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Folate pathway gene alterations in patients with neural tube defects
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Dive into the research topics of 'Folate pathway gene alterations in patients with neural tube defects'. Together they form a unique fingerprint.
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Keyphrases
Gene Alteration
100%
Neural Tube Defects
100%
Pathway Genes
100%
Folate Receptor
100%
Folate Pathway
100%
Receptor Gene
50%
MTHFR C677T
50%
Heterozygosity
25%
Homozygosity
25%
Coding Region
25%
Risk Factors
25%
Amino Acids
25%
Protective Mechanism
25%
Etiology
25%
Exon 3
25%
Folate
25%
3′-untranslated Region (3′-UTR)
25%
Genetic Risk
25%
Occurrence Risk
25%
Recurrence Risk
25%
Carboxyl Terminus
25%
Molecular Genetic Analysis
25%
Genetic Association
25%
Specific mutation
25%
Reductase
25%
Inborn Errors
25%
Pseudogene
25%
Periconceptional Supplementation
25%
GPI-anchored Protein (GPI-AP)
25%
Anchor Region
25%
Homocysteine Metabolism
25%
Molecular Variation
25%
Exon 7
25%
Folate Metabolism
25%
Nascent Protein
25%
Gene Conversion
25%
A1298C Polymorphism
25%
Biochemistry, Genetics and Molecular Biology
Gene Mutation
100%
Folic Acid
100%
Neural Tube
100%
Folate Receptor
100%
Receptor Gene
50%
Heterozygosity
25%
Homozygosity
25%
Coding Region
25%
Homocysteine
25%
Amino Acids
25%
Oxidoreductase
25%
Metabolic Pathway
25%
C-Terminus
25%
3' Untranslated Region
25%
Genetic Risk
25%
Exon
25%
Genetic Association
25%
Molecular Genetics
25%
Reductase
25%
Pseudogene
25%
Gene Conversion
25%