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The role of biostimulated endometrial organoids by low level laser therapy in regeneration the ablated endometrium in mice / Mona Elsayed Mahmoud Badawy Gebril ; Supervised Mohamed Amr Hussein Elnoury , Osama Fekry Ahmed , Tamer Fouad Taha Hussein

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Mona Elsayed Mahmoud Badawy Gebril , 2021Description: 146 P. : charts , facsimiles ; 25cmOther title:
  • دور بطانة الرحم المخلقة المعرضة للعلاج بالليزر المنخفض المستوى لتجديد بطانة الرحم المدمرة للفئران [Added title page title]
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Dissertation note: Thesis (Ph.D.) - Cairo University - National Institute of Laser Enhanced Science - Department of Laser Application in Medical Biological Summary: Objective: Studying the effect Low Level Laser Therapy on the mice epithelial endometrial organoids regarding cell proliferation, endometrial regeneration, and endometrial receptivity. Studying the role of epithelial progesterone receptors (PGR) on implantation and endometrial receptivity using genetically modified mice model with only epithelial deletion of PGR (ePGR- KO).Study design: the in vitro part was to generate mice epithelial organoid model and testing LLLT using He:NE 632.8 nm device and testing cell proliferation and organoid function markers then culturing organoids with DUM to test the regeneration ability of organoids to endometrial tissue and the effect of LLLT on regeneration.The genetically modified animal model ePGR -KO, to test ePGR effect on endometrial receptivity and implantation. Both stages are testing the morphological and hormonal aspects of endometrial receptivity Results: LLLT proved to have a proliferative effect on the epithelial mouse organoids confirmed by Ki67 and PCNA IHC and ePGR are a mandatory mediator that regulate both endometrial epithelial and stromal function for successful implantation. Conclusion: LLLT and organoids are a promising modality to treat Asherman syndrome correcting the morphology of the endometrium for receptive uterus. Also, our results address a critical role of epithelial PGR for uterine receptivity and embryo attachment in early pregnancy
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.24.03.Ph.D2021.Mo.R (Browse shelf(Opens below)) Not for loan 01010110085331000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.24.03.Ph.D2021.Mo.R (Browse shelf(Opens below)) 85331.CD Not for loan 01020110085331000

Thesis (Ph.D.) - Cairo University - National Institute of Laser Enhanced Science - Department of Laser Application in Medical Biological

Objective: Studying the effect Low Level Laser Therapy on the mice epithelial endometrial organoids regarding cell proliferation, endometrial regeneration, and endometrial receptivity. Studying the role of epithelial progesterone receptors (PGR) on implantation and endometrial receptivity using genetically modified mice model with only epithelial deletion of PGR (ePGR- KO).Study design: the in vitro part was to generate mice epithelial organoid model and testing LLLT using He:NE 632.8 nm device and testing cell proliferation and organoid function markers then culturing organoids with DUM to test the regeneration ability of organoids to endometrial tissue and the effect of LLLT on regeneration.The genetically modified animal model ePGR -KO, to test ePGR effect on endometrial receptivity and implantation. Both stages are testing the morphological and hormonal aspects of endometrial receptivity Results: LLLT proved to have a proliferative effect on the epithelial mouse organoids confirmed by Ki67 and PCNA IHC and ePGR are a mandatory mediator that regulate both endometrial epithelial and stromal function for successful implantation. Conclusion: LLLT and organoids are a promising modality to treat Asherman syndrome correcting the morphology of the endometrium for receptive uterus. Also, our results address a critical role of epithelial PGR for uterine receptivity and embryo attachment in early pregnancy

Issued also as CD

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