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查看斯高帕斯 (Scopus) 概要
劉 孜孜
副研究員
腫瘤惡化卓越研究中心
h-index
h10-index
h5-index
2404
引文
28
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508
引文
11
h-指數
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65
引文
5
h-指數
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1989 …
2022
每年研究成果
概覽
指紋
網路
研究成果
(68)
類似的個人檔案
(6)
指紋
查看啟用 Tze-Tze Liu 的研究主題。這些主題標籤來自此人的作品。共同形成了獨特的指紋。
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Keyphrases
6-pyruvoyltetrahydropterin Synthase
90%
Taiwan
84%
Methylmalonic Acidemia
56%
Chinese Patients
51%
Tetrahydrobiopterin
48%
Hyperphenylalaninemia
44%
Newborn Screening
38%
Glucose-6-phosphate Dehydrogenase (G6PD)
28%
Gene mutation
28%
Phenylketonuria
27%
Mutant Alleles
24%
Expressed Sequence Tags
24%
Tandem Mass Spectrometry
24%
East Asia
23%
Taiwanese
22%
Mutation Spectrum
21%
PTS Gene
20%
Bile Duct
19%
Propionic Acidemia
19%
Genome Sequencing
19%
Genotype
19%
Molecular Epidemiology
18%
Mosquito Vectors
18%
Kaposi's Sarcoma-associated Herpesvirus
18%
MMACHC
18%
Human Immunodeficiency Virus Type 1 (HIV-1)
18%
Sirtuin 1 (SIRT1)
18%
Charcot-Marie-Tooth Disease
18%
Mycoplasma Fermentans
18%
Draft Genome Sequence
18%
Primary Cutaneous Amyloidosis
18%
Armigeres Subalbatus
18%
Klebsiella Pneumoniae (K. pneumoniae)
18%
BH4 Deficiency
18%
Propionyl-CoA Carboxylase
17%
Sequence Analysis
16%
Mutation Analysis
16%
Novel mutation
16%
Prenatal Diagnosis
14%
East Asian Population
14%
Transcriptome
14%
Founder Effect
14%
Exome Sequencing
14%
Cirrhosis
14%
AIDS Patients
14%
Repetitive Sequences
14%
Frequent mutation
13%
Neonatal Screening
13%
Tetrahydrobiopterin Deficiency
13%
Complementary DNA (cDNA)
13%
Biochemistry, Genetics and Molecular Biology
Synthase
100%
Sapropterin
61%
Allele
50%
Phenylketonuria
32%
Gene Mutation
31%
Wild Type
29%
Newborn Screening
28%
Exome Sequencing
27%
Gene Expression
25%
Enzyme
22%
Oxidoreductase
22%
Homocystinuria
21%
Cancer Cell
20%
PTS (Gene)
20%
Propionic Acidemia
19%
DNA Sequence
19%
Human Herpesvirus 8
18%
Amyloidosis
18%
Glucose-6-Phosphate Dehydrogenase
18%
Expressed Sequence Tag
18%
Human Immunodeficiency Virus 1
18%
Founder Effect
18%
Amino Acids
17%
Oxygenase
17%
Propionyl-CoA Carboxylase
17%
Haplotype
16%
Missense Mutation
15%
Single-Nucleotide Polymorphism
15%
Reductase
15%
Genetics
14%
Genotyping
14%
Cell Proliferation
14%
Microsatellite
14%
Genomics
14%
Histone
14%
Phenylalanine Hydroxylase
13%
Codon
13%
Phylogeny
13%
Cladistics
13%
Autosomal Dominant Inheritance
12%
Transfer RNA
12%
Gene Function
11%
Screening
11%
Tumor Necrosis Factor
11%
Exon
11%
Genome Organization
11%
Methylation
11%
Gene Linkage
11%
MicroRNA
10%
Tandem Mass Spectrometry
10%
Medicine and Dentistry
Newborn Screening
46%
Disease
35%
6 Pyruvoyltetrahydropterin Synthase
27%
Glucose-6-Phosphate Dehydrogenase Deficiency
23%
Tandem Mass Spectrometry
21%
Neonatal Infant
19%
Bile Duct
18%
Methylmalonic aciduria
18%
Glucose 6 Phosphate Dehydrogenase
18%
Methylmalonic Acidemia
18%
Tumor Necrosis Factor
13%
Screening
13%
Hyperphenylalaninemia
13%
Liver Cirrhosis
12%
Phenylketonuria
12%
Homocystinuria
11%
Enteritis
11%
Interleukin 10
10%
Muscle Atrophy
10%
5-Hydroxytryptophan
10%
Patient Referral
10%
Neonate
9%
Tetrahydrobiopterin Deficiency
9%
Levodopa
9%
Extracorporeal Membrane Oxygenation
9%
Endocannabinoid
9%
Multifocal Motor Neuropathy
9%
Acute Respiratory Distress Syndrome
9%
Primary Effusion Lymphoma
9%
Dried Blood Spot
9%
Propionic Acidemia
9%
Argipressin Receptor
9%
Nephrogenic Diabetes Insipidus
9%
Sirtuin1
9%
Hepatocellular Carcinoma
9%
Cobalamin
9%
Mycobacterium Tuberculosis
9%
Somatic Mutation
9%
Autosomal Dominant Inheritance
9%
Tandem Mass Spectrometry
9%
Endotoxemia
9%
Portal Hypertension
9%
Hyperammonemia
9%
Dysbiosis
9%
Diuretic Agent
9%
Ascites
9%
Sirtuin 1
9%
Short Chain Fatty Acid
9%
Human Herpesvirus 8
9%
Endocrine Therapy
9%