1.Prosthetic rehabilitation in patient with soft palatal defect.
Myung Woo CHANG ; Jong jin KIM ; John D PIRO ; Robert F WRIGHT
The Journal of Korean Academy of Prosthodontics 1999;37(1):134-138
No abstract available.
Humans
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Rehabilitation*
2.Follicular stimulating hormone enhances Notch 1 expression in SK-OV-3 ovarian cancer cells.
Young Han PARK ; Su Jin KIM ; Byung Hoon JEONG ; Thomas J HERZOG ; Jason WRIGHT ; Jan KITAJEWSKI ; Chae Chun RHIM ; Pong Rheem JANG ; Jung Bae KANG ; Sung Ju KIM
Journal of Gynecologic Oncology 2010;21(2):119-124
OBJECTIVE: Notch is known as a transmembranous receptor family with four homologous forms - Notch 1, Notch 2, Notch 3, and Notch 4 and related to cell fate regulation and angiogenesis. The purpose is to investigate the effect of follicular stimulating hormone (FSH) on the Notch 1 expression and proliferation in ovarian cancer cells. METHODS: Human ovarian cancer cell line, SK-OV-3 and FSH were used. XTT cell proliferation and cell migration assay were carried out with FSH 100 mIU/mL and Notch 1 siRNA. Western blots and reverse transcriptase-polymerase chain reactions (RT-PCR) were carried out to determine the expression level of the Notch 1 protein and mRNA with FSH treatment in 0, 1, 5, 10, 100, 200, 300 mIU/mL concentrations. Immunofluorescent (IF) stains were performed in SK-OV-3 cell cultures with FSH 100 mIU/mL. Student-t tests were used in statistical analyses. RESULTS: The SK-OV-3 have Notch 1 receptors in their natural status. FSH stimulated SK-OV-3 cells in XTT cell proliferation and cell migration assays and notch 1 siRNA inhibited. The expression level of Notch 1 protein and mRNA were increased in a dose dependent pattern according to FSH concentrations compared to untreated cells. IF stains also showed brighter Notch1 expressions in the FSH treated cells compared to the control cells. CONCLUSION: FSH enhances proliferation & migration and Notch 1 signaling in SK-OV-3 cells. The Notch signaling probably supports one of the cell proliferating mechanisms of FSH in ovarian cancer cells.
Blotting, Western
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Cell Culture Techniques
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Cell Line
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Cell Migration Assays
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Cell Proliferation
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Coloring Agents
;
Humans
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Ovarian Neoplasms
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RNA, Messenger
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RNA, Small Interfering
3.Cohort profile: investigating SARS-CoV-2 infection and the health and psychosocial impact of the COVID-19 pandemic in the Canadian CHILD Cohort
Rilwan AZEEZ ; Larisa LOTOSKI ; Aimée DUBEAU ; Natalie RODRIGUEZ ; Myrtha E. REYNA ; Tyler FREITAS ; Stephanie GOGUEN ; Maria MEDELEANU ; Geoffrey L. WINSOR ; Fiona S. L. BRINKMAN ; Emily E. CAMERON ; Leslie ROOS ; Elinor SIMONS ; Theo J. MORAES ; Piush J. MANDHANE ; Stuart E. TURVEY ; Shelly BOLOTIN ; Kim WRIGHT ; Deborah MCNEIL ; David M. PATRICK ; Jared BULLARD ; Marc-André LANGLOIS ; Corey R. ARNOLD ; Yannick GALIPEAU ; Martin PELCHAT ; Natasha DOUCAS ; Padmaja SUBBARAO ; Meghan B. AZAD
Epidemiology and Health 2023;45(1):e2023091-
The coronavirus disease 2019 (COVID-19) pandemic has affected all Canadian families, with some impacted differently than others. Our study aims to: (1) determine the prevalence and transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection among Canadian families, (2) identify predictors of infection susceptibility and severity of SARS-CoV-2, and (3) identify health and psychosocial impacts of the COVID-19 pandemic. This study builds upon the CHILD Cohort Study, an ongoing multi-ethnic general population prospective cohort consisting of 3,454 Canadian families with children born in Vancouver, Edmonton, Manitoba, and Toronto between 2009 and 2012. During the pandemic, CHILD households were invited to participate in the CHILD COVID-19 Add-On Study involving: (1) brief biweekly surveys about COVID-19 symptoms and testing; (2) quarterly questionnaires assessing COVID-19 exposure and testing, vaccination status, physical and mental health, and pandemic-driven life changes; and (3) in-home biological sampling kits to collect blood and stool. In total, 1,462 households (5,378 participants) consented to the CHILD COVID-19 Add-On Study: 2,803 children (mean±standard deviation [SD], 9.0±2.7 years; range, 0-17 years) and 2,576 adults (mean±SD, 43.0±6.5 years; range, 18-85 years). We will leverage the wealth of pre-pandemic CHILD data to identify risk and resilience factors for susceptibility and severity to the direct and indirect pandemic effects. Our short-term findings will inform key stakeholders and knowledge users to shape current and future pandemic responses. Additionally, this study provides a unique resource to study the long-term impacts of the pandemic as the CHILD Cohort Study continues.