Richard J. Gibbons - Search Results

Year	Number of Results
2003	3
2004	4
2005	5
2006	4
2007	3
2008	3
2009	4
2010	4
2011	5
2012	4
2013	4
2014	4
2015	5
2016	4
2017	3
2018	5
2019	4
2020	2
2021	2
2022	1
2023	1
2024	0

1

Induction of the alternative lengthening of telomeres pathway by trapping of proteins on DNA.

Rose AM, Goncalves T, Cunniffe S, Geiller HEB, Kent T, Shepherd S, Ratnaweera M, O'Sullivan RJ, Gibbons RJ, Clynes D. Rose AM, et al. Among authors: gibbons rj. Nucleic Acids Res. 2023 Jul 21;51(13):6509-6527. doi: 10.1093/nar/gkad150. Nucleic Acids Res. 2023. PMID: 36940725 Free PMC article.

2

The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin.

Truch J, Downes DJ, Scott C, Gür ER, Telenius JM, Repapi E, Schwessinger R, Gosden M, Brown JM, Taylor S, Cheong PL, Hughes JR, Higgs DR, Gibbons RJ. Truch J, et al. Among authors: gibbons rj. Nat Commun. 2022 Jun 17;13(1):3485. doi: 10.1038/s41467-022-31194-7. Nat Commun. 2022. PMID: 35710802 Free PMC article.

3

A gain-of-function single nucleotide variant creates a new promoter which acts as an orientation-dependent enhancer-blocker.

Bozhilov YK, Downes DJ, Telenius J, Marieke Oudelaar A, Olivier EN, Mountford JC, Hughes JR, Gibbons RJ, Higgs DR. Bozhilov YK, et al. Among authors: gibbons rj. Nat Commun. 2021 Jun 21;12(1):3806. doi: 10.1038/s41467-021-23980-6. Nat Commun. 2021. PMID: 34155213 Free PMC article.

4

Genetic and functional insights into CDA-I prevalence and pathogenesis.

Olijnik AA, Roy NBA, Scott C, Marsh JA, Brown J, Lauschke K, Ask K, Roberts N, Downes DJ, Brolih S, Johnson E, Xella B, Proven M, Hipkiss R, Ryan K, Frisk P, Mäkk J, Stattin EM, Sadasivam N, McIlwaine L, Hill QA, Renella R, Hughes JR, Gibbons RJ, Groth A, McHugh PJ, Higgs DR, Buckle VJ, Babbs C. Olijnik AA, et al. Among authors: gibbons rj. J Med Genet. 2021 Mar;58(3):185-195. doi: 10.1136/jmedgenet-2020-106880. Epub 2020 Jun 9. J Med Genet. 2021. PMID: 32518175 Free PMC article.

5

An evolutionarily ancient mechanism for regulation of hemoglobin expression in vertebrate red cells.

Miyata M, Gillemans N, Hockman D, Demmers JAA, Cheng JF, Hou J, Salminen M, Fisher CA, Taylor S, Gibbons RJ, Ganis JJ, Zon LI, Grosveld F, Mulugeta E, Sauka-Spengler T, Higgs DR, Philipsen S. Miyata M, et al. Among authors: gibbons rj. Blood. 2020 Jul 16;136(3):269-278. doi: 10.1182/blood.2020004826. Blood. 2020. PMID: 32396940 Free PMC article.

6

ATRX Contributes to MeCP2-Mediated Pericentric Heterochromatin Organization during Neural Differentiation.

Marano D, Fioriniello S, Fiorillo F, Gibbons RJ, D'Esposito M, Della Ragione F. Marano D, et al. Among authors: gibbons rj. Int J Mol Sci. 2019 Oct 29;20(21):5371. doi: 10.3390/ijms20215371. Int J Mol Sci. 2019. PMID: 31671722 Free PMC article.

7

Persistence of skewed X-chromosome inactivation in pre-B acute lymphoblastic leukemia of a female ATRX mutation carrier.

Bradley CP, Chen C, Oetjen KA, Yan C, Panjwani R, Hauffe S, Calvo KR, Yuan C, Patel PA, Montgomery ND, Foster MC, Battiwalla M, Barrett AJ, Gibbons RJ, Ito S. Bradley CP, et al. Among authors: gibbons rj. Blood Adv. 2019 Sep 10;3(17):2627-2631. doi: 10.1182/bloodadvances.2019000013. Blood Adv. 2019. PMID: 31501157 Free PMC article.

8

Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide Donors.

Moir-Meyer G, Cheong PL, Olijnik AA, Brown J, Knight S, King A, Kurita R, Nakamura Y, Gibbons RJ, Higgs DR, Buckle VJ, Babbs C. Moir-Meyer G, et al. Among authors: gibbons rj. Methods Protoc. 2018 Jul 30;1(3):28. doi: 10.3390/mps1030028. Methods Protoc. 2018. PMID: 31164570 Free PMC article.

9

The macroH2A1.2 histone variant links ATRX loss to alternative telomere lengthening.

Kim J, Sun C, Tran AD, Chin PJ, Ruiz PD, Wang K, Gibbons RJ, Gamble MJ, Liu Y, Oberdoerffer P. Kim J, et al. Among authors: gibbons rj. Nat Struct Mol Biol. 2019 Mar;26(3):213-219. doi: 10.1038/s41594-019-0192-3. Epub 2019 Mar 4. Nat Struct Mol Biol. 2019. PMID: 30833786 Free PMC article.

10

Refining the Primrose syndrome phenotype: A study of five patients with ZBTB20 de novo variants and a review of the literature.

Cleaver R, Berg J, Craft E, Foster A, Gibbons RJ, Hobson E, Lachlan K, Naik S, Sampson JR, Sharif S, Smithson S; Deciphering Developmental Disorders Study; Parker MJ, Tatton-Brown K. Cleaver R, et al. Among authors: gibbons rj. Am J Med Genet A. 2019 Mar;179(3):344-349. doi: 10.1002/ajmg.a.61024. Epub 2019 Jan 13. Am J Med Genet A. 2019. PMID: 30637921 Review.

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