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[Genetics of endocrine tumours]
scientific article published on 01 December 2005
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
[Genetics of endocrine tumours]
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
author name string
A Calender
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
S Dupasquier
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
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28 January 2020
M Cordier
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
C X Zhang
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
Groupe d'Etude des Tumeurs Endocrines
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
publication date
1 December 2005
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
published in
Annales de Pathologie
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
volume
25
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
page(s)
463-486
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
cites work
Molecular genetics of multiple endocrine neoplasia types 1 and 2.
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Crossref
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7 January 2021
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Surgical treatment of hyperparathyroidism in patients with multiple endocrine neoplasia type 1
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Crossref
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7 January 2021
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[Gastrinomas in multiple endocrine neoplasia type-1. A 127-case cohort study from the endocrine tumor group (ETG)]
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Crossref
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https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
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Adrenal involvement in multiple endocrine neoplasia type 1
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Crossref
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https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
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Thymic carcinoids in multiple endocrine neoplasia type 1
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Crossref
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https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
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Bronchopulmonary carcinoid in multiple endocrine neoplasia type 1.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cutaneous tumors in patients with multiple endocrine neoplasia type 1 show allelic deletion of the MEN1 gene.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
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Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma.
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Crossref
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https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Gastric carcinoid tumors in multiple endocrine neoplasia-1 patients with Zollinger-Ellison syndrome can be symptomatic, demonstrate aggressive growth, and require surgical treatment.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
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inferred from DOI database lookup
Guidelines for diagnosis and therapy of MEN type 1 and type 2.
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Crossref
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https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of the gene for multiple endocrine neoplasia-type 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Functional characterization of a promoter region in the human MEN1 tumor suppressor gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Menin, the product of the MEN1 gene, is a nuclear protein
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type 1 gene, in cell lines and human tissues
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Menin molecular interactions: insights into normal functions and tumorigenesis.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterozygous Men1 mutant mice develop a range of endocrine tumors mimicking multiple endocrine neoplasia type 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic ablation of the tumor suppressor menin causes lethality at mid-gestation with defects in multiple organs.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Menin is a regulator of the stress response in Drosophila melanogaster
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Stable overexpression of MEN1 suppresses tumorigenicity of RAS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The menin tumor suppressor protein is an essential oncogenic cofactor for MLL-associated leukemogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The tumor suppressor menin regulates hematopoiesis and myeloid transformation by influencing Hox gene expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The tumor suppressor protein menin interacts with NF-kappaB proteins and inhibits NF-kappaB-mediated transactivation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin and TGF-beta superfamily member signaling via the Smad pathway in pituitary, parathyroid and osteoblast
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin suppresses osteoblast differentiation by antagonizing the AP-1 factor, JunD
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Direct binding of DNA by tumor suppressor menin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple tumor suppressor pathways negatively regulate telomerase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional interaction between tumor suppressor menin and activator of S-phase kinase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Menin, the multiple endocrine neoplasia type 1 gene product, exhibits GTP-hydrolyzing activity in the presence of the tumor metastasis suppressor nm23
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 32-kilodalton subunit of replication protein A interacts with menin, the product of the MEN1 tumor suppressor gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Enhanced sensitivity to alkylating agent in lymphocytes from patients with multiple endocrine neoplasia type 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin's interaction with glial fibrillary acidic protein and vimentin suggests a role for the intermediate filament network in regulating menin activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin, a tumor suppressor, associates with nonmuscle myosin II-A heavy chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reduction of menin expression enhances cell proliferation and is tumorigenic in intestinal epithelial cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin induces apoptosis in murine embryonic fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transfection of the multiple endocrine neoplasia type 1 gene to a human endocrine pancreatic tumor cell line inhibits cell growth and affects expression of JunD, delta-like protein 1/preadipocyte factor-1, proliferating cell nuclear antigen, and QM/
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transcription factor JunD, deprived of menin, switches from growth suppressor to growth promoter
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin regulates pancreatic islet growth by promoting histone methylation and expression of genes encoding p27Kip1 and p18INK4c
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evaluation of denaturing high performance liquid chromatography for the mutational analysis of the MEN1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin missense mutants associated with multiple endocrine neoplasia type 1 are rapidly degraded via the ubiquitin-proteasome pathway
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of mutations in patients with multiple endocrine neoplasia type 1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of multiple endocrine neoplasia type 1 in young patients with apparently sporadic primary hyperparathyroidism or pancreaticoduodenal endocrine tumours
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RET Mutation Screening in Familial Cutaneous Lichen Amyloidosis and in Skin Amyloidosis Associated With Multiple Endocrine Neoplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biological effects of the dual phenotypic Janus mutation of ret cosegregating with both multiple endocrine neoplasia type 2 and Hirschsprung's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The RET receptor: function in development and dysfunction in congenital malformation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dysfunction of the RET receptor in human cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transforming ability of MEN2A-RET requires activation of the phosphatidylinositol 3-kinase/AKT signaling pathway.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mice expressing a dominant-negative Ret mutation phenocopy human Hirschsprung disease and delineate a direct role of Ret in spermatogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The RET receptor is linked to stress response pathways
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A targeting mutation of tyrosine 1062 in Ret causes a marked decrease of enteric neurons and renal hypoplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development of medullary thyroid carcinoma in transgenic mice expressing the RET protooncogene altered by a multiple endocrine neoplasia type 2A mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple endocrine neoplasia type 2B mutation in human RET oncogene induces medullary thyroid carcinoma in transgenic mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RET(Men2B)-transgene produces sympathoadrenal tumors but does not prevent intestinal aganglionosis in gdnf-/- or gfr alpha-1(-/-) mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inducible dimerization of RET reveals a specific AKT deregulation in oncogenic signaling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Minireview: RET: normal and abnormal functions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression profiles provide insights into early malignant potential and skeletal abnormalities in multiple endocrine neoplasia type 2B syndrome tumors.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline Homozygous Mutations at Codon 804 in theRETProtooncogene in Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia Type 2A Patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a novel point mutation in the RET gene (Ala883Thr), which is associated with medullary thyroid carcinoma phenotype only in homozygous condition
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
When should thyroidectomy be performed in familial medullary thyroid carcinoma gene carriers with non-cysteine RET mutations?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial medullary thyroid carcinoma with noncysteine ret mutations: phenotype-genotype relationship in a large series of patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial medullary thyroid carcinoma: not a distinct entity? Genotype-phenotype correlation in a large family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pancreatic involvement in von Hippel–Lindau disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative sequence analysis of the VHL tumor suppressor gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular basis for stabilization of the von Hippel-Lindau (VHL) tumor suppressor protein by components of the VHL ubiquitin ligase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A tumor-specific gene therapy strategy targeting dysregulation of the VHL/HIF pathway in renal cell carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of a von Hippel Lindau pathway involved in extracellular matrix remodeling, cell invasion, and angiogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
von Hippel-Lindau tumor suppressor protein regulates the assembly of intercellular junctions in renal cancer cells through hypoxia-inducible factor-independent mechanisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of von Hippel-Lindau protein causes cell density dependent deregulation of CyclinD1 expression through hypoxia-inducible factor.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Jade-1, a candidate renal tumor suppressor that promotes apoptosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
von Hippel-Lindau partner Jade-1 is a transcriptional co-activator associated with histone acetyltransferase activity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NF1 tumor suppressor gene function: narrowing the GAP
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The NF1 tumor suppressor critically regulates TSC2 and mTOR.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Perturbations of the AKT signaling pathway in human cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tuberous sclerosis: a GAP at the crossroads of multiple signaling pathways
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hamartin and tuberin: working together for tumour suppression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The parafibromin tumor suppressor protein is part of a human Paf1 complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a functional bipartite nuclear localization signal in the tumor suppressor parafibromin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial cytopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial SDHD gene is required for early embryogenesis, and its partial deficiency results in persistent carotid body glomus cell activation with full responsiveness to hypoxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic testing in pheochromocytoma or functional paraganglioma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0242-6498%2805%2986161-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0242-6498(05)86161-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
PubMed publication ID
16735973
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16735973
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16735973%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 January 2020
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