Harding B - Search Results

1

Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31.

Williamson C, Cavaco BM, Jauch A, Dixon PH, Forbes S, Harding B, Holtgreve-Grez H, Schoell B, Pereira MC, Font AP, Loureiro MM, Sobrinho LG, Santos MA, Thakker RV. Williamson C, et al. Among authors: harding b. J Bone Miner Res. 1999 Feb;14(2):230-9. doi: 10.1359/jbmr.1999.14.2.230. J Bone Miner Res. 1999. PMID: 9933477 Free article.

2

Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1.

Bassett JH, Rashbass P, Harding B, Forbes SA, Pannett AA, Thakker RV. Bassett JH, et al. Among authors: harding b. J Bone Miner Res. 1999 Jan;14(1):3-10. doi: 10.1359/jbmr.1999.14.1.3. J Bone Miner Res. 1999. PMID: 9893060 Free article.

3

Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13.

Stacey JM, Turner JJ, Harding B, Nesbit MA, Kotanko P, Lhotta K, Puig JG, Torres RJ, Thakker RV. Stacey JM, et al. Among authors: harding b. J Clin Endocrinol Metab. 2003 Jan;88(1):464-70. doi: 10.1210/jc.2002-021268. J Clin Endocrinol Metab. 2003. PMID: 12519891

4

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene.

Cavaco BM, Guerra L, Bradley KJ, Carvalho D, Harding B, Oliveira A, Santos MA, Sobrinho LG, Thakker RV, Leite V. Cavaco BM, et al. Among authors: harding b. J Clin Endocrinol Metab. 2004 Apr;89(4):1747-52. doi: 10.1210/jc.2003-031016. J Clin Endocrinol Metab. 2004. PMID: 15070940

5

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.

Pang JT, Lloyd SE, Wooding C, Farren B, Pottinger B, Harding B, Leigh SE, Pook MA, Benham FJ, Gillett GT, Taggart RT, Thakker RV. Pang JT, et al. Among authors: harding b. Hum Genet. 1996 Jun;97(6):732-41. doi: 10.1007/BF02346182. Hum Genet. 1996. PMID: 8641689

6

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: harding b. Hum Genet. 1997 Sep;100(3-4):481-5. doi: 10.1007/s004390050538. Hum Genet. 1997. PMID: 9272177

7

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: harding b. Am J Hum Genet. 1998 Feb;62(2):232-44. doi: 10.1086/301729. Am J Hum Genet. 1998. PMID: 9463336 Free PMC article.

8

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.

Pannett AA, Kennedy AM, Turner JJ, Forbes SA, Cavaco BM, Bassett JH, Cianferotti L, Harding B, Shine B, Flinter F, Maidment CG, Trembath R, Thakker RV. Pannett AA, et al. Among authors: harding b. Clin Endocrinol (Oxf). 2003 May;58(5):639-46. doi: 10.1046/j.1365-2265.2003.01765.x. Clin Endocrinol (Oxf). 2003. PMID: 12699448

9

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.

Bradley KJ, Cavaco BM, Bowl MR, Harding B, Cranston T, Fratter C, Besser GM, Conceição Pereira M, Davie MW, Dudley N, Leite V, Sadler GP, Seller A, Thakker RV. Bradley KJ, et al. Among authors: harding b. Clin Endocrinol (Oxf). 2006 Mar;64(3):299-306. doi: 10.1111/j.1365-2265.2006.02460.x. Clin Endocrinol (Oxf). 2006. PMID: 16487440

10

Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families.

Thakker RV, Wooding C, Pang JT, Farren B, Harding B, Anderson DC, Besser GM, Bouloux P, Brenton DP, Buchanan KD. Thakker RV, et al. Among authors: harding b. Ann Hum Genet. 1993 Jan;57(1):17-25. doi: 10.1111/j.1469-1809.1993.tb00883.x. Ann Hum Genet. 1993. PMID: 8101435

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