Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

MSX1

msh homeo box homolog 1 (Drosophila)HYD1msh (Drosophila) homeo box homolog 1 (formerly homeo box 7)


Gene MSX1 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Humans

610.0

Population Surveillance

21.0

Animals

280.0

Chromosome Mapping

80.0

Chromosomes, Human, Pair 4/*genetics

44.0

Cleft Palate/*genetics/pathology

337.0

Family Health

50.0

Female

310.0

Homeodomain Proteins/*genetics

204.0

Linkage Disequilibrium

30.0

Male

300.0

Microsatellite Repeats

80.0

Pedigree

130.0

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

310.0

*Transcription Factors

231.0

Adolescent

70.0

Adult

120.0

Amino Acid Substitution

30.0

Anodontia/*genetics

738.0

Child

100.0

Child, Preschool

40.0

DNA Mutational Analysis

30.0

Genes, Dominant

70.0

Genes, Homeobox

55.0

Linkage (Genetics)

70.0

Middle Aged

30.0

Odontogenesis/genetics

228.0

Polymorphism, Single-Stranded Conformational

30.0

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

400.0

*Transcription, Genetic

30.0

Chile

58.0

Cleft Lip/*genetics

1117.0

Cleft Palate/*genetics

1014.0

Genetic Markers

60.0

Linkage Disequilibrium/genetics

21.0

Monte Carlo Method

34.0

Transcription Factors/*genetics

90.0

Alleles

90.0

Comparative Study

90.0

Genetic Predisposition to Disease/*genetics

30.0

Genotype

160.0

Lod Score

70.0

*Chromosome Mapping

20.0

Genetic Markers/genetics

30.0

Homeodomain Proteins/genetics

104.0

Linkage (Genetics)/genetics

20.0

Models, Genetic

20.0

Statistics, Nonparametric

20.0

Transforming Growth Factor alpha/genetics

311.0

Chromosomes, Human, Pair 14/genetics

22.0

DNA/genetics

30.0

DNA-Binding Proteins/*genetics

50.0

Exons/genetics

30.0

Genes, Dominant/genetics

21.0

Genetic Heterogeneity

31.0

Mutation/*genetics

20.0

Phenotype

100.0

Polymorphism, Genetic/genetics

40.0

Sequence Analysis, DNA

20.0

Cleft Lip/complications/*genetics

240.0

Cleft Palate/complications/*genetics

240.0

*Linkage Disequilibrium

31.0

Molecular Sequence Data

130.0

Polymerase Chain Reaction

60.0

Case-Control Studies

100.0

Chi-Square Distribution

40.0

Cleft Lip/epidemiology/*genetics

225.0

Cleft Palate/epidemiology/*genetics

225.0

Infant

30.0

Infant, Newborn

50.0

Logistic Models

30.0

Maryland/epidemiology

323.0

Nuclear Family

20.0

Transforming Growth Factor beta/genetics

33.0

Genetics, Population

20.0

Haplotypes/*genetics

21.0

Introns/genetics

20.0

Transforming Growth Factor alpha/*genetics

24.0

Risk Factors

60.0

Amino Acid Sequence

60.0

Cattle

20.0

Cell Line

40.0

Chickens

20.0

Embryonic and Fetal Development

20.0

*Gene Expression Regulation, Developmental

20.0

Heterozygote

30.0

Mice

190.0

Mice, Knockout

60.0

Rats

20.0

Sequence Alignment

20.0

Sequence Homology, Amino Acid

40.0

Environment

22.0

Pregnancy

40.0

Transforming Growth Factor beta/*genetics

33.0

Base Sequence

100.0

In Situ Hybridization

60.0

Linkage (Genetics)/*genetics

20.0

Syndrome

60.0

Craniofacial Abnormalities/*genetics

26.0

English Abstract

30.0

Gene Expression Regulation, Developmental

50.0

Maxillofacial Development/*genetics

266.0

Mice, Transgenic

30.0

Mutation

30.0

Reverse Transcriptase Polymerase Chain Reaction

20.0

DNA-Binding Proteins/genetics/*physiology

31.0

Gene Expression Regulation

20.0

Transcription Factors/genetics/*physiology

21.0

Cell Division

30.0

Homeodomain Proteins/*genetics/metabolism

22.0

Tumor Cells, Cultured

20.0

Cell Differentiation

30.0

Gene Expression

30.0

Time Factors

20.0

*Trans-Activators

20.0

DNA-Binding Proteins/genetics

50.0

Transcription Factors/genetics

40.0

Binding Sites

30.0

Consensus Sequence

20.0

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

40.0

European Continental Ancestry Group

20.0

Receptors, Fibroblast Growth Factor/genetics

23.0

Immunohistochemistry

20.0

Signal Transduction

20.0

*Chromosomes, Human, Pair 4

52.0

European Continental Ancestry Group/genetics

40.0

Gene Frequency

40.0

Extremities/embryology

38.0

Tooth Abnormalities/*genetics

218.0

Exons

20.0

Point Mutation

30.0

Variation (Genetics)

20.0

Genes, Homeobox/genetics

310.0

Mutation/genetics

30.0

Signal Transduction/physiology

20.0

Organ Culture Techniques

20.0

Proteins/*genetics

20.0

Genes, Homeobox/*genetics

23.0

Limb Deformities, Congenital/epidemiology/*genetics

2100.0

Philippines

26.0

Chimera

21.0

Chromosomes, Human, Pair 4

32.0

*Genes, Homeobox

52.0

Bone Morphogenetic Proteins/genetics/*metabolism

211.0

Morphogenesis/genetics

25.0

Finland

20.0

Cleft Lip/*genetics/pathology

228.0

Genes, Recessive

20.0

Anodontia/complications/*genetics

2100.0

Mesoderm/metabolism

22.0

Trans-Activators/*metabolism

20.0