Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

F8

coagulation factor VIII, procoagulant component (hemophilia A)FVIII, Factor VIIIF8B, DXS1253E, HEMA


Gene F8 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Animals

50.0

Humans

520.0

Adult

190.0

Aged

40.0

Female

310.0

Male

300.0

Middle Aged

80.0

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

210.0

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

100.0

Vascular Endothelial Growth Factor A

30.0

Vascular Endothelial Growth Factors

30.0

English Abstract

50.0

Pregnancy

20.0

Laterality/*physiology

26.0

Motor Cortex/*physiology

315.0

Movement/*physiology

25.0

Adolescent

100.0

*Theta Rhythm

240.0

Base Sequence

60.0

Factor VIII/*genetics

615.0

Hemophilia A/*genetics

419.0

*Inversion, Chromosome

22.0

Molecular Sequence Data

60.0

Pedigree

70.0

Recombination, Genetic

30.0

Repetitive Sequences, Nucleic Acid

30.0

Analysis of Variance

40.0

Regression Analysis

40.0

*Brain Mapping

24.0

Child

70.0

Electroencephalography

31.0

*Electroencephalography

1110.0

Fourier Analysis

23.0

Electrostatics

21.0

*Point Mutation

20.0

Time Factors

20.0

Mice

40.0

Rats

20.0

Structure-Activity Relationship

20.0

Mice, Inbred BALB C

20.0

Reaction Time/physiology

22.0

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

20.0

Brain/*physiology

21.0

*Databases, Factual

23.0

Gene Frequency

30.0

Inversion, Chromosome

23.0

Linkage (Genetics)

60.0

Sex Factors

30.0

Electrodes

24.0

Blotting, Southern

20.0

Reference Values

20.0

Amino Acid Sequence

20.0

Restriction Mapping

20.0

Cerebral Cortex/physiopathology

28.0

Cells, Cultured

20.0

Magnetic Resonance Imaging

20.0

Chromosome Mapping

20.0

DNA Probes

30.0

Genetic Markers

60.0

*X Chromosome

80.0

*Chromosome Deletion

20.0

DNA/*genetics

20.0

Genes, Recessive

20.0

*Linkage (Genetics)

30.0

Polymorphism, Restriction Fragment Length

40.0

Parietal Lobe/physiology

233.0

Fimbriae, Bacterial/*immunology

222.0

Serotyping

20.0

*Chromosome Mapping

20.0

Fragile X Syndrome/*genetics

21.0