Genes, Neurofibromatosis 1
"Genes, Neurofibromatosis 1" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Tumor suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome.
| Descriptor ID |
D016514
|
| MeSH Number(s) |
G05.360.340.024.340.375.249.340 G05.360.340.024.340.415.400.340
|
| Concept/Terms |
Genes, Neurofibromatosis 1- Genes, Neurofibromatosis 1
- Genes, nf 1
- Gene, nf 1
- nf 1 Gene
- nf 1 Genes
- nf1 Genes
- Neurofibromatosis 1 Genes
- Neurofibromatosis 1 Gene
- Genes, nf1
- Gene, nf1
- nf1 Gene
|
Below are MeSH descriptors whose meaning is more general than "Genes, Neurofibromatosis 1".
Below are MeSH descriptors whose meaning is more specific than "Genes, Neurofibromatosis 1".
This graph shows the total number of publications written about "Genes, Neurofibromatosis 1" by people in this website by year, and whether "Genes, Neurofibromatosis 1" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Genes, Neurofibromatosis 1" by people in Profiles.
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Evaluation of somatic mutations in tibial pseudarthrosis samples in neurofibromatosis type 1. J Med Genet. 2015 Apr; 52(4):256-61.
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Pilocytic astrocytoma: a disease with evolving molecular heterogeneity. J Child Neurol. 2013 May; 28(5):625-32.
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Elucidating distinct roles for NF1 in melanomagenesis. Cancer Discov. 2013 Mar; 3(3):338-49.
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Neurofibromatosis 2011: a report of the Children's Tumor Foundation annual meeting. Acta Neuropathol. 2012 Mar; 123(3):369-80.
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Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome. JAMA. 2009 Nov 18; 302(19):2111-8.
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Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1. Anticancer Res. 2009 Apr; 29(4):1255-62.
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Somatic mitochondrial DNA mutations in neurofibromatosis type 1-associated tumors. Mol Cancer Res. 2004 Aug; 2(8):433-41.
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NF1 inactivation cooperates with N-ras in in vivo lymphogenesis activating Erk by a mechanism independent of its Ras-GTPase accelerating activity. Oncogene. 1998 Oct 01; 17(13):1705-16.
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Nf1 deficiency causes Ras-mediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia. Nat Genet. 1996 Feb; 12(2):137-43.
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The neurofibromatosis type 1 (NF1) tumor suppressor gene and myeloid leukemia. Curr Top Microbiol Immunol. 1996; 211:233-9.