PMID- 10966852
OWN - NLM
STAT- MEDLINE
DCOM- 20001018
LR  - 20051116
IS  - 1044-579X (Print)
IS  - 1044-579X (Linking)
VI  - 10
IP  - 4
DP  - 2000 Aug
TI  - Multiple endocrine neoplasia type 1.
PG  - 299-312
AB  - The recent cloning of the gene responsible for multiple endocrine neoplasia type 
      1 (MEN 1) has opened new avenues for both clinical and basic science research in 
      the field of endocrine oncology. A large amount of genetic information, 
      particularly those in relation to germline and somatic mutations, has since been 
      published during the last 2 years. This new knowledge has provided important 
      insights into its gene function. The significance of these advances in relation 
      to clinical management and future directions for research is discussed.
CI  - Copyright 2000 Academic Press.
FAU - Ki Wong, F
AU  - Ki Wong F
AD  - Department of Molecular Medicine, CMM L8:01, Karolinska Hospital, Stockholm, 
      S-17176, Sweden.
FAU - Burgess, J
AU  - Burgess J
FAU - Nordenskjold, M
AU  - Nordenskjold M
FAU - Larsson, C
AU  - Larsson C
FAU - Tean Teh, B
AU  - Tean Teh B
LA  - eng
PT  - Journal Article
PT  - Review
PL  - England
TA  - Semin Cancer Biol
JT  - Seminars in cancer biology
JID - 9010218
RN  - 0 (Neoplasm Proteins)
SB  - IM
MH  - Animals
MH  - Chromosome Mapping
MH  - Cloning, Molecular
MH  - Genotype
MH  - Humans
MH  - Multiple Endocrine Neoplasia Type 1/*genetics
MH  - Mutation/genetics
MH  - Neoplasm Proteins/metabolism
MH  - Phenotype
MH  - Risk Factors
RF  - 102
EDAT- 2000/09/01 11:00
MHDA- 2000/10/21 11:01
CRDT- 2000/09/01 11:00
PHST- 2000/09/01 11:00 [pubmed]
PHST- 2000/10/21 11:01 [medline]
PHST- 2000/09/01 11:00 [entrez]
AID - S1044-579X(00)90150-0 [pii]
AID - 10.1006/scbi.2000.0150 [doi]
PST - ppublish
SO  - Semin Cancer Biol. 2000 Aug;10(4):299-312. doi: 10.1006/scbi.2000.0150.