Compounds > tyrosine

tyrosine and Microcephaly

tyrosine has been researched along with Microcephaly in 15 studies

Research

Studies (15)

Timeframe	Studies, this research(%)	All Research%
pre-1990	11 (73.33)	18.7374
1990's	1 (6.67)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (13.33)	24.3611
2020's	1 (6.67)	2.80

Authors

Authors	Studies
Arai, Y; Fujiki, M; Fujinami, H; Hanada, R; Hanada, T; Hikida, T; Kobayashi, T; Morisaki, I; Penninger, JM; Shimizu, N; Shiraishi, H	1
Andrieux, A; Barbier, EL; Bauer, P; Blair, EM; Bosc, C; Couly, S; Deloulme, JC; Denarier, E; Deshpande, C; Elmonairy, AA; Gory-Fauré, S; Heemeryck, P; Jayawant, S; Loong, L; Martin, HC; Maurice, T; Moutin, MJ; Murthy, S; Pagnamenta, AT; Peris, L; Siddiqui, A; Taylor, JC; Uszynski, I; Vossier, F; Walker, I	1
Cross, SH; Ferland, RJ; Hu, J; Lian, G; Lu, J; Sheen, VL; Zhang, J	1
Diwan, BA; Joshi, PN; Mulherkar, L	1
Levy, HL; Waisbren, SE	1
Jarosch, E; Plöchl, E; Rittinger, O	1
Erickson, AM; Kaplan, GN; Levy, HL	1
Lenke, RR; Levy, HL	1
al-Awadi, SA; al-Ghanim, MM; al-Najdi, K; el-Badramany, MH; Farag, TI; Girish, Y; Uma, R; Usha, R	1
Ampola, MG; Bailey, IV; Benacerraf, B; Doherty, LB; Levy, HL; Rohr, FJ; Waisbren, SE	1
O'Halloran, MT; Yu, JS	2
Bost, M; Boucharlat, J; Favier, A; Ledru, J; Ratel, M; Serre, JC	1
Huntley, CC; Stevenson, RE	1
Anderson, JA; Fisch, RO; Walker, WA	1

Other Studies

15 other study(ies) available for tyrosine and Microcephaly

Article	Year
Modeling a human CLP1 mutation in mouse identifies an accumulation of tyrosine pre-tRNA fragments causing pontocerebellar hypoplasia type 10. Biochemical and biophysical research communications, 2021, 09-17, Volume: 570 Topics: Amino Acid Sequence; Animals; Base Sequence; Cerebellar Diseases; Fibroblasts; Humans; Introns; Mice, Inbred C57BL; Mice, Inbred ICR; Microcephaly; Models, Biological; Motor Activity; Motor Neurons; Mutation; Nuclear Proteins; Phenotype; Phosphotransferases; RNA Precursors; RNA, Transfer; Transcription Factors; Tyrosine	2021
Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice. Human molecular genetics, 2019, 10-15, Volume: 28, Issue:20 Topics: Animals; Brain; Carrier Proteins; Cell Cycle Proteins; Cognitive Dysfunction; Female; Humans; Immunoblotting; Magnetic Resonance Imaging; Mice; Microcephaly; Neurons; Tubulin; Tyrosine	2019
Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012, May-30, Volume: 32, Issue:22 Topics: Age Factors; Animals; Bromodeoxyuridine; CDC2 Protein Kinase; Cell Cycle; Cell Cycle Proteins; Cell Differentiation; Cell Proliferation; Cells, Cultured; Cerebral Cortex; Contractile Proteins; Cyclin B1; DNA-Binding Proteins; Embryo, Mammalian; Filamins; Flow Cytometry; Gene Expression Regulation, Enzymologic; Immunoprecipitation; In Situ Nick-End Labeling; Ki-67 Antigen; Mice; Mice, Transgenic; Microcephaly; Microfilament Proteins; Neural Stem Cells; Nuclear Proteins; Periventricular Nodular Heterotopia; Phosphorylation; Protein-Tyrosine Kinases; T-Box Domain Proteins; Tyrosine	2012
A study of the mode of action of chloramphenicol on the chick morphogenesis. Experientia, 1967, Nov-15, Volume: 23, Issue:11 Topics: Abnormalities, Drug-Induced; Aminobenzoates; Animals; Chick Embryo; Chloramphenicol; Heart Defects, Congenital; Lactates; Microcephaly; Nervous System Malformations; Phenylalanine; Tyrosine	1967
Effects of untreated maternal phenylketonuria and hyperphenylalaninemia on the fetus. The New England journal of medicine, 1983, Nov-24, Volume: 309, Issue:21 Topics: Abortion, Spontaneous; Birth Weight; Body Weight; Child; Child, Preschool; Congenital Abnormalities; Female; Fetal Blood; Fetus; Humans; Infant; Infant, Newborn; Intellectual Disability; Intelligence; Male; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1983
[Maternal phenylketonuria]. Padiatrie und Padologie, 1984, Volume: 19, Issue:1 Topics: Child; Chromatography, Thin Layer; Female; Heterozygote; Humans; Infant, Newborn; Intellectual Disability; Male; Maternal-Fetal Exchange; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1984
Comparison of treated and untreated pregnancies in a mother with phenylketonuria. The Journal of pediatrics, 1982, Volume: 100, Issue:6 Topics: Abortion, Spontaneous; Adult; Child; Child, Preschool; Female; Humans; Intellectual Disability; Microcephaly; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1982
Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies. The New England journal of medicine, 1980, Nov-20, Volume: 303, Issue:21 Topics: Abortion, Spontaneous; Birth Weight; Female; Heart Defects, Congenital; Humans; Infant, Newborn; Intellectual Disability; Intelligence; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1980
Late diagnosis of phenylketonuria in a Bedouin mother. American journal of medical genetics, 1992, Dec-01, Volume: 44, Issue:6 Topics: Abortion, Habitual; Adult; Child, Preschool; Female; Fetal Diseases; Heart Defects, Congenital; Humans; Infant; Intellectual Disability; Male; Maternal-Fetal Exchange; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1992
New England Maternal PKU Project: prospective study of untreated and treated pregnancies and their outcomes. The Journal of pediatrics, 1987, Volume: 110, Issue:3 Topics: Adolescent; Adult; Female; Fetal Blood; Fetal Diseases; Humans; Infant, Newborn; Microcephaly; Patient Compliance; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Prenatal Diagnosis; Prognosis; Tyrosine	1987
Children of mothers with phenylketonuria. Lancet (London, England), 1970, Jan-31, Volume: 1, Issue:7640 Topics: Adolescent; Adult; Child; Child, Preschool; Diet Therapy; Family Planning Services; Female; Growth Disorders; Heart Defects, Congenital; Heterozygote; Homozygote; Humans; Intellectual Disability; Male; Microcephaly; Middle Aged; Phenylalanine; Phenylketonurias; Seizures; Strabismus; Tyrosine	1970
[2 new cases of microcephalic children with intrauterine growth retardation born of phenylketonuric mothers]. Annales medico-psychologiques, 1972, Volume: 2, Issue:4 Topics: Birth Weight; Chromatography, Ion Exchange; Female; Growth Disorders; Humans; Infant; Male; Mental Disorders; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1972
Maternal phenylketonuria. Course of two pregnancies. Obstetrics and gynecology, 1969, Volume: 34, Issue:5 Topics: Adult; Amniotic Fluid; Birth Weight; Chromatography; Female; Growth; Heart Defects, Congenital; Hemorrhage; Humans; Infant, Newborn; Intellectual Disability; Lung; Lymphangiectasis; Male; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine; Umbilical Cord; Vagina	1969
Atypical phenylketonuria in a family with a phenylketonuric mother. Pediatrics, 1970, Volume: 46, Issue:5 Topics: Adult; Alleles; Child; Female; Genes, Regulator; Heterozygote; Humans; Infant, Newborn; Male; Microcephaly; Milk, Human; Mixed Function Oxygenases; Phenotype; Phenylalanine; Phenylketonurias; Phenylpyruvic Acids; Tyrosine	1970
Prenatal and postnatal developmental consequences of maternal phenylketonuria. Pediatrics, 1966, Volume: 37, Issue:6 Topics: Adult; Birth Weight; Congenital Abnormalities; Female; Fetal Diseases; Humans; Infant, Newborn; Intellectual Disability; Male; Maternal-Fetal Exchange; Microcephaly; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Tyrosine	1966