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Survival Motor Neuron Protein Interaction Partners in Drosophila melanogaster
Survival Motor Neuron Protein Interaction Partners in Drosophila melanogaster

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자료유형  
 학위논문
Control Number  
0014996834
International Standard Book Number  
9780438033368
Dewey Decimal Classification Number  
574
Main Entry-Personal Name  
Gray, Kelsey Marie.
Publication, Distribution, etc. (Imprint  
[Sl] : The University of North Carolina at Chapel Hill, 2018
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2018
Physical Description  
139 p
General Note  
Source: Dissertation Abstracts International, Volume: 79-10(E), Section: B.
General Note  
Advisers: Arnold G. Matera
Dissertation Note  
Thesis (Ph.D.)--The University of North Carolina at Chapel Hill, 2018.
Summary, Etc.  
요약Spinal Muscular Atrophy (SMA) is a neuromuscular disorder that results from biallelic loss-of-function mutations in the human survival motor neuron 1 (SMN1) gene. Tissue-specific and housekeeping functions have been ascribed to SMN
Summary, Etc.  
요약We also identified Slmb, SkpA, and Cullin 1 as being highly enriched in Flag-SMN samples as compared to the control sample. Together, these proteins comprise the SCFSlmb E3 ubiquitin ligase. These interactions were verified in Drosophila S2 cell
Summary, Etc.  
요약We identified additional protein interactions of SMN with CG2941, nucleosome assembly protein 1 (Nap1), and Bendless (Ben). Each of these interactions was verified in cell culture or using antibodies generated specifically for the protein of int
Summary, Etc.  
요약We have examined SMN protein interactions in the context of developing Drosophila melanogaster embryos, with follow-up studies in mouse, and human systems. When SMN is unable to self-oligomerize, the Slmb degron is highly accessible, and thus S
Subject Added Entry-Topical Term  
Molecular biology
Subject Added Entry-Topical Term  
Genetics
Added Entry-Corporate Name  
The University of North Carolina at Chapel Hill Genetics and Molecular Biology
Host Item Entry  
Dissertation Abstracts International. 79-10B(E).
Host Item Entry  
Dissertation Abstract International
Electronic Location and Access  
로그인을 한후 보실 수 있는 자료입니다.
Control Number  
joongbu:553265

MARC

 008190618s2018                                          c    eng  d
■001000014996834
■00520190102171315
■020    ▼a9780438033368
■035    ▼a(MiAaPQ)AAI10744561
■035    ▼a(MiAaPQ)unc:17501
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a574
■1001  ▼aGray,  Kelsey  Marie.
■24510▼aSurvival  Motor  Neuron  Protein  Interaction  Partners  in    Drosophila  melanogaster
■260    ▼a[Sl]▼bThe  University  of  North  Carolina  at  Chapel  Hill▼c2018
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2018
■300    ▼a139  p
■500    ▼aSource:  Dissertation  Abstracts  International,  Volume:  79-10(E),  Section:  B.
■500    ▼aAdvisers:  Arnold  G.  Matera
■5021  ▼aThesis  (Ph.D.)--The  University  of  North  Carolina  at  Chapel  Hill,  2018.
■520    ▼aSpinal  Muscular  Atrophy  (SMA)  is  a  neuromuscular  disorder  that  results  from  biallelic  loss-of-function  mutations  in  the  human  survival  motor  neuron  1  (SMN1)  gene.  Tissue-specific  and  housekeeping  functions  have  been  ascribed  to  SMN
■520    ▼aWe  also  identified  Slmb,  SkpA,  and  Cullin  1  as  being  highly  enriched  in  Flag-SMN  samples  as  compared  to  the  control  sample.  Together,  these  proteins  comprise  the  SCFSlmb  E3  ubiquitin  ligase.  These  interactions  were  verified  in  Drosophila  S2  cell
■520    ▼aWe  identified  additional  protein  interactions  of  SMN  with  CG2941,  nucleosome  assembly  protein  1  (Nap1),  and  Bendless  (Ben).  Each  of  these  interactions  was  verified  in  cell  culture  or  using  antibodies  generated  specifically  for  the  protein  of  int
■520    ▼aWe  have  examined  SMN  protein  interactions  in  the  context  of  developing    Drosophila  melanogaster  embryos,  with  follow-up  studies  in  mouse,  and  human  systems.  When  SMN  is  unable  to  self-oligomerize,  the  Slmb  degron  is  highly  accessible,  and  thus  S
■590    ▼aSchool  code:  0153.
■650  4▼aMolecular  biology
■650  4▼aGenetics
■690    ▼a0307
■690    ▼a0369
■71020▼aThe  University  of  North  Carolina  at  Chapel  Hill▼bGenetics  and  Molecular  Biology.
■7730  ▼tDissertation  Abstracts  International▼g79-10B(E).
■773    ▼tDissertation  Abstract  International
■790    ▼a0153
■791    ▼aPh.D.
■792    ▼a2018
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T14996834▼nKERIS
■980    ▼a201812▼f2019

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