glycine has been researched along with Embryopathies in 11 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "The X-linked form of Alport syndrome is associated with mutations in the COL4A5 gene encoding the alpha 5-chain of type IV collagen." | 1.29 | A nonsense mutation in the COL4A5 collagen gene in a family with X-linked juvenile Alport syndrome. ( Heiskari, N; Hertz, JM; Jensen, UB; Tryggvason, K; Zhou, J, 1995) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (27.27) | 18.7374 |
| 1990's | 5 (45.45) | 18.2507 |
| 2000's | 3 (27.27) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Paupe, A | 1 |
| Bidat, L | 1 |
| Sonigo, P | 1 |
| Lenclen, R | 1 |
| Molho, M | 1 |
| Ville, Y | 1 |
| Cheillan, D | 1 |
| Salomons, GS | 1 |
| Acquaviva, C | 1 |
| Boisson, C | 1 |
| Roth, P | 1 |
| Cordier, MP | 1 |
| François, L | 1 |
| Jakobs, C | 1 |
| Vianey-Saban, C | 1 |
| von Wendt, L | 1 |
| Similä, S | 1 |
| Ruokonen, A | 1 |
| Hartikainen-Sorri, AL | 1 |
| Williams, C | 1 |
| Mallard, C | 1 |
| Tan, W | 1 |
| Johnston, B | 1 |
| Gunn, A | 1 |
| Marks, K | 1 |
| Gluckman, P | 1 |
| Hertz, JM | 1 |
| Heiskari, N | 1 |
| Zhou, J | 1 |
| Jensen, UB | 1 |
| Tryggvason, K | 1 |
| Freisinger, P | 1 |
| Ala-Kokko, L | 1 |
| LeGuellec, D | 1 |
| Franc, S | 1 |
| Bouvier, R | 1 |
| Ritvaniemi, P | 1 |
| Prockop, DJ | 1 |
| Bonaventure, J | 1 |
| Ljubić, A | 1 |
| Cvetković, M | 1 |
| Sulović, V | 1 |
| Novakov, A | 1 |
| Kokai, D | 1 |
| Bujko, M | 1 |
| Jovanović, T | 1 |
| Vukolić, D | 1 |
| Ilas, J | 1 |
| Mühl, A | 1 |
| Stöckler-Ipsiroglu, S | 1 |
| Shigematsu, Y | 1 |
| Kikawa, Y | 1 |
| Sudo, M | 1 |
| Kanaoka, H | 1 |
| Fujioka, M | 1 |
| Dan, M | 1 |
| Cole, RJ | 1 |
| Regan, T | 1 |
| Tarbutt, RG | 1 |
| Mestyán, J | 1 |
| Fekete, M | 1 |
| Járai, I | 1 |
| Sulyok, E | 1 |
| Imhof, S | 1 |
| Soltész, G | 1 |
11 other studies available for glycine and Embryopathies
| Article | Year |
|---|---|
Prenatal diagnosis of hypoplasia of the corpus callosum in association with non-ketotic hyperglycinemia.
Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Amino Acid Metabolism, Inborn Errors; Electroe | 2002 |
Prenatal diagnosis of guanidinoacetate methyltransferase deficiency: increased guanidinoacetate concentrations in amniotic fluid.
Topics: Amniocentesis; Amniotic Fluid; Creatine; Female; Fetal Diseases; Gestational Age; Glycine; Guanidino | 2006 |
Problems of prenatal diagnosis of non-ketotic hyperglycinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Amniotic Fluid; Female; Fetal Diseases; Glycine | 1983 |
Perinatal brain injury. Pathophysiology and therapeutic intervention.
Topics: Animals; Animals, Newborn; Brain; Brain Injuries; Electroencephalography; Fetal Diseases; Flunarizin | 1995 |
A nonsense mutation in the COL4A5 collagen gene in a family with X-linked juvenile Alport syndrome.
Topics: Adult; Base Sequence; Chromosome Deletion; Collagen; DNA; DNA Primers; Exons; Female; Fetal Diseases | 1995 |
Mutation in the COL2A1 gene in a patient with hypochondrogenesis. Expression of mutated COL2A1 gene is accompanied by expression of genes for type I procollagen in chondrocytes.
Topics: Adult; Amino Acid Sequence; Base Sequence; Cartilage Diseases; Collagen; DNA; Electrophoresis, Polya | 1994 |
Essential and nonessential amino acids in appropriate and small for gestational age fetuses with congenital cytomegalovirus infection.
Topics: Cordocentesis; Cytomegalovirus Infections; Female; Fetal Blood; Fetal Diseases; Fetal Growth Retarda | 1997 |
Guanidinoacetate methyltransferase (GAMT) deficiency: non-invasive enzymatic diagnosis of a newly recognized inborn error of metabolism.
Topics: Amniotic Fluid; Cells, Cultured; Chromatography, High Pressure Liquid; Creatine; Female; Fetal Disea | 2000 |
Prenatal diagnosis of isovaleric acidemia by fast atom bombardment and tandem mass spectrometry.
Topics: Amniotic Fluid; Carnitine; Female; Fetal Diseases; Glycine; Hemiterpenes; Humans; Isovaleryl-CoA Deh | 1991 |
Haemoglobin synthesis in reticulocytes of prenatal f-f anaemic mice.
Topics: Anemia, Hypochromic; Animals; Carbon Isotopes; Female; Fetal Diseases; Genotype; Glycine; Heme; Hemo | 1972 |
The postnatal changes in the circulating free amino acid pool in the newborn infant. II. The plasma amino acid ratio in intrauterine malnutrition (small for dates' full-term, preterm and twin infants).
Topics: Amino Acids; Birth Weight; Chromatography, Paper; Female; Fetal Diseases; Gestational Age; Glutamine | 1969 |