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Regulatory Mechanisms of the Anti-cancer Cgamp-sting Pathway- [electronic resource]
Regulatory Mechanisms of the Anti-cancer Cgamp-sting Pathway- [electronic resource]

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자료유형  
 학위논문
Control Number  
0016932002
International Standard Book Number  
9798379657185
Dewey Decimal Classification Number  
600
Main Entry-Personal Name  
Ritchie, Christopher.
Publication, Distribution, etc. (Imprint  
[S.l.] : Stanford University., 2023
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2023
Physical Description  
1 online resource(131 p.)
General Note  
Source: Dissertations Abstracts International, Volume: 84-12, Section: B.
General Note  
Advisor: Gao, Alex;Kim, Peter;Li, Lingyin.
Dissertation Note  
Thesis (Ph.D.)--Stanford University, 2023.
Restrictions on Access Note  
This item must not be sold to any third party vendors.
Summary, Etc.  
요약Throughout our lifetimes, our bodies encounter a plethora of threats on the cellular level, including pathogen infection, cellular damage, and the development of cancer. When these threats are not properly detected, they can lead to serious health problems, including death. Thankfully, our cells are pre-programmed with an array of innate immune pathways that can quickly respond to threats by detecting specific molecular danger signals that indicate a threat is present. Of these innate immune pathways, the cGAMP-STING pathway is on the forefront of the immune response due to its ability to detect mislocalized double stranded DNA (dsDNA). Since mislocalized dsDNA is a danger signal nearly ubiquitous with cellular threats, the cGAMP-STING pathway is essential for responding to most threats, including pathogen infection, cellular damage, and cancer. Given the extensive role of the cGAMP-STING pathway in defending against threats, regulation of the pathway is crucial to ensure its proper function. In this work, I show how intercellular pathway activation is regulated through cell-type specific transporters of the pathway's agonist, cGAMP, and how intracellular pathway activation is regulated through the E3-ubiquitin ligase PELI2.
Subject Added Entry-Topical Term  
Infections.
Subject Added Entry-Topical Term  
Cancer.
Subject Added Entry-Topical Term  
Endoplasmic reticulum.
Subject Added Entry-Topical Term  
Biochemistry.
Subject Added Entry-Topical Term  
Polymerization.
Subject Added Entry-Topical Term  
Binding sites.
Subject Added Entry-Topical Term  
Cytokines.
Subject Added Entry-Topical Term  
Autophagy.
Subject Added Entry-Topical Term  
Genes.
Subject Added Entry-Topical Term  
Apoptosis.
Subject Added Entry-Topical Term  
Cell cycle.
Subject Added Entry-Topical Term  
Polymers.
Subject Added Entry-Topical Term  
Dendritic cells.
Subject Added Entry-Topical Term  
Regulation.
Subject Added Entry-Topical Term  
Bacterial infections.
Subject Added Entry-Topical Term  
Lymphocytes.
Subject Added Entry-Topical Term  
Antigens.
Subject Added Entry-Topical Term  
Phosphorylation.
Subject Added Entry-Topical Term  
Viral infections.
Subject Added Entry-Topical Term  
Enzymes.
Subject Added Entry-Topical Term  
Interferon.
Subject Added Entry-Topical Term  
Transcription factors.
Subject Added Entry-Topical Term  
Cellular biology.
Subject Added Entry-Topical Term  
Immunology.
Subject Added Entry-Topical Term  
Pathology.
Subject Added Entry-Topical Term  
Pharmaceutical sciences.
Subject Added Entry-Topical Term  
Polymer chemistry.
Subject Added Entry-Topical Term  
Virology.
Added Entry-Corporate Name  
Stanford University.
Host Item Entry  
Dissertations Abstracts International. 84-12B.
Host Item Entry  
Dissertation Abstract International
Electronic Location and Access  
로그인을 한후 보실 수 있는 자료입니다.
Control Number  
joongbu:643225

MARC

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■0820  ▼a600
■1001  ▼aRitchie,  Christopher.
■24510▼aRegulatory  Mechanisms  of  the  Anti-cancer  Cgamp-sting  Pathway▼h[electronic  resource]
■260    ▼a[S.l.]▼bStanford  University.  ▼c2023
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2023
■300    ▼a1  online  resource(131  p.)
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  84-12,  Section:  B.
■500    ▼aAdvisor:  Gao,  Alex;Kim,  Peter;Li,  Lingyin.
■5021  ▼aThesis  (Ph.D.)--Stanford  University,  2023.
■506    ▼aThis  item  must  not  be  sold  to  any  third  party  vendors.
■520    ▼aThroughout  our  lifetimes,  our  bodies  encounter  a  plethora  of  threats  on  the  cellular  level,  including  pathogen  infection,  cellular  damage,  and  the  development  of  cancer.  When  these  threats  are  not  properly  detected,  they  can  lead  to  serious  health  problems,  including  death.  Thankfully,  our  cells  are  pre-programmed  with  an  array  of  innate  immune  pathways  that  can  quickly  respond  to  threats  by  detecting  specific  molecular  danger  signals  that  indicate  a  threat  is  present.  Of  these  innate  immune  pathways,  the  cGAMP-STING  pathway  is  on  the  forefront  of  the  immune  response  due  to  its  ability  to  detect  mislocalized  double  stranded  DNA  (dsDNA).  Since  mislocalized  dsDNA  is  a  danger  signal  nearly  ubiquitous  with  cellular  threats,  the  cGAMP-STING  pathway  is  essential  for  responding  to  most  threats,  including  pathogen  infection,  cellular  damage,  and  cancer.  Given  the  extensive  role  of  the  cGAMP-STING  pathway  in  defending  against  threats,  regulation  of  the  pathway  is  crucial  to  ensure  its  proper  function.  In  this  work,  I  show  how  intercellular  pathway  activation  is  regulated  through  cell-type  specific  transporters  of  the  pathway's  agonist,  cGAMP,  and  how  intracellular  pathway  activation  is  regulated  through  the  E3-ubiquitin  ligase  PELI2.
■590    ▼aSchool  code:  0212.
■650  4▼aInfections.
■650  4▼aCancer.
■650  4▼aEndoplasmic  reticulum.
■650  4▼aBiochemistry.
■650  4▼aPolymerization.
■650  4▼aBinding  sites.
■650  4▼aCytokines.
■650  4▼aAutophagy.
■650  4▼aGenes.
■650  4▼aApoptosis.
■650  4▼aCell  cycle.
■650  4▼aPolymers.
■650  4▼aDendritic  cells.
■650  4▼aRegulation.
■650  4▼aBacterial  infections.
■650  4▼aLymphocytes.
■650  4▼aAntigens.
■650  4▼aPhosphorylation.
■650  4▼aViral  infections.
■650  4▼aEnzymes.
■650  4▼aInterferon.
■650  4▼aTranscription  factors.
■650  4▼aCellular  biology.
■650  4▼aImmunology.
■650  4▼aPathology.
■650  4▼aPharmaceutical  sciences.
■650  4▼aPolymer  chemistry.
■650  4▼aVirology.
■690    ▼a0487
■690    ▼a0379
■690    ▼a0982
■690    ▼a0571
■690    ▼a0572
■690    ▼a0495
■690    ▼a0720
■71020▼aStanford  University.
■7730  ▼tDissertations  Abstracts  International▼g84-12B.
■773    ▼tDissertation  Abstract  International
■790    ▼a0212
■791    ▼aPh.D.
■792    ▼a2023
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T16932002▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.
■980    ▼a202402▼f2024

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