Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

DRPLA

dentatorubral-pallidoluysian atrophy (atrophin-1)ATN1, B37


Gene DRPLA gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Animals

50.0

Humans

330.0

Mice

20.0

Mice, Transgenic

20.0

Alleles

80.0

DNA/genetics

20.0

Gene Frequency

70.0

Nerve Tissue Proteins/genetics

72.0

Nuclear Proteins/genetics

72.0

Proteins/*genetics

20.0

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

280.0

Trinucleotide Repeat Expansion/*genetics

58.0

Trinucleotide Repeats/*genetics

22.0

Aged

70.0

Magnetic Resonance Imaging

20.0

Male

180.0

Middle Aged

140.0

Pedigree

80.0

Adult

120.0

Female

170.0

Mutation

80.0

Trinucleotide Repeats/genetics

23.0

Case-Control Studies

20.0

Huntington Disease/*genetics

24.0

Nerve Tissue Proteins/*genetics

40.0

Nuclear Proteins/*genetics

30.0

Polymerase Chain Reaction

80.0

*Trinucleotide Repeat Expansion

511.0

Comparative Study

50.0

Adolescent

40.0

Age of Onset

60.0

Calcium Channels/genetics

518.0

Child

20.0

DNA Mutational Analysis

40.0

Proteins/genetics

50.0

Phenotype

40.0

*Genes, Dominant

20.0

Spinocerebellar Ataxias/*genetics

210.0

Trinucleotide Repeats

54.0

Child, Preschool

20.0

Genetic Counseling

21.0

Haplotypes

20.0

Microsatellite Repeats/genetics

20.0

Cerebellar Ataxia/*complications

2100.0

English Abstract

40.0

Amino Acid Sequence

20.0

Cell Line

20.0

Molecular Sequence Data

40.0

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

80.0

Machado-Joseph Disease/genetics

266.0

Genes, Dominant

20.0

Spinocerebellar Degenerations/*genetics

317.0

*Trinucleotide Repeats

54.0

DNA Primers

20.0

Huntington Disease/genetics

211.0

Organ Specificity

20.0

Reproducibility of Results

20.0

Chromosome Mapping

20.0

Genotype

20.0

Base Sequence

30.0

Sequence Alignment

20.0

Species Specificity

20.0

Brain Diseases/*genetics

240.0

Nervous System Diseases/*genetics

26.0