fibrillin

[US]/[ˈfɪbrɪlɪn]/
[UK]/[ˈfɪbrɪlɪn]/
Frequency: Very High

Translation

n. En stor glykoprotein, der er den primære komponent i ekstracellulær matrix mikrofibriller, vigtig for strukturel integritet i bindevæv; En genetisk lidelse karakteriseret ved skeletabnormaliteter, synsproblemer og kardiovaskulære problemer, forårsaget af mutationer i FBN1-genet.

Phrases & Collocations

fibrillin gene

fibrillin gen

fibrillin deficiency

fibrillin mangel

fibrillin-rich tissues

fibrillinrige væv

containing fibrillin

indeholdende fibrillin

fibrillin aggregates

fibrillinklumpe

fibrillin mutations

fibrillintmutationer

fibrillin-1

fibrillin-1

fibrillin network

fibrillinnetsværk

fibrillin deposition

fibrillindeposition

fibrillin related

fibrillinrelateret

Example Sentences

researchers are studying the role of fibrillin in connective tissue development.

Forskere studerer fibrillins rolle i udviklingen af bindevæv.

mutations in the fibrillin gene can lead to marfan syndrome.

Mutationer i fibrillin-genet kan føre til Marfans syndrom.

fibrillin forms microfibrils, which are crucial for tissue elasticity.

Fibrillin danner mikrofibriller, som er afgørende for vævs elasticitet.

the absence of fibrillin can weaken the aorta and other blood vessels.

Fraværet af fibrillin kan svække aorta og andre blodkar.

genetic testing can identify mutations affecting fibrillin production.

Genetisk testning kan identificere mutationer, der påvirker fibrillinproduktionen.

fibrillin-containing microfibrils provide structural support to tissues.

Fibrillinholdige mikrofibriller giver strukturel støtte til væv.

diagnosis of marfan syndrome often involves assessing fibrillin levels.

Diagnosen af Marfans syndrom involverer ofte vurdering af fibrillinniveauer.

fibrillin interacts with other extracellular matrix proteins to maintain tissue integrity.

Fibrillin interagerer med andre ekstracellulære matrixproteiner for at opretholde vævs integritet.

the severity of marfan syndrome varies depending on the fibrillin mutation.

Sværhedsgraden af Marfans syndrom varierer afhængigt af fibrillin-mutationen.

scientists are investigating new therapies targeting fibrillin deficiencies.

Forskere undersøger nye terapier, der sigter mod fibrillindefekter.

fibrillin’s role in maintaining the structure of the eye lens is also being studied.

Fibrillins rolle i at opretholde strukturen af øjets linse studeres også.

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