Показ 1 - 9 результатів із 9 для пошуку 'Playford, R', час виконання запиту: 0.02сек.
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1
Once you start, you can't stop. за авторством Ashrafian, H, Taylor-Robinson, S, Calam, J, Playford, R
Опубліковано 2002Journal article -
2
Novel presentation of coeliac disease after following the Atkins' low carbohydrate diet. за авторством van Heel, D, Dart, J, Nichols, S, Jewell, D, Playford, R
Опубліковано 2005Journal article -
3
Synergy between TLR9 and NOD2 innate immune responses is lost in genetic Crohn's disease. за авторством van Heel, D, Ghosh, S, Hunt, K, Mathew, C, Forbes, A, Jewell, D, Playford, R
Опубліковано 2005Journal article -
4
A common CTLA4 haplotype associated with coeliac disease за авторством Hunt, K, McGovern, D, Kumar, P, Ghosh, S, Travis, S, Walters, J, Jewell, D, Playford, R, van Heel, D
Опубліковано 2005Conference item -
5
A common CTLA4 haplotype associated with coeliac disease. за авторством Hunt, K, McGovern, D, Kumar, P, Ghosh, S, Travis, S, Walters, JR, Jewell, D, Playford, R, van Heel, D
Опубліковано 2005Journal article -
6
Lack of association of MYO9B genetic variants with coeliac disease in a British cohort. за авторством Hunt, K, Monsuur, A, McArdle, W, Kumar, P, Travis, S, Walters, JR, Jewell, D, Strachan, D, Playford, R, Wijmenga, C, van Heel, D
Опубліковано 2006Journal article -
7
Mutated epithelial cadherin is associated with increased tumorigenicity and loss of adhesion and of responsiveness to the motogenic trefoil factor 2 in colon carcinoma cells. за авторством Efstathiou, J, Liu, D, Wheeler, J, Kim, H, Beck, N, Ilyas, M, Karayiannakis, A, Mortensen, N, Kmiot, W, Playford, R, Pignatelli, M, Bodmer, W
Опубліковано 1999Journal article -
8
Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease. за авторством van Heel, D, Ghosh, S, Butler, M, Hunt, K, Lundberg, A, Ahmad, T, McGovern, D, Onnie, C, Negoro, K, Goldthorpe, S, Foxwell, B, Mathew, C, Forbes, A, Jewell, D, Playford, R
Опубліковано 2005Journal article -
9
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. за авторством van Heel, D, Franke, L, Hunt, K, Gwilliam, R, Zhernakova, A, Inouye, M, Wapenaar, M, Barnardo, M, Bethel, G, Holmes, G, Feighery, C, Jewell, D, Kelleher, D, Kumar, P, Travis, S, Walters, JR, Sanders, D, Howdle, P, Swift, J, Playford, R, McLaren, WM, Mearin, M, Mulder, C, McManus, R, McGinnis, R
Опубліковано 2007Journal article