Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

F7

coagulation factor VII (serum prothrombin conversion accelerator)


Gene F7 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Adult

200.0

Female

320.0

Humans

460.0

Laterality/*physiology

26.0

Male

280.0

Motor Cortex/*physiology

210.0

Adolescent

110.0

English Abstract

30.0

*Theta Rhythm

240.0

Animals

80.0

CHO Cells

20.0

Hamsters

30.0

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

210.0

Child

110.0

Analysis of Variance

20.0

Electroencephalography

20.0

Statistics, Nonparametric

20.0

*Electroencephalography

1211.0

Fourier Analysis

23.0

Middle Aged

90.0

Factor VII/*genetics

770.0

Factor VII Deficiency/*genetics

550.0

Amino Acid Substitution

20.0

Base Sequence

30.0

DNA Mutational Analysis

30.0

Genotype

50.0

In Vitro

20.0

Models, Molecular

20.0

*Mutation

20.0

Mutation, Missense

20.0

Phenotype

50.0

Point Mutation

30.0

Polymerase Chain Reaction

40.0

Protein Conformation

30.0

Case-Control Studies

20.0

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

20.0

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

60.0

Time Factors

20.0

Predictive Value of Tests

20.0

Factor VII Deficiency/blood/*genetics

2100.0

Heterozygote

30.0

*Polymorphism, Genetic

30.0

Transfection

30.0

Aged

40.0

Angiotensin II Type 1 Receptor Blockers/*therapeutic use

225.0

Benzimidazoles/*therapeutic use

216.0

Double-Blind Method

20.0

Hypertension/*prevention & control

220.0

Tetrazoles/*therapeutic use

213.0

Regression Analysis

30.0

Comparative Study

40.0

Child, Preschool

20.0

Electrodes

24.0

Molecular Sequence Data

30.0

Mutagenesis, Site-Directed

20.0

Cerebral Cortex/physiopathology

28.0

Magnetic Resonance Imaging

20.0

Pedigree

30.0

Sex Factors

20.0

Mice

20.0

Electrophoresis, Starch Gel

21.0

*Hemoglobins, Abnormal

211.0

Infant, Newborn

20.0

Amino Acids/analysis

20.0