Dahia PL - Search Results

1

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.

Qin Y, Yao L, King EE, Buddavarapu K, Lenci RE, Chocron ES, Lechleiter JD, Sass M, Aronin N, Schiavi F, Boaretto F, Opocher G, Toledo RA, Toledo SP, Stiles C, Aguiar RC, Dahia PL. Qin Y, et al. Among authors: dahia pl. Nat Genet. 2010 Mar;42(3):229-33. doi: 10.1038/ng.533. Epub 2010 Feb 14. Nat Genet. 2010. PMID: 20154675 Free PMC article.

2

Molecular and immunohistochemical analysis of P53 in phaeochromocytoma.

Dahia PL, Aguiar RC, Tsanaclis AM, Bendit I, Bydlowski SP, Abelin NM, Toledo SP. Dahia PL, et al. Br J Cancer. 1995 Nov;72(5):1211-3. doi: 10.1038/bjc.1995.487. Br J Cancer. 1995. PMID: 7577469 Free PMC article.

3

Low cord blood levels of catecholamine from a newborn of a pheochromocytoma patient.

Dahia PL, Hayashida CY, Strunz C, Abelin N, Toledo SP. Dahia PL, et al. Eur J Endocrinol. 1994 Mar;130(3):217-9. doi: 10.1530/eje.0.1300217. Eur J Endocrinol. 1994. PMID: 8156092

4

Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas.

Aguiar RC, Dahia PL, Sill H, Toledo SP, Goldman JM, Cross NC. Aguiar RC, et al. Among authors: dahia pl. Clin Endocrinol (Oxf). 1996 Jul;45(1):93-6. Clin Endocrinol (Oxf). 1996. PMID: 8796144

5

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PL, O'Riordan JL, Toledo SP, et al. Eng C, et al. Among authors: dahia pl. J Med Genet. 1995 Dec;32(12):934-7. doi: 10.1136/jmg.32.12.934. J Med Genet. 1995. PMID: 8825918 Free PMC article.

6

Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas.

Dahia PL, Toledo SP, Mulligan LM, Maher ER, Grossman AB, Eng C. Dahia PL, et al. Cancer Res. 1997 Jan 15;57(2):310-3. Cancer Res. 1997. PMID: 9000574

7

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.

Liaw D, Marsh DJ, Li J, Dahia PL, Wang SI, Zheng Z, Bose S, Call KM, Tsou HC, Peacocke M, Eng C, Parsons R. Liaw D, et al. Among authors: dahia pl. Nat Genet. 1997 May;16(1):64-7. doi: 10.1038/ng0597-64. Nat Genet. 1997. PMID: 9140396

8

PTEN is inversely correlated with the cell survival factor Akt/PKB and is inactivated via multiple mechanismsin haematological malignancies.

Dahia PL, Aguiar RC, Alberta J, Kum JB, Caron S, Sill H, Marsh DJ, Ritz J, Freedman A, Stiles C, Eng C. Dahia PL, et al. Hum Mol Genet. 1999 Feb;8(2):185-93. doi: 10.1093/hmg/8.2.185. Hum Mol Genet. 1999. PMID: 9931326

9

Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations.

Duerr EM, Gimm O, Neuberg DS, Kum JB, Clifford SC, Toledo SP, Maher ER, Dahia PL, Eng C. Duerr EM, et al. Among authors: dahia pl. J Clin Endocrinol Metab. 1999 Sep;84(9):3207-11. doi: 10.1210/jcem.84.9.5961. J Clin Endocrinol Metab. 1999. PMID: 10487688

10

Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas.

Aguiar RC, Cox G, Pomeroy SL, Dahia PL. Aguiar RC, et al. Among authors: dahia pl. J Clin Endocrinol Metab. 2001 Jun;86(6):2890-4. doi: 10.1210/jcem.86.6.7547. J Clin Endocrinol Metab. 2001. PMID: 11397905

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