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Development and Validation of the Human Rosette Array for Neural Tube Defect Risk Screening.
紀錄類型:
書目-語言資料,手稿 : Monograph/item
正題名/作者:
Development and Validation of the Human Rosette Array for Neural Tube Defect Risk Screening./
作者:
Lundin, Brady F.
面頁冊數:
1 online resource (98 pages)
附註:
Source: Dissertations Abstracts International, Volume: 85-11, Section: B.
Contained By:
Dissertations Abstracts International85-11B.
標題:
Bioengineering. -
電子資源:
click for full text (PQDT)
ISBN:
9798382404998
Development and Validation of the Human Rosette Array for Neural Tube Defect Risk Screening.
Lundin, Brady F.
Development and Validation of the Human Rosette Array for Neural Tube Defect Risk Screening.
- 1 online resource (98 pages)
Source: Dissertations Abstracts International, Volume: 85-11, Section: B.
Thesis (Ph.D.)--The University of Wisconsin - Madison, 2024.
Includes bibliographical references
Neural tube defects are the second most common congenital malformation and inflict significant morbidity and mortality upon affected patients. The mechanisms by with they form are unclear and traditional methods of studying the nascent central nervous system have significant limitations. Neural organoids have revolutionized how human neurodevelopmental disorders are studied. Yet, their utility for screening complex neural tube defect etiologies and potential prophylactics is limited by a lack of scalable and quantifiable derivation formats. Here, a brief introduction to neural tube formation and an overview of the known causes of neural tube defects is presented. Then a survey of the rapidly developing field of neural organoids is provided. After which, we describe the Rosette Array platform's ability to be used as an off-the-shelf, 96-well plate assay that standardizes incipient forebrain and spinal cord organoid morphogenesis as micropatterned, 3-D, singularly polarized neural rosette tissues. Rosette Arrays are seeded from cryopreserved human pluripotent stem cells, cultured over 6-8 days, and immunostained images can be quantified using artificial intelligence-based software. We demonstrate the platform's suitability for screening genetic and environmental factors known to cause neural tube defect risk. Lastly, the discussion closes by considering the implications of the platform's development and screening results and future research directions regarding understanding and preventing neural tube defect formation.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2024
Mode of access: World Wide Web
ISBN: 9798382404998Subjects--Topical Terms:
598252
Bioengineering.
Subjects--Index Terms:
Disease modelingIndex Terms--Genre/Form:
554714
Electronic books.
Development and Validation of the Human Rosette Array for Neural Tube Defect Risk Screening.
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Neural tube defects are the second most common congenital malformation and inflict significant morbidity and mortality upon affected patients. The mechanisms by with they form are unclear and traditional methods of studying the nascent central nervous system have significant limitations. Neural organoids have revolutionized how human neurodevelopmental disorders are studied. Yet, their utility for screening complex neural tube defect etiologies and potential prophylactics is limited by a lack of scalable and quantifiable derivation formats. Here, a brief introduction to neural tube formation and an overview of the known causes of neural tube defects is presented. Then a survey of the rapidly developing field of neural organoids is provided. After which, we describe the Rosette Array platform's ability to be used as an off-the-shelf, 96-well plate assay that standardizes incipient forebrain and spinal cord organoid morphogenesis as micropatterned, 3-D, singularly polarized neural rosette tissues. Rosette Arrays are seeded from cryopreserved human pluripotent stem cells, cultured over 6-8 days, and immunostained images can be quantified using artificial intelligence-based software. We demonstrate the platform's suitability for screening genetic and environmental factors known to cause neural tube defect risk. Lastly, the discussion closes by considering the implications of the platform's development and screening results and future research directions regarding understanding and preventing neural tube defect formation.
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