Thakker RV - Search Results

1

Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers.

Lemos MC, Harding B, Reed AA, Jeyabalan J, Walls GV, Bowl MR, Sharpe J, Wedden S, Moss JE, Ross A, Davidson D, Thakker RV. Lemos MC, et al. Among authors: thakker rv. J Endocrinol. 2009 Oct;203(1):133-42. doi: 10.1677/JOE-09-0124. Epub 2009 Jul 8. J Endocrinol. 2009. PMID: 19587266

2

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. Ann Hum Genet. 1993 Jan;57(1):17-25. doi: 10.1111/j.1469-1809.1993.tb00883.x. Ann Hum Genet. 1993. PMID: 8101435

3

Prolactinoma presenting in identical twins with multiple endocrine neoplasia type 1.

Flanagan DE, Armitage M, Clein GP, Thakker RV. Flanagan DE, et al. Among authors: thakker rv. Clin Endocrinol (Oxf). 1996 Jul;45(1):117-20. Clin Endocrinol (Oxf). 1996. PMID: 8846498

4

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

5

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

6

Metastatic parathyroid carcinoma in the MEN2A syndrome.

Jenkins PJ, Satta MA, Simmgen M, Drake WM, Williamson C, Lowe DG, Britton K, Chew SL, Thakker RV, Besser GM. Jenkins PJ, et al. Among authors: thakker rv. Clin Endocrinol (Oxf). 1997 Dec;47(6):747-51. doi: 10.1046/j.1365-2265.1997.3421147.x. Clin Endocrinol (Oxf). 1997. PMID: 9497883

7

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: thakker rv. 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.

8

Absence of mutations in the growth hormone (GH)-releasing hormone receptor gene in GH-secreting pituitary adenomas.

Salvatori R, Thakker RV, Lopes MB, Fan X, Eswara JR, Ellison D, Lees P, Harding B, Yang I, Levine MA. Salvatori R, et al. Among authors: thakker rv. Clin Endocrinol (Oxf). 2001 Mar;54(3):301-7. doi: 10.1046/j.1365-2265.2001.01213.x. Clin Endocrinol (Oxf). 2001. PMID: 11298081

9

X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene.

Christie PT, Harding B, Nesbit MA, Whyte MP, Thakker RV. Christie PT, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2001 Aug;86(8):3840-4. doi: 10.1210/jcem.86.8.7730. J Clin Endocrinol Metab. 2001. PMID: 11502821

10

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: thakker rv. J Clin Endocrinol Metab. 2002 Jun;87(6):2688-93. doi: 10.1210/jcem.87.6.8607. J Clin Endocrinol Metab. 2002. PMID: 12050235

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