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In-patient physiotherapy for adults on veno-venous extracorporeal membrane oxygenation - United Kingdom ECMO Physiotherapy Network: A consensus agreement for best practice.

Journal of the Intensive Care Society

Eden A, Purkiss C, Cork G, Baddeley A, Morris K, Carey L, Brown M, McGarrigle L, Kennedy S.
PMID: 29118833
J Intensive Care Soc. 2017 Aug;18(3):212-220. doi: 10.1177/1751143717705801. Epub 2017 Jun 14.

Clinical specialist physiotherapists from the five severe respiratory failure centres in England where respiratory extracorporeal membrane oxygenation (ECMO) is practiced have established this consensus agreement for physiotherapy best practice. The severe respiratory failure centres are Wythenshawe Hospital, Manchester; Glenfield...

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Eden A, Purkiss C, Cork G, et al. In-patient physiotherapy for adults on veno-venous extracorporeal membrane oxygenation - United Kingdom ECMO Physiotherapy Network: A consensus agreement for best practice. J Intensive Care Soc. 2017;18(3):212-220doi: 10.1177/1751143717705801.
Eden, A., Purkiss, C., Cork, G., Baddeley, A., Morris, K., Carey, L., Brown, M., McGarrigle, L., & Kennedy, S. (2017). In-patient physiotherapy for adults on veno-venous extracorporeal membrane oxygenation - United Kingdom ECMO Physiotherapy Network: A consensus agreement for best practice. Journal of the Intensive Care Society, 18(3), 212-220. https://doi.org/10.1177/1751143717705801
Eden, Allaina, et al. "In-patient physiotherapy for adults on veno-venous extracorporeal membrane oxygenation - United Kingdom ECMO Physiotherapy Network: A consensus agreement for best practice." Journal of the Intensive Care Society vol. 18,3 (2017): 212-220. doi: https://doi.org/10.1177/1751143717705801
Eden A, Purkiss C, Cork G, Baddeley A, Morris K, Carey L, Brown M, McGarrigle L, Kennedy S. In-patient physiotherapy for adults on veno-venous extracorporeal membrane oxygenation - United Kingdom ECMO Physiotherapy Network: A consensus agreement for best practice. J Intensive Care Soc. 2017 Aug;18(3):212-220. doi: 10.1177/1751143717705801. Epub 2017 Jun 14. PMID: 29118833; PMCID: PMC5665141.
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Investigation of RadFET response to X-ray and electron beams.

Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine

Yilmaz E, Kahraman A, McGarrigle AM, Vasovic N, Yegen D, Jaksic A.
PMID: 28622597
Appl Radiat Isot. 2017 Sep;127:156-160. doi: 10.1016/j.apradiso.2017.06.004. Epub 2017 Jun 08.

The irradiation response of Radiation Sensing Field Effect Transistor (RadFET), also known as MOSFET/pMOS dosimeter, to high energy X-rays and electron beams was investigated. The threshold voltages before and after irradiation were measured and the trap densities in the...

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Yilmaz E, Kahraman A, McGarrigle AM, et al. Investigation of RadFET response to X-ray and electron beams. Appl Radiat Isot. 2017;127:156-160doi: 10.1016/j.apradiso.2017.06.004.
Yilmaz, E., Kahraman, A., McGarrigle, A. M., Vasovic, N., Yegen, D., & Jaksic, A. (2017). Investigation of RadFET response to X-ray and electron beams. Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 127156-160. https://doi.org/10.1016/j.apradiso.2017.06.004
Yilmaz, E, et al. "Investigation of RadFET response to X-ray and electron beams." Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine vol. 127 (2017): 156-160. doi: https://doi.org/10.1016/j.apradiso.2017.06.004
Yilmaz E, Kahraman A, McGarrigle AM, Vasovic N, Yegen D, Jaksic A. Investigation of RadFET response to X-ray and electron beams. Appl Radiat Isot. 2017 Sep;127:156-160. doi: 10.1016/j.apradiso.2017.06.004. Epub 2017 Jun 08. PMID: 28622597.
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Stereoselective organocatalyzed glycosylations - thiouracil, thioureas and monothiophthalimide act as Brønsted acid catalysts at low loadings.

Chemical science

Bradshaw GA, Colgan AC, Allen NP, Pongener I, Boland MB, Ortin Y, McGarrigle EM.
PMID: 30713648
Chem Sci. 2018 Oct 22;10(2):508-514. doi: 10.1039/c8sc02788a. eCollection 2019 Jan 14.

Thiouracil catalyzes stereoselective glycosylations with galactals in loadings as low as 0.1 mol%. It is proposed that in these glycosylations thiouracil, monothiophthalimide, and the previously reported catalyst, Schreiner's thiourea, do not operate

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Bradshaw GA, Colgan AC, Allen NP, et al. Stereoselective organocatalyzed glycosylations - thiouracil, thioureas and monothiophthalimide act as Brønsted acid catalysts at low loadings. Chem Sci. 2018;10(2):508-514doi: 10.1039/c8sc02788a.
Bradshaw, G. A., Colgan, A. C., Allen, N. P., Pongener, I., Boland, M. B., Ortin, Y., & McGarrigle, E. M. (2019). Stereoselective organocatalyzed glycosylations - thiouracil, thioureas and monothiophthalimide act as Brønsted acid catalysts at low loadings. Chemical science, 10(2), 508-514. https://doi.org/10.1039/c8sc02788a
Bradshaw, G A, et al. "Stereoselective organocatalyzed glycosylations - thiouracil, thioureas and monothiophthalimide act as Brønsted acid catalysts at low loadings." Chemical science vol. 10,2 (2019): 508-514. doi: https://doi.org/10.1039/c8sc02788a
Bradshaw GA, Colgan AC, Allen NP, Pongener I, Boland MB, Ortin Y, McGarrigle EM. Stereoselective organocatalyzed glycosylations - thiouracil, thioureas and monothiophthalimide act as Brønsted acid catalysts at low loadings. Chem Sci. 2018 Oct 22;10(2):508-514. doi: 10.1039/c8sc02788a. eCollection 2019 Jan 14. PMID: 30713648; PMCID: PMC6334493.
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Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering.

Cell reports

Hamilton JR, Tsuchida CA, Nguyen DN, Shy BR, McGarrigle ER, Sandoval Espinoza CR, Carr D, Blaeschke F, Marson A, Doudna JA.
PMID: 34077734
Cell Rep. 2021 Jun 01;35(9):109207. doi: 10.1016/j.celrep.2021.109207.

As genome engineering advances cell-based therapies, a versatile approach to introducing both CRISPR-Cas9 ribonucleoproteins (RNPs) and therapeutic transgenes into specific cells would be transformative. Autologous T cells expressing a chimeric antigen receptor (CAR) manufactured by viral transduction are approved...

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Hamilton JR, Tsuchida CA, Nguyen DN, et al. Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering. Cell Rep. 2021;35(9):109207doi: 10.1016/j.celrep.2021.109207.
Hamilton, J. R., Tsuchida, C. A., Nguyen, D. N., Shy, B. R., McGarrigle, E. R., Sandoval Espinoza, C. R., Carr, D., Blaeschke, F., Marson, A., & Doudna, J. A. (2021). Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering. Cell reports, 35(9), 109207. https://doi.org/10.1016/j.celrep.2021.109207
Hamilton, Jennifer R, et al. "Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering." Cell reports vol. 35,9 (2021): 109207. doi: https://doi.org/10.1016/j.celrep.2021.109207
Hamilton JR, Tsuchida CA, Nguyen DN, Shy BR, McGarrigle ER, Sandoval Espinoza CR, Carr D, Blaeschke F, Marson A, Doudna JA. Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering. Cell Rep. 2021 Jun 01;35(9):109207. doi: 10.1016/j.celrep.2021.109207. PMID: 34077734; PMCID: PMC8236216.
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Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering.

Cell reports

Hamilton JR, Tsuchida CA, Nguyen DN, Shy BR, McGarrigle ER, Sandoval Espinoza CR, Carr D, Blaeschke F, Marson A, Doudna JA.
PMID: 34077734
Cell Rep. 2021 Jun 01;35(9):109207. doi: 10.1016/j.celrep.2021.109207.

As genome engineering advances cell-based therapies, a versatile approach to introducing both CRISPR-Cas9 ribonucleoproteins (RNPs) and therapeutic transgenes into specific cells would be transformative. Autologous T cells expressing a chimeric antigen receptor (CAR) manufactured by viral transduction are approved...

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Hamilton JR, Tsuchida CA, Nguyen DN, et al. Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering. Cell Rep. 2021;35(9):109207doi: 10.1016/j.celrep.2021.109207.
Hamilton, J. R., Tsuchida, C. A., Nguyen, D. N., Shy, B. R., McGarrigle, E. R., Sandoval Espinoza, C. R., Carr, D., Blaeschke, F., Marson, A., & Doudna, J. A. (2021). Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering. Cell reports, 35(9), 109207. https://doi.org/10.1016/j.celrep.2021.109207
Hamilton, Jennifer R, et al. "Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering." Cell reports vol. 35,9 (2021): 109207. doi: https://doi.org/10.1016/j.celrep.2021.109207
Hamilton JR, Tsuchida CA, Nguyen DN, Shy BR, McGarrigle ER, Sandoval Espinoza CR, Carr D, Blaeschke F, Marson A, Doudna JA. Targeted delivery of CRISPR-Cas9 and transgenes enables complex immune cell engineering. Cell Rep. 2021 Jun 01;35(9):109207. doi: 10.1016/j.celrep.2021.109207. PMID: 34077734; PMCID: PMC8236216.
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Predictors of Listening-Related Fatigue Across the Adult Life Span.

Psychological science

McGarrigle R, Knight S, Hornsby BWY, Mattys S.
PMID: 34751602
Psychol Sci. 2021 Nov 09;9567976211016410. doi: 10.1177/09567976211016410. Epub 2021 Nov 09.

Listening-related fatigue is a potentially serious negative consequence of an aging auditory and cognitive system. However, the impact of age on listening-related fatigue and the factors underpinning any such effect remain unexplored. Using data from a large sample of...

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McGarrigle R, Knight S, Hornsby BWY, et al. Predictors of Listening-Related Fatigue Across the Adult Life Span. Psychol Sci. 2021;9567976211016410doi: 10.1177/09567976211016410.
McGarrigle, R., Knight, S., Hornsby, B. W. Y., & Mattys, S. (2021). Predictors of Listening-Related Fatigue Across the Adult Life Span. Psychological science, 9567976211016410. https://doi.org/10.1177/09567976211016410
McGarrigle, Ronan, et al. "Predictors of Listening-Related Fatigue Across the Adult Life Span." Psychological science vol. (2021): 9567976211016410. doi: https://doi.org/10.1177/09567976211016410
McGarrigle R, Knight S, Hornsby BWY, Mattys S. Predictors of Listening-Related Fatigue Across the Adult Life Span. Psychol Sci. 2021 Nov 09;9567976211016410. doi: 10.1177/09567976211016410. Epub 2021 Nov 09. PMID: 34751602.
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Non-contrast CT at comparable dose to an abdominal radiograph in patients with acute renal colic; impact of iterative reconstruction on image quality and diagnostic performance.

Insights into imaging

McLaughlin PD, Murphy KP, Hayes SA, Carey K, Sammon J, Crush L, O'Neill F, Normoyle B, McGarrigle AM, Barry JE, Maher MM.
PMID: 24500656
Insights Imaging. 2014 Apr;5(2):217-30. doi: 10.1007/s13244-014-0310-z. Epub 2014 Feb 07.

OBJECTIVES: The aim was to assess the performance of low-dose non-contrast CT of the urinary tract (LD-CT) acquired at radiation exposures close to that of abdominal radiography using adaptive statistical iterative reconstruction (ASiR).METHODS: Thirty-three patients with clinically suspected renal...

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McLaughlin PD, Murphy KP, Hayes SA, et al. Non-contrast CT at comparable dose to an abdominal radiograph in patients with acute renal colic; impact of iterative reconstruction on image quality and diagnostic performance. Insights Imaging. 2014;5(2):217-30doi: 10.1007/s13244-014-0310-z.
McLaughlin, P. D., Murphy, K. P., Hayes, S. A., Carey, K., Sammon, J., Crush, L., O'Neill, F., Normoyle, B., McGarrigle, A. M., Barry, J. E., & Maher, M. M. (2014). Non-contrast CT at comparable dose to an abdominal radiograph in patients with acute renal colic; impact of iterative reconstruction on image quality and diagnostic performance. Insights into imaging, 5(2), 217-30. https://doi.org/10.1007/s13244-014-0310-z
McLaughlin, P D, et al. "Non-contrast CT at comparable dose to an abdominal radiograph in patients with acute renal colic; impact of iterative reconstruction on image quality and diagnostic performance." Insights into imaging vol. 5,2 (2014): 217-30. doi: https://doi.org/10.1007/s13244-014-0310-z
McLaughlin PD, Murphy KP, Hayes SA, Carey K, Sammon J, Crush L, O'Neill F, Normoyle B, McGarrigle AM, Barry JE, Maher MM. Non-contrast CT at comparable dose to an abdominal radiograph in patients with acute renal colic; impact of iterative reconstruction on image quality and diagnostic performance. Insights Imaging. 2014 Apr;5(2):217-30. doi: 10.1007/s13244-014-0310-z. Epub 2014 Feb 07. PMID: 24500656; PMCID: PMC3999367.
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Chalcogenides as organocatalysts.

Chemical reviews

McGarrigle EM, Myers EL, Illa O, Shaw MA, Riches SL, Aggarwal VK.
PMID: 18072810
Chem Rev. 2007 Dec;107(12):5841-83. doi: 10.1021/cr068402y.

No abstract available.

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McGarrigle EM, Myers EL, Illa O, et al. Chalcogenides as organocatalysts. Chem Rev. 2007;107(12):5841-83doi: 10.1021/cr068402y.
McGarrigle, E. M., Myers, E. L., Illa, O., Shaw, M. A., Riches, S. L., & Aggarwal, V. K. (2007). Chalcogenides as organocatalysts. Chemical reviews, 107(12), 5841-83. https://doi.org/10.1021/cr068402y
McGarrigle, Eoghan M, et al. "Chalcogenides as organocatalysts." Chemical reviews vol. 107,12 (2007): 5841-83. doi: https://doi.org/10.1021/cr068402y
McGarrigle EM, Myers EL, Illa O, Shaw MA, Riches SL, Aggarwal VK. Chalcogenides as organocatalysts. Chem Rev. 2007 Dec;107(12):5841-83. doi: 10.1021/cr068402y. PMID: 18072810.
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Synthesis and application of easily recyclable thiomorpholines for use in sulfur ylide mediated asymmetric epoxidation of aldehydes.

Chemistry, an Asian journal

Hansch M, Illa O, McGarrigle EM, Aggarwal VK.
PMID: 18604816
Chem Asian J. 2008 Sep 01;3(8):1657-63. doi: 10.1002/asia.200800174.

Chiral nonracemic thiomorpholines have been synthesized in four to six steps from limonene or achiral alkenes using alpha-methylbenzylamine to control absolute stereochemistry. These aminosulfides have been used to generate sulfur ylides, which have been applied in the asymmetric epoxidation...

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Hansch M, Illa O, McGarrigle EM, et al. Synthesis and application of easily recyclable thiomorpholines for use in sulfur ylide mediated asymmetric epoxidation of aldehydes. Chem Asian J. 2008;3(8):1657-63doi: 10.1002/asia.200800174.
Hansch, M., Illa, O., McGarrigle, E. M., & Aggarwal, V. K. (2008). Synthesis and application of easily recyclable thiomorpholines for use in sulfur ylide mediated asymmetric epoxidation of aldehydes. Chemistry, an Asian journal, 3(8), 1657-63. https://doi.org/10.1002/asia.200800174
Hansch, Markus, et al. "Synthesis and application of easily recyclable thiomorpholines for use in sulfur ylide mediated asymmetric epoxidation of aldehydes." Chemistry, an Asian journal vol. 3,8 (2008): 1657-63. doi: https://doi.org/10.1002/asia.200800174
Hansch M, Illa O, McGarrigle EM, Aggarwal VK. Synthesis and application of easily recyclable thiomorpholines for use in sulfur ylide mediated asymmetric epoxidation of aldehydes. Chem Asian J. 2008 Sep 01;3(8):1657-63. doi: 10.1002/asia.200800174. PMID: 18604816.
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Synthesis of P-stereogenic phosphorus compounds. Asymmetric oxidation of phosphines under Appel conditions.

Journal of the American Chemical Society

Bergin E, O'Connor CT, Robinson SB, McGarrigle EM, O'Mahony CP, Gilheany DG.
PMID: 17630743
J Am Chem Soc. 2007 Aug 08;129(31):9566-7. doi: 10.1021/ja072925l. Epub 2007 Jul 14.

No abstract available.

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Bergin E, O'Connor CT, Robinson SB, et al. Synthesis of P-stereogenic phosphorus compounds. Asymmetric oxidation of phosphines under Appel conditions. J Am Chem Soc. 2007;129(31):9566-7doi: 10.1021/ja072925l.
Bergin, E., O'Connor, C. T., Robinson, S. B., McGarrigle, E. M., O'Mahony, C. P., & Gilheany, D. G. (2007). Synthesis of P-stereogenic phosphorus compounds. Asymmetric oxidation of phosphines under Appel conditions. Journal of the American Chemical Society, 129(31), 9566-7. https://doi.org/10.1021/ja072925l
Bergin, Enda, et al. "Synthesis of P-stereogenic phosphorus compounds. Asymmetric oxidation of phosphines under Appel conditions." Journal of the American Chemical Society vol. 129,31 (2007): 9566-7. doi: https://doi.org/10.1021/ja072925l
Bergin E, O'Connor CT, Robinson SB, McGarrigle EM, O'Mahony CP, Gilheany DG. Synthesis of P-stereogenic phosphorus compounds. Asymmetric oxidation of phosphines under Appel conditions. J Am Chem Soc. 2007 Aug 08;129(31):9566-7. doi: 10.1021/ja072925l. Epub 2007 Jul 14. PMID: 17630743.
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Structural changes in alginate-based microspheres exposed to in vivo environment as revealed by confocal Raman microscopy.

Scientific reports

Kroneková Z, Pelach M, Mazancová P, Uhelská L, Treľová D, Rázga F, Némethová V, Szalai S, Chorvát D, McGarrigle JJ, Omami M, Isa D, Ghani S, Majková E, Oberholzer J, Raus V, Šiffalovič P, Lacík I.
PMID: 29374272
Sci Rep. 2018 Jan 26;8(1):1637. doi: 10.1038/s41598-018-20022-y.

A next-generation cure for type 1 diabetes relies on immunoprotection of insulin-producing cells, which can be achieved by their encapsulation in microspheres made of non-covalently crosslinked hydrogels. Treatment success is directly related to the microsphere structure that is characterized...

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Kroneková Z, Pelach M, Mazancová P, et al. Structural changes in alginate-based microspheres exposed to in vivo environment as revealed by confocal Raman microscopy. Sci Rep. 2018;8(1):1637doi: 10.1038/s41598-018-20022-y.
Kroneková, Z., Pelach, M., Mazancová, P., Uhelská, L., Treľová, D., Rázga, F., Némethová, V., Szalai, S., Chorvát, D., McGarrigle, J. J., Omami, M., Isa, D., Ghani, S., Majková, E., Oberholzer, J., Raus, V., Šiffalovič, P., & Lacík, I. (2018). Structural changes in alginate-based microspheres exposed to in vivo environment as revealed by confocal Raman microscopy. Scientific reports, 8(1), 1637. https://doi.org/10.1038/s41598-018-20022-y
Kroneková, Zuzana, et al. "Structural changes in alginate-based microspheres exposed to in vivo environment as revealed by confocal Raman microscopy." Scientific reports vol. 8,1 (2018): 1637. doi: https://doi.org/10.1038/s41598-018-20022-y
Kroneková Z, Pelach M, Mazancová P, Uhelská L, Treľová D, Rázga F, Némethová V, Szalai S, Chorvát D, McGarrigle JJ, Omami M, Isa D, Ghani S, Majková E, Oberholzer J, Raus V, Šiffalovič P, Lacík I. Structural changes in alginate-based microspheres exposed to in vivo environment as revealed by confocal Raman microscopy. Sci Rep. 2018 Jan 26;8(1):1637. doi: 10.1038/s41598-018-20022-y. PMID: 29374272; PMCID: PMC5785987.
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Stereoselective β-mannosylations and β-rhamnosylations from glycosyl hemiacetals mediated by lithium iodide.

Chemical science

Pongener I, Pepe DA, Ruddy JJ, McGarrigle EM.
PMID: 34377400
Chem Sci. 2021 Jul 05;12(29):10070-10075. doi: 10.1039/d1sc01300a. eCollection 2021 Jul 28.

Stereoselective β-mannosylation is one of the most challenging problems in the synthesis of oligosaccharides. Herein, a highly selective synthesis of β-mannosides and β-rhamnosides from glycosyl hemi-acetals is reported, following a one-pot chlorination, iodination, glycosylation sequence employing cheap oxalyl chloride,...

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Pongener I, Pepe DA, Ruddy JJ, et al. Stereoselective β-mannosylations and β-rhamnosylations from glycosyl hemiacetals mediated by lithium iodide. Chem Sci. 2021;12(29):10070-10075doi: 10.1039/d1sc01300a.
Pongener, I., Pepe, D. A., Ruddy, J. J., & McGarrigle, E. M. (2021). Stereoselective β-mannosylations and β-rhamnosylations from glycosyl hemiacetals mediated by lithium iodide. Chemical science, 12(29), 10070-10075. https://doi.org/10.1039/d1sc01300a
Pongener, Imlirenla, et al. "Stereoselective β-mannosylations and β-rhamnosylations from glycosyl hemiacetals mediated by lithium iodide." Chemical science vol. 12,29 (2021): 10070-10075. doi: https://doi.org/10.1039/d1sc01300a
Pongener I, Pepe DA, Ruddy JJ, McGarrigle EM. Stereoselective β-mannosylations and β-rhamnosylations from glycosyl hemiacetals mediated by lithium iodide. Chem Sci. 2021 Jul 05;12(29):10070-10075. doi: 10.1039/d1sc01300a. eCollection 2021 Jul 28. PMID: 34377400; PMCID: PMC8317664.
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