genetic mutation
genetisk mutation
DNA mutation
DNA mutation
cell mutation
cellemutation
chromosome mutation
kromosommutation
gene mutation
gen mutation
mutation breeding
mutationsavl
mutation rate
mutationshastighed
point mutation
punktmutation
induced mutation
induceret mutation
mutation frequency
mutationsfrekvens
mutation theory
mutationsteori
missense mutation
feilmutasjon
bud mutation
knopmutation
the mutation of ethnic politics into nationalist politics.
transformationen af etnisk politik til nationalistisk politik.
Gene mutations are alterations in the DNA code.
Gene mutationer er ændringer i DNA-koden.
Technique of mutation breeding in gladiola was studied by meansof electron beam.
Teknikken for mutationsavl i gladiolus blev undersøgt ved hjælp af elektronstråle.
Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.
Milde mutationer i XPF forårsager den cancer-udsatte syndrom xeroderma pigmentosum.
Abstract： Technique of mutation breeding in gladiola was studied by means of electron beam.
Abstract: Teknikken for mutationsavl i gladiolus blev undersøgt ved hjælp af elektronstråle.
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
Formål at identificere COL7A1 genmutationen i en familie med dystrofi epidermolysis bullosa pruriginosa.
Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.
Resultater En 13389G-sletning i exon 6 blev karakteriseret hos proband, og denne mutation førte til forskydning af læserammen.
We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.
Vi fandt en recessiv kataraktmutation, der opstod spontant i en KUNMING outbred musestamme.
a modern Darwinian theory that explains new species in terms of genetic mutations
en moderne darwinistisk teori, der forklarer nye arter i form af genetiske mutationer.
CONCLUSION: Base pair substitution mutation and frame shift mutation were caused by folpet in Ames test.And DNA breakage in human PMNC might be induced by folpet.
KONKLUSION: Basepar substitutionsmutation og forskydningsmutation blev forårsaget af folpet i Ames-testen. Og DNA-skader i humane PMNC kan muligvis være induceret af folpet.
This indicats that gamma ray irradiation can increase the frequency of mutations and produces special types of flower in Godetia grandiflora breeding.
Dette indikerer, at gamma-strålingsbestråling kan øge mutationsfrekvensen og producere specielle typer blomster i avlen af Godetia grandiflora.
In addition, no back mutation to obtain a maximal complexity (i.e. λ-resistant and sensitive species coexistence) or original ecology (i.e. original λ-lysogen) for the evolution occurs.
Derudover sker der ingen tilbagegående mutation for at opnå maksimal kompleksitet (dvs. sameksistens af λ-resistente og følsomme arter) eller oprindelig økologi (dvs. oprindelig λ-lysogen) for udviklingen.
Methods Morulae of four mutation hairless mice and one cataract mouse were transplanted into uterus using embryonic transfer method.
Metoder: Morulaer fra fire mutation hairless mus og én kataraktmus blev transplanteret ind i livmoderen ved hjælp af embryotransfermetoden.
JianYang Tangelo,a new citrus hybrid cultivar,originated from a bud mutation of a tangelo cultivar introduced from abroad.
JianYang Tangelo, en ny citrus hybrid cultivar, stammer fra en knopmutation af en tangelo cultivar introduceret udefra.
Allelotype analysis was done at five short tandem repeat markers (D17S855, D17S1322, D17S1323, D17S1326, and D17S1327) in or adjacent to BRCA1 on the recurrent mutation carriers.
Allelotypeanalyse blev udført på fem korte tandem-repeat-markører (D17S855, D17S1322, D17S1323, D17S1326 og D17S1327) i eller ved siden af BRCA1 hos tilbagevendende mutationsbærere.
At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.
Mindst nogle af de mutationer, der er ansvarlige for dette synstab, varierede mellem de 29 populationer af hulefisk, der er kendt for at eksistere.
Cleidocranial dysostosis or Cleidocranial dysplasia is a hereditary congenital abnormality of humans due to haploinsufficiency caused by mutations in the CBFA1 gene.
Cleidocraniel dysostose eller cleidocraniel dysplasi er en arvelig medfødt abnormitet hos mennesker, der skyldes haploinsufficiens forårsaget af mutationer i CBFA1-genet.
High-level quinolone resistance require mutations in both DNA gyrase gene and topoisomerase Ⅳ gene. ② Bacterial cell wall is the barrier for the entry of antibiotics.
Høj-niveau quinoloneresistens kræver mutationer i både DNA gyrase gen og topoisomerase Ⅳ gen. ② Bakteriel cellevæg er barrieren for antibiotikas indtrængen.
AIM: To investigate if there are disease-specific mutations within the dentin phosphoprotein in two dentinogenesis imperfecta type Ⅱfamilies,and analyse the nucleotide polymorphism in DPP region.
AIM: At undersøge, om der er sygdomsspecifikke mutationer i dentin phosphoprotein i to dentinogenesis imperfecta type Ⅱfamilier, og at analysere nukleotidpolymorfismen i DPP-regionen.
The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.
Ethephons mutationspotential blev undersøgt ved hjælp af micronucleus-testen af knoglemarvs polychromatofile erythroblast-celler (PCE) og spermform-abnormitetstesten hos mus.
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