WordNet
- 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
- (of genes) producing its characteristic phenotype only when its allele is identical
PrepTutorEJDIC
- 〈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
- 後退する,退行の / (遺伝が)劣性の / 劣性遺伝形質
UpToDate Contents
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- 1. 成人における小脳性運動失調の概要 overview of cerebellar ataxia in adults
- 2. 遺伝性の魚鱗癬の概要 overview of the inherited ichthyoses
- 3. メンデル遺伝の概要 overview of mendelian inheritance
- 4. 遺伝性運動失調の概要 overview of the hereditary ataxias
- 5. 家族性筋萎縮性側索硬化症 familial amyotrophic lateral sclerosis
English Journal
- Are all the previously reported genetic variants in limb girdle muscular dystrophy genes pathogenic?
- Di Fruscio G1,2, Garofalo A1,2, Mutarelli M2, Savarese M1,2, Nigro V1,2.
- European journal of human genetics : EJHG.Eur J Hum Genet.2016 Jan;24(1):73-7. doi: 10.1038/ejhg.2015.76. Epub 2015 Apr 22.
- Hundreds of variants in autosomal genes associated with the limb girdle muscular dystrophies (LGMDs) have been reported as being causative. However, in most cases the proof of pathogenicity derives from their non-occurrence in hundreds of healthy controls and/or from segregation studies in small fam
- PMID 25898921
- Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing.
- Weber S1, Büscher AK1, Hagmann H2, Liebau MC2,3, Heberle C4, Ludwig M5, Rath S4, Alberer M6, Beissert A7, Zenker M8, Hoyer PF1, Konrad M9, Klein HG4, Hoefele J10.
- Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2016 Jan;31(1):73-81. doi: 10.1007/s00467-015-3167-6. Epub 2015 Aug 7.
- BACKGROUND: Steroid-resistant nephrotic syndrome (SRNS) is a severe cause of progressive renal disease. Genetic forms of SRNS can present with autosomal recessive or autosomal dominant inheritance. Recent studies have identified mutations in multiple podocyte genes responsible for SRNS. Improved seq
- PMID 26248470
- 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
Japanese Journal
- ファブリー病と腎移植
- 祖父江 理
- 日本臨床腎移植学会雑誌 = Journal of Japanese Society for Clinical Renal Transplantation 3(1), 23-30, 2015-07
- NAID 40020550800
- 遺伝子解析による血友病保因者診断の意義
- 篠澤 圭子
- 日本血栓止血学会誌 26(5), 549-556, 2015
- 要約：血友病は，X 染色体の第VIII 因子または第IX 因子の遺伝子変異を病因とする出血性疾患である．X連鎖劣性遺伝形式をとり，通常，患者は男性である．保因者とは，2 本のX 染色体（対立遺伝子）のうち1 本に病因遺伝子変異をもつ女性と定義する．保因者は通常は無症候性であるが，保因者全体の約1/3 に過多月経，鼻出血，術後出血や産後出血などの出血症状がある．確定保因者は，家系から保因者であること …
- NAID 130005102993
- Genetic Diagnosis via Whole Exome Sequencing in Taiwanese Patients with Hypertriglyceridemia
- Chiou Kuan-Rau,Chen Chung-Yung,Charng Min-ji
- Journal of Atherosclerosis and Thrombosis 22(9), 887-900, 2015
- … Based on the WES findings, we extended the study to genotype 65 unrelated adult index patients with a fasting serum triglyceride level of ＞500 mg/dL and 125 normal controls using polymerase chain reaction.Results: Using WES alignment, variant calling and annotation, 15 presumptive causal variants were initially identified, including 13 cases by the autosomal dominant model and two cases by the autosomal recessive model. …
- NAID 130005099302
Related Links
- Legend: Mechanisms of recessive and dominant inheritance. Recessive Inheritance Both parents carry a normal gene (N), and a faulty, recessive, gene (n). The parents, although carriers, are unaffected by the faulty gene. Their ...
- Translate recessive inheritance into another language Relevant Questions How Are Recessive Traits... When Recessive Gene For ... How Are Recessive Disord... What Is Dominate And Rec... What Is Autosomal Recess... How Is ...
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★リンクテーブル★
| リンク元 | 「劣性遺伝」「劣性遺伝形式」 |
| 関連記事 | 「inheritance」「recessive」 |
「劣性遺伝」
「劣性遺伝形式」
「inheritance」
- n.
「recessive」
- adj.
- 劣性の、劣性遺伝性の