fibrillin gene
纖維蛋白基因
fibrillin deficiency
纖維蛋白缺乏
fibrillin-rich tissues
富含纖維蛋白的組織
containing fibrillin
含有纖維蛋白
fibrillin aggregates
纖維蛋白聚集體
fibrillin mutations
纖維蛋白突變
fibrillin-1
纖維蛋白-1
fibrillin network
纖維蛋白網絡
fibrillin deposition
纖維蛋白沉積
fibrillin related
與纖維蛋白相關
researchers are studying the role of fibrillin in connective tissue development.
研究人員正在研究纖維蛋白在結締組織發育中的作用。
mutations in the fibrillin gene can lead to marfan syndrome.
纖維蛋白基因的突變可能導致馬凡氏症。
fibrillin forms microfibrils, which are crucial for tissue elasticity.
纖維蛋白形成微纖毛，對於組織彈性至關重要。
the absence of fibrillin can weaken the aorta and other blood vessels.
纖維蛋白的缺失會削弱主動脈和其他血管。
genetic testing can identify mutations affecting fibrillin production.
基因檢測可以識別影響纖維蛋白生成的突變。
fibrillin-containing microfibrils provide structural support to tissues.
含有纖維蛋白的微纖毛為組織提供結構支持。
diagnosis of marfan syndrome often involves assessing fibrillin levels.
馬凡氏症的診斷通常涉及評估纖維蛋白水平。
fibrillin interacts with other extracellular matrix proteins to maintain tissue integrity.
纖維蛋白與其他細胞外基質蛋白相互作用以維持組織完整性。
the severity of marfan syndrome varies depending on the fibrillin mutation.
馬凡氏症的嚴重程度取決於纖維蛋白突變。
scientists are investigating new therapies targeting fibrillin deficiencies.
科學家們正在研究針對纖維蛋白缺乏的新療法。
fibrillin’s role in maintaining the structure of the eye lens is also being studied.
纖維蛋白在維持眼睛晶狀體結構中的作用也正在研究中。
fibrillin gene
纖維蛋白基因
fibrillin deficiency
纖維蛋白缺乏
fibrillin-rich tissues
富含纖維蛋白的組織
containing fibrillin
含有纖維蛋白
fibrillin aggregates
纖維蛋白聚集體
fibrillin mutations
纖維蛋白突變
fibrillin-1
纖維蛋白-1
fibrillin network
纖維蛋白網絡
fibrillin deposition
纖維蛋白沉積
fibrillin related
與纖維蛋白相關
researchers are studying the role of fibrillin in connective tissue development.
研究人員正在研究纖維蛋白在結締組織發育中的作用。
mutations in the fibrillin gene can lead to marfan syndrome.
纖維蛋白基因的突變可能導致馬凡氏症。
fibrillin forms microfibrils, which are crucial for tissue elasticity.
纖維蛋白形成微纖毛，對於組織彈性至關重要。
the absence of fibrillin can weaken the aorta and other blood vessels.
纖維蛋白的缺失會削弱主動脈和其他血管。
genetic testing can identify mutations affecting fibrillin production.
基因檢測可以識別影響纖維蛋白生成的突變。
fibrillin-containing microfibrils provide structural support to tissues.
含有纖維蛋白的微纖毛為組織提供結構支持。
diagnosis of marfan syndrome often involves assessing fibrillin levels.
馬凡氏症的診斷通常涉及評估纖維蛋白水平。
fibrillin interacts with other extracellular matrix proteins to maintain tissue integrity.
纖維蛋白與其他細胞外基質蛋白相互作用以維持組織完整性。
the severity of marfan syndrome varies depending on the fibrillin mutation.
馬凡氏症的嚴重程度取決於纖維蛋白突變。
scientists are investigating new therapies targeting fibrillin deficiencies.
科學家們正在研究針對纖維蛋白缺乏的新療法。
fibrillin’s role in maintaining the structure of the eye lens is also being studied.
纖維蛋白在維持眼睛晶狀體結構中的作用也正在研究中。
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