 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
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 | | 2005 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2021 | 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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Klein-Tasman BP, Lee K, Thompson HL, Janusz J, Payne JM, Pardej S, de Blank P, Kennedy T, Janke KM, Castillo AD, Walsh KS. Recommendations for Measurement of Attention Outcomes in Preschoolers With Neurofibromatosis. Neurology. 2021 08 17; 97(7 Suppl 1):S81-S90.
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Sant DW, Margraf RL, Stevenson DA, Grossmann AH, Viskochil DH, Hanson H, Everitt MD, Rios JJ, Elefteriou F, Hennessey T, Mao R. 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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Johannessen CM, Johnson BW, Williams SM, Chan AW, Reczek EE, Lynch RC, Rioth MJ, McClatchey A, Ryeom S, Cichowski K. TORC1 is essential for NF1-associated malignancies. Curr Biol. 2008 Jan 08; 18(1):56-62.
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Inagaki H, Ohye T, Kogo H, Yamada K, Kowa H, Shaikh TH, Emanuel BS, Kurahashi H. Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates. Hum Mutat. 2005 Oct; 26(4):332-42.
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Luna-Fineman S, Shannon KM, Lange BJ. Childhood monosomy 7: epidemiology, biology, and mechanistic implications. Blood. 1995 Apr 15; 85(8):1985-99.
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