MOLEKULÁRIS BIOLÓGIA SZAKTERÜLET

AJÁNLÁSI LISTA A 'FAMILIARIS TUMORSZINDRÓMÁK' TÉMAKÖRBEN


Alaplista

Igaz P, Rácz K , Tóth M, Cserepes É, Ésik O, Kiss R, Perner F, Gláz E, Tulassay Zs. Molekuláris genetikai módszerekkel igazolt ret-protoonkogén mutáció magyar MEN2A család esetében. Orv Hetil 1999;140(7):355-357.

Couch, Vicki MS, Lindor Noralene M, Karnes Pamela, Michels Virginia V. von Hippel-Lindau disease. Mayo Clinic Proceedings 2000;75(3):265-272.

Marsh DJ, Theodosopoulos G, Howell V, Richardson AL, Benn DE, Proos AL, Eng C, Robinson BG. Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography. Neoplasia (New York) 2001;3(3):236-44.

Nguyen L, Niccoli-Sire P, Caron P, Bastie D, Maes, B, Henry J-F, Conte-Devolx B. Phaeochromocytoma a multiplex endokrin neoplasia II. típusában: egy előre tervezett vizsgálat Pheochromocytoma in multiple endocrine neoplasia type 2: a prospective study. Eur J Endocrinol 2001;(144):37-44.



Ajánlott lista

Hayward N. New developments in melanoma genetics. Current Oncology Reports 2000;2(4):300-6.

Chiefari E, Chiarela R, Crocetti U, Tardio B, Arturi F, Russo D, Trischitta V, Filetti S, Zingrillo M. A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN2A and FMTC. Hormone & Metabolic Research 2001;33(1):52-6.

Lore F, Talidis F, Di Cairano G, Renieri A. Multiple endocrine neoplasia type 2A syndromes mya be associated with renal malformations. Journal of Internal Medcine 2001;250(1):37-42.

Aguiar RC, Cox G, Pomeroy SL, Dahia PL. Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas. J Clin Endocrinol Metab 2001;86(6):2890-4.

Kimmelman A, Liang BC. Familial neurogenic tumor syndromes. Hematol Oncol Clin North Am 2001;15(6):1073-84.

Lynch HT, McComb RD, Osborn NK, Wolpert PA, Lynch JF, Wszolek ZK, Sidransky D, Steg RE. Predominance of brain tumors in an extended Li-Fraumeni (SBLA) kindred, including a case of Sturge-Weber syndrome. Cancer 2000;88(2):433-9.

Lehmann TA, Haffy BG, Carbone CJ, Bishop LR, Gumbs AA, Krishnan S, Shields PG, Modali R, Turner BC. Elevated frequency and functional activity of a specific germ-line p53 intron mutation in a familial breast cancer. Cancer Res 2000;60(4):1062-9.

Pannett AA, Thakker RV. Somatic mutations in MEN type 1 tumors, consistent with the Knudson "two-hit" hypothesis. J of Clinical Endocrinology and Metabolism 2001;86(9):4371-4.