A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype.
about
The dark matter of the cancer genome: aberrations in regulatory elements, untranslated regions, splice sites, non-coding RNA and synonymous mutationsMEN1, MEN4, and Carney Complex: Pathology and Molecular GeneticsTemozolomide and pasireotide treatment for aggressive pituitary adenoma: expertise at a tertiary care center.uORFdb--a comprehensive literature database on eukaryotic uORF biology.Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.Assessment of selective mRNA translation in mammalian cells by polysome profilingEarly Onset Primary Hyperparathyroidism Associated with a Novel Germline Mutation in CDKN1B.Pituitary gigantism: update on molecular biology and managementA constitutive active MAPK/ERK pathway due to BRAFV600E positively regulates AHR pathway in PTC.Comprehensive translational control of tyrosine kinase expression by upstream open reading frames.The non-canonical functions of p27(Kip1) in normal and tumor biology.The genetic background of acromegaly.The regulatory potential of upstream open reading frames in eukaryotic gene expression.Genetic mutations in sporadic pituitary adenomas--what to screen for?The role of genetic and epigenetic changes in pituitary tumorigenesis.New potential targets for treatment of Cushing's disease: epithelial growth factor receptor and cyclin-dependent kinases.Multiple Endocrine Neoplasia: A Genetically Diverse Group of Familial Tumor Syndromes.Genetics of gigantism and acromegaly.Genetics of Hyperparathyroidism, Including Parathyroid Cancer.hnRNPs and ELAVL1 cooperate with uORFs to inhibit protein translation.Functional characterization of a CDKN1B mutation in a Sardinian kindred with multiple endocrine neoplasia type 4 (MEN4).Expression of p27(Kip1) and p18(Ink4c) in human multiple endocrine neoplasia type 1-related pancreatic neuroendocrine tumors.Loss-of-function uORF mutations in human malignancies.MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism.A giant? Think of genetics: growth hormone-producing adenomas in the young are almost always the result of genetic defects.MEN4 and CDKN1B mutations: the latest of the MEN syndromes.Genetics of Cushing's Syndrome.Early onset acromegaly associated with a novel deletion in CDKN1B 5'UTR region.Landscape of CDKN1B Mutations in Luminal Breast Cancer and Other Hormone-Driven Human TumorsTranslation acrobatics: how cancer cells exploit alternate modes of translational initiationThe Importance of an Early and Accurate MEN1 DiagnosisCell Cycle Regulators and Lineage-Specific Therapeutic Targets for Cushing Disease
P2860
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P2860
A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype.
description
2013 nî lūn-bûn
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2013 թուականի Մարտին հրատարակուած գիտական յօդուած
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2013 թվականի մարտին հրատարակված գիտական հոդված
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
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name
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@ast
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@en
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@nl
type
label
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@ast
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@en
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@nl
prefLabel
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@ast
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@en
A novel mutation in the upstre ...... gene causes a MEN4 phenotype.
@nl
P2093
P2860
P50
P1433
P1476
A novel mutation in the upstre ...... B gene causes a MEN4 phenotype
@en
P2093
Elena Pardi
Filomena Cetani
Franco Mantero
Sara Bobisse
Sergio Ferasin
P2860
P304
P356
10.1371/JOURNAL.PGEN.1003350
P50
P577
2013-03-21T00:00:00Z