Dr Mark C Hirst
机构: Visiting fellow, Open University (Retired)
每年引用次数
引用次数
引用: 4,198
H-指数: 30
I10-指数 : 44
出版物: 100
Encyclopaedia of Life Sciences. Print version. 20 volumes. 14,288 pages.
PT Matsudaira , Baset Wood , G Phillips , RM Atlas
(Vol.2001). Nature Publishing Group: London. (2001)
2001
Encyclopedia of Life Sciences. Print version (26 volumes)
PT Matsudaira , G Phillips , RM Atlas , JW Silvertown
(Vol.1-26). Nature Publishing Group/Wiley: London/Chichester. (2007)
2007
Dopamine restores cortical function Huntington's disease mice
SC Vatsavayai , GM Dallerac , DM Cummings , MC Hirst
Journal of Neurology, Neurosurgery, and Psychiatry
2005
B24 Dysfunctional dopaminergic neurones and biphasic activity-dependent dopamine release in mouse models of Huntington's disease
KPSJ Murphy , GM Dallerac , AJ Milnerwood , DM Cummings
Journal of Neurology, Neurosurgery, and Psychiatry 83
2012
PL 3O7
S Hake , PA Hamel , BL Gallie , RA Phillips
Altered dopaminergic function in a mouse model of Huntington's disease
GM Dallerac , AJ Milner , DM Cummings , SC Vatsavayai
BMJ PUBLISHING GROUP 76 ? -?
2005
Is the progression of Huntington's disease determined by somatic CAG repeat instability?
SC Vatsavayai , GM Dallerac , AJ Milner , DM Cummings
BMJ PUBLISHING GROUP 76 ? -?
2005
Physical mapping studies in Xq27 to Xq28-analysis of a novel DNA marker close to the fragile site
MV Bell , MC Hirst , R Mckinnon , JEV Watson
Cytogenetics and Cell Genetics 51 960 -960
3
1989
Identification oftheFRAXE fragile site intwo families ascertained forX linked mental retardation
GA Flynn , MC Hirst , SJ Knight , JN Macpherson
78
1993
Instability of a (CGG)98 repeat in the Fmr1 promoter
CJM Bontekoe , CE Bakker , IM Nieuwenhuizen , H van Der Linde
Human Molecular Genetics 10 ( 16) 1693 -1699
119
2001
FRAXE MENTAL-RETARDATION ASSOCIATED WITH TRINUCLEOTIDE REPEAT EXPANSION AND HYPERMETHYLATION OF A CPG ISLAND IN XQ28
SJL Knight , AV Flannery , MC Hirst , L Campbell
AMERICAN JOURNAL OF HUMAN GENETICS 53 ( 3) 79 -79
1
1993
Modelling genetic instability of the human FMR1 trinucleotide repeat
MC Hirst , PJ White
AMERICAN JOURNAL OF HUMAN GENETICS 61 ( 4) A310 -A310
1997
THE GENETICAL SOCIETY
MC Hirst , DJ Porteous , I Hickey , S Jones
Heredity 60 311 -319
1988
The identification of a third fragile site, FRAXF, in Xq27 — q28 distal to both FRAXA and FRAXE
M.C. Hirst , A. Barnicoat , G. Flynn , Q. Wang
Human Molecular Genetics 2 ( 2) 197 -200
64
1993
Impaired Long-Term Potentiation in the Prefrontal Cortex of Huntington’s Disease Mouse Models: Rescue by D1 Dopamine Receptor Activation
G.M. Dallérac , S.C. Vatsavayai , D.M. Cummings , A.J. Milnerwood
Neurodegenerative Diseases 8 ( 4) 230 -239
33
2011
Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome
M.V. Bell , M.C. Hirst , Y. Nakahori , R.N. MacKinnon
Cell 64 ( 4) 861 -866
303
1991
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
S.J.L. Knight , A.V. Flannery , M.C. Hirst , L. Campbell
Cell 74 ( 1) 127 -134
646
1993
Linear order of new and established DNA markers around the fragile site at Xq27.3.
M.C. Hirst , A. Roche , T.J. Flint , R.N. MacKinnon
Genomics 10 ( 1) 243 -249
28
1991
A YAC contig across the fragile X site defines the region of fragility.
M.C. Hirst , K. Rack , Y. Nakahori , A. Roche
Nucleic Acids Research 19 ( 12) 3283 -3288
29
1991
Molecular heterogeneity of the fragile X syndrome.
Y. Nakahori , S.J.L. Knight , J. Holland , C. Schwartz
Nucleic Acids Research 19 ( 16) 4355 -4359
93
1991