Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

NOTCH3

Notch homolog 3 (Drosophila)CASILNotch (Drosophila) homolog 3


Gene NOTCH3 gene interaction
View Neighborhood Gene

Result number fewer <<<< << < ALL > >> >>> more

MeSH term
FrequencyCondition_Probility

Adult

150.0

Aged

110.0

Base Sequence

60.0

Cerebral Infarction/*genetics

337.0

DNA Mutational Analysis

70.0

Dementia, Multi-Infarct/*genetics

990.0

English Abstract

70.0

Exons/genetics

40.0

Female

200.0

Genes, Dominant

30.0

Humans

590.0

Male

210.0

Middle Aged

200.0

Molecular Sequence Data

100.0

*Mutation, Missense

40.0

Pedigree

70.0

Point Mutation/genetics

20.0

Proto-Oncogene Proteins/*genetics

161.0

Receptors, Cell Surface/*genetics

41.0

Animals

240.0

Blotting, Northern

40.0

Cell Differentiation/drug effects

20.0

Ligands

70.0

Mice

200.0

Proto-Oncogene Proteins/genetics/metabolism

21.0

RNA, Messenger/metabolism

30.0

Research Support, U.S. Gov't, P.H.S.

100.0

*Transcription Factors

110.0

Magnetic Resonance Imaging

131.0

Phenotype

50.0

Proto-Oncogene Proteins/genetics

81.0

*Receptors, Cell Surface

338.0

Child

40.0

Flow Cytometry

20.0

Gene Deletion

20.0

*Gene Expression Regulation, Neoplastic

20.0

Homeodomain Proteins/genetics

31.0

Membrane Proteins/genetics/metabolism

21.0

Mice, Transgenic

40.0

Proto-Oncogene Proteins/genetics/*metabolism

41.0

RNA, Messenger/genetics/metabolism

20.0

Research Support, Non-U.S. Gov't

480.0

Comparative Study

80.0

Receptors, Cell Surface/genetics/*physiology

23.0

Signal Transduction

50.0

Transfection

20.0

Chromosome Aberrations

20.0

Gene Frequency

20.0

Signal Transduction/genetics

31.0

Blood Flow Velocity

22.0

Time Factors

20.0

*Ultrasonography, Doppler, Transcranial

250.0

Sensitivity and Specificity

40.0

Skin/pathology

31.0

Cells, Cultured

40.0

Mutation/*genetics

20.0

Protein Binding

20.0

Proteins/*metabolism

20.0

Proto-Oncogene Proteins/*genetics/metabolism

32.0

*Signal Transduction

40.0

Brain/pathology

51.0

Exons

40.0

*Mutation

60.0

Polymerase Chain Reaction

40.0

Alleles

30.0

Mutation

140.0

Amino Acid Sequence

60.0

Cysteine/genetics

21.0

Family Health

40.0

Gene Expression Regulation, Developmental

40.0

Immunohistochemistry

90.0

In Situ Hybridization

60.0

Dementia, Multi-Infarct/*diagnosis/genetics

2100.0

Genotype

30.0

Risk Factors

20.0

Protein Structure, Tertiary

20.0

Adolescent

40.0

Child, Preschool

20.0

Infant

20.0

RNA, Messenger/genetics

20.0

Receptors, Cell Surface/metabolism

20.0

Reverse Transcriptase Polymerase Chain Reaction

40.0

Age of Onset

40.0

Models, Genetic

30.0

*Genes, Dominant

20.0

Muscle, Smooth, Vascular/metabolism

23.0

Point Mutation/*genetics

20.0

Japan/epidemiology

30.0

Sequence Analysis, DNA

20.0

Cell Differentiation/genetics

20.0

Cell Division/genetics

20.0

Epidermal Growth Factor/genetics

34.0

Linkage (Genetics)

20.0

Mice, Knockout

40.0

Arginine/genetics

21.0

Polymorphism, Single-Stranded Conformational

30.0

Cell Count

20.0

*Cell Differentiation

31.0

Epithelial Cells/*cytology/metabolism

212.0

Chromosomes, Human, Pair 19/*genetics

22.0

Karyotyping

20.0

RNA, Messenger/analysis

20.0

Receptors, Cell Surface/genetics/*metabolism

21.0

Tumor Cells, Cultured

50.0

Up-Regulation

30.0

Mutation, Missense

20.0

Polymorphism, Genetic

20.0

Sequence Homology, Amino Acid

50.0

Gene Expression

20.0

Protein Biosynthesis

30.0

Repressor Proteins/biosynthesis

214.0

Cerebral Arterial Diseases/*genetics

2100.0

Proteins/genetics

30.0

Rats

40.0

Cell Lineage

20.0

Case-Control Studies

20.0

Cell Differentiation

20.0

Chromosome Mapping

20.0

Chromosomes, Artificial, Yeast

20.0

Chromosomes, Human, Pair 19

21.0

Receptors, Cell Surface/biosynthesis

25.0

Sequence Homology, Nucleic Acid

20.0

Cell Line

20.0

Gene Expression Regulation

20.0

Sequence Alignment

20.0

*Transcription, Genetic

20.0

Diagnosis, Differential

20.0