Genes, Neurofibromatosis 2
"Genes, Neurofibromatosis 2" 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 22. Mutation or loss of these genes causes NEUROFIBROMATOSIS 2.
Descriptor ID |
D016515
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MeSH Number(s) |
G05.360.340.024.340.375.249.345 G05.360.340.024.340.415.400.345
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Concept/Terms |
Genes, Neurofibromatosis 2- Genes, Neurofibromatosis 2
- Genes, nf 2
- Gene, nf 2
- nf 2 Gene
- nf 2 Genes
- nf2 Genes
- Neurofibromatosis 2 Genes
- Gene, Neurofibromatosis 2
- Neurofibromatosis 2 Gene
- Genes, nf2
- Gene, nf2
- nf2 Gene
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Below are MeSH descriptors whose meaning is more general than "Genes, Neurofibromatosis 2".
Below are MeSH descriptors whose meaning is more specific than "Genes, Neurofibromatosis 2".
This graph shows the total number of publications written about "Genes, Neurofibromatosis 2" by people in this website by year, and whether "Genes, Neurofibromatosis 2" 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 |
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1996 | 0 | 1 | 1 | 1997 | 1 | 0 | 1 | 2000 | 0 | 2 | 2 | 2014 | 1 | 0 | 1 | 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genes, Neurofibromatosis 2" by people in Profiles.
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Paintal A, Tjota MY, Wang P, Fitzpatrick C, Wanjari P, Stadler WM, Gallan AJ, Segal J, Antic T. NF2-mutated Renal Carcinomas Have Common Morphologic Features Which Overlap With Biphasic Hyalinizing Psammomatous Renal Cell Carcinoma: A Comprehensive Study of 14 Cases. Am J Surg Pathol. 2022 05 01; 46(5):617-627.
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Gavilan HS, Kulikauskas RM, Gutmann DH, Fehon RG. In vivo functional analysis of the human NF2 tumor suppressor gene in Drosophila. PLoS One. 2014; 9(3):e90853.
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Lim DJ, Rubenstein AE, Evans DG, Jacks T, Seizinger BG, Baser ME, Beebe D, Brackmann DE, Chiocca EA, Fehon RG, Giovannini M, Glazer R, Gusella JF, Gutmann DH, Korf B, Lieberman F, Martuza R, McClatchey AI, Parry DM, Pulst SM, Ramesh V, Ramsey WJ, Ratner N, Rutkowski JL, Ruttledge M, Weinstein DE. Advances in neurofibromatosis 2 (NF2): a workshop report. J Neurogenet. 2000 Jun; 14(2):63-106.
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McCartney BM, Kulikauskas RM, LaJeunesse DR, Fehon RG. The neurofibromatosis-2 homologue, Merlin, and the tumor suppressor expanded function together in Drosophila to regulate cell proliferation and differentiation. Development. 2000 Mar; 127(6):1315-24.
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Fehon RG, Oren T, LaJeunesse DR, Melby TE, McCartney BM. Isolation of mutations in the Drosophila homologues of the human Neurofibromatosis 2 and yeast CDC42 genes using a simple and efficient reverse-genetic method. Genetics. 1997 May; 146(1):245-52.
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McCartney BM, Fehon RG. Distinct cellular and subcellular patterns of expression imply distinct functions for the Drosophila homologues of moesin and the neurofibromatosis 2 tumor suppressor, merlin. J Cell Biol. 1996 May; 133(4):843-52.
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