James A Quinn

Prof. James A Quinn

University of Liverpool, Liverpool, United Kingdom
orcid

Research Focus & Metrics

Academic Career Length

42Years (1985-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2019 in The Lancet Neurology
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Journal Article
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MNMike A Nalls
Mike A Nalls
CBCornelis Blauwendraat
Cornelis Blauwendraat
KHKarl Heilbron
Karl Heilbron
SBSara Bandres-Ciga
Sara Bandres-Ciga
DCDiana Chang
Diana Chang
FZFutao Zhang
Futao Zhang

1 June 1996 in Cellular and Molecular Neurobiology
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Journal Article
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George FinkGeorge Fink
George Fink
BSBarbara E. H. Sumner
Barbara E. H. Sumner
RRRoberta Rosie
Roberta Rosie
OGOliver Grace
Oliver Grace
JQJames A Quinn
James A Quinn

21 December 1999 in Proceedings of the National Academy of Sciences
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AMAlasdair MacKenzie
Alasdair MacKenzie
JQJames A Quinn
James A Quinn
Polymorphic regions consisting of a variable number of tandem repeats within intron 2 of the gene coding for the serotonin transporter protein 5-HTT have been associated with susceptibility to affective disorders. We have cloned two of these intronic polymorphisms, Stin2.10 and Stin2.12, into an expression vector containing a heterologous minimal promoter and the bacterial LacZ reporter gene. These constructs were then used to produce transgenic mice. In embryonic day 10.5 embryos, both Stin2.10 and Stin2.12 produced consistent β-galactosidase expression in the embryonic midbrain, hindbrain, and spinal cord floor plate. However, we observed that the levels of β-galactosidase expression produced by both the Stin2.10 and Stin2.12 within the rostral hindbrain differed significantly at embryonic day 10.5. Our data suggest that these polymorphic variable number of tandem repeats regions act as transcriptional regulators and have allele-dependent differential enhancer-like properties within an area of the hindbrain where the 5-HTT gene is known to be transcribed at this stage of development.

10 September 1999 in FEBS Letters
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CFC.E. Fiskerstrand
C.E. Fiskerstrand
ELE.A. Lovejoy
E.A. Lovejoy
JQJames A Quinn
James A Quinn

1 August 2010 in American Journal of Psychiatry
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Journal Article
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CLCathryn Lewis
Cathryn Lewis
MNMandy Y. Ng
Mandy Y. Ng
ABAmy W. Butler
Amy W. Butler
SCSarah Cohen-Woods
Sarah Cohen-Woods
RURudolf Uher
Rudolf Uher
PMPeter McGuffin
Peter McGuffin

1 January 1985 in Nucleic Acids Research
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Journal Article
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JQJames A Quinn
James A Quinn
DMDuncan J. McGeoch
Duncan J. McGeoch
In the long unique region of the genome of herpes simplex virus type 1 (HSV-1), the genes for DNA polymerase and the major DNA binding protein are arranged in a head to head manner, with an origin of DNA replication (termed OriL) located between them. This paper reports an 8400 base pair DNA sequence containing both genes and the origin, obtained mostly by M13/dideoxy analysis of plasmid cloned fragments. Amino acid sequences of the two proteins were deduced. Homologues of both genes were detected in the genome sequence of the distantly related Epstein-Barr virus (EBV). Arrangement of these HSV-1 and EBV genes differs in genome location and in relative orientation. A part of HSV-1 DNA polymerase was found to be similar to a sequence in adenovirus 2 DNA polymerase, but the significance of this is unclear. Since a DNA sequence in the locality of OriL deletes on plasmid cloning, this region was analysed using virus DNA. A palindrome with 72-residue arms was found, which shows great similarity to the better characterized origin, OriS.