cysteine has been researched along with Embryopathies in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (57.14) | 18.7374 |
| 1990's | 2 (28.57) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akdemir, ZC; Azamian, MS; Belmont, JW; Braxton, A; Chandarana, J; D'Alessandro, LC; Ding, Y; Eldomery, MK; Eng, CM; Gibbs, RA; Hanchard, NA; Harel, T; Holtzman, J; Jhangiani, SN; Kois, C; Lupski, JR; Miller, K; Muzny, DM; Rijhsinghani, A; Rosenfeld, JA; Sack, V; Shur, N; Vetrini, F; Yang, Y | 1 |
| MEEKER, IA | 1 |
| Bonaventure, J; Cetta, G; Delezoide, AL; Rossi, A; Superti-Furga, A | 1 |
| Brodie, SG; Kitoh, H; Lipson, M; Sifry-Platt, M; Wilcox, WR | 1 |
| Becker, FL; Garvin, AJ; Horger, EO; Jacobson, C; Kroll, WA; Pellett, OL; Schneider, JA; Spear, GS; Verroust, FM; Wong, VG | 1 |
| Bradley, KH; Schneider, JA; Schulman, JD; Seegmiller, JE | 1 |
| Ho, OL; Olney, JW; Rhee, V; Schainker, B | 1 |
7 other study(ies) available for cysteine and Embryopathies
| Article | Year |
|---|---|
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
Topics: Alleles; Amino Acid Motifs; Amino Acid Sequence; Animals; Caenorhabditis elegans; Cysteine; Exome; Female; Fetal Diseases; Functional Laterality; Heart Defects, Congenital; Heterotaxy Syndrome; Homozygote; Humans; Infant, Newborn; Introns; Male; Membrane Proteins; Mice; Middle Aged; Models, Molecular; Mutation; Mutation, Missense; Oryzias; Pedigree; RNA Splicing; Situs Inversus | 2016 |
ACETYLCYSTEINE USED TO LIQUEFY INSPISSATED MECONIUM CAUSING INTESTINAL OBSTRUCTION IN THE NEWBORN.
Topics: Acetylcysteine; Cysteine; Cystic Fibrosis; Fetal Diseases; Hernia, Umbilical; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intestinal Obstruction; Intestinal Perforation; Meconium; Peritonitis; Surgical Procedures, Operative | 1964 |
Undersulfation of cartilage proteoglycans ex vivo and increased contribution of amino acid sulfur to sulfation in vitro in McAlister dysplasia/atelosteogenesis type 2.
Topics: Anion Transport Proteins; Biological Transport; Carrier Proteins; Cells, Cultured; Chondrocytes; Chondroitin Sulfates; Chromatography, High Pressure Liquid; Chromatography, Ion Exchange; Cysteine; Disaccharides; Electrophoresis, Agar Gel; Fetal Diseases; Fetus; Growth Plate; Humans; Membrane Transport Proteins; Osteochondrodysplasias; Polymorphism, Restriction Fragment Length; Proteoglycans; Sulfate Transporters; Sulfates | 1997 |
Thanatophoric dysplasia type I with syndactyly.
Topics: Cysteine; Fetal Diseases; Humans; Male; Point Mutation; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Syndactyly; Thanatophoric Dysplasia; Tyrosine | 1998 |
Prenatal diagnosis of cystinosis.
Topics: Amniocentesis; Amniotic Fluid; Autoradiography; Cells, Cultured; Chromatography, Thin Layer; Crystallization; Cysteine; Cystine; Cystinosis; Electrophoresis, Paper; Female; Fetal Diseases; Fetus; Gestational Age; Humans; Kidney; Liver; Placenta; Pregnancy; Prenatal Diagnosis; Retina; Spleen; Thymus Gland | 1974 |
Cystine, cysteine, and glutathione metabolism in normal and cystinotic fibroblasts in vitro, and in cultured normal amniotic fluid cells.
Topics: Amniotic Fluid; Cells, Cultured; Cysteine; Cystine; Cystinosis; Female; Fetal Diseases; Fibroblasts; Glutathione; Half-Life; Heterozygote; Humans; Kinetics; Pregnancy; Skin; Sulfur Isotopes | 1972 |
Cysteine-induced brain damage in infant and fetal rodents.
Topics: Animals; Animals, Newborn; Brain; Brain Damage, Chronic; Cysteine; Female; Fetal Diseases; Maternal-Fetal Exchange; Mice; Nerve Degeneration; Pregnancy; Rats | 1972 |