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Search results 1 to 100 out of 730 for Tyrp1

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0.057s
Type Details Score
Gene
Type: gene
Organism: Not Specified
Gene
Type: gene
Organism: human
Gene
Type: gene
Organism: chicken
Gene
Type: gene
Organism: macaque, rhesus
Gene
Type: gene
Organism: frog, western clawed
Gene
Type: gene
Organism: cattle
Gene
Type: gene
Organism: goat
Gene
Type: gene
Organism: rat
Gene
Type: gene
Organism: dog, domestic
Gene
Type: gene
Organism: chimpanzee
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Publication  
First Author: Lu H
Year: 2011
Journal: Mol Vis
Title: Complex interactions of Tyrp1 in the eye.
Volume: 17
Pages: 2455-68
Publication
First Author: Kobayashi T
Year: 1998
Journal: J Biol Chem
Title: Tyrosinase stabilization by Tyrp1 (the brown locus protein).
Volume: 273
Issue: 48
Pages: 31801-5
Publication
First Author: Yatsu A
Year: 2013
Journal: J Invest Dermatol
Title: Syntaxin-3 is required for melanosomal localization of Tyrp1 in melanocytes.
Volume: 133
Issue: 9
Pages: 2237-46
Publication
First Author: Schmutz SM
Year: 2002
Journal: Mamm Genome
Title: TYRP1 and MC1R genotypes and their effects on coat color in dogs.
Volume: 13
Issue: 7
Pages: 380-7
Publication
First Author: Smyth IM
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Genomic anatomy of the Tyrp1 (brown) deletion complex.
Volume: 103
Issue: 10
Pages: 3704-9
Publication
First Author: Kobayashi T
Year: 2007
Journal: J Cell Sci
Title: Direct interaction of tyrosinase with Tyrp1 to form heterodimeric complexes in vivo.
Volume: 120
Issue: Pt 24
Pages: 4261-8
Publication
First Author: Tamura K
Year: 2009
Journal: Mol Biol Cell
Title: Varp is a novel Rab32/38-binding protein that regulates Tyrp1 trafficking in melanocytes.
Volume: 20
Issue: 12
Pages: 2900-8
Publication
First Author: Simpson EH
Year: 2000
Journal: Mamm Genome
Title: A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23.
Volume: 11
Issue: 1
Pages: 58-63
Publication
First Author: Chang B
Year: 1999
Journal: Nat Genet
Title: Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.
Volume: 21
Issue: 4
Pages: 405-9
Publication  
First Author: Lu H
Year: 2016
Journal: Mol Vis
Title: Iris transillumination defect and its gene modulators do not correlate with intraocular pressure in the BXD family of mice.
Volume: 22
Pages: 224-33
Publication
First Author: Roy Chowdhury U
Year: 2022
Journal: Invest Ophthalmol Vis Sci
Title: Effect of ATP-sensitive Potassium Channel Openers on Intraocular Pressure in Ocular Hypertensive Animal Models.
Volume: 63
Issue: 2
Pages: 15
Publication
First Author: Di Pietro SM
Year: 2006
Journal: Mol Biol Cell
Title: BLOC-1 interacts with BLOC-2 and the AP-3 complex to facilitate protein trafficking on endosomes.
Volume: 17
Issue: 9
Pages: 4027-38
Publication
First Author: Kenny EE
Year: 2012
Journal: Science
Title: Melanesian blond hair is caused by an amino acid change in TYRP1.
Volume: 336
Issue: 6081
Pages: 554
Publication
First Author: John SW
Year: 1999
Journal: J Glaucoma
Title: Mouse genetics: a tool to help unlock the mechanisms of glaucoma.
Volume: 8
Issue: 6
Pages: 400-12
Publication
First Author: Inman DM
Year: 2006
Journal: Invest Ophthalmol Vis Sci
Title: Quantitative correlation of optic nerve pathology with ocular pressure and corneal thickness in the DBA/2 mouse model of glaucoma.
Volume: 47
Issue: 3
Pages: 986-96
Publication  
First Author: Anderson MG
Year: 2001
Journal: BMC Genet
Title: Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice.
Volume: 2
Pages: 1
Publication  
First Author: Rohowetz LJ
Year: 2021
Journal: Front Neurosci
Title: The Contribution of Anterior Segment Abnormalities to Changes in Intraocular Pressure in the DBA/2J Mouse Model of Glaucoma: DBA/2J-Gpnmb +/SjJ Mice as Critical Controls.
Volume: 15
Pages: 801184
Publication
First Author: Jakobs TC
Year: 2005
Journal: J Cell Biol
Title: Retinal ganglion cell degeneration is topological but not cell type specific in DBA/2J mice.
Volume: 171
Issue: 2
Pages: 313-25
Publication  
First Author: Liu Y
Year: 2023
Journal: Front Neurosci
Title: Parvalbumin expression changes with retinal ganglion cell degeneration.
Volume: 17
Pages: 1227116
Publication
First Author: Fernández-Sánchez L
Year: 2014
Journal: Invest Ophthalmol Vis Sci
Title: Loss of outer retinal neurons and circuitry alterations in the DBA/2J mouse.
Volume: 55
Issue: 9
Pages: 6059-72
Publication
First Author: Zhou X
Year: 2005
Journal: J Biol Chem
Title: Involvement of inflammation, degradation, and apoptosis in a mouse model of glaucoma.
Volume: 280
Issue: 35
Pages: 31240-8
Publication  
First Author: Wilson GN
Year: 2016
Journal: Front Neurosci
Title: Early Cytoskeletal Protein Modifications Precede Overt Structural Degeneration in the DBA/2J Mouse Model of Glaucoma.
Volume: 10
Pages: 494
Publication
First Author: Setty SR
Year: 2007
Journal: Mol Biol Cell
Title: BLOC-1 is required for cargo-specific sorting from vacuolar early endosomes toward lysosome-related organelles.
Volume: 18
Issue: 3
Pages: 768-80
Publication  
First Author: Nivison MP
Year: 2017
Journal: Exp Neurol
Title: Age-related accumulation of phosphorylated mitofusin 2 protein in retinal ganglion cells correlates with glaucoma progression.
Volume: 296
Pages: 49-61
Publication
First Author: Anderson MG
Year: 2002
Journal: Nat Genet
Title: Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice.
Volume: 30
Issue: 1
Pages: 81-5
Publication
First Author: Lye-Barthel M
Year: 2013
Journal: Invest Ophthalmol Vis Sci
Title: Morphology of astrocytes in a glaucomatous optic nerve.
Volume: 54
Issue: 2
Pages: 909-17
Publication
First Author: Beermann F
Year: 1999
Journal: Cell Mol Biol (Noisy-le-grand)
Title: The tyrosinase related protein-1 (Tyrp1) promoter in transgenic experiments: targeted expression to the retinal pigment epithelium.
Volume: 45
Issue: 7
Pages: 961-8
Publication  
First Author: Howell GR
Year: 2007
Journal: BMC Genet
Title: Absence of glaucoma in DBA/2J mice homozygous for wild-type versions of Gpnmb and Tyrp1.
Volume: 8
Pages: 45
Publication
First Author: Onojafe IF
Year: 2018
Journal: Invest Ophthalmol Vis Sci
Title: Minimal Efficacy of Nitisinone Treatment in a Novel Mouse Model of Oculocutaneous Albinism, Type 3.
Volume: 59
Issue: 12
Pages: 4945-4952
Publication
First Author: Buchanan RA
Year: 2019
Journal: Invest Ophthalmol Vis Sci
Title: Meox2 Haploinsufficiency Accelerates Axonal Degeneration in DBA/2J Glaucoma.
Volume: 60
Issue: 10
Pages: 3283-3296
Publication
First Author: Libby RT
Year: 2005
Journal: PLoS Genet
Title: Susceptibility to neurodegeneration in a glaucoma is modified by Bax gene dosage.
Volume: 1
Issue: 1
Pages: 17-26
Publication
First Author: Brooks BP
Year: 2007
Journal: Invest Ophthalmol Vis Sci
Title: Analysis of ocular hypopigmentation in Rab38cht/cht mice.
Volume: 48
Issue: 9
Pages: 3905-13
Publication      
First Author: Medical Research Council (MRC) Harwell
Year: 2012
Journal: MGI Direct Data Submission
Title: Direct Data Submission 2012/03/01
Publication
First Author: King R
Year: 2018
Journal: PLoS Genet
Title: Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma.
Volume: 14
Issue: 1
Pages: e1007145
Publication
First Author: Loftus SK
Year: 2002
Journal: Proc Natl Acad Sci U S A
Title: Mutation of melanosome protein RAB38 in chocolate mice.
Volume: 99
Issue: 7
Pages: 4471-6
Publication
First Author: Trantow CM
Year: 2011
Journal: Invest Ophthalmol Vis Sci
Title: Microarray analysis of iris gene expression in mice with mutations influencing pigmentation.
Volume: 52
Issue: 1
Pages: 237-48
Publication
First Author: Suda M
Year: 2022
Journal: Sci Rep
Title: Glycoprotein nonmetastatic melanoma protein B regulates lysosomal integrity and lifespan of senescent cells.
Volume: 12
Issue: 1
Pages: 6522
Publication
First Author: Harder JM
Year: 2020
Journal: J Neuroinflammation
Title: Complement peptide C3a receptor 1 promotes optic nerve degeneration in DBA/2J mice.
Volume: 17
Issue: 1
Pages: 336
Publication
First Author: Barabas P
Year: 2011
Journal: Invest Ophthalmol Vis Sci
Title: Missing optomotor head-turning reflex in the DBA/2J mouse.
Volume: 52
Issue: 9
Pages: 6766-73
Publication      
First Author: RIKEN BioResource Center/RIKEN Genomic Sciences Center
Year: 2008
Journal: PhenoSITE, World Wide Web (URL: http://www.brc.riken.jp/lab/gsc/mouse/)
Title: A Large Scale Mutagenesis Program in RIKEN GSC
Publication
First Author: Harun-Or-Rashid M
Year: 2018
Journal: J Neurosci
Title: Structural and Functional Rescue of Chronic Metabolically Stressed Optic Nerves through Respiration.
Volume: 38
Issue: 22
Pages: 5122-5139
Publication
First Author: Shen AL
Year: 2017
Journal: PLoS One
Title: Retinal pathology in the PPCD1 mouse.
Volume: 12
Issue: 10
Pages: e0185094
Publication
First Author: Fortin A
Year: 2010
Journal: Genes Brain Behav
Title: Positional cloning of a quantitative trait locus contributing to pain sensitivity: possible mediation by Tyrp1.
Volume: 9
Issue: 8
Pages: 856-67
Publication  
First Author: Anderson MG
Year: 2006
Journal: BMC Biol
Title: Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma.
Volume: 4
Pages: 20
Publication
First Author: Costin GE
Year: 2003
Journal: J Cell Sci
Title: Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4.
Volume: 116
Issue: Pt 15
Pages: 3203-12
Publication
First Author: Peters J
Year: 2003
Journal: Mutat Res
Title: Biochemical and recessive visible specific locus responses of C3H/HeH to fractionated, acute radiation.
Volume: 543
Issue: 2
Pages: 137-43
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus caroli
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus pahari
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus spretus
Publication
First Author: Shibahara S
Year: 1986
Journal: Nucleic Acids Res
Title: Cloning and expression of cDNA encoding mouse tyrosinase.
Volume: 14
Issue: 6
Pages: 2413-27
Publication
First Author: Halaban R
Year: 1990
Journal: Proc Natl Acad Sci U S A
Title: Murine and human b locus pigmentation genes encode a glycoprotein (gp75) with catalase activity.
Volume: 87
Issue: 12
Pages: 4809-13
Publication
First Author: Zdarsky E
Year: 1990
Journal: Genetics
Title: The molecular basis of brown, an old mouse mutation, and of an induced revertant to wild type.
Volume: 126
Issue: 2
Pages: 443-9
Publication
First Author: Crabbe JC
Year: 1996
Journal: Addict Biol
Title: Quantitative trait locus gene mapping: a new method for locating alcohol response genes.
Volume: 1
Issue: 3
Pages: 229-35
Publication
First Author: Buck KJ
Year: 1997
Journal: J Neurosci
Title: Quantitative trait loci involved in genetic predisposition to acute alcohol withdrawal in mice.
Volume: 17
Issue: 10
Pages: 3946-55
Publication
First Author: Hollander WF
Year: 1977
Journal: J Hered
Title: Meander tail: a recessive mutant located in chromosome 4 of the mouse.
Volume: 68
Issue: 6
Pages: 403-6
Publication
First Author: Green MC
Year: 1972
Journal: Science
Title: Cribriform degeneration (cri): a new recessive neurological mutation in the mouse.
Volume: 176
Issue: 4036
Pages: 800-3
Publication
First Author: Penna D
Year: 1998
Journal: Oncogene
Title: Tumors of the retinal pigment epithelium metastasize to inguinal lymph nodes and spleen in tyrosinase-related protein 1/SV40 T antigen transgenic mice.
Volume: 17
Issue: 20
Pages: 2601-7
Publication  
First Author: Sweet HO
Year: 1985
Journal: Mouse News Lett
Title: Clasper (cla)
Volume: 73
Pages: 18
Publication  
First Author: Kelly EM
Year: 1968
Journal: Mouse News Lett
Title: Dominant reduced ear, E (orBe)
Volume: 38
Pages: 31
Publication
First Author: Bell JA
Year: 1995
Journal: Mamm Genome
Title: A high-resolution map of the brown (b, Tyrp1) deletion complex of mouse chromosome 4.
Volume: 6
Issue: 6
Pages: 389-95
Publication
First Author: Miller DS
Year: 1955
Journal: J Hered
Title: Cordovan, a new allele of black and brown color in the mouse.
Volume: 46
Issue: 6
Pages: 293-96
Publication
First Author: MacDOWELL EC
Year: 1950
Journal: J Hered
Title: "Light"--a new mouse color.
Volume: 41
Issue: 2
Pages: 35-6
Publication
First Author: Jackson IJ
Year: 1990
Journal: Genetics
Title: Characterization of TRP-1 mRNA levels in dominant and recessive mutations at the mouse brown (b) locus.
Volume: 126
Issue: 2
Pages: 451-9
Publication  
First Author: PIERRO LJ
Year: 1963
Journal: J Exp Zool
Title: EFFECTS OF THE LIGHT MUTATION OF MOUSE COAT COLOR ON EYE PIGMENTATION.
Volume: 153
Pages: 81-7
Publication
First Author: Johnson R
Year: 1992
Journal: Nat Genet
Title: Light is a dominant mouse mutation resulting in premature cell death.
Volume: 1
Issue: 3
Pages: 226-9
Publication
First Author: Cable J
Year: 1993
Journal: Pigment Cell Res
Title: Light (Blt), a mutation that causes melanocyte death, affects stria vascularis function in the mouse inner ear.
Volume: 6
Issue: 4 Pt 1
Pages: 215-25
Publication
First Author: Javerzat S
Year: 1998
Journal: Mamm Genome
Title: White-based brown (Tyrp1B-w) is a dominant mutation causing reduced hair pigmentation owing to a chromosomal inversion.
Volume: 9
Issue: 6
Pages: 469-71
Publication  
First Author: Hunsicker PR
Year: 1969
Journal: Mouse News Lett
Title: White-based brown, BW.
Volume: 40
Pages: 41
Publication
First Author: Raymond S
Year: 1994
Journal: Genet Res
Title: Molecular characterization of the mouse Bw mutation causing premature melanocyte death - melanocytes and early development
Volume: 63
Issue: 2
Pages: 155 (Abstr)
Publication  
First Author: Little CC
Year: 1916
Journal: Am Naturalist
Title: The occurrence of three recognized coat mutations in mice
Volume: 50
Pages: 335-349
Publication
First Author: Rittenhouse E
Year: 1968
Journal: Dev Biol
Title: Genetic effect on fine structure and development of pigment granules in mouse hair bulb melanocytes. I. The b and d loci.
Volume: 17
Issue: 4
Pages: 351-65
Publication      
First Author: Purrington T
Year: 2014
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for ca-los
Publication      
First Author: Reyna C
Year: 2016
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for butter