Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 95 entries
Sorted by: Best Match Show Resources per page
Sound-proofing the surgery.

The Practitioner

Rathbone A.
PMID: 5666174
Practitioner. 1968 Mar;Suppl 6:19-24.

No abstract available.

Cite
Rathbone A. Sound-proofing the surgery. Practitioner. 1968;Suppl 6:19-24
Rathbone, A. (1968). Sound-proofing the surgery. The Practitioner, Suppl 6:19-24.
Rathbone, A. "Sound-proofing the surgery." The Practitioner vol. (1968): Suppl 6:19-24.
Rathbone A. Sound-proofing the surgery. Practitioner. 1968 Mar;Suppl 6:19-24. PMID: 5666174.
Copy Download .nbib Format: NLM
The Lilian Greg Occupation Centre for Defective Children.

Studies in mental inefficiency

Rathbone E.
PMID: 28909953
Stud Ment Ineffic. 1920 Oct 15;1(4):78-81.

No abstract available.

Cite
Rathbone E. The Lilian Greg Occupation Centre for Defective Children. Stud Ment Ineffic. 1920;1(4):78-81
Rathbone, E. (1920). The Lilian Greg Occupation Centre for Defective Children. Studies in mental inefficiency, 1(4), 78-81.
Rathbone, Elfrida. "The Lilian Greg Occupation Centre for Defective Children." Studies in mental inefficiency vol. 1,4 (1920): 78-81.
Rathbone E. The Lilian Greg Occupation Centre for Defective Children. Stud Ment Ineffic. 1920 Oct 15;1(4):78-81. PMID: 28909953; PMCID: PMC5109065.
Copy Download .nbib Format: NLM
The application of co-melt-extruded poly(ε-caprolactone) as a controlled release drug delivery device when combined with novel bioactive drug candidates: Membrane permeation and Hanson dissolution studies.

Results in pharma sciences

Gardyne SJ, Mucalo MR, Rathbone MJ.
PMID: 25755986
Results Pharma Sci. 2011 Nov 25;1(1):80-7. doi: 10.1016/j.rinphs.2011.11.002. eCollection 2011 May.

Eight bioactive drug compounds (abamectin, amoxicillin, dexamethasone, dexamethasone valerate, ketoprofen, melatonin, oestradiol 17β, and oestradiol benzoate) were combined via melt extrusion and disc pressing processes with a polycaprolactone (PCL) matrix and were then evaluated and compared via membrane diffusion...

Cite
Gardyne SJ, Mucalo MR, Rathbone MJ. The application of co-melt-extruded poly(ε-caprolactone) as a controlled release drug delivery device when combined with novel bioactive drug candidates: Membrane permeation and Hanson dissolution studies. Results Pharma Sci. 2011;1(1):80-7doi: 10.1016/j.rinphs.2011.11.002.
Gardyne, S. J., Mucalo, M. R., & Rathbone, M. J. (2011). The application of co-melt-extruded poly(ε-caprolactone) as a controlled release drug delivery device when combined with novel bioactive drug candidates: Membrane permeation and Hanson dissolution studies. Results in pharma sciences, 1(1), 80-7. https://doi.org/10.1016/j.rinphs.2011.11.002
Gardyne, Stephen J, et al. "The application of co-melt-extruded poly(ε-caprolactone) as a controlled release drug delivery device when combined with novel bioactive drug candidates: Membrane permeation and Hanson dissolution studies." Results in pharma sciences vol. 1,1 (2011): 80-7. doi: https://doi.org/10.1016/j.rinphs.2011.11.002
Gardyne SJ, Mucalo MR, Rathbone MJ. The application of co-melt-extruded poly(ε-caprolactone) as a controlled release drug delivery device when combined with novel bioactive drug candidates: Membrane permeation and Hanson dissolution studies. Results Pharma Sci. 2011 Nov 25;1(1):80-7. doi: 10.1016/j.rinphs.2011.11.002. eCollection 2011 May. PMID: 25755986; PMCID: PMC4150627.
Copy Download .nbib Format: NLM
Preliminary in vitro toxicological evaluation of a series of 2-pyridylcarboxamidrazone candidate anti-tuberculosis compounds: II(1).

Environmental toxicology and pharmacology

Coleman MD, Rathbone DL, Endersby CR, Hovey MC, Tims KJ, Lambert PA, Billington DC.
PMID: 10925069
Environ Toxicol Pharmacol. 2000 Mar 01;8(3):167-172. doi: 10.1016/s1382-6689(00)00037-5.

The in vitro toxicity of two amidrazones I [N(1)-(3-benzyloxy-4-methoxybenzylidene)-pyridine-2-carboxamidrazone] and II [N(1)-(4-benzyloxy-3-methoxybenzylidene)-pyridine-2-carboxamidrazone] and their precursors PI (3-benzyloxy-4-methoxybenzaldehyde) and PII (4-benzyloxy-3-methoxybenzaldehyde) was determined using a rat liver metabolism system with human mononuclear leucocytes (MNL) as target cells. The minimum inhibitory...

Cite
Coleman MD, Rathbone DL, Endersby CR, et al. Preliminary in vitro toxicological evaluation of a series of 2-pyridylcarboxamidrazone candidate anti-tuberculosis compounds: II(1). Environ Toxicol Pharmacol. 2000;8(3):167-172doi: 10.1016/s1382-6689(00)00037-5.
Coleman, M. D., Rathbone, D. L., Endersby, C. R., Hovey, M. C., Tims, K. J., Lambert, P. A., & Billington, D. C. (2000). Preliminary in vitro toxicological evaluation of a series of 2-pyridylcarboxamidrazone candidate anti-tuberculosis compounds: II(1). Environmental toxicology and pharmacology, 8(3), 167-172. https://doi.org/10.1016/s1382-6689(00)00037-5
Coleman, et al. "Preliminary in vitro toxicological evaluation of a series of 2-pyridylcarboxamidrazone candidate anti-tuberculosis compounds: II(1)." Environmental toxicology and pharmacology vol. 8,3 (2000): 167-172. doi: https://doi.org/10.1016/s1382-6689(00)00037-5
Coleman MD, Rathbone DL, Endersby CR, Hovey MC, Tims KJ, Lambert PA, Billington DC. Preliminary in vitro toxicological evaluation of a series of 2-pyridylcarboxamidrazone candidate anti-tuberculosis compounds: II(1). Environ Toxicol Pharmacol. 2000 Mar 01;8(3):167-172. doi: 10.1016/s1382-6689(00)00037-5. PMID: 10925069.
Copy Download .nbib Format: NLM
Observation of the symmetry-forbidden 5sigmau-->ksigmau CS2 transition: a vibrationally driven photoionization resonance.

Physical review letters

Rathbone GJ, Poliakoff ED, Bozek JD, Lucchese RR.
PMID: 15089534
Phys Rev Lett. 2004 Apr 09;92(14):143002. doi: 10.1103/PhysRevLett.92.143002. Epub 2004 Apr 08.

Vibrationally resolved photoelectron spectroscopy and Schwinger calculations are used to characterize a new resonance phenomenon in the 5sigma(u)-->ksigma(u) photoionization of CS2. This resonant channel is symmetry forbidden, yet is observable because it is activated by the antisymmetric stretching vibration....

Cite
Rathbone GJ, Poliakoff ED, Bozek JD, et al. Observation of the symmetry-forbidden 5sigmau-->ksigmau CS2 transition: a vibrationally driven photoionization resonance. Phys Rev Lett. 2004;92(14):143002doi: 10.1103/PhysRevLett.92.143002.
Rathbone, G. J., Poliakoff, E. D., Bozek, J. D., & Lucchese, R. R. (2004). Observation of the symmetry-forbidden 5sigmau-->ksigmau CS2 transition: a vibrationally driven photoionization resonance. Physical review letters, 92(14), 143002. https://doi.org/10.1103/PhysRevLett.92.143002
Rathbone, G J, et al. "Observation of the symmetry-forbidden 5sigmau-->ksigmau CS2 transition: a vibrationally driven photoionization resonance." Physical review letters vol. 92,14 (2004): 143002. doi: https://doi.org/10.1103/PhysRevLett.92.143002
Rathbone GJ, Poliakoff ED, Bozek JD, Lucchese RR. Observation of the symmetry-forbidden 5sigmau-->ksigmau CS2 transition: a vibrationally driven photoionization resonance. Phys Rev Lett. 2004 Apr 09;92(14):143002. doi: 10.1103/PhysRevLett.92.143002. Epub 2004 Apr 08. PMID: 15089534.
Copy Download .nbib Format: NLM
Photoelectron trapping in N2O 7sigma-->ksigma resonant ionization.

The Journal of chemical physics

Rathbone GJ, Poliakoff ED, Bozek JD, Toffoli D, Lucchese RR.
PMID: 16035835
J Chem Phys. 2005 Jul 01;123(1):014307. doi: 10.1063/1.1946738.

Vibrationally resolved photoelectron spectroscopy of the N2O+(A 2Sigma+) state is used to compare the dependence of the photoelectron dynamics on molecular geometry for two shape resonances in the same ionization channel. Spectra are acquired over the photon energy range...

Cite
Rathbone GJ, Poliakoff ED, Bozek JD, et al. Photoelectron trapping in N2O 7sigma-->ksigma resonant ionization. J Chem Phys. 2005;123(1):014307doi: 10.1063/1.1946738.
Rathbone, G. J., Poliakoff, E. D., Bozek, J. D., Toffoli, D., & Lucchese, R. R. (2005). Photoelectron trapping in N2O 7sigma-->ksigma resonant ionization. The Journal of chemical physics, 123(1), 014307. https://doi.org/10.1063/1.1946738
Rathbone, G J, et al. "Photoelectron trapping in N2O 7sigma-->ksigma resonant ionization." The Journal of chemical physics vol. 123,1 (2005): 014307. doi: https://doi.org/10.1063/1.1946738
Rathbone GJ, Poliakoff ED, Bozek JD, Toffoli D, Lucchese RR. Photoelectron trapping in N2O 7sigma-->ksigma resonant ionization. J Chem Phys. 2005 Jul 01;123(1):014307. doi: 10.1063/1.1946738. PMID: 16035835.
Copy Download .nbib Format: NLM
Electronically forbidden (5sigmau-->ksigmau) photoionization of CS2: mode-specific electronic-vibrational coupling.

The Journal of chemical physics

Rathbone GJ, Poliakoff ED, Bozek JD, Lucchese RR.
PMID: 15740373
J Chem Phys. 2005 Feb 08;122(6):064308. doi: 10.1063/1.1850474.

Vibrationally resolved photoelectron spectroscopy of the CS(2) (+)(B (2)Sigma(u) (+)) state is used to show how nontotally symmetric vibrations "activate" a forbidden electronic transition in the photoionization continuum, specifically, a 5sigma(u)-->ksigma(u) shape resonance, that would be inaccessible in the...

Cite
Rathbone GJ, Poliakoff ED, Bozek JD, et al. Electronically forbidden (5sigmau-->ksigmau) photoionization of CS2: mode-specific electronic-vibrational coupling. J Chem Phys. 2005;122(6):064308doi: 10.1063/1.1850474.
Rathbone, G. J., Poliakoff, E. D., Bozek, J. D., & Lucchese, R. R. (2005). Electronically forbidden (5sigmau-->ksigmau) photoionization of CS2: mode-specific electronic-vibrational coupling. The Journal of chemical physics, 122(6), 064308. https://doi.org/10.1063/1.1850474
Rathbone, G J, et al. "Electronically forbidden (5sigmau-->ksigmau) photoionization of CS2: mode-specific electronic-vibrational coupling." The Journal of chemical physics vol. 122,6 (2005): 064308. doi: https://doi.org/10.1063/1.1850474
Rathbone GJ, Poliakoff ED, Bozek JD, Lucchese RR. Electronically forbidden (5sigmau-->ksigmau) photoionization of CS2: mode-specific electronic-vibrational coupling. J Chem Phys. 2005 Feb 08;122(6):064308. doi: 10.1063/1.1850474. PMID: 15740373.
Copy Download .nbib Format: NLM
Ion chemistry of 1H-1,2,3-triazole.

The journal of physical chemistry. B

Ichino T, Andrews DH, Rathbone GJ, Misaizu F, Calvi RM, Wren SW, Kato S, Bierbaum VM, Lineberger WC.
PMID: 17960930
J Phys Chem B. 2008 Jan 17;112(2):545-57. doi: 10.1021/jp074824f. Epub 2007 Oct 26.

A combination of experimental methods, photoelectron-imaging spectroscopy, flowing afterglow-photoelectron spectroscopy and the flowing afterglow-selected ion flow tube technique, and electronic structure calculations at the B3LYP/6-311++G(d,p) level of density functional theory (DFT) have been employed to study the mechanism of...

Cite
Ichino T, Andrews DH, Rathbone GJ, et al. Ion chemistry of 1H-1,2,3-triazole. J Phys Chem B. 2007;112(2):545-57doi: 10.1021/jp074824f.
Ichino, T., Andrews, D. H., Rathbone, G. J., Misaizu, F., Calvi, R. M., Wren, S. W., Kato, S., Bierbaum, V. M., & Lineberger, W. C. (2008). Ion chemistry of 1H-1,2,3-triazole. The journal of physical chemistry. B, 112(2), 545-57. https://doi.org/10.1021/jp074824f
Ichino, Takatoshi, et al. "Ion chemistry of 1H-1,2,3-triazole." The journal of physical chemistry. B vol. 112,2 (2008): 545-57. doi: https://doi.org/10.1021/jp074824f
Ichino T, Andrews DH, Rathbone GJ, Misaizu F, Calvi RM, Wren SW, Kato S, Bierbaum VM, Lineberger WC. Ion chemistry of 1H-1,2,3-triazole. J Phys Chem B. 2008 Jan 17;112(2):545-57. doi: 10.1021/jp074824f. Epub 2007 Oct 26. PMID: 17960930.
Copy Download .nbib Format: NLM
Novel protein targets for organophosphorus pesticides in rat brain.

Environmental toxicology and pharmacology

Murray A, Rathbone AJ, Ray DE.
PMID: 21783511
Environ Toxicol Pharmacol. 2005 May;19(3):451-4. doi: 10.1016/j.etap.2004.12.006. Epub 2005 Jan 26.

We report preliminary results from a proteomic search for rat brain protein targets adducted by organophosphorous pesticides. Azamethaphos, chlorfenvinphos, diazinon, malathion and chlorpyrifos oxons (in rat brain homogenates) or pirimiphos-methyl (after systemic treatment) were tested at levels producing no...

Cite
Murray A, Rathbone AJ, Ray DE. Novel protein targets for organophosphorus pesticides in rat brain. Environ Toxicol Pharmacol. 2005;19(3):451-4doi: 10.1016/j.etap.2004.12.006.
Murray, A., Rathbone, A. J., & Ray, D. E. (2005). Novel protein targets for organophosphorus pesticides in rat brain. Environmental toxicology and pharmacology, 19(3), 451-4. https://doi.org/10.1016/j.etap.2004.12.006
Murray, Andrea, et al. "Novel protein targets for organophosphorus pesticides in rat brain." Environmental toxicology and pharmacology vol. 19,3 (2005): 451-4. doi: https://doi.org/10.1016/j.etap.2004.12.006
Murray A, Rathbone AJ, Ray DE. Novel protein targets for organophosphorus pesticides in rat brain. Environ Toxicol Pharmacol. 2005 May;19(3):451-4. doi: 10.1016/j.etap.2004.12.006. Epub 2005 Jan 26. PMID: 21783511.
Copy Download .nbib Format: NLM
Effects of glutathione, N-acetyl-cysteine, α-lipoic acid and dihydrolipoic acid on the cytotoxicity of a 2-pyridylcarboxamidrazone antimycobacterial agent in human mononuclear leucocytes in vitro.

Environmental toxicology and pharmacology

Coleman MD, Khan N, Welton G, Lambert PA, Tims KJ, Rathbone DL.
PMID: 21782725
Environ Toxicol Pharmacol. 2004 Jul;17(3):143-8. doi: 10.1016/j.etap.2004.04.002.

A series of antioxidants was used to explore the cytotoxicity of one particularly toxic antimycobacterial 2-pyridylcarboxamidrazone anti-tuberculosis agent against human mononuclear leucocytes (MNL), in comparison with isoniazid (INH) to aid future compound design. INH caused a significant reduction of...

Cite
Coleman MD, Khan N, Welton G, et al. Effects of glutathione, N-acetyl-cysteine, α-lipoic acid and dihydrolipoic acid on the cytotoxicity of a 2-pyridylcarboxamidrazone antimycobacterial agent in human mononuclear leucocytes in vitro. Environ Toxicol Pharmacol. 2004;17(3):143-8doi: 10.1016/j.etap.2004.04.002.
Coleman, M. D., Khan, N., Welton, G., Lambert, P. A., Tims, K. J., & Rathbone, D. L. (2004). Effects of glutathione, N-acetyl-cysteine, α-lipoic acid and dihydrolipoic acid on the cytotoxicity of a 2-pyridylcarboxamidrazone antimycobacterial agent in human mononuclear leucocytes in vitro. Environmental toxicology and pharmacology, 17(3), 143-8. https://doi.org/10.1016/j.etap.2004.04.002
Coleman, Michael D, et al. "Effects of glutathione, N-acetyl-cysteine, α-lipoic acid and dihydrolipoic acid on the cytotoxicity of a 2-pyridylcarboxamidrazone antimycobacterial agent in human mononuclear leucocytes in vitro." Environmental toxicology and pharmacology vol. 17,3 (2004): 143-8. doi: https://doi.org/10.1016/j.etap.2004.04.002
Coleman MD, Khan N, Welton G, Lambert PA, Tims KJ, Rathbone DL. Effects of glutathione, N-acetyl-cysteine, α-lipoic acid and dihydrolipoic acid on the cytotoxicity of a 2-pyridylcarboxamidrazone antimycobacterial agent in human mononuclear leucocytes in vitro. Environ Toxicol Pharmacol. 2004 Jul;17(3):143-8. doi: 10.1016/j.etap.2004.04.002. PMID: 21782725.
Copy Download .nbib Format: NLM
Veterinary drug delivery.

Journal of pharmacy & bioallied sciences

McDowell A, Rathbone MJ.
PMID: 24459396
J Pharm Bioallied Sci. 2014 Jan;6(1):1. doi: 10.4103/0975-7406.124299.

No abstract available.

Cite
McDowell A, Rathbone MJ. Veterinary drug delivery. J Pharm Bioallied Sci. 2014;6(1):1doi: 10.4103/0975-7406.124299.
McDowell, A., & Rathbone, M. J. (2014). Veterinary drug delivery. Journal of pharmacy & bioallied sciences, 6(1), 1. https://doi.org/10.4103/0975-7406.124299
McDowell, Arlene, and Rathbone, Michael J. "Veterinary drug delivery." Journal of pharmacy & bioallied sciences vol. 6,1 (2014): 1. doi: https://doi.org/10.4103/0975-7406.124299
McDowell A, Rathbone MJ. Veterinary drug delivery. J Pharm Bioallied Sci. 2014 Jan;6(1):1. doi: 10.4103/0975-7406.124299. PMID: 24459396; PMCID: PMC3895286.
Copy Download .nbib Format: NLM
Root Filling.

The American journal of dental science

Rathbone WR.
PMID: 30750195
Am J Dent Sci. 1900 Feb;33(10):458-460.

No abstract available.

Cite
Rathbone WR. Root Filling. Am J Dent Sci. 1900;33(10):458-460
Rathbone, W. R. (1900). Root Filling. The American journal of dental science, 33(10), 458-460.
Rathbone, W R. "Root Filling." The American journal of dental science vol. 33,10 (1900): 458-460.
Rathbone WR. Root Filling. Am J Dent Sci. 1900 Feb;33(10):458-460. PMID: 30750195; PMCID: PMC6067286.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 95 entries