Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 1 |
2021 | 2 |
2022 | 1 |
2023 | 1 |
2024 | 1 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Striated preferentially expressed gene deficiency leads to mitochondrial dysfunction in developing cardiomyocytes.
Basic Res Cardiol. 2024 Feb;119(1):151-168. doi: 10.1007/s00395-023-01029-7. Epub 2023 Dec 26.
Basic Res Cardiol. 2024.
PMID: 38145999
Free PMC article.
CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.
Bray D, Hook H, Zhao R, Keenan JL, Penvose A, Osayame Y, Mohaghegh N, Chen X, Parameswaran S, Kottyan LC, Weirauch MT, Siggers T.
Bray D, et al. Among authors: zhao r.
Cell Genom. 2022 Feb 9;2(2):100098. doi: 10.1016/j.xgen.2022.100098.
Cell Genom. 2022.
PMID: 35252945
Free PMC article.
Item in Clipboard
High-Throughput Analysis of the Cell and DNA Site-Specific Binding of Native NF-κB Dimers Using Nuclear Extract Protein-Binding Microarrays (NextPBMs).
Hook H, Zhao RW, Bray D, Keenan JL, Siggers T.
Hook H, et al. Among authors: zhao rw.
Methods Mol Biol. 2021;2366:43-66. doi: 10.1007/978-1-0716-1669-7_4.
Methods Mol Biol. 2021.
PMID: 34236632
Item in Clipboard
Decision-Making and Relationship Competence When Reporting Suspected Physical Abuse and Child Neglect: An Objective Structured Clinical Evaluation.
Tufford L, Lee B, Bogo M, Wenghofer E, Etherington C, Thieu V, Zhao R.
Tufford L, et al. Among authors: zhao r.
Clin Soc Work J. 2021;49(2):256-270. doi: 10.1007/s10615-020-00785-6. Epub 2021 Feb 6.
Clin Soc Work J. 2021.
PMID: 33583967
Free PMC article.
Item in Clipboard
Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome.
Blackburn PR, Xu Z, Tumelty KE, Zhao RW, Monis WJ, Harris KG, Gass JM, Cousin MA, Boczek NJ, Mitkov MV, Cappel MA, Francomano CA, Parisi JE, Klee EW, Faqeih E, Alkuraya FS, Layne MD, McDonnell NB, Atwal PS.
Blackburn PR, et al. Among authors: zhao rw.
Am J Hum Genet. 2018 Apr 5;102(4):696-705. doi: 10.1016/j.ajhg.2018.02.018. Epub 2018 Mar 29.
Am J Hum Genet. 2018.
PMID: 29606302
Free PMC article.
Item in Clipboard
Cite
Cite