- 少遺伝子による、オリゴジーンの、主働遺伝子の
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- 1. ネフロン癆の遺伝学および病因 genetics and pathogenesis of nephronophthisis
- 2. 喘息の遺伝学 genetics of asthma
- 3. 先天性性腺刺激ホルモン放出ホルモン欠乏症（特発性低ゴナドトロピン性性腺機能低下） congenital gonadotropin releasing hormone deficiency idiopathic hypogonadotropic hypogonadism
- 4. ネフロン癆の臨床症状、診断、および治療 clinical manifestations diagnosis and treatment of nephronophthisis
English Journal
- Identification of novel hereditary cancer genes by whole exome sequencing.
- Sokolenko AP1, Suspitsin EN1, Kuligina ESh2, Bizin IV3, Frishman D4, Imyanitov EN5.
- Cancer letters.Cancer Lett.2015 Dec 28;369(2):274-88. doi: 10.1016/j.canlet.2015.09.014. Epub 2015 Sep 30.
- Whole exome sequencing (WES) provides a powerful tool for medical genetic research. Several dozens of WES studies involving patients with hereditary cancer syndromes have already been reported. WES led to breakthrough in understanding of the genetic basis of some exceptionally rare syndromes; for ex
- PMID 26427841
- Bardet-Biedl syndrome: Is it only cilia dysfunction?
- Novas R1, Cardenas-Rodriguez M1, Irigoín F2, Badano JL3.
- FEBS letters.FEBS Lett.2015 Nov 14;589(22):3479-91. doi: 10.1016/j.febslet.2015.07.031. Epub 2015 Jul 29.
- Bardet-Biedl syndrome (BBS) is a genetically heterogeneous, pleiotropic disorder, characterized by both congenital and late onset defects. From the analysis of the mutational burden in patients to the functional characterization of the BBS proteins, this syndrome has become a model for both understa
- PMID 26231314
- Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.
- Tarlarini C1, Lunetta C2, Mosca L1, Avemaria F1, Riva N3, Mantero V4, Maestri E2, Quattrini A3, Corbo M2,5, Melazzini MG2, Penco S1.
- European journal of neurology.Eur J Neurol.2015 Nov;22(11):1474-81. doi: 10.1111/ene.12772. Epub 2015 Jul 15.
- BACKGROUND AND PURPOSE: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease. Approximately 5%-10% of cases are familial (FALS) and the remaining are sporadic (SALS). To date FUS mutations are responsible for 4%-6% of familial cases as well as 0.7%-1.8% of sporadic cases.METHODS:
- PMID 26176978
Japanese Journal
- Effects of estrogens on proliferation and differentiation of neural stem/progenitor cells
- OKADA Makiko,MURASE Koichi,MAKINO Akihisa,NAKAJIMA Mitsunari,KAKU Teppei,FURUKAWA Shoei,FURUKAWA Yoshiko
- Biomedical Research 29(3), 163-170, 2008
- … however, this ratio did not change when the cells were stimulated with platelet-derived growth factor (PDGF), a mitogen for oligodendrocyte precursors, or with neurotrophin-3, an oligogenic factor for glial progenitor cells. …
- NAID 130004470710
- 骨粗鬆症のゲノム医学--遺伝的素因解明へ向けたゲノム学応用への期待 (特集 骨・破壊と再生のゲノム医学)
- 江面 陽一
- ゲノム医学 6(1), 13-16, 2006-02
- NAID 40007163885
- Partial resistance of pepper to bacterial wilt is oligogenic and stable under tropical conditions
- LAFORTUNE D.
- Plant Dis. 89, 501-506, 2005
- NAID 30027623596
Related Links
- oligogenic [ol′igōjen′ik] Etymology: Gk, oligos + genein, to produce pertaining to hereditary characteristics produced by one or only a few genes. oligogenic ... Whereas sequencing to date has mainly been limited to unraveling single ...
- oligogenic (comparative more oligogenic, superlative most oligogenic) (genetics, of a trait) Determined by but a small number of genes. Retrieved from "https://en.wiktionary.org/w/index.php?title=oligogenic&oldid=26756872" : ...
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★リンクテーブル★
| リンク元 | 「主働遺伝子」「オリゴジーン」「少遺伝子」「oligogene」 |
「主働遺伝子」
「オリゴジーン」
- 英
- oligogene、oligogenic
- 関
- 主働遺伝子、少遺伝子
「少遺伝子」
- 英
- oligogenic
- 関
- オリゴジーン、主働遺伝子