Page last updated: 2024-08-17

lysine and Chromosome Deletion

lysine has been researched along with Chromosome Deletion in 19 studies

Research

Studies (19)

TimeframeStudies, this research(%)All Research%
pre-19903 (15.79)18.7374
1990's10 (52.63)18.2507
2000's1 (5.26)29.6817
2010's4 (21.05)24.3611
2020's1 (5.26)2.80

Authors

AuthorsStudies
de Vries, BBA; Devilee, L; Frega, M; Gabriele, M; Hommersom, M; Klein Gunnewiek, TM; Koolen, DA; Lewerissa, EI; Linda, K; Nadif Kasri, N; Oudakker, A; Schoenmaker, C; Schubert, D; Testa, G; Ulferts, E; van Bokhoven, H; Verboven, AHA1
Benevento, M; Dubos, A; Feil, R; Habibi, E; Herault, Y; Iacono, G; Kasri, NN; Kleefstra, T; Mandoli, A; Méziane, H; Riet, F; Selloum, M; Stunnenberg, HG; van Bokhoven, H; Zhou, H1
Cao, Q; Chen, GJ; Cheng, J; Lin, L; Liu, A; Ma, K; Matas, E; Wang, W; Wang, X; Wang, ZJ; Wei, J; Yan, Z; Zhang, F; Zheng, Y1
Farina, A; Gurvich, N; Hurwitz, J; Menendez, S; Nimer, SD; Perna, F; Voza, F1
Arai, M; Arinami, T; Ichikawa, T; Itokawa, M; Iwayama, Y; Maekawa, M; Miyashita, M; Toyosima, M; Toyota, T; Yoshikawa, T1
Christensen, E; de Koning, TJ; Dorland, L; Hoffmann, GF; Knerr, I; Müller, P; Rascher, W; Trautmann, U; Trefz, FK; Wündisch, GF; Zschocke, J1
Assmann, G; Fielding, CJ; Haas, J; Mahley, RW; Menzel, HJ; Ogawa, Y; Rall, SC; Steinmetz, A; Utermann, G; Weisgraber, KH1
Andria, G; Borsani, G; Castaldo, P; Incerti, B; Rossi, E; Sebastio, G; Sperandeo, MP; Taglialatela, M; Zollo, M; Zuffardi, O1
Ashford, AJ; Dobberstein, B; High, S; Lütcke, H; Römisch, K1
Hirata, H; Kagawa, Y; Kawamura, M; Mutoh, Y; Nakanishi, M; Noguchi, S; Ohta, T1
Costa, FF; Sonati, MF; Zago, MA1
Andresen, BS; Bross, P; Christensen, E; Engst, S; Gregersen, N; Kelly, D; Kølvraa, S; Rüdiger, N; Strauss, AW; Winter, V1
Megee, PC; Mittman, BA; Morgan, BA; Smith, MM1
Davis, AE; Kramer, J; Parad, RB; Rosen, FS; Strunk, RC1
de Murcia, G; Gradwohl, G; Keith, G; Ménissier-de Murcia, J; Molinete, M; Muller, S; Penning, C; Poch, O; Simonin, F1
Asada, M; Hasegawa, Y; Iijima, A; Kitoh, K; Nagasu, T; Shikata, Y; Wakabayashi, T1
Higgins, E; Laughrea, M1
Chuang, J; Jentoft, J; Smith, LM; Zull, JE1
Gorinchuk, GF; Maliuta, SS; Shevchenko, TN; Timashova, EO1

Other Studies

19 other study(ies) available for lysine and Chromosome Deletion

ArticleYear
Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders.
    Autophagy, 2022, Volume: 18, Issue:2

    Topics: Abnormalities, Multiple; Autophagosomes; Autophagy; Chromosome Deletion; Chromosomes, Human, Pair 17; Epigenesis, Genetic; Humans; Intellectual Disability; Lysine; Lysosomes; Reactive Oxygen Species; Sirolimus; Superoxide Dismutase-1; TOR Serine-Threonine Kinases

2022
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome.
    Nucleic acids research, 2018, 06-01, Volume: 46, Issue:10

    Topics: Animals; Animals, Newborn; Cadherins; Chromosome Deletion; Chromosomes, Human, Pair 9; Cognitive Dysfunction; Craniofacial Abnormalities; Disease Models, Animal; Gene Expression Regulation; Heart Defects, Congenital; Hippocampus; Histone-Lysine N-Methyltransferase; Histones; Intellectual Disability; Lysine; Male; Methylation; Mice, Knockout

2018
Inhibition of EHMT1/2 rescues synaptic and cognitive functions for Alzheimer's disease.
    Brain : a journal of neurology, 2019, 03-01, Volume: 142, Issue:3

    Topics: Alzheimer Disease; Animals; Chromosome Deletion; Cognition; Cognition Disorders; Cognitive Dysfunction; Disease Models, Animal; DNA Methylation; Epigenesis, Genetic; Hippocampus; Histocompatibility Antigens; Histone-Lysine N-Methyltransferase; Histones; Humans; Lysine; Memory Disorders; Methylation; Mice; Mice, Transgenic; Prefrontal Cortex; Synapses

2019
L3MBTL1 polycomb protein, a candidate tumor suppressor in del(20q12) myeloid disorders, is essential for genome stability.
    Proceedings of the National Academy of Sciences of the United States of America, 2010, Dec-28, Volume: 107, Issue:52

    Topics: Blotting, Western; Cell Cycle; Cell Line; Cell Line, Tumor; Cell Proliferation; Chromosomal Proteins, Non-Histone; Chromosome Deletion; Chromosomes, Human, Pair 20; DNA Damage; DNA Replication; Genomic Instability; HEK293 Cells; Histones; Humans; Immunoprecipitation; K562 Cells; Lysine; Methylation; Myeloproliferative Disorders; Neoplasm Proteins; Protein Binding; Repressor Proteins; Retinoblastoma Protein; RNA Interference; Tumor Suppressor Proteins

2010
Schizophrenia with the 22q11.2 deletion and additional genetic defects: case history.
    The British journal of psychiatry : the journal of mental science, 2011, Volume: 199, Issue:3

    Topics: Adult; Arginine; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Exotropia; Female; Frameshift Mutation; Genetic Predisposition to Disease; Homeodomain Proteins; Humans; Lactoylglutathione Lyase; Lysine; Polymerase Chain Reaction; Schizophrenia; Transcription Factors

2011
Glutaric aciduria type III: a distinctive non-disease?
    Journal of inherited metabolic disease, 2002, Volume: 25, Issue:6

    Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chromosome Deletion; Diarrhea; Fasting; Female; Glutarates; Humans; Liver; Lysine; Male; Pipecolic Acids; Riboflavin

2002
Abnormal lecithin:cholesterol acyltransferase activation by a human apolipoprotein A-I variant in which a single lysine residue is deleted.
    The Journal of biological chemistry, 1984, Aug-25, Volume: 259, Issue:16

    Topics: Adult; Amino Acids; Apolipoprotein A-I; Apolipoproteins; Chromosome Deletion; Enzyme Activation; Female; Genetic Variation; Humans; Lipoproteins, HDL; Lysine; Male; Middle Aged; Pedigree; Peptide Fragments; Phosphatidylcholine-Sterol O-Acyltransferase; Protein Conformation

1984
The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome.
    Genomics, 1998, Apr-15, Volume: 49, Issue:2

    Topics: Abnormalities, Multiple; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acid Sequence; Amino Acid Transport Systems, Basic; Animals; Blotting, Northern; Carrier Proteins; Chromosome Deletion; Chromosome Mapping; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Dinucleotide Repeats; Female; Humans; Lysine; Membrane Proteins; Molecular Sequence Data; Oocytes; Sequence Analysis, DNA; Syndrome; Tetralogy of Fallot; Velopharyngeal Insufficiency; Xenopus

1998
The methionine-rich domain of the 54 kDa subunit of signal recognition particle is sufficient for the interaction with signal sequences.
    The EMBO journal, 1992, Volume: 11, Issue:4

    Topics: Animals; Azirines; Benzoates; Binding Sites; Cell-Free System; Chromosome Deletion; Cross-Linking Reagents; Cycloheximide; Lysine; Macromolecular Substances; Methionine; Molecular Weight; Prolactin; Protein Biosynthesis; Protein Precursors; Protein Sorting Signals; Ribonucleoproteins; Ribosomes; Signal Recognition Particle; Transcription, Genetic

1992
The 'lysine cluster' in the N-terminal region of Na+/K(+)-ATPase alpha-subunit is not involved in ATPase activity.
    Biochimica et biophysica acta, 1991, Aug-23, Volume: 1059, Issue:2

    Topics: Adenosine Triphosphatases; Amino Acid Sequence; Animals; Base Sequence; Chromosome Deletion; Kidney; Lysine; Microsomes; Molecular Sequence Data; Plasmids; Ranidae; Sequence Homology, Nucleic Acid; Sodium-Potassium-Exchanging ATPase; Torpedo; Xenopus

1991
Hemoglobin Stanleyville II (alpha 78 Asn----Lys) is associated with a 3.7-kb alpha-globin gene deletion.
    Human genetics, 1991, Volume: 86, Issue:3

    Topics: Asparagine; Chromosome Deletion; Chromosome Mapping; DNA; Female; Genetic Carrier Screening; Globins; Hemoglobins, Abnormal; Homozygote; Humans; Leukocytes; Lysine; Male; Polymorphism, Restriction Fragment Length

1991
Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli.
    Human genetics, 1991, Volume: 86, Issue:6

    Topics: Acyl-CoA Dehydrogenases; Base Sequence; Blotting, Northern; Blotting, Western; Cells, Cultured; Chromosome Deletion; Cloning, Molecular; DNA; DNA Mutational Analysis; Escherichia coli; Female; Glutamine; Humans; Lysine; Male; Molecular Sequence Data; Mutation; Pedigree; Polymerase Chain Reaction; RNA, Messenger

1991
Genetic analysis of histone H4: essential role of lysines subject to reversible acetylation.
    Science (New York, N.Y.), 1990, Feb-16, Volume: 247, Issue:4944

    Topics: Acetylation; Alleles; Cell Cycle; Chromosome Deletion; Codon; Glutamine; Histones; Lysine; Mutation; Plasmids; Protein Processing, Post-Translational; Saccharomyces cerevisiae

1990
Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation site.
    Proceedings of the National Academy of Sciences of the United States of America, 1990, Volume: 87, Issue:17

    Topics: Amino Acid Sequence; Angioedema; Base Sequence; Cell-Free System; Chromosome Deletion; Complement C1 Inactivator Proteins; Electrophoresis, Polyacrylamide Gel; Glycosylation; Humans; Lysine; Molecular Sequence Data; Molecular Weight; Protein Biosynthesis; RNA, Messenger

1990
Expression and site-directed mutagenesis of the catalytic domain of human poly(ADP-ribose)polymerase in Escherichia coli. Lysine 893 is critical for activity.
    The Journal of biological chemistry, 1990, Nov-05, Volume: 265, Issue:31

    Topics: Amino Acid Sequence; Animals; Base Sequence; Cattle; Chromosome Deletion; Cloning, Molecular; Escherichia coli; Humans; Lysine; Molecular Sequence Data; Mutagenesis, Site-Directed; Oligonucleotide Probes; Poly(ADP-ribose) Polymerases; Recombinant Proteins; Sequence Homology, Nucleic Acid; Thymus Gland; Transcription, Genetic

1990
Deletion of lysine 84 to lysine 89 enhances the cytotoxicity and the receptor binding affinity of human lymphotoxin.
    The Journal of biological chemistry, 1990, May-05, Volume: 265, Issue:13

    Topics: Amino Acid Sequence; Animals; Cell Line; Cell Survival; Chromosome Deletion; Circular Dichroism; Cloning, Molecular; Escherichia coli; Genes; Genetic Vectors; Humans; Kinetics; Lymphotoxin-alpha; Lysine; Mice; Molecular Sequence Data; Mutation; Protein Conformation; Receptors, Cell Surface; Restriction Mapping; Sequence Homology, Nucleic Acid

1990
Delta Lys120, a mutation which destabilizes the ribosome-binding domain of ribosomal protein L7/L12.
    Biochemistry and cell biology = Biochimie et biologie cellulaire, 1990, Volume: 68, Issue:5

    Topics: Amino Acid Sequence; Ammonium Chloride; Base Sequence; Binding Sites; Centrifugation, Density Gradient; Chlorides; Chromosome Deletion; Cloning, Molecular; Electrophoresis; Escherichia coli; Ethanol; Lithium; Lithium Chloride; Lysine; Molecular Sequence Data; Mutation; Ribosomal Proteins; Ribosomes

1990
Deletion of lysine 13 alters the structure and function of parathyroid hormone.
    Molecular and cellular endocrinology, 1987, Volume: 51, Issue:3

    Topics: Amino Acid Sequence; Animals; Cattle; Chromatography, High Pressure Liquid; Chromosome Deletion; Cyanogen Bromide; Hydrogen-Ion Concentration; Lysine; Magnetic Resonance Spectroscopy; Parathyroid Hormone; Peptide Fragments; Protein Conformation; Structure-Activity Relationship

1987
[The induction of auxotrophic mutations for riboflavin by the integration of plasmid pLRS33 into the chromosome of Bacillus subtilis].
    Genetika, 1988, Volume: 24, Issue:8

    Topics: Bacillus subtilis; Chromosome Deletion; Chromosomes, Bacterial; DNA, Bacterial; Lysine; Mutation; Operon; Plasmids; Recombination, Genetic; Restriction Mapping; Riboflavin; Transformation, Bacterial

1988