Absence of mutations in human ubiquitin fusion-degradation protein gene in tetralogy of Fallot

Keyphrases

• Protein-coding Genes 100%
• Tetralogy of Fallot 100%
• Ubiquitin Fusion 100%
• UFD1L 75%
• Sequence Analysis 50%
• Human Chromosomes 50%
• 22q11.2 Deletion Syndrome 50%
• Cardiovascular System 25%
• Mobility Shift 25%
• Single nucleotide Polymorphism 25%
• Mouse Embryo 25%
• Gene-deficient Mice 25%
• Causal Role 25%
• Screening Analysis 25%
• Exon 4 25%
• Chromosome 22q11.2 Deletion Syndrome 25%
• Conotruncal Defects 25%
• Chromosome 22q11.2 25%
• Fetal Development 25%
• Flanking Sequence 25%
• Congenital Disorders 25%
• Mutation Screening 25%
• Cranial Neural Crest 25%
• Branchial Arch 25%
• Mutation Sequence 25%
• Aortic Arch Anomalies 25%
• Heteroduplex Analysis 25%
• Cardiac Neural Crest 25%
• Gene Dosage Analysis 25%
• Congenital Cardiovascular Malformations 25%
• Chromosome Deletion 25%
• Pharyngeal Pouch 25%
• Nucleotide Variation 25%
• Tetralogy of Fallot with Pulmonary Atresia 25%

Biochemistry, Genetics and Molecular Biology

• Human Chromosome 100%
• Protein Catabolism 100%
• Ubiquitin 100%
• Exon 50%
• Protein Sequencing 50%
• Single-Nucleotide Polymorphism 50%
• Shotgun Sequencing 50%
• Intron 50%
• DNA Flanking Region 50%
• Gene Dosage 50%
• Heteroduplex Analysis 50%
• Cranial Neural Crest 50%
• Fetus Development 50%

Medicine and Dentistry

• Ubiquitin 100%
• Protein Degradation 100%
• Tetralogy of Fallot 100%
• Chromosome Deletion 22q11 60%
• Human Chromosome 40%
• Protein Sequencing 20%
• Sequence Analysis 20%
• Mouse Embryo 20%
• Exon 20%
• Intron 20%
• Single Nucleotide Polymorphism 20%
• Congenital Disorder 20%
• Cardiovascular Malformation 20%
• Gene Dosage 20%
• Disease 20%
• Chromosome Deletion 20%
• DNA Flanking Region 20%
• Branchial Arch 20%
• Aortic Arch Anomaly 20%
• Heteroduplex Analysis 20%
• Pulmonary Atresia 20%
• Fetus Development 20%
• Cranial Neural Crest 20%
• Cardiovascular System 20%