The place of fault in Grotius's conception of liability for wrongdoing by Sampson, J

The limits of natural law: liability for wrongdoing in the Inleidinge by Sampson, J

Crystal structure analysis of anti-V2 mAb 2158 suggests a conformational epitope involving an N-linked glycan by Spurrier B, Pan R, Sampson J, Williams C, Gorny M, Zolla-Pazner S, Kong X

P04-42. Molecular design of a mimotope that preserves conserved structural elements of the HIV-1 V3 crown by Zollla-Pazner S, Gorny MK, Williams C, Sampson J, Totrov M, Jiang X, Kong X

Guidelines for industrially-based multiple case studies in software engineering by Verner, J.M., Sampson, J., Tosic, V., Abu Bakar, Nur Azzah, Kitchenham, B.A.

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Risk of all-cause mortality associated with nonfatal AIDS and serious non-AIDS events among adults infected with HIV. by Neuhaus, J, Angus, B, Kowalska, J, La Rosa, A, Sampson, J, Wentworth, D, Mocroft, A

An exploratory comparison of genetic counselling protocols for HNPCC predictive testing. by Brain, K, Sivell, S, Bennert, K, Howell, L, France, L, Jordan, S, Rogers, M, Gray, J, Sampson, J

Diagnosis of invasive pneumococcal disease among children in Kenya with enzyme-linked immunosorbent assay for immunoglobulin G antibodies to pneumococcal surface adhesin A. by Scott, J, Mlacha, Z, Nyiro, J, Njenga, S, Lewa, P, Obiero, J, Otieno, H, Sampson, J, Carlone, G

Characterization of mutations in patients with multiple endocrine neoplasia type 1. by Bassett, J, Forbes, SA, Pannett, A, Lloyd, SE, Christie, P, Wooding, C, Harding, B, Besser, G, Edwards, C, Monson, J, Sampson, J, Wass, J, Wheeler, M, Thakker, R

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome. by Nesbit, M, Bowl, MR, Harding, B, Ali, A, Ayala, A, Crowe, C, Dobbie, A, Hampson, G, Holdaway, I, Levine, M, McWilliams, R, Rigden, S, Sampson, J, Williams, A, Thakker, R

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. by Ylikorkala, A, Avizienyte, E, Tomlinson, I, Tiainen, M, Roth, S, Loukola, A, Hemminki, A, Johansson, M, Sistonen, P, Markie, D, Neale, K, Phillips, R, Zauber, P, Twama, T, Sampson, J, Järvinen, H, Mäkelä, T, Aaltonen, L

Clinical studies of multiple endocrine neoplasia type 1 (MEN1) (vol 89, pg 653, 1996) by Trump, D, Farren, B, Wooding, C, Pang, J, Besser, G, Buchanan, K, Edwards, C, Heath, D, Jackson, C, Jansen, S, Lips, K, Monson, J, OHalloran, D, Sampson, J, Shalet, S, Wheeler, M, Zink, A, Thakker, R

Clinical studies of multiple endocrine neoplasia type 1 (MEN1) by Trump, D, Farren, B, Wooding, C, Pang, J, Besser, G, Buchanan, K, Edwards, C, Heath, D, Jackson, C, Jansen, S, Lips, K, Monson, J, O'Halloran, D, Sampson, J, Shalet, S, Wheeler, M, Zink, A, Thakker, R

Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q. by Lamlum, H, Al Tassan, N, Jaeger, E, Frayling, I, Sieber, O, Reza, F, Eckert, M, Rowan, A, Barclay, E, Atkin, W, Williams, C, Gilbert, J, Cheadle, J, Bell, J, Houlston, R, Bodmer, W, Sampson, J, Tomlinson, I

Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. by Olschwang, S, Markie, D, Seal, S, Neale, K, Phillips, R, Cottrell, S, Ellis, I, Hodgson, S, Zauber, P, Spigelman, A, Iwama, T, Loff, S, McKeown, C, Marchese, C, Sampson, J, Davies, S, Talbot, I, Wyke, J, Thomas, G, Bodmer, W, Hemminki, A, Avizienyte, E, de la Chapelle, A, Aaltonen, L, Tomlinson, I

THE POLYCYSTIC KIDNEY-DISEASE-1 GENE ENCODES A 14-KB TRANSCRIPT AND LIES WITHIN A DUPLICATED REGION ON CHROMOSOME-16 by Ward, C, Peral, B, Hughes, J, Thomas, S, Gamble, V, Maccarthy, A, Sloanestanley, J, Buckle, V, Kearney, L, Higgs, D, Ratcliffe, P, Harris, P, Roelfsema, J, Spruit, L, Saris, J, Dauwerse, H, Peters, D, Breuning, M, Nellist, M, Brookcarter, P, Maheshwar, M, Cordeiro, I, Santos, H, Cabral, P, Sampson, J

Large-scale fine mapping of the HNF1B locus and prostate cancer risk. by Berndt, S, Sampson, J, Yeager, M, Jacobs, K, Wang, Z, Hutchinson, A, Chung, C, Orr, N, Wacholder, S, Chatterjee, N, Yu, K, Kraft, P, Feigelson, H, Thun, M, Diver, W, Albanes, D, Virtamo, J, Weinstein, S, Schumacher, F, Cancel-Tassin, G, Cussenot, O, Valeri, A, Andriole, G, Crawford, E, Haiman, C

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33. by Wang, Z, Zhu, B, Zhang, M, Parikh, H, Jia, J, Chung, C, Sampson, J, Hoskins, J, Hutchinson, A, Burdette, L, Ibrahim, A, Hautman, C, Raj, P, Abnet, C, Adjei, A, Ahlbom, A, Albanes, D, Allen, N, Ambrosone, C, Aldrich, M, Amiano, P, Amos, C, Andersson, U, Andriole, G, Andrulis, I

Protocolised non-invasive compared with invasive weaning from mechanical ventilation for adults in intensive care: the Breathe RCT. by Perkins, G, Mistry, D, Lall, R, Gao-Smith, F, Snelson, C, Hart, N, Camporota, L, Varley, J, Carle, C, Paramasivam, E, Hoddell, B, De Paeztron, A, Dosanjh, S, Sampson, J, Blair, L, Couper, K, McAuley, D, Young, J, Walsh, T, Blackwood, B, Rose, L, Lamb, S, Dritsaki, M, Maredza, M, Khan, I, Petrou, S, Gates, S

People of the British Isles: preliminary analysis of genotypes and surnames in a UK-control population by Winney, B, Boumertit, A, Day, T, Davison, D, Echeta, C, Evseeva, I, Hutnik, K, Leslie, S, Nicodemus, K, Royrvik, E, Tonks, S, Yang, X, Cheshire, J, Longley, P, Mateos, P, Groom, A, Relton, C, Bishop, D, Black, K, Northwood, E, Parkinson, L, Frayling, T, Steele, A, Sampson, J, King, T, Dixon, R, Middleton, D, Jennings, B, Bowden, R, Donnelly, P, Bodmer, W