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Measurement of dynamic cell-induced 3D displacement fields .

Biomedical optics express

Mulligan JA, Bordeleau F, Reinhart-King CA, Adie SG.
PMID: 28271010
Biomed Opt Express. 2017 Jan 27;8(2):1152-1171. doi: 10.1364/BOE.8.001152. eCollection 2017 Feb 01.

Traction force microscopy (TFM) is a method used to study the forces exerted by cells as they sense and interact with their environment. Cell forces play a role in processes that take place over a wide range of spatiotemporal...

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Mulligan JA, Bordeleau F, Reinhart-King CA, et al. Measurement of dynamic cell-induced 3D displacement fields . Biomed Opt Express. 2017;8(2):1152-1171doi: 10.1364/BOE.8.001152.
Mulligan, J. A., Bordeleau, F., Reinhart-King, C. A., & Adie, S. G. (2017). Measurement of dynamic cell-induced 3D displacement fields . Biomedical optics express, 8(2), 1152-1171. https://doi.org/10.1364/BOE.8.001152
Mulligan, Jeffrey A, et al. "Measurement of dynamic cell-induced 3D displacement fields ." Biomedical optics express vol. 8,2 (2017): 1152-1171. doi: https://doi.org/10.1364/BOE.8.001152
Mulligan JA, Bordeleau F, Reinhart-King CA, Adie SG. Measurement of dynamic cell-induced 3D displacement fields . Biomed Opt Express. 2017 Jan 27;8(2):1152-1171. doi: 10.1364/BOE.8.001152. eCollection 2017 Feb 01. PMID: 28271010; PMCID: PMC5330596.
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Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study.

BMJ open

Esplen MJ, Cappelli M, Wong J, Bottorff JL, Hunter J, Carroll J, Dorval M, Wilson B, Allanson J, Semotiuk K, Aronson M, Bordeleau L, Charlemagne N, Meschino W.
PMID: 23485718
BMJ Open. 2013 Mar 13;3(3). doi: 10.1136/bmjopen-2012-002227.

OBJECTIVES: To develop a brief, reliable and valid instrument to screen psychosocial risk among those who are undergoing genetic testing for Adult-Onset Hereditary Disease (AOHD).DESIGN: A prospective two-phase cohort study.SETTING: 5 genetic testing centres for AOHD, such as cancer,...

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Esplen MJ, Cappelli M, Wong J, et al. Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study. BMJ Open. 2013;3(3)doi: 10.1136/bmjopen-2012-002227.
Esplen, M. J., Cappelli, M., Wong, J., Bottorff, J. L., Hunter, J., Carroll, J., Dorval, M., Wilson, B., Allanson, J., Semotiuk, K., Aronson, M., Bordeleau, L., Charlemagne, N., & Meschino, W. (2013). Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study. BMJ open, 3(3), . https://doi.org/10.1136/bmjopen-2012-002227
Esplen, Mary Jane, et al. "Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study." BMJ open vol. 3,3 (2013). doi: https://doi.org/10.1136/bmjopen-2012-002227
Esplen MJ, Cappelli M, Wong J, Bottorff JL, Hunter J, Carroll J, Dorval M, Wilson B, Allanson J, Semotiuk K, Aronson M, Bordeleau L, Charlemagne N, Meschino W. Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study. BMJ Open. 2013 Mar 13;3(3). doi: 10.1136/bmjopen-2012-002227. PMID: 23485718; PMCID: PMC3612753.
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Diversity of integrating conjugative elements in actinobacteria: Coexistence of two mechanistically different DNA-translocation systems.

Mobile genetic elements

Bordeleau E, Ghinet MG, Burrus V.
PMID: 22934248
Mob Genet Elements. 2012 Mar 01;2(2):119-124. doi: 10.4161/mge.20498.

Conjugation is certainly the most widespread and promiscuous mechanism of horizontal gene transfer in bacteria. During conjugation, DNA translocation across membranes of two cells forming a mating pair is mediated by two types of mobile genetic elements: conjugative plasmids...

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Bordeleau E, Ghinet MG, Burrus V. Diversity of integrating conjugative elements in actinobacteria: Coexistence of two mechanistically different DNA-translocation systems. Mob Genet Elements. 2012;2(2):119-124doi: 10.4161/mge.20498.
Bordeleau, E., Ghinet, M. G., & Burrus, V. (2012). Diversity of integrating conjugative elements in actinobacteria: Coexistence of two mechanistically different DNA-translocation systems. Mobile genetic elements, 2(2), 119-124. https://doi.org/10.4161/mge.20498
Bordeleau, Eric, et al. "Diversity of integrating conjugative elements in actinobacteria: Coexistence of two mechanistically different DNA-translocation systems." Mobile genetic elements vol. 2,2 (2012): 119-124. doi: https://doi.org/10.4161/mge.20498
Bordeleau E, Ghinet MG, Burrus V. Diversity of integrating conjugative elements in actinobacteria: Coexistence of two mechanistically different DNA-translocation systems. Mob Genet Elements. 2012 Mar 01;2(2):119-124. doi: 10.4161/mge.20498. PMID: 22934248; PMCID: PMC3429521.
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Agreement Analysis between Vive and Vicon Systems to Monitor Lumbar Postural Changes.

Sensors (Basel, Switzerland)

van der Veen SM, Bordeleau M, Pidcoe PE, France CR, Thomas JS.
PMID: 31438520
Sensors (Basel). 2019 Aug 21;19(17). doi: 10.3390/s19173632.

Immersive virtual reality has recently developed into a readily available system that allows for full-body tracking. Can this affordable system be used for component tracking to advance or replace expensive kinematic systems for motion analysis in the clinic? The...

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van der Veen SM, Bordeleau M, Pidcoe PE, et al. Agreement Analysis between Vive and Vicon Systems to Monitor Lumbar Postural Changes. Sensors (Basel). 2019;19(17)doi: 10.3390/s19173632.
van der Veen, S. M., Bordeleau, M., Pidcoe, P. E., France, C. R., & Thomas, J. S. (2019). Agreement Analysis between Vive and Vicon Systems to Monitor Lumbar Postural Changes. Sensors (Basel, Switzerland), 19(17), . https://doi.org/10.3390/s19173632
van der Veen, Susanne M, et al. "Agreement Analysis between Vive and Vicon Systems to Monitor Lumbar Postural Changes." Sensors (Basel, Switzerland) vol. 19,17 (2019). doi: https://doi.org/10.3390/s19173632
van der Veen SM, Bordeleau M, Pidcoe PE, France CR, Thomas JS. Agreement Analysis between Vive and Vicon Systems to Monitor Lumbar Postural Changes. Sensors (Basel). 2019 Aug 21;19(17). doi: 10.3390/s19173632. PMID: 31438520; PMCID: PMC6749183.
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Clinical doses of radiation reduce collagen matrix stiffness.

APL bioengineering

Miller JP, Borde BH, Bordeleau F, Zanotelli MR, LaValley DJ, Parker DJ, Bonassar LJ, Pannullo SC, Reinhart-King CA.
PMID: 31069314
APL Bioeng. 2018 Apr 03;2(3):031901. doi: 10.1063/1.5018327. eCollection 2018 Sep.

Cells receive mechanical cues from their extracellular matrix (ECM), which direct migration, differentiation, apoptosis, and in some cases, the transition to a cancerous phenotype. As a result, there has been significant research to develop methods to tune the mechanical...

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Miller JP, Borde BH, Bordeleau F, et al. Clinical doses of radiation reduce collagen matrix stiffness. APL Bioeng. 2018;2(3):031901doi: 10.1063/1.5018327.
Miller, J. P., Borde, B. H., Bordeleau, F., Zanotelli, M. R., LaValley, D. J., Parker, D. J., Bonassar, L. J., Pannullo, S. C., & Reinhart-King, C. A. (2018). Clinical doses of radiation reduce collagen matrix stiffness. APL bioengineering, 2(3), 031901. https://doi.org/10.1063/1.5018327
Miller, Joseph P, et al. "Clinical doses of radiation reduce collagen matrix stiffness." APL bioengineering vol. 2,3 (2018): 031901. doi: https://doi.org/10.1063/1.5018327
Miller JP, Borde BH, Bordeleau F, Zanotelli MR, LaValley DJ, Parker DJ, Bonassar LJ, Pannullo SC, Reinhart-King CA. Clinical doses of radiation reduce collagen matrix stiffness. APL Bioeng. 2018 Apr 03;2(3):031901. doi: 10.1063/1.5018327. eCollection 2018 Sep. PMID: 31069314; PMCID: PMC6324208.
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Origin and formation of the royal fat body of the higher termite queens.

Journal of morphology

Han SH, Bordereau C.
PMID: 30089346
J Morphol. 1982 Jul;173(1):17-28. doi: 10.1002/jmor.1051730103.

The formation of the royal fat body was studied by electron microscopy in three species of higher termites (Macrotermes bellicosus, Macrotermes subhyalinus, and Cubitermes fungifaber). The swarming alate imago has a storage fat body typical of most insects. In...

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Han SH, Bordereau C. Origin and formation of the royal fat body of the higher termite queens. J Morphol. 1982;173(1):17-28doi: 10.1002/jmor.1051730103.
Han, S. H., & Bordereau, C. (1982). Origin and formation of the royal fat body of the higher termite queens. Journal of morphology, 173(1), 17-28. https://doi.org/10.1002/jmor.1051730103
Han, Sun Heat, and Bordereau, Christian. "Origin and formation of the royal fat body of the higher termite queens." Journal of morphology vol. 173,1 (1982): 17-28. doi: https://doi.org/10.1002/jmor.1051730103
Han SH, Bordereau C. Origin and formation of the royal fat body of the higher termite queens. J Morphol. 1982 Jul;173(1):17-28. doi: 10.1002/jmor.1051730103. PMID: 30089346.
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Classification of Qualitative Fieldnotes Collected During Quantitative Sensory Testing: A Step Towards the Development of a New Mixed Methods Approach in Pain Research.

Journal of pain research

Bordeleau M, Léonard G, Gauthier L, Ferland CE, Backonja M, Vollert J, Marchand S, Jackson P, Cantin L, Prud'Homme M.
PMID: 34434059
J Pain Res. 2021 Aug 18;14:2501-2511. doi: 10.2147/JPR.S301655. eCollection 2021.

PURPOSE: Quantitative sensory testing (QST) is a standardized method to assess somatosensory function. The collection of qualitative information, during the QST procedure, could be an interesting way to facilitate the characterization of altered sensory perception and the identification of...

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Bordeleau M, Léonard G, Gauthier L, et al. Classification of Qualitative Fieldnotes Collected During Quantitative Sensory Testing: A Step Towards the Development of a New Mixed Methods Approach in Pain Research. J Pain Res. 2021;14:2501-2511doi: 10.2147/JPR.S301655.
Bordeleau, M., Léonard, G., Gauthier, L., Ferland, C. E., Backonja, M., Vollert, J., Marchand, S., Jackson, P., Cantin, L., & Prud'Homme, M. (2021). Classification of Qualitative Fieldnotes Collected During Quantitative Sensory Testing: A Step Towards the Development of a New Mixed Methods Approach in Pain Research. Journal of pain research, 142501-2511. https://doi.org/10.2147/JPR.S301655
Bordeleau, Martine, et al. "Classification of Qualitative Fieldnotes Collected During Quantitative Sensory Testing: A Step Towards the Development of a New Mixed Methods Approach in Pain Research." Journal of pain research vol. 14 (2021): 2501-2511. doi: https://doi.org/10.2147/JPR.S301655
Bordeleau M, Léonard G, Gauthier L, Ferland CE, Backonja M, Vollert J, Marchand S, Jackson P, Cantin L, Prud'Homme M. Classification of Qualitative Fieldnotes Collected During Quantitative Sensory Testing: A Step Towards the Development of a New Mixed Methods Approach in Pain Research. J Pain Res. 2021 Aug 18;14:2501-2511. doi: 10.2147/JPR.S301655. eCollection 2021. PMID: 34434059; PMCID: PMC8380625.
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Remote, proactive, telephone based management of toxicity in outpatients during adjuvant or neoadjuvant chemotherapy for early stage breast cancer: pragmatic, cluster randomised trial.

BMJ (Clinical research ed.)

Krzyzanowska MK, Julian JA, Gu CS, Powis M, Li Q, Enright K, Howell D, Earle CC, Gandhi S, Rask S, Brezden-Masley C, Dent S, Hajra L, Freeman O, Spadafora S, Hamm C, Califaretti N, Trudeau M, Levine MN, Amir E, Bordeleau L, Chiarotto JA, Elser C, Husain J, Laferriere N, Rahim Y, Robinson AG, Vandenberg T, Grunfeld E.
PMID: 34880055
BMJ. 2021 Dec 08;375:e066588. doi: 10.1136/bmj-2021-066588.

OBJECTIVE: To evaluate the effectiveness of remote proactive management of toxicities during chemotherapy for early stage breast cancer.DESIGN: Pragmatic, cluster randomised trial.SETTING: 20 cancer centres in Ontario, Canada, allocated by covariate constrained randomisation to remote management of toxicities or...

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Krzyzanowska MK, Julian JA, Gu CS, et al. Remote, proactive, telephone based management of toxicity in outpatients during adjuvant or neoadjuvant chemotherapy for early stage breast cancer: pragmatic, cluster randomised trial. BMJ. 2021;375:e066588doi: 10.1136/bmj-2021-066588.
Krzyzanowska, M. K., Julian, J. A., Gu, C. S., Powis, M., Li, Q., Enright, K., Howell, D., Earle, C. C., Gandhi, S., Rask, S., Brezden-Masley, C., Dent, S., Hajra, L., Freeman, O., Spadafora, S., Hamm, C., Califaretti, N., Trudeau, M., Levine, M. N., Amir, E., Bordeleau, L., Chiarotto, J. A., Elser, C., Husain, J., Laferriere, N., Rahim, Y., Robinson, A. G., Vandenberg, T., & Grunfeld, E. (2021). Remote, proactive, telephone based management of toxicity in outpatients during adjuvant or neoadjuvant chemotherapy for early stage breast cancer: pragmatic, cluster randomised trial. BMJ (Clinical research ed.), 375e066588. https://doi.org/10.1136/bmj-2021-066588
Krzyzanowska, Monika K, et al. "Remote, proactive, telephone based management of toxicity in outpatients during adjuvant or neoadjuvant chemotherapy for early stage breast cancer: pragmatic, cluster randomised trial." BMJ (Clinical research ed.) vol. 375 (2021): e066588. doi: https://doi.org/10.1136/bmj-2021-066588
Krzyzanowska MK, Julian JA, Gu CS, Powis M, Li Q, Enright K, Howell D, Earle CC, Gandhi S, Rask S, Brezden-Masley C, Dent S, Hajra L, Freeman O, Spadafora S, Hamm C, Califaretti N, Trudeau M, Levine MN, Amir E, Bordeleau L, Chiarotto JA, Elser C, Husain J, Laferriere N, Rahim Y, Robinson AG, Vandenberg T, Grunfeld E. Remote, proactive, telephone based management of toxicity in outpatients during adjuvant or neoadjuvant chemotherapy for early stage breast cancer: pragmatic, cluster randomised trial. BMJ. 2021 Dec 08;375:e066588. doi: 10.1136/bmj-2021-066588. PMID: 34880055.
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An evaluation of memory and attention in BRCA mutation carriers using an online cognitive assessment tool.

Cancer

Kotsopoulos J, Kim SJ, Armel S, Bordeleau L, Foulkes WD, McKinnon W, Panchal S, Cohen SA, Sun S, Sun P, McKetton L, Troyer AK, Narod SA.
PMID: 34077552
Cancer. 2021 Sep 01;127(17):3183-3193. doi: 10.1002/cncr.33654. Epub 2021 Jun 02.

BACKGROUND: The objective of this study was to evaluate the impact of various surgical, hormonal, and lifestyle factors on memory and attention in women with a BRCA1 or BRCA2 mutation.METHODS: BRCA mutation carriers enrolled in a longitudinal study were...

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Kotsopoulos J, Kim SJ, Armel S, et al. An evaluation of memory and attention in BRCA mutation carriers using an online cognitive assessment tool. Cancer. 2021;127(17):3183-3193doi: 10.1002/cncr.33654.
Kotsopoulos, J., Kim, S. J., Armel, S., Bordeleau, L., Foulkes, W. D., McKinnon, W., Panchal, S., Cohen, S. A., Sun, S., Sun, P., McKetton, L., Troyer, A. K., & Narod, S. A. (2021). An evaluation of memory and attention in BRCA mutation carriers using an online cognitive assessment tool. Cancer, 127(17), 3183-3193. https://doi.org/10.1002/cncr.33654
Kotsopoulos, Joanne, et al. "An evaluation of memory and attention in BRCA mutation carriers using an online cognitive assessment tool." Cancer vol. 127,17 (2021): 3183-3193. doi: https://doi.org/10.1002/cncr.33654
Kotsopoulos J, Kim SJ, Armel S, Bordeleau L, Foulkes WD, McKinnon W, Panchal S, Cohen SA, Sun S, Sun P, McKetton L, Troyer AK, Narod SA. An evaluation of memory and attention in BRCA mutation carriers using an online cognitive assessment tool. Cancer. 2021 Sep 01;127(17):3183-3193. doi: 10.1002/cncr.33654. Epub 2021 Jun 02. PMID: 34077552.
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Author Correction: Energetic costs regulated by cell mechanics and confinement are predictive of migration path during decision-making.

Nature communications

Zanotelli MR, Rahman-Zaman A, VanderBurgh JA, Taufalele PV, Jain A, Erickson D, Bordeleau F, Reinhart-King CA.
PMID: 31797873
Nat Commun. 2019 Dec 04;10(1):5619. doi: 10.1038/s41467-019-13655-8.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Zanotelli MR, Rahman-Zaman A, VanderBurgh JA, et al. Author Correction: Energetic costs regulated by cell mechanics and confinement are predictive of migration path during decision-making. Nat Commun. 2019;10(1):5619doi: 10.1038/s41467-019-13655-8.
Zanotelli, M. R., Rahman-Zaman, A., VanderBurgh, J. A., Taufalele, P. V., Jain, A., Erickson, D., Bordeleau, F., & Reinhart-King, C. A. (2019). Author Correction: Energetic costs regulated by cell mechanics and confinement are predictive of migration path during decision-making. Nature communications, 10(1), 5619. https://doi.org/10.1038/s41467-019-13655-8
Zanotelli, Matthew R, et al. "Author Correction: Energetic costs regulated by cell mechanics and confinement are predictive of migration path during decision-making." Nature communications vol. 10,1 (2019): 5619. doi: https://doi.org/10.1038/s41467-019-13655-8
Zanotelli MR, Rahman-Zaman A, VanderBurgh JA, Taufalele PV, Jain A, Erickson D, Bordeleau F, Reinhart-King CA. Author Correction: Energetic costs regulated by cell mechanics and confinement are predictive of migration path during decision-making. Nat Commun. 2019 Dec 04;10(1):5619. doi: 10.1038/s41467-019-13655-8. PMID: 31797873; PMCID: PMC6893040.
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Neuropathobiology of COVID-19: The Role for Glia.

Frontiers in cellular neuroscience

Tremblay ME, Madore C, Bordeleau M, Tian L, Verkhratsky A.
PMID: 33304243
Front Cell Neurosci. 2020 Nov 11;14:592214. doi: 10.3389/fncel.2020.592214. eCollection 2020.

SARS-CoV-2, which causes the Coronavirus Disease 2019 (COVID-19) pandemic, has a brain neurotropism through binding to the receptor angiotensin-converting enzyme 2 expressed by neurones and glial cells, including astrocytes and microglia. Systemic infection which accompanies severe cases of COVID-19...

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Tremblay ME, Madore C, Bordeleau M, et al. Neuropathobiology of COVID-19: The Role for Glia. Front Cell Neurosci. 2020;14:592214doi: 10.3389/fncel.2020.592214.
Tremblay, M. E., Madore, C., Bordeleau, M., Tian, L., & Verkhratsky, A. (2020). Neuropathobiology of COVID-19: The Role for Glia. Frontiers in cellular neuroscience, 14592214. https://doi.org/10.3389/fncel.2020.592214
Tremblay, Marie-Eve, et al. "Neuropathobiology of COVID-19: The Role for Glia." Frontiers in cellular neuroscience vol. 14 (2020): 592214. doi: https://doi.org/10.3389/fncel.2020.592214
Tremblay ME, Madore C, Bordeleau M, Tian L, Verkhratsky A. Neuropathobiology of COVID-19: The Role for Glia. Front Cell Neurosci. 2020 Nov 11;14:592214. doi: 10.3389/fncel.2020.592214. eCollection 2020. PMID: 33304243; PMCID: PMC7693550.
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National Cancer Institute Breast Cancer Steering Committee Working Group Report on Meaningful and Appropriate End Points for Clinical Trials in Metastatic Breast Cancer.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology

Seidman AD, Bordeleau L, Fehrenbacher L, Barlow WE, Perlmutter J, Rubinstein L, Wedam SB, Hershman DL, Hayes JF, Butler LP, Smith ML, Regan MM, Beaver JA, Amiri-Kordestani L, Rastogi P, Zujewski JA, Korde LA.
PMID: 30212295
J Clin Oncol. 2018 Nov 10;36(32):3259-3268. doi: 10.1200/JCO.18.00242. Epub 2018 Sep 13.

PURPOSE: To provide evidence-based consensus recommendations on choice of end points for clinical trials in metastatic breast cancer, with a focus on biologic subtype and line of therapy.METHODS: The National Cancer Institute Breast Cancer Steering Committee convened a working...

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Seidman AD, Bordeleau L, Fehrenbacher L, et al. National Cancer Institute Breast Cancer Steering Committee Working Group Report on Meaningful and Appropriate End Points for Clinical Trials in Metastatic Breast Cancer. J Clin Oncol. 2018;36(32):3259-3268doi: 10.1200/JCO.18.00242.
Seidman, A. D., Bordeleau, L., Fehrenbacher, L., Barlow, W. E., Perlmutter, J., Rubinstein, L., Wedam, S. B., Hershman, D. L., Hayes, J. F., Butler, L. P., Smith, M. L., Regan, M. M., Beaver, J. A., Amiri-Kordestani, L., Rastogi, P., Zujewski, J. A., & Korde, L. A. (2018). National Cancer Institute Breast Cancer Steering Committee Working Group Report on Meaningful and Appropriate End Points for Clinical Trials in Metastatic Breast Cancer. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 36(32), 3259-3268. https://doi.org/10.1200/JCO.18.00242
Seidman, Andrew D, et al. "National Cancer Institute Breast Cancer Steering Committee Working Group Report on Meaningful and Appropriate End Points for Clinical Trials in Metastatic Breast Cancer." Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 36,32 (2018): 3259-3268. doi: https://doi.org/10.1200/JCO.18.00242
Seidman AD, Bordeleau L, Fehrenbacher L, Barlow WE, Perlmutter J, Rubinstein L, Wedam SB, Hershman DL, Hayes JF, Butler LP, Smith ML, Regan MM, Beaver JA, Amiri-Kordestani L, Rastogi P, Zujewski JA, Korde LA. National Cancer Institute Breast Cancer Steering Committee Working Group Report on Meaningful and Appropriate End Points for Clinical Trials in Metastatic Breast Cancer. J Clin Oncol. 2018 Nov 10;36(32):3259-3268. doi: 10.1200/JCO.18.00242. Epub 2018 Sep 13. PMID: 30212295; PMCID: PMC7351338.
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