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Can academic distress be predicted prior to dental school.

The Journal of the American College of Dentists

Horton PS.
PMID: 274480
J Am Coll Dent. 1978 Apr;45(2):111-9.

No abstract available.

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Horton PS. Can academic distress be predicted prior to dental school. J Am Coll Dent. 1978;45(2):111-9
Horton, P. S. (1978). Can academic distress be predicted prior to dental school. The Journal of the American College of Dentists, 45(2), 111-9.
Horton, P S. "Can academic distress be predicted prior to dental school." The Journal of the American College of Dentists vol. 45,2 (1978): 111-9.
Horton PS. Can academic distress be predicted prior to dental school. J Am Coll Dent. 1978 Apr;45(2):111-9. PMID: 274480.
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Crystal structure of 2-amino-7-hy-droxy-4-(4-hy-droxy-phen-yl)-4H-chromene-3-carbo-nitrile.

Acta crystallographica. Section E, Crystallographic communications

Horton PN, Akkurt M, Mohamed SK, Younes SH, Albayati MR.
PMID: 26396789
Acta Crystallogr E Crystallogr Commun. 2015 Jul 08;71:o546-7. doi: 10.1107/S2056989015012815. eCollection 2015 Aug 01.

In the title compound, C16H12N2O3, the chromene ring system is nearly planar [maximum deviation from the mean plane = 0.057 (1) Å], and is almost perpendicular to the benzene ring, with a dihedral angle of 85.29 (5)°. In the...

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Horton PN, Akkurt M, Mohamed SK, et al. Crystal structure of 2-amino-7-hy-droxy-4-(4-hy-droxy-phen-yl)-4H-chromene-3-carbo-nitrile. Acta Crystallogr E Crystallogr Commun. 2015;71:o546-7doi: 10.1107/S2056989015012815.
Horton, P. N., Akkurt, M., Mohamed, S. K., Younes, S. H., & Albayati, M. R. (2015). Crystal structure of 2-amino-7-hy-droxy-4-(4-hy-droxy-phen-yl)-4H-chromene-3-carbo-nitrile. Acta crystallographica. Section E, Crystallographic communications, 71o546-7. https://doi.org/10.1107/S2056989015012815
Horton, Peter N, et al. "Crystal structure of 2-amino-7-hy-droxy-4-(4-hy-droxy-phen-yl)-4H-chromene-3-carbo-nitrile." Acta crystallographica. Section E, Crystallographic communications vol. 71 (2015): o546-7. doi: https://doi.org/10.1107/S2056989015012815
Horton PN, Akkurt M, Mohamed SK, Younes SH, Albayati MR. Crystal structure of 2-amino-7-hy-droxy-4-(4-hy-droxy-phen-yl)-4H-chromene-3-carbo-nitrile. Acta Crystallogr E Crystallogr Commun. 2015 Jul 08;71:o546-7. doi: 10.1107/S2056989015012815. eCollection 2015 Aug 01. PMID: 26396789; PMCID: PMC4571389.
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Chromophore-labelled, luminescent platinum complexes: syntheses, structures, and spectroscopic properties.

Dalton transactions (Cambridge, England : 2003)

Stacey OJ, Ward BD, Coles SJ, Horton PN, Pope SJ.
PMID: 27241625
Dalton Trans. 2016 Jun 21;45(25):10297-307. doi: 10.1039/c6dt01335j.

Ligands based upon 4-carboxamide-2-phenylquinoline derivatives have been synthesised with solubilising octyl hydrocarbon chains and tethered aromatic chromophores to give naphthyl (), anthracenyl () and pyrenyl () ligand variants, together with a non-chromophoric analogue () for comparison. (1)H NMR spectroscopic...

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Stacey OJ, Ward BD, Coles SJ, et al. Chromophore-labelled, luminescent platinum complexes: syntheses, structures, and spectroscopic properties. Dalton Trans. 2016;45(25):10297-307doi: 10.1039/c6dt01335j.
Stacey, O. J., Ward, B. D., Coles, S. J., Horton, P. N., & Pope, S. J. (2016). Chromophore-labelled, luminescent platinum complexes: syntheses, structures, and spectroscopic properties. Dalton transactions (Cambridge, England : 2003), 45(25), 10297-307. https://doi.org/10.1039/c6dt01335j
Stacey, Oliver J, et al. "Chromophore-labelled, luminescent platinum complexes: syntheses, structures, and spectroscopic properties." Dalton transactions (Cambridge, England : 2003) vol. 45,25 (2016): 10297-307. doi: https://doi.org/10.1039/c6dt01335j
Stacey OJ, Ward BD, Coles SJ, Horton PN, Pope SJ. Chromophore-labelled, luminescent platinum complexes: syntheses, structures, and spectroscopic properties. Dalton Trans. 2016 Jun 21;45(25):10297-307. doi: 10.1039/c6dt01335j. PMID: 27241625.
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From Ligand to Phosphor: Rapid, Machine-Assisted Synthesis of Substituted Iridium(III) Pyrazolate Complexes with Tuneable Luminescence.

Chemistry (Weinheim an der Bergstrasse, Germany)

Groves LM, Schotten C, Beames J, Platts JA, Coles SJ, Horton PN, Browne DL, Pope SJA.
PMID: 28543913
Chemistry. 2017 Jul 12;23(39):9407-9418. doi: 10.1002/chem.201701551. Epub 2017 Jun 21.

A first-generation machine-assisted approach towards the preparation of hybrid ligand/metal materials has been developed. A comparison of synthetic approaches demonstrates that incorporation of both flow chemistry and microwave heating can be successfully applied to the rapid synthesis of a...

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Groves LM, Schotten C, Beames J, et al. From Ligand to Phosphor: Rapid, Machine-Assisted Synthesis of Substituted Iridium(III) Pyrazolate Complexes with Tuneable Luminescence. Chemistry. 2017;23(39):9407-9418doi: 10.1002/chem.201701551.
Groves, L. M., Schotten, C., Beames, J., Platts, J. A., Coles, S. J., Horton, P. N., Browne, D. L., & Pope, S. J. A. (2017). From Ligand to Phosphor: Rapid, Machine-Assisted Synthesis of Substituted Iridium(III) Pyrazolate Complexes with Tuneable Luminescence. Chemistry (Weinheim an der Bergstrasse, Germany), 23(39), 9407-9418. https://doi.org/10.1002/chem.201701551
Groves, Lara M, et al. "From Ligand to Phosphor: Rapid, Machine-Assisted Synthesis of Substituted Iridium(III) Pyrazolate Complexes with Tuneable Luminescence." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 23,39 (2017): 9407-9418. doi: https://doi.org/10.1002/chem.201701551
Groves LM, Schotten C, Beames J, Platts JA, Coles SJ, Horton PN, Browne DL, Pope SJA. From Ligand to Phosphor: Rapid, Machine-Assisted Synthesis of Substituted Iridium(III) Pyrazolate Complexes with Tuneable Luminescence. Chemistry. 2017 Jul 12;23(39):9407-9418. doi: 10.1002/chem.201701551. Epub 2017 Jun 21. PMID: 28543913.
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The relationship between Photosystem II intrinsic quantum yield and millisecond luminescence in thylakoids.

Photosynthesis research

Rees D, Horton P, Schreiber U.
PMID: 24317709
Photosynth Res. 1993 Aug;37(2):131-8. doi: 10.1007/BF02187471.

The relationship between charge recombination at Photosystem II (PS II), as indicated by millisecond luminescence, and PS II quantum yield was studied in spinach thylakoids during electron flow to methylviologen. Under the low magnesium conditions used, a decrease in...

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Rees D, Horton P, Schreiber U. The relationship between Photosystem II intrinsic quantum yield and millisecond luminescence in thylakoids. Photosynth Res. 1993;37(2):131-8doi: 10.1007/BF02187471.
Rees, D., Horton, P., & Schreiber, U. (1993). The relationship between Photosystem II intrinsic quantum yield and millisecond luminescence in thylakoids. Photosynthesis research, 37(2), 131-8. https://doi.org/10.1007/BF02187471
Rees, D, et al. "The relationship between Photosystem II intrinsic quantum yield and millisecond luminescence in thylakoids." Photosynthesis research vol. 37,2 (1993): 131-8. doi: https://doi.org/10.1007/BF02187471
Rees D, Horton P, Schreiber U. The relationship between Photosystem II intrinsic quantum yield and millisecond luminescence in thylakoids. Photosynth Res. 1993 Aug;37(2):131-8. doi: 10.1007/BF02187471. PMID: 24317709.
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Generation of oscillatory behavior in the Laisk model of photosynthetic carbon assimilation.

Photosynthesis research

Horton P, Nicholson H.
PMID: 24435636
Photosynth Res. 1987 Jan;12(2):129-43. doi: 10.1007/BF00047943.

The metabolic pathways in photosynthesis are modelled as an interconnected series of chemical reactions representing the electron transfer system, the carbon reduction cycle and starch and sucrose synthesis according to the model of Laisk and Walker [Proc R Soc...

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Horton P, Nicholson H. Generation of oscillatory behavior in the Laisk model of photosynthetic carbon assimilation. Photosynth Res. 1987;12(2):129-43doi: 10.1007/BF00047943.
Horton, P., & Nicholson, H. (1987). Generation of oscillatory behavior in the Laisk model of photosynthetic carbon assimilation. Photosynthesis research, 12(2), 129-43. https://doi.org/10.1007/BF00047943
Horton, P, and Nicholson, H. "Generation of oscillatory behavior in the Laisk model of photosynthetic carbon assimilation." Photosynthesis research vol. 12,2 (1987): 129-43. doi: https://doi.org/10.1007/BF00047943
Horton P, Nicholson H. Generation of oscillatory behavior in the Laisk model of photosynthetic carbon assimilation. Photosynth Res. 1987 Jan;12(2):129-43. doi: 10.1007/BF00047943. PMID: 24435636.
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Ultrasound-detectable grey scale synovitis predicts future fulfilment of the 2010 ACR/EULAR RA classification criteria in patients with new-onset undifferentiated arthritis.

RMD open

Horton SC, Tan AL, Wakefield RJ, Freeston JE, Buch MH, Emery P.
PMID: 28469936
RMD Open. 2017 Mar 30;3(1):e000394. doi: 10.1136/rmdopen-2016-000394. eCollection 2017.

OBJECTIVE: To determine the clinical outcomes for patients with new-onset undifferentiated arthritis (UA), not fulfilling the 2010 American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) rheumatoid arthritis (RA) classification criteria, and the clinical and imaging predictors of disease...

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Horton SC, Tan AL, Wakefield RJ, et al. Ultrasound-detectable grey scale synovitis predicts future fulfilment of the 2010 ACR/EULAR RA classification criteria in patients with new-onset undifferentiated arthritis. RMD Open. 2017;3(1):e000394doi: 10.1136/rmdopen-2016-000394.
Horton, S. C., Tan, A. L., Wakefield, R. J., Freeston, J. E., Buch, M. H., & Emery, P. (2017). Ultrasound-detectable grey scale synovitis predicts future fulfilment of the 2010 ACR/EULAR RA classification criteria in patients with new-onset undifferentiated arthritis. RMD open, 3(1), e000394. https://doi.org/10.1136/rmdopen-2016-000394
Horton, Sarah C, et al. "Ultrasound-detectable grey scale synovitis predicts future fulfilment of the 2010 ACR/EULAR RA classification criteria in patients with new-onset undifferentiated arthritis." RMD open vol. 3,1 (2017): e000394. doi: https://doi.org/10.1136/rmdopen-2016-000394
Horton SC, Tan AL, Wakefield RJ, Freeston JE, Buch MH, Emery P. Ultrasound-detectable grey scale synovitis predicts future fulfilment of the 2010 ACR/EULAR RA classification criteria in patients with new-onset undifferentiated arthritis. RMD Open. 2017 Mar 30;3(1):e000394. doi: 10.1136/rmdopen-2016-000394. eCollection 2017. PMID: 28469936; PMCID: PMC5387989.
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An Investigation of the Sustained Component of Nonphotochemical Quenching of Chlorophyll Fluorescence in Isolated Chloroplasts and Leaves of Spinach.

Plant physiology

Ruban AV, Horton P.
PMID: 12228504
Plant Physiol. 1995 Jun;108(2):721-726. doi: 10.1104/pp.108.2.721.

The slowly reversible component of nonphotochemical quenching of Chl fluorescence, ql, has been investigated in intact leaves and chloroplasts of spinach (Spinacia oleracea). In leaves, between 50 and 100% of ql (defined as the quenching that remained after at...

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Ruban AV, Horton P. An Investigation of the Sustained Component of Nonphotochemical Quenching of Chlorophyll Fluorescence in Isolated Chloroplasts and Leaves of Spinach. Plant Physiol. 1995;108(2):721-726doi: 10.1104/pp.108.2.721.
Ruban, A. V., & Horton, P. (1995). An Investigation of the Sustained Component of Nonphotochemical Quenching of Chlorophyll Fluorescence in Isolated Chloroplasts and Leaves of Spinach. Plant physiology, 108(2), 721-726. https://doi.org/10.1104/pp.108.2.721
Ruban, A. V., and Horton, P.. "An Investigation of the Sustained Component of Nonphotochemical Quenching of Chlorophyll Fluorescence in Isolated Chloroplasts and Leaves of Spinach." Plant physiology vol. 108,2 (1995): 721-726. doi: https://doi.org/10.1104/pp.108.2.721
Ruban AV, Horton P. An Investigation of the Sustained Component of Nonphotochemical Quenching of Chlorophyll Fluorescence in Isolated Chloroplasts and Leaves of Spinach. Plant Physiol. 1995 Jun;108(2):721-726. doi: 10.1104/pp.108.2.721. PMID: 12228504; PMCID: PMC157393.
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Dynamics of Xanthophyll-Cycle Activity in Different Antenna Subcomplexes in the Photosynthetic Membranes of Higher Plants (The Relationship between Zeaxanthin Conversion and Nonphotochemical Fluorescence Quenching).

Plant physiology

Farber A, Young AJ, Ruban AV, Horton P, Jahns P.
PMID: 12223884
Plant Physiol. 1997 Dec;115(4):1609-1618. doi: 10.1104/pp.115.4.1609.

The generation of nonphotochemical quenching of chlorophyll fluorescence (qN) in the antenna of photosystem II (PSII) is accompanied by the de-epoxidation of violaxanthin to antheraxanthin and zeaxanthin. The function of zeaxanthin in two mechanisms of qN, energy-dependent quenching (qE)...

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Farber A, Young AJ, Ruban AV, et al. Dynamics of Xanthophyll-Cycle Activity in Different Antenna Subcomplexes in the Photosynthetic Membranes of Higher Plants (The Relationship between Zeaxanthin Conversion and Nonphotochemical Fluorescence Quenching). Plant Physiol. 1997;115(4):1609-1618doi: 10.1104/pp.115.4.1609.
Farber, A., Young, A. J., Ruban, A. V., Horton, P., & Jahns, P. (1997). Dynamics of Xanthophyll-Cycle Activity in Different Antenna Subcomplexes in the Photosynthetic Membranes of Higher Plants (The Relationship between Zeaxanthin Conversion and Nonphotochemical Fluorescence Quenching). Plant physiology, 115(4), 1609-1618. https://doi.org/10.1104/pp.115.4.1609
Farber, A., et al. "Dynamics of Xanthophyll-Cycle Activity in Different Antenna Subcomplexes in the Photosynthetic Membranes of Higher Plants (The Relationship between Zeaxanthin Conversion and Nonphotochemical Fluorescence Quenching)." Plant physiology vol. 115,4 (1997): 1609-1618. doi: https://doi.org/10.1104/pp.115.4.1609
Farber A, Young AJ, Ruban AV, Horton P, Jahns P. Dynamics of Xanthophyll-Cycle Activity in Different Antenna Subcomplexes in the Photosynthetic Membranes of Higher Plants (The Relationship between Zeaxanthin Conversion and Nonphotochemical Fluorescence Quenching). Plant Physiol. 1997 Dec;115(4):1609-1618. doi: 10.1104/pp.115.4.1609. PMID: 12223884; PMCID: PMC158627.
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Practical synthesis of chiral vinylphosphine oxides by direct nucleophilic substitution. Stereodivergent synthesis of aminophosphine ligands.

The Journal of organic chemistry

Oliana M, King F, Horton PN, Hursthouse MB, Hii KK.
PMID: 16526799
J Org Chem. 2006 Mar 17;71(6):2472-9. doi: 10.1021/jo052575q.

[reaction: see text] A practical synthesis of optically pure alkylphenylvinylphosphine oxides is described, utilizing a nucleophilic displacement at phosphorus to install the vinyl moiety. The products were used to prepare classes of P-stereogenic aminophosphine (PN) and aminohydroxyphosphine (PNO) ligands....

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Oliana M, King F, Horton PN, et al. Practical synthesis of chiral vinylphosphine oxides by direct nucleophilic substitution. Stereodivergent synthesis of aminophosphine ligands. J Org Chem. 2006;71(6):2472-9doi: 10.1021/jo052575q.
Oliana, M., King, F., Horton, P. N., Hursthouse, M. B., & Hii, K. K. (2006). Practical synthesis of chiral vinylphosphine oxides by direct nucleophilic substitution. Stereodivergent synthesis of aminophosphine ligands. The Journal of organic chemistry, 71(6), 2472-9. https://doi.org/10.1021/jo052575q
Oliana, Marco, et al. "Practical synthesis of chiral vinylphosphine oxides by direct nucleophilic substitution. Stereodivergent synthesis of aminophosphine ligands." The Journal of organic chemistry vol. 71,6 (2006): 2472-9. doi: https://doi.org/10.1021/jo052575q
Oliana M, King F, Horton PN, Hursthouse MB, Hii KK. Practical synthesis of chiral vinylphosphine oxides by direct nucleophilic substitution. Stereodivergent synthesis of aminophosphine ligands. J Org Chem. 2006 Mar 17;71(6):2472-9. doi: 10.1021/jo052575q. PMID: 16526799.
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VITAMIN A AND CAROTENE. II. VITAMIN A AND CAROTENE METABOLISM IN DIABETICS AND NORMALS.

The Journal of clinical investigation

Murrill WA, Horton PB, Leiberman E, Newburgh LH.
PMID: 16694847
J Clin Invest. 1941 Jul;20(4):395-400. doi: 10.1172/JCI101234.

No abstract available.

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Murrill WA, Horton PB, Leiberman E, et al. VITAMIN A AND CAROTENE. II. VITAMIN A AND CAROTENE METABOLISM IN DIABETICS AND NORMALS. J Clin Invest. 1941;20(4):395-400doi: 10.1172/JCI101234.
Murrill, W. A., Horton, P. B., Leiberman, E., & Newburgh, L. H. (1941). VITAMIN A AND CAROTENE. II. VITAMIN A AND CAROTENE METABOLISM IN DIABETICS AND NORMALS. The Journal of clinical investigation, 20(4), 395-400. https://doi.org/10.1172/JCI101234
Murrill, W A, et al. "VITAMIN A AND CAROTENE. II. VITAMIN A AND CAROTENE METABOLISM IN DIABETICS AND NORMALS." The Journal of clinical investigation vol. 20,4 (1941): 395-400. doi: https://doi.org/10.1172/JCI101234
Murrill WA, Horton PB, Leiberman E, Newburgh LH. VITAMIN A AND CAROTENE. II. VITAMIN A AND CAROTENE METABOLISM IN DIABETICS AND NORMALS. J Clin Invest. 1941 Jul;20(4):395-400. doi: 10.1172/JCI101234. PMID: 16694847; PMCID: PMC435071.
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Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions.

Dalton transactions (Cambridge, England : 2003)

Dervisi A, Koursarou D, Ooi LL, Horton PN, Hursthouse MB.
PMID: 17146536
Dalton Trans. 2006 Dec 28;(48):5717-24. doi: 10.1039/b609607g. Epub 2006 Oct 18.

The synthesis of the benzyl phosphinothioether derivatives Ph(2)PCH(2)CH(Et)SR and their corresponding palladium complexes are reported, where R = CH(2)Ph, R = CH(2)-3,5-Me-C(6)H(3) and R = 1-CH(2)C(10)H(7)(5). Crystallographic data obtained for the complexes Pd(3)Cl(2) and Pd(4)Cl(2) show intra- and inter-molecular...

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Dervisi A, Koursarou D, Ooi LL, et al. Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions. Dalton Trans. 2006;(48):5717-24doi: 10.1039/b609607g.
Dervisi, A., Koursarou, D., Ooi, L. L., Horton, P. N., & Hursthouse, M. B. (2006). Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions. Dalton transactions (Cambridge, England : 2003), (48), 5717-24. https://doi.org/10.1039/b609607g
Dervisi, Athanasia, et al. "Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions." Dalton transactions (Cambridge, England : 2003) vol. ,48 (2006): 5717-24. doi: https://doi.org/10.1039/b609607g
Dervisi A, Koursarou D, Ooi LL, Horton PN, Hursthouse MB. Synthesis and characterisation of benzyl phosphino-thioether and -thiolato Pd(II) complexes and their applications in Suzuki coupling reactions. Dalton Trans. 2006 Dec 28;(48):5717-24. doi: 10.1039/b609607g. Epub 2006 Oct 18. PMID: 17146536.
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Showing 1 to 12 of 325 entries