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Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

ASS

argininosuccinate synthetaseASS1, CTLN1


Gene ASS gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Female

310.0

Humans

710.0

Pregnancy

20.0

Age Factors

20.0

Animals

170.0

Animals, Newborn

20.0

Argininosuccinate Synthase/genetics/metabolism

2100.0

Blotting, Northern

50.0

Carbamoyl-Phosphate Synthase (Ammonia)/genetics/metabolism

2100.0

Male

340.0

*Membrane Transport Proteins

40.0

Mice

90.0

*Mitochondrial Proteins

42.0

RNA, Messenger/analysis

30.0

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

460.0

Amino Acid Sequence

90.0

Base Sequence

120.0

DNA Primers

20.0

Molecular Sequence Data

180.0

Sequence Homology, Amino Acid

20.0

Adult

210.0

Aged

80.0

Middle Aged

150.0

Aged, 80 and over

40.0

Arginine/metabolism

35.0

Citrulline/metabolism

333.0

English Abstract

40.0

Mutation

30.0

Chromosome Banding

20.0

Chromosomes, Human, Pair 9

42.0

Comparative Study

60.0

In Situ Hybridization, Fluorescence/*methods

22.0

Translocation, Genetic

20.0

Arginine/*metabolism

24.0

Brain/*metabolism

20.0

Adolescent

80.0

Age of Onset

50.0

Blotting, Western

20.0

Child

60.0

DNA Mutational Analysis

40.0

Liver/enzymology

50.0

*Mutation

50.0

Disease Models, Animal

50.0

Dose-Response Relationship, Drug

30.0

Genotype

20.0

Immunohistochemistry

30.0

Kinetics

20.0

Mice, Knockout

20.0

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

150.0

Alleles

50.0

Amino Acids/blood

24.0

Homozygote

20.0

Mice, Mutant Strains

20.0

Argininosuccinate Synthase/*deficiency/*genetics

2100.0

Infant

50.0

Polymerase Chain Reaction

90.0

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

20.0

Argininosuccinate Synthase/deficiency/genetics

2100.0

Cloning, Molecular

30.0

Argininosuccinate Synthase/*deficiency

3100.0

Citrulline/*blood

1386.0

Liver/enzymology/pathology

318.0

Amino Acid Metabolism, Inborn Errors/*genetics/metabolism

250.0

Chromosome Mapping

90.0

*Chromosomes, Human, Pair 9

135.0

Consanguinity

30.0

Genes, Recessive

30.0

Genetic Markers

80.0

Infant, Newborn

70.0

Sequence Alignment

30.0

Transcription, Genetic

20.0

Urea/metabolism

48.0

Ammonia/blood

411.0

Argininosuccinate Synthase/*deficiency/metabolism

3100.0

Argininosuccinate Synthase/genetics

466.0

Child, Preschool

50.0

DNA/genetics

30.0

Linkage (Genetics)

40.0

Lod Score

50.0

Pedigree

120.0

Phenotype

30.0

Dystonia Musculorum Deformans/*genetics

315.0

Haplotypes

40.0

Jews/*genetics

42.0

Polymorphism, Genetic

20.0

Biopsy

30.0

Chromosome Disorders

20.0

Blotting, Southern

20.0

Genetic Screening

30.0

Heterozygote

20.0

RNA, Messenger/metabolism

20.0

Urea/*metabolism

29.0

Amino Acid Metabolism, Inborn Errors/*genetics

25.0

Argininosuccinate Synthase/*genetics

888.0

Gene Expression/genetics

20.0

Recombination, Genetic

30.0

Benzoic Acid

222.0

Ethnic Groups

20.0

Genes, Dominant

20.0

Sequence Analysis, DNA

20.0

Tumor Cells, Cultured

20.0

Enzyme-Linked Immunosorbent Assay

20.0

Mutation/*genetics

20.0

Polymorphism, Restriction Fragment Length

40.0

*Linkage (Genetics)

50.0

Aspartic Acid/metabolism

27.0

Cell Division/drug effects

20.0

DNA/*genetics

20.0

Hela Cells

20.0

DNA Probes

20.0

Hamsters

40.0

Hybrid Cells

30.0

Sequence Homology, Nucleic Acid

20.0

Argininosuccinate Synthase/*metabolism

266.0

Cell Line

40.0

Ligases/*genetics

32.0

Liver/*enzymology

30.0

Argininosuccinate Synthase/*deficiency/genetics

266.0

Citrulline/*blood/metabolism

2100.0

Ligases/*deficiency

440.0