externí odkaz:
https://doaj.org/article/33bd5d09e8bc4889bac131cdfd30c35a
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
Autor:
Ramaswamy K. Iyer, Stauffer Daniel, Alex Yashchenko, Robin Baker, Aaron Black, Amber D. Gaither, Alina Khromykh, Dale L. Bodian, Elisabeth Klein, Rajiv Baveja, Benjamin D. Solomon, John E. Niederhuber, Greg Eley, Joseph G. Vockley, Irina Remsburg, Radhika Hastak, Kathi Huddleston
Publikováno v:
Pediatrics. 137:492A-492A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24aec4fc8bb5c85ea4ba798fd862fdbf
https://doi.org/10.1542/peds.137.supplement_3.492a
https://doi.org/10.1542/peds.137.supplement_3.492a