Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

DM1

dystrophia myotonica 1 (includes dystrophia myotonia protein kinase)


Gene DM1 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Animals

340.0

Humans

1480.0

Genes, Dominant

20.0

*Microsatellite Repeats

31.0

Phenotype

110.0

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

1000.0

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

360.0

*Trinucleotide Repeat Expansion

818.0

Adult

700.0

Base Sequence

180.0

Case-Control Studies

110.0

DNA/genetics

30.0

Male

930.0

Myotonic Dystrophy/classification/complications/*genetics

2100.0

Risk Factors

80.0

Diabetes Mellitus, Type 1/*complications

27.0

Dose-Response Relationship, Drug

20.0

Double-Blind Method

20.0

Aged

220.0

DNA/analysis/genetics

21.0

Female

850.0

Middle Aged

400.0

Myotonic Dystrophy/*genetics/*physiopathology

2100.0

English Abstract

130.0

Brain/metabolism

20.0

Fibroblasts/metabolism

20.0

Gene Expression Profiling

20.0

Mice

210.0

Mice, Knockout

60.0

Molecular Sequence Data

160.0

Muscle, Skeletal/metabolism

31.0

Myotonic Dystrophy/*genetics/pathology

450.0

Polymerase Chain Reaction

110.0

Transfection

20.0

Tumor Cells, Cultured

20.0

Alleles

110.0

Child

270.0

Genetic Markers

50.0

Genotype

60.0

HLA-DR Antigens/*genetics

30.0

Pedigree

100.0

Blotting, Southern

50.0

DNA Primers

80.0

Mice, Transgenic

90.0

Proteins/genetics

20.0

Trinucleotide Repeat Expansion/*genetics

1016.0

Treatment Outcome

20.0

Amino Acid Sequence

80.0

*Drosophila Proteins

30.0

Myotonic Dystrophy/*genetics

1624.0

Nuclear Proteins/*genetics/metabolism

21.0

Phylogeny

30.0

RNA, Messenger/metabolism

60.0

Child, Preschool

170.0

Infant

130.0

Infant, Newborn

50.0

Pregnancy

60.0

European Continental Ancestry Group/genetics

20.0

Protein-Serine-Threonine Kinases/*genetics

103.0

Reference Values

100.0

Trinucleotide Repeats/*genetics

56.0

Adolescent

340.0

In Vitro

20.0

Regression Analysis

40.0

Blotting, Western

70.0

Cells, Cultured

120.0

Enzyme-Linked Immunosorbent Assay

20.0

Immunohistochemistry

70.0

Organ Specificity

30.0

RNA, Messenger/genetics/metabolism

60.0

Reverse Transcriptase Polymerase Chain Reaction

60.0

Transgenes/genetics

22.0

Age Factors

80.0

Diabetes Mellitus, Type 1/*epidemiology

466.0

Genes, Dominant/genetics

21.0

Homeodomain Proteins/genetics

31.0

Protein-Serine-Threonine Kinases/genetics

75.0

*Gene Expression Regulation

30.0

Myotonic Dystrophy/etiology/*genetics

2100.0

Trinucleotide Repeat Expansion

513.0

Family Health

40.0

Sequence Analysis, DNA

20.0

Trinucleotide Repeat Expansion/genetics

512.0

Trinucleotide Repeats/genetics

711.0

Gene Frequency

20.0

Nuclear Proteins/*genetics

20.0

*Trinucleotide Repeats

43.0

Age of Onset

80.0

Disease Progression

40.0

Lymphocytes/metabolism

20.0

Mutation/*genetics

20.0

Time Factors

50.0

Comparative Study

250.0

Prognosis

30.0

Cell Nucleus/metabolism

40.0

Electrophoresis, Polyacrylamide Gel

20.0

Gene Expression

40.0

In Situ Hybridization, Fluorescence

60.0

Blood Glucose/analysis

40.0

Diabetes Mellitus, Type 1/*metabolism

35.0

Hemoglobin A, Glycosylated/analysis

30.0

Sex Factors

20.0

Autoantibodies/blood

31.0

Antibody Specificity

30.0

Cell Division

20.0

In Situ Hybridization

50.0

Muscle, Skeletal/*metabolism/pathology

212.0

Fasting

20.0

Insulin/therapeutic use

21.0

Sex Distribution

41.0

Cell Line

60.0

Cloning, Molecular

50.0

Sequence Homology, Amino Acid

40.0

*Founder Effect

32.0

Haplotypes/*genetics

21.0

Insulin Resistance/*genetics

22.0

Myotonic Dystrophy/*genetics/physiopathology

266.0

RNA/genetics

21.0

Receptor, Insulin/*genetics

25.0

Chromosome Mapping

30.0

Linkage Disequilibrium

20.0

Mutation

100.0

Myotonic Dystrophy/*genetics/metabolism

250.0

*Gene Expression Regulation, Developmental

20.0

3' Untranslated Regions/genetics

33.0

Fluorescent Antibody Technique, Indirect

20.0

Protein Binding

20.0

RNA-Binding Proteins/genetics/*metabolism

23.0

Body Composition

31.0

Electric Impedance

23.0

Insulin/blood

30.0

Statistics, Nonparametric

30.0

Variation (Genetics)

20.0

Glucose Clamp Technique/methods

2100.0

Brain/*pathology

31.0

Clinical Trials, Phase I

23.0

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

30.0

RNA-Binding Proteins/genetics

47.0

Questionnaires

50.0

Reproducibility of Results

20.0

*Alleles

20.0

Haplotypes/genetics

20.0

Mutation/genetics

20.0

*Chromosome Mapping

20.0

Chromosomes, Human, Pair 19

42.0

Diagnosis, Differential

20.0

Cell Differentiation/*physiology

20.0

Gene Expression Regulation, Developmental

20.0

Calorimetry, Indirect

35.0

Magnetic Resonance Spectroscopy

20.0

Hela Cells

20.0

Follow-Up Studies

20.0

Prevalence

80.0

Exons/genetics

20.0

*Genetic Predisposition to Disease

20.0

Genetic Predisposition to Disease

20.0

Predictive Value of Tests

50.0

*Seasons

37.0

Mice, SCID

20.0

Mosaicism

22.0

*Diabetes Mellitus, Type 1

250.0

Neurologic Examination

21.0

*Pregnancy Complications

25.0

Prospective Studies

30.0

Muscle, Skeletal/pathology

23.0

Child Welfare

28.0

Diabetes Mellitus, Type 1/*complications/epidemiology

2100.0

Statistics

20.0

Retrospective Studies

40.0

Severity of Illness Index

70.0

Genomic Instability

212.0

Blood Glucose/*metabolism

31.0

Aged, 80 and over

40.0

Alternative Splicing/*genetics

21.0

Glucose/metabolism

20.0

Genetic Markers/genetics

20.0

Blotting, Northern/methods

23.0

Myotonic Dystrophy/genetics/*metabolism

266.0

RNA/*metabolism

23.0

Muscle, Skeletal/physiopathology

315.0

Neoplasm Transplantation

20.0

Transplantation, Heterologous

20.0

Myotonic Dystrophy/*genetics/*psychology

266.0

Socioeconomic Factors

21.0

Sequence Homology, Nucleic Acid

20.0

Myotonic Dystrophy/*complications/genetics

266.0

Blotting, Northern

40.0

Disease Models, Animal

30.0

Binding Sites

20.0

*Repetitive Sequences, Nucleic Acid

20.0

Models, Biological

20.0

Protein Biosynthesis

20.0

*Chromosomes, Human, Pair 3

30.0

Hamsters

20.0

*DNA-Binding Proteins

30.0

Mice, Inbred C57BL

20.0

Body Mass Index

30.0

Cross-Over Studies

20.0

Promoter Regions (Genetics)

30.0

Cross-Sectional Studies

30.0

Hemoglobin A, Glycosylated/metabolism

21.0

Blood Glucose

22.0

C-Peptide/blood

21.0

Haplotypes

20.0

Introns

20.0

Myotonic Dystrophy/classification/*genetics

2100.0

Base Pairing

23.0

Seasons

21.0

Diabetes Mellitus, Type 1/*genetics/immunology

23.0

HLA-DQ Antigens/*genetics

20.0

Histocompatibility Testing

20.0

Polymorphism, Genetic/genetics

20.0

Thyroid Function Tests

22.0

*Sex Characteristics

21.0

Vibration

214.0

Incidence

30.0

Disability Evaluation

25.0

Cell Differentiation

30.0

Protein-Serine-Threonine Kinases/*genetics/metabolism

23.0