Zobrazeno 1 - 10
of 491
pro vyhledávání: '"Spurr N"'
Autor:
Parsons, S. F., Mallinson, G., Holmes, C. H., Houlihan, J. M., Simpson, K. L., Mawby, W. J., Spurr, N. K., Warne, D., Barclay, A. N., Anstee, D. J.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1995 Jun 01. 92(12), 5496-5500.
Externí odkaz:
https://www.jstor.org/stable/2367543
Autor:
Solomon, E., Hiorns, L. R., Spurr, N., Kurkinen, M., Barlow, D., Hogan, B. L. M., Dalgleish, R.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1985 May . 82(10), 3330-3334.
Externí odkaz:
https://www.jstor.org/stable/25577
Autor:
Weller, P. A., Ogryzko, E. P., Corben, E. B., Zhidkova, N. I., Patel, B., Price, G. J., Spurr, N. K., Koteliansky, V. E., Critchley, D. R.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1990 Aug 01. 87(15), 5667-5671.
Externí odkaz:
https://www.jstor.org/stable/2354984
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1989 Aug . 86(16), 6211-6214.
Externí odkaz:
https://www.jstor.org/stable/34296
Autor:
Isaacs, A. M., Oliver, P. L., Jones, E. L., Jeans, A., Potter, A., Hovik, B. H., Patrick Nolan, Vizor, L., Glenister, P., Simon, A. K., Gray, I. C., Spurr, N. K., Brown, S. D. M., Hunter, A. J., Davies, K. E.
Publikováno v:
Scopus-Elsevier
The robotic mouse is an autosomal dominant mutant that arose from a large-scale chemical mutagenesis program. It has a jerky, ataxic gait and develops adult-onset Purkinje cell loss in the cerebellum in a striking region-specific pattern, as well as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c33cf95dbb4197f772e603409d1ebcd5
https://ora.ox.ac.uk/objects/uuid:dae41685-9654-4aa3-a94a-b2da6a124287
https://ora.ox.ac.uk/objects/uuid:dae41685-9654-4aa3-a94a-b2da6a124287
Autor:
Spurr, N, Blanton, S, Bookstein, R, Clarke, R, Cottingham, R, Daiger, S, Drayna, D, Faber, P, Horrigan, S, Kas, K, Kirchgessner, C, Kumar, S, Leach, R, Luedecke, H, Nakamura, Y, Pebusque, M, Ranta, S, Sim, E, Sullivan, L, Takle, L, Vance, J, Wagner, M, Wells, D, Westbrook, C, Yaremko, L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::8b18965e26a3a6cd3a8857a5790af5b0
https://ora.ox.ac.uk/objects/uuid:4fa8746e-1763-4c6e-acb1-fe7657624a7d
https://ora.ox.ac.uk/objects/uuid:4fa8746e-1763-4c6e-acb1-fe7657624a7d
Publikováno v:
Europe PubMed Central
In response to cell-free conditioned medium derived from the human bladder carcinoma line T24 (T24 SN), we found greatly reduced incorporation of tritiated thymidine and uridine ([3H]TdR, [3H]UR) by the human carcinoma lines UCHNCu (small-cell lung c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3feda6067c404ab4845b040ee67225a1
https://ora.ox.ac.uk/objects/uuid:238414e4-db3c-47ee-980e-cf8ac669742d
https://ora.ox.ac.uk/objects/uuid:238414e4-db3c-47ee-980e-cf8ac669742d
Autor:
White, J. A., McAlpine, P. J., Antonarakis, Stylianos, Cann, H., Eppig, J. T., Frazer, K., Frezal, J., Lancet, D., Nahmias, J., Pearson, P., Peters, J., Scott, A., Scott, Hamish Steele, Spurr, N., Talbot, C., Jr., Povey, S.
Publikováno v:
Genomics, Vol. 45, No 2 (1997) pp. 468-471
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::09b680552bd8f26f65871f44b9fcf55f
https://pubmed.ncbi.nlm.nih.gov/9344684
https://pubmed.ncbi.nlm.nih.gov/9344684
Autor:
Cox, S A, Attwood, J, Bryant, S P, Bains, R, Povey, S, Rebello, M, Kapsetaki, M, Moschonas, N K, Grzeschik, K H, Otto, M, Dixon, M, Sudworth, H E, Kooy, R F, Wright, A, Teague, P, Terrenato, L, Vergnaud, Gilles, Monfouilloux, S, Weissenbach, J, Alibert, O, Dib, C, Fauré, S, Bakker, E, Pearson, Nathaniel M., Spurr, N K
Publikováno v:
Annals of Human Genetics
Annals of Human Genetics, Wiley, 1996, 60 (Pt 6), pp.447-86
Annals of Human Genetics, 1996, 60 (Pt 6), pp.447-86
Annals of Human Genetics, Wiley, 1996, 60 (Pt 6), pp.447-86
Annals of Human Genetics, 1996, 60 (Pt 6), pp.447-86
International audience; Meiotic breakpoint panels for human chromosomes 2, 3, 4, 5, 6, 7, 8, 9, 10, 13, 14, 15, 17, 18, 20 and X were constructed from genotypes from the CEPH reference families. Each recombinant chromosome included has a breakpoint w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::574f17165dcce09647c2bcdf49cdff69
https://pubmed.ncbi.nlm.nih.gov/9024576
https://pubmed.ncbi.nlm.nih.gov/9024576
Autor:
SPURR, N, BLANTON, S, BOOKSTEIN, R, CLARKE, R, COTTINGHAM, R, DAIGER, S, DRAYNA, D, FABER, P, HORRIGAN, S, KAS, K, KIRCHGESSNER, C, KUMAR, S, LEACH, R, LUEDECKE, H, NAKAMURA, Y, PEBUSQUE, M, RANTA, S, SIM, E, SULLIVAN, L, TAKLE, L, VANCE, J, WAGNER, M, WELLS, D, WESTBROOK, C, YAREMKO, L, ZALETAYEV, D, ZUFFARDI, O, WOOD, S
Publikováno v:
CYTOGENETICS AND CELL GENETICS. 68(3-4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::8cf4bf67f98c8db6d059021774a96981
http://ora.ox.ac.uk/objects/uuid:4fa8746e-1763-4c6e-acb1-fe7657624a7d
http://ora.ox.ac.uk/objects/uuid:4fa8746e-1763-4c6e-acb1-fe7657624a7d