Inheritable forms of medullary thyroid carcinoma

Anne Bachelot; Francesca Lombardo; Eric Baudin; Jean Michel Bidart; Martin Schlumberger

doi:10.1016/S0300-9084(01)01364-5

Inheritable forms of medullary thyroid carcinoma

Anne Bachelot, Francesca Lombardo, Eric Baudin, Jean Michel Bidart, Martin Schlumberger

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

16 Citations (Scopus)

Résumé

Medullary thyroid carcinoma (MTC) arises from parafollicular or C cells of the thyroid that produce calcitonin. It accounts for 5-10% of all thyroid cancers. Hereditary MTC represents 20-30% of all MTCs. It can be transmitted with an autosomal dominant pattern, either as a single entity, familial MTC, or it can arise as part of a multiple endocrine neoplasia (MEN) syndrome type 2A or 2B. The identification of hereditary MTC has been facilitated in recent years by the direct analysis of the ret proto-oncogene.

langue originale	Anglais
Pages (de - à)	61-66
Nombre de pages	6
journal	Biochimie
Volume	84
Numéro de publication	1
Les DOIs	https://doi.org/10.1016/S0300-9084(01)01364-5
état	Publié - 1 janv. 2002

Accès au document

10.1016/S0300-9084(01)01364-5

Autres fichiers et liens

Lien vers la publication dans Scopus

Contient cette citation

@article{0372d957f3ff4584b4ae576e980363ce,

title = "Inheritable forms of medullary thyroid carcinoma",

abstract = "Medullary thyroid carcinoma (MTC) arises from parafollicular or C cells of the thyroid that produce calcitonin. It accounts for 5-10% of all thyroid cancers. Hereditary MTC represents 20-30% of all MTCs. It can be transmitted with an autosomal dominant pattern, either as a single entity, familial MTC, or it can arise as part of a multiple endocrine neoplasia (MEN) syndrome type 2A or 2B. The identification of hereditary MTC has been facilitated in recent years by the direct analysis of the ret proto-oncogene.",

keywords = "Calcitonin, Medullary thyroid carcinoma, RET gene",

author = "Anne Bachelot and Francesca Lombardo and Eric Baudin and Bidart, {Jean Michel} and Martin Schlumberger",

year = "2002",

month = jan,

day = "1",

doi = "10.1016/S0300-9084(01)01364-5",

language = "English",

volume = "84",

pages = "61--66",

journal = "Biochimie",

issn = "0300-9084",

number = "1",

}

TY - JOUR

T1 - Inheritable forms of medullary thyroid carcinoma

AU - Bachelot, Anne

AU - Lombardo, Francesca

AU - Baudin, Eric

AU - Bidart, Jean Michel

AU - Schlumberger, Martin

PY - 2002/1/1

Y1 - 2002/1/1

N2 - Medullary thyroid carcinoma (MTC) arises from parafollicular or C cells of the thyroid that produce calcitonin. It accounts for 5-10% of all thyroid cancers. Hereditary MTC represents 20-30% of all MTCs. It can be transmitted with an autosomal dominant pattern, either as a single entity, familial MTC, or it can arise as part of a multiple endocrine neoplasia (MEN) syndrome type 2A or 2B. The identification of hereditary MTC has been facilitated in recent years by the direct analysis of the ret proto-oncogene.

AB - Medullary thyroid carcinoma (MTC) arises from parafollicular or C cells of the thyroid that produce calcitonin. It accounts for 5-10% of all thyroid cancers. Hereditary MTC represents 20-30% of all MTCs. It can be transmitted with an autosomal dominant pattern, either as a single entity, familial MTC, or it can arise as part of a multiple endocrine neoplasia (MEN) syndrome type 2A or 2B. The identification of hereditary MTC has been facilitated in recent years by the direct analysis of the ret proto-oncogene.

KW - Calcitonin

KW - Medullary thyroid carcinoma

KW - RET gene

UR - http://www.scopus.com/inward/record.url?scp=0036256094&partnerID=8YFLogxK

U2 - 10.1016/S0300-9084(01)01364-5

DO - 10.1016/S0300-9084(01)01364-5

M3 - Article

C2 - 11900877

AN - SCOPUS:0036256094

SN - 0300-9084

VL - 84

SP - 61

EP - 66

JO - Biochimie

JF - Biochimie

IS - 1

ER -