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
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MeSH Number(s) |
G05.360.340.024.340.375.249.340 G05.360.340.024.340.415.400.340
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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 |
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2004 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
2012 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genes, Neurofibromatosis 1" by people in Profiles.
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Recent Advances in the Diagnosis and Pathogenesis of Neurofibromatosis Type 1 (NF1)-associated Peripheral Nervous System Neoplasms. Adv Anat Pathol. 2018 Sep; 25(5):353-368.
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Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development. Dis Model Mech. 2012 Nov; 5(6):881-94.
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Genetically engineered mouse models shed new light on the pathogenesis of neurofibromatosis type I-related neoplasms of the peripheral nervous system. Brain Res Bull. 2012 May 01; 88(1):58-71.
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Tumor suppressor mutations and growth factor signaling in the pathogenesis of NF1-associated peripheral nerve sheath tumors. I. The role of tumor suppressor mutations. J Neuropathol Exp Neurol. 2004 Nov; 63(11):1115-23.