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「Genes」の共起表現一覧(2語左が「and」)

該当件数 : 44



This is done by screening and mapping genes until no new genes are found.
It will decrease rRNA and other genes transcription but will increase transcription
allows identification of gene networks and how genes are regulated.
CEA and related genes make up the CEA family belonging to the immuno
ABCG5 and ABCG8 genes encode for two proteins sterolin-1 and -2, res
Transcription of Period and Cryptochrome genes, therefore, is inhibited, the protein levels o
SAA1 and SAA2 genes are regulated in liver cells by the proinflamm
AB bioreporters contain only the luxA and luxB genes, which together are responsible for generating
and B2, are expressed from the LMNB1 and LMNB2 genes on 5q23 and 19q13, respectively.
s IS063 ) is located between the ompN and ydbK genes in E. coli.
eron as a segment between the promoter and the genes of the operon.
indicates that mutations in the LAT2 and TAT1 genes might be involved in causing this syndrome
witch is located upstream of the metA and metC genes in Agrobacterium tumefaciens, and other methio
Although it is agreed that the gabT and gabD genes encode a transaminase and dehydrogenase, respe
ly an evolutionary fusion of the ACLA and ACLB genes probably occurred early in the evolutionary hi
en used in genetics to transfer and select-for genes of interest from one organism into the chromos
rs around the role of cell cycle and apoptotic genes in cancer progression and as targets for the d
y to the junction between the second and third genes of the sdh operon (sdhD and sdhA).
nuclease restriction analysis of uidA and uidR genes in Escherichia coli K-12: determination of tra
This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcriptio
ked the malaria surface antigens RIFIN and VAR genes or in locations that are known for being recom
In fact all predicted metK and ahcY genes within Chlorobi bacteria as of 2010 are preced
tion is often utilized to silence and regulate genes without changing the original DNA sequence, an
ophy of Medicine and Ethics and Biotechnology: Genes and Stem Cells .
I and COUP-TFII encoded by the NR2F1 and NR2F2 genes respectively.
autoimmune diseases evaporated as DR3 and DQ2 genes were characterized.
Both the gabD and gabT genes were shown, in various experiments, to be indu
etabolism in P. stipitis, so the XYL1 and XYL2 genes it uses to produce the proteins required to br
length that is found between the yghK and glcB genes in the genomes of Escherichia coli and Shigell
slated region (3'UTR) of the HoxB1a and HoxB3a genes, which are important in anterior-posterior pat
are able to ferment D-xylose the XYL1 and XYL2 genes of P. stipitis coding for the XR and XDH respe
eam discovered mutations in the BRAF and ERBB2 genes in approximately 60 per cent of malignant mela
length that is found between the abgR and ydaL genes in Escherichia coli and Shigella flexneri.
The pylT and pylS genes are part of an operon of Methanosarcina barker
psn, irp2 and ybtP (transport and biosynthetic genes) promoters but represses expression of its own
length that is found between the tar and cheW genes in the genomes of Escherichia coli and Shigell
e conserved as far back as the ced-3 and ced-4 genes in C. elegans, the organism in which several c
duces expression of metallothioneins and other genes involved in metal homeostasis in response to h
The C/EBPα, -β, -γ and -δ genes are intronless and C/EBPε and -ζ have respecti
stored in the Study Database, and significant genes discovered from the results can be queried in
ering, the tumor-promoting and opine-synthesis genes are removed from the T-DNA and replaced with a
pression of approximately 2000 human and mouse genes, including glycosyltransferases, glycan-bindin
ile in mouse of the co-regulated Meg3 and Dlk1 genes suggests a causative role in the pathologies f
g for certain mutations in the BRCA1 and BRCA2 genes which cause hereditary breast cancer; develope
                                                                                                   


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