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单词 alloalbuminaemia
释义

alloalbuminaemiaalloalbuminemian.

Brit. /ˌaləʊˌalbjᵿmᵻˈniːmɪə/, U.S. /ˌæloʊælˌbjuməˈnimiə/
Forms: 1900s– alloalbuminaemia, 1900s– alloalbuminemia (chiefly U.S.).
Origin: Formed within English, by derivation. Etymons: allo- comb. form, albumin n., -aemia suffix.
Etymology: < allo- comb. form + albumin n. + -aemia suffix. Compare slightly later alloalbumin n.
Biochemistry and Genetics.
The condition of having a genetically determined variant form of albumin in the blood; an instance of this.
ΚΠ
1968 B. S. Blumberg et al. in Jrnl. Amer. Med. Assoc. 15 Jan. 181/1 The term ‘alloalbuminemia’ (from the Greek allo meaning different) is recommended for the condition in which the individual has an albumin variant different from common albumin A.
1982 Brit. Med. Jrnl. 18 Sept. 812/2 The effect of an albumin variant (as in alloalbuminaemia, bisalbuminaemia) will be less predictable: the alloalbumin may bind either warfarin or its competing drugs differently from the albumin-A normally present.
2010 Translational Res. 155 118/1 Mutations in this gene [for human serum albumin] may cause the presence of 2 circulating forms of the protein (bisalbuminemia or alloalbuminemia).
This is a new entry (OED Third Edition, September 2012; most recently modified version published online December 2021).
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n.1968
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更新时间:2024/12/22 16:54:19