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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 1
2012 2
2013 2
2014 1
2015 3
2016 4
2017 1
2018 3
2019 2
2020 4
2021 5
2022 4
2023 5
2024 0

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35 results

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Page 1
Pancytopenia and thrombosis defects in zebrafish mutants of Fanconi anemia genes.
Raman R, Ramanagoudr-Bhojappa R, Dhinoja S, Ramaswami M, Carrington B, Jagadeeswaran P, Chandrasekharappa SC. Raman R, et al. Among authors: carrington b. Blood Cells Mol Dis. 2022 Mar;93:102640. doi: 10.1016/j.bcmd.2021.102640. Epub 2021 Dec 29. Blood Cells Mol Dis. 2022. PMID: 34991062 Free PMC article.
Compound heterozygous KCTD7 variants in progressive myoclonus epilepsy.
Burke EA, Sturgeon M, Zastrow DB, Fernandez L, Prybol C, Marwaha S, Frothingham EP, Ward PA, Eng CM, Fresard L, Montgomery SB, Enns GM, Fisher PG, Wolfe LA, Harding B, Carrington B, Bishop K, Sood R, Huang Y, Elkahloun A, Toro C, Bassuk AG, Wheeler MT, Markello TC, Gahl WA, Malicdan MCV. Burke EA, et al. Among authors: carrington b. J Neurogenet. 2021 Mar-Jun;35(2):74-83. doi: 10.1080/01677063.2021.1892095. Epub 2021 May 10. J Neurogenet. 2021. PMID: 33970744
CRISPRz: a database of zebrafish validated sgRNAs.
Varshney GK, Zhang S, Pei W, Adomako-Ankomah A, Fohtung J, Schaffer K, Carrington B, Maskeri A, Slevin C, Wolfsberg T, Ledin J, Sood R, Burgess SM. Varshney GK, et al. Among authors: carrington b. Nucleic Acids Res. 2016 Jan 4;44(D1):D822-6. doi: 10.1093/nar/gkv998. Epub 2015 Oct 4. Nucleic Acids Res. 2016. PMID: 26438539 Free PMC article.
Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development.
Bresciani E, Carrington B, Yu K, Kim EM, Zhen T, Guzman VS, Broadbridge E, Bishop K, Kirby M, Harper U, Wincovitch S, Dell'Orso S, Sartorelli V, Sood R, Liu P. Bresciani E, et al. Among authors: carrington b. Blood Adv. 2021 Dec 14;5(23):4949-4962. doi: 10.1182/bloodadvances.2020003969. Blood Adv. 2021. PMID: 34492681 Free PMC article.
A novel de novo TP63 mutation in whole-exome sequencing of a Syrian family with Oral cleft and ectrodactyly.
Simpson CL, Kimble DC, Chandrasekharappa SC; NISC Comparative Sequencing Program; Alqosayer K, Holzinger E, Carrington B, McElderry J, Sood R, Al-Souqi G, Albacha-Hejazi H, Bailey-Wilson JE. Simpson CL, et al. Among authors: carrington b. Mol Genet Genomic Med. 2023 Aug;11(8):e2179. doi: 10.1002/mgg3.2179. Epub 2023 Apr 18. Mol Genet Genomic Med. 2023. PMID: 37070724 Free PMC article.
35 results