Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 289 entries
Sorted by: Best Match Show Resources per page
Facile synthesis of SnO2-PbS nanocomposites with controlled structure for applications in photocatalysis.

Nanoscale

Kar A, Sain S, Rossouw D, Knappett BR, Pradhan SK, Wheatley AE.
PMID: 26765053
Nanoscale. 2016 Feb 07;8(5):2727-39. doi: 10.1039/c5nr07036h.

Recent studies have shown that SnO2-based nanocomposites offer excellent electrical, optical, and electrochemical properties. In this article, we present the facile and cost-effective fabrication, characterization and testing of a new SnO2-PbS nanocomposite photocatalyst designed to overcome low photocatalytic efficiency...

Cite
Kar A, Sain S, Rossouw D, et al. Facile synthesis of SnO2-PbS nanocomposites with controlled structure for applications in photocatalysis. Nanoscale. 2016;8(5):2727-39doi: 10.1039/c5nr07036h.
Kar, A., Sain, S., Rossouw, D., Knappett, B. R., Pradhan, S. K., & Wheatley, A. E. (2016). Facile synthesis of SnO2-PbS nanocomposites with controlled structure for applications in photocatalysis. Nanoscale, 8(5), 2727-39. https://doi.org/10.1039/c5nr07036h
Kar, Arik, et al. "Facile synthesis of SnO2-PbS nanocomposites with controlled structure for applications in photocatalysis." Nanoscale vol. 8,5 (2016): 2727-39. doi: https://doi.org/10.1039/c5nr07036h
Kar A, Sain S, Rossouw D, Knappett BR, Pradhan SK, Wheatley AE. Facile synthesis of SnO2-PbS nanocomposites with controlled structure for applications in photocatalysis. Nanoscale. 2016 Feb 07;8(5):2727-39. doi: 10.1039/c5nr07036h. PMID: 26765053.
Copy Download .nbib Format: NLM
Non-standardised treatment rooms present an obstacle to efficient and prompt patient care.

Clinical medicine (London, England)

Tunney R, Shillito S, Wheatley E.
PMID: 26026020
Clin Med (Lond). 2015 Jun;15:s26. doi: 10.7861/clinmedicine.15-3-s26. Epub 2015 May 29.

No abstract available.

Cite
Tunney R, Shillito S, Wheatley E. Non-standardised treatment rooms present an obstacle to efficient and prompt patient care. Clin Med (Lond). 2015;15:s26doi: 10.7861/clinmedicine.15-3-s26.
Tunney, R., Shillito, S., & Wheatley, E. (2015). Non-standardised treatment rooms present an obstacle to efficient and prompt patient care. Clinical medicine (London, England), 15s26. https://doi.org/10.7861/clinmedicine.15-3-s26
Tunney, Ruth, et al. "Non-standardised treatment rooms present an obstacle to efficient and prompt patient care." Clinical medicine (London, England) vol. 15 (2015): s26. doi: https://doi.org/10.7861/clinmedicine.15-3-s26
Tunney R, Shillito S, Wheatley E. Non-standardised treatment rooms present an obstacle to efficient and prompt patient care. Clin Med (Lond). 2015 Jun;15:s26. doi: 10.7861/clinmedicine.15-3-s26. Epub 2015 May 29. PMID: 26026020.
Copy Download .nbib Format: NLM
"I've got a lot to do and i don't think i'll have the time": Gender differences in late adolescents' narratives of the future.

Journal of youth and adolescence

Greene AL, Wheatley SM.
PMID: 24264169
J Youth Adolesc. 1992 Dec;21(6):667-86. doi: 10.1007/BF01538738.

The present study examined gender differences in late adolescents' future narratives.Thirty-nine male and 43 female late adolescents (M=20.01 years) completed 90-minute individual interviews assessing dimensional and thematic aspects of the future narrative as well as psychological profile characteristics (abstract...

Cite
Greene AL, Wheatley SM. "I've got a lot to do and i don't think i'll have the time": Gender differences in late adolescents' narratives of the future. J Youth Adolesc. 1992;21(6):667-86doi: 10.1007/BF01538738.
Greene, A. L., & Wheatley, S. M. (1992). "I've got a lot to do and i don't think i'll have the time": Gender differences in late adolescents' narratives of the future. Journal of youth and adolescence, 21(6), 667-86. https://doi.org/10.1007/BF01538738
Greene, A L, and Wheatley, S M. ""I've got a lot to do and i don't think i'll have the time": Gender differences in late adolescents' narratives of the future." Journal of youth and adolescence vol. 21,6 (1992): 667-86. doi: https://doi.org/10.1007/BF01538738
Greene AL, Wheatley SM. "I've got a lot to do and i don't think i'll have the time": Gender differences in late adolescents' narratives of the future. J Youth Adolesc. 1992 Dec;21(6):667-86. doi: 10.1007/BF01538738. PMID: 24264169.
Copy Download .nbib Format: NLM
Mitral valve replacement with mechanical or bioprosthetic valve.

Multimedia manual of cardiothoracic surgery : MMCTS

Wheatley D, Will M.
PMID: 24264717
Multimed Man Cardiothorac Surg. 2005 Jan 01;2005(425):mmcts.2004.001024. doi: 10.1510/mmcts.2004.001024.

A presentation on the technique of mitral valve replacement is shown: exposure and excision of the diseased mitral valve is demonstrated along with the use of sub-annular and supra-annular interrupted suture techniques for securing biological and mechanical mitral prostheses....

Cite
Wheatley D, Will M. Mitral valve replacement with mechanical or bioprosthetic valve. Multimed Man Cardiothorac Surg. 2005;2005(425):mmcts.2004.001024doi: 10.1510/mmcts.2004.001024.
Wheatley, D., & Will, M. (2005). Mitral valve replacement with mechanical or bioprosthetic valve. Multimedia manual of cardiothoracic surgery : MMCTS, 2005(425), mmcts.2004.001024. https://doi.org/10.1510/mmcts.2004.001024
Wheatley, David, and Will, Malcolm. "Mitral valve replacement with mechanical or bioprosthetic valve." Multimedia manual of cardiothoracic surgery : MMCTS vol. 2005,425 (2005): mmcts.2004.001024. doi: https://doi.org/10.1510/mmcts.2004.001024
Wheatley D, Will M. Mitral valve replacement with mechanical or bioprosthetic valve. Multimed Man Cardiothorac Surg. 2005 Jan 01;2005(425):mmcts.2004.001024. doi: 10.1510/mmcts.2004.001024. PMID: 24264717.
Copy Download .nbib Format: NLM
Ethane-1,2-diphosphonic acid as a building block in supramolecular chemistry; a pillared-layer framework and framework-encapsulated cations.

Acta crystallographica. Section B, Structural science

Wheatley PS, Lough AJ, Ferguson G, Burchell CJ, Glidewell C.
PMID: 11173372
Acta Crystallogr B. 2001 Feb;57:95-102. doi: 10.1107/s0108768100014841.

The 1:1 adduct of piperazine and ethane-1,2-diphosphonic acid is a salt [C(4)H(12)N(2)](2+).[C(2)H(6)O(6)P(2)](2-), in which both ions lie across centres of inversion in space group P2(1)/c. The anions are linked by a single type of O-H...O hydrogen bond [O...O, 2.562...

Cite
Wheatley PS, Lough AJ, Ferguson G, et al. Ethane-1,2-diphosphonic acid as a building block in supramolecular chemistry; a pillared-layer framework and framework-encapsulated cations. Acta Crystallogr B. 2001;57:95-102doi: 10.1107/s0108768100014841.
Wheatley , P. S., Lough , A. J., Ferguson , G., Burchell , C. J., & Glidewell , C. (2001). Ethane-1,2-diphosphonic acid as a building block in supramolecular chemistry; a pillared-layer framework and framework-encapsulated cations. Acta crystallographica. Section B, Structural science, 5795-102. https://doi.org/10.1107/s0108768100014841
Wheatley , P S, et al. "Ethane-1,2-diphosphonic acid as a building block in supramolecular chemistry; a pillared-layer framework and framework-encapsulated cations." Acta crystallographica. Section B, Structural science vol. 57 (2001): 95-102. doi: https://doi.org/10.1107/s0108768100014841
Wheatley PS, Lough AJ, Ferguson G, Burchell CJ, Glidewell C. Ethane-1,2-diphosphonic acid as a building block in supramolecular chemistry; a pillared-layer framework and framework-encapsulated cations. Acta Crystallogr B. 2001 Feb;57:95-102. doi: 10.1107/s0108768100014841. PMID: 11173372.
Copy Download .nbib Format: NLM
How tainted is medicine?.

Lancet (London, England)

Wheatley D.
PMID: 12049887
Lancet. 2002 May 18;359(9319):1775-6. doi: 10.1016/S0140-6736(02)08618-X.

No abstract available.

Cite
Wheatley D. How tainted is medicine?. Lancet. 2002;359(9319):1775-6doi: 10.1016/S0140-6736(02)08618-X.
Wheatley, D. (2002). How tainted is medicine?. Lancet (London, England), 359(9319), 1775-6. https://doi.org/10.1016/S0140-6736(02)08618-X
Wheatley, David. "How tainted is medicine?." Lancet (London, England) vol. 359,9319 (2002): 1775-6. doi: https://doi.org/10.1016/S0140-6736(02)08618-X
Wheatley D. How tainted is medicine?. Lancet. 2002 May 18;359(9319):1775-6. doi: 10.1016/S0140-6736(02)08618-X. PMID: 12049887.
Copy Download .nbib Format: NLM
The general practitioner research group.

The Practitioner

WHEATLEY D.
PMID: 13844269
Practitioner. 1960 Apr;184:500-3.

No abstract available.

Cite
WHEATLEY D. The general practitioner research group. Practitioner. 1960;184:500-3
WHEATLEY, D. (1960). The general practitioner research group. The Practitioner, 184500-3.
WHEATLEY, D. "The general practitioner research group." The Practitioner vol. 184 (1960): 500-3.
WHEATLEY D. The general practitioner research group. Practitioner. 1960 Apr;184:500-3. PMID: 13844269.
Copy Download .nbib Format: NLM
Fast racemisation and slow epimerisation of laterally lithiated amides: stereochemical evidence for the mechanism of inversion of amide-substituted benzyllithiums.

Chemical communications (Cambridge, England)

Clayden J, Stimson CC, Keenan M, Wheatley AE.
PMID: 14737562
Chem Commun (Camb). 2004 Jan 21;(2):228-9. doi: 10.1039/b310963a. Epub 2003 Dec 05.

Tertiary 1-naphthamides racemise much more slowly than their laterally lithiated derivatives, and the relative rates of racemisation and epimerisation of these derivatives indicate that the lithium-bearing stereogenic centre inverts via a "conducted tour" mechanism, in which the lithium cation...

Cite
Clayden J, Stimson CC, Keenan M, et al. Fast racemisation and slow epimerisation of laterally lithiated amides: stereochemical evidence for the mechanism of inversion of amide-substituted benzyllithiums. Chem Commun (Camb). 2003;(2):228-9doi: 10.1039/b310963a.
Clayden, J., Stimson, C. C., Keenan, M., & Wheatley, A. E. (2004). Fast racemisation and slow epimerisation of laterally lithiated amides: stereochemical evidence for the mechanism of inversion of amide-substituted benzyllithiums. Chemical communications (Cambridge, England), (2), 228-9. https://doi.org/10.1039/b310963a
Clayden, Jonathan, et al. "Fast racemisation and slow epimerisation of laterally lithiated amides: stereochemical evidence for the mechanism of inversion of amide-substituted benzyllithiums." Chemical communications (Cambridge, England) vol. ,2 (2004): 228-9. doi: https://doi.org/10.1039/b310963a
Clayden J, Stimson CC, Keenan M, Wheatley AE. Fast racemisation and slow epimerisation of laterally lithiated amides: stereochemical evidence for the mechanism of inversion of amide-substituted benzyllithiums. Chem Commun (Camb). 2004 Jan 21;(2):228-9. doi: 10.1039/b310963a. Epub 2003 Dec 05. PMID: 14737562.
Copy Download .nbib Format: NLM
Role of Hepatic Stellate Cells in the Early Phase of Liver Regeneration in Rat: Formation of Tight Adhesion to Parenchymal Cells.

Comparative hepatology

Mabuchi A, Mullaney I, Sheard P, Hessian P, Zimmermann A, Senoo H, Wheatley AM.
PMID: 14960181
Comp Hepatol. 2004 Jan 14;3:S29. doi: 10.1186/1476-5926-2-S1-S29.

We investigated activation mechanisms of hepatic stellate cells (HSCs) that are known to play pivotal roles in the regeneration process after 70% partial hepatectomy (PHx). Parenchymal liver cells (PLCs) and non-parenchymal cells (NPLCs) were isolated and purified from the...

Cite
Mabuchi A, Mullaney I, Sheard P, et al. Role of Hepatic Stellate Cells in the Early Phase of Liver Regeneration in Rat: Formation of Tight Adhesion to Parenchymal Cells. Comp Hepatol. 2004;3:S29doi: 10.1186/1476-5926-2-S1-S29.
Mabuchi, A., Mullaney, I., Sheard, P., Hessian, P., Zimmermann, A., Senoo, H., & Wheatley, A. M. (2004). Role of Hepatic Stellate Cells in the Early Phase of Liver Regeneration in Rat: Formation of Tight Adhesion to Parenchymal Cells. Comparative hepatology, 3S29. https://doi.org/10.1186/1476-5926-2-S1-S29
Mabuchi, Ayako, et al. "Role of Hepatic Stellate Cells in the Early Phase of Liver Regeneration in Rat: Formation of Tight Adhesion to Parenchymal Cells." Comparative hepatology vol. 3 (2004): S29. doi: https://doi.org/10.1186/1476-5926-2-S1-S29
Mabuchi A, Mullaney I, Sheard P, Hessian P, Zimmermann A, Senoo H, Wheatley AM. Role of Hepatic Stellate Cells in the Early Phase of Liver Regeneration in Rat: Formation of Tight Adhesion to Parenchymal Cells. Comp Hepatol. 2004 Jan 14;3:S29. doi: 10.1186/1476-5926-2-S1-S29. PMID: 14960181; PMCID: PMC2410248.
Copy Download .nbib Format: NLM
Use of deuterium labeling studies to determine the stereochemical outcome of palladium migrations during an asymmetric intermolecular Heck reaction.

The Journal of organic chemistry

Wheatley BM, Keay BA.
PMID: 17705545
J Org Chem. 2007 Sep 14;72(19):7253-9. doi: 10.1021/jo071119u. Epub 2007 Aug 18.

A series of deuterium labeling experiments showed that Pd migrations during an intermolecular asymmetric Heck reaction between phenyl triflate and various deuterated 2,3-dihydrofurans (2b, 2c, 2d, 2e) occurs exclusively by either syn-1,2-dyotropic shifts or a syn-chain-walking mechanism; no evidence...

Cite
Wheatley BM, Keay BA. Use of deuterium labeling studies to determine the stereochemical outcome of palladium migrations during an asymmetric intermolecular Heck reaction. J Org Chem. 2007;72(19):7253-9doi: 10.1021/jo071119u.
Wheatley, B. M., & Keay, B. A. (2007). Use of deuterium labeling studies to determine the stereochemical outcome of palladium migrations during an asymmetric intermolecular Heck reaction. The Journal of organic chemistry, 72(19), 7253-9. https://doi.org/10.1021/jo071119u
Wheatley, Bronwen M M, and Keay, Brian A. "Use of deuterium labeling studies to determine the stereochemical outcome of palladium migrations during an asymmetric intermolecular Heck reaction." The Journal of organic chemistry vol. 72,19 (2007): 7253-9. doi: https://doi.org/10.1021/jo071119u
Wheatley BM, Keay BA. Use of deuterium labeling studies to determine the stereochemical outcome of palladium migrations during an asymmetric intermolecular Heck reaction. J Org Chem. 2007 Sep 14;72(19):7253-9. doi: 10.1021/jo071119u. Epub 2007 Aug 18. PMID: 17705545.
Copy Download .nbib Format: NLM
Syntheses, structures and magnetic properties of Mn(II) dimers [CpMn(micro-X)]2(Cp = C5H5; X = RNH, R1R2N, C[triple bond]CR).

Dalton transactions (Cambridge, England : 2003)

Alvarez CS, Boss SR, Burley JC, Humphry SM, Layfield RA, Kowenicki RA, McPartlin M, Rawson JM, Wheatley AE, Wood PT, Wright DS.
PMID: 15510266
Dalton Trans. 2004 Nov 07;(21):3481-7. doi: 10.1039/B409135C. Epub 2004 Sep 21.

Manganocene, Cp(2)Mn, has been employed as a precursor in the synthesis of a range of Mn(II) dimers of the type [CpMn(micro-X)](2)[X = 8-NHC(9)H(6)N (1), N(Ph)(C(5)H(4)N)(2), N(4-EtC(6)H(4))(C(5)H(4)N)(3) and C[triple bond]CPh (4)] as well as the bis-adduct [Cp(2)Mn[HN=C(NMe(2))(2)](2)](5). The solid-state structures...

Cite
Alvarez CS, Boss SR, Burley JC, et al. Syntheses, structures and magnetic properties of Mn(II) dimers [CpMn(micro-X)]2(Cp = C5H5; X = RNH, R1R2N, C[triple bond]CR). Dalton Trans. 2004;(21):3481-7doi: 10.1039/B409135C.
Alvarez, C. S., Boss, S. R., Burley, J. C., Humphry, S. M., Layfield, R. A., Kowenicki, R. A., McPartlin, M., Rawson, J. M., Wheatley, A. E., Wood, P. T., & Wright, D. S. (2004). Syntheses, structures and magnetic properties of Mn(II) dimers [CpMn(micro-X)]2(Cp = C5H5; X = RNH, R1R2N, C[triple bond]CR). Dalton transactions (Cambridge, England : 2003), (21), 3481-7. https://doi.org/10.1039/B409135C
Alvarez, Carmen Soria, et al. "Syntheses, structures and magnetic properties of Mn(II) dimers [CpMn(micro-X)]2(Cp = C5H5; X = RNH, R1R2N, C[triple bond]CR)." Dalton transactions (Cambridge, England : 2003) vol. ,21 (2004): 3481-7. doi: https://doi.org/10.1039/B409135C
Alvarez CS, Boss SR, Burley JC, Humphry SM, Layfield RA, Kowenicki RA, McPartlin M, Rawson JM, Wheatley AE, Wood PT, Wright DS. Syntheses, structures and magnetic properties of Mn(II) dimers [CpMn(micro-X)]2(Cp = C5H5; X = RNH, R1R2N, C[triple bond]CR). Dalton Trans. 2004 Nov 07;(21):3481-7. doi: 10.1039/B409135C. Epub 2004 Sep 21. PMID: 15510266.
Copy Download .nbib Format: NLM
Limitations associated with the use of the pipelle sampler.

Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology

Heatley MK.
PMID: 15512127
J Obstet Gynaecol. 1998 Jul;18(4):398. doi: 10.1080/01443619867308.

No abstract available.

Cite
Heatley MK. Limitations associated with the use of the pipelle sampler. J Obstet Gynaecol. 1998;18(4):398doi: 10.1080/01443619867308.
Heatley, M. K. (1998). Limitations associated with the use of the pipelle sampler. Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology, 18(4), 398. https://doi.org/10.1080/01443619867308
Heatley, M K. "Limitations associated with the use of the pipelle sampler." Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology vol. 18,4 (1998): 398. doi: https://doi.org/10.1080/01443619867308
Heatley MK. Limitations associated with the use of the pipelle sampler. J Obstet Gynaecol. 1998 Jul;18(4):398. doi: 10.1080/01443619867308. PMID: 15512127.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 289 entries