MEN1 gene mutations are a rare event in patients with sporadic neuroendocrine tumors (Q38455820)

3 September 2017

title

MEN1 gene mutations are a rare event in patients with sporadic neuroendocrine tumors (English)

1 reference

3 September 2017

C Asteria

1

1 reference

3 September 2017

M Anagni

2

1 reference

3 September 2017

L Fugazzola

3

1 reference

3 September 2017

G Faglia

4

1 reference

3 September 2017

P Vezzadini

5

1 reference

3 September 2017

P Beck-Peccoz

6

1 reference

3 September 2017

language of work or name

1 reference

1 August 2002

1 reference

European Journal of Internal Medicine

3 September 2017

published in

1 reference

3 September 2017

volume

13

1 reference

3 September 2017

issue

5

1 reference

3 September 2017

page(s)

319-323

1 reference

The classification of carcinoid tum ours

3 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Genetic aspects of adenomatosis of endocrine glands

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Positional cloning of the gene for multiple endocrine neoplasia-type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Mutations in the MEN I gene in sporadic neuroendocrine tumours of gastroenteropancreatic system

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Mutations and allelic deletions of the MEN1 gene are associated with a subset of sporadic endocrine pancreatic and neuroendocrine tumors and not restricted to foregut neoplasms

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

MEN1 gene mutations in sporadic neuroendocrine tumors of foregut derivation

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Molecular genetics of neuroendocrine tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Lack of MEN1 gene mutations in 27 sporadic insulinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1: Additional information for mutational screening

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Characterization of mutations in patients with multiple endocrine neoplasia type 1.

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Comparative genomic hybridization identifies loss of 18q22-qter as an early and specific event in tumorigenesis of midgut carcinoids

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Chromosome 18 deletions are common events in classical midgut carcinoid tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

Carcinoid tumors: molecular genetics, tumor biology, and update of diagnosis and treatment

1 reference

https://api.crossref.org/works/10.1016%2FS0953-6205%2802%2900064-X

7 January 2021

10.1016/S0953-6205(02)00064-X

Identifiers

DOI

1 reference

3 September 2017

1 reference