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Efficient Generation of Primordial Germ Cells and CRISPR Perturbation Screens Identify Epigenetic Regulators Impacting Primordial Germ Cell Development
Efficient Generation of Primordial Germ Cells and CRISPR Perturbation Screens Identify Epi...
Efficient Generation of Primordial Germ Cells and CRISPR Perturbation Screens Identify Epigenetic Regulators Impacting Primordial Germ Cell Development

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자료유형  
 학위논문 서양
최종처리일시  
20250211151028
ISBN  
9798382840239
DDC  
574
저자명  
Li, Liangdao.
서명/저자  
Efficient Generation of Primordial Germ Cells and CRISPR Perturbation Screens Identify Epigenetic Regulators Impacting Primordial Germ Cell Development
발행사항  
[Sl] : Cornell University, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
165 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-12, Section: B.
주기사항  
Advisor: Schimenti, John.
학위논문주기  
Thesis (Ph.D.)--Cornell University, 2024.
초록/해제  
요약In mammalian development, the process of gametogenesis begins with a group of germline precursors known as primordial germ cells (PGCs), which emerge shortly after embryo implantation. These PGCs undertake a migration through the developing hindgut to ultimately reach and populate the embryonic gonads. In vitro modeling of this complex developmental process offers a non-invasive method to study the molecular mechanisms governing gametogenesis. This is particularly significant for understanding the genetic and epigenetic underpinnings of infertility, which can inform advancements in assisted reproductive technologies (ART), including gene correction techniques and the optimization of in vitro gametogenesis (IVG). My thesis will concentrate on refining this in vitro model for generating mouse PGCs, aiming to make the process more efficient and scalable. An important aspect of my research will involve utilizing CRISPR technology for perturbation screens, designed to identify key epigenetic regulators that play a crucial role in PGC development. By enhancing our understanding of these regulators and the overall process of PGC development, my research could provide valuable insights and tools for improving ART and IVG.
일반주제명  
Biology
일반주제명  
Cellular biology
일반주제명  
Genetics
키워드  
Assisted reproductive technologies
키워드  
Primordial germ cells
키워드  
Infertility
키워드  
Gametogenesis begins
키워드  
Epigenetic regulators
기타저자  
Cornell University Biomedical and Biological Sciences
기본자료저록  
Dissertations Abstracts International. 85-12B.
전자적 위치 및 접속  
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MARC

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■0820  ▼a574
■1001  ▼aLi,  Liangdao.▼0(orcid)0000-0001-9266-5103
■24510▼aEfficient  Generation  of  Primordial  Germ  Cells  and  CRISPR  Perturbation  Screens  Identify  Epigenetic  Regulators  Impacting  Primordial  Germ  Cell  Development
■260    ▼a[Sl]▼bCornell  University▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a165  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-12,  Section:  B.
■500    ▼aAdvisor:  Schimenti,  John.
■5021  ▼aThesis  (Ph.D.)--Cornell  University,  2024.
■520    ▼aIn  mammalian  development,  the  process  of  gametogenesis  begins  with  a  group  of  germline  precursors  known  as  primordial  germ  cells  (PGCs),  which  emerge  shortly  after  embryo  implantation.  These  PGCs  undertake  a  migration  through  the  developing  hindgut  to  ultimately  reach  and  populate  the  embryonic  gonads.  In  vitro  modeling  of  this  complex  developmental  process  offers  a  non-invasive  method  to  study  the  molecular  mechanisms  governing  gametogenesis.  This  is  particularly  significant  for  understanding  the  genetic  and  epigenetic  underpinnings  of  infertility,  which  can  inform  advancements  in  assisted  reproductive  technologies  (ART),  including  gene  correction  techniques  and  the  optimization  of  in  vitro  gametogenesis  (IVG).  My  thesis  will  concentrate  on  refining  this  in  vitro  model  for  generating  mouse  PGCs,  aiming  to  make  the  process  more  efficient  and  scalable.  An  important  aspect  of  my  research  will  involve  utilizing  CRISPR  technology  for  perturbation  screens,  designed  to  identify  key  epigenetic  regulators  that  play  a  crucial  role  in  PGC  development.  By  enhancing  our  understanding  of  these  regulators  and  the  overall  process  of  PGC  development,  my  research  could  provide  valuable  insights  and  tools  for  improving  ART  and  IVG.
■590    ▼aSchool  code:  0058.
■650  4▼aBiology
■650  4▼aCellular  biology
■650  4▼aGenetics
■653    ▼aAssisted  reproductive  technologies
■653    ▼aPrimordial  germ  cells
■653    ▼aInfertility
■653    ▼aGametogenesis  begins
■653    ▼aEpigenetic  regulators
■690    ▼a0306
■690    ▼a0379
■690    ▼a0369
■71020▼aCornell  University▼bBiomedical  and  Biological  Sciences.
■7730  ▼tDissertations  Abstracts  International▼g85-12B.
■790    ▼a0058
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17160487▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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