aspartic acid has been researched along with Malabsorption Syndromes in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (33.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Fiser, A; Goldman, ID; Min, SH; Russell, L; Shin, DS; Zhao, R | 1 |
Brook, A; Davachi, B; Esmaili, M; Kianifar, HR; Talebi, S; Tavakkol-Afshari, J | 1 |
Grävinghoff, J; Hütter, HJ | 1 |
3 other study(ies) available for aspartic acid and Malabsorption Syndromes
Article | Year |
---|---|
Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption.
Topics: Amino Acid Substitution; Aspartic Acid; Child; DNA Mutational Analysis; Folic Acid; Homozygote; Humans; Infant, Newborn; Malabsorption Syndromes; Mutation, Missense; Pakistan; Protein Stability; Proton-Coupled Folate Transporter | 2010 |
D28G mutation in congenital glucose-galactose malabsorption.
Topics: Aspartic Acid; Female; Galactose; Glucose; Glycine; Humans; Infant, Newborn; Malabsorption Syndromes; Male; Mutation; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Sodium-Glucose Transporter 1 | 2007 |
[Acylase activity of human small intestinal mucosa in malabsorption syndrome].
Topics: Amidohydrolases; Anilides; Aspartic Acid; Celiac Disease; Child, Preschool; Humans; Infant; Intestinal Mucosa; Jejunum; Malabsorption Syndromes; Methionine | 1978 |