Thomas HB - Search Results

1

Bi-allelic FRA10AC1 variants in a multisystem human syndrome.

Banka S, Shalev S, Park SM, Wood KA, Thomas HB, Wright HL, Alyahya M, Bankier S, Alimi O, Chervinsky E, Zeef LAH, O'Keefe RT. Banka S, et al. Among authors: thomas hb. Brain. 2022 Oct 21;145(10):e86-e89. doi: 10.1093/brain/awac262. Brain. 2022. PMID: 35871492 No abstract available.

2

RNA-seq reveals activation of both common and cytokine-specific pathways following neutrophil priming.

Wright HL, Thomas HB, Moots RJ, Edwards SW. Wright HL, et al. Among authors: thomas hb. PLoS One. 2013;8(3):e58598. doi: 10.1371/journal.pone.0058598. Epub 2013 Mar 6. PLoS One. 2013. PMID: 23554905 Free PMC article. Clinical Trial.

3

Interferon gene expression signature in rheumatoid arthritis neutrophils correlates with a good response to TNFi therapy.

Wright HL, Thomas HB, Moots RJ, Edwards SW. Wright HL, et al. Among authors: thomas hb. Rheumatology (Oxford). 2015 Jan;54(1):188-93. doi: 10.1093/rheumatology/keu299. Epub 2014 Aug 13. Rheumatology (Oxford). 2015. PMID: 25125592

4

A lack of confirmation with alternative assays questions the validity of IL-17A expression in human neutrophils using immunohistochemistry.

Tamarozzi F, Wright HL, Thomas HB, Edwards SW, Taylor MJ. Tamarozzi F, et al. Among authors: thomas hb. Immunol Lett. 2014 Dec;162(2 Pt B):194-8. doi: 10.1016/j.imlet.2014.10.025. Epub 2014 Oct 28. Immunol Lett. 2014. PMID: 25445614 Free article. Clinical Trial.

5

Whose Gene Is It Anyway? The Effect of Preparation Purity on Neutrophil Transcriptome Studies.

Thomas HB, Moots RJ, Edwards SW, Wright HL. Thomas HB, et al. PLoS One. 2015 Sep 24;10(9):e0138982. doi: 10.1371/journal.pone.0138982. eCollection 2015. PLoS One. 2015. PMID: 26401909 Free PMC article.

6

Disease modeling of core pre-mRNA splicing factor haploinsufficiency.

Wood KA, Rowlands CF, Qureshi WMS, Thomas HB, Buczek WA, Briggs TA, Hubbard SJ, Hentges KE, Newman WG, O'Keefe RT. Wood KA, et al. Among authors: thomas hb. Hum Mol Genet. 2019 Nov 15;28(22):3704-3723. doi: 10.1093/hmg/ddz169. Hum Mol Genet. 2019. PMID: 31304552 Free PMC article.

7

A homozygous missense variant in CHRM3 associated with familial urinary bladder disease.

Beaman GM, Galatà G, Teik KW, Urquhart JE, Aishah A, O'Sullivan J, Bhaskar SS, Wood KA, Thomas HB, O'Keefe RT, Woolf AS, Stuart HM, Newman WG. Beaman GM, et al. Among authors: thomas hb. Clin Genet. 2019 Dec;96(6):515-520. doi: 10.1111/cge.13631. Epub 2019 Sep 11. Clin Genet. 2019. PMID: 31441039 Free PMC article.

8

Advanced Methods for the Analysis of Altered Pre-mRNA Splicing in Yeast and Disease.

Thomas HB, O'Keefe RT. Thomas HB, et al. Methods Mol Biol. 2019;2049:131-140. doi: 10.1007/978-1-4939-9736-7_8. Methods Mol Biol. 2019. PMID: 31602609

9

EFTUD2 missense variants disrupt protein function and splicing in mandibulofacial dysostosis Guion-Almeida type.

Thomas HB, Wood KA, Buczek WA, Gordon CT, Pingault V, Attié-Bitach T, Hentges KE, Varghese VC, Amiel J, Newman WG, O'Keefe RT. Thomas HB, et al. Hum Mutat. 2020 Aug;41(8):1372-1382. doi: 10.1002/humu.24027. Epub 2020 May 3. Hum Mutat. 2020. PMID: 32333448

10

Modelling the developmental spliceosomal craniofacial disorder Burn-McKeown syndrome using induced pluripotent stem cells.

Wood KA, Rowlands CF, Thomas HB, Woods S, O'Flaherty J, Douzgou S, Kimber SJ, Newman WG, O'Keefe RT. Wood KA, et al. Among authors: thomas hb. PLoS One. 2020 Jul 31;15(7):e0233582. doi: 10.1371/journal.pone.0233582. eCollection 2020. PLoS One. 2020. PMID: 32735620 Free PMC article.

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