Gene DMD function profile ��Ʈw

Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol

Gene Name	Aliases	Previous_Symbol
DMD	dystrophin (muscular dystrophy, Duchenne and Becker types)	BMD, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272	dystrophin (muscular dystrophy, Duchenne and Becker types), includes DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272

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MeSH term

Frequency	Condition_Probility
Animals	23	0.0
Exons	12	0.0
Female	72	0.0
Humans	147	0.0
In Vitro	3	0.0
Male	91	0.0
Research Support, Non-U.S. Gov't	86	0.0
Sequence Deletion	2	0.0
Middle Aged	21	0.0
RNA, Messenger/analysis	2	0.0
English Abstract	20	0.0
*Gene Therapy	3	0.0
Adolescent	42	0.0
Adult	50	0.0
Electrocardiography	3	0.0
Child	56	0.0
Creatine Kinase/blood	14	12.0
Fibrin Fibrinogen Degradation Products/metabolism	2	2.0
Regression Analysis	4	0.0
Blotting, Western	3	0.0
Child, Preschool	32	0.0
Mice	15	0.0
Muscle, Skeletal/metabolism	2	1.0
Base Sequence	13	0.0
Gene Expression	2	0.0
Infant	13	0.0
Reverse Transcriptase Polymerase Chain Reaction	2	0.0
Amino Acid Sequence	3	0.0
Infant, Newborn	9	0.0
Linkage (Genetics)	10	0.0
Molecular Sequence Data	10	0.0
Muscular Dystrophies/genetics	4	18.0
Mutation	7	0.0
Phenotype	6	0.0
X Chromosome	8	1.0
Alleles	4	0.0
Dystrophin/*genetics	9	37.0
Introns	2	0.0
Muscular Dystrophy, Duchenne/*genetics	3	75.0
Polymerase Chain Reaction	15	0.0
Polymorphism, Genetic	2	0.0
Recombination, Genetic	2	0.0
Research Support, U.S. Gov't, Non-P.H.S.	5	0.0
X Chromosome/genetics	2	1.0
Chromosome Deletion	7	1.0
Genotype	2	0.0
Japan	3	0.0
Karyotyping	6	0.0
Microsatellite Repeats	2	0.0
X Chromosome/*genetics	6	1.0
Blotting, Southern	12	0.0
*Gene Deletion	8	0.0
Genes, Recessive	2	0.0
Syndrome	9	0.0
*X Chromosome	24	2.0
Case-Control Studies	2	0.0
Kinetics	3	0.0
Research Support, U.S. Gov't, P.H.S.	17	0.0
Dystrophin/metabolism	2	20.0
Mice, Transgenic	2	0.0
Microscopy, Electron	4	0.0
Muscular Dystrophies/*genetics/metabolism/pathology	2	66.0
Mutation/genetics	2	0.0
Utrophin	3	11.0
Exons/genetics	2	0.0
Gene Deletion	3	0.0
Polymerase Chain Reaction/*methods	3	0.0
Comparative Study	15	0.0
Muscle, Skeletal/*metabolism	2	1.0
Sex Chromosome Aberrations/*genetics	2	3.0
Muscular Dystrophy, Duchenne/*complications	2	100.0
Heterozygote Detection	6	1.0
Muscular Dystrophies/*genetics	23	27.0
Prenatal Diagnosis	6	3.0
Chromosome Mapping	17	0.0
DNA/genetics	7	0.0
Family Health	2	0.0
Lod Score	3	0.0
Mental Retardation/*genetics	4	1.0
Pedigree	18	0.0
Creatine Kinase/*blood	15	37.0
Isoenzymes	5	2.0
Muscular Dystrophies/*enzymology	8	72.0
Binding Sites	2	0.0
Creatine Kinase/*metabolism	3	23.0
Crosses, Genetic	5	0.0
Mice, Inbred C57BL	4	0.0
Mice, Mutant Strains	2	0.0
Adenosinetriphosphatase/analysis	2	15.0
Age Factors	7	0.0
In Situ Hybridization	2	0.0
*Transcription, Genetic	2	0.0
Aged	7	0.0
*Dosage Compensation (Genetics)	2	1.0
Heterozygote	13	0.0
DNA Primers	2	0.0
Gene Rearrangement	2	0.0
Pregnancy	11	0.0
Immunohistochemistry	5	0.0
*Mutation	3	0.0
Genetic Markers	8	0.0
Genetic Vectors	2	0.0
Biopsy	2	0.0
Muscles/pathology	4	10.0
Genes	2	0.0
Cells, Cultured	6	0.0
Fluorescent Antibody Technique	2	0.0
Muscles/*pathology	2	8.0
Cloning, Molecular	2	0.0
DNA/*genetics	3	0.0
Genome, Human	4	0.0
Image Processing, Computer-Assisted	2	0.0
Repetitive Sequences, Nucleic Acid	2	0.0
Restriction Mapping	2	0.0
DNA	3	0.0
*Point Mutation	2	0.0
Adrenal Insufficiency/*genetics	3	27.0
Glycerol Kinase/*deficiency	5	83.0
DNA Probes	9	0.0
Muscular Dystrophies/diagnosis/*genetics	4	40.0
Asian Continental Ancestry Group	2	0.0
*Linkage (Genetics)	2	0.0
Chromosomes, Fungal	3	4.0
Cosmids	3	0.0
Gene Library	2	0.0
Glycerol Kinase/deficiency/*genetics	2	40.0
Muscular Dystrophies/*diagnosis/genetics	6	75.0
Cell Line	4	0.0
*Genetic Markers	2	0.0
Muscles/*metabolism	3	4.0
Risk Factors	2	0.0
DNA Probes/genetics	2	1.0
*Polymorphism, Restriction Fragment Length	3	0.0
Muscular Dystrophies/*metabolism	2	40.0
Calcium/blood	2	0.0
*Chromosome Mapping	2	0.0
Polymorphism, Restriction Fragment Length	7	0.0
Nucleic Acid Hybridization	5	0.0
Time Factors	5	0.0
*Polymorphism, Genetic	2	0.0
Sequence Homology, Nucleic Acid	2	0.0
Adrenal Insufficiency/congenital/*genetics	2	40.0
Chromosome Banding	4	0.0
*Chromosome Deletion	8	1.0
Dystrophin/genetics	2	11.0
Glycerol Kinase/*deficiency/genetics	2	50.0
Heterozygote Detection/*methods	6	11.0
Prenatal Diagnosis/*methods	2	1.0
Risk	8	0.0
*Diseases in Twins	2	6.0
Dystrophin	6	100.0
Twins, Monozygotic	2	2.0
Muscle Proteins/genetics	2	2.0
Phosphotransferases/*deficiency	6	35.0
Indoles/*therapeutic use	2	1.0
*DNA Probes	3	6.0
Genetic Counseling	3	1.0
Muscles/*enzymology	3	3.0
Muscular Dystrophies/enzymology/*genetics	3	100.0
Gene Frequency	2	0.0
Probability	3	0.0
Heterozygote Detection/methods	3	12.0
*Prenatal Diagnosis	2	0.0
Enzyme Tests	4	5.0
Immunoenzyme Techniques	2	0.0
Reference Values	4	0.0
*Exertion	2	1.0
Muscular Dystrophies/*blood	5	62.0
Organ Specificity	2	0.0
Glucosephosphate Dehydrogenase/genetics	2	2.0
Double-Blind Method	2	0.0
Muscular Dystrophies/*enzymology/pathology	2	100.0
Erythrocyte Membrane/*analysis	2	9.0
Muscular Dystrophies/*blood/genetics	2	100.0
Isoenzymes/*blood	3	6.0
Muscles/enzymology	3	5.0
Erythrocytes/*enzymology	3	0.0
Fetal Blood/enzymology	2	13.0
Myoglobin/*blood	4	50.0
Muscular Dystrophies/*enzymology/genetics	5	71.0
Aging	2	0.0
Radioimmunoassay	2	0.0
*Heterozygote Detection	2	1.0
Pyruvate Kinase/*blood	2	25.0
*Regeneration	2	7.0