O'Kelly I[au] - Search Results

Year	Number of Results
1998	1
1999	2
2000	2
2001	3
2002	2
2003	2
2004	1
2005	2
2006	2
2007	1
2008	1
2011	1
2012	1
2013	3
2014	2
2015	3
2016	2
2017	1
2018	1
2019	1
2020	2
2021	1

1

Tebentafusp, A TCR/Anti-CD3 Bispecific Fusion Protein Targeting gp100, Potently Activated Antitumor Immune Responses in Patients with Metastatic Melanoma.

Middleton MR, McAlpine C, Woodcock VK, Corrie P, Infante JR, Steven NM, Evans TRJ, Anthoney A, Shoushtari AN, Hamid O, Gupta A, Vardeu A, Leach E, Naidoo R, Stanhope S, Lewis S, Hurst J, O'Kelly I, Sznol M. Middleton MR, et al. Among authors: o kelly i. Clin Cancer Res. 2020 Nov 15;26(22):5869-5878. doi: 10.1158/1078-0432.CCR-20-1247. Epub 2020 Aug 18. Clin Cancer Res. 2020. PMID: 32816891 Free article.

2

Ursodeoxycholic acid inhibits uptake and vasoconstrictor effects of taurocholate in human placenta.

Lofthouse EM, Torrens C, Manousopoulou A, Nahar M, Cleal JK, O'Kelly IM, Sengers BG, Garbis SD, Lewis RM. Lofthouse EM, et al. Among authors: o kelly im. FASEB J. 2019 Jul;33(7):8211-8220. doi: 10.1096/fj.201900015RR. Epub 2019 Mar 28. FASEB J. 2019. PMID: 30922127 Free PMC article.

3

A 5' UTR GGN repeat controls localisation and translation of a potassium leak channel mRNA through G-quadruplex formation.

Maltby CJ, Schofield JPR, Houghton SD, O'Kelly I, Vargas-Caballero M, Deinhardt K, Coldwell MJ. Maltby CJ, et al. Among authors: o kelly i. Nucleic Acids Res. 2020 Sep 25;48(17):9822-9839. doi: 10.1093/nar/gkaa699. Nucleic Acids Res. 2020. PMID: 32870280 Free PMC article.

4

Endocytosis as a mode to regulate functional expression of two-pore domain potassium (K₂p) channels.

O'Kelly I. O'Kelly I. Pflugers Arch. 2015 May;467(5):1133-42. doi: 10.1007/s00424-014-1641-9. Epub 2014 Nov 22. Pflugers Arch. 2015. PMID: 25413469 Free PMC article. Review.

5

Estrone sulphate uptake by the microvillous membrane of placental syncytiotrophoblast is coupled to glutamate efflux.

Lofthouse EM, Cleal JK, O'Kelly IM, Sengers BG, Lewis RM. Lofthouse EM, et al. Among authors: o kelly im. Biochem Biophys Res Commun. 2018 Nov 17;506(1):237-242. doi: 10.1016/j.bbrc.2018.10.074. Epub 2018 Oct 19. Biochem Biophys Res Commun. 2018. PMID: 30343886 Free PMC article.

6

Airway chemotransduction: from oxygen sensor to cellular effector.

Kemp PJ, Lewis A, Hartness ME, Searle GJ, Miller P, O'Kelly I, Peers C. Kemp PJ, et al. Among authors: o kelly i. Am J Respir Crit Care Med. 2002 Dec 15;166(12 Pt 2):S17-24. doi: 10.1164/rccm.2206009. Am J Respir Crit Care Med. 2002. PMID: 12471084 Review.

7

Potassium leak channels and the KCNK family of two-P-domain subunits.

Goldstein SA, Bockenhauer D, O'Kelly I, Zilberberg N. Goldstein SA, et al. Among authors: o kelly i. Nat Rev Neurosci. 2001 Mar;2(3):175-84. doi: 10.1038/35058574. Nat Rev Neurosci. 2001. PMID: 11256078 Free article. Review.

8

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LCA, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'Lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, FitzPatrick DR; UK10K Consortium, Wilson DI, Mital S, Hurles ME. Al Turki S, et al. Among authors: o kelly im. Am J Hum Genet. 2016 Mar 3;98(3):592. doi: 10.1016/j.ajhg.2016.02.016. Epub 2016 Mar 3. Am J Hum Genet. 2016. PMID: 28863274 Free PMC article. No abstract available.

9

Rare variants in NR2F2 cause congenital heart defects in humans.

Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LC, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Low J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, Fitzpatrick DF; UK10K Consortium, Wilson DI, Mital S, Hurles ME. Al Turki S, et al. Among authors: o kelly im. Am J Hum Genet. 2014 Apr 3;94(4):574-85. doi: 10.1016/j.ajhg.2014.03.007. Am J Hum Genet. 2014. PMID: 24702954 Free PMC article.

10

AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis.

Andreoletti G, Seaby EG, Dewing JM, O'Kelly I, Lachlan K, Gilbert RD, Ennis S. Andreoletti G, et al. Among authors: o kelly i. J Med Genet. 2017 Apr;54(4):269-277. doi: 10.1136/jmedgenet-2016-104100. Epub 2016 Nov 3. J Med Genet. 2017. PMID: 27811305 Free PMC article.

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