英语词汇“progeria”的意思、用法、释义、翻译、读音、例句、短语、词组-英语词典

是什么意思

早衰，早老，儿童的早衰症；

英英释义

progeria[ pr?u'd?iri:? ]

n.a rare abnormality marked by premature aging (grey hair and wrinkled skin and stooped posture) in a child

学习怎么用

权威例句

Progeria syndromes and ageing: what is the connection?
Hutchinson-Gilford progeria syndrome: review of the phenotype
Lamin a truncation in Hutchinson-Gilford progeria
Phenotype and Course of Hutchinson–Gilford Progeria Syndrome
A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects
Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndrome.
Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson–Gilford progeria syndrome
A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation
Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson鈥揋ilford progeria syndrome

单词	progeria
释义	progeria 听听怎么读英 [pr??'d???r??] 美 [pro?'d??r?r] 是什么意思 n. 早衰，早老，儿童的早衰症；英英释义 progeria[ pr?u'd?iri:? ] n.a rare abnormality marked by premature aging (grey hair and wrinkled skin and stooped posture) in a child 学习怎么用权威例句 Progeria syndromes and ageing: what is the connection? Hutchinson-Gilford progeria syndrome: review of the phenotype Lamin a truncation in Hutchinson-Gilford progeria Phenotype and Course of Hutchinson–Gilford Progeria Syndrome A Human iPSC Model of Hutchinson Gilford Progeria Reveals Vascular Smooth Muscle and Mesenchymal Stem Cell Defects Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndrome. Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson–Gilford progeria syndrome A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson鈥揋ilford progeria syndrome
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