tyrosine has been researched along with Albinism, Oculocutaneous in 19 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 10 (52.63) | 18.2507 |
2000's | 4 (21.05) | 29.6817 |
2010's | 5 (26.32) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abraham, L; Bilandžija, H; Jeffery, WR; Ma, L; Renner, KJ | 1 |
Abu-Asab, MS; Adams, DR; Aderemi, JO; Albert, JS; Alur, RP; Bernardini, IM; Brooks, BP; Chan, CC; Cogliati, T; Megan, LH; Melch, MG; Onojafe, IF | 1 |
Bilandžija, H; Jeffery, WR; Ma, L; Parkhurst, A | 1 |
Hirobe, T; Ishikawa, A | 1 |
Brixen, K; Brondum-Nielsen, K; Bygum, A; Ek, J; Grønskov, K; Rosenberg, T; Sand, A; Scheller, R | 1 |
Adams, DR; Alur, RP; Bernardini, IM; Brilliant, MH; Brooks, BP; Chan, CC; Dolinska, MB; Gahl, WA; Onojafe, IF; Sergeev, YV; Simeonov, DR; Zhang, J | 1 |
Cheng, E; Halaban, R; Hebert, DN | 1 |
Ni-Komatsu, L; Orlow, SJ | 1 |
Hutton, SM; Spritz, RA | 1 |
Fukai, K; Jong, MT; Lee, ST; Nicholls, RD; Spritz, RA | 1 |
Spritz, RA | 1 |
Bailin, T; Bennett, DC; Ho, L; Lee, ST; Spritz, RA; Sviderskaya, EV | 1 |
Orlow, SJ | 1 |
Käsmann, B; Ruprecht, KW | 1 |
Bennett, DC; Easty, DJ; Kwon, BS; Orlow, SJ; Rosemblat, S; Sviderskaya, EV; Wilson, A | 1 |
Bennett, DC; Furumura, M; Hearing, VJ; Potterf, SB; Santis, C; Sviderskaya, EV | 1 |
Aquaron, R | 1 |
Schallreuter, KU | 1 |
Hearing, VJ; Jiménez, M; Tsukamoto, K | 1 |
5 review(s) available for tyrosine and Albinism, Oculocutaneous
Article | Year |
---|---|
Molecular genetics of oculocutaneous albinism.
Topics: Albinism, Oculocutaneous; Amino Acid Sequence; Base Sequence; Humans; Molecular Sequence Data; Mutation; Tyrosine | 1993 |
Albinism: an update.
Topics: Albinism; Albinism, Ocular; Albinism, Oculocutaneous; Eye; Genetic Linkage; Hair; Humans; Mutation; Skin Pigmentation; Tyrosine; X Chromosome | 1997 |
Tradition of basic and applied pigment cell research in Marseilles.
Topics: Agaricales; Albinism, Oculocutaneous; Biochemistry; Boston; Cameroon; Catecholamines; Chromosomes, Human, Pair 15; France; Genetic Heterogeneity; History, 20th Century; Humans; Melanins; Melanocytes; Monophenol Monooxygenase; Plant Proteins; Thyroid Hormones; Tyrosine | 1999 |
A review of recent advances on the regulation of pigmentation in the human epidermis.
Topics: Albinism, Oculocutaneous; alpha-MSH; Biopterins; Dihydroxyphenylalanine; Enzyme Activation; Epidermis; Humans; Hydrogen Peroxide; Hydrogen-Ion Concentration; Intramolecular Oxidoreductases; Keratinocytes; Melanocytes; Melanosomes; Membrane Glycoproteins; Membrane Proteins; Monophenol Monooxygenase; Oxidative Stress; Oxidoreductases; Phenylalanine; Phenylalanine Hydroxylase; Pro-Opiomelanocortin; Proteins; Racial Groups; Recombinant Fusion Proteins; Skin Pigmentation; Transfection; Tyrosine; Tyrosine 3-Monooxygenase; Vitiligo | 1999 |
The nature of tyrosinase isozymes.
Topics: Albinism, Oculocutaneous; Animals; Catalase; Dihydroxyphenylalanine; Genes; Glycoproteins; Isoenzymes; Melanins; Melanocytes; Mice; Mice, Mutant Strains; Monophenol Monooxygenase; Multigene Family; Pigmentation Disorders; Tyrosine | 1992 |
14 other study(ies) available for tyrosine and Albinism, Oculocutaneous
Article | Year |
---|---|
Behavioural changes controlled by catecholaminergic systems explain recurrent loss of pigmentation in cavefish.
Topics: Activity Cycles; Albinism, Oculocutaneous; Anesthesia; Anesthetics; Animals; Biological Evolution; Catecholamines; Characidae; Fish Proteins; Norepinephrine; Pigmentation; Tyrosine | 2018 |
Minimal Efficacy of Nitisinone Treatment in a Novel Mouse Model of Oculocutaneous Albinism, Type 3.
Topics: Administration, Oral; Albinism, Oculocutaneous; Animals; Blotting, Western; Cyclohexanones; Disease Models, Animal; Enzyme Inhibitors; Genotyping Techniques; Melanins; Melanosomes; Membrane Glycoproteins; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Inbred DBA; Microscopy, Electron, Transmission; Nitrobenzoates; Oxidoreductases; Real-Time Polymerase Chain Reaction; Treatment Outcome; Tyrosine | 2018 |
A potential benefit of albinism in Astyanax cavefish: downregulation of the oca2 gene increases tyrosine and catecholamine levels as an alternative to melanin synthesis.
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-tyrosine induces melanocyte differentiation in novel pink-eyed dilution castaneus mouse mutant showing age-related pigmentation.
Topics: Aging; Albinism, Oculocutaneous; Animals; Cell Differentiation; Cell Proliferation; Intramolecular Oxidoreductases; Melanocytes; Membrane Glycoproteins; Mice; Microphthalmia-Associated Transcription Factor; Monophenol Monooxygenase; Oxidoreductases; Primary Cell Culture; RNA, Messenger; Tyrosine; Up-Regulation | 2015 |
Birth prevalence and mutation spectrum in danish patients with autosomal recessive albinism.
Topics: Adolescent; Adult; Aged; Albinism, Oculocutaneous; Alleles; Antigens, Neoplasm; Antiporters; Child; Child, Preschool; Chromatography, High Pressure Liquid; Denmark; DNA Mutational Analysis; Female; Genes, Recessive; Humans; Infant; Male; Membrane Glycoproteins; Membrane Transport Proteins; Middle Aged; Mutation; Oxidoreductases; Pedigree; Phenotype; Prevalence; Registries; Retrospective Studies; Reverse Transcriptase Polymerase Chain Reaction; Tyrosine | 2009 |
Nitisinone improves eye and skin pigmentation defects in a mouse model of oculocutaneous albinism.
Topics: Albinism, Oculocutaneous; Animals; Cyclohexanones; Disease Models, Animal; Enzyme Inhibitors; Enzyme Stability; Eye Color; Female; Humans; Melanins; Melanocytes; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Microscopy, Electron, Transmission; Models, Molecular; Monophenol Monooxygenase; Mutation; Nitrobenzoates; Pregnancy; Skin Pigmentation; Tyrosine | 2011 |
Coexpression of wild-type tyrosinase enhances maturation of temperature-sensitive tyrosinase mutants.
Topics: Albinism, Oculocutaneous; Animals; Cells, Cultured; Dihydroxyphenylalanine; Enzyme Stability; Glycosylation; Humans; Mice; Monophenol Monooxygenase; Mutation; Pigmentation; Temperature; Tyrosine | 2002 |
Heterologous expression of tyrosinase recapitulates the misprocessing and mistrafficking in oculocutaneous albinism type 2: effects of altering intracellular pH and pink-eyed dilution gene expression.
Topics: Albinism, Oculocutaneous; Biological Transport; Blotting, Western; Cell Line; Endoplasmic Reticulum; Endosomes; Epithelial Cells; Gene Expression; Golgi Apparatus; Humans; Hydrogen-Ion Concentration; Intracellular Fluid; Lysosomes; Melanins; Membrane Transport Proteins; Microscopy, Fluorescence; Monophenol Monooxygenase; Pigment Epithelium of Eye; Transfection; Tyrosine | 2006 |
Comprehensive analysis of oculocutaneous albinism among non-Hispanic caucasians shows that OCA1 is the most prevalent OCA type.
Topics: Albinism, Oculocutaneous; Antigens, Neoplasm; gp100 Melanoma Antigen; Guanine Nucleotide Exchange Factors; Humans; Membrane Glycoproteins; Membrane Proteins; Membrane Transport Proteins; Mutation; Oxidoreductases; Prevalence; Proteins; Tyrosine; White People | 2008 |
Organization and sequence of the human P gene and identification of a new family of transport proteins.
Topics: Albinism, Oculocutaneous; Alleles; Amino Acid Sequence; Animals; Bacterial Proteins; Base Sequence; Carrier Proteins; Chromosome Mapping; Chromosomes, Human, Pair 15; Ethnicity; Exons; Genes; Genes, Recessive; Humans; Membrane Proteins; Membrane Transport Proteins; Mice; Molecular Sequence Data; Multigene Family; Polymerase Chain Reaction; Promoter Regions, Genetic; Racial Groups; Sequence Alignment; Sequence Homology, Amino Acid; Species Specificity; Tyrosine | 1995 |
Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequences.
Topics: Albinism, Oculocutaneous; Animals; Carrier Proteins; Cell Division; Cell Line; DNA, Complementary; Female; Genetic Complementation Test; Genotype; Humans; Hypopigmentation; Male; Melanocytes; Membrane Proteins; Membrane Transport Proteins; Mice; Mice, Mutant Strains; Phenotype; Pigmentation; Tyrosine | 1997 |
Might the refractive state in oculocutaneous albino patients be a clue for distinguishing between tyrosinase-positive and tyrosinase-negative forms of oculocutaneous albinism?
Topics: Adolescent; Adult; Aged; Albinism, Oculocutaneous; Child; Child, Preschool; Humans; Hyperopia; Infant; Middle Aged; Myopia; Refraction, Ocular; Tyrosine | 1996 |
Melanosomal defects in melanocytes from mice lacking expression of the pink-eyed dilution gene: correction by culture in the presence of excess tyrosine.
Topics: Albinism, Oculocutaneous; Animals; Carrier Proteins; Enzyme Induction; gp100 Melanoma Antigen; Intramolecular Oxidoreductases; Melanins; Melanocytes; Membrane Glycoproteins; Membrane Proteins; Membrane Transport Proteins; Mice; Mice, Mutant Strains; Monophenol Monooxygenase; Morphogenesis; Oxidoreductases; Protein Biosynthesis; Proteins; RNA, Messenger; Tyrosine | 1998 |
Normal tyrosine transport and abnormal tyrosinase routing in pink-eyed dilution melanocytes.
Topics: Albinism, Oculocutaneous; Animals; Biological Transport; Carrier Proteins; Cell Line; Melanins; Melanocytes; Membrane Proteins; Mice; Mice, Inbred C57BL; Monophenol Monooxygenase; Mutation; Phenotype; Pigmentation; Subcellular Fractions; Tyrosine | 1998 |