「Double Stranded」の共起表現一覧(1語右で並び替え)
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genome length is 16000 nt, and the DNA is | double-stranded and circular. |
es, naturally occurring DNA molecules are | double-stranded and RNA molecules are single-stranded. |
rmed between the two strands of DNA and a | double-stranded break in a DNA molecule leaves a 3'OH end |
homologous chromosome, triggering the DNA | double-stranded break repair system, which "repairs" the |
nerated from the other end of the initial | double-stranded break. |
iposide causes dose-dependent single- and | double-stranded breaks in DNA and DNA-protein cross-links |
Meiotic recombination initiates with | double-stranded breaks that are introduced into the DNA b |
then digest the 5' ends generated by the | double-stranded breaks to produce 3' single-stranded DNA |
ys a role in transcription, DNA repair of | double-stranded breaks, and recombination. |
d may introduce either single stranded or | double-stranded breaks. |
stranded origin (SSO) DNA to make another | double-stranded circle. |
oins the ends to make another molecule of | double-stranded circular DNA. |
The | double-stranded DNA molecules are also typically much lon |
Coccolithovirus is a giant | double-stranded DNA virus that infects Emiliania huxleyi, |
nt of the dissociation-characteristics of | double-stranded DNA during heating. |
Depurinated bases in | double-stranded DNA are efficiently repaired by portions |
ranscription, a process that produces new | double-stranded DNA from the viral genome's single-strand |
elting profile of the hybridized DNA, the | double-stranded DNA is bound to a column and the mixture |
When a | double-stranded DNA molecule has suffered a break in both |
their subsequent paper, “Translocation of | double-stranded DNA through membrane-adapted phi29 motor |
heating a reaction-mixture that contains | double-stranded DNA sequences and measuring dissociation |
V40 ori in mammalian cells, ColE1 ori for | double-stranded DNA replication or f1 ori for single-stra |
ide are related to the relative number of | double-stranded DNA breaks produced in cells, which are a |
ion," in which one strand of a homologous | double-stranded DNA is displaced by the RecA-associated s |
m, the average extinction coefficient for | double-stranded DNA is 0.020 (μg/ml)-1 cm-1, for single-s |
eaks generated by topoisomerase I; lethal | double-stranded DNA breaks occur when the topoisomerase I |
NA strand into an antisense DNA to form a | double-stranded DNA intermediate. |
Anti-dsDNA ( | double-stranded DNA) |
ementary DNA (cDNA) and ultimately dsDNA ( | double-stranded DNA) with full LTRs. |
de 5'-monophosphates, but does not digest | double-stranded DNA, double-stranded RNA, or DNA / RNA hy |
It acts on single-stranded DNA, | double-stranded DNA, and chromatin. |
nvert RPA-bound, single stranded DNA into | double-stranded DNA, an enzyme activity termed "annealing |
The stain preferentially binds to | double-stranded DNA, but will stain single-stranded DNA w |
ch is transverse electron transport along | double-stranded DNA, its implications in the biology of D |
T, which pairs with deoxyadenosine (A) in | double-stranded DNA. |
A, which pairs with deoxythymidine (T) in | double-stranded DNA. |
nd contains a single molecule of circular | double-stranded DNA. |
rry their genetic material in the form of | double-stranded DNA. |
sponds to a concentration of 50 μg/ml for | double-stranded DNA. |
rocedure by binding directly to single or | double-stranded DNA. |
o dissociate and reanneal, forming hybrid | double-stranded DNA. |
two single strands of DNA combine to form | double-stranded DNA. |
mperature, the DNA will exist stably in a | double-stranded form. |
G4 structures much more efficiently than | double-stranded nucleic acid. |
one of the two complementary strands of a | double-stranded nucleotide polymer, in the strand which i |
broken one as a template to bring the two | double-stranded pieces into correct alignment for rejoini |
It catalyzes the unwinding of | double-stranded plasmid DNA that has been nicked at the r |
specifically recognize adenosines within | double-stranded regions of pre-mRNAs and deaminate them t |
nome of the virus consists of two linear, | double-stranded RNA molecules. |
erization of the mechanical properties of | double-stranded RNA |
ly single-stranded RNA (ssRNA) but may be | double-stranded RNA (dsRNA). |
These have | double-stranded RNA genomes and are therefore group III v |
n of an argonaute protein in complex with | double-stranded RNA PDB 1YTU. |
e classification, which means they have a | double-stranded RNA genome. |
r RNA replication in RNA viruses, such as | double-stranded RNA viruses. |
se-2 (RED2, or ADARB2) is a member of the | double-stranded RNA (dsRNA) adenosine deaminase family of |
oRNAs and small temporal RNAs and produce | double-stranded RNA using small interfering RNAs as prime |
ease in the RNase III family that cleaves | double-stranded RNA (dsRNA) and pre-microRNA (miRNA) into |
however-some viruses have genomes made of | double-stranded RNA and other viruses have single-strande |
or RpoS is mediated by the formation of a | double-stranded RNA stem-loop structure in the upstream r |
NA oligos resulting from cleavage of long | double-stranded RNA (dsRNA) with an endoribonuclease such |
viruses can encode proteins that bind to | double-stranded RNA (dsRNA) to prevent the activity of RN |
EIF2AK2: the | double-stranded RNA-dependent kinase (PKR) |
onds, creating stable, at least partially | double-stranded RNA-like structures, similar to ribozymes |
Double-stranded RNA-specific editase B2 is an enzyme that | |
dissecting dsRNA into the 21nt strech of | double-stranded RNA. |
RNase V1 is non-sequence specific for | double-stranded RNAs. |
RNA (Reverse transcriptase requires this | double-stranded segment as a primer to start its operatio |
mplementarity, all the information in the | double-stranded sequence of a DNA helix is duplicated on |
ng as a backup system when Rdp1-generated | double-stranded siRNA precursors are lost. |
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