全部文献期刊学位论文会议报纸专利标准年鉴图书|学者科研项目
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作者:Idit Bejarano-Achache , Liran Levy ...
来源:[J].Clinical Therapeutics(IF 2.23), 2012, Vol.34 (4), pp.811-823Elsevier
摘要:Abstract(#br)Background(#br)The cytochrome P450 (CYP) 4F2 isozyme has been reported to metabolize vitamin K 1 in vitro, and the V433M polymorphism in the CYP4F2 gene has been associated with reduced vitamin K 1 metabolism and the need for a higher maintenance dosage in patients r...
作者:... Aby Lewin , Idit Bejarano-Achache , Anat Blumenfeld
来源:[J].Pediatric and Developmental Pathology(IF 0.859), 1999, Vol.2 (5), pp.404-414Springer
摘要:ABSTRACT(#br) Oculocutaneous albinism type I (OCA I) comprises autosomal recessive syndromes of hypopigmentation and low vision, caused by the lack of tyrosinase activity. Affected families seek genetic counseling and prenatal diagnosis as preventive measures. Until recently, pre...
作者:Idit Bejarano-Achache , Mordechai Muszkat
来源:[J].European Journal of Clinical Pharmacology(IF 2.741), 2012, Vol.68 (5), pp.617-627Springer
摘要:Abstract(#br) Objective(#br)Warfarin responsiveness is characterized by marked interindividual variability. A major portion of this variability is attributed to CYP2C 9 and VKORC1 polymorphisms, but almost 50% is still unaccounted for. This paper reports the first prospectiv...

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