Zobrazeno 1 - 10
of 149
pro vyhledávání: '"Dejian, Zhao"'
Transcriptomic identification of genes expressed in invasive S. aureus diabetic foot ulcer infection
Autor:
Taiwo Samuel Agidigbi, Hyuk-Kwon Kwon, James R. Knight, Dejian Zhao, Francis Y. Lee, Irvin Oh
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 13 (2023)
IntroductionInfection in diabetic foot ulcers (DFUs) is one of the major complications associated with patients with diabetes. Staphylococcus aureus is the most common offending pathogen in patients with infected DFU. Previous studies have suggested
Externí odkaz:
https://doaj.org/article/1d0790a8ddcd40daa84e487e567c4597
Autor:
Hellen Weinschutz Mendes, Uma Neelakantan, Yunqing Liu, Sarah E. Fitzpatrick, Tianying Chen, Weimiao Wu, April Pruitt, David S. Jin, Priyanka Jamadagni, Marina Carlson, Cheryl M. Lacadie, Kristen D. Enriquez, Ningshan Li, Dejian Zhao, Sundas Ijaz, Catalina Sakai, Christina Szi, Brendan Rooney, Marcus Ghosh, Ijeoma Nwabudike, Andrea Gorodezky, Sumedha Chowdhury, Meeraal Zaheer, Sarah McLaughlin, Joseph M. Fernandez, Jia Wu, Jeffrey A. Eilbott, Brent Vander Wyk, Jason Rihel, Xenophon Papademetris, Zuoheng Wang, Ellen J. Hoffman
Publikováno v:
Cell Reports, Vol 42, Iss 3, Pp 112243- (2023)
Summary: Advancing from gene discovery in autism spectrum disorders (ASDs) to the identification of biologically relevant mechanisms remains a central challenge. Here, we perform parallel in vivo functional analysis of 10 ASD genes at the behavioral,
Externí odkaz:
https://doaj.org/article/7996517e63554f8b8dc40a353d5ba4fb
Autor:
Guillermo I. Drelichman, Nicolas Fernández Escobar, Barbara C. Soberon, Nora F. Basack, Joaquin Frabasil, Andrea B. Schenone, Gabriel Aguilar, Maria S. Larroudé, James R. Knight, Dejian Zhao, Jiapeng Ruan, Pramod K. Mistry
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss , Pp 100820- (2021)
Gaucher disease is renowned for extreme phenotypic diversity that does not show consistent genotype/phenotype correlations. In Argentina, a national collaborative group, Grupo Argentino de Diagnóstico y Tratamiento de la Enfermedad de Gaucher, GADTE
Externí odkaz:
https://doaj.org/article/98b4f2892f6c4590959c830cdc82cef0
Autor:
Wei Zheng, Dejian Zhao, Hui Zhang, Prameladevi Chinnasamy, Nicholas Sibinga, Jeffrey W. Pollard
Publikováno v:
Wellcome Open Research, Vol 6 (2021)
Background: Metastatic breast cancer cells recruit macrophages (metastasis-associated macrophages, or MAMs) to facilitate their seeding, survival and outgrowth. However, a comprehensive understanding of the gene expression program in MAMs and how thi
Externí odkaz:
https://doaj.org/article/83a6b7fec207418181a2ef9007ecd23b
Autor:
Dejian Zhao, Deyou Zheng
Publikováno v:
BMC Bioinformatics, Vol 19, Iss 1, Pp 1-13 (2018)
Abstract Background Noises and artifacts may arise in several steps of the next-generation sequencing (NGS) process. Recently, an NGS library preparation method called SMART, or Switching Mechanism At the 5′ end of the RNA Transcript, is introduced
Externí odkaz:
https://doaj.org/article/44b1585116074d499ab93ab203739bc4
Autor:
Wei Zheng, Dejian Zhao, Hui Zhang, Prameladevi Chinnasamy, Nicholas Sibinga, Jeffrey W. Pollard
Publikováno v:
Wellcome Open Research, Vol 6 (2021)
Background: Metastatic breast cancer cells recruit macrophages (metastasis-associated macrophages, or MAMs) to facilitate their seeding, survival and outgrowth. However, a comprehensive understanding of the gene expression program in MAMs and how thi
Externí odkaz:
https://doaj.org/article/c1e2bf6bdfac4ca6826641018bf785c6
Autor:
Nagarjuna R, Cheemarla, Amelia, Hanron, Joseph R, Fauver, Jason, Bishai, Timothy A, Watkins, Anderson F, Brito, Dejian, Zhao, Tara, Alpert, Chantal B F, Vogels, Albert I, Ko, Wade L, Schulz, Marie L, Landry, Nathan D, Grubaugh, David, van Dijk, Ellen F, Foxman
Publikováno v:
The Lancet Microbe. 4:e38-e46
Symptomatic patients who test negative for common viruses are an important possible source of unrecognised or emerging pathogens, but metagenomic sequencing of all samples is inefficient because of the low likelihood of finding a pathogen in any give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25bd778901287c9134316290fed323a5
https://doi.org/10.1016/s2666-5247(22)00296-8
https://doi.org/10.1016/s2666-5247(22)00296-8
Autor:
Hengfei Qin, Ruihong Jian, Jirong Bai, Jianghong Tang, Yue Zhou, Binglong Zhu, Dejian Zhao, Zhijiang Ni, Liangbiao Wang, Weiqiao Liu, Quanfa Zhou, Xi Li
Publikováno v:
ACS Omega, Vol 3, Iss 1, Pp 1350-1356 (2018)
Externí odkaz:
https://doaj.org/article/8e0f65a23e614e5e93d686949ce2e716
Publikováno v:
BMC Genomics, Vol 18, Iss 1, Pp 1-18 (2017)
Abstract Background Monoallelic expression of autosomal genes has been implicated in human psychiatric disorders. However, there is a paucity of allelic expression studies in human brain cells at the single cell and genome wide levels. Results In thi
Externí odkaz:
https://doaj.org/article/2d6b798741c94971adde04b51f08e045
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-12 (2017)
Abstract Background Rett syndrome (RTT) is a severe, neurodevelopmental disorder primarily affecting girls, characterized by progressive loss of cognitive, social, and motor skills after a relatively brief period of typical development. It is usually
Externí odkaz:
https://doaj.org/article/d753d06279ca414d927eadfdbf521734