phenylalanine has been researched along with Abnormalities, Autosome in 23 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 14 (60.87) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (26.09) | 29.6817 |
| 2010's | 3 (13.04) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Canella, L; Kudejova, P; Röhrmoser, A; Schmid, E; Schmid, TE; Wagner, FM | 1 |
| Ahring, K; Almeida, MF; Belanger-Quintana, A; Blau, N; Burlina, A; Cleary, M; Coskum, T; Dokoupil, K; Evans, S; Feillet, F; Giżewska, M; Gokmen Ozel, H; Kamieńska, E; Lammardo, AM; Lotz-Havla, AS; MacDonald, A; Maillot, F; Muntau, AC; Puchwein-Schwepcke, A; Robert, M; Rocha, JC; Santra, S; Skeath, R; Strączek, K; Trefz, FK; van Dam, E; van Rijn, M; van Spronsen, F; Vijay, S | 1 |
| Dal Cin, P; Hernandez, JM; Kuo, FC; Leon, A; Longtine, JA; Staropoli, JF | 1 |
| Hara, K; Nishizawa, M; Onodera, O; Shimohata, T; Takado, Y; Tokiguchi, S | 1 |
| Berciano, J; Combarros, O; Domínguez-Perles, R; Gallardo, E; García, A; García-Barredo, R; Illa, I; Infante, J | 1 |
| Finke, CM; Gangat, N; Ketterling, RP; Knudson, RA; Lasho, TL; Li, CY; Pardanani, A; Strand, J; Tefferi, A | 1 |
| Kakuda, H; Kasai, M; Tsukamoto, Y | 1 |
| Ackermann, J; Assmann, I; Drach, J; Hübl, W; Ludwig, H; Schuster-Kolbe, J; Strasser, K; Zojer, N | 1 |
| de Verneuil, H; Ged, C; Herrero, C; Lecha, M; Mascaro, JM; Mendez, M; Ozalla, D | 1 |
| Winokur, B | 1 |
| Gopalan, HN | 1 |
| Watanabe, S | 1 |
| Barbacid, M; Carrasco, L; Vazquez, D | 1 |
| Kaji, A; Otaka, T; Tanaka, S | 1 |
| Cabrer, B; Modolell, J; Vázquez, D | 1 |
| Spirin, AS | 1 |
| Kaji, A; Ranu, RS | 1 |
| Seller, MJ | 1 |
| Ishitsuka, H; Kaji, A | 1 |
| Grützner, IP; Spivey, BE; Yazawa, K | 1 |
| Göttinger, E | 1 |
| Gowans, CS; McBride, AC | 1 |
| Millington-Ward, AM | 1 |
2 review(s) available for phenylalanine and Abnormalities, Autosome
| Article | Year |
|---|---|
[Structural bases of ribosome functions].
Topics: Cell-Free System; Chromosome Aberrations; Magnesium; Molecular Biology; Nucleoproteins; Peptide Chain Elongation, Translational; Phenylalanine; Poly U; Protein Biosynthesis; Ribosomes; RNA, Ribosomal; RNA, Transfer | 1974 |
Heredity and strabismus.
Topics: Chromosome Aberrations; Chromosome Disorders; Diseases in Twins; Eye Abnormalities; Female; Genes, Dominant; Genes, Recessive; Genetics, Population; Humans; Male; Phenotype; Phenylalanine; Phenylketonurias; Pigmentation; Sex Factors; Strabismus; United States | 1970 |
21 other study(ies) available for phenylalanine and Abnormalities, Autosome
| Article | Year |
|---|---|
The effectiveness of the high-LET radiations from the boron neutron capture [10B(n,α) 7Li] reaction determined for induction of chromosome aberrations and apoptosis in lymphocytes of human blood samples.
Topics: Apoptosis; Borohydrides; Boron; Boron Compounds; Boron Neutron Capture Therapy; Chromosome Aberrations; Dose-Response Relationship, Radiation; Female; Humans; Isotopes; Linear Energy Transfer; Lithium; Lymphocytes; Male; Neutrons; Phenylalanine; Radiation-Sensitizing Agents; Sulfhydryl Compounds | 2015 |
The challenges of managing coexistent disorders with phenylketonuria: 30 cases.
Topics: Adolescent; Adult; Autoimmune Diseases; Biopterins; Child; Child, Preschool; Chromosome Aberrations; Consanguinity; Diet; Disease Management; Europe; Female; Gastrointestinal Diseases; Humans; Infant; Male; Phenylalanine; Phenylketonurias; Pregnancy; Retrospective Studies; Turkey | 2015 |
Translocation t(1;9) is a recurrent cytogenetic abnormality associated with progression of essential thrombocythemia patients displaying the JAK2 V617F mutation.
Topics: Aged; Aged, 80 and over; Amino Acid Substitution; Chromosome Aberrations; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 9; Cohort Studies; Disease Progression; Female; Humans; Janus Kinase 2; Male; Middle Aged; Mutation, Missense; Phenylalanine; Recurrence; Thrombocythemia, Essential; Translocation, Genetic; Valine | 2011 |
New mutation in the non-gigantic exon of SACS in Japanese siblings.
Topics: Adult; Amino Acid Substitution; Atrophy; Cerebellum; Chromosome Aberrations; Consanguinity; Exons; Female; Gait Ataxia; Genes, Recessive; Heat-Shock Proteins; Homozygote; Humans; Leucine; Male; Middle Aged; Mutation; Phenylalanine; Sequence Analysis, DNA; Siblings | 2007 |
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.
Topics: Adipose Tissue; Adult; Aged; Amino Acid Substitution; Atrophy; Biopsy; Chromosome Aberrations; Codon; Connectin; Creatine Kinase; Cytoskeletal Proteins; DNA Mutational Analysis; Electromyography; Exons; Female; Genes, Dominant; Genetic Carrier Screening; Humans; Leg; Magnetic Resonance Imaging; Male; Microfilament Proteins; Middle Aged; Muscle Proteins; Muscle Weakness; Muscle, Skeletal; Muscular Atrophy; Muscular Diseases; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; Neurologic Examination; Pedigree; Phenotype; Phenylalanine; Serine | 2008 |
Cytogenetic studies at diagnosis in polycythemia vera: clinical and JAK2V617F allele burden correlates.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; Bone Marrow Cells; Chromosome Aberrations; Disease-Free Survival; Female; Humans; Janus Kinase 2; Male; Middle Aged; Phenylalanine; Polycythemia Vera; Prognosis; Retrospective Studies; Valine | 2008 |
Construction of a Bacillus subtilis (natto) with high productivity of vitamin K2 (menaquinone-7) by analog resistance.
Topics: Alanine; Animals; Bacillus subtilis; Chromosome Aberrations; Cricetinae; Cricetulus; Drug Resistance, Bacterial; Food Industry; Genetic Engineering; Glycine max; Industrial Microbiology; Mutation; Naphthols; p-Fluorophenylalanine; Phenylalanine; Rats; Toxicity Tests; Vitamin K 2 | 2001 |
Chromosomal aberrations are shared by malignant plasma cells and a small fraction of circulating CD19+ cells in patients with myeloma and monoclonal gammopathy of undetermined significance.
Topics: Aged; Aged, 80 and over; Antigens, CD19; Bone Marrow Examination; Chromosome Aberrations; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 17; Clone Cells; Disease Progression; Disulfides; Gene Deletion; Genes, Immunoglobulin; Genes, p53; Genes, Retinoblastoma; Humans; Immunoglobulin G; Immunoglobulin Light Chains; Immunohistochemistry; In Situ Hybridization, Fluorescence; Membrane Glycoproteins; Middle Aged; Multiple Myeloma; Paraproteinemias; Phenylalanine; Plasma Cells; Polymerase Chain Reaction; Proteoglycans; RNA, Messenger; Syndecan-1; Syndecans; T-Lymphocytes | 2002 |
Description of a new mutation in hepatoerythropoietic porphyria and prenatal exclusion of a homozygous fetus.
Topics: Amino Acid Substitution; Child, Preschool; Chromosome Aberrations; Codon; Consanguinity; Female; Genes, Recessive; Genetic Carrier Screening; Homozygote; Humans; Leucine; Male; Mutation; Phenylalanine; Porphyria, Erythropoietic; Pregnancy; Prenatal Diagnosis; Uroporphyrinogen Decarboxylase | 2002 |
Subnormality and its relation to psychiatry.
Topics: Adult; Brain; Child; Child Development; Chromosome Aberrations; Chromosome Disorders; Homocystinuria; Humans; Intellectual Disability; Intelligence; Mental Disorders; Metabolism, Inborn Errors; Norepinephrine; Phenethylamines; Phenylalanine; Phenylketonurias; Psychoanalysis; Psychophysiologic Disorders; Psychotic Disorders; Schizophrenia; Serotonin; Sex Chromosome Aberrations | 1974 |
Amino acid induced changes of puffing patterns in Chironomus salivary gland chromosomes.
Topics: Amino Acids; Animals; Chromosome Aberrations; Chromosomes; Deoxyadenosines; Dinitrophenols; Diptera; DNA; Larva; Metamorphosis, Biological; Phenylalanine; Salivary Glands; Tritium; Tryptophan; Uridine | 1973 |
Interaction of siomycin with the acceptor site of Escherichia coli ribosomes.
Topics: Anti-Bacterial Agents; Binding Sites; Chromosome Aberrations; Escherichia coli; Magnesium; Peptides; Phenylalanine; Puromycin; Quaternary Ammonium Compounds; Ribosomes; RNA, Transfer; Tetracycline | 1972 |
The trichodermin group of antibiotics, inhibitors of peptide bond formation by eukaryotic ribosomes.
Topics: Anti-Bacterial Agents; Carbon Isotopes; Chromosome Aberrations; Fusarium; Humans; In Vitro Techniques; Kinetics; Leucine; Palatine Tonsil; Peptide Chain Elongation, Translational; Peptide Elongation Factors; Phenylalanine; Protein Binding; Ribosomes; RNA, Transfer; Saccharomyces cerevisiae; Terpenes; Tritium | 1973 |
Further studies on the mechanism of erythromycin action.
Topics: Acylation; Binding Sites; Carbon Isotopes; Carbon Radioisotopes; Centrifugation, Density Gradient; Chromosome Aberrations; Erythromycin; Escherichia coli; Fusidic Acid; Guanosine Triphosphate; Peptide Elongation Factors; Phenylalanine; Protein Binding; Puromycin; Ribosomes; RNA, Transfer | 1973 |
The stoichiometry of ribosomal translocation.
Topics: Acetates; Binding Sites; Chromosome Aberrations; Escherichia coli; Fusidic Acid; Guanosine Triphosphate; Kinetics; Peptide Chain Elongation, Translational; Peptide Elongation Factors; Phenylalanine; Phosphorus Radioisotopes; Ribosomes; RNA, Transfer; Tritium | 1973 |
Evidence for specific inhibition of translocation of aminoacyl-transfer ribonucleic acid by the pretreatment of ribosomes of Bacillus subtilis with p-chloromercuribenzoate.
Topics: Bacillus subtilis; Binding Sites; Carbon Isotopes; Cell-Free System; Centrifugation, Density Gradient; Chloromercuribenzoates; Chromatography, Gel; Chromosome Aberrations; Chromosomes, Bacterial; Escherichia coli; Genetics, Microbial; Magnesium; Mercaptoethanol; Peptide Biosynthesis; Peptide Chain Elongation, Translational; Phenylalanine; Poly U; Puromycin; Ribosomes; RNA, Transfer | 1972 |
Some observations on the blood levels of phenylalanine in dilute mice and a comparison between human phenylketonuria and the disease of mice homozygous for the dilute lethal gene.
Topics: Age Factors; Animals; Chromosome Aberrations; Chromosome Disorders; Disease Models, Animal; Drug Tolerance; Female; Genes, Lethal; Homozygote; Humans; Male; Metabolic Clearance Rate; Mice; Phenylalanine; Phenylketonurias; Sex Factors; Time Factors | 1972 |
Release of tRNA from ribosomes by a factor other than G factor.
Topics: Carbon Isotopes; Chromatography; Chromosome Aberrations; Erythromycin; Escherichia coli; Hot Temperature; Phenylalanine; Ribosomes; RNA, Bacterial; RNA, Transfer | 1970 |
[Toxicology of chemical sweetening agents].
Topics: Abnormalities, Drug-Induced; Animals; Blood Coagulation Disorders; Chemical and Drug Induced Liver Injury; Chromosome Aberrations; Chromosome Disorders; Cyclamates; Cyclohexylamines; Depression, Chemical; Esters; Guinea Pigs; Humans; Kidney Diseases; Mice; Pancreatic Diseases; Peptides; Phenylalanine; Photosensitivity Disorders; Rats; Saccharin; Sweetening Agents; Tolbutamide; Triazoles; Urinary Bladder Neoplasms | 1971 |
The induction of gene mutation and chromosome aberration in Chlamydomonas eugametos by a phenylalanine analog.
Topics: Chromosome Aberrations; Eukaryota; Mutation; Phenylalanine | 1969 |
A vegetative insatability in Aspergillus nidulans.
Topics: Aspergillus; Chromosome Aberrations; Crosses, Genetic; Gene Frequency; Phenotype; Phenylalanine; Recombination, Genetic; Sulfates | 1967 |