arginine has been researched along with Malabsorption Syndromes in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (16.67) | 29.6817 |
| 2010's | 2 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cai, W; Del Castillo, MD; Fernandez-Gomez, B; Martinez-Saez, N; Uribarri, J | 1 |
| Assaraf, YG; Berman, B; Bessler, H; Drori, S; Glaser, F; Jansen, G; Lasry, I; Sharkia, M; Sofer, Y; Straussberg, R | 1 |
| Assaraf, YG; Berman, B; Glaser, F; Jansen, G; Lasry, I | 1 |
| Chang, MH; Diop-Bove, N; Fulterer, A; Goldman, ID; Mahadeo, K; Romero, MF; Shin, D; Teo, J; Unal, ES; Zhao, R | 1 |
| BLAIR, A; FOX, M; ROSENBERG, LE; SEGAL, S; THIER, SO | 1 |
| Clifton, JA | 1 |
| Fujimoto, A; Higami, S; Matsuoka, O; Omura, K; Yamanaka, N | 1 |
| Costin, G; Kogut, MD | 1 |
| Madge, DS | 1 |
| Agus, SG; Di Sant'Agnese, PA; Kattwinkel, J; Laster, L; Taussig, LM | 1 |
| Launiala, K | 1 |
| Miura, R; Oyanagi, K; Yamanouchi, T | 1 |
12 other study(ies) available for arginine and Malabsorption Syndromes
| Article | Year |
|---|---|
In vitro formation of Maillard reaction products during simulated digestion of meal-resembling systems.
Topics: Amino Acids; Arginine; Biological Availability; Carbohydrates; Digestion; Fructosamine; Fructose; Glucose; Intestines; Lysine; Maillard Reaction; Malabsorption Syndromes; Meals; Proteins; Starch; Sugars | 2019 |
A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function.
Topics: Amino Acid Sequence; Animals; Arginine; Base Sequence; Binding Sites; Carrier Proteins; Cell Membrane; Child; CHO Cells; Consanguinity; Cricetinae; Cricetulus; DNA Primers; Folate Receptors, GPI-Anchored; Folic Acid; Homozygote; Humans; Hydrogen-Ion Concentration; In Vitro Techniques; Malabsorption Syndromes; Methotrexate; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Point Mutation; Protein Conformation; Receptors, Cell Surface; Recombinant Proteins; Sequence Homology, Amino Acid; Transfection | 2008 |
Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding.
Topics: Amino Acid Sequence; Arginine; Folic Acid; Humans; Intestinal Absorption; Malabsorption Syndromes; Membrane Transport Proteins; Models, Molecular; Molecular Sequence Data; Mutation; Protein Conformation; Proton-Coupled Folate Transporter | 2009 |
Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption.
Topics: Amino Acid Substitution; Animals; Arginine; Folic Acid; Folic Acid Antagonists; Glutamates; Glutamine; Guanine; HeLa Cells; Humans; Hydrogen-Ion Concentration; Malabsorption Syndromes; Molecular Sequence Data; Mutagenesis, Site-Directed; Oocytes; Patch-Clamp Techniques; Pemetrexed; Proton-Coupled Folate Transporter; Protons; Tetrahydrofolates; Xenopus laevis | 2010 |
CYSTINURIA: DEFECTIVE INTESTINAL TRANSPORT OF DIBASIC AMINO ACIDS AND CYSTINE.
Topics: Amino Acids, Diamino; Arginine; Biological Transport; Carbon Isotopes; Cystine; Cystinuria; Genetics, Medical; Humans; Jejunum; Kidney; Lysine; Malabsorption Syndromes; Sulfur Isotopes | 1965 |
[Some hereditary disorders of intestinal resorption with renal dysfunction].
Topics: Arginine; Child; Chlorides; Cystine; Cystinuria; Diarrhea; Female; Galactose; Glucose; Hartnup Disease; Humans; Infant, Newborn; Intestinal Absorption; Kidney Diseases; Lysine; Malabsorption Syndromes; Male; Pedigree; Tryptophan | 1976 |
Lysine malabsorption syndrome: a new type of transport defect.
Topics: Amino Acids; Arginine; Cystine; Female; Humans; Infant; Infant, Newborn; Intestinal Absorption; Lysine; Malabsorption Syndromes; Ornithine | 1976 |
Carbohydrate intolerance in gonadal dysgenesis: evidence for insulin resistance and hyperglucagonemia.
Topics: Adolescent; Adult; Aging; Arginine; Blood Glucose; Body Weight; Child; Glucagon; Glucose Tolerance Test; Gonadal Dysgenesis; Growth Hormone; Humans; Insulin; Insulin Resistance; Malabsorption Syndromes; Male; Obesity; Tolbutamide | 1985 |
Malabsorption in C57 mice experimentally infected with Johne's disease.
Topics: Animals; Arginine; Body Weight; Cecum; Female; Galactose; Glucose; Hexoses; Histidine; Intestinal Absorption; Intestine, Large; Intestine, Small; Malabsorption Syndromes; Male; Mice; Mice, Inbred Strains; Mycobacterium Infections; Organ Size; Paratuberculosis; Proteins; Rectum; Water | 1971 |
The use of L-arginine and sodium bicarbonate in the treatment of malabsorption due to cystic fibrosis.
Topics: Adolescent; Adult; Arginine; Bicarbonates; Body Weight; Carotenoids; Child; Cystic Fibrosis; Duodenum; Fats; Feces; Humans; Intestinal Secretions; Malabsorption Syndromes; Nitrogen; Pancreatic Extracts; Peptide Hydrolases; Sodium | 1972 |
The effect of unabsorbed sucrose- or mannitol-induced accelerated transit on absorption in the human small intestine.
Topics: Arginine; Child, Preschool; Female; Humans; Infant; Intestinal Absorption; Intestine, Small; Malabsorption Syndromes; Mannitol; Mathematics; Methods; Palmitic Acids; Perfusion; Sucrose; Time Factors; Xylose | 1969 |
Congenital lysinuria: a new inherited transport disorder of dibasic amino acids.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Arginine; Biological Transport; Child; Chromatography, Thin Layer; Consanguinity; Cystine; Cystinuria; Diarrhea; Female; Growth; Humans; Intellectual Disability; Lysine; Malabsorption Syndromes; Ornithine; Renal Aminoacidurias; Vomiting | 1970 |