Dictionnaire français - anglais

sciences naturelles et appliquées - acta.es
L'hyperglycérolémie familiale au saguenay-lac-saint-jean : étude démogénétique et origine de la mutation n288d du gène de la glycérol kinaseUne mutation ponctuelle (N288D), associée à l'expression de l'hyperglycérolémie familiale, a été identifiée dans le gène de la glycérol kinase (GK) au sein de la population du Saguenay-Lac-Saint-Jean...
général - core.ac.uk - PDF: core.ac.uk
mutation ponctuelle
sciences naturelles et appliquées - acta.es iate.europa.eu
Mutation ponctuelle mutation n'affectant qu'un seul nucléotide.

Single point mutation–a mutation that involves a single nucleotide.

général - CCMatrix (Wikipedia + CommonCrawl)
Différence entre la mutation Frameshift et la mutation ponctuelle

Difference between Point Mutation and Frameshift Mutation

général - CCMatrix (Wikipedia + CommonCrawl)
Un autre type de mutation ponctuelle est la mutation frameshift.

The third kind of point mutation is a frameshift mutation.

général - CCMatrix (Wikipedia + CommonCrawl)
La mutation ponctuelle se trouve en posititon 604 et/ou en position 610.

The point mutation either is at position 604 or 610, or both positions.

chimie - wipo.int
La présente invention concerne, entre autres, une méthode de criblage de la présence d'une mutation ponctuelle dans le gène ACCase, ladite mutation ponctuelle pouvant conférer une résistance aux herbicides à une espèce végétale.

The present invention relates, inter alia, to a method of screening for the presence of a point mutation in the ACCase gene, said point mutation being capable of conferring herbicide resistance on a plant species.

sciences naturelles et appliquées - wipo.int
Incidence du génotype du gène du récepteur à la ryanodine (ryr 1) associé à la sensibilité au stress dans 5 filières porcines belges.
Le syndrome de stress chez le porc est dû à une mutation ponctuelle au niveau du gène Ryr1 codantpour le récepteur à la ryanodine....
...peer reviewedaudience: researcher, professional, studentPorcine stress syndrome is related to a point mutation in Ryr1 gene encoding the ryanodin receptor....
général - core.ac.uk - PDF: orbi.ulg.ac.be
Molecular determinism of limb development : contribution of new technologies for genome study
... Dans la majorité des cas, l’événement génétique responsable est une mutation ponctuelle située dans des gènes codant des facteurs de transcription ou dans des régulateurs transcriptionnels....
... In most of the cases, the genetic event involved is a point mutation in the genes coding transcriptionnal factor or regulatory sequence....
général - core.ac.uk -
Antithrombin iii deficiency in indian patients with deep vein thrombosis: identification of first india based at variants including a novel point mutation (t280a) that leads to aggregation... We also report a novel point mutation at position g.7549...
santé / technologie et réglementation technique / droit civil - core.ac.uk - PDF: figshare.com
Antithrombin iii deficiency in indian patients with deep vein thrombosis: identification of first india based at variants including a novel point mutation (t280a) that leads to aggregation.... We also report a novel point mutation at position g.7549...
 PDF: doaj.org
Construction and characterization of two infectious molecular clones of encephalomyocarditis virus.... pDA contained a single point mutation at position 1720 within the "puff" region of capsid protein 1AB that was derived from the nondiabetogenic variant of EMC virus (EMC-B)....
Configuration of templates used for evaluating the sensitivity of siba for point mutation(s).Eight additional templates harboring different numbers of point mutation(s) 1–4 were synthesized....
In silico driven redesign of a clinically relevant antibody for the treatment of gd2 positive tumors.... Based on in silico scanning mutagenesis of the 12 interacting amino acids from the docked 3F8:GD2 model, a single point mutation (Heavy Chain: Gly54Ile) was engineered into a humanized 3F8 (hu3F8) MoAb and found to have a 6-9 fold enhancement in antibody-dependent cell-mediated cytotoxicity...
 PDF: doaj.org
mutation ponctuelle
sciences naturelles et appliquées - iate.europa.eu
Dopa-responsive dystonia with a novel initiation codon mutation in the gch1 gene misdiagnosed as cerebral palsy... Genetic analysis by using PCR-direct sequencing revealed a novel initiation codon mutation (c.1A>T;...
général - core.ac.uk - PDF: www.pubmedcentral.nih.gov
Mitochondrial encephalomyopathy and complex iii deficiency associated with a stop-codon mutation in the cytochrome b gene ... Sequence analysis revealed a stop-codon mutation (G15242A) in the mtDNA-encoded cytochrome b gene, resulting in loss of the last 215 amino acids of cytochrome b....
Crispr-induced exon skipping is dependent on premature termination codon mutations... By analyzing 22 gene-edited rabbit lines generated using CRISPR/Cas9, we provide evidence of exon skipping at high frequency in premature termination codon-mutated rabbits but not in the rabbits with a premature termination codon mutation in exon 1 rabbits with non-frameshift or missense mutations....
 PDF: doaj.org
An initiation codon mutation (aug----gug) of the human alpha 1-globin gene. structural characterization and evidence for a mild thalassemic phenotype.... In a previous study we described a nondeletion alpha-thalassemia defect in the alpha 2-globin gene resulting from an AUG----ACG initiation codon mutation....
An initiation codon mutation (aug-- gug) of the human al-globin gene structural characterization and evidence for a mild thalassemic phenotype... In a previous study we described a nondeletion a-thalassemia de-fect in the a2-globin gene resulting from an AUG-- ACG initiation codon mutation....
sciences naturelles et appliquées - iate.europa.eu
An investigation of mutagenic activities of some 9- substituedphenanthrene derivatives with ames / salmonella / microsome test... In the absence of metabolic activation, while only one of the compounds were causing frame-shift mutations, two of them were determined to induce base pair substitution mutations....
général - core.ac.uk - PDF: doaj.org
Determination of the rate of base-pair substitution and insertion mutations in retrovirus replication.... We determined that the mutation rate for a single base pair substitution during replication of this avian retrovirus is 2 x 10(-5) per base pair per replication cycle and the insertion rate is 10(-7) per base pair per replication...
sciences naturelles et appliquées - iate.europa.eu
Development of method to derive variation pattern in neuraminidase enzyme of influenza-a virus and predict the most probable upcoming subtype.... In this study, the variation pattern followed by the neuraminidase enzyme of thedpathogen has been derived using the concept of substitution mutation....
général - core.ac.uk - PDF: doaj.org
Inhibition of a k9/k36 demethylase by an h3.3 point mutation found in paediatric glioblastoma...H3.3 G34R substitution mutation, which is found in paediatric gliomas, causes changes in H3K9me3 and H3K36me3 by interfering with the KDM4 family of K9/K36 demethylases
 PDF: doaj.org
Variation in base-substitution mutation in experimental and natural lineages of caenorhabditis nematodes... Our findings show that base-substitution mutation processes in these closely related animal lineages are mostly stable but differ from natural polymorphism patterns in these two species
The structure and function of a cis-acting element located upstream of the ires that influences coxsackievirus b3 rna translation ... The deletion or substitution mutation at this apical loop resulted in significant decrease in IRES activity....
Yeast two-hybrid assay for pehab1- interacting proteins.... (a-d) indicated negative control; yeast harbored PeHAB1 and PePYL4; Supplied interacting pairs that served as positive control; yeast harbored PePYL4 and PeHAB1 of substitution mutation W420A and yeast harbored PeHAB1 and PePYL4 of substitution mutation P124S....
sciences naturelles et appliquées - iate.europa.eu
Current status of aedes aegypti insecticide resistance development from banjarmasin, kalimantan, indonesia... Molecular analysis of voltage-gated sodium channel (Vgsc) gene showed significant association of V1016G gene point mutation in resistance Ae....
général - core.ac.uk - PDF: doaj.org
Short communication analysis of p16 gene deletion and point mutation in breast carcinomaSummary We looked for p16 gene deletion by Southern analysis and p16 gene point mutation by single-stranded conformation polymorphism (SSCP) analysis and direct sequencing of DNA from fresh tumour samples of 35 and 33 breast carcinomas respectively....
 PDF: ftp:
Analysis of p16 gene deletion and point mutation in breast carcinoma.We looked for p16 gene deletion by Southern analysis and p16 gene point mutation by single-stranded conformation polymorphism (SSCP) analysis and direct sequencing of DNA from fresh tumour samples of 35 and 33 breast carcinomas respectively....
Angelman syndrome and isovaleric acidemia: what is the link?... Such association was due to paternal uniparental isodisomy (UPD) of chromosome 15 in which the proband inherited two paternal copies of an IVA gene point mutation....
 PDF: doaj.org
Clinical study of dmd gene point mutation causing becker muscular dystrophyBackground DMD gene point mutation, mainly nonsense mutation, always cause the most severe Duchenne muscular dystrophy (DMD)....
 PDF: doaj.org

Exemples français - anglais

santé / sciences naturelles et appliquées / activité agricole / environnement / informatique et traitement des données - acta.es
institutions de l'union européenne et fonction publique européenne / pouvoir exécutif et administration publique / union européenne / éducation - iate.europa.eu
droit / institutions financières et crédit - iate.europa.eu
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général - eur-lex.europa.eu

Traductions en contexte français - anglais

Un autre type de mutation ponctuelle est la mutation frameshift.

Another type of mutation is the frameshift mutation.

général - CCMatrix (Wikipedia + CommonCrawl)
Un autre type de mutation ponctuelle est la mutation frameshift.

Another type of gene mutation is the frameshift mutation.

général - CCMatrix (Wikipedia + CommonCrawl)
Mutation ponctuelle terme générique désignant une mutation qui affecte seulement une petite séquence d'ADN (petites insertions, délétions et substitutions d'une base par une autre).

Commonly used to package DNA cloned onto a lambda vector (separated by cos sites) into infectious lambda particles.

général - eur-lex.europa.eu
Une mutation ponctuelle qui donne naissance à un codon d'arrêt est appelé une mutation non-sens.

And a mutation to for a stop code-on is called a nonsense mutation.

général - CCMatrix (Wikipedia + CommonCrawl)
Une mutation ponctuelle qui donne naissance à un codon d'arrêt est appelée une mutation non-sens.

And a mutation to for a stop code-on is called a nonsense mutation.

général - CCMatrix (Wikipedia + CommonCrawl)
La mutation ponctuelle peut éliminer et/ou modifier un site de glycosylation ou un site de clivage enzymatique.

The point mutation may remove and/or alter a glycosylation site or an enzyme cleavage site.

santé - wipo.int
Et vous avez raison, ce n'est probablement pas une mutation ponctuelle.

You’re right, and it’s likely not to change on a measurable scale.

général - CCMatrix (Wikipedia + CommonCrawl)
La mutation ponctuelle peut éliminer et/ou modifier un site de glycosylation ou un site de clivage enzymatique.

The point mutation may remove and/or alter a glycosylation site or an enzyme cleavage site.

chimie - wipo.int
Une mutation ponctuelle dans le gène CD18 responsable de l'apparition d'une déficience d'adhésion leucocytaire chez les bovins et une mutation silencieuse liée à cette dernière ont été identifiées.

A point mutation in the CD18 gene responsible for causing bovine leukocyte adhesion deficiency (BLAD) and a silent mutation linked thereto have been identified.

sciences naturelles et appliquées - wipo.int
Le procédé est efficace car il permet de détecter une mutation ponctuelle simple ainsi que des variations d'insertion et de délétion.

The method is effective in detecting a single point mutation as well as insertion and deletion variations.

sciences naturelles et appliquées - wipo.int
La mutation est une mutation ponctuelle du gène CRY1, ce qui signifie qu'une seule "lettre" de ses instructions génétiques est désactivée.

The mutation is a single-point mutation in the CRY1 gene, meaning just one “letter” in its genetic instructions is off.

général - CCMatrix (Wikipedia + CommonCrawl)
La mutation est une mutation ponctuelle du gène CRY1, ce qui signifie qu'une seule "lettre" de ses instructions génétiques est désactivée.

They identified the mutation as a single-point mutation in the CRY1 gene, which means that one “letter” in the gene’s instructions is off.

général - CCMatrix (Wikipedia + CommonCrawl)
La mutation est une mutation ponctuelle du gène CRY1, ce qui signifie qu'une seule "lettre" de ses instructions génétiques est désactivée.

The mutation is a single-point mutation in the CRY1 gene, meaning just one "letter" in its genetic instructions is off.

général - CCMatrix (Wikipedia + CommonCrawl)
La mutation est une mutation ponctuelle du gène CRY1, ce qui signifie qu'une seule "lettre" de ses instructions génétiques est désactivée.

The mutation found is a single-point mutation in the CRY1 gene, meaning just one letter in its genetic instructions is incorrect.

général - CCMatrix (Wikipedia + CommonCrawl)
Dans la famille Marsili, une mutation ponctuelle empêche le gène d’exprimer la protéine cruciale.

In the Marsili family, a point mutation prevents the gene from expressing the crucial protein.

général - CCMatrix (Wikipedia + CommonCrawl)


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