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Data from: Translational selection frequently overcomes genetic drift in shaping synonymous codon usage patterns in vertebrates
负责人:
关键词:
translational selection mutational bias vertebrates synonymous codon usage genetic drift
DOI:
doi:10.5061/dryad.4k887
摘要:
on of translational selection in vertebrates has proven to be a challenging task, obscured by small long-term effective population sizes in larger animals and the existence
Data from: Exploring the selective constraint on the sizes of insertions and deletions in 5’ untranslated regions in mammals
负责人:
关键词:
Selective constraint;Mus musculus;5' untranslated region;upstream start codon;Homo Sapiens;upstream open reading frame;5'UTR;indel
DOI:
doi:10.5061/dryad.vh3dm
摘要:
regulatory elements are present. Results: We design the Indel Selection Index to measure the selective constraint on non-3n indels in 5'UTRs. The index controls
Data from: Gene expression levels are correlated with synonymous codon usage, amino acid composition and gene architecture in the red flour beetle
负责人:
关键词:
translational selection;gene structure;size\/complexity score;Tribolium castaneum;tRNA abundance
DOI:
doi:10.5061/dryad.r0t1q
摘要:
expression on synonymous codon usage, amino acid composition and gene structure in the red flour beetle, Tribolium castaneum. Consistent with the action of translational selection
Data from: A nutrient-driven tRNA modification alters translational fidelity and genome-wide protein coding across an animal genus
负责人:
关键词:
translational selection queuosine codon usage tRNA modification Akashi selection score
DOI:
doi:10.5061/dryad.1jn88
摘要:
, genes maximally expressed at each stage display selection for codons that are most accurate given stage-specific queuosine modificati
Data from: TAK-071, a muscarinic M1 receptor positive allosteric modulator, attenuates scopolamine-induced quantitative electroencephalogra
负责人:
Kurimoto, Emi
关键词:
Monkeys Cognitive impairment Alzheimer's disease Electroencephalography Biomarkers Animal cognition Cholinergics Oral administration
DOI:
doi:10.5061/dryad.qp313np
摘要:
by scopolamine, a non-selective muscarinic receptor antagonist, with reduced side effects on gastrointestinal function in rats. In this study, we explored change
Data from: Cell death and survival due to cytotoxic exposure modeled as a two-state Ising system
负责人:
关键词:
Ising model;cytotoxicity;Chemotherapy;cancer cell
DOI:
doi:10.5061/dryad.4qrfj6q6d
摘要:
nt to judiciously choose a drug type, its dosage, and schedule for optimized drug selection and administration. Consequently, the precise mathematical formulati
LIM Domain Kinase 1 (LIMK1), Human Kinase Domain; A Target Enabling Package
负责人:
Eidarus Salah;;Beltrami, Alessandra;;Apirat Chaikuad;;Hanke, Thomas;;Kashima, Risa;;Canning, Peter;;Knapp, Susanne Muller;;Knaus, Petra;;Hata, Akiko
关键词:
Structural Genomics Drug Discovery Chemical Biology
DOI:
doi:10.5287/bodleian:zg5naqjyk
摘要:
Loss of the translational repressor FMRP in fragile X syndrome causes upregulation of the type II BMP receptor BMPR2 and its non-canonical signal
Human Lim Domain Kinase 1 (Limk1), Kinase Domain; A Target Enabling Package
负责人:
关键词:
protein target enabling package disease structure cancer neuropsychiatry neuro neurological genetic disorders metabolic diseases oncology
DOI:
doi:10.5281/zenodo.1287260
摘要:
Loss of the translational repressor FMRP in fragile X syndrome causes upregulation of the type II BMP receptor BMPR2 and its non-canonical signal
Human Lim Domain Kinase 1 (Limk1), Kinase Domain; A Target Enabling Package
负责人:
关键词:
protein target enabling package disease structure cancer neuropsychiatry neuro neurological genetic disorders metabolic diseases oncology
DOI:
doi:10.5281/zenodo.1241027
摘要:
Loss of the translational repressor FMRP in fragile X syndrome causes upregulation of the type II BMP receptor BMPR2 and its non-canonical signal
Human LIM domain kinase 1 (LIMK1), kinase domain; A Target Enabling Package
负责人:
关键词:
protein target enabling package disease structure cancer neuropsychiatry neuro neurological genetic disorders metabolic diseases oncology
DOI:
doi:10.5281/zenodo.1219706
摘要:
Loss of the translational repressor FMRP in fragile X syndrome causes upregulation of the type II BMP receptor BMPR2 and its non-canonical signal

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