tyrosine and Albinism

tyrosine has been researched along with Albinism in 33 studies

Research

Studies (33)

TimeframeStudies, this research(%)All Research%
pre-199023 (69.70)18.7374
1990's7 (21.21)18.2507
2000's2 (6.06)29.6817
2010's1 (3.03)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bilandžija, H; Jeffery, WR; Ma, L; Parkhurst, A1
Decatur, CL; Lopez, VM; Lynch, RM; McKay, BS; Stamer, WD1
Dahle, J; Kvam, E1
KUGELMAN, TP; VAN SCOTT, EJ1
SCHULTZE-JENA, BS1
HAWKINS, GR; MAZZARELLA, M; ZIPKIN, I1
Lamoreux, ML; Murray, M; Pawelek, JM1
King, RA; Olds, DP1
Klein, LE; Nordlund, JJ1
Assensio, AM; Cascone, C; Fracassi, A; Giardini, O; Lubrano, R; Parisi, SG1
Beermann, F; Grund, C; Kelsey, G; Ruppert, S; Schütz, G; Tanguay, RM1
al-Dhalimy, M; Burlingame, T; Finegold, M; Grompe, M; Kennaway, NG; Ou, CN; Soriano, P1
Kelsey, G; Schütz, G1
Orlow, SJ1
Alonso, D; Barroso, JB; Bentura, ML; Campbell, RO; Esteban, FJ; Fernández, AP; Leza, JC; Lizasoain, I; Martínez-Murillo, R; Moro, MA; Pedrosa, JA; Peinado, MA; Richart, A; Rodrigo, J; Santacana, M; Serrano, J; Uttenthal, LO; Valderrama, R1
Laviolette, P; Voulot, C1
Mojamdar, MV; Shah, VC; Sharma, KS1
Holdener-Kenny, B; Magnuson, T; Sharan, SK1
Giebel, LB; King, RA; Spritz, RA; Strunk, KM1
Irons, M; Levy, HL1
Dogliotti, M1
Li, JP; Pomerantz, SH1
Fuzeau-Braesch, S1
Nace, GW; Richards, CM; Smith-Gill, SJ1
Bergsma, DR; Niswander, JD; White, JG; Witkop, CJ; Workman, PL1
Kroll, S; Toussaint, W; Zebisch, P2
Balda, BR; Lukacs, I1
Fellman, JH; Gaudin, D1
Nance, WE; Rawls, RF; White, JG; Witkop, CJ1
Nance, WE; Rawls, RF; Witkop, CJ1
Desnick, S; Jackson, CE; Nance, WE; White, JG; Witkop, CJ1
Bamshad, J1

Reviews

5 review(s) available for tyrosine and Albinism

ArticleYear
Lessons from lethal albino mice.
    Current opinion in genetics & development, 1993, Volume: 3, Issue:2

    Topics: Albinism; Animals; Animals, Newborn; Gene Deletion; Gene Expression Regulation; Genes, Lethal; Humans; Hydrolases; Liver; Mice; Mice, Mutant Strains; Mice, Transgenic; Models, Biological; Organ Specificity; Phenotype; Transcription Factors; Transcription, Genetic; Tyrosine

1993
Albinism: an update.
    Seminars in cutaneous medicine and surgery, 1997, Volume: 16, Issue:1

    Topics: Albinism; Albinism, Ocular; Albinism, Oculocutaneous; Eye; Genetic Linkage; Hair; Humans; Mutation; Skin Pigmentation; Tyrosine; X Chromosome

1997
Mouse albino-deletions: from genetics to genes in development.
    BioEssays : news and reviews in molecular, cellular and developmental biology, 1992, Volume: 14, Issue:12

    Topics: Albinism; Animals; Embryonic and Fetal Development; Eye Color; Gastrula; Gene Expression Regulation, Developmental; Genes; Genes, Lethal; Hair Color; Melanins; Mesoderm; Mice; Mice, Mutant Strains; Sequence Deletion; Tyrosine

1992
Metabolic syndromes with dermatologic manifestations.
    Clinical reviews in allergy, 1986, Volume: 4, Issue:1

    Topics: Albinism; Alkaptonuria; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Amino Acids; Biotinidase; Carbohydrate Metabolism; Eczema; Hartnup Disease; Homocystinuria; Humans; Keratosis; Menkes Kinky Hair Syndrome; Metabolic Diseases; Phenylketonurias; Porphyrias; Skin Diseases; Steryl-Sulfatase; Sulfatases; Tyrosine; Urea

1986
[Molecular biologic aspects in dermatology demonstrated by some hereditary enzyme defects].
    Zeitschrift fur Haut- und Geschlechtskrankheiten, 1968, Dec-01, Volume: 43, Issue:23

    Topics: Albinism; Alkaptonuria; Anemia, Sickle Cell; Chromosomes; Hartnup Disease; Humans; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Models, Chemical; Molecular Biology; Phenylalanine; Phenylketonurias; Porphyrias; Skin Diseases; Tyrosine

1968

Other Studies

28 other study(ies) available for tyrosine and Albinism

ArticleYear
A potential benefit of albinism in Astyanax cavefish: downregulation of the oca2 gene increases tyrosine and catecholamine levels as an alternative to melanin synthesis.
    PloS one, 2013, Volume: 8, Issue:11

    Topics: Albinism; Albinism, Oculocutaneous; Animals; Base Sequence; Brain; Catecholamines; Chromatography, High Pressure Liquid; DNA Primers; Down-Regulation; Enzyme-Linked Immunosorbent Assay; Fishes; In Situ Hybridization; Kidney; Melanins; Polymerase Chain Reaction; Tyrosine

2013
L-DOPA is an endogenous ligand for OA1.
    PLoS biology, 2008, Sep-30, Volume: 6, Issue:9

    Topics: Albinism; Animals; Autocrine Communication; Calcium; Cell Line; Dopamine; Dopamine Agents; Eye Proteins; Humans; Levodopa; Ligands; Membrane Glycoproteins; Monophenol Monooxygenase; Nerve Growth Factors; Pigment Epithelium of Eye; Protease Inhibitors; Receptors, Dopamine; Serpins; Signal Transduction; Tyrosine

2008
Pigmented melanocytes are protected against ultraviolet-A-induced membrane damage.
    The Journal of investigative dermatology, 2003, Volume: 121, Issue:3

    Topics: Albinism; Animals; Antioxidants; Cell Line, Transformed; Cell Membrane; Cell Membrane Permeability; Glutathione; Lipid Peroxidation; Melanins; Melanocytes; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Reactive Oxygen Species; Skin Pigmentation; Thiobarbituric Acid Reactive Substances; Tyrosine; Ultraviolet Rays

2003
Tyrosinase activity in melanocytes of human albinos.
    The Journal of investigative dermatology, 1961, Volume: 37

    Topics: Albinism; Chromatophores; Humans; Melanocytes; Monophenol Monooxygenase; Oxidoreductases; Tyrosine

1961
[Hereditary enzyme defects of amino acid metabolism].
    Ergebnisse der inneren Medizin und Kinderheilkunde, 1962, Volume: 18

    Topics: Albinism; Alkaptonuria; Amino Acids; Humans; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proteins; Tryptophan; Tyrosine

1962
THE TYROSINE, TRYPTOPHAN AND PROTEIN CONTENT OF HUMAN PAROTID SALIVA IN ORAL AND SYSTEMIC DISEASE. USE OF ULTRAVIOLET ABSORPTION TECHNICS.
    International series of monographs on oral biology, 1964, Volume: 3

    Topics: Albinism; Arthritis, Rheumatoid; Biomedical Research; Dental Caries; Gingival Diseases; Humans; Parotid Gland; Periodontal Diseases; Proteins; Saliva; Salivation; Sialorrhea; Sjogren's Syndrome; Spectrum Analysis; Tryptophan; Tyrosine; Uric Acid

1964
New regulatory factors for melanogenesis: developmental changes in neonatal mice of various genotypes.
    Developmental biology, 1983, Volume: 100, Issue:1

    Topics: Albinism; Animals; Animals, Newborn; Dihydroxyphenylalanine; Indoles; Melanins; Mice; Mice, Inbred AKR; Mice, Inbred C57BL; Skin; Tyrosine

1983
Tyrosine uptake in normal and albino hairbulbs.
    Archives of dermatological research, 1984, Volume: 276, Issue:5

    Topics: Albinism; Biological Transport, Active; Hair; Hair Color; Humans; In Vitro Techniques; Melanins; Melanocytes; Monophenol Monooxygenase; Tyrosine

1984
Genetic basis of pigmentation and its disorders.
    International journal of dermatology, 1981, Volume: 20, Issue:10

    Topics: Albinism; Animals; Cell Differentiation; Color; Humans; Lentigo; Melanins; Melanocytes; Melanoma; Mice; Monophenol Monooxygenase; Nevus; Phenylalanine; Pigmentation; Pigmentation Disorders; Skin; Syndrome; Tyrosine

1981
[Oculocutaneous albinism and tyrosinuria. Description of a clinical case].
    Minerva pediatrica, 1983, Volume: 35, Issue:3

    Topics: Albinism; Amino Acid Metabolism, Inborn Errors; Humans; Infant; Male; Tyrosine

1983
Rescue of mice homozygous for lethal albino deletions: implications for an animal model for the human liver disease tyrosinemia type 1.
    Genes & development, 1993, Volume: 7, Issue:12A

    Topics: Albinism; Animals; Disease Models, Animal; Gene Deletion; Gene Expression; Homozygote; Humans; Hydrolases; Hypoglycemia; Liver; Liver Diseases; Mice; Mice, Transgenic; Phenotype; Tyrosine

1993
Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice.
    Genes & development, 1993, Volume: 7, Issue:12A

    Topics: Albinism; Animals; Animals, Newborn; Base Sequence; Cells, Cultured; Endoplasmic Reticulum; Gene Deletion; Gene Expression; Hydrolases; Liver Diseases; Mice; Microscopy, Electron; Molecular Sequence Data; Phenotype; RNA, Messenger; Tyrosine

1993
Neuronal and inducible nitric oxide synthase and nitrotyrosine immunoreactivities in the cerebral cortex of the aging rat.
    Microscopy research and technique, 1998, Oct-01, Volume: 43, Issue:1

    Topics: Aging; Albinism; Animals; Blotting, Western; Cerebral Cortex; Immunohistochemistry; Male; Nerve Tissue Proteins; Nitric Oxide Synthase; Nitric Oxide Synthase Type I; Nitric Oxide Synthase Type II; Rats; Rats, Wistar; Tyrosine

1998
[Tyrosinases of the pigmented portions of the eye in 4 species of rodent].
    Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles, 1976, Jul-05, Volume: 283, Issue:1

    Topics: Albinism; Animals; Catechol Oxidase; Cricetinae; Electrophoresis, Polyacrylamide Gel; Eye; Guinea Pigs; Molecular Weight; Monophenol Monooxygenase; Oxidation-Reduction; Rabbits; Rats; Retinal Pigments; Rodentia; Species Specificity; Tyrosine

1976
A comparative study on tyrosine metabolism in livers of albino & black mice.
    Indian journal of biochemistry & biophysics, 1976, Volume: 13, Issue:3

    Topics: Albinism; Animals; Liver; Mice; Skin Pigmentation; Tyrosine

1976
Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.
    The New England journal of medicine, 1990, Jun-14, Volume: 322, Issue:24

    Topics: Adult; Albinism; Base Sequence; Blotting, Southern; DNA; Exons; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Tyrosine

1990
Actinic keratoses in Bantu albinos. Clinical experiences with the topical use of 5-fluoro-uracil.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1973, Nov-17, Volume: 47, Issue:45

    Topics: Adult; Albinism; Carcinoma, Basal Cell; Carcinoma, Squamous Cell; Catechol Oxidase; Child; Female; Fluorouracil; Humans; Keratosis; Male; Middle Aged; Ointments; Skin Neoplasms; Sunlight; Tyrosine

1973
Tyrosinase in the skin of albino hamsters and mice.
    Nature, 1974, Nov-15, Volume: 252, Issue:5480

    Topics: Albinism; Animals; Catechol Oxidase; Cricetinae; Hydroxylation; Mice; Mice, Inbred AKR; Skin; Tyrosine

1974
[Effects of injections of different substrates and an enzyme inhibitor on pigmentation in normal and albino Locusta migratoria L. (Orthop.)].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1974, Volume: 168, Issue:10-11-12

    Topics: Albinism; Amino Acids; Animals; Ascorbic Acid; Benserazide; Folic Acid; Grasshoppers; Nialamide; Pigmentation; Reserpine; Tryptophan; Tyrosine

1974
Genetic and metabolic bases of two "albino" phenotypes in the leopard frog, Rana pipiens.
    The Journal of experimental zoology, 1972, Volume: 180, Issue:2

    Topics: Albinism; Animals; Anura; Catechol Oxidase; Chromatophores; Crosses, Genetic; Culture Techniques; Dihydroxyphenylalanine; Female; Genes, Recessive; Larva; Male; Melanins; Melanocytes; Metamorphosis, Biological; Mexico; Michigan; Phenotype; Pigmentation; Rana pipiens; Tyrosine

1972
Tyrosinase positive oculocutaneous albinism among the Zuni and the Brandywine triracial isolate: biochemical and clinical characteristics and fertility.
    American journal of physical anthropology, 1972, Volume: 36, Issue:3

    Topics: Adolescent; Adult; Age Factors; Aged; Albinism; Catechol Oxidase; Child; Child, Preschool; Copper; Female; Fertility; Hair; Humans; Indians, North American; Infant; Male; Microscopy, Electron; Middle Aged; New Mexico; Pigmentation; Tyrosine

1972
[Hereditary amino acid metabolism disorders. Indications for early diagnosis].
    Fortschritte der Medizin, 1972, Apr-13, Volume: 90, Issue:11

    Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Cystathionine; Cystinosis; Diagnosis, Differential; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine

1972
[Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
    Fortschritte der Medizin, 1972, Apr-13, Volume: 90, Issue:11

    Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Clinical Laboratory Techniques; Cystathionine; Cystinosis; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine

1972
The biosynthesis of DOPA in albino skin.
    Biochimica et biophysica acta, 1967, Jun-13, Volume: 141, Issue:1

    Topics: Albinism; Animals; Carbon Isotopes; Catechol Oxidase; Chelating Agents; Dihydroxyphenylalanine; Electrophoresis; Female; Pigmentation; Rats; Skin; Solubility; Tritium; Tyrosine

1967
Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity.
    American journal of human genetics, 1970, Volume: 22, Issue:1

    Topics: Albinism; Black People; Catechol Oxidase; Child, Preschool; Female; Gene Frequency; Genes, Recessive; Hair; Heterozygote; Humans; Iris; Male; Melanins; Melanocyte-Stimulating Hormones; Microscopy, Electron; Mutation; North Carolina; Pedigree; Phenotype; Tyrosine; White People

1970
Genetic and biochemical evidence for two forms of oculocutaneous albinism in man.
    Birth defects original article series, 1971, Volume: 7, Issue:3

    Topics: Albinism; Child; Female; Genes, Recessive; Hair; Humans; Male; Pedigree; Phenotype; Tyrosine

1971
Classification of albinism in man.
    Birth defects original article series, 1971, Volume: 7, Issue:8

    Topics: Adolescent; Adult; Albinism; Animals; Blood Platelets; Bone Marrow Cells; Child; Child, Preschool; Female; Hair; Hemorrhagic Disorders; Humans; Macrophages; Male; Melanocyte-Stimulating Hormones; Mice; Microphthalmos; Mononuclear Phagocyte System; Skin Pigmentation; Syndrome; Tyrosine; Visual Acuity

1971
Cutaneous manifestations of disorders of metabolism of phenylalanine-tyrosine.
    Missouri medicine, 1971, Volume: 68, Issue:6

    Topics: Albinism; Amino Acid Metabolism, Inborn Errors; Humans; Phenylalanine; Pigmentation Disorders; Skin Manifestations; Tyrosine

1971