Mr John McAbney

  • Technician (Cardiovascular & Metabolic Health Professional Services)

telephone: 01413304483
email: John.McAbney@glasgow.ac.uk

Lab 440, West Medical Building, ICAMS, CMVLS, University of Glasgow, G12 8QQ

Import to contacts

Publications

List by: Type | Date

Jump to: 2023 | 2010 | 2007 | 2004 | 2003 | 2002
Number of items: 8.

2023

Sykes, R. A. et al. (2023) Vascular mechanisms of post-COVID-19 conditions: rho-kinase is a novel target for therapy. European Heart Journal: Cardiovascular Pharmacotherapy, 9(4), pp. 371-386. (doi: 10.1093/ehjcvp/pvad025) (PMID:37019821) (PMCID:PMC10236521)

2010

Burton, P. et al. (2010) Erythro-9-(2-hydroxy-3-nonyl)adenine (EHNA) blocks differentiation and maintains the expression of pluripotency markers in human embryonic stem cells. Biochemical Journal, 432(3), pp. 575-584. (doi: 10.1042/BJ20100726)

Burton, P. et al. (2010) Identification and characterization of small-molecule ligands that maintain pluripotency of human embryonic stem cells. Biochemical Society Transactions, 38(4), pp. 1058-1061. (doi: 10.1042/BST0381058)

2007

Veitch, N.J. , Ennis, M., McAbney, J.P., Shelbourne, P.F. and Monckton, D.G. (2007) Inherited CAG center dot CTG allele length is a major modifier of somatic mutation length variability in Huntington disease. DNA Repair, 6(6), pp. 789-796. (doi: 10.1016/j.dnarep.2007.01.002)

2004

Gomes-Pereira, M., Fortune, M.T., Ingram, L., McAbney, J.P. and Monckton, D.G. (2004) Pms2 is a genetic enhancer of trinucleotide CAG·CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion. Human Molecular Genetics, 13(16), 1815 -1825. (doi: 10.1093/hmg/ddh186)

Martorell, L., Gamez, J., Cayuela, M.L., Gould, F.K., McAbney, J.P., Ashizawa, T., Monckton, D.G. and Baiget, M. (2004) Germline mutational dynamics in myotonic dystrophy type 1 males: Allele length and age effects. Neurology, 62(2), 269 -274.

2003

Libby, R.T. et al. (2003) Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice. Human Molecular Genetics, 12(1), 41 -50. (doi: 10.1093/hmg/ddg006)

2002

Abbruzzese, A., Costanzi Porrini, S., Mariani, B., Gould, F.K., McAbney, J.P., Monckton, D.G. , Ashizawa, T. and Giacanelli, M. (2002) Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1. Annals of Neurology, 52(4), 435 -441. (doi: 10.1002/ana.10304)

This list was generated on Thu Nov 7 14:12:51 2024 GMT.
Jump to: Articles
Number of items: 8.

Articles

Sykes, R. A. et al. (2023) Vascular mechanisms of post-COVID-19 conditions: rho-kinase is a novel target for therapy. European Heart Journal: Cardiovascular Pharmacotherapy, 9(4), pp. 371-386. (doi: 10.1093/ehjcvp/pvad025) (PMID:37019821) (PMCID:PMC10236521)

Burton, P. et al. (2010) Erythro-9-(2-hydroxy-3-nonyl)adenine (EHNA) blocks differentiation and maintains the expression of pluripotency markers in human embryonic stem cells. Biochemical Journal, 432(3), pp. 575-584. (doi: 10.1042/BJ20100726)

Burton, P. et al. (2010) Identification and characterization of small-molecule ligands that maintain pluripotency of human embryonic stem cells. Biochemical Society Transactions, 38(4), pp. 1058-1061. (doi: 10.1042/BST0381058)

Veitch, N.J. , Ennis, M., McAbney, J.P., Shelbourne, P.F. and Monckton, D.G. (2007) Inherited CAG center dot CTG allele length is a major modifier of somatic mutation length variability in Huntington disease. DNA Repair, 6(6), pp. 789-796. (doi: 10.1016/j.dnarep.2007.01.002)

Gomes-Pereira, M., Fortune, M.T., Ingram, L., McAbney, J.P. and Monckton, D.G. (2004) Pms2 is a genetic enhancer of trinucleotide CAG·CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion. Human Molecular Genetics, 13(16), 1815 -1825. (doi: 10.1093/hmg/ddh186)

Martorell, L., Gamez, J., Cayuela, M.L., Gould, F.K., McAbney, J.P., Ashizawa, T., Monckton, D.G. and Baiget, M. (2004) Germline mutational dynamics in myotonic dystrophy type 1 males: Allele length and age effects. Neurology, 62(2), 269 -274.

Libby, R.T. et al. (2003) Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice. Human Molecular Genetics, 12(1), 41 -50. (doi: 10.1093/hmg/ddg006)

Abbruzzese, A., Costanzi Porrini, S., Mariani, B., Gould, F.K., McAbney, J.P., Monckton, D.G. , Ashizawa, T. and Giacanelli, M. (2002) Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1. Annals of Neurology, 52(4), 435 -441. (doi: 10.1002/ana.10304)

This list was generated on Thu Nov 7 14:12:51 2024 GMT.