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Jakeman David L.
Associate Professor
Dalhousie University
,
Economics, Econometrics and Finance
电子邮件
JD963470
dal
ca
网站
https://www.scopus.com/authid/detail.url?authorId=6603963470
h-index
h10-index
h5-index
2197
引用
30
H-指数
根据储存在 Pure 的刊物以及来自 Scopus 的引用文献数量计算
392
引用
12
H-指数
根据储存在 Pure 的刊物以及来自 Scopus 的引用文献数量计算
14
引用
3
H-指数
根据储存在 Pure 的刊物以及来自 Scopus 的引用文献数量计算
1994 …
2023
每年的科研成果
综述
指纹
网络
科研成果
(95)
新闻 / 媒体
(1)
相似简介
(6)
指纹
深入其中 Jakeman David L. 为活跃的研究主题。这些主题标签来自此人的成果。它们共同形成唯一的指纹。
分类
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Biochemistry, Genetics and Molecular Biology
Enzyme
100%
Nucleotide Sugar
74%
Anabolism
63%
Phosphoglycerate Kinase
55%
Glycosyltransferase
48%
Streptomyces Venezuelae
46%
Amino Acids
43%
Active Site
41%
Enzyme Activity
34%
Synthase
34%
Enzyme Specificity
32%
Glyceric Acid
32%
Glucose 1-Phosphate
30%
Uridine Diphosphate
30%
Rhamnose
27%
Nucleoside Triphosphate
27%
Streptococcus
27%
Transition State Analog
27%
Glycoside Hydrolase
27%
Signaling Peptide
27%
Phosphoglucomutase
27%
Escherichia coli
27%
Precursor
25%
Mannose
24%
Polyketide
23%
Glycosylation
22%
Pyrophosphate
20%
Dehydratase
20%
Oligosaccharide
20%
Bacterial Cell Wall
20%
Reprogramming
20%
Fucose
20%
Hexose
20%
Gene Cluster
20%
Cytotoxicity
20%
Glycosyl
20%
Synthesis
20%
Cancer Cell
18%
Antimicrobial Activity
18%
Nucleotide Metabolism
18%
Streptococcus mutans
18%
Nucleoside
18%
Structure Activity Relation
16%
Secondary Metabolite
16%
Nucleophilicity
15%
Glycopeptide
13%
Enzyme Assay
13%
Glycosidic Linkage
13%
Binding Protein
13%
Antibiotic Resistance
13%
Chemistry
Jadomycin
69%
Amino Acid
34%
Occurrence in Nature
27%
Nucleotide-Sugar
27%
Digitoxose
27%
NMR Spectroscopy
27%
Hexose
20%
Enzymatic Reaction
20%
Stereochemistry
18%
Jadomycin B
16%
Electrospray Ionization Mass Spectrometry
16%
Substrate Specificity
15%
Nucleoside Triphosphate
13%
Sugar Phosphate
13%
L-Rhamnose
13%
Deoxyribonucleic Acid
13%
Transition State Analog
13%
Nucleoside
13%
Nucleoside Triphosphate Analogue
13%
Phenylalanine
13%
Triazole
13%
Nucleotides Synthesis
13%
Antimicrobial Agent
13%
Ornithine
13%
Rotational Echo Double Resonance
13%
Nucleoside Tetraphosphate
13%
Quantum Mechanical Method
13%
Thymidine
13%
Jadomycin A
13%
Diastereomer
13%
Rotational Resonance
13%
Stereoselective Synthesis
13%
Glucopyranose
13%
Shikimate
13%
Sodium Fluoride
13%
Phosphoenolpyruvate
13%
Magnesium
13%
Phosphoryl
13%
UDP
13%
Ribonucleoside Triphosphate
13%
19F NMR Spectrum
13%
Phosphoglycerate
13%
31P{1H}-NMR Spectrum
13%
Lineshape
13%
Triphosphate(5-)
13%
Furan
13%
Alkyne
9%
D-Mannose
9%
L-Fucose
9%
Glyphosate
9%
Keyphrases
Jadomycin
55%
Glucose-1-phosphate
27%
Enzyme Synthesis
27%
Phosphoglycerate Kinase
27%
Phosphonate Analogues
23%
Natural Products
22%
Nucleotide Sugars
22%
Nucleotidylyltransferase
18%
Isosteric
18%
Difluoro
16%
Streptomyces Venezuelae
15%
5-enolpyruvylshikimate-3-phosphate Synthase
13%
Kinetic Evaluation
13%
Coupled Enzyme Assay
13%
Phosphate Analog
13%
Glycopeptide Synthesis
13%
Nucleoside Tetraphosphate
13%
Protein Binding Study
13%
Transition State Conformation
13%
Phenanthroviridin
13%
Transition State Analogue
13%
Fluorophosphonate
13%
Triphosphate Analogues
13%
Uridine Diphosphate
13%
Digitoxose
13%
Nucleoside Triphosphates
13%
Nucleoside Monophosphates
13%
Phosphorylase
13%
Triazole
13%
Saccharopolyspora Erythraea
13%
Glycoside Hydrolase Family 3
13%
Semisynthesis
13%
N-acetylglucosaminidase
13%
Herbaspirillum Seropedicae
13%
Biomolecular
13%
Substrate Analog
13%
Non-enveloped Virus
13%
Myristoylation
13%
Peptide Motif
13%
Synthetase
13%
GalP
13%
Chemoenzymatic Synthesis
13%
Mechanistic Probes
13%
Structure-based Design
13%
Nucleotide Synthesis
13%
Ornithine
13%
Ketose
13%
Monofluorination
13%
Quorum Sensing Molecules
13%
Mutarotation
13%
