sulfur has been researched along with Metabolism, Inborn Errors in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (70.00) | 18.7374 |
| 1990's | 2 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kožich, V; Stabler, S | 1 |
| Eto, Y; Numaguchi, S; Rennert, OM; Tahara, T | 1 |
| Armier, J; Benoit, A; Marionnet, C; Quilliet, X; Sarasin, A; Stary, A | 1 |
| Alapetite, C; Benoit, A; Moustacchi, E; Sarasin, A | 1 |
| Abroms, IF; Carney, M; Cloherty, JP; Johnson, JL; Mandell, R; Rajagopalan, KV; Robb, RM; Shih, VE | 1 |
| Mudd, SH | 1 |
| Rüdiger, HW; Wöhler, W | 1 |
| Barthélémy, JP; Bousquet, B; Civatte, J; Dreux, C; Larregue, M | 1 |
| Bernard, JF; Boivin, P; Tursz, T; Verdier, F | 1 |
2 review(s) available for sulfur and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism.
Topics: Amino Acids, Sulfur; Animals; Brain Diseases; Cysteine; Glutathione; Homocysteine; Homocystinuria; Humans; Hydrogen Sulfide; Liver; Metabolic Diseases; Metabolism, Inborn Errors; Methionine; Methionine Adenosyltransferase; Methylation; S-Adenosylmethionine; Sulfites; Sulfur; Sulfur Compounds | 2020 |
Diseases of sulphur metabolism: implications for the methionine-homocysteine cycle, and vitamin responsiveness.
Topics: Adolescent; Cystathionine beta-Synthase; Homocysteine; Homocystinuria; Humans; Metabolism, Inborn Errors; Methionine; Methylation; Pyridoxine; Sulfur | 1979 |
8 other study(ies) available for sulfur and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo.
Topics: Cells, Cultured; Fibroblasts; Humans; Metabolism, Inborn Errors; Sulfatases; Sulfur | 1980 |
Recovery of normal DNA repair and mutagenesis in trichothiodystrophy cells after transduction of the XPD human gene.
Topics: Cell Line, Transformed; Colony-Forming Units Assay; DNA Helicases; DNA Repair; DNA-Binding Proteins; Fibroblasts; Genetic Complementation Test; Hair Diseases; Humans; Intellectual Disability; Metabolism, Inborn Errors; Mutagenesis; Photosensitivity Disorders; Protein Biosynthesis; Proteins; Recombinant Fusion Proteins; Sulfur; Transcription Factors; Transfection; Ultraviolet Rays; Xeroderma Pigmentosum; Xeroderma Pigmentosum Group D Protein | 1996 |
The comet assay as a repair test for prenatal diagnosis of Xeroderma pigmentosum and trichothiodystrophy.
Topics: Cells, Cultured; DNA Damage; DNA Repair; Electrophoresis; Female; Fetus; Hair Diseases; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Microscopy, Fluorescence; Pregnancy; Prenatal Diagnosis; Sulfur; Ultraviolet Rays; Xeroderma Pigmentosum | 1997 |
Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism.
Topics: Amino Acids, Sulfur; Child, Preschool; Cysteine; Hemiplegia; Humans; Lens Subluxation; Male; Metabolism, Inborn Errors; Methionine; Oxidoreductases; Sulfites; Sulfur | 1977 |
Sulphur in biology. General discussion.
Topics: Animals; Biological Transport; Energy Metabolism; Escherichia coli; Iron-Sulfur Proteins; Liver; Metabolism, Inborn Errors; Methionine; Oxidation-Reduction; Salmonella typhimurium; Sulfates; Sulfides; Sulfur; Thiobacillus; Thiosulfate Sulfurtransferase; Thiosulfates | 1979 |
[Prenatal diagnosis of metabolic abnormalities in cell cultures (author's transl)].
Topics: Amniotic Fluid; Autoradiography; Carbon Dioxide; Carbon Radioisotopes; Cell Line; Cells, Cultured; Culture Media; Cytodiagnosis; Female; Fibroblasts; Galactose; Galactosemias; Humans; Lesch-Nyhan Syndrome; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Mucopolysaccharidoses; Pregnancy; Prenatal Diagnosis; Sulfur | 1975 |
[Pellagroid syndrome with vitamin B6 deficiency. Biological and clinical study of a case].
Topics: Amino Acids; Cystine; Humans; Indoleacetic Acids; Liver Cirrhosis; Male; Metabolism, Inborn Errors; Methionine; Middle Aged; Pellagra; Serotonin; Sulfur; Taurine; Tryptophan; Vitamin B 6 Deficiency; Xanthurenates | 1972 |
[Sulfhemoglobin and glutathione peroxidase deficiency].
Topics: Acetanilides; Cyanosis; Erythrocytes; Female; Glutathione; Humans; Metabolism, Inborn Errors; Middle Aged; Peroxidases; Phenacetin; Sulfhemoglobin; Sulfhemoglobinemia; Sulfur; Thiosulfates | 1974 |