WordNet
- the means of connection between things linked in series (同)nexus
- a unit of length equal to 1/100 of a chain
- an interconnecting circuit between two or more locations for the purpose of transmitting and receiving data (同)data link
- a fastener that serves to join or connect; "the walls are held together with metal links placed in the wet mortar during construction" (同)linkup, tie, tie-in
- (computing) an instruction that connects one part of a program or an element on a list to another program or list
- that which is inherited; a title or property or estate that passes by law to the heir on the death of the owner (同)heritage
- (genetics) attributes acquired via biological heredity from the parents (同)hereditary pattern
- any attribute or immaterial possession that is inherited from ancestors; "my only inheritance was my mothers blessing"; "the worlds heritage of knowledge" (同)heritage
- hereditary succession to a title or an office or property (同)heritage
- the 24th letter of the Roman alphabet (同)x, ex
PrepTutorEJDIC
- (鎖の)『輪』,環 / 鎖のようにつながったソーセージの一節 / (…と)つなぐ物(人),(…との)きずな,つながり《+『with』(『to』)+『名』》 / 《複数形で》=cuff links / …‘を'『つなぎ合わせる』,連結する;(…と)…‘を'つなぐ《+『名』+『with』(『to』)+『名』》 / (…と)結合する,つながる《+[『up』(『together』)]『with』+『名』》
- たいまつ
- 〈U〉『相続』,継承 / 〈C〉『遺産』,相続財産 / 〈C〉(両親・前任者・前代などから)受け継いだもの
- Christ / Christian
- x-axis
UpToDate Contents
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- 1. メンデル遺伝の概要 overview of mendelian inheritance
- 2. 単一遺伝子性疾患の非メンデル遺伝のパターン non mendelian inheritance patterns of monogenic diseases
- 3. ペリツェウス・メルツバッハー病 pelizaeus merzbacher disease
- 4. 点頭てんかんの病因および発症機序 etiology and pathogenesis of infantile spasms
- 5. 知的障害（精神遅滞）をもつ成人のプライマリケア primary care of the adult with intellectual disability mental retardation
English Journal
- Wiskott-Aldrich syndrome presenting with a clinical picture mimicking juvenile myelomonocytic leukaemia.
- Yoshimi A, Kamachi Y, Imai K, Watanabe N, Nakadate H, Kanazawa T, Ozono S, Kobayashi R, Yoshida M, Kobayashi C, Hama A, Muramatsu H, Sasahara Y, Jakob M, Morio T, Ehl S, Manabe A, Niemeyer C, Kojima S.SourceDepartment of Paediatrics and Adolescent Medicine, University of Freiburg, Freiburg, Germany. ayami.yoshimi@uniklinik-freiburg.de.
- Pediatric blood & cancer.Pediatr Blood Cancer.2013 May;60(5):836-41. doi: 10.1002/pbc.24359. Epub 2012 Sep 28.
- BACKGROUND: Wiskott-Aldrich syndrome (WAS) is a rare X-linked immunodeficiency caused by defects of the WAS protein (WASP) gene. Patients with WAS typically demonstrate micro-thrombocytopenia.PROCEDURES: The report describes seven male infants with WAS that initially presented with leukocytosis, mon
- PMID 23023736
- HER2 stabilizes survivin while concomitantly down-regulating survivin gene transcription by suppressing Notch cleavage.
- Ju JH, Yang W, Oh S, Nam K, Lee KM, Noh DY, Shin I.Source*Department of Life Science, Hanyang University, Seoul 133-791, Korea.
- The Biochemical journal.Biochem J.2013 Apr 1;451(1):123-34. doi: 10.1042/BJ20121716.
- In breast cancer, the HER2 (human epidermal growth factor receptor 2) receptor tyrosine kinase is associated with extremely poor prognosis and survival. Notch signalling has a key role in cell-fate decisions, especially in cancer-initiating cells. The Notch intracellular domain produced by Notch cle
- PMID 23323858
Japanese Journal
- Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations
- RAMESH Raakhee,CHEN Huijia,KUKULA Anna,WAKELING Emma L.,RUSTIN Malcolm H. A.,MCLEAN W. H. Irwin
- Journal of dermatological science 64(3), 159-162, 2011-12-01
- NAID 10030893475
- 常染色体性 Alport 症候群
- 岡 政史,野津 寛大,飯島 一誠,松尾 雅文
- 日本小児腎臓病学会雑誌 = Japanese journal of pediatric nephrology 23(1), 8-12, 2010-04-15
- Alport症候群 (AS) は感音性難聴を伴う遺伝性進行性腎疾患である。高頻度に末期腎不全に至るとされ臨床的に重要な疾患であるが，その臨床像，自然予後は十分には解明されていない。今回，分子遺伝学的特徴および近年報告された家族性良性血尿症候群との関連について，常染色体性Alport症候群を中心に概要をまとめる。
- NAID 10026412082
- Alport 症候群
- 野津 寛大,飯島 一誠,松尾 雅文
- 日本小児腎臓病学会雑誌 = Japanese journal of pediatric nephrology 21(2), 117-121, 2008-11-15
- … 中でも最も頻度の高い，X染色体連鎖型Alport症候群を中心に概要をまとめる。 …
- NAID 10025170337
Related Links
- X-linked in·her·i·tance the pattern of inheritance that may result from a mutant gene on an X chromosome. X-linked inheritance, a pattern of inheritance in which the transmission of traits varies according to the sex of the person ...
- X-Linked Inheritance Traits that are determined by alleles carried on the X chromosome are referred to as X-linked. X-linked alleles require a specific notation: Xc or X+ where the “+” represents the dominant allele and the lowercase ...
Related Pictures
★リンクテーブル★
| リンク元 | 「伴性遺伝」「X連鎖遺伝」「sex-linked inheritance」 |
| 関連記事 | 「link」「inheritance」「linked」「X」 |
「伴性遺伝」
「X連鎖遺伝」
「sex-linked inheritance」
「link」
- n.
- v.
- 関連づける、連結する、連接する
- 関
- associate、association、attach、bearing、bind、catenate、catenation、concatenation、connect、connection、correlate、correlation、implicate、implication、join、juncture、ligate、ligation、linkage、linked、pertinent、reference、relate、relation、relationship、relative、relevance、relevant
「inheritance」
- n.
「linked」
- adj.
- 連鎖の、連鎖的な、連鎖性の