C1s欠損症
WordNet
- the 3rd letter of the Roman alphabet (同)c
- (music) the keynote of the scale of C major
- a general-purpose programing language closely associated with the UNIX operating system
PrepTutorEJDIC
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
- carbonの化学記号
UpToDate Contents
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- 1. 止血の概要 overview of hemostasis
- 2. 補体系の遺伝性疾患 inherited disorders of the complement system
- 3. 補体経路 complement pathways
- 4. 補体系の制御因子および受容体 regulators and receptors of the complement system
- 5. 補体系の概要および臨床的評価 overview and clinical assessment of the complement system
English Journal
- ELISA to measure neutralizing capacity of anti-C1-inhibitor antibodies in plasma of angioedema patients.
- Engel R1, Rensink I2, Roem D1, Brouwer M1, Kalei A2, Perry D3, Zeerleder S4, Wouters D1, Hamann D5.
- Journal of immunological methods.J Immunol Methods.2015 Nov;426:114-9. doi: 10.1016/j.jim.2015.08.011. Epub 2015 Aug 28.
- BACKGROUND: Neutralizing autoantibodies (NAbs) against plasma serpin C1-inhibitor (C1-inh) are implicated in the rare disorder, acquired angioedema (AAE). There is insufficient understanding of the process of antibody formation and its correlation with disease progression and severity. We have devel
- PMID 26318839
- Classical pathway deficiencies - A short analytical review.
- Truedsson L1.
- Molecular immunology.Mol Immunol.2015 Nov;68(1):14-9. doi: 10.1016/j.molimm.2015.05.007. Epub 2015 May 30.
- Deficiencies in the classical pathway of complement activation have some common features but show also great differences. Deficiencies of each of the components (C1q, C1s, C1r, C4 and C2) imply increased susceptibility to bacterial infections. They are also associated with increased risk to develop
- PMID 26038300
- Functional analysis of matriptase-2 mutations and domains: insights into the molecular basis of iron-refractory iron deficiency anemia.
- McDonald CJ1, Ostini L1, Bennett N1, Subramaniam N1, Hooper J2, Velasco G3, Wallace DF1, Subramaniam VN4.
- American journal of physiology. Cell physiology.Am J Physiol Cell Physiol.2015 Apr 1;308(7):C539-47. doi: 10.1152/ajpcell.00264.2014. Epub 2015 Jan 14.
- Mutations in the TMPRSS6 gene are associated with severe iron-refractory iron deficiency anemia resulting from an overexpression of hepcidin, the key regulator of iron homeostasis. The matriptase (MT)-2 protein (encoded by the TMPRSS6 gene) regulates hepcidin expression by cleaving hemojuvelin [HJV/
- PMID 25588876
Japanese Journal
- 井上 直和,斎藤 俊行,増田 理亜子,鈴木 好夫,大富 美智子,崎山 比早子
- 日本分子生物学会年会プログラム・講演要旨集 21, 691, 1998-12-01
- NAID 10002920540
Related Links
- Inoue et al. (1998) reported a patient with selective C1s deficiency resulting from a homozygous mutation in the C1S gene (120580.0001). In a 27-month-old girl with multiple autoimmune diseases, Dragon-Durey et al ...
- From NCBI Gene: Complement component c1s deficiency EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2 From UniProt: Complement component C1s deficiency (C1SD): A rare defect resulting in C1 ...
★リンクテーブル★
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- 英
- C1s deficiency
- 関
- C1s
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- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve
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