Sta znaci na Engleskom GENU - prevod na Енглеском S

Именица
gene
džin
gen
gena
genetski
džina
генске
genea

Примери коришћења Genu на Српском и њихови преводи на Енглески

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To je u ljudskom genu.
This is in human's gene.
Mutacije u genu fibrilina-2 su povezane sa Bealovim sindrom.
Mutations in the fibrillin-2 gene have been linked to Beal's Syndrome.
Mutacija je na genu P53.
There's a mutation in the p53 gene.
Tvoje medicinske podatke, psihološki profil,mutacije u tvom MAO-A genu.
Your medical data, your psychological profile,the mutations in your MAO-A gene.
Postoji mutacija u genu i jedan od njih mutira kako bi pratio sebičnu strategiju.
There's a mutation in the gene and one of them mutates to follow a selfish strategy.
Ali ako nema nikakve anomalije u genu.
But if there's no abnormality in the gene.
I pronašli su mutaciju u jednoj bazi u genu koji kontroliše programiranu ćelijsku smrt.
And what they find is a single-point mutation in a gene responsible for controlling programmed cell death.
Nedostaje li nekoliko baznih parova u genu 178?
Missing a couple of base pairs in gene 178?
Ukoliko imate ovako štetnu mutaciju u tom genu, imate 90 odsto šanse da obolite od raka u svom životu.
If you have this deleterious mutation in this gene, you're 90 percent likely to get cancer in your life.
Ova prelepa boja kose nastaje mutacijom u jednom MC1R genu.
Your red hair is caused by a mutation in your MC1R gene.
Po nekim hipotezama mutacije u CFTR genu mogu da pruže selektivnu prednost heterozigotnim individuama.
It has been hypothesized that mutations in the CFTR gene may confer a selective advantage to heterozygous individuals.
Ipak mislimo da znamo koja mutacija u tom genu izaziva bolest.
But we think we know what the mutation is in that gene causing the disease.
Ono što su oni pronašli su određeni, idemo ih nazvati neparnim proteinima,koji imaju jedinstvene konfiguracije u roditeljskom genu.
What they've found are certain, let's call them odd proteins,that have unique configurations in the parent gene.
Pre 10 000 godina pored Crnog Mora,desila se mutacija u jednom genu koja je dovela do plavih očiju.
So about 10,000 years ago by the Black Sea,we had one mutation in one gene which led to blue eyes.
Vlasnik je imao defekt na poziciji 370 na svom glukozidnom beta kiselinskom genu.
The owner had a genetic defect at position 370 on his glucosidase beta acid gene.
Hajde da sekvenciramo genom ovog deteta." I pronašli su mutaciju u jednoj bazi u genu koji kontroliše programiranu ćelijsku smrt.
And what they find is a single-point mutation in a gene responsible for controlling programmed cell death.
Mada je specifična funkcija tog nuklearnog receptora nije bila još potpuno karakterisana,neke njegove uloge proizilaze iz literature o genu miša.
Although the specific functions of this nuclear receptor have not been fully characterized yet,some roles emerge from the literature on the mouse gene.
I pronašli su čitav niz mutacija u genu koji zovemo SPR, koji, između ostalog, diktira proizvodnju serotonina.
What they found was a series of mutations in a gene called SPR, which is responsible for producing serotonin, among other things.
Tu je Dr. Horner sa Oxforda koji ima interesantan rad na tiroidnom genu srodnih peptida.
There's a Dr. Horner at Oxford who's doing interesting work on calcitonin gene related peptide.
Ona je prezentovala istraživanje obavlljeno u našem Centru, sa naslovom" Funkcionalna anotacija proteina:primena na MYBL2, genu uključenom u nastanak i razvoj kancera". APR 2018Vlada i Branka na Biocuration konferenciji u ŠangajuVlada i Branka su učestvovali na Biocuration konferenciji u Šangaju, Kina.
She presented a research done in our Center, titled"Functional annotation of proteins:application on MYBL2, a gene involved in the onset and progression of cancer". APR 2018Vlada and Branka on Biocuration Conference in ShanghaiVlada and Branka attended the Biocuration Conference in Shanghai, China.
Kako neko doživljava miris određenog muškarca, zavisi od varijacija u specifičnom genu OR7D4.
How one perceives its smell appears to have a lot to do with variations in one odor receptor gene called OR7D4.
Ali, tokom studije je otkriveno da ljudi sa kratkim alelima na genu 5-HTTLPR, pokazuju pozitivne reakcije i češće se smeju.
But it was discovered during a study that people with a short allele of the 5-HTTLPR gene show positive reactions such as smiling and laughing more often.
Broj transkripcionih faktora nađenih u organizmu raste sa veličinom genoma, i veći genomi teže daimaju veći broj transkripcionih faktora po genu.
The number of transcription factors found within an organism increases with genome size, andlarger genomes tend to have more transcription factors per gene.
Evo kako funkcioniše u laboratoriji:naučnici dizajniraju RNK„ vodiča” tako da odgovara genu koji žele da izmene, i vezuju ga za kas 9.
Here's how it works in the lab:scientists design a“guide” RNA to match the gene they want to edit, and attach it to Cas9.
RORγt( ili RORγ2)- nastaje iz iRNK identičnom sa RORγ, izuzev da su dva 5'- najbliža eksona zamenjena sa alternativnim eksonom,lociranim nizvodno u genu.
RORγt(also known as RORγ2)- produced from an mRNA identical to that of RORγ, except that the two 5'-most exons are replaced by an alternative exon,located downstream in the gene.
Sad, istog meseca kada je moja laboratorija objavila naše otkriće o imunom genu pirinča, moj prijatelj i kolega Dejv Mekil je svratio do moje kancelarije.
Now, the same month that my laboratory published our discovery on the rice immunity gene, my friend and colleague Dave Mackill stopped by my office.
Pod ovim uslovima, FOXO protein označen plavom bojom je premešten u nukleus-- taj maleni pregradak u sredini ćelije-- i sedi na genu sa kojim je povezan.
Under those conditions, the FOXO protein in blue has gone into the nucleus-- that little compartment there in the middle of the cell-- and it's sitting down on a gene binding to it.
Računarski gen se u budućnosti može primeniti za korekciju negativnih mutacija u genu ili grupi gena koji mogu da izazovu fenotipe bolesti.
Computational genes might be used in the future to correct aberrant mutations in a gene or group of genes that can trigger disease phenotypes.
Mnogi od ovih poremećaja uzrokovani su naslednim bolestima i zato hoćemo da pokušamo što bolje darazumemo koje mutacije u genu izazivaju bolest.
So blindness is a big problem, and a lot of these blind disorders come from inherited diseases, so we want to try andbetter understand which mutations in the gene cause the disease.
To znači damikrookolina i kontekst koji okružuje ove ćelije, u stvari govore genu raka i ćeliji raka šta da rade.
That means that microenvironment andthe context which surrounds those cells actually are telling the cancer gene and the cancer cell what to do.
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