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Spin Textures of Exciton-Polaritons in a Tunable Microcavity with Large TE-TM Splitting.

Physical review letters

Dufferwiel S, Li F, Cancellieri E, Giriunas L, Trichet AA, Whittaker DM, Walker PM, Fras F, Clarke E, Smith JM, Skolnick MS, Krizhanovskii DN.
PMID: 26705642
Phys Rev Lett. 2015 Dec 11;115(24):246401. doi: 10.1103/PhysRevLett.115.246401. Epub 2015 Dec 08.

We report an extended family of spin textures of zero-dimensional exciton-polaritons spatially confined in tunable open microcavity structures. The transverse-electric-transverse-magnetic (TE-TM) splitting, which is enhanced in the open cavity structures, leads to polariton eigenstates carrying quantized spin vortices. Depending...

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Dufferwiel S, Li F, Cancellieri E, et al. Spin Textures of Exciton-Polaritons in a Tunable Microcavity with Large TE-TM Splitting. Phys Rev Lett. 2015;115(24):246401doi: 10.1103/PhysRevLett.115.246401.
Dufferwiel, S., Li, F., Cancellieri, E., Giriunas, L., Trichet, A. A., Whittaker, D. M., Walker, P. M., Fras, F., Clarke, E., Smith, J. M., Skolnick, M. S., & Krizhanovskii, D. N. (2015). Spin Textures of Exciton-Polaritons in a Tunable Microcavity with Large TE-TM Splitting. Physical review letters, 115(24), 246401. https://doi.org/10.1103/PhysRevLett.115.246401
Dufferwiel, S, et al. "Spin Textures of Exciton-Polaritons in a Tunable Microcavity with Large TE-TM Splitting." Physical review letters vol. 115,24 (2015): 246401. doi: https://doi.org/10.1103/PhysRevLett.115.246401
Dufferwiel S, Li F, Cancellieri E, Giriunas L, Trichet AA, Whittaker DM, Walker PM, Fras F, Clarke E, Smith JM, Skolnick MS, Krizhanovskii DN. Spin Textures of Exciton-Polaritons in a Tunable Microcavity with Large TE-TM Splitting. Phys Rev Lett. 2015 Dec 11;115(24):246401. doi: 10.1103/PhysRevLett.115.246401. Epub 2015 Dec 08. PMID: 26705642.
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Clustering, hierarchical organization, and the topography of abstract and concrete nouns.

Frontiers in psychology

Troche J, Crutch S, Reilly J.
PMID: 24808876
Front Psychol. 2014 Apr 28;5:360. doi: 10.3389/fpsyg.2014.00360. eCollection 2014.

The empirical study of language has historically relied heavily upon concrete word stimuli. By definition, concrete words evoke salient perceptual associations that fit well within feature-based, sensorimotor models of word meaning. In contrast, many theorists argue that abstract words...

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Troche J, Crutch S, Reilly J. Clustering, hierarchical organization, and the topography of abstract and concrete nouns. Front Psychol. 2014;5:360doi: 10.3389/fpsyg.2014.00360.
Troche, J., Crutch, S., & Reilly, J. (2014). Clustering, hierarchical organization, and the topography of abstract and concrete nouns. Frontiers in psychology, 5360. https://doi.org/10.3389/fpsyg.2014.00360
Troche, Joshua, et al. "Clustering, hierarchical organization, and the topography of abstract and concrete nouns." Frontiers in psychology vol. 5 (2014): 360. doi: https://doi.org/10.3389/fpsyg.2014.00360
Troche J, Crutch S, Reilly J. Clustering, hierarchical organization, and the topography of abstract and concrete nouns. Front Psychol. 2014 Apr 28;5:360. doi: 10.3389/fpsyg.2014.00360. eCollection 2014. PMID: 24808876; PMCID: PMC4009417.
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Gene Expression Profiling of Ewing Sarcoma Tumors Reveals the Prognostic Importance of Tumor-Stromal Interactions: A Report from the Children's Oncology Group.

The journal of pathology. Clinical research

Volchenboum SL, Andrade J, Huang L, Barkauskas DA, Krailo M, Womer RB, Ranft A, Potratz J, Dirksen U, Triche TJ, Lawlor ER.
PMID: 26052443
J Pathol Clin Res. 2015 Apr;1(2):83-94. doi: 10.1002/cjp2.9.

Relapse of Ewing sarcoma (ES) can occur months or years after initial remission and salvage therapy for relapsed disease is usually ineffective. Thus, there is great need to develop biomarkers that can predict which patients are at risk for...

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Volchenboum SL, Andrade J, Huang L, et al. Gene Expression Profiling of Ewing Sarcoma Tumors Reveals the Prognostic Importance of Tumor-Stromal Interactions: A Report from the Children's Oncology Group. J Pathol Clin Res. 2015;1(2):83-94doi: 10.1002/cjp2.9.
Volchenboum, S. L., Andrade, J., Huang, L., Barkauskas, D. A., Krailo, M., Womer, R. B., Ranft, A., Potratz, J., Dirksen, U., Triche, T. J., & Lawlor, E. R. (2015). Gene Expression Profiling of Ewing Sarcoma Tumors Reveals the Prognostic Importance of Tumor-Stromal Interactions: A Report from the Children's Oncology Group. The journal of pathology. Clinical research, 1(2), 83-94. https://doi.org/10.1002/cjp2.9
Volchenboum, Samuel L, et al. "Gene Expression Profiling of Ewing Sarcoma Tumors Reveals the Prognostic Importance of Tumor-Stromal Interactions: A Report from the Children's Oncology Group." The journal of pathology. Clinical research vol. 1,2 (2015): 83-94. doi: https://doi.org/10.1002/cjp2.9
Volchenboum SL, Andrade J, Huang L, Barkauskas DA, Krailo M, Womer RB, Ranft A, Potratz J, Dirksen U, Triche TJ, Lawlor ER. Gene Expression Profiling of Ewing Sarcoma Tumors Reveals the Prognostic Importance of Tumor-Stromal Interactions: A Report from the Children's Oncology Group. J Pathol Clin Res. 2015 Apr;1(2):83-94. doi: 10.1002/cjp2.9. PMID: 26052443; PMCID: PMC4457396.
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Salmonella enterica Serotype Arizonae Meningitis in a Neonate.

Case reports in pediatrics

Lakew W, Girma A, Triche E.
PMID: 24187642
Case Rep Pediatr. 2013;2013:813495. doi: 10.1155/2013/813495. Epub 2013 Sep 30.

Typhoidal and nontyphoidal salmonella infections are common causes of gastroenteritis in the community. However, salmonella only rarely causes invasive infections like meningitis. We report a 13-day-old female neonate with signs and symptoms of meningitis whose cerebrospinal fluid (CSF) culture...

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Lakew W, Girma A, Triche E. Salmonella enterica Serotype Arizonae Meningitis in a Neonate. Case Rep Pediatr. 2013;2013:813495doi: 10.1155/2013/813495.
Lakew, W., Girma, A., & Triche, E. (2013). Salmonella enterica Serotype Arizonae Meningitis in a Neonate. Case reports in pediatrics, 2013813495. https://doi.org/10.1155/2013/813495
Lakew, Wubishet, et al. "Salmonella enterica Serotype Arizonae Meningitis in a Neonate." Case reports in pediatrics vol. 2013 (2013): 813495. doi: https://doi.org/10.1155/2013/813495
Lakew W, Girma A, Triche E. Salmonella enterica Serotype Arizonae Meningitis in a Neonate. Case Rep Pediatr. 2013;2013:813495. doi: 10.1155/2013/813495. Epub 2013 Sep 30. PMID: 24187642; PMCID: PMC3800626.
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Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.

Nature medicine

Bolouri H, Farrar JE, Triche T, Ries RE, Lim EL, Alonzo TA, Ma Y, Moore R, Mungall AJ, Marra MA, Zhang J, Ma X, Liu Y, Liu Y, Auvil JMG, Davidsen TM, Gesuwan P, Hermida LC, Salhia B, Capone S, Ramsingh G, Zwaan CM, Noort S, Piccolo SR, Kolb EA, Gamis AS, Smith MA, Gerhard DS, Meshinchi S.
PMID: 30705421
Nat Med. 2019 Mar;25(3):530. doi: 10.1038/s41591-019-0369-7.

In the version of this article originally published, the color key in Fig. 1a was wrong. In the Cytogenetics key, the box over t(8;21) originally was green. It should have been red, matching the color of the sections of...

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Bolouri H, Farrar JE, Triche T, et al. Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions. Nat Med. 2019;25(3):530doi: 10.1038/s41591-019-0369-7.
Bolouri, H., Farrar, J. E., Triche, T., Ries, R. E., Lim, E. L., Alonzo, T. A., Ma, Y., Moore, R., Mungall, A. J., Marra, M. A., Zhang, J., Ma, X., Liu, Y., Liu, Y., Auvil, J. M. G., Davidsen, T. M., Gesuwan, P., Hermida, L. C., Salhia, B., Capone, S., Ramsingh, G., Zwaan, C. M., Noort, S., Piccolo, S. R., Kolb, E. A., Gamis, A. S., Smith, M. A., Gerhard, D. S., & Meshinchi, S. (2019). Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions. Nature medicine, 25(3), 530. https://doi.org/10.1038/s41591-019-0369-7
Bolouri, Hamid, et al. "Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions." Nature medicine vol. 25,3 (2019): 530. doi: https://doi.org/10.1038/s41591-019-0369-7
Bolouri H, Farrar JE, Triche T, Ries RE, Lim EL, Alonzo TA, Ma Y, Moore R, Mungall AJ, Marra MA, Zhang J, Ma X, Liu Y, Liu Y, Auvil JMG, Davidsen TM, Gesuwan P, Hermida LC, Salhia B, Capone S, Ramsingh G, Zwaan CM, Noort S, Piccolo SR, Kolb EA, Gamis AS, Smith MA, Gerhard DS, Meshinchi S. Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions. Nat Med. 2019 Mar;25(3):530. doi: 10.1038/s41591-019-0369-7. PMID: 30705421; PMCID: PMC7747938.
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Therapeutic opportunities for pain medicines via targeting of specific translation signaling mechanisms.

Neurobiology of pain (Cambridge, Mass.)

Megat S, Price TJ.
PMID: 30211342
Neurobiol Pain. 2018 Aug-Dec;4:8-19. doi: 10.1016/j.ynpai.2018.02.001. Epub 2018 Feb 23.

As the population of the world ages and as more and more people survive diseases that used to be primary causes of mortality, the incidence of severe chronic pain in most of the world has risen dramatically. This type...

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Megat S, Price TJ. Therapeutic opportunities for pain medicines via targeting of specific translation signaling mechanisms. Neurobiol Pain. 2018;4:8-19doi: 10.1016/j.ynpai.2018.02.001.
Megat, S., & Price, T. J. (2018). Therapeutic opportunities for pain medicines via targeting of specific translation signaling mechanisms. Neurobiology of pain (Cambridge, Mass.), 48-19. https://doi.org/10.1016/j.ynpai.2018.02.001
Megat, Salim, and Price, Theodore J. "Therapeutic opportunities for pain medicines via targeting of specific translation signaling mechanisms." Neurobiology of pain (Cambridge, Mass.) vol. 4 (2018): 8-19. doi: https://doi.org/10.1016/j.ynpai.2018.02.001
Megat S, Price TJ. Therapeutic opportunities for pain medicines via targeting of specific translation signaling mechanisms. Neurobiol Pain. 2018 Aug-Dec;4:8-19. doi: 10.1016/j.ynpai.2018.02.001. Epub 2018 Feb 23. PMID: 30211342; PMCID: PMC6130820.
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Ultrafast Near-Infrared Light-triggered Intracellular Uncaging to Probe Cell Signaling.

Advanced functional materials

Li X, Che Z, Mazhar K, Price TJ, Qin Z.
PMID: 29176940
Adv Funct Mater. 2017 Mar 17;27(11). doi: 10.1002/adfm.201605778. Epub 2017 Feb 01.

The possibility of regulating cell signaling with high spatial and temporal resolution within individual cells and complex cellular networks has important implications in biomedicine. In this report, we demonstrate a general strategy that uses near-infrared tissue-penetrating laser pulses to...

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Li X, Che Z, Mazhar K, et al. Ultrafast Near-Infrared Light-triggered Intracellular Uncaging to Probe Cell Signaling. Adv Funct Mater. 2017;27(11)doi: 10.1002/adfm.201605778.
Li, X., Che, Z., Mazhar, K., Price, T. J., & Qin, Z. (2017). Ultrafast Near-Infrared Light-triggered Intracellular Uncaging to Probe Cell Signaling. Advanced functional materials, 27(11), . https://doi.org/10.1002/adfm.201605778
Li, Xiuying, et al. "Ultrafast Near-Infrared Light-triggered Intracellular Uncaging to Probe Cell Signaling." Advanced functional materials vol. 27,11 (2017). doi: https://doi.org/10.1002/adfm.201605778
Li X, Che Z, Mazhar K, Price TJ, Qin Z. Ultrafast Near-Infrared Light-triggered Intracellular Uncaging to Probe Cell Signaling. Adv Funct Mater. 2017 Mar 17;27(11). doi: 10.1002/adfm.201605778. Epub 2017 Feb 01. PMID: 29176940; PMCID: PMC5697715.
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The Purified Extract from the Medicinal Plant .

Cells

Smith E, Palethorpe HM, Tomita Y, Pei JV, Townsend AR, Price TJ, Young JP, Yool AJ, Hardingham JE.
PMID: 30037060
Cells. 2018 Jul 21;7(7). doi: 10.3390/cells7070081.

Aquaporin-1 (AQP1), a transmembrane pore-forming molecule, facilitates the rapid movement of water and small solutes across cell membranes. We have previously shown that bacopaside II, an extract from the medicinal herb

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Smith E, Palethorpe HM, Tomita Y, et al. The Purified Extract from the Medicinal Plant . Cells. 2018;7(7)doi: 10.3390/cells7070081.
Smith, E., Palethorpe, H. M., Tomita, Y., Pei, J. V., Townsend, A. R., Price, T. J., Young, J. P., Yool, A. J., & Hardingham, J. E. (2018). The Purified Extract from the Medicinal Plant . Cells, 7(7), . https://doi.org/10.3390/cells7070081
Smith, Eric, et al. "The Purified Extract from the Medicinal Plant ." Cells vol. 7,7 (2018). doi: https://doi.org/10.3390/cells7070081
Smith E, Palethorpe HM, Tomita Y, Pei JV, Townsend AR, Price TJ, Young JP, Yool AJ, Hardingham JE. The Purified Extract from the Medicinal Plant . Cells. 2018 Jul 21;7(7). doi: 10.3390/cells7070081. PMID: 30037060; PMCID: PMC6070819.
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Mesenchymal stem cells increase proliferation but do not change quiescent state of osteosarcoma cells: Potential implications according to the tumor resection status.

Journal of bone oncology

Avril P, Le Nail LR, Brennan MÁ, Rosset P, De Pinieux G, Layrolle P, Heymann D, Perrot P, Trichet V.
PMID: 26998421
J Bone Oncol. 2015 Dec 12;5(1):5-14. doi: 10.1016/j.jbo.2015.11.002. eCollection 2016 Mar.

Conventional therapy of primary bone tumors includes surgical excision with wide resection, which leads to physical and aesthetic defects. For reconstruction of bone and joints, allografts can be supplemented with mesenchymal stem cells (MSCs). Similarly, adipose tissue transfer (ATT)...

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Avril P, Le Nail LR, Brennan MÁ, et al. Mesenchymal stem cells increase proliferation but do not change quiescent state of osteosarcoma cells: Potential implications according to the tumor resection status. J Bone Oncol. 2015;5(1):5-14doi: 10.1016/j.jbo.2015.11.002.
Avril, P., Le Nail, L. R., Brennan, M. �. �., Rosset, P., De Pinieux, G., Layrolle, P., Heymann, D., Perrot, P., & Trichet, V. (2016). Mesenchymal stem cells increase proliferation but do not change quiescent state of osteosarcoma cells: Potential implications according to the tumor resection status. Journal of bone oncology, 5(1), 5-14. https://doi.org/10.1016/j.jbo.2015.11.002
Avril, Pierre, et al. "Mesenchymal stem cells increase proliferation but do not change quiescent state of osteosarcoma cells: Potential implications according to the tumor resection status." Journal of bone oncology vol. 5,1 (2016): 5-14. doi: https://doi.org/10.1016/j.jbo.2015.11.002
Avril P, Le Nail LR, Brennan MÁ, Rosset P, De Pinieux G, Layrolle P, Heymann D, Perrot P, Trichet V. Mesenchymal stem cells increase proliferation but do not change quiescent state of osteosarcoma cells: Potential implications according to the tumor resection status. J Bone Oncol. 2015 Dec 12;5(1):5-14. doi: 10.1016/j.jbo.2015.11.002. eCollection 2016 Mar. PMID: 26998421; PMCID: PMC4782020.
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Visual-auditory differences in duration discrimination of intervals in the subsecond and second range.

Frontiers in psychology

Rammsayer TH, Borter N, Troche SJ.
PMID: 26579013
Front Psychol. 2015 Oct 26;6:1626. doi: 10.3389/fpsyg.2015.01626. eCollection 2015.

A common finding in time psychophysics is that temporal acuity is much better for auditory than for visual stimuli. The present study aimed to examine modality-specific differences in duration discrimination within the conceptual framework of the Distinct Timing Hypothesis....

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Rammsayer TH, Borter N, Troche SJ. Visual-auditory differences in duration discrimination of intervals in the subsecond and second range. Front Psychol. 2015;6:1626doi: 10.3389/fpsyg.2015.01626.
Rammsayer, T. H., Borter, N., & Troche, S. J. (2015). Visual-auditory differences in duration discrimination of intervals in the subsecond and second range. Frontiers in psychology, 61626. https://doi.org/10.3389/fpsyg.2015.01626
Rammsayer, Thomas H, et al. "Visual-auditory differences in duration discrimination of intervals in the subsecond and second range." Frontiers in psychology vol. 6 (2015): 1626. doi: https://doi.org/10.3389/fpsyg.2015.01626
Rammsayer TH, Borter N, Troche SJ. Visual-auditory differences in duration discrimination of intervals in the subsecond and second range. Front Psychol. 2015 Oct 26;6:1626. doi: 10.3389/fpsyg.2015.01626. eCollection 2015. PMID: 26579013; PMCID: PMC4620148.
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Tumor Variant Identification That Accounts for the Unique Molecular Landscape of Pediatric Malignancies.

JNCI cancer spectrum

Lorentzian A, Biegel JA, Ostrow DG, Rolf N, Liu CC, Rassekh SR, Deyell RJ, Triche T, Schultz KR, Rozmus J, Reid GSD, Lim CJ, Lange PF, Maxwell CA.
PMID: 30976750
JNCI Cancer Spectr. 2018 Oct;2(4):pky079. doi: 10.1093/jncics/pky079. Epub 2019 Jan 25.

Precision oncology trials for pediatric cancers require rapid and accurate detection of genetic alterations. Tumor variant identification should interrogate the distinctive driver genes and more frequent copy number variants and gene fusions that are characteristics of pediatric tumors. Here,...

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Lorentzian A, Biegel JA, Ostrow DG, et al. Tumor Variant Identification That Accounts for the Unique Molecular Landscape of Pediatric Malignancies. JNCI Cancer Spectr. 2019;2(4):pky079doi: 10.1093/jncics/pky079.
Lorentzian, A., Biegel, J. A., Ostrow, D. G., Rolf, N., Liu, C. C., Rassekh, S. R., Deyell, R. J., Triche, T., Schultz, K. R., Rozmus, J., Reid, G. S. D., Lim, C. J., Lange, P. F., & Maxwell, C. A. (2018). Tumor Variant Identification That Accounts for the Unique Molecular Landscape of Pediatric Malignancies. JNCI cancer spectrum, 2(4), pky079. https://doi.org/10.1093/jncics/pky079
Lorentzian, Amanda, et al. "Tumor Variant Identification That Accounts for the Unique Molecular Landscape of Pediatric Malignancies." JNCI cancer spectrum vol. 2,4 (2018): pky079. doi: https://doi.org/10.1093/jncics/pky079
Lorentzian A, Biegel JA, Ostrow DG, Rolf N, Liu CC, Rassekh SR, Deyell RJ, Triche T, Schultz KR, Rozmus J, Reid GSD, Lim CJ, Lange PF, Maxwell CA. Tumor Variant Identification That Accounts for the Unique Molecular Landscape of Pediatric Malignancies. JNCI Cancer Spectr. 2018 Oct;2(4):pky079. doi: 10.1093/jncics/pky079. Epub 2019 Jan 25. PMID: 30976750; PMCID: PMC6447067.
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Brain metastasis in advanced colorectal cancer: results from the South Australian metastatic colorectal cancer (SAmCRC) registry.

Cancer biology & medicine

Tapia Rico G, Price TJ, Karapetis C, Piantadosi C, Padbury R, Roy A, Maddern G, Moore J, Carruthers S, Roder D, Townsend AR.
PMID: 29372103
Cancer Biol Med. 2017 Nov;14(4):371-376. doi: 10.20892/j.issn.2095-3941.2017.0068.

OBJECTIVE: Brain metastasis is considered rare in metastatic colorectal cancer (mCRC); thus, surveillance imaging does not routinely include the brain. The reported incidence of brain metastases ranges from 0.6% to 3.2%.METHODS: The South Australian mCRC Registry (SAmCRC) was analyzed...

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Tapia Rico G, Price TJ, Karapetis C, et al. Brain metastasis in advanced colorectal cancer: results from the South Australian metastatic colorectal cancer (SAmCRC) registry. Cancer Biol Med. 2017;14(4):371-376doi: 10.20892/j.issn.2095-3941.2017.0068.
Tapia Rico, G., Price, T. J., Karapetis, C., Piantadosi, C., Padbury, R., Roy, A., Maddern, G., Moore, J., Carruthers, S., Roder, D., & Townsend, A. R. (2017). Brain metastasis in advanced colorectal cancer: results from the South Australian metastatic colorectal cancer (SAmCRC) registry. Cancer biology & medicine, 14(4), 371-376. https://doi.org/10.20892/j.issn.2095-3941.2017.0068
Tapia Rico, Gonzalo, et al. "Brain metastasis in advanced colorectal cancer: results from the South Australian metastatic colorectal cancer (SAmCRC) registry." Cancer biology & medicine vol. 14,4 (2017): 371-376. doi: https://doi.org/10.20892/j.issn.2095-3941.2017.0068
Tapia Rico G, Price TJ, Karapetis C, Piantadosi C, Padbury R, Roy A, Maddern G, Moore J, Carruthers S, Roder D, Townsend AR. Brain metastasis in advanced colorectal cancer: results from the South Australian metastatic colorectal cancer (SAmCRC) registry. Cancer Biol Med. 2017 Nov;14(4):371-376. doi: 10.20892/j.issn.2095-3941.2017.0068. PMID: 29372103; PMCID: PMC5785167.
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Showing 1 to 12 of 176 entries