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The construction of professional identity

professional

Caza BB, Creary S.
GSID: YwMHifsa0lwJ
BB Caza, S Creary - Perspectives on contemporary professional …, 2016 - elgaronline.com

… In the next section we discuss professional identities … professional identity around multiple professional bases. Finally, we discuss the implications for the modern form of professional …

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Caza, B. B., & Creary, S. (2016). The construction of professional identity. In Perspectives on contemporary professional work. Edward Elgar Publishing.
Caza, Brianna Barker, and Stephanie Creary. "The construction of professional identity." Perspectives on contemporary professional work. Edward Elgar Publishing, 2016.
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Testicular and epididymal toxicity: Pathogenesis and potential mechanisms of toxicity.

Spermatogenesis

Creasy DM, Chapin RE.
PMID: 26413392
Spermatogenesis. 2015 Jan 13;4(2):e1005511. doi: 10.1080/21565562.2014.1005511. eCollection 2014.

No abstract available.

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Creasy DM, Chapin RE. Testicular and epididymal toxicity: Pathogenesis and potential mechanisms of toxicity. Spermatogenesis. 2015;4(2):e1005511doi: 10.1080/21565562.2014.1005511.
Creasy, D. M., & Chapin, R. E. (2014). Testicular and epididymal toxicity: Pathogenesis and potential mechanisms of toxicity. Spermatogenesis, 4(2), e1005511. https://doi.org/10.1080/21565562.2014.1005511
Creasy, D M, and Chapin, R E. "Testicular and epididymal toxicity: Pathogenesis and potential mechanisms of toxicity." Spermatogenesis vol. 4,2 (2014): e1005511. doi: https://doi.org/10.1080/21565562.2014.1005511
Creasy DM, Chapin RE. Testicular and epididymal toxicity: Pathogenesis and potential mechanisms of toxicity. Spermatogenesis. 2015 Jan 13;4(2):e1005511. doi: 10.1080/21565562.2014.1005511. eCollection 2014. PMID: 26413392; PMCID: PMC4581047.
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THE DISTRIBUTION OF LIFE-HISTORY VARIATION IN THE DAPHNIA PULEX COMPLEX.

Evolution; international journal of organic evolution

Lynch M, Spitze K, Crease T.
PMID: 28564335
Evolution. 1989 Dec;43(8):1724-1736. doi: 10.1111/j.1558-5646.1989.tb02622.x.

In the midwestern United States the Daphnia pulex complex consists of a mosaic of sexual and asexual populations, providing a useful model system for studying the evolutionary forces underlying the maintenance of sex. One asexual and two sexual populations...

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Lynch M, Spitze K, Crease T. THE DISTRIBUTION OF LIFE-HISTORY VARIATION IN THE DAPHNIA PULEX COMPLEX. Evolution. 1989;43(8):1724-1736doi: 10.1111/j.1558-5646.1989.tb02622.x.
Lynch, M., Spitze, K., & Crease, T. (1989). THE DISTRIBUTION OF LIFE-HISTORY VARIATION IN THE DAPHNIA PULEX COMPLEX. Evolution; international journal of organic evolution, 43(8), 1724-1736. https://doi.org/10.1111/j.1558-5646.1989.tb02622.x
Lynch, Michael, et al. "THE DISTRIBUTION OF LIFE-HISTORY VARIATION IN THE DAPHNIA PULEX COMPLEX." Evolution; international journal of organic evolution vol. 43,8 (1989): 1724-1736. doi: https://doi.org/10.1111/j.1558-5646.1989.tb02622.x
Lynch M, Spitze K, Crease T. THE DISTRIBUTION OF LIFE-HISTORY VARIATION IN THE DAPHNIA PULEX COMPLEX. Evolution. 1989 Dec;43(8):1724-1736. doi: 10.1111/j.1558-5646.1989.tb02622.x. PMID: 28564335.
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Corrigendum.

Parasitology today (Personal ed.)

Creasey A.
PMID: 10377535
Parasitol Today. 1999 Jul;15(7):300. doi: 10.1016/s0169-4758(99)01475-1.

No abstract available.

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Creasey A. Corrigendum. Parasitol Today. 1999;15(7):300doi: 10.1016/s0169-4758(99)01475-1.
Creasey, A. (1999). Corrigendum. Parasitology today (Personal ed.), 15(7), 300. https://doi.org/10.1016/s0169-4758(99)01475-1
Creasey. "Corrigendum." Parasitology today (Personal ed.) vol. 15,7 (1999): 300. doi: https://doi.org/10.1016/s0169-4758(99)01475-1
Creasey A. Corrigendum. Parasitol Today. 1999 Jul;15(7):300. doi: 10.1016/s0169-4758(99)01475-1. PMID: 10377535.
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Methylenecyclopropane Rearrangement as a Probe for Free Radical Substituent Effects. sigma (*) Values for Potent Radical-Stabilizing Nitrogen-Containing Substituents.

The Journal of organic chemistry

Creary X, Engel PS, Kavaluskas N, Pan L, Wolf A.
PMID: 11674633
J Org Chem. 1999 Jul 23;64(15):5634-5643. doi: 10.1021/jo990732d.

A series of nitrogen-containing 2-aryl-3,3-dimethylmethylenecyclopropanes have been prepared and rearrangement rates to the corresponding 2-arylisopropylidenecyclopropanes have been measured. These rates are dependent on the nature of the nitrogen-containing group in the para-position of the aryl group. Rearrangement rates have...

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Creary X, Engel PS, Kavaluskas N, et al. Methylenecyclopropane Rearrangement as a Probe for Free Radical Substituent Effects. sigma (*) Values for Potent Radical-Stabilizing Nitrogen-Containing Substituents. J Org Chem. 1999;64(15):5634-5643doi: 10.1021/jo990732d.
Creary, X., Engel, P. S., Kavaluskas, N., Pan, L., & Wolf, A. (1999). Methylenecyclopropane Rearrangement as a Probe for Free Radical Substituent Effects. sigma (*) Values for Potent Radical-Stabilizing Nitrogen-Containing Substituents. The Journal of organic chemistry, 64(15), 5634-5643. https://doi.org/10.1021/jo990732d
Creary, Xavier, et al. "Methylenecyclopropane Rearrangement as a Probe for Free Radical Substituent Effects. sigma (*) Values for Potent Radical-Stabilizing Nitrogen-Containing Substituents." The Journal of organic chemistry vol. 64,15 (1999): 5634-5643. doi: https://doi.org/10.1021/jo990732d
Creary X, Engel PS, Kavaluskas N, Pan L, Wolf A. Methylenecyclopropane Rearrangement as a Probe for Free Radical Substituent Effects. sigma (*) Values for Potent Radical-Stabilizing Nitrogen-Containing Substituents. J Org Chem. 1999 Jul 23;64(15):5634-5643. doi: 10.1021/jo990732d. PMID: 11674633.
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Radical stabilizing ability of the ferrocenyl and cyclobutadieneiron tricarbonyl groups.

Organic letters

Creary X.
PMID: 10891232
Org Lett. 2000 Jul 13;2(14):2069-72. doi: 10.1021/ol000119c.

Computational studies indicate that ferrocenyl-substituted methyl radicals owe their stability to a spin delocalization mechanism involving Fe and a major contribution from an eta(4) form. Cyclobutadieneiron tricarbonyl substituted methyl radicals are also calculated to be highly stabilized by spin...

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Creary X. Radical stabilizing ability of the ferrocenyl and cyclobutadieneiron tricarbonyl groups. Org Lett. 2000;2(14):2069-72doi: 10.1021/ol000119c.
Creary, X. (2000). Radical stabilizing ability of the ferrocenyl and cyclobutadieneiron tricarbonyl groups. Organic letters, 2(14), 2069-72. https://doi.org/10.1021/ol000119c
Creary. "Radical stabilizing ability of the ferrocenyl and cyclobutadieneiron tricarbonyl groups." Organic letters vol. 2,14 (2000): 2069-72. doi: https://doi.org/10.1021/ol000119c
Creary X. Radical stabilizing ability of the ferrocenyl and cyclobutadieneiron tricarbonyl groups. Org Lett. 2000 Jul 13;2(14):2069-72. doi: 10.1021/ol000119c. PMID: 10891232.
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A Dilution Plate Counting Method for Certain Strains of Bacterium tularense.

Journal of bacteriology

Snyder TL, Engley FB, Penfield RA, Creasy JC.
PMID: 16561170
J Bacteriol. 1946 Aug;52(2):241-2.

No abstract available.

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Snyder TL, Engley FB, Penfield RA, et al. A Dilution Plate Counting Method for Certain Strains of Bacterium tularense. J Bacteriol. 1946;52(2):241-2
Snyder, T. L., Engley, F. B., Penfield, R. A., & Creasy, J. C. (1946). A Dilution Plate Counting Method for Certain Strains of Bacterium tularense. Journal of bacteriology, 52(2), 241-2.
Snyder, T L, et al. "A Dilution Plate Counting Method for Certain Strains of Bacterium tularense." Journal of bacteriology vol. 52,2 (1946): 241-2.
Snyder TL, Engley FB, Penfield RA, Creasy JC. A Dilution Plate Counting Method for Certain Strains of Bacterium tularense. J Bacteriol. 1946 Aug;52(2):241-2. PMID: 16561170; PMCID: PMC518172.
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Choosing Detectors for the SSC: SSC officials are inching toward choosing the two large-scale experiments that will be done in the machine--a decision that will influence physics for at least a decade.

Science (New York, N.Y.)

Crease R.
PMID: 17734693
Science. 1990 Dec 21;250(4988):1648-50. doi: 10.1126/science.250.4988.1648.

No abstract available.

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Crease R. Choosing Detectors for the SSC: SSC officials are inching toward choosing the two large-scale experiments that will be done in the machine--a decision that will influence physics for at least a decade. Science. 1990;250(4988):1648-50doi: 10.1126/science.250.4988.1648.
Crease, R. (1990). Choosing Detectors for the SSC: SSC officials are inching toward choosing the two large-scale experiments that will be done in the machine--a decision that will influence physics for at least a decade. Science (New York, N.Y.), 250(4988), 1648-50. https://doi.org/10.1126/science.250.4988.1648
Crease, R. "Choosing Detectors for the SSC: SSC officials are inching toward choosing the two large-scale experiments that will be done in the machine--a decision that will influence physics for at least a decade." Science (New York, N.Y.) vol. 250,4988 (1990): 1648-50. doi: https://doi.org/10.1126/science.250.4988.1648
Crease R. Choosing Detectors for the SSC: SSC officials are inching toward choosing the two large-scale experiments that will be done in the machine--a decision that will influence physics for at least a decade. Science. 1990 Dec 21;250(4988):1648-50. doi: 10.1126/science.250.4988.1648. PMID: 17734693.
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Hydroxy-beta-thiolactams to oxazole-2-thiones. A novel DMSO-promoted oxidation.

Organic letters

Creary X, Losch A.
PMID: 18844362
Org Lett. 2008 Nov 06;10(21):4975-8. doi: 10.1021/ol802050a. Epub 2008 Oct 10.

3-Aryl-3-hydroxy-1-methylazetidine-2-thiones react with HCl in DMSO to give 3-methyl-5-aryloxazole-2-thiones. Substituent effects correlate with rate effects on hydrolyses of acetals of benzaldehyde. An (17)O labeling experiment indicates that the oxygen atom of the product is derived from the hydroxyl group....

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Creary X, Losch A. Hydroxy-beta-thiolactams to oxazole-2-thiones. A novel DMSO-promoted oxidation. Org Lett. 2008;10(21):4975-8doi: 10.1021/ol802050a.
Creary, X., & Losch, A. (2008). Hydroxy-beta-thiolactams to oxazole-2-thiones. A novel DMSO-promoted oxidation. Organic letters, 10(21), 4975-8. https://doi.org/10.1021/ol802050a
Creary, Xavier, and Losch, Andrea. "Hydroxy-beta-thiolactams to oxazole-2-thiones. A novel DMSO-promoted oxidation." Organic letters vol. 10,21 (2008): 4975-8. doi: https://doi.org/10.1021/ol802050a
Creary X, Losch A. Hydroxy-beta-thiolactams to oxazole-2-thiones. A novel DMSO-promoted oxidation. Org Lett. 2008 Nov 06;10(21):4975-8. doi: 10.1021/ol802050a. Epub 2008 Oct 10. PMID: 18844362.
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Effects of mono-(2-ethylhexyl) phthalate and mono-n-pentyl phthalate on the ultrastructural morphology of rat Sertoli cells in Sertoli/germ cell co-cultures: Correlation with the in vivo effects of di-n-pentyl phthalate.

Toxicology in vitro : an international journal published in association with BIBRA

Creasy DM, Beech LM, Gray TJ.
PMID: 20702342
Toxicol In Vitro. 1988;2(2):83-95. doi: 10.1016/0887-2333(88)90018-5.

The effects of mono-(2-ethylhexyl) phthalate (MEHP) and mono-n-pentyl phthalate (MPP) on the ultrastructure of Sertoli cells in primary co-cultures of rat Sertoli and germ cells has been examined and compared with the in vivo effects of di-n-pentyl phthalate (DPP)...

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Creasy DM, Beech LM, Gray TJ. Effects of mono-(2-ethylhexyl) phthalate and mono-n-pentyl phthalate on the ultrastructural morphology of rat Sertoli cells in Sertoli/germ cell co-cultures: Correlation with the in vivo effects of di-n-pentyl phthalate. Toxicol In Vitro. 1988;2(2):83-95doi: 10.1016/0887-2333(88)90018-5.
Creasy, D. M., Beech, L. M., & Gray, T. J. (1988). Effects of mono-(2-ethylhexyl) phthalate and mono-n-pentyl phthalate on the ultrastructural morphology of rat Sertoli cells in Sertoli/germ cell co-cultures: Correlation with the in vivo effects of di-n-pentyl phthalate. Toxicology in vitro : an international journal published in association with BIBRA, 2(2), 83-95. https://doi.org/10.1016/0887-2333(88)90018-5
Creasy, D M, et al. "Effects of mono-(2-ethylhexyl) phthalate and mono-n-pentyl phthalate on the ultrastructural morphology of rat Sertoli cells in Sertoli/germ cell co-cultures: Correlation with the in vivo effects of di-n-pentyl phthalate." Toxicology in vitro : an international journal published in association with BIBRA vol. 2,2 (1988): 83-95. doi: https://doi.org/10.1016/0887-2333(88)90018-5
Creasy DM, Beech LM, Gray TJ. Effects of mono-(2-ethylhexyl) phthalate and mono-n-pentyl phthalate on the ultrastructural morphology of rat Sertoli cells in Sertoli/germ cell co-cultures: Correlation with the in vivo effects of di-n-pentyl phthalate. Toxicol In Vitro. 1988;2(2):83-95. doi: 10.1016/0887-2333(88)90018-5. PMID: 20702342.
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Peach Mesocarp Explant Enlargement and Callus Production in vitro.

Science (New York, N.Y.)

Sommer NF, Bradley MV, Creasy MT.
PMID: 17750873
Science. 1962 Apr 20;136(3512):264-5. doi: 10.1126/science.136.3512.264.

Explants from fruits of the peach were stimulated to grow by cell enlargement, cell division, or both when placed on media containing kinetin. Callus cultures have been obtained, even occasionally from ripening fruits, long after cessation of normal cell...

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Sommer NF, Bradley MV, Creasy MT. Peach Mesocarp Explant Enlargement and Callus Production in vitro. Science. 1962;136(3512):264-5doi: 10.1126/science.136.3512.264.
Sommer, N. F., Bradley, M. V., & Creasy, M. T. (1962). Peach Mesocarp Explant Enlargement and Callus Production in vitro. Science (New York, N.Y.), 136(3512), 264-5. https://doi.org/10.1126/science.136.3512.264
Sommer, N F, et al. "Peach Mesocarp Explant Enlargement and Callus Production in vitro." Science (New York, N.Y.) vol. 136,3512 (1962): 264-5. doi: https://doi.org/10.1126/science.136.3512.264
Sommer NF, Bradley MV, Creasy MT. Peach Mesocarp Explant Enlargement and Callus Production in vitro. Science. 1962 Apr 20;136(3512):264-5. doi: 10.1126/science.136.3512.264. PMID: 17750873.
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Systematic repression of beta-silyl carbocation stabilization.

The Journal of organic chemistry

Creary X, Kochly ED.
PMID: 19203235
J Org Chem. 2009 Mar 06;74(5):2134-44. doi: 10.1021/jo802722z.

Solvolysis of 1-(trimethylsilylmethyl)cyclopropyl mesylate in CD(3)CO(2)D gives ring-opened products as well as methylenecyclopropane. The rate enhancement due to the beta-trimethylsilyl group is a factor of about 10(6). The large stabilizing effect of a beta-silyl group (which can cause rate...

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Creary X, Kochly ED. Systematic repression of beta-silyl carbocation stabilization. J Org Chem. 2009;74(5):2134-44doi: 10.1021/jo802722z.
Creary, X., & Kochly, E. D. (2009). Systematic repression of beta-silyl carbocation stabilization. The Journal of organic chemistry, 74(5), 2134-44. https://doi.org/10.1021/jo802722z
Creary, Xavier, and Kochly, Elizabeth D. "Systematic repression of beta-silyl carbocation stabilization." The Journal of organic chemistry vol. 74,5 (2009): 2134-44. doi: https://doi.org/10.1021/jo802722z
Creary X, Kochly ED. Systematic repression of beta-silyl carbocation stabilization. J Org Chem. 2009 Mar 06;74(5):2134-44. doi: 10.1021/jo802722z. PMID: 19203235.
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Showing 1 to 12 of 119 entries