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Year Number of Results
2016 1
2017 6
2018 11
2019 15
2020 2
2021 1
2024 0

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33 results

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Page 1
An essential role for the Zn2+ transporter ZIP7 in B cell development.
Anzilotti C, Swan DJ, Boisson B, Deobagkar-Lele M, Oliveira C, Chabosseau P, Engelhardt KR, Xu X, Chen R, Alvarez L, Berlinguer-Palmini R, Bull KR, Cawthorne E, Cribbs AP, Crockford TL, Dang TS, Fearn A, Fenech EJ, de Jong SJ, Lagerholm BC, Ma CS, Sims D, van den Berg B, Xu Y, Cant AJ, Kleiner G, Leahy TR, de la Morena MT, Puck JM, Shapiro RS, van der Burg M, Chapman JR, Christianson JC, Davies B, McGrath JA, Przyborski S, Santibanez Koref M, Tangye SG, Werner A, Rutter GA, Padilla-Parra S, Casanova JL, Cornall RJ, Conley ME, Hambleton S. Anzilotti C, et al. Nat Immunol. 2019 Mar;20(3):350-361. doi: 10.1038/s41590-018-0295-8. Epub 2019 Feb 4. Nat Immunol. 2019. PMID: 30718914 Free PMC article.
Sequencing of human genomes with nanopore technology.
Bowden R, Davies RW, Heger A, Pagnamenta AT, de Cesare M, Oikkonen LE, Parkes D, Freeman C, Dhalla F, Patel SY, Popitsch N, Ip CLC, Roberts HE, Salatino S, Lockstone H, Lunter G, Taylor JC, Buck D, Simpson MA, Donnelly P. Bowden R, et al. Nat Commun. 2019 Apr 23;10(1):1869. doi: 10.1038/s41467-019-09637-5. Nat Commun. 2019. PMID: 31015479 Free PMC article.
Reconstruction of the Global Neural Crest Gene Regulatory Network In Vivo.
Williams RM, Candido-Ferreira I, Repapi E, Gavriouchkina D, Senanayake U, Ling ITC, Telenius J, Taylor S, Hughes J, Sauka-Spengler T. Williams RM, et al. Dev Cell. 2019 Oct 21;51(2):255-276.e7. doi: 10.1016/j.devcel.2019.10.003. Dev Cell. 2019. PMID: 31639368 Free PMC article.
Low-Bias RNA Sequencing of the HIV-2 Genome from Blood Plasma.
James KL, de Silva TI, Brown K, Whittle H, Taylor S, McVean G, Esbjörnsson J, Rowland-Jones SL. James KL, et al. J Virol. 2018 Dec 10;93(1):e00677-18. doi: 10.1128/JVI.00677-18. Print 2019 Jan 1. J Virol. 2018. PMID: 30333167 Free PMC article.
An ontogenetic switch drives the positive and negative selection of B cells.
Xu X, Deobagkar-Lele M, Bull KR, Crockford TL, Mead AJ, Cribbs AP, Sims D, Anzilotti C, Cornall RJ. Xu X, et al. Proc Natl Acad Sci U S A. 2020 Feb 18;117(7):3718-3727. doi: 10.1073/pnas.1915247117. Epub 2020 Feb 4. Proc Natl Acad Sci U S A. 2020. PMID: 32019891 Free PMC article.
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.
Turnpenny PD, Wright MJ, Sloman M, Caswell R, van Essen AJ, Gerkes E, Pfundt R, White SM, Shaul-Lotan N, Carpenter L, Schaefer GB, Fryer A, Innes AM, Forbes KP, Chung WK, McLaughlin H, Henderson LB, Roberts AE, Heath KE, Paumard-Hernández B, Gener B; DDD study; Fawcett KA, Gjergja-Juraški R, Pilz DT, Fry AE. Turnpenny PD, et al. Am J Hum Genet. 2018 Nov 1;103(5):786-793. doi: 10.1016/j.ajhg.2018.09.012. Epub 2018 Oct 18. Am J Hum Genet. 2018. PMID: 30343942 Free PMC article.
33 results