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Year Number of Results
1995 1
1996 2
1997 2
1998 2
1999 3
2000 1
2001 3
2002 3
2003 2
2005 1
2024 0

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Page 1
Multiple endocrine neoplasia type 1.
Pannett AA, Thakker RV. Pannett AA, et al. Endocr Relat Cancer. 1999 Dec;6(4):449-73. doi: 10.1677/erc.0.0060449. Endocr Relat Cancer. 1999. PMID: 10730900 Review.
Menin interacts directly with the homeobox-containing protein Pem.
Lemmens IH, Forsberg L, Pannett AA, Meyen E, Piehl F, Turner JJ, Van de Ven WJ, Thakker RV, Larsson C, Kas K. Lemmens IH, et al. Among authors: pannett aa. Biochem Biophys Res Commun. 2001 Aug 17;286(2):426-31. doi: 10.1006/bbrc.2001.5405. Biochem Biophys Res Commun. 2001. PMID: 11500056
The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred.
Cavaco BM, Barros L, Pannett AA, Ruas L, Carvalheiro M, Ruas MM, Krausz T, Santos MA, Sobrinho LG, Leite V, Thakker RV. Cavaco BM, et al. Among authors: pannett aa. QJM. 2001 Apr;94(4):213-22. doi: 10.1093/qjmed/94.4.213. QJM. 2001. PMID: 11294964
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.
Carpten JD, Robbins CM, Villablanca A, Forsberg L, Presciuttini S, Bailey-Wilson J, Simonds WF, Gillanders EM, Kennedy AM, Chen JD, Agarwal SK, Sood R, Jones MP, Moses TY, Haven C, Petillo D, Leotlela PD, Harding B, Cameron D, Pannett AA, Höög A, Heath H 3rd, James-Newton LA, Robinson B, Zarbo RJ, Cavaco BM, Wassif W, Perrier ND, Rosen IB, Kristoffersson U, Turnpenny PD, Farnebo LO, Besser GM, Jackson CE, Morreau H, Trent JM, Thakker RV, Marx SJ, Teh BT, Larsson C, Hobbs MR. Carpten JD, et al. Among authors: pannett aa. Nat Genet. 2002 Dec;32(4):676-80. doi: 10.1038/ng1048. Epub 2002 Nov 18. Nat Genet. 2002. PMID: 12434154
Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1.
Turner JJ, Leotlela PD, Pannett AA, Forbes SA, Bassett JH, Harding B, Christie PT, Bowen-Jones D, Ellard S, Hattersley A, Jackson CE, Pope R, Quarrell OW, Trembath R, Thakker RV. Turner JJ, et al. Among authors: pannett aa. J Clin Endocrinol Metab. 2002 Jun;87(6):2688-93. doi: 10.1210/jcem.87.6.8607. J Clin Endocrinol Metab. 2002. PMID: 12050235
Characterization of mutations in patients with multiple endocrine neoplasia type 1.
Bassett JH, Forbes SA, Pannett AA, Lloyd SE, Christie PT, Wooding C, Harding B, Besser GM, Edwards CR, Monson JP, Sampson J, Wass JA, Wheeler MH, Thakker RV. Bassett JH, et al. Among authors: pannett aa. Am J Hum Genet. 1998 Feb;62(2):232-44. doi: 10.1086/301729. Am J Hum Genet. 1998. PMID: 9463336 Free PMC article.
Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).
Forbes SA, Pannett AA, Bassett JH, Harding B, Wooding C, Thakker RV, Butler R, Ogilvie D, Anand R, Gaudray P, Weber G, Larsson C, Zhang CX, Calender A, Höppener JW, Lips CJ, Kas K. Forbes SA, et al. Among authors: pannett aa. Hum Genet. 1997 Sep;100(3-4):481-5. doi: 10.1007/s004390050538. Hum Genet. 1997. PMID: 9272177
20 results