No association between FADS polymorphisms and atopic diseases in children from the GINI and LISA birth cohorts.

Singmann P; Rzehak P; Berdel D; Wichmann HE; Heinrich J

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No association between FADS polymorphisms and atopic diseases in children from the GINI and LISA birth cohorts.

机译：GINI和LISA出生队列儿童的FADS多态性与特应性疾病之间没有关联。

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(PUFA) in the development of atopic diseases is commonly discussed (1, 2).Also defects in the PUFA generating pathway (delta6 desat-uration) have been suggested to be involved in atopic patients of early onset (1). PUFA have crucial functions in the organism; for example, they are precursors of major inflammatory mediators (2).

机译：（PUFA）在特应性疾病的发展中被广泛讨论（1，2）.PUFA产生途径（delta6脱饱和）的缺陷也被认为与早发性特应性患者有关（1）。 PUFA在生物体中具有至关重要的功能;例如，它们是主要炎症介质的前体（2）。

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《Allergy》 |2010年第12期|共3页
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Singmann P; Rzehak P; Berdel D; Wichmann HE; Heinrich J;
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正文语种 eng
中图分类医学免疫学;
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1. No association between FADS polymorphisms and atopic diseases in children from the GINI and LISA birth cohorts. [J] . Singmann P, Rzehak P, Berdel D, Allergy . 2010,第12期

机译：GINI和LISA出生队列儿童的FADS多态性与特应性疾病之间没有关联。
2. FADS gene cluster polymorphisms: important modulators of fatty acid levels and their impact on atopic diseases. [J] . Lattka E, Illig T, Heinrich J, Journal of nutrigenetics and nutrigenomics. . 2009,第3期

机译：FADS基因簇多态性：脂肪酸水平的重要调节剂及其对特应性疾病的影响。
3. FADS gene cluster polymorphisms: important modulators of fatty acid levels and their impact on atopic diseases. [J] . Lattka E, Illig T, Heinrich J, Journal of nutrigenetics and nutrigenomics. . 2009,第3期

机译：FADS基因簇多态性：脂肪酸水平的重要调节剂及其对特应性疾病的影响。
4. Association of CYP2D6 and ADRB1 Single Nucleotide Polymorphisms and Response to Beta Blocker Therapy in a Patient Sample Set with Cardiovascular Diseases from Romania [C] . Andrada Camelia Guta, Liana Gabriela Gruescu Molecular Medicine TRI-CON. . 2014

机译：CYP2D6和ADRB1单核苷酸多态性和对患者样本中β受体疗法的响应与来自罗马尼亚的心血管疾病
5. Risk factors for atopic diseases in a Czech birth cohort [D] . Yap, Poh-Sin. 2007

机译：捷克出生队列中特应性疾病的危险因素
6. Cytokine gene polymorphisms and atopic disease in two European cohorts. (ECRHS-Basel and SAPALDIA) [O] . M Imboden, A Nieters, AJ Bircher, 2006

机译：欧洲两个队列中的细胞因子基因多态性和特应性疾病。（ECRHS-巴塞尔协议和SAPALDIA）
7. Associations of genotype variants of single nucleotide polymorphism of gene orosomucoid-1-like-protein 3 and atopic diseases at children. [O] . V. O. Dytiatkovsky, O. E. Abaturov, N. V. Naumenko, 2019

机译：基因核苷酸-1样蛋白3和儿童特应性疾病的单核苷酸多态性基因型变体的关联。

No association between FADS polymorphisms and atopic diseases in children from the GINI and LISA birth cohorts.

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