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Showing 1 to 12 of 247 entries
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Servant Hearts.

Operative dentistry

Platt JA.
PMID: 26779674
Oper Dent. 2016 Jan-Feb;41(1):1. doi: 10.2341/1559-2863-41.1.1.

No abstract available.

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Platt JA. Servant Hearts. Oper Dent. 2016;41(1):1doi: 10.2341/1559-2863-41.1.1.
Platt, J. A. (2016). Servant Hearts. Operative dentistry, 41(1), 1. https://doi.org/10.2341/1559-2863-41.1.1
Platt, J A. "Servant Hearts." Operative dentistry vol. 41,1 (2016): 1. doi: https://doi.org/10.2341/1559-2863-41.1.1
Platt JA. Servant Hearts. Oper Dent. 2016 Jan-Feb;41(1):1. doi: 10.2341/1559-2863-41.1.1. PMID: 26779674.
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Corrigendum: Adiponectin receptor 1 conserves docosahexaenoic acid and promotes photoreceptor cell survival.

Nature communications

Rice DS, Calandria JM, Gordon WC, Jun B, Zhou Y, Gelfman CM, Li S, Jin M, Knott EJ, Chang B, Abuin A, Issa T, Potter D, Platt KA, Bazan NG.
PMID: 25962704
Nat Commun. 2015 May 12;6:7225. doi: 10.1038/ncomms8225.

No abstract available.

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Rice DS, Calandria JM, Gordon WC, et al. Corrigendum: Adiponectin receptor 1 conserves docosahexaenoic acid and promotes photoreceptor cell survival. Nat Commun. 2015;6:7225doi: 10.1038/ncomms8225.
Rice, D. S., Calandria, J. M., Gordon, W. C., Jun, B., Zhou, Y., Gelfman, C. M., Li, S., Jin, M., Knott, E. J., Chang, B., Abuin, A., Issa, T., Potter, D., Platt, K. A., & Bazan, N. G. (2015). Corrigendum: Adiponectin receptor 1 conserves docosahexaenoic acid and promotes photoreceptor cell survival. Nature communications, 67225. https://doi.org/10.1038/ncomms8225
Rice, Dennis S, et al. "Corrigendum: Adiponectin receptor 1 conserves docosahexaenoic acid and promotes photoreceptor cell survival." Nature communications vol. 6 (2015): 7225. doi: https://doi.org/10.1038/ncomms8225
Rice DS, Calandria JM, Gordon WC, Jun B, Zhou Y, Gelfman CM, Li S, Jin M, Knott EJ, Chang B, Abuin A, Issa T, Potter D, Platt KA, Bazan NG. Corrigendum: Adiponectin receptor 1 conserves docosahexaenoic acid and promotes photoreceptor cell survival. Nat Commun. 2015 May 12;6:7225. doi: 10.1038/ncomms8225. PMID: 25962704; PMCID: PMC4462836.
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Implications of muon anomalous magnetic moment for supersymmetric dark matter.

Physical review letters

Baltz EA, Gondolo P.
PMID: 11384406
Phys Rev Lett. 2001 May 28;86(22):5004-7. doi: 10.1103/PhysRevLett.86.5004.

The anomalous magnetic moment of the muon has recently been measured to be in conflict with the standard model prediction with an excess of 2.6sigma. Taking the excess at face value as a measurement of the supersymmetric contribution, we...

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Baltz EA, Gondolo P. Implications of muon anomalous magnetic moment for supersymmetric dark matter. Phys Rev Lett. 2001;86(22):5004-7doi: 10.1103/PhysRevLett.86.5004.
Baltz, E. A., & Gondolo, P. (2001). Implications of muon anomalous magnetic moment for supersymmetric dark matter. Physical review letters, 86(22), 5004-7. https://doi.org/10.1103/PhysRevLett.86.5004
Baltz, E A, and Gondolo, P. "Implications of muon anomalous magnetic moment for supersymmetric dark matter." Physical review letters vol. 86,22 (2001): 5004-7. doi: https://doi.org/10.1103/PhysRevLett.86.5004
Baltz EA, Gondolo P. Implications of muon anomalous magnetic moment for supersymmetric dark matter. Phys Rev Lett. 2001 May 28;86(22):5004-7. doi: 10.1103/PhysRevLett.86.5004. PMID: 11384406.
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Re: biologic and biochemical analyses of p16(INK4a) mutations from primary tumors.

Journal of the National Cancer Institute

Hansson J, Hashemi J, Linder S, Platz A.
PMID: 10793120
J Natl Cancer Inst. 2000 May 03;92(9):758A-759.

No abstract available.

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Hansson J, Hashemi J, Linder S, et al. Re: biologic and biochemical analyses of p16(INK4a) mutations from primary tumors. J Natl Cancer Inst. 2000;92(9):758A-759
Hansson, J., Hashemi, J., Linder, S., & Platz, A. (2000). Re: biologic and biochemical analyses of p16(INK4a) mutations from primary tumors. Journal of the National Cancer Institute, 92(9), 758A-759.
Hansson, et al. "Re: biologic and biochemical analyses of p16(INK4a) mutations from primary tumors." Journal of the National Cancer Institute vol. 92,9 (2000): 758A-759.
Hansson J, Hashemi J, Linder S, Platz A. Re: biologic and biochemical analyses of p16(INK4a) mutations from primary tumors. J Natl Cancer Inst. 2000 May 03;92(9):758A-759. PMID: 10793120.
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Evidence for specific solvation of two halocarbene amides.

Journal of the American Chemical Society

Tippmann EM, Platz MS, Svir IB, Klymenko OV.
PMID: 15125668
J Am Chem Soc. 2004 May 12;126(18):5750-62. doi: 10.1021/ja039693k.

Laser flash photolysis (LFP, 308 nm) of endo-10-halo-10'-N,N-dimethylcarboxamidetricyclo[4.3.1.0]-deca-2,4-diene (1Cl and 1F) releases indan and halocarbene amide (2Cl and 2F). Although the carbenes are not UV-vis active, they react rapidly with pyridine to form ylides (4Cl, 4F), which are readily...

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Tippmann EM, Platz MS, Svir IB, et al. Evidence for specific solvation of two halocarbene amides. J Am Chem Soc. 2004;126(18):5750-62doi: 10.1021/ja039693k.
Tippmann, E. M., Platz, M. S., Svir, I. B., & Klymenko, O. V. (2004). Evidence for specific solvation of two halocarbene amides. Journal of the American Chemical Society, 126(18), 5750-62. https://doi.org/10.1021/ja039693k
Tippmann, Eric M, et al. "Evidence for specific solvation of two halocarbene amides." Journal of the American Chemical Society vol. 126,18 (2004): 5750-62. doi: https://doi.org/10.1021/ja039693k
Tippmann EM, Platz MS, Svir IB, Klymenko OV. Evidence for specific solvation of two halocarbene amides. J Am Chem Soc. 2004 May 12;126(18):5750-62. doi: 10.1021/ja039693k. PMID: 15125668.
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Ultrafast carbene-carbene isomerization.

Journal of the American Chemical Society

Wang J, Burdzinski G, Kubicki J, Gustafson TL, Platz MS.
PMID: 18366167
J Am Chem Soc. 2008 Apr 23;130(16):5418-9. doi: 10.1021/ja8002827. Epub 2008 Mar 26.

The photochemistry of two isomeric aryl diazo ketones was investigated by fs time-resolved UV-vis and IR spectroscopies. Both diazo ketone excited states decompose in less than 300 fs by multiple pathways. One pathway involves concerted Wolff rearrangement and nitrogen...

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Wang J, Burdzinski G, Kubicki J, et al. Ultrafast carbene-carbene isomerization. J Am Chem Soc. 2008;130(16):5418-9doi: 10.1021/ja8002827.
Wang, J., Burdzinski, G., Kubicki, J., Gustafson, T. L., & Platz, M. S. (2008). Ultrafast carbene-carbene isomerization. Journal of the American Chemical Society, 130(16), 5418-9. https://doi.org/10.1021/ja8002827
Wang, Jin, et al. "Ultrafast carbene-carbene isomerization." Journal of the American Chemical Society vol. 130,16 (2008): 5418-9. doi: https://doi.org/10.1021/ja8002827
Wang J, Burdzinski G, Kubicki J, Gustafson TL, Platz MS. Ultrafast carbene-carbene isomerization. J Am Chem Soc. 2008 Apr 23;130(16):5418-9. doi: 10.1021/ja8002827. Epub 2008 Mar 26. PMID: 18366167.
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Reaction of benzoylnitrene with anions: formation of an intermediate in the Hofmann rearrangement.

Organic letters

Mandel SM, Platz MS.
PMID: 16288512
Org Lett. 2005 Nov 24;7(24):5385-7. doi: 10.1021/ol051985y.

[reaction: see text] Nucleophilic anions react rapidly with benzoylnitrene to form a species involved in the Hofmann rearrangement. This species has been detected by time-resolved infrared spectroscopy.

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Mandel SM, Platz MS. Reaction of benzoylnitrene with anions: formation of an intermediate in the Hofmann rearrangement. Org Lett. 2005;7(24):5385-7doi: 10.1021/ol051985y.
Mandel, S. M., & Platz, M. S. (2005). Reaction of benzoylnitrene with anions: formation of an intermediate in the Hofmann rearrangement. Organic letters, 7(24), 5385-7. https://doi.org/10.1021/ol051985y
Mandel, Sarah M, and Platz, Matthew S. "Reaction of benzoylnitrene with anions: formation of an intermediate in the Hofmann rearrangement." Organic letters vol. 7,24 (2005): 5385-7. doi: https://doi.org/10.1021/ol051985y
Mandel SM, Platz MS. Reaction of benzoylnitrene with anions: formation of an intermediate in the Hofmann rearrangement. Org Lett. 2005 Nov 24;7(24):5385-7. doi: 10.1021/ol051985y. PMID: 16288512.
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Circular dichroism spectra and the molecular arrangement of bacteriochlorophylls in the reaction centers of photosynthetic bacteria.

Proceedings of the National Academy of Sciences of the United States of America

Sauer K, Dratz EA, Coyne L.
PMID: 16591686
Proc Natl Acad Sci U S A. 1968 Sep;61(1):17-24. doi: 10.1073/pnas.61.1.17.

No abstract available.

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Sauer K, Dratz EA, Coyne L. Circular dichroism spectra and the molecular arrangement of bacteriochlorophylls in the reaction centers of photosynthetic bacteria. Proc Natl Acad Sci U S A. 1968;61(1):17-24doi: 10.1073/pnas.61.1.17.
Sauer, K., Dratz, E. A., & Coyne, L. (1968). Circular dichroism spectra and the molecular arrangement of bacteriochlorophylls in the reaction centers of photosynthetic bacteria. Proceedings of the National Academy of Sciences of the United States of America, 61(1), 17-24. https://doi.org/10.1073/pnas.61.1.17
Sauer, K, et al. "Circular dichroism spectra and the molecular arrangement of bacteriochlorophylls in the reaction centers of photosynthetic bacteria." Proceedings of the National Academy of Sciences of the United States of America vol. 61,1 (1968): 17-24. doi: https://doi.org/10.1073/pnas.61.1.17
Sauer K, Dratz EA, Coyne L. Circular dichroism spectra and the molecular arrangement of bacteriochlorophylls in the reaction centers of photosynthetic bacteria. Proc Natl Acad Sci U S A. 1968 Sep;61(1):17-24. doi: 10.1073/pnas.61.1.17. PMID: 16591686; PMCID: PMC285898.
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Study of singlet and triplet 2,6-difluorophenylnitrene by time-resolved infrared spectroscopy.

The journal of physical chemistry. A

Mandel S, Liu J, Hadad CM, Platz MS.
PMID: 16833595
J Phys Chem A. 2005 Mar 31;109(12):2816-21. doi: 10.1021/jp045254b.

The solution-phase photochemistry of 2,6-difluorophenyl azide was studied by time-resolved infrared (TRIR) spectroscopy. A vibrational band of singlet 2,6-difluorophenyl nitrene (1N) was observed at 1404 cm(-1) between 243 and 283 K. At ambient temperature, it was not possible to...

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Mandel S, Liu J, Hadad CM, et al. Study of singlet and triplet 2,6-difluorophenylnitrene by time-resolved infrared spectroscopy. J Phys Chem A. 2005;109(12):2816-21doi: 10.1021/jp045254b.
Mandel, S., Liu, J., Hadad, C. M., & Platz, M. S. (2005). Study of singlet and triplet 2,6-difluorophenylnitrene by time-resolved infrared spectroscopy. The journal of physical chemistry. A, 109(12), 2816-21. https://doi.org/10.1021/jp045254b
Mandel, Sarah, et al. "Study of singlet and triplet 2,6-difluorophenylnitrene by time-resolved infrared spectroscopy." The journal of physical chemistry. A vol. 109,12 (2005): 2816-21. doi: https://doi.org/10.1021/jp045254b
Mandel S, Liu J, Hadad CM, Platz MS. Study of singlet and triplet 2,6-difluorophenylnitrene by time-resolved infrared spectroscopy. J Phys Chem A. 2005 Mar 31;109(12):2816-21. doi: 10.1021/jp045254b. PMID: 16833595.
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Some Properties of Phytochrome Isolated From Dark-grown Oat Seedlings (Avena sativa L.).

Plant physiology

Briggs WR, Zollinger WD, Platz BB.
PMID: 16656907
Plant Physiol. 1968 Aug;43(8):1239-43. doi: 10.1104/pp.43.8.1239.

Phytochrome was partially purified from etiolated seedlings of Avena sativa L. Several properties of the red-absorbing (P(R)) and far-red absorbing (P(FR)) forms of the pigment were compared. The 2 forms could not be shown to differ with respect to...

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Briggs WR, Zollinger WD, Platz BB. Some Properties of Phytochrome Isolated From Dark-grown Oat Seedlings (Avena sativa L.). Plant Physiol. 1968;43(8):1239-43doi: 10.1104/pp.43.8.1239.
Briggs, W. R., Zollinger, W. D., & Platz, B. B. (1968). Some Properties of Phytochrome Isolated From Dark-grown Oat Seedlings (Avena sativa L.). Plant physiology, 43(8), 1239-43. https://doi.org/10.1104/pp.43.8.1239
Briggs, W R, et al. "Some Properties of Phytochrome Isolated From Dark-grown Oat Seedlings (Avena sativa L.)." Plant physiology vol. 43,8 (1968): 1239-43. doi: https://doi.org/10.1104/pp.43.8.1239
Briggs WR, Zollinger WD, Platz BB. Some Properties of Phytochrome Isolated From Dark-grown Oat Seedlings (Avena sativa L.). Plant Physiol. 1968 Aug;43(8):1239-43. doi: 10.1104/pp.43.8.1239. PMID: 16656907; PMCID: PMC1087000.
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Ultrafast study of the photochemistry of 2-azidonitrobenzene.

Organic letters

McCulla RD, Burdzinski G, Platz MS.
PMID: 16597129
Org Lett. 2006 Apr 13;8(8):1637-40. doi: 10.1021/ol0602452.

[reaction: see text] Ultrafast time-resolved studies of the photochemistry of 2-azidonitrobenzene demonstrate that the lifetimes of excited singlet 2-azidonitrobenzene and 2-nitrophenylnitrene are 500 fs and 8.3 ps, respectively, in solution at ambient temperature. The singlet nitrene is a discrete...

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McCulla RD, Burdzinski G, Platz MS. Ultrafast study of the photochemistry of 2-azidonitrobenzene. Org Lett. 2006;8(8):1637-40doi: 10.1021/ol0602452.
McCulla, R. D., Burdzinski, G., & Platz, M. S. (2006). Ultrafast study of the photochemistry of 2-azidonitrobenzene. Organic letters, 8(8), 1637-40. https://doi.org/10.1021/ol0602452
McCulla, Ryan D, et al. "Ultrafast study of the photochemistry of 2-azidonitrobenzene." Organic letters vol. 8,8 (2006): 1637-40. doi: https://doi.org/10.1021/ol0602452
McCulla RD, Burdzinski G, Platz MS. Ultrafast study of the photochemistry of 2-azidonitrobenzene. Org Lett. 2006 Apr 13;8(8):1637-40. doi: 10.1021/ol0602452. PMID: 16597129.
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Ultrafast spectroscopy of arylchlorodiazirines: Hammett correlations of excited state lifetimes.

Journal of the American Chemical Society

Zhang Y, Wang L, Moss RA, Platz MS.
PMID: 19883052
J Am Chem Soc. 2009 Nov 25;131(46):16652-3. doi: 10.1021/ja907915z.

Experimental and computational studies suggest that 375 nm excitation of arylchlorodiazirines furnishes their S(1) excited states with lengthened C-N bonds, a positive charge at the para and diazirine carbon atoms, and a negative charge at the nitrogen atoms. These...

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Zhang Y, Wang L, Moss RA, et al. Ultrafast spectroscopy of arylchlorodiazirines: Hammett correlations of excited state lifetimes. J Am Chem Soc. 2009;131(46):16652-3doi: 10.1021/ja907915z.
Zhang, Y., Wang, L., Moss, R. A., & Platz, M. S. (2009). Ultrafast spectroscopy of arylchlorodiazirines: Hammett correlations of excited state lifetimes. Journal of the American Chemical Society, 131(46), 16652-3. https://doi.org/10.1021/ja907915z
Zhang, Yunlong, et al. "Ultrafast spectroscopy of arylchlorodiazirines: Hammett correlations of excited state lifetimes." Journal of the American Chemical Society vol. 131,46 (2009): 16652-3. doi: https://doi.org/10.1021/ja907915z
Zhang Y, Wang L, Moss RA, Platz MS. Ultrafast spectroscopy of arylchlorodiazirines: Hammett correlations of excited state lifetimes. J Am Chem Soc. 2009 Nov 25;131(46):16652-3. doi: 10.1021/ja907915z. PMID: 19883052.
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Showing 1 to 12 of 247 entries