lysine has been researched along with Abnormalities, Congenital in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Afenjar, A; Banka, S; Barish, S; Bellen, HJ; Blyth, M; Choufani, S; Costain, G; Cytrynbaum, C; Deshwar, AR; Haldeman-Englert, C; Hayes, I; Haynes, D; Huang, Y; Jobling, R; Kanca, O; Keren, B; Le Quesne Stabej, P; Mao, X; Mignot, C; Nil, Z; Prescott, T; Robin-Renaldo, F; Shinawi, M; Sisco, K; Tveten, K; Vøllo, A; Wangler, MF; Wegner, DJ; Weksberg, R; Wheeler, PG; Wilson, C; Yamamoto, S; Yap, P; Zhang, X; Zon, J | 1 |
| Alaee, F; Bowcock, AM; Desruisseau, DM; Dobbs, MB; Gurnett, CA; Hecht, JT; Kruse, LM; Wise, CA | 1 |
| Eriksson, UJ; Gittenberger-de Groot, AC; Molin, DG; Roest, PA; Schalkwijk, CG; van Iperen, L; Wentzel, P | 1 |
| Escobedo, JO; Lim, S; Samoei, GK; Sibrian-Vazquez, M; Strongin, RM | 1 |
| Fujimoto, M; Fukami, M; Hasegawa, T; Koitabashi, Y; Ogata, T; Soneda, S | 1 |
| Hayde, M; Lischka, A; Pollak, A; Salzer, HR | 1 |
6 other study(ies) available for lysine and Abnormalities, Congenital
| Article | Year |
|---|---|
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.
Topics: Congenital Abnormalities; Developmental Disabilities; Drosophila; Drosophila Proteins; Gain of Function Mutation; Histone-Lysine N-Methyltransferase; Histones; Humans; Lysine; Methylation; Methyltransferases; Neoplasms | 2023 |
Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation.
Topics: Alleles; Amino Acid Sequence; Amino Acid Substitution; Case-Control Studies; Chromosome Mapping; Chromosomes, Human, Pair 5; Congenital Abnormalities; Conserved Sequence; Female; Gene Frequency; Genes, Dominant; Genetic Linkage; Genetic Markers; Haplotypes; Heterozygote; Humans; Lod Score; Lower Extremity Deformities, Congenital; Lysine; Male; Models, Molecular; Molecular Sequence Data; Mutation; Mutation, Missense; Paired Box Transcription Factors; Pedigree; Polymorphism, Single Nucleotide; Radiography; Transcription Factors | 2008 |
Specific local cardiovascular changes of Nepsilon-(carboxymethyl)lysine, vascular endothelial growth factor, and Smad2 in the developing embryos coincide with maternal diabetes-induced congenital heart defects.
Topics: Animals; Congenital Abnormalities; Disease Models, Animal; Embryo, Mammalian; Female; Glycation End Products, Advanced; Heart Defects, Congenital; Humans; Infant, Newborn; Lysine; Pregnancy; Pregnancy in Diabetics; Rats; Rats, Sprague-Dawley; Risk Factors; Smad2 Protein; Vascular Endothelial Growth Factor A; Wound Healing | 2009 |
Homocystamides promote free-radical and oxidative damage to proteins.
Topics: Alzheimer Disease; Cardiovascular Diseases; Congenital Abnormalities; Free Radicals; Homocysteine; Humans; Hydrogen Bonding; Kinetics; Lysine; Osteoporosis; Oxidative Stress; Protein Processing, Post-Translational; Renal Insufficiency; Serum Albumin | 2010 |
Association of micropenis with Pro185Ala polymorphism of the gene for aryl hydrocarbon receptor repressor involved in dioxin signaling.
Topics: Adolescent; Alanine; Arginine; Basic Helix-Loop-Helix Transcription Factors; Case-Control Studies; Child; Child, Preschool; Congenital Abnormalities; Dioxins; Gene Frequency; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Lysine; Male; Penis; Polymorphism, Genetic; Proline; Receptors, Aryl Hydrocarbon; Repressor Proteins; Signal Transduction | 2005 |
Non-enzymatic glycation of fetal tissue in diabetic pregnancy. Estimation of the glucitollysine content of umbilical cord extracts.
Topics: Adult; Congenital Abnormalities; Female; Humans; Infant, Newborn; Lysine; Pregnancy; Pregnancy in Diabetics; Umbilical Cord | 1988 |