Up-and-Coming Experimental Drug Options for Metastatic Colorectal Cancer by Cimino SK, Eng C

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A luohan from Yixian in the Heritage Museum: Some Parallels in Material Usage with the Longquanwu and Liuliqu kilns near Beijing by Wood, N, Doherty, C, Menshikova, M, Eng, C, Smithies, R

Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas. by Dahia, P, Toledo, S, Mulligan, L, Maher, E, Grossman, AB, Eng, C

Xylometazoline hydrochloride 0.1 per cent versus physiological saline in nasal surgical aftercare: a randomised, single-blinded, comparative clinical trial. by Humphreys, MR, Grant, D, McKean, SA, Eng, C, Townend, J, Evans, A

Severe TMD/AMKL with GATA1 mutation in a stillborn fetus with Down syndrome. by Heald, B, Hilden, J, Zbuk, K, Norton, A, Vyas, P, Theil, K, Eng, C

Inflammatory aetiology of human myometrial activation tested using directed graphs. by Andrew M Bisits, Roger Smith, Sam Mesiano, George Yeo, Kenneth Kwek, David MacIntyre, Eng C Chan

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Germline PTEN mutations in Cowden syndrome-like families. by Marsh, D, Dahia, P, Caron, S, Kum, J, Frayling, I, Tomlinson, I, Hughes, K, Eeles, R, Hodgson, S, Murday, V, Houlston, R, Eng, C

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis by Kokko, A, Laiho, P, Lehtonen, R, Korja, S, Carvajal-Carmona, L, Järvinen, H, Mecklin, J, Eng, C, Schleutker, J, Tomlinson, I, Vahteristo, P, Aaltonen, L

Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility. by Astuti, D, Hart-Holden, N, Latif, F, Lalloo, F, Black, G, Lim, C, Moran, A, Grossman, AB, Hodgson, S, Freemont, A, Ramsden, R, Eng, C, Evans, D, Maher, E

Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci. by Stratakis, C, Kirschner, L, Taymans, SE, Tomlinson, I, Marsh, D, Torpy, D, Giatzakis, C, Eccles, D, Theaker, J, Houlston, R, Blouin, J, Antonarakis, SE, Basson, C, Eng, C, Carney, J

Immune dysregulation and defects in mucosal B cell homeostasis in patients with PTEN hamartoma tumor syndrome by Heindl, M, Haendel, N, Ngeow, J, Kionke, J, Wittekind, C, Kamprad, M, Hoffmeister, A, Ehl, S, Rensing-Ehl, A, Maul, J, Loddenkemper, C, Reifenberger, J, Aretz, S, Kiess, W, Eng, C, Uhlig, H

Autoimmunity, intestinal lymphoid hyperplasia, and defects in mucosal B-cell homeostasis in patients with PTEN hamartoma tumor syndrome. by Heindl, M, Händel, N, Ngeow, J, Kionke, J, Wittekind, C, Kamprad, M, Rensing-Ehl, A, Ehl, S, Reifenberger, J, Loddenkemper, C, Maul, J, Hoffmeister, A, Aretz, S, Kiess, W, Eng, C, Uhlig, H

Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndrome. by Bevan, S, Woodford-Richens, K, Rozen, P, Eng, C, Young, J, Dunlop, M, Neale, K, Phillips, R, Markie, D, Rodriguez-Bigas, M, Leggett, B, Sheridan, E, Hodgson, S, Iwama, T, Eccles, D, Bodmer, W, Houlston, R, Tomlinson, I

Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases. by Houlston, R, Bevan, S, Williams, A, Young, J, Dunlop, M, Rozen, P, Eng, C, Markie, D, Woodford-Richens, K, Rodriguez-Bigas, M, Leggett, B, Neale, K, Phillips, R, Sheridan, E, Hodgson, S, Iwama, T, Eccles, D, Bodmer, W, Tomlinson, I

An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome. by Jaeger, E, Woodford-Richens, K, Lockett, M, Rowan, A, Sawyer, E, Heinimann, K, Rozen, P, Murday, V, Whitelaw, S, Ginsberg, A, Atkin, W, Lynch, H, Southey, M, Debinski, H, Eng, C, Bodmer, W, Talbot, I, Hodgson, S, Thomas, H, Tomlinson, I

Mutation screening of fumarate hydratase by multiplex ligation-dependent probe amplification: detection of exonic deletion in a patient with leiomyomatosis and renal cell cancer. by Ahvenainen, T, Lehtonen, H, Lehtonen, R, Vahteristo, P, Aittomäki, K, Baynam, G, Dommering, C, Eng, C, Gruber, S, Grönberg, H, Harvima, R, Herva, R, Hietala, M, Kujala, M, Kääriäinen, H, Sunde, L, Vierimaa, O, Pollard, P, Tomlinson, I, Björck, E, Aaltonen, L, Launonen, V

Unregulated smooth-muscle myosin in human intestinal neoplasia. by Alhopuro, P, Phichith, D, Tuupanen, S, Sammalkorpi, H, Nybondas, M, Saharinen, J, Robinson, J, Yang, Z, Chen, L, Orntoft, T, Mecklin, J, Järvinen, H, Eng, C, Moeslein, G, Shibata, D, Houlston, R, Lucassen, A, Tomlinson, I, Launonen, V, Ristimäki, A, Arango, D, Karhu, A, Sweeney, H, Aaltonen, L

Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome. by Marsh, D, Roth, S, Lunetta, K, Hemminki, A, Dahia, P, Sistonen, P, Zheng, Z, Caron, S, van Orsouw, N, Bodmer, W, Cottrell, SE, Dunlop, MG, Eccles, D, Hodgson, S, Järvinen, H, Kellokumpu, I, Markie, D, Neale, K, Phillips, R, Rozen, P, Syngal, S, Vijg, J, Tomlinson, I, Aaltonen, L, Eng, C

Analysis of genetic and phenotypic heterogeneity in juvenile polyposis. by Woodford-Richens, K, Bevan, S, Churchman, M, Dowling, B, Jones, D, Norbury, C, Hodgson, S, Desai, D, Neale, K, Phillips, R, Young, J, Leggett, B, Dunlop, M, Rozen, P, Eng, C, Markie, D, Rodriguez-Bigas, M, Sheridan, E, Iwama, T, Eccles, D, Smith, G, Kim, J, Kim, K, Sampson, JR, Evans, G

Analysis of genetic and phenotypic heterogeneity in juvenile polyposis by Woodford-Richens, K, Tomlinson, P, Bevan, S, Houlston, R, Churchman, M, Dowling, B, Jones, D, Norbury, C, Hodgson, S, Desai, D, Neale, K, Phillips, R, Young, J, Leggett, B, Dunlop, M, Rozen, P, Eng, C, Markie, D, Rodriguez-Bigas, M, Sheridan, E, Iwama, T, Eccles, D, Smith, G, Kim, J, Kim, K