tyrosine and Abnormalities, Autosome

tyrosine has been researched along with Abnormalities, Autosome in 9 studies

Research

Studies (9)

Timeframe	Studies, this research(%)	All Research%
pre-1990	6 (66.67)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (22.22)	29.6817
2010's	1 (11.11)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Honda, T; Morii, M; Nakayama, Y; Suzuki, K; Yamaguchi, N	1
Lee, KA	1
Jorquera, R; Tanguay, RM	1
Gallasch, G; Jaeger, W; Lutz, P; Schmidt, H; Schnyder, UW	1
Finegold, MJ	1
Jones, B; Jones, JE; Lizarralde, G; Seal, US	1
Malinin, GI	1
van der Horst, JL; Wadman, SK	1
Hansen, S; Hardwick, DF; Perry, TL; Pohlmann, L; Warrington, PD	1

Reviews

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

Article	Year
Ewings family oncoproteins: drunk, disorderly and in search of partners. Cell research, 2007, Volume: 17, Issue:4 Topics: Cell Transformation, Neoplastic; Chromosome Aberrations; Humans; Mutation; Oncogene Proteins, Fusion; Phosphorylation; Protein Binding; Protein Folding; Proto-Oncogene Protein c-fli-1; RNA-Binding Protein EWS; Sarcoma, Ewing; Transcription Factors; Transcriptional Activation; Tyrosine	2007
Cholestatic syndromes in infancy. Perspectives in pediatric pathology, 1976, Volume: 3 Topics: Anemia, Hemolytic; Bile; Bile Ducts; Cholestasis; Chromosome Aberrations; Chromosome Disorders; Fasting; Fructose Intolerance; Galactosemias; Histiocytosis, Langerhans-Cell; Humans; Infant; Infant, Newborn; Infections; Jaundice, Neonatal; Liver; Liver Cirrhosis; Niemann-Pick Diseases; Nutritional Physiological Phenomena; Syndrome; Tyrosine	1976

Article

Year

Ewings family oncoproteins: drunk, disorderly and in search of partners.

Cell research, 2007, Volume: 17, Issue:4

Topics: Cell Transformation, Neoplastic; Chromosome Aberrations; Humans; Mutation; Oncogene Proteins, Fusion; Phosphorylation; Protein Binding; Protein Folding; Proto-Oncogene Protein c-fli-1; RNA-Binding Protein EWS; Sarcoma, Ewing; Transcription Factors; Transcriptional Activation; Tyrosine

2007

Cholestatic syndromes in infancy.

Perspectives in pediatric pathology, 1976, Volume: 3

Topics: Anemia, Hemolytic; Bile; Bile Ducts; Cholestasis; Chromosome Aberrations; Chromosome Disorders; Fasting; Fructose Intolerance; Galactosemias; Histiocytosis, Langerhans-Cell; Humans; Infant; Infant, Newborn; Infections; Jaundice, Neonatal; Liver; Liver Cirrhosis; Niemann-Pick Diseases; Nutritional Physiological Phenomena; Syndrome; Tyrosine

1976

Other Studies

7 other study(ies) available for tyrosine and Abnormalities, Autosome

Article	Year
v-Src-driven transformation is due to chromosome abnormalities but not Src-mediated growth signaling. Scientific reports, 2018, 01-18, Volume: 8, Issue:1 Topics: Animals; Cell Adhesion; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Transformation, Neoplastic; Chromosome Aberrations; Cyclin-Dependent Kinase Inhibitor Proteins; Gene Expression Regulation; Humans; Mice; NIH 3T3 Cells; Oncogene Protein pp60(v-src); Phosphorylation; Signal Transduction; Tyrosine	2018
Fumarylacetoacetate, the metabolite accumulating in hereditary tyrosinemia, activates the ERK pathway and induces mitotic abnormalities and genomic instability. Human molecular genetics, 2001, Aug-15, Volume: 10, Issue:17 Topics: Acetoacetates; Animals; Cell Line; Chromosome Aberrations; Cricetinae; Fluorescent Antibody Technique; G2 Phase; Glutathione; Golgi Apparatus; HeLa Cells; Humans; MAP Kinase Signaling System; Mitogen-Activated Protein Kinase Kinases; Mitogen-Activated Protein Kinases; Mitosis; Phosphorylation; Protein Serine-Threonine Kinases; Reactive Oxygen Species; Spindle Apparatus; Tyrosine; Tyrosinemias	2001
[Tyrosinemia and Richner-Hanhart syndrome (an autosomal recessive hereditary metabolic disease of childhood with bilateral dendritic pseudokeratitis, keratosis palmaris et plantaris and mental deficiency)]. Bericht uber die Zusammenkunft. Deutsche Ophthalmologische Gesellschaft, 1978, Issue:75 Topics: Amino Acid Metabolism, Inborn Errors; Child; Chromosome Aberrations; Chromosome Disorders; Genes, Recessive; Humans; Intellectual Disability; Keratitis, Dendritic; Keratoderma, Palmoplantar; Syndrome; Tyrosine	1978
Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis. The Journal of clinical endocrinology and metabolism, 1966, Volume: 26, Issue:11 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, Gel; Chromosome Aberrations; Chromosome Disorders; Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Immunodiffusion; Iodine Radioisotopes; Male; Mosaicism; Thyroglobulin; Thyroid Function Tests; Thyroxine; Triiodothyronine; Tyrosine; Ultracentrifugation	1966
Cytochemical observations on the adenovirus type-12-transformed hamster-embryo cell cultures. Journal of the National Cancer Institute, 1969, Volume: 43, Issue:3 Topics: Adenoviridae; Animals; Carbohydrates; Cell Nucleus; Chromosome Aberrations; Cricetinae; Culture Techniques; Cytopathogenic Effect, Viral; Cytoplasmic Granules; DNA; Embryo, Mammalian; Golgi Apparatus; Histocytochemistry; Proteins; RNA; Staining and Labeling; Transformation, Genetic; Tyrosine	1969
A variant form of branched-chain keto aciduria. Acta paediatrica Scandinavica, 1971, Volume: 60, Issue:5 Topics: Amino Acids; Child Behavior Disorders; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Diet Therapy; Dietary Proteins; Female; Heterozygote; Humans; Infant; Intellectual Disability; Isoleucine; Keto Acids; Leucine; Male; Maple Syrup Urine Disease; Methionine; Motor Skills; Pedigree; Phenylketonurias; Tyrosine; Valine	1971
Methionine induction of experimental tyrosinaemia. Journal of mental deficiency research, 1967, Volume: 11, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Chromosome Aberrations; Chromosome Disorders; Guinea Pigs; Methionine; Pancreas; Tyrosine	1967