罹患同胞対連鎖解析、罹患同胞対連鎖解析法

WordNet

form a pair or pairs; "The two old friends paired off" (同)pair off, partner off, couple
a set of two similar things considered as a unit (同)brace
a poker hand with 2 cards of the same value
two people considered as a unit
arrange in pairs; "Pair these numbers" (同)geminate
occur in pairs (同)geminate
have an effect upon; "Will the new rules affect me?" (同)impact, bear upon, bear on, touch_on, touch
act physically on; have an effect upon; "the medicine affects my heart rate"
the conscious subjective aspect of feeling or emotion
have an emotional or cognitive impact upon; "This child impressed me as unusually mature"; "This behavior struck me as odd" (同)impress, move, strike
an investigation of the component parts of a whole and their relations in making up the whole
the abstract separation of a whole into its constituent parts in order to study the parts and their relations (同)analytic thinking
a branch of mathematics involving calculus and the theory of limits; sequences and series and integration and differentiation
a form of literary criticism in which the structure of a piece of writing is analyzed
the use of closed-class words instead of inflections: e.g., `the father of the bride instead of `the brides father
an associative relation
(genetics) traits that tend to be inherited together as a consequence of an association between their genes; all of the genes of a given chromosome are linked (where one goes they all go) (同)gene linkage
a mechanical system of rods or springs or pivots that transmits power or motion
the act of linking things together
acted upon; influenced
speaking or behaving in an artificial way to make an impression (同)unnatural

PrepTutorEJDIC

(二つで一つに用いられる物の)『組』,『対』《+『of』+『名』》 / (対になる部分からなる物の)『1個』《+『of』+『名』》 / 《集合的に》《複数扱い》夫婦,婚約中の男女;(動物の)つがい《+『of』+『名』》 / 《集合的に》《複数扱い》(同種または何かの関係のある物の)二人(二つ,2頭など)の組《+『of』+『名』》 / …‘を'二人(2個)ずつ組にする《+『名』+『off』(『up』),+『off』(『up』)+『名』》,(…と)…‘を'組にする《+『名』+『with』+『名』》 / (…と)…‘を'結婚させる《+『名』+[『up』]『with』+『名』》 / 二人(2個)ずつ組になる《+『off』(『up』)》
…‘に'『影響する』,作用する / 〈人〉‘の'『心を動かす』,'を'感動させる / 〈人,人の健康など〉'を'冒す
…‘の'ふりをする,'を'装う / …'を'好む,好んでする(用いる,身につける)
(内容・状況などの)『分析』,分解;(詳細な)検討 / (化学・物理で)分析;《米》(心理学で)[精神]分析;(数学で)解析
〈C〉鎖の輪 / 〈U〉連結(結合)の状態(仕方)
影響された,作用を受けた / 感動した / (病気などに)冒された
気どった,きざな

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 喘息の遺伝学 genetics of asthma
2. 遺伝的変異の概要 overview of genetic variation
3. アルツハイマー病の遺伝学 genetics of alzheimer disease
4. 遺伝学用語集 glossary of genetic terms
5. 不整脈原性右室心筋症：解剖学、組織学、病因、および遺伝学 arrhythmogenic right ventricular cardiomyopathy anatomy histology pathogenesis and genetics

English Journal

Variations in ORAI1 Gene Associated with Kawasaki Disease.

Onouchi Y1,2, Fukazawa R3, Yamamura K4, Suzuki H5, Kakimoto N5, Suenaga T5, Takeuchi T5, Hamada H6, Honda T6, Yasukawa K6, Terai M6, Ebata R7, Higashi K8, Saji T9, Kemmotsu Y9, Takatsuki S9, Ouchi K10, Kishi F11, Yoshikawa T12, Nagai T13, Hamamoto K14, Sato Y15, Honda A16, Kobayashi H16, Sato J17, Shibuta S18, Miyawaki M18, Oishi K19, Yamaga H20, Aoyagi N21, Yoshiyama M22, Miyashita R23, Murata Y24, Fujino A25, Ozaki K1, Kawasaki T26, Abe J27, Seki M28, Kobayashi T29, Arakawa H28, Ogawa S3, Hara T4, Hata A2, Tanaka T1,30.
PloS one.PLoS One.2016 Jan 20;11(1):e0145486. doi: 10.1371/journal.pone.0145486. eCollection 2016.
Kawasaki disease (KD; MIM#61175) is a systemic vasculitis syndrome with unknown etiology which predominantly affects infants and children. Recent findings of susceptibility genes for KD suggest possible involvement of the Ca(2+)/NFAT pathway in the pathogenesis of KD. ORAI1 is a Ca(2+) release activ
PMID 26789410

Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.

Onodera K1, Arimura Y1, Isshiki H1, Kawakami K1, Nagaishi K2, Yamashita K1, Yamamoto E1, Niinuma T3, Naishiro Y4, Suzuki H3, Imai K5, Shinomura Y1.
PloS one.PLoS One.2015 Sep 16;10(9):e0137801. doi: 10.1371/journal.pone.0137801. eCollection 2015.
BACKGROUND: The common disease-common variant hypothesis is insufficient to explain the complexities of Crohn's disease (CD) genetics; therefore, rare variants are expected to be important in the disease. We explored rare variants associated with susceptibility to CD in Japanese individuals by perso
PMID 26375822

Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia.

Brucato N1, DeLisi LE, Fisher SE, Francks C.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.Am J Med Genet B Neuropsychiatr Genet.2014 Oct;165B(7):555-63. doi: 10.1002/ajmg.b.32258. Epub 2014 Aug 11.
Epigenetic effects on psychiatric traits remain relatively under-studied, and it remains unclear what the sizes of individual epigenetic effects may be, or how they vary between different clinical populations. The gene LRRTM1 (chromosome 2p12) has previously been linked and associated with schizophr
PMID 25111784

Japanese Journal

Mathematical basis of affected sib-pair analysis : an extension to X-linked loci

TSUKAMOTO Yasuo,KOMAI Koichiro,TSUMIYAMA Ken,SAKAI Yoshitada,SHIOZAWA Shunichi
Modern rheumatology 20(4), 370-375, 2010-08-01
NAID 10026691476

A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12

Onouchi Yoshihiro,Tamari Mayumi,Takahashi Atsushi [他],TSUNODA Tatsuhiko,YASHIRO Mayumi,NAKAMURA Yoshikazu,YANAGAWA Hiroshi,WAKUI Keiko,FUKUSHIMA Yoshimitsu,KAWASAKI Tomisaku,NAKAMURA Yusuke,HATA Akira
Journal of human genetics 52(2), 179-190, 2007-02-01
NAID 10018514642

Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?

Krischek Boris,Narita Akira,Akagawa Hiroyuki [他],KASUYA Hidetoshi,TAJIMA Atsushi,ONDA Hideaki,YONEYAMA Taku,HORI Tomokatsu,INOUE Ituro
Journal of human genetics 51(5), 491-494, 2006-05-01
NAID 10019168190

Related Pictures

★リンクテーブル★

リンク元	「罹患同胞対連鎖解析」「罹患同胞対連鎖解析法」
関連記事	「linkage」「affect」「pair」「analysis」「paired」