phenylalanine has been researched along with Amino Acid Transport Disorder, Neutral in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (86.67) | 18.7374 |
| 1990's | 2 (13.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ersser, RS; Seakins, JW | 1 |
| Dove, WF; Shedlovsky, A; Symula, DJ | 1 |
| Dove, WF; Guillery, EN; Shedlovsky, A; Symula, DJ | 1 |
| Asatoor, AM; Navab, F | 1 |
| Narayanan, HS; Rao, BS; Reddy, GN | 1 |
| Levy, HL | 2 |
| Silk, DB | 1 |
| Brown, DA; Gaha, TJ; McLeay, AC; Smith, A; Wilcken, B | 1 |
| Balda, BR; Lukacs, I | 1 |
| Milne, MD | 1 |
| Alpers, DH; Bartoscas, CS; Bixby, EM; Shih, VE; Thier, SO | 1 |
| Asatoor, AM; Bandoh, JK; Lant, AF; Milne, MD; Navab, F | 1 |
| Asatoor, AM; Cheng, B; Edwards, KD; Lant, AF; Matthews, DM; Milne, MD; Navab, F; Richards, AJ | 2 |
5 review(s) available for phenylalanine and Amino Acid Transport Disorder, Neutral
| Article | Year |
|---|---|
Genetic screening.
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine | 1973 |
Progress report. Peptide absorption in man.
Topics: Amino Acids; Betaine; Biological Transport, Active; Cystinuria; Dietary Proteins; Gelatin; Glycine; Hartnup Disease; Humans; Hydrolysis; Intestinal Absorption; Intestinal Mucosa; Kinetics; Methionine; Milk Proteins; Models, Biological; Nutritional Physiological Phenomena; Peptides; Phenylalanine; Structure-Activity Relationship | 1974 |
Neonatal screening for inborn errors of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Biological Assay; Chromatography, Paper; Evaluation Studies as Topic; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant, Newborn; Leucine; Maple Syrup Urine Disease; Mass Screening; Methionine; Methods; Phenylalanine; Phenylketonurias; Pregnancy; Tyrosine | 1974 |
[Molecular biologic aspects in dermatology demonstrated by some hereditary enzyme defects].
Topics: Albinism; Alkaptonuria; Anemia, Sickle Cell; Chromosomes; Hartnup Disease; Humans; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Models, Chemical; Molecular Biology; Phenylalanine; Phenylketonurias; Porphyrias; Skin Diseases; Tyrosine | 1968 |
Transport of amino acids and peptides in the gut and the kidney.
Topics: Adult; Alanine; Amino Acids; Animals; Biological Transport, Active; Digestive System; Glycine; Hartnup Disease; Histidine; Humans; Hydrolysis; Intestinal Absorption; Kidney; Kidney Tubules; Leucine; Lysine; Methionine; Peptides; Phenylalanine; Proteins; Rats; Serine; Threonine; Tryptophan; Valine | 1971 |
10 other study(ies) available for phenylalanine and Amino Acid Transport Disorder, Neutral
| Article | Year |
|---|---|
Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.
Topics: Amino Acids; Hartnup Disease; Histidine; Humans; Infant, Newborn; Intestinal Absorption; Kidney Function Tests; Lysine; Male; Nicotinic Acids; Phenylalanine; Tyrosine | 1967 |
Genetic mapping of hph2, a mutation affecting amino acid transport in the mouse.
Topics: Animals; Biological Transport; Chromosome Mapping; Crosses, Genetic; Disease Models, Animal; Hartnup Disease; Humans; Mice; Mice, Inbred C57BL; Mutation; Phenylalanine | 1997 |
A candidate mouse model for Hartnup disorder deficient in neutral amino acid transport.
Topics: Animals; Biological Transport; Blood Glucose; Disease Models, Animal; Glycosuria; Hartnup Disease; Humans; Kidney; Mice; Phenylalanine | 1997 |
Studies on intestinal absorption of amino acids and a dipeptide in a case of Hartnup disease.
Topics: Adult; Alanine; Amino Acids; Chromatography, Paper; Dipeptides; Female; Hartnup Disease; Histidine; Humans; Intestinal Absorption; Intestine, Small; Niacinamide; Phenylalanine; Radiography; Tryptophan | 1970 |
A clinical and biochemical survey of 729 cases of mental subnormality.
Topics: Angiomatosis; Child; Child, Preschool; Congenital Hypothyroidism; Down Syndrome; Female; Hartnup Disease; Humans; India; Infant; Intellectual Disability; Laurence-Moon Syndrome; Lipidoses; Male; Marfan Syndrome; Microcephaly; Mucopolysaccharidoses; Phenylalanine; Phenylketonurias; Sex Factors; Syphilis, Congenital | 1971 |
Screening for metabolic diseases in New South Wales.
Topics: Australia; Biological Assay; Chromatography, Paper; Cystathionine; Cystinuria; Female; Hartnup Disease; Homocystinuria; Humans; Infant, Newborn; Male; Mass Screening; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Seasons | 1973 |
Studies of intestinal transport defect in Hartnup disease.
Topics: Adolescent; Biological Transport; Carbon Isotopes; Child; Culture Techniques; Feces; Genes, Recessive; Hartnup Disease; Humans; Intellectual Disability; Intestinal Mucosa; Jejunum; Leucine; Lysine; Male; Methionine; Phenylalanine; Proline; Tryptophan | 1971 |
Absorption of amino acids and the dipeptide, carnosine, from the gut in normal subjects and a case of Hartnup disease.
Topics: Alanine; Amino Acids; Dipeptides; Hartnup Disease; Histidine; Humans; Intestinal Absorption; Phenylalanine | 1969 |
Intestinal absorption of two dipeptides in Hartnup disease.
Topics: Adult; Animals; Dipeptides; Female; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Phenylalanine; Rats; Tryptophan | 1970 |
Intestinal absorption of dipeptides and corresponding free amino acids in Hartnup disease.
Topics: Amino Acids; Animals; Dipeptides; Glycine; Hartnup Disease; Humans; Intestinal Absorption; Intestine, Small; Phenylalanine; Rats; Tryptophan | 1970 |