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Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial.

Frontiers in public health

Keene KL, Chen WM, Chen F, Williams SR, Elkhatib SD, Hsu FC, Mychaleckyj JC, Doheny KF, Pugh EW, Ling H, Laurie CC, Gogarten SM, Madden EB, Worrall BB, Sale MM.
PMID: 25147783
Front Public Health. 2014 Aug 06;2:112. doi: 10.3389/fpubh.2014.00112. eCollection 2014.

BACKGROUND: B vitamins play an important role in homocysteine metabolism, with vitamin deficiencies resulting in increased levels of homocysteine and increased risk for stroke. We performed a genome-wide association study (GWAS) in 2,100 stroke patients from the Vitamin Intervention...

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Keene KL, Chen WM, Chen F, et al. Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial. Front Public Health. 2014;2:112doi: 10.3389/fpubh.2014.00112.
Keene, K. L., Chen, W. M., Chen, F., Williams, S. R., Elkhatib, S. D., Hsu, F. C., Mychaleckyj, J. C., Doheny, K. F., Pugh, E. W., Ling, H., Laurie, C. C., Gogarten, S. M., Madden, E. B., Worrall, B. B., & Sale, M. M. (2014). Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial. Frontiers in public health, 2112. https://doi.org/10.3389/fpubh.2014.00112
Keene, Keith L, et al. "Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial." Frontiers in public health vol. 2 (2014): 112. doi: https://doi.org/10.3389/fpubh.2014.00112
Keene KL, Chen WM, Chen F, Williams SR, Elkhatib SD, Hsu FC, Mychaleckyj JC, Doheny KF, Pugh EW, Ling H, Laurie CC, Gogarten SM, Madden EB, Worrall BB, Sale MM. Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial. Front Public Health. 2014 Aug 06;2:112. doi: 10.3389/fpubh.2014.00112. eCollection 2014. PMID: 25147783; PMCID: PMC4123605.
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Winter Depression: Integrating mood, circadian rhythms, and the sleep/wake and light/dark cycles into a bio-psycho-social-environmental model.

Sleep medicine clinics

Lewy AJ, Emens JS, Songer JB, Sims N, Laurie AL, Fiala SC, Buti AL.
PMID: 20160896
Sleep Med Clin. 2009 Jun 01;4(2):285-299. doi: 10.1016/j.jsmc.2009.02.003.

The phase shift hypothesis (PSH) states that most patients with SAD become depressed in the winter because of a delay in circadian rhythms with respect to the sleep/wake cycle: According to the PSH, these patients should preferentially respond to...

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Lewy AJ, Emens JS, Songer JB, et al. Winter Depression: Integrating mood, circadian rhythms, and the sleep/wake and light/dark cycles into a bio-psycho-social-environmental model. Sleep Med Clin. 2009;4(2):285-299doi: 10.1016/j.jsmc.2009.02.003.
Lewy, A. J., Emens, J. S., Songer, J. B., Sims, N., Laurie, A. L., Fiala, S. C., & Buti, A. L. (2009). Winter Depression: Integrating mood, circadian rhythms, and the sleep/wake and light/dark cycles into a bio-psycho-social-environmental model. Sleep medicine clinics, 4(2), 285-299. https://doi.org/10.1016/j.jsmc.2009.02.003
Lewy, Alfred J, et al. "Winter Depression: Integrating mood, circadian rhythms, and the sleep/wake and light/dark cycles into a bio-psycho-social-environmental model." Sleep medicine clinics vol. 4,2 (2009): 285-299. doi: https://doi.org/10.1016/j.jsmc.2009.02.003
Lewy AJ, Emens JS, Songer JB, Sims N, Laurie AL, Fiala SC, Buti AL. Winter Depression: Integrating mood, circadian rhythms, and the sleep/wake and light/dark cycles into a bio-psycho-social-environmental model. Sleep Med Clin. 2009 Jun 01;4(2):285-299. doi: 10.1016/j.jsmc.2009.02.003. PMID: 20160896; PMCID: PMC2768314.
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Differential downregulation of e-cadherin and desmoglein by epidermal growth factor.

Dermatology research and practice

Chavez MG, Buhr CA, Petrie WK, Wandinger-Ness A, Kusewitt DF, Hudson LG.
PMID: 22312325
Dermatol Res Pract. 2012;2012:309587. doi: 10.1155/2012/309587. Epub 2012 Jan 16.

Modulation of cell : cell junctions is a key event in cutaneous wound repair. In this study we report that activation of the epidermal growth factor (EGF) receptor disrupts cell : cell adhesion, but with different kinetics and fates...

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Chavez MG, Buhr CA, Petrie WK, et al. Differential downregulation of e-cadherin and desmoglein by epidermal growth factor. Dermatol Res Pract. 2012;2012:309587doi: 10.1155/2012/309587.
Chavez, M. G., Buhr, C. A., Petrie, W. K., Wandinger-Ness, A., Kusewitt, D. F., & Hudson, L. G. (2012). Differential downregulation of e-cadherin and desmoglein by epidermal growth factor. Dermatology research and practice, 2012309587. https://doi.org/10.1155/2012/309587
Chavez, Miquella G, et al. "Differential downregulation of e-cadherin and desmoglein by epidermal growth factor." Dermatology research and practice vol. 2012 (2012): 309587. doi: https://doi.org/10.1155/2012/309587
Chavez MG, Buhr CA, Petrie WK, Wandinger-Ness A, Kusewitt DF, Hudson LG. Differential downregulation of e-cadherin and desmoglein by epidermal growth factor. Dermatol Res Pract. 2012;2012:309587. doi: 10.1155/2012/309587. Epub 2012 Jan 16. PMID: 22312325; PMCID: PMC3270554.
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Continuous Irrigation with Hydrogen Peroxide as a Treatment for Septic Sinuses, Etc.

The Hospital

Laurie RD.
PMID: 29814389
Hospital (Lond 1886). 1910 Jan 29;47(1226):515.

No abstract available.

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Laurie RD. Continuous Irrigation with Hydrogen Peroxide as a Treatment for Septic Sinuses, Etc. Hospital (Lond 1886). 1910;47(1226):515
Laurie, R. D. (1910). Continuous Irrigation with Hydrogen Peroxide as a Treatment for Septic Sinuses, Etc. The Hospital, 47(1226), 515.
Laurie, R Douglas. "Continuous Irrigation with Hydrogen Peroxide as a Treatment for Septic Sinuses, Etc." The Hospital vol. 47,1226 (1910): 515.
Laurie RD. Continuous Irrigation with Hydrogen Peroxide as a Treatment for Septic Sinuses, Etc. Hospital (Lond 1886). 1910 Jan 29;47(1226):515. PMID: 29814389; PMCID: PMC5202587.
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Using zebrafish larval models to study brain injury, locomotor and neuroinflammatory outcomes following intracerebral haemorrhage.

F1000Research

Crilly S, Njegic A, Laurie SE, Fotiou E, Hudson G, Barrington J, Webb K, Young HL, Badrock AP, Hurlstone A, Rivers-Auty J, Parry-Jones AR, Allan SM, Kasher PR.
PMID: 30473780
F1000Res. 2018 Oct 08;7:1617. doi: 10.12688/f1000research.16473.2. eCollection 2018.

Intracerebral haemorrhage (ICH) is a devastating condition with limited treatment options, and current understanding of pathophysiology is incomplete. Spontaneous cerebral bleeding is a characteristic of the human condition that has proven difficult to recapitulate in existing pre-clinical rodent models....

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Crilly S, Njegic A, Laurie SE, et al. Using zebrafish larval models to study brain injury, locomotor and neuroinflammatory outcomes following intracerebral haemorrhage. F1000Res. 2018;7:1617doi: 10.12688/f1000research.16473.2.
Crilly, S., Njegic, A., Laurie, S. E., Fotiou, E., Hudson, G., Barrington, J., Webb, K., Young, H. L., Badrock, A. P., Hurlstone, A., Rivers-Auty, J., Parry-Jones, A. R., Allan, S. M., & Kasher, P. R. (2018). Using zebrafish larval models to study brain injury, locomotor and neuroinflammatory outcomes following intracerebral haemorrhage. F1000Research, 71617. https://doi.org/10.12688/f1000research.16473.2
Crilly, Siobhan, et al. "Using zebrafish larval models to study brain injury, locomotor and neuroinflammatory outcomes following intracerebral haemorrhage." F1000Research vol. 7 (2018): 1617. doi: https://doi.org/10.12688/f1000research.16473.2
Crilly S, Njegic A, Laurie SE, Fotiou E, Hudson G, Barrington J, Webb K, Young HL, Badrock AP, Hurlstone A, Rivers-Auty J, Parry-Jones AR, Allan SM, Kasher PR. Using zebrafish larval models to study brain injury, locomotor and neuroinflammatory outcomes following intracerebral haemorrhage. F1000Res. 2018 Oct 08;7:1617. doi: 10.12688/f1000research.16473.2. eCollection 2018. PMID: 30473780; PMCID: PMC6234746.
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Clinical Notes.

Glasgow medical journal

Laurie JA.
PMID: 30432024
Glasgow Med J. 1853 Oct;1(3):339-359.

No abstract available.

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Laurie JA. Clinical Notes. Glasgow Med J. 1853;1(3):339-359
Laurie, J. A. (1853). Clinical Notes. Glasgow medical journal, 1(3), 339-359.
Laurie, James A. "Clinical Notes." Glasgow medical journal vol. 1,3 (1853): 339-359.
Laurie JA. Clinical Notes. Glasgow Med J. 1853 Oct;1(3):339-359. PMID: 30432024; PMCID: PMC5767401.
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A Charge to Academic Chairs.

JAMA internal medicine

Jacobs LG.
PMID: 33871572
JAMA Intern Med. 2021 Aug 01;181(8):1136. doi: 10.1001/jamainternmed.2021.0843.

No abstract available.

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Jacobs LG. A Charge to Academic Chairs. JAMA Intern Med. 2021;181(8):1136doi: 10.1001/jamainternmed.2021.0843.
Jacobs, L. G. (2021). A Charge to Academic Chairs. JAMA internal medicine, 181(8), 1136. https://doi.org/10.1001/jamainternmed.2021.0843
Jacobs, Laurie G. "A Charge to Academic Chairs." JAMA internal medicine vol. 181,8 (2021): 1136. doi: https://doi.org/10.1001/jamainternmed.2021.0843
Jacobs LG. A Charge to Academic Chairs. JAMA Intern Med. 2021 Aug 01;181(8):1136. doi: 10.1001/jamainternmed.2021.0843. PMID: 33871572.
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A Charge to Academic Chairs.

JAMA internal medicine

Jacobs LG.
PMID: 33871572
JAMA Intern Med. 2021 Aug 01;181(8):1136. doi: 10.1001/jamainternmed.2021.0843.

No abstract available.

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Jacobs LG. A Charge to Academic Chairs. JAMA Intern Med. 2021;181(8):1136doi: 10.1001/jamainternmed.2021.0843.
Jacobs, L. G. (2021). A Charge to Academic Chairs. JAMA internal medicine, 181(8), 1136. https://doi.org/10.1001/jamainternmed.2021.0843
Jacobs, Laurie G. "A Charge to Academic Chairs." JAMA internal medicine vol. 181,8 (2021): 1136. doi: https://doi.org/10.1001/jamainternmed.2021.0843
Jacobs LG. A Charge to Academic Chairs. JAMA Intern Med. 2021 Aug 01;181(8):1136. doi: 10.1001/jamainternmed.2021.0843. PMID: 33871572.
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Estimation of secondary household attack rates for emergent spike L452R SARS-CoV-2 variants detected by genomic surveillance at a community-based testing site in San Francisco.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

Peng J, Liu J, Mann SA, Mitchell AM, Laurie MT, Sunshine S, Pilarowski G, Ayscue P, Kistler A, Vanaerschot M, Li LM, McGeever A, Chow ED, Marquez C, Nakamura R, Rubio L, Chamie G, Jones D, Jacobo J, Rojas S, Rojas S, Tulier-Laiwa V, Black D, Martinez J, Naso J, Schwab J, Petersen M, Havlir D, DeRisi J.
PMID: 33788923
Clin Infect Dis. 2021 Mar 31; doi: 10.1093/cid/ciab283. Epub 2021 Mar 31.

BACKGROUND: Sequencing of the SARS-CoV-2 viral genome from patient samples is an important epidemiological tool for monitoring and responding to the pandemic, including the emergence of new mutations in specific communities.METHODS: SARS-CoV-2 genomic sequences were generated from positive samples...

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Peng J, Liu J, Mann SA, et al. Estimation of secondary household attack rates for emergent spike L452R SARS-CoV-2 variants detected by genomic surveillance at a community-based testing site in San Francisco. Clin Infect Dis. 2021;doi: 10.1093/cid/ciab283.
Peng, J., Liu, J., Mann, S. A., Mitchell, A. M., Laurie, M. T., Sunshine, S., Pilarowski, G., Ayscue, P., Kistler, A., Vanaerschot, M., Li, L. M., McGeever, A., Chow, E. D., Marquez, C., Nakamura, R., Rubio, L., Chamie, G., Jones, D., Jacobo, J., Rojas, S., Rojas, S., Tulier-Laiwa, V., Black, D., Martinez, J., Naso, J., Schwab, J., Petersen, M., Havlir, D., DeRisi, J. (2021). Estimation of secondary household attack rates for emergent spike L452R SARS-CoV-2 variants detected by genomic surveillance at a community-based testing site in San Francisco. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, . https://doi.org/10.1093/cid/ciab283
Peng, James, et al. "Estimation of secondary household attack rates for emergent spike L452R SARS-CoV-2 variants detected by genomic surveillance at a community-based testing site in San Francisco." Clinical infectious diseases : an official publication of the Infectious Diseases Society of America vol. (2021). doi: https://doi.org/10.1093/cid/ciab283
Peng J, Liu J, Mann SA, Mitchell AM, Laurie MT, Sunshine S, Pilarowski G, Ayscue P, Kistler A, Vanaerschot M, Li LM, McGeever A, Chow ED, Marquez C, Nakamura R, Rubio L, Chamie G, Jones D, Jacobo J, Rojas S, Rojas S, Tulier-Laiwa V, Black D, Martinez J, Naso J, Schwab J, Petersen M, Havlir D, DeRisi J. Estimation of secondary household attack rates for emergent spike L452R SARS-CoV-2 variants detected by genomic surveillance at a community-based testing site in San Francisco. Clin Infect Dis. 2021 Mar 31; doi: 10.1093/cid/ciab283. Epub 2021 Mar 31. PMID: 33788923; PMCID: PMC8083548.
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Intention to Receive a COVID-19 Vaccine by HIV Status Among a Population-Based Sample of Women and Gender Diverse Individuals in British Columbia, Canada.

AIDS and behavior

Kaida A, Brotto LA, Murray MCM, Côté HCF, Albert AY, Nicholson V, Gormley R, Gordon S, Booth A, Smith LW, Baaske A, Galea LAM, Sadarangani M, Ogilvie GS.
PMID: 35020094
AIDS Behav. 2022 Jan 12; doi: 10.1007/s10461-022-03577-w. Epub 2022 Jan 12.

COVID-19 vaccination is recommended for people living with HIV (PLWH), among whom social inequities and co-morbidities may drive risks of COVID-19 infection and outcome severity. Among a provincial (British Columbia) sample, we determined the prevalence of COVID-19 vaccine intention...

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Kaida A, Brotto LA, Murray MCM, et al. Intention to Receive a COVID-19 Vaccine by HIV Status Among a Population-Based Sample of Women and Gender Diverse Individuals in British Columbia, Canada. AIDS Behav. 2022;doi: 10.1007/s10461-022-03577-w.
Kaida, A., Brotto, L. A., Murray, M. C. M., Côté, H. C. F., Albert, A. Y., Nicholson, V., Gormley, R., Gordon, S., Booth, A., Smith, L. W., Baaske, A., Galea, L. A. M., Sadarangani, M., & Ogilvie, G. S. (2022). Intention to Receive a COVID-19 Vaccine by HIV Status Among a Population-Based Sample of Women and Gender Diverse Individuals in British Columbia, Canada. AIDS and behavior, . https://doi.org/10.1007/s10461-022-03577-w
Kaida, Angela, et al. "Intention to Receive a COVID-19 Vaccine by HIV Status Among a Population-Based Sample of Women and Gender Diverse Individuals in British Columbia, Canada." AIDS and behavior vol. (2022). doi: https://doi.org/10.1007/s10461-022-03577-w
Kaida A, Brotto LA, Murray MCM, Côté HCF, Albert AY, Nicholson V, Gormley R, Gordon S, Booth A, Smith LW, Baaske A, Galea LAM, Sadarangani M, Ogilvie GS. Intention to Receive a COVID-19 Vaccine by HIV Status Among a Population-Based Sample of Women and Gender Diverse Individuals in British Columbia, Canada. AIDS Behav. 2022 Jan 12; doi: 10.1007/s10461-022-03577-w. Epub 2022 Jan 12. PMID: 35020094.
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Sexual violence victimization among American college students studying abroad.

Journal of American college health : J of ACH

Pedersen ER, DiGuiseppi G, Klein DJ, Davis JP, Farris C, D'Amico EJ, LaBrie JW, Griffin BA.
PMID: 34398702
J Am Coll Health. 2021 Aug 16;1-10. doi: 10.1080/07448481.2021.1950733. Epub 2021 Aug 16.

OBJECTIVE: Research has just begun to identify American college students who study abroad as a group at-risk for sexual violence victimization. The purpose of the current study was to examine the context of these incidents.

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Pedersen ER, DiGuiseppi G, Klein DJ, et al. Sexual violence victimization among American college students studying abroad. J Am Coll Health. 2021;1-10doi: 10.1080/07448481.2021.1950733.
Pedersen, E. R., DiGuiseppi, G., Klein, D. J., Davis, J. P., Farris, C., D'Amico, E. J., LaBrie, J. W., & Griffin, B. A. (2021). Sexual violence victimization among American college students studying abroad. Journal of American college health : J of ACH, 1-10. https://doi.org/10.1080/07448481.2021.1950733
Pedersen, Eric R, et al. "Sexual violence victimization among American college students studying abroad." Journal of American college health : J of ACH vol. (2021): 1-10. doi: https://doi.org/10.1080/07448481.2021.1950733
Pedersen ER, DiGuiseppi G, Klein DJ, Davis JP, Farris C, D'Amico EJ, LaBrie JW, Griffin BA. Sexual violence victimization among American college students studying abroad. J Am Coll Health. 2021 Aug 16;1-10. doi: 10.1080/07448481.2021.1950733. Epub 2021 Aug 16. PMID: 34398702.
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SARS-CoV-2 variant exposures elicit antibody responses with differential cross-neutralization of established and emerging strains including Delta and Omicron.

The Journal of infectious diseases

Laurie MT, Liu J, Sunshine S, Peng J, Black D, Mitchell AM, Mann SA, Pilarowski G, Zorn KC, Rubio L, Bravo S, Marquez C, Sabatino JJ, Mittl K, Petersen M, Havlir D, DeRisi J.
PMID: 34979030
J Infect Dis. 2022 Jan 03; doi: 10.1093/infdis/jiab635. Epub 2022 Jan 03.

The wide spectrum of SARS-CoV-2 variants with phenotypes impacting transmission and antibody sensitivity necessitates investigation of the immune response to different spike protein versions. Here, we compare the neutralization of variants of concern, including B.1.617.2 (Delta) and B.1.1.529 (Omicron)...

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Laurie MT, Liu J, Sunshine S, et al. SARS-CoV-2 variant exposures elicit antibody responses with differential cross-neutralization of established and emerging strains including Delta and Omicron. J Infect Dis. 2022;doi: 10.1093/infdis/jiab635.
Laurie, M. T., Liu, J., Sunshine, S., Peng, J., Black, D., Mitchell, A. M., Mann, S. A., Pilarowski, G., Zorn, K. C., Rubio, L., Bravo, S., Marquez, C., Sabatino, J. J., Mittl, K., Petersen, M., Havlir, D., & DeRisi, J. (2022). SARS-CoV-2 variant exposures elicit antibody responses with differential cross-neutralization of established and emerging strains including Delta and Omicron. The Journal of infectious diseases, . https://doi.org/10.1093/infdis/jiab635
Laurie, Matthew T, et al. "SARS-CoV-2 variant exposures elicit antibody responses with differential cross-neutralization of established and emerging strains including Delta and Omicron." The Journal of infectious diseases vol. (2022). doi: https://doi.org/10.1093/infdis/jiab635
Laurie MT, Liu J, Sunshine S, Peng J, Black D, Mitchell AM, Mann SA, Pilarowski G, Zorn KC, Rubio L, Bravo S, Marquez C, Sabatino JJ, Mittl K, Petersen M, Havlir D, DeRisi J. SARS-CoV-2 variant exposures elicit antibody responses with differential cross-neutralization of established and emerging strains including Delta and Omicron. J Infect Dis. 2022 Jan 03; doi: 10.1093/infdis/jiab635. Epub 2022 Jan 03. PMID: 34979030.
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Showing 13 to 24 of 199 entries