Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

A B C D E F G H I J K L M N O P Q R X Y Z



Gene Symbol
Gene NameAliasesPrevious_Symbol

MPZ

myelin protein zero (Charcot-Marie-Tooth neuropathy 1B)HMSNIB


Gene MPZ gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

English Abstract

60.0

Humans

480.0

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

390.0

Animals

50.0

Charcot-Marie-Tooth Disease/diagnosis/*genetics

216.0

Connexins/*genetics

116.0

Female

280.0

Male

270.0

Myelin P0 Protein/*genetics

1862.0

Myelin Proteins/*genetics

109.0

Pedigree

130.0

Point Mutation

30.0

Polymorphism, Genetic

40.0

Polymorphism, Single-Stranded Conformational

50.0

Adult

170.0

Base Sequence

30.0

Charcot-Marie-Tooth Disease/*genetics

107.0

Comparative Study

50.0

Connexins/genetics

817.0

DNA Mutational Analysis/*methods

32.0

Mutation/*genetics

40.0

Myelin Proteins/genetics

712.0

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

80.0

Sensitivity and Specificity

20.0

Amino Acid Substitution

20.0

DNA Primers

20.0

Exons

50.0

Genes, Dominant

20.0

Hereditary Motor and Sensory Neuropathies/*genetics/physiopathology

342.0

Chromosomes, Human, Pair 17/*genetics

21.0

Cohort Studies

30.0

DNA Mutational Analysis

80.0

Gene Duplication

42.0

Genetic Screening

40.0

Genotype

30.0

Hereditary Motor and Sensory Neuropathies/*genetics

49.0

Italy

20.0

Myelin P0 Protein/genetics

853.0

Phenotype

100.0

Adolescent

40.0

Charcot-Marie-Tooth Disease/*genetics/pathology

428.0

Child

30.0

Electrophysiology

30.0

*Point Mutation

60.0

Amino Acid Sequence

40.0

Molecular Sequence Data

60.0

*Mutation

70.0

Charcot-Marie-Tooth Disease/genetics/*pathology

350.0

Middle Aged

110.0

Myelin P0 Protein/*genetics/metabolism

3100.0

DNA Mutational Analysis/methods

20.0

DNA-Binding Proteins/*genetics

20.0

Heterozygote

30.0

Homozygote

20.0

Mice

20.0

Chromosomes, Human, Pair 17

30.0

Myelin Sheath/*pathology

222.0

Peripheral Nerves/pathology

29.0

Restriction Mapping

20.0

Charcot-Marie-Tooth Disease/genetics

28.0

Polymerase Chain Reaction

20.0

Mutation

70.0

Sural Nerve/pathology

511.0

Aged

30.0

Biopsy

30.0

Electromyography

21.0

Family Health

20.0

Myelin P0 Protein/chemistry/*genetics

240.0

Protein Structure, Tertiary

20.0

Child, Preschool

40.0

Gene Deletion

30.0

Age of Onset

30.0

Charcot-Marie-Tooth Disease/classification/diagnosis/*genetics

266.0

Multigene Family

20.0

Neural Conduction

44.0

X Chromosome

20.0

Intestinal Absorption

21.0

Charcot-Marie-Tooth Disease/*genetics/*pathology/physiopathology

250.0

Axons/pathology

26.0

Muscle, Skeletal/physiopathology

210.0

Japan

20.0