Endocrine cancer

Citations 11-20 of 46 total displayed.

Short reports
A pleiomorphic GH pituitary adenoma from a Carney complex patient displays universal allelic loss at the protein kinase A regulatory subunit 1A (PRKARIA) locus

I Bossis, A Voutetakis, L Matyakhina, S Pack, M Abu-Asab, I Bourdeau, K J Griffin, N Courcoutsakis, S Stergiopoulos, D Batista, M Tsokos, C A Stratakis
J. Med. Genet. 2004; 41: 596-600. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer

J D McKay, D Thompson, F Lesueur, K Stankov, A Pastore, C Watfah, S Strolz, G Riccabona, R Moncayo, G Romeo, D E Goldgar
J. Med. Genet. 2004; 41: 407-412. [Abstract] [Full text] [PDF] [Request Permissions]  

Short reports
Inhibin -subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers

C A Longui, S H V Lemos-Marini, B Figueiredo, B B Mendonca, M Castro, R Liberatore, Jr, C Watanabe, C L P Lancellotti, M N Rocha, M B Melo, O Monte, L E P Calliari, G Guerra-Junior, M T M Baptista, L Sbragia-Neto, A C Latronico, A Moreira, A M D Tardelli, A Nigri, S E Taymans, C A Stratakis
J. Med. Genet. 2004; 41: 354-359. [Abstract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
Genetic and epigenetic profile of sporadic pheochromocytomas

A Cascon, S Ruiz-Llorente, M F Fraga, R Leton, D Telleria, J Sastre, J Jose Diez, G Martinez Diaz-Guerra, J A Diaz Perez, J Benitez, M Esteller, M Robledo
J. Med. Genet. 2004; 41: e30. [Extract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)

A Villablanca, A Calender, L Forsberg, A Höög, J-D Cheng, D Petillo, C Bauters, K Kahnoski, T Ebeling, P Salmela, A-L Richardson, L Delbridge, A Meyrier, C Proye, J D Carpten, B T Teh, B G Robinson, C Larsson
J. Med. Genet. 2004; 41: e32. [Extract] [Full text] [PDF] [Request Permissions]  

Original articles
Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications

J Warner, M Epstein, A Sweet, D Singh, J Burgess, S Stranks, P Hill, D Perry-Keene, D Learoyd, B Robinson, P Birdsey, E Mackenzie, B T Teh, J B Prins, J Cardinal
J. Med. Genet. 2004; 41: 155-160. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Akt activation and localisation correlate with tumour invasion and oncogene expression in thyroid cancer

V Vasko, M Saji, E Hardy, M Kruhlak, A Larin, V Savchenko, M Miyakawa, O Isozaki, H Murakami, T Tsushima, K D Burman, C De Micco, M D Ringel
J. Med. Genet. 2004; 41: 161-170. [Abstract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
Novel germline mutations in the adenomatous polyposis coli gene in Polish families with familial adenomatous polyposis

A Plawski, J Lubinski, T Banasiewicz, J Paszkowski, D Lipinski, A Strembalska, G Kurzawski, T Byrski, S Zajaczek, D Hodorowicz-Zaniewska, T Gach, I Brozek, D Nowakowska, E Czkwaniec, P Krokowicz, M Drews, J Zeyland, W Juzwa, R Slomski
J. Med. Genet. 2004; 41: e11. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Chinese patients with sporadic Hirschsprung’s disease are predominantly represented by a single RET haplotype

M-M Garcia-Barceló, M-H Sham, V C-H Lui, B L-S Chen, Y-Q Song, W-S Lee, S-K Yung, G Romeo, P K-H Tam
J. Med. Genet. 2003; 40: e122. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
PTEN hamartoma tumour syndrome: variability of an entity

J H M Merks, L S de Vries, X-P Zhou, P Nikkels, P G Barth, C Eng, R C M Hennekam
J. Med. Genet. 2003; 40: e111. [Extract] [Full text] [PDF] [Request Permissions]