lysine has been researched along with Abnormalities, Autosome in 13 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 9 (69.23) | 18.7374 |
1990's | 1 (7.69) | 18.2507 |
2000's | 3 (23.08) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Carvalho, MA; Dapic, V; Galán-Caridad, JM; Melendez, J; Monteiro, AN; Rios-Doria, J; Velkova, A | 1 |
Sakaguchi, A; Steward, R | 1 |
Bongiorni, S; Pasqualini, B; Prantera, G; Singh, PB; Taranta, M | 1 |
Ezquieta Zubicaray, B; González Gancedo, P; Gracia Bouthelier, R; Iguacel, AO; Jariego Fente, CM; Varela Junquera, JM | 1 |
Cohen-Solal, M; Creyssel, R; Delphin, D; Gaillard, L; Rosa, J | 1 |
Friedman, M; MacGregor, JT; Tucker, JD; Wehr, CM; Wilson, RE; Ziderman, II | 1 |
Cotton, RG; Milstein, C; Secher, DS | 1 |
Lichtenstein, JR; Martin, GR; McKusick, VA; Nigra, TP; Sussman, M | 1 |
Blouquit, Y; Cohen-Solal, M; Creyssel, R; Gaillard, L; Garel, MC; Gibaud, A; Rosa, J; Thillet, J | 1 |
Leder, P | 1 |
Colombo, JP | 1 |
Dayras, JC; Lejeune, J; See, G | 1 |
Daniel, WL | 1 |
2 review(s) available for lysine and Abnormalities, Autosome
Article | Year |
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The elongation reactions in protein synthesis.
Topics: Alanine; Amino Acyl-tRNA Synthetases; Bacterial Proteins; Binding Sites; Chromosome Aberrations; Lysine; Methionine; Models, Biological; Peptide Chain Elongation, Translational; Peptide Elongation Factors; Peptide Initiation Factors; Protein Binding; Protein Biosynthesis; Puromycin; Ribosomes; RNA, Bacterial; RNA, Messenger; RNA, Transfer | 1973 |
Congenital disorders of the urea cycle and ammonia detoxication.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Brain; Chromosome Aberrations; Fetus; Humans; Liver; Lysine; Metabolism, Inborn Errors; Urea | 1971 |
11 other study(ies) available for lysine and Abnormalities, Autosome
Article | Year |
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Ectopic expression of histone H2AX mutants reveals a role for its post-translational modifications.
Topics: Amino Acid Substitution; Apoptosis; Blotting, Western; Cell Cycle; Cell Line; Chromosome Aberrations; Fluorescent Antibody Technique; Green Fluorescent Proteins; HCT116 Cells; HeLa Cells; Histones; Humans; Immunoprecipitation; Lysine; Mutation; Phosphorylation; Proteasome Endopeptidase Complex; Protein Processing, Post-Translational; Recombinant Fusion Proteins; Serine; Transfection; Ubiquitination | 2009 |
Aberrant monomethylation of histone H4 lysine 20 activates the DNA damage checkpoint in Drosophila melanogaster.
Topics: Anaphase-Promoting Complex-Cyclosome; Animals; Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome; Brain; Cell Cycle; Cell Cycle Proteins; Checkpoint Kinase 1; Chromosome Aberrations; Cyclin B; DNA Breaks, Double-Stranded; DNA Damage; Down-Regulation; Drosophila melanogaster; Drosophila Proteins; Histone-Lysine N-Methyltransferase; Histones; Lysine; Methylation; Mitosis; Mutation; Neurons; Protein Kinases; Protein Serine-Threonine Kinases; Ubiquitin-Protein Ligase Complexes | 2007 |
Epigenetic regulation of facultative heterochromatinisation in Planococcus citri via the Me(3)K9H3-HP1-Me(3)K20H4 pathway.
Topics: Animals; Chromosome Aberrations; Embryo, Nonmammalian; Epigenesis, Genetic; Genomic Imprinting; Hemiptera; Heterochromatin; Histones; Insect Proteins; Lysine; Male; Metaphase; Methylation; Nuclear Proteins; RNA, Double-Stranded; Signal Transduction | 2007 |
[Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population].
Topics: Achondroplasia; Arginine; Asparagine; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 4; Genetic Counseling; Glycine; Humans; Lysine; Osteochondrodysplasias; Phenotype; Point Mutation; Protein-Tyrosine Kinases; Receptors, Fibroblast Growth Factor; RNA, Transfer, Amino Acid-Specific; Spain | 1999 |
[Lyon hemoglobin: discovery of an abnormal hemoglobin due to deletion of aminoacids (beta 17-18 (A 14-15) lys-val equals 0)].
Topics: Adolescent; Amino Acid Sequence; Anemia, Hypochromic; Blood Protein Electrophoresis; Chromatography; Chromosome Aberrations; Genes, Dominant; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Kinetics; Lysine; Male; Mutation; Oxygen; Valine | 1975 |
Non-clastogenicity in mouse bone marrow of fructose/lysine and other sugar/amino acid browning products with in vitro genotoxicity.
Topics: Animals; Bone Marrow; Chromosome Aberrations; Cricetinae; Female; Fructose; Lysine; Maillard Reaction; Male; Mice; Micronucleus Tests; Mutagenicity Tests; Salmonella typhimurium | 1989 |
Variability of immunoglobulins.
Topics: Amino Acid Sequence; Animals; Antibody-Producing Cells; Autoradiography; Biological Evolution; Chromosome Aberrations; Clone Cells; Culture Techniques; Epitopes; Genes; Genetic Variation; Humans; Hybrid Cells; Immunoglobulins; Isoelectric Focusing; Lysine; Mice; Molecular Conformation; Multiple Myeloma; Mutation; Myeloma Proteins; Rats; Species Specificity | 1974 |
Hydroxylysine-deficient skin collagen in a patient with a form of the Ehlers-Danlos syndrome.
Topics: Chromosome Aberrations; Chromosome Disorders; Collagen Diseases; Ehlers-Danlos Syndrome; Female; Fibroblasts; Genes, Recessive; Humans; Hydroxylysine; Ketoglutaric Acids; Lysine; Male; Middle Aged; Mixed Function Oxygenases; Pedigree; Procollagen-Proline Dioxygenase | 1974 |
Haemoglobin Lyon (beta17-18 (A 14-15) Lys-Val leads to O). Determination by sequenator analysis.
Topics: Amino Acid Sequence; Amino Acids; Blood Protein Electrophoresis; Cellulose; Chloromercuribenzoates; Chromatography, Gas; Chromatography, Ion Exchange; Chromatography, Thin Layer; Chromosome Aberrations; Female; France; Hemoglobins, Abnormal; Humans; Lysine; Male; Microchemistry; Oxyhemoglobins; Pedigree; Peptide Fragments; Protein Binding; Trypsin; Valine | 1974 |
[Cystinuria-lysinuria with dwarfism, facial dysmorphy, muscle hypoplasia and psychomotor retardation].
Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Consanguinity; Cystinuria; Dwarfism; Face; Female; Humans; Infant; Karyotyping; Lysine; Muscular Diseases; Pedigree; Psychomotor Disorders | 1970 |
A genetic and biochemical investigation of primary microcephaly.
Topics: Adult; Blood Proteins; Chromosome Aberrations; Chromosomes, Human, 1-3; Chromosomes, Human, 16-18; Female; Humans; Leucine; Lysine; Male; Metabolism, Inborn Errors; Microcephaly; Pregnancy; Proteins | 1971 |