Jump to content

Gillian Bates: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous editNext edit →
Content deleted Content added
VisualWikitext
ce
Rescuing 2 sources and tagging 0 as dead. #IABot (v1.2)
Line 34: Line 34:


==Research==
==Research==
Bates's research has focused on [[Huntington's disease]]. She was one of the group who first cloned the [[Huntingtin|Huntington's disease gene]].<ref name="Macdonald1993">{{cite journal|last1=Macdonald|first1=M|title=A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes|journal=Cell|volume=72|issue=6|year=1993|pages=971–983|doi=10.1016/0092-8674(93)90585-E}}</ref><ref name="MangiariniSathasivam1996">{{cite journal|last1=Mangiarini|first1=Laura|last2=Sathasivam|first2=Kirupa|last3=Seller|first3=Mary|last4=Cozens|first4=Barbara|last5=Harper|first5=Alex|last6=Hetherington|first6=Colin|last7=Lawton|first7=Martin|last8=Trottier|first8=Yvon|last9=Lehrach|first9=Hans|last10=Davies|first10=Stephen W|last11=Bates|first11=Gillian P|title=Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic Mice|journal=Cell|volume=87|issue=3|year=1996|pages=493–506|doi=10.1016/S0092-8674(00)81369-0}}</ref> She also created the first mouse model of the disease, the R6/2 mouse, an important step in understanding the pathogenesis of Huntington's.<ref name=RS_bio>[http://royalsociety.org/publication.asp?id=7705 Royal Society: New Fellows - 2007: Amos - Bruce] (accessed 6 January 2009) {{dead|date=June 2016}}</ref>
Bates's research has focused on [[Huntington's disease]]. She was one of the group who first cloned the [[Huntingtin|Huntington's disease gene]].<ref name="Macdonald1993">{{cite journal|last1=Macdonald|first1=M|title=A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes|journal=Cell|volume=72|issue=6|year=1993|pages=971–983|doi=10.1016/0092-8674(93)90585-E}}</ref><ref name="MangiariniSathasivam1996">{{cite journal|last1=Mangiarini|first1=Laura|last2=Sathasivam|first2=Kirupa|last3=Seller|first3=Mary|last4=Cozens|first4=Barbara|last5=Harper|first5=Alex|last6=Hetherington|first6=Colin|last7=Lawton|first7=Martin|last8=Trottier|first8=Yvon|last9=Lehrach|first9=Hans|last10=Davies|first10=Stephen W|last11=Bates|first11=Gillian P|title=Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic Mice|journal=Cell|volume=87|issue=3|year=1996|pages=493–506|doi=10.1016/S0092-8674(00)81369-0}}</ref> She also created the first mouse model of the disease, the R6/2 mouse, an important step in understanding the pathogenesis of Huntington's.<ref name=RS_bio>[http://royalsociety.org/publication.asp?id=7705 Royal Society: New Fellows - 2007: Amos - Bruce](accessed 6 January 2009) {{wayback|url=http://royalsociety.org/publication.asp?id=7705 |date=20080609233936 }}</ref>


Prior to joining UCL in 2016, Bates was the head of the [[Neurogenetics]] Research Group at [[King's College London]].<ref name="kings-bates">{{cite web|title=King's College London - Gillian Bates|url=http://www.kcl.ac.uk/lsm/research/divisions/gmm/departments/mmg/researchgroups/bateslab/index.aspx|website=www.kcl.ac.uk|accessdate=10 June 2016}}</ref>
Prior to joining UCL in 2016, Bates was the head of the [[Neurogenetics]] Research Group at [[King's College London]].<ref name="kings-bates">{{cite web|title=King's College London - Gillian Bates|url=http://www.kcl.ac.uk/lsm/research/divisions/gmm/departments/mmg/researchgroups/bateslab/index.aspx|website=www.kcl.ac.uk|accessdate=10 June 2016}}</ref>


==Awards and honours==
==Awards and honours==
Bates has been elected a fellow of the [[Academy of Medical Sciences]] (1999) and a member of the [[European Molecular Biology Organisation]] (2002).<ref>http://people.embo.org/profile/gillian-bates</ref><ref name=AMS_bio>[http://www.acmedsci.ac.uk/p59fid374.html Academy of Medical Sciences: Fellows: Professor Gillian Bates] (accessed 6 January 2009)</ref><ref>[http://www.embo.org/communities/searchMembers.php EMBO: Search for an EMBO member] (accessed 6 January 2009)</ref> She was elected a Fellow of the [[Royal Society]] in 2007 and to its Council in 2011.<ref name=RS_bio/><ref name=RSCouncil>{{cite web|title=Council of the Royal Society|url=http://royalsociety.org/about-us/governance/council/|accessdate=5 November 2012}}</ref> In 1998, she was awarded the Royal Society Glaxo Wellcome Award jointly with Stephen Davies, for the "discovery of the cause of Huntington's Disease".<ref>[http://royalsociety.org/page.asp?id=1779 Royal Society: GlaxoSmithKline previous winners 2005 - 1980] (accessed 6 January 2009) {{dead|date=June 2016}}</ref>
Bates has been elected a fellow of the [[Academy of Medical Sciences]] (1999) and a member of the [[European Molecular Biology Organisation]] (2002).<ref>http://people.embo.org/profile/gillian-bates</ref><ref name=AMS_bio>[http://www.acmedsci.ac.uk/p59fid374.html Academy of Medical Sciences: Fellows: Professor Gillian Bates] (accessed 6 January 2009)</ref><ref>[http://www.embo.org/communities/searchMembers.php EMBO: Search for an EMBO member] (accessed 6 January 2009)</ref> She was elected a Fellow of the [[Royal Society]] in 2007 and to its Council in 2011.<ref name=RS_bio/><ref name=RSCouncil>{{cite web|title=Council of the Royal Society|url=http://royalsociety.org/about-us/governance/council/|accessdate=5 November 2012}}</ref> In 1998, she was awarded the Royal Society Glaxo Wellcome Award jointly with Stephen Davies, for the "discovery of the cause of Huntington's Disease".<ref>[http://royalsociety.org/page.asp?id=1779 Royal Society: GlaxoSmithKline previous winners 2005 - 1980](accessed 6 January 2009) {{wayback|url=http://royalsociety.org/page.asp?id=1779 |date=20080609053756 }}</ref>


==References==
==References==

Revision as of 22:23, 8 September 2016

Gillian Bates
Born (1956-05-19) May 19, 1956 (age 68)[1]
NationalityBritish
Alma mater
Known forCo-discovering cause of Huntington's disease
Awards
Scientific career
FieldsNeurogenetics
Institutions
ThesisMolecular approaches towards the fine genetic mapping of human chromosomes : with special reference to the cystic fibrosis gene (1987)
Websitewww.ucl.ac.uk/ion/departments/sobell/Research/GBates

Gillian Patricia Bates (born 19 May 1956)[1] FMedSci FRS is a British biologist. She is distinguished for her research into the molecular basis of Huntington's disease and in 1998 was awarded the GlaxoSmithKline Prize as a co-discoverer of the cause of this disease. As of 2016, she is Professor of Neurogenetics at UCL Institute of Neurology and the co-director of UCL Huntington's Disease Centre.[2][3]

Education

Bates was educated at Kenilworth Grammar School and the University of Sheffield where she graduated with a Bachelor of Science degree in 1979.[1] She completed her postgraduate study at Birkbeck College, London where she was awarded a Master of Science degree in 1984 followed by St Mary's Hospital Medical School where she was awarded a PhD 1987 for genetic mapping of the cystic fibrosis gene.[1][4]

Research

Bates's research has focused on Huntington's disease. She was one of the group who first cloned the Huntington's disease gene.[5][6] She also created the first mouse model of the disease, the R6/2 mouse, an important step in understanding the pathogenesis of Huntington's.[7]

Prior to joining UCL in 2016, Bates was the head of the Neurogenetics Research Group at King's College London.[8]

Awards and honours

Bates has been elected a fellow of the Academy of Medical Sciences (1999) and a member of the European Molecular Biology Organisation (2002).[9][10][11] She was elected a Fellow of the Royal Society in 2007 and to its Council in 2011.[7][12] In 1998, she was awarded the Royal Society Glaxo Wellcome Award jointly with Stephen Davies, for the "discovery of the cause of Huntington's Disease".[13]

References

  1. ^ a b c d http://ukwhoswho.com/view/article/oupww/whoswho/U6775
  2. ^ "Prof. G. Bates". www.ucl.ac.uk. Retrieved 10 June 2016.
  3. ^ Gillian Bates's publications indexed by the Scopus bibliographic database. (subscription required)
  4. ^ Bates, Gillian Patricia (1987). Molecular approaches towards the fine genetic mapping of human chromosomes : with special reference to the cystic fibrosis gene (PhD thesis). University of London. OCLC 940163599.
  5. ^ Macdonald, M (1993). "A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes". Cell. 72 (6): 971–983. doi:10.1016/0092-8674(93)90585-E.
  6. ^ Mangiarini, Laura; Sathasivam, Kirupa; Seller, Mary; Cozens, Barbara; Harper, Alex; Hetherington, Colin; Lawton, Martin; Trottier, Yvon; Lehrach, Hans; Davies, Stephen W; Bates, Gillian P (1996). "Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic Mice". Cell. 87 (3): 493–506. doi:10.1016/S0092-8674(00)81369-0.
  7. ^ a b Royal Society: New Fellows - 2007: Amos - Bruce(accessed 6 January 2009) Template:Wayback
  8. ^ "King's College London - Gillian Bates". www.kcl.ac.uk. Retrieved 10 June 2016.
  9. ^ http://people.embo.org/profile/gillian-bates
  10. ^ Academy of Medical Sciences: Fellows: Professor Gillian Bates (accessed 6 January 2009)
  11. ^ EMBO: Search for an EMBO member (accessed 6 January 2009)
  12. ^ "Council of the Royal Society". Retrieved 5 November 2012.
  13. ^ Royal Society: GlaxoSmithKline previous winners 2005 - 1980(accessed 6 January 2009) Template:Wayback
Retrieved from "https://en.wikipedia.org/w/index.php?title=Gillian_Bates&oldid=738429561"