Page last updated: 2024-08-17

lysine and Abnormalities, Autosome

lysine has been researched along with Abnormalities, Autosome in 13 studies

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19909 (69.23)18.7374
1990's1 (7.69)18.2507
2000's3 (23.08)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Carvalho, MA; Dapic, V; Galán-Caridad, JM; Melendez, J; Monteiro, AN; Rios-Doria, J; Velkova, A1
Sakaguchi, A; Steward, R1
Bongiorni, S; Pasqualini, B; Prantera, G; Singh, PB; Taranta, M1
Ezquieta Zubicaray, B; González Gancedo, P; Gracia Bouthelier, R; Iguacel, AO; Jariego Fente, CM; Varela Junquera, JM1
Cohen-Solal, M; Creyssel, R; Delphin, D; Gaillard, L; Rosa, J1
Friedman, M; MacGregor, JT; Tucker, JD; Wehr, CM; Wilson, RE; Ziderman, II1
Cotton, RG; Milstein, C; Secher, DS1
Lichtenstein, JR; Martin, GR; McKusick, VA; Nigra, TP; Sussman, M1
Blouquit, Y; Cohen-Solal, M; Creyssel, R; Gaillard, L; Garel, MC; Gibaud, A; Rosa, J; Thillet, J1
Leder, P1
Colombo, JP1
Dayras, JC; Lejeune, J; See, G1
Daniel, WL1

Reviews

2 review(s) available for lysine and Abnormalities, Autosome

ArticleYear
The elongation reactions in protein synthesis.
    Advances in protein chemistry, 1973, Volume: 27

    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.
    Monographs in paediatrics, 1971, Volume: 1

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Brain; Chromosome Aberrations; Fetus; Humans; Liver; Lysine; Metabolism, Inborn Errors; Urea

1971

Other Studies

11 other study(ies) available for lysine and Abnormalities, Autosome

ArticleYear
Ectopic expression of histone H2AX mutants reveals a role for its post-translational modifications.
    Cancer biology & therapy, 2009, Volume: 8, Issue:5

    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.
    The Journal of cell biology, 2007, Jan-15, Volume: 176, Issue:2

    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.
    Journal of cell science, 2007, Mar-15, Volume: 120, Issue:Pt 6

    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].
    Medicina clinica, 1999, Mar-06, Volume: 112, Issue:8

    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)].
    Pediatrie, 1975, Volume: 30, Issue:2

    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.
    Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 1989, Volume: 27, Issue:11

    Topics: Animals; Bone Marrow; Chromosome Aberrations; Cricetinae; Female; Fructose; Lysine; Maillard Reaction; Male; Mice; Micronucleus Tests; Mutagenicity Tests; Salmonella typhimurium

1989
Variability of immunoglobulins.
    Annales d'immunologie, 1974, Volume: 125C, Issue:1-2

    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.
    The Journal of bone and joint surgery. American volume, 1974, Volume: 56, Issue:6

    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.
    Biochimica et biophysica acta, 1974, Jun-07, Volume: 351, Issue:2

    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].
    Annales de pediatrie, 1970, Nov-02, Volume: 17, Issue:11

    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.
    American journal of mental deficiency, 1971, Volume: 75, Issue:6

    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