- 関
- neurofibromatosis 1 gene
WordNet
- (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" (同)cistron, factor
- the 14th letter of the Roman alphabet (同)n
- informal term for information; "give me the gen on your new line of computers"
PrepTutorEJDIC
- 遺伝子
- nitrogenの化学記号
UpToDate Contents
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English Journal
- NF1 Mutations Prevalent but Not Clinically Relevant.
- [No authors listed]
- Cancer discovery.Cancer Discov.2015 Aug 17. [Epub ahead of print]
- Whole-exome sequencing of 213 tumor samples shows that NF1 is mutated in 13.1% of melanomas. The gene is usually mutated in tumors that don't carry mutations in BRAF or NRAS, and it may be a cancer driver. However, loss of the gene didn't predict whether RAS activity increased or whether cell lines
- PMID 26283687
- Decoding NF1 Intragenic Copy-Number Variations.
- Hsiao MC1, Piotrowski A2, Callens T1, Fu C1, Wimmer K3, Claes KB4, Messiaen L5.
- American journal of human genetics.Am J Hum Genet.2015 Aug 6;97(2):238-49. doi: 10.1016/j.ajhg.2015.06.002. Epub 2015 Jul 16.
- Genomic rearrangements can cause both Mendelian and complex disorders. Currently, several major mechanisms causing genomic rearrangements, such as non-allelic homologous recombination (NAHR), non-homologous end joining (NHEJ), fork stalling and template switching (FoSTeS), and microhomology-mediated
- PMID 26189818
- Identification and functional analysis of early gene expression induced by circadian light-resetting in Drosophila.
- Adewoye AB1, Kyriacou CP2, Tauber E3.
- BMC genomics.BMC Genomics.2015 Aug 1;16:570. doi: 10.1186/s12864-015-1787-7.
- BACKGROUND: The environmental light-dark cycle is the dominant cue that maintains 24-h biological rhythms in multicellular organisms. In Drosophila, light entrainment is mediated by the photosensitive protein CRYPTOCHROME, but the role and extent of transcription regulation in light resetting of the
- PMID 26231660
Japanese Journal
- A novel RET gene mutation in a patient with apparently sporadic pheochromocytoma
- Development of a practical NF1 genetic testing method through the pilot analysis of five Japanese families with neurofibromatosis type 1
- A novel RET gene mutation in a patient with apparently sporadic pheochromocytoma
Related Links
- Complete information for NF1 gene (protein-coding), neurofibromin 1, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium ... Disorders / Diseases for NF1 gene ...
- neurofibromatosis type 1 - caused by mutations in the NF1 gene More than 1,000 NF1 mutations that cause neurofibromatosis type 1 have been identified. Most of these mutations are unique to a particular family. Many NF1 ...
★リンクテーブル★
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- 英
- neurofibromatosis 1 gene、NF1 gene
- 関
- NF1遺伝子
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- 英
- NF1 gene
- 関
- 神経線維腫症1型遺伝子
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- 関
- NF1 gene
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- 同
- neurofibromatosis type 1
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神経線維腫症 neurofibromatosis