(Q28249576)

multiple endocrine neoplasia type 1

inferred from title

1 reference

Manuel C Lemos

1

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Rajesh Thakker

object named as

Rajesh V Thakker

series ordinal

2

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language of work or name

English

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publication date

January 2008

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published in

Human Mutation

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volume

29

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page(s)

22-32

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issue

1

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cites work

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin molecular interactions: insights into normal functions and tumorigenesis.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin and its interacting proteins: elucidation of menin function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Splicing in action: assessing disease causing sequence changes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Hyperparathyroidism presenting as the first lesion in multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Identification of MEN1 gene mutations in families with MEN 1 and related disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Heterozygous Men1 mutant mice develop a range of endocrine tumors mimicking multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Genetic ablation of the tumor suppressor menin causes lethality at mid-gestation with defects in multiple organs.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Somatic mutations of the MEN1 tumor suppressor gene detected in sporadic angiofibromas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Expression of the MEN-1 gene in a large kindred with multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Multiple endocrine neoplasia type 1 interacts with forkhead transcription factor CHES1 in DNA damage response

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Multiple endocrine neoplasia type 1 in France: clinical and genetic studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Functional studies of the MEN1 gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Lack of MEN1 gene mutations in 27 sporadic insulinomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Nomenclature for the description of human sequence variations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Lethality of multiple endocrine neoplasia type I

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin links estrogen receptor activation to histone H3K4 trimethylation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

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/10.1002%2FHUMU.20605

7 January 2021

Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

MEN1 gene mutations in sporadic neuroendocrine tumors of foregut derivation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin uncouples Elk-1, JunD and c-Jun phosphorylation from MAP kinase activation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

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/10.1002%2FHUMU.20605

7 January 2021

MEN1 gene mutation analysis of sporadic adrenocortical lesions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

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/10.1002%2FHUMU.20605

7 January 2021

Menin, the product of the MEN1 gene, is a nuclear protein

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Novel germline mutations of the MEN1 gene in Japanese patients with multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Multiple endocrine neoplasia type 1 variant with frequent prolactinoma and rare gastrinoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Somatic mutation of the MEN1 gene in parathyroid tumours.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

The tumor suppressor protein menin interacts with NF-kappaB proteins and inhibits NF-kappaB-mediated transactivation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Nonsense-mediated decay approaches the clinic

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Reconstituted expression of menin in Men1-deficient mouse Leydig tumour cells induces cell cycle arrest and apoptosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Characteristics of the Danish families with multiple endocrine neoplasia type 1.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin regulates pancreatic islet growth by promoting histone methylation and expression of genes encoding p27Kip1 and p18INK4c

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Heterogeneity at the 5'-end of MEN1 transcripts

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Stable overexpression of MEN1 suppresses tumorigenicity of RAS.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Applying nonsense-mediated mRNA decay research to the clinic: progress and challenges

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Direct binding of DNA by tumor suppressor menin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Tumor suppressor menin: the essential role of nuclear localization signal domains in coordinating gene expression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

GTPase inhibiting mutations activate the alpha chain of Gs and stimulate adenylyl cyclase in human pituitary tumours.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

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/10.1002%2FHUMU.20605

7 January 2021

Menin interacts directly with the homeobox-containing protein Pem

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Multiple tumor suppressor pathways negatively regulate telomerase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Multiple endocrine neoplasia syndromes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Broad tumor spectrum in a mouse model of multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin's interaction with glial fibrillary acidic protein and vimentin suggests a role for the intermediate filament network in regulating menin activity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Loss of wild-type MEN1 gene expression in multiple endocrine neoplasia type 1-associated parathyroid adenoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Two G protein oncogenes in human endocrine tumors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Multiple endocrine neoplasia type 1: clinical and genetic topics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Frequency of somatic MEN1 gene mutations in monoclonal parathyroid tumours of patients with primary hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin and MLL cooperatively regulate expression of cyclin-dependent kinase inhibitors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin, a tumor suppressor, associates with nonmuscle myosin II-A heavy chain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin, a gene product responsible for multiple endocrine neoplasia type 1, interacts with the putative tumor metastasis suppressor nm23

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Genomic variants in exons and introns: identifying the splicing spoilers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Multiple endocrine neoplasia type 1.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Mouse JunD negatively regulates fibroblast growth and antagonizes transformation by ras.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

jun-D: a third member of the jun gene family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Somatic mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in patients with sporadic, nonfamilial primary hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Genome-wide analysis of menin binding provides insights into MEN1 tumorigenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Analysis of the MEN1 gene in sporadic pituitary adenomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Functional interaction between tumor suppressor menin and activator of S-phase kinase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Isolated familial somatotropinoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Tumor deletion mapping on chromosome 11q13 in eight families with isolated familial somatotropinoma and in 15 sporadic somatotropinomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Inactivation of menin, the product of the multiple endocrine neoplasia type 1 gene, inhibits the commitment of multipotential mesenchymal stem cells into the osteoblast lineage

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin is required for bone morphogenetic protein 2- and transforming growth factor beta-regulated osteoblastic differentiation through interaction with Smads and Runx2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

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

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Characterization of the mouse Men1 gene and its expression during development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

The 32-kilodalton subunit of replication protein A interacts with menin, the product of the MEN1 tumor suppressor gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Frequent Occurrence of an Intron 4 Mutation in Multiple Endocrine Neoplasia Type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Pituitary adenoma predisposition caused by germline mutations in the AIP gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Multiple endocrine neoplasia 1 gene alterations in MEN1-associated and sporadic lipomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Genetic aspects of adenomatosis of endocrine glands

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Cause of death in multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin, the multiple endocrine neoplasia type 1 gene product, exhibits GTP-hydrolyzing activity in the presence of the tumor metastasis suppressor nm23

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Menin missense mutants associated with multiple endocrine neoplasia type 1 are rapidly degraded via the ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021

Suppression of insulin-induced AP-1 transactivation by menin accompanies inhibition of c-Fos induction.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20605

7 January 2021