Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nicola J. Craig"'
Autor:
Steven D. Bryce, Vivienne Morrison, Nicola J. Craig, Nicholas R. Forsyth, Sara A. Fitzsimmons, Hazel Ireland, Andrew P. Cuthbert, Robert F. Newbold, E. Kenneth Parkinson
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 4, Iss 6, Pp 544-550 (2002)
Human chromosome 4 was previously shown to elicit features of senescence when introduced into cell lines that map to complementation group B for senescence, including HeLa cells. Subsequently, a DNA segment encoding the pseudogene Mortality Factor 4
Externí odkaz:
https://doaj.org/article/a6179be447d349699fd49d61c5fd5ae5
Autor:
E. Kenneth Parkinson, Nicholas R. Forsyth, Robert F. Newbold, Katrina E. Gordon, Sara A. Fitzsimmons, Hazel Ireland, Steven D. Bryce, Vivienne Morrison, Sally Dowen, Andrew P. Cuthbert, Nighean I Barr, Nicola J. Craig
Publikováno v:
Oncogene. 21:5135-5147
Squamous cell carcinoma (SCC) immortality is associated with p53 and INK4A dysfunction, high levels of telomerase and loss of heterozygosity (LOH) of other chromosomes, including chromosome 4. To test for a functional cancer mortality gene on human c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::336d5227b44aca3a4b60615a4e446fa0
https://doi.org/10.1038/sj.onc.1205688
https://doi.org/10.1038/sj.onc.1205688
Autor:
Andrew S. McCallion, Maurice Canham, Kim L. Hawker, María B. Durán Alonso, Thora A. Glencorse, Raymond J. MacDonald, D.P. Gilmore, Anthony P. Payne, Mary T. Gardiner, Nicola J. Craig, N.K. Bennett, J.M Campbell, Denise Donald, David Russell, Kirsty Maitland, Paul G. Shiels, R G Sutcliffe, R. Wayne Davies
Publikováno v:
Nature neuroscience. 4(11)
Rats harboring the agu mutation have altered behavior1 and brain pathology1 resembling human Parkinsonian syndromes2; notably, they have a movement disorder and age-progressive dysfunction and death of neurons in the midbrain (substantia nigra pars c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b907263a3437d626980df65241bb60b
https://pubmed.ncbi.nlm.nih.gov/11600890
https://pubmed.ncbi.nlm.nih.gov/11600890
Autor:
Nicola J. Craig, R G Sutcliffe, Alison J McVie, Sandra M. Burridge, Richard H. Wilson, Jennifer Varley, Bill Brintnell, A Michael Wallace, Martin W. McBride
Publikováno v:
Genomics. 61(3)
Seven members of the human 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene family (HGMW-approved symbols HSD3BP1-HSD3BP5) have been cloned and physically mapped. HSD3B1 and 2 express 3beta-HSD enzymes; HSD3Bpsi1-5 are unprocessed pseudogenes that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5e6f5ec4192a5cef9ede6a4b71fd3d8
https://pubmed.ncbi.nlm.nih.gov/10552929
https://pubmed.ncbi.nlm.nih.gov/10552929
Autor:
Sara A. Fitzsimmons, Nicholas R. Forsyth, E. Kenneth Parkinson, Robert F. Newbold, Nicola J. Craig, Andrew P. Cuthbert, Vivienne Morrison, Hazel Ireland, Steven D. Bryce
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 4, Iss 6, Pp 544-550 (2002)
Human chromosome 4 was previously shown to elicit features of senescence when introduced into cell lines that map to complementation group B for senescence, including HeLa cells. Subsequently, a DNA segment encoding the pseudogene Mortality Factor 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70094da7f37a01ee8da851175d11aa65