| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1034/J.1600-0749.2003.00067.X |
| P8608 | Fatcat ID | release_gawykyq7lnf6rnnmosgikz6n7u |
| P698 | PubMed publication ID | 12859616 |
| P5875 | ResearchGate publication ID | 6582959 |
| P2093 | author name string | Dorothy C Bennett | |
| M Lynn Lamoreux | |||
| P2860 | cites work | Pmel17 initiates premelanosome morphogenesis within multivesicular bodies | Q24291864 |
| Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene | Q24292277 | ||
| The Hermansky-Pudlak syndrome 1 (HPS1) and HPS4 proteins are components of two complexes, BLOC-3 and BLOC-4, involved in the biogenesis of lysosome-related organelles | Q24298696 | ||
| Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability | Q24300451 | ||
| SLUG (SNAI2) deletions in patients with Waardenburg disease | Q24319901 | ||
| Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism | Q24337545 | ||
| Rab27a is an essential component of melanosome receptor for myosin Va | Q24524137 | ||
| A di-leucine-based motif in the cytoplasmic tail of LIMP-II and tyrosinase mediates selective binding of AP-3. | Q24533159 | ||
| Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice | Q24538566 | ||
| Identification of a human melanoma antigen recognized by tumor-infiltrating lymphocytes associated with in vivo tumor rejection | Q24561706 | ||
| A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice | Q24602264 | ||
| Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus | Q24633925 | ||
| Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium | Q28145744 | ||
| Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1) | Q28208164 | ||
| Tyrp1 and oculocutaneous albinism type 3 | Q28214493 | ||
| An essential role for ectodomain shedding in mammalian development | Q77544828 | ||
| From Agouti to Pomc--100 years of fat blonde mice | Q78199439 | ||
| Obesity in the mouse model of pro-opiomelanocortin deficiency responds to peripheral melanocortin | Q78199477 | ||
| The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene | Q28239757 | ||
| Polymerization of 5,6-dihydroxyindole-2-carboxylic acid to melanin by the pmel 17/silver locus protein | Q28277065 | ||
| The leaden gene product is required with Rab27a to recruit myosin Va to melanosomes in melanocytes | Q28506301 | ||
| Spongiform degeneration in mahoganoid mutant mice | Q28506434 | ||
| Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice | Q28513043 | ||
| Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6 | Q28585075 | ||
| Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human | Q28590831 | ||
| The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene | Q28594610 | ||
| A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism | Q33552077 | ||
| Biochemical control of melanogenesis and melanosomal organization | Q33760835 | ||
| Identification of the albino mutation of mouse tyrosinase by analysis of an in vitro revertant | Q33786384 | ||
| Mutation of melanosome protein RAB38 in chocolate mice | Q34048569 | ||
| The inbred mouse in pigmentation research: significance of a congenic developmental system | Q34128441 | ||
| Melanophilin, the product of the leaden locus, is required for targeting of myosin-Va to melanosomes | Q34313682 | ||
| Ocular albinism type 1: more than meets the eye. | Q34363477 | ||
| The melanosome: membrane dynamics in black and white | Q34389530 | ||
| How the zebrafish gets its stripes | Q34488840 | ||
| Agouti: from mouse to man, from skin to fat. | Q34523557 | ||
| Chediak-Higashi Syndrome: a rare disorder of lysosomes and lysosome related organelles | Q34722897 | ||
| The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome | Q34874723 | ||
| Hermansky-Pudlak syndrome: vesicle formation from yeast to man. | Q35009608 | ||
| Human and mouse disorders of pigmentation | Q35145880 | ||
| Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene | Q35223876 | ||
| Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes | Q35619461 | ||
| Genetics of dark skin in mice | Q35963838 | ||
| Cloning and expression of cDNA encoding mouse tyrosinase | Q36424864 | ||
| Tyrosinase related protein 1 (TRP1) functions as a DHICA oxidase in melanin biosynthesis. | Q37639625 | ||
| Pink-eyed dilution protein modulates arsenic sensitivity and intracellular glutathione metabolism. | Q39691845 | ||
| Genetics, development, and malignancy of melanocytes. | Q40839996 | ||
| KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential | Q42515610 | ||
| Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice | Q42665432 | ||
| The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS. | Q47881745 | ||
| The mouse silver locus encodes a single transcript truncated by the silver mutation. | Q47901792 | ||
| bcl-2 Protein Expression in Cutaneous Malignant Melanoma and Benign Melanocytic Nevi | Q50764553 | ||
| Strain-specific white-spotting patterns in laboratory mice. | Q52172190 | ||
| NEMO/IKK gamma-deficient mice model incontinentia pigmenti. | Q52540121 | ||
| MAP kinase links the transcription factor Microphthalmia to c-Kit signalling in melanocytes | Q59096765 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 333-344 | |
| P577 | publication date | 2003-08-01 | |
| P1433 | published in | Pigment Cell & Melanoma Research | Q762851 |
| P1476 | title | The color loci of mice--a genetic century | |
| P478 | volume | 16 |
| Q36700627 | 9-cis retinoic acid is the ALDH1A1 product that stimulates melanogenesis |
| Q24606634 | A -defensin mutation causes black coat color in domestic dogs |
| Q39084617 | A coiled-coil domain of melanophilin is essential for Myosin Va recruitment and melanosome transport in melanocytes. |
| Q33622891 | A composite six bp in-frame deletion in the melanocortin 1 receptor (MC1R) gene is associated with the Japanese brindling coat colour in rabbits (Oryctolagus cuniculus) |
| Q44150153 | A comprehensive analysis reveals mutational spectra and common alleles in Chinese patients with oculocutaneous albinism |
| Q40239443 | A conserved transcriptional enhancer that specifies Tyrp1 expression to melanocytes |
| Q41334841 | A gene duplication affecting expression of the ovine ASIP gene is responsible for white and black sheep |
| Q24648719 | A genomewide association study of skin pigmentation in a South Asian population |
| Q36339182 | A novel locus on chromosome 1 underlies the evolution of a melanic plumage polymorphism in a wild songbird |
| Q33492479 | A potent activator of melanogenesis identified from small-molecule screening |
| Q57103804 | A window on the genetics of evolution: MC1R and plumage colouration in birds |
| Q53309916 | ARP101 inhibits α-MSH-stimulated melanogenesis by regulation of autophagy in melanocytes. |
| Q33886501 | Adaptation of human skin color in various populations |
| Q38385307 | Adaptive reptile color variation and the evolution of the Mc1r gene |
| Q33294069 | Adaptive variation in beach mice produced by two interacting pigmentation genes |
| Q42134614 | Adrenal function and MC1R gene analysis in a prepubertal girl with generalized hyperpigmentation: case report |
| Q40536387 | Agonist-independent, high constitutive activity of the human melanocortin 1 receptor. |
| Q41993614 | Agouti protein, mahogunin, and attractin in pheomelanogenesis and melanoblast-like alteration of melanocytes: a cAMP-independent pathway |
| Q46612763 | Agouti signalling protein (ASIP) gene: molecular cloning, sequence characterisation and tissue distribution in domestic goose |
| Q33908592 | Allele-specific genetic interactions between Mitf and Kit affect melanocyte development |
| Q41951821 | An extensive candidate gene approach to speciation: diversity, divergence and linkage disequilibrium in candidate pigmentation genes across the European crow hybrid zone |
| Q34016272 | An iterative genetic and dynamical modelling approach identifies novel features of the gene regulatory network underlying melanocyte development. |
| Q36391821 | An unstable targeted allele of the mouse Mitf gene with a high somatic and germline reversion rate. |
| Q28288300 | Analysis of cultured human melanocytes based on polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P loci |
| Q36008833 | Analysis of ocular hypopigmentation in Rab38cht/cht mice |
| Q33553784 | Application of selection mapping to identify genomic regions associated with dairy production in sheep |
| Q40044479 | Association of the SLC45A2 gene with physiological human hair colour variation |
| Q36967843 | BACE2 processes PMEL to form the melanosome amyloid matrix in pigment cells |
| Q27348522 | Basonuclin-2 requirements for zebrafish adult pigment pattern development and female fertility |
| Q58450115 | Biogenesis of Melanosomes |
| Q36955006 | Candidate Gene Analysis Suggests Untapped Genetic Complexity in Melanin-Based Pigmentation in Birds |
| Q35854948 | Candidate genes for colour and vision exhibit signals of selection across the pied flycatcher (Ficedula hypoleuca) breeding range |
| Q36272951 | Cellular and ultrastructural characterization of the grey-morph phenotype in southern right whales (Eubalaena australis). |
| Q39236244 | Childhood malnutrition is associated with a reduction in the total melanin content of scalp hair |
| Q47259002 | Coat colour in mouse populations selected for weight gain: support for hitchhiking, not pleiotropy |
| Q52623380 | Coat colours in the Massese sheep breed are associated with mutations in the agouti signalling protein (ASIP) and melanocortin 1 receptor (MC1R) genes. |
| Q92929685 | Coloration in Mammals |
| Q42147605 | Comparative Transcriptome Analysis of Mink (Neovison vison) Skin Reveals the Key Genes Involved in the Melanogenesis of Black and White Coat Colour |
| Q64239166 | Comparative analyses identify genomic features potentially involved in the evolution of birds-of-paradise |
| Q104736915 | Comparative transcriptomics reveals the molecular genetic basis of pigmentation loss in Sinocyclocheilus cavefishes |
| Q57242494 | Compelling evidence that a single nucleotide substitution in TYRP1 is responsible for coat-colour polymorphism in a free-living population of Soay sheep |
| Q21283863 | Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans |
| Q36521086 | Constitutive gray hair in mice induced by melanocyte-specific deletion of c-Myc |
| Q37416476 | DNA reviews: predicting phenotype |
| Q36119087 | Darkness descends with two Rabs. |
| Q33997907 | Development of a linkage map and mapping of phenotypic polymorphisms in a free-living population of Soay sheep (Ovis aries) |
| Q24644487 | Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus) |
| Q36161681 | Differential recognition of a dileucine-based sorting signal by AP-1 and AP-3 reveals a requirement for both BLOC-1 and AP-3 in delivery of OCA2 to melanosomes |
| Q34231940 | Diversity of human hair pigmentation as studied by chemical analysis of eumelanin and pheomelanin |
| Q24804161 | Dorsoventral patterning of the mouse coat by Tbx15 |
| Q34886367 | Dual loss of ER export and endocytic signals with altered melanosome morphology in the silver mutation of Pmel17 |
| Q28509225 | Effects of G-protein mutations on skin color |
| Q27308079 | Endothelin Receptor B2 (EDNRB2) Gene Is Associated with Spot Plumage Pattern in Domestic Ducks (Anas platyrhynchos) |
| Q37510079 | Endothelin receptor B2 (EDNRB2) is responsible for the tyrosinase-independent recessive white (mo(w) ) and mottled (mo) plumage phenotypes in the chicken. |
| Q22122008 | Epistasis--the essential role of gene interactions in the structure and evolution of genetic systems |
| Q35027899 | Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse |
| Q35960776 | Evolutionary genetics as a tool to target genes involved in phenotypes of medical relevance |
| Q45841491 | Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism |
| Q37412247 | FIG4, Charcot-Marie-Tooth disease, and hypopigmentation: a role for phosphoinositides in melanosome biogenesis? |
| Q90118621 | Female-biased dispersal and non-random gene flow of MC1R variants do not result in a migration load in barn owls |
| Q35567778 | Ferritin H subunit gene is specifically expressed in melanophore precursor-derived white pigment cells in which reflecting platelets are formed from stage II melanosomes in the periodic albino mutant of Xenopus laevis |
| Q56996726 | Follicular vitiligo: a new form of vitiligo |
| Q34762915 | Functional interactions between OCA2 and the protein complexes BLOC-1, BLOC-2, and AP-3 inferred from epistatic analyses of mouse coat pigmentation |
| Q30489895 | Functional neurons and melanocytes induced from immortal lines of postnatal neural crest-like stem cells |
| Q92836239 | Gene Structure and Sequence Polymorphism of the Coat Color Gene, Mc1r, in the Black-Bellied Vole (Eothenomys melanogaster) |
| Q38497846 | Gene expression profile in white alpaca (Vicugna pacos) skin |
| Q43800754 | Genetic and phenotypic studies of the dark-like mutant mouse |
| Q33249314 | Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma |
| Q33294507 | Genetic effects on coat colour in cattle: dilution of eumelanin and phaeomelanin pigments in an F2-Backcross Charolais x Holstein population |
| Q37119877 | Genetic modulation of the iris transillumination defect: a systems genetics analysis using the expanded family of BXD glaucoma strains |
| Q37252489 | Genetic variation of the cutaneous HPA axis: an analysis of UVB-induced differential responses |
| Q34604038 | Genetics of Sex-linked yellow in the Syrian hamster |
| Q36528520 | Genetics, development and evolution of adaptive pigmentation in vertebrates |
| Q35974854 | Genome Wide Association Study Identifies New Loci Associated with Undesired Coat Color Phenotypes in Saanen Goats |
| Q36365208 | Genome-Wide Scan for Adaptive Divergence and Association with Population-Specific Covariates |
| Q33389875 | Genome-wide siRNA-based functional genomics of pigmentation identifies novel genes and pathways that impact melanogenesis in human cells. |
| Q38922460 | Genomic differentiation between Asturiana de los Valles, Avileña-Negra Ibérica, Bruna dels Pirineus, Morucha, Pirenaica, Retinta and Rubia Gallega cattle breeds. |
| Q51985326 | High levels of melanin-related metabolites in plasma from pink-eyed dilution mice. |
| Q37849841 | How are proliferation and differentiation of melanocytes regulated? |
| Q36314397 | Human melanocyte biology, toxicology, and pathology |
| Q46301864 | Hybrid speciation in sparrows II: a role for sex chromosomes? |
| Q37587673 | IFN-γ signaling maintains skin pigmentation homeostasis through regulation of melanosome maturation |
| Q36173698 | Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani population. |
| Q30946082 | Identification of Genes Expressed in Hyperpigmented Skin Using Meta-Analysis of Microarray Data Sets |
| Q27303686 | Identification of QTL for UV-protective eye area pigmentation in cattle by progeny phenotyping and genome-wide association analysis |
| Q37584550 | Identification of a major locus interacting with MC1R and modifying black coat color in an F₂ Nellore-Angus population. |
| Q28589778 | Identification of a novel point mutation of mouse proto-oncogene c-kit through N-ethyl-N-nitrosourea mutagenesis |
| Q49156766 | Identification of miR-145 as a key regulator of the pigmentary process |
| Q35041982 | Identification of novel transcripts and noncoding RNAs in bovine skin by deep next generation sequencing |
| Q36730790 | Immunohistochemistry and in situ hybridization in the study of human skin melanocytes |
| Q41450300 | In ovo gene manipulation of melanocytes and their adjacent keratinocytes during skin pigmentation of chicken embryos |
| Q57643659 | Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4 |
| Q33285294 | Informatic and genomic analysis of melanocyte cDNA libraries as a resource for the study of melanocyte development and function |
| Q34694810 | Interspecies difference in the regulation of melanocyte development by SOX10 and MITF. |
| Q79401867 | Investigation of the role of the agouti signaling protein gene (ASIP) in coat color evolution in primates |
| Q38230708 | Ion transport in pigmentation |
| Q33821226 | Iris phenotypes and pigment dispersion caused by genes influencing pigmentation |
| Q37159545 | Isolation of 4,5-O-Dicaffeoylquinic Acid as a Pigmentation Inhibitor Occurring in Artemisia capillaris Thunberg and Its Validation In Vivo |
| Q35970143 | Liver X Receptor-α polymorphisms (rs11039155 and rs2279238) are associated with susceptibility to vitiligo |
| Q39230073 | Liver X receptor activation inhibits melanogenesis through the acceleration of ERK-mediated MITF degradation |
| Q24294239 | MART-1 is required for the function of the melanosomal matrix protein PMEL17/GP100 and the maturation of melanosomes |
| Q37529296 | MC1R genotype and plumage colouration in the zebra finch (Taeniopygia guttata): population structure generates artefactual associations |
| Q51595009 | MC1R-dependent, melanin-based colour polymorphism is associated with cell-mediated response in the Eleonora's falcon. |
| Q35624663 | Mammalian paramutation: a tail's tale? |
| Q81607608 | Medaka double mutants for color interfere and leucophore free: characterization of the xanthophore-somatolactin relationship using the leucophore free gene |
| Q33489634 | Melanism in peromyscus is caused by independent mutations in agouti |
| Q50796079 | Melanoblasts on the move: Rac1 sets the pace. |
| Q26745953 | Melanocortin 1 Receptor: Structure, Function, and Regulation |
| Q24316155 | Melanocortin-1 receptor signaling markedly induces the expression of the NR4A nuclear receptor subgroup in melanocytic cells |
| Q34562487 | Melanocortin-1 receptor structure and functional regulation. |
| Q37861902 | Melanocyte stem cells: a melanocyte reservoir in hair follicles for hair and skin pigmentation |
| Q28587784 | Melanocytes and pigmentation are affected in dopachrome tautomerase knockout mice |
| Q24647195 | Melanosomes--dark organelles enlighten endosomal membrane transport |
| Q30486283 | Mice with mutations of Dock7 have generalized hypopigmentation and white-spotting but show normal neurological function |
| Q34143012 | MicroRNA-218 inhibits melanogenesis by directly suppressing microphthalmia-associated transcription factor expression. |
| Q37100856 | Microarray analysis sheds light on the dedifferentiating role of agouti signal protein in murine melanocytes via the Mc1r |
| Q33583915 | Microarray-based analysis of the differential expression of melanin synthesis genes in dark and light-muzzle Korean cattle |
| Q37183418 | Modifying skin pigmentation - approaches through intrinsic biochemistry and exogenous agents |
| Q28585860 | Molecular basis of the extreme dilution mottled mouse mutation: a combination of coding and noncoding genomic alterations |
| Q55514055 | Molecular cloning and characterization of the endothelin 3 gene in black bone sheep. |
| Q48062814 | Molecular cloning, sequence identification and tissue expression profile of three novel genes Sfxn1, Snai2 and Cno from Black-boned sheep (Ovis aries) |
| Q36476144 | Mouse coat color mutations: from fancy mice to functional genomics |
| Q39497919 | Mutations in dopachrome tautomerase (Dct) affect eumelanin/pheomelanin synthesis, but do not affect intracellular trafficking of the mutant protein |
| Q48472647 | NGS-based 100-gene panel of hypopigmentation identifies mutations in Chinese Hermansky-Pudlak syndrome patients |
| Q30010991 | Natural selection in avian protein-coding genes expressed in brain |
| Q33584524 | Networks and pathways in pigmentation, health, and disease |
| Q28590740 | Neural crest cell deficiency of c-myc causes skull and hearing defects |
| Q37361948 | New insights into melanosome transport in vertebrate pigment cells. |
| Q34563018 | Not just black and white: pigment pattern development and evolution in vertebrates |
| Q36117464 | Notch signaling via Hes1 transcription factor maintains survival of melanoblasts and melanocyte stem cells |
| Q34204896 | On the way to functional agro biodiversity: coat colour gene variability in goats. |
| Q28076932 | PMEL Amyloid Fibril Formation: The Bright Steps of Pigmentation |
| Q51495687 | Pale and dark reddish melanic tawny owls differentially regulate the level of blood circulating POMC prohormone in relation to environmental conditions. |
| Q36034930 | Peri-implantation lethality in mice carrying megabase-scale deletion on 5qc3.3 is caused by Exoc1 null mutation |
| Q38109037 | Phenotypes from ancient DNA: approaches, insights and prospects |
| Q42631348 | Pheomelanin coat colour dilution in French cattle breeds is not correlated with the TYR, TYRP1 and DCT transcription levels |
| Q28245280 | Physiological factors that regulate skin pigmentation |
| Q38016481 | Piebaldism |
| Q46025636 | Pigment phenotype and biogeographical ancestry from ancient skeletal remains: inferences from multiplexed autosomal SNP analysis. |
| Q33730665 | Pigmentation pathway evolution after whole-genome duplication in fish |
| Q51022428 | Polymorphisms of four pigmentation genes (SLC45A2, SLC24A5, MC1R and TYRP1) among eleven endogamous populations of India. |
| Q33379083 | Predicting unobserved phenotypes for complex traits from whole-genome SNP data |
| Q50474486 | Preliminary study on eye colour in Japanese macaques (Macaca fuscata) in their natural habitat. |
| Q33605413 | Protein interaction network topology uncovers melanogenesis regulatory network components within functional genomics datasets |
| Q36500613 | QTL analysis of modifiers for pigmentary disorder in rats carrying Ednrb sl mutations |
| Q43130488 | Rab1A regulates anterograde melanosome transport by recruiting kinesin-1 to melanosomes through interaction with SKIP. |
| Q36119125 | Rab38 and Rab32 control post-Golgi trafficking of melanogenic enzymes |
| Q41448358 | Refractive errors, visual impairment, and the use of low-vision devices in albinism in Malawi |
| Q50455720 | Regulating melanosome transfer: who's driving the bus? |
| Q46607661 | Regulation of melanoblast and retinal pigment epithelium development by Xenopus laevis Mitf |
| Q44666427 | Regulation of tyrosinase processing and trafficking by organellar pH and by proteasome activity |
| Q57485237 | Seeing spots: quantifying mother-offspring similarity and assessing fitness consequences of coat pattern traits in a wild population of giraffes () |
| Q57614838 | Selection and microevolution of coat pattern are cryptic in a wild population of sheep |
| Q33567668 | Sequence polymorphism in candidate genes for differences in winter plumage between Scottish and Scandinavian Willow Grouse (Lagopus lagopus) |
| Q61544715 | Sequence variation in the coding region of the melanocortin-1 receptor gene (MC1R) is not associated with plumage variation in the blue-crowned manakin (Lepidothrix coronata) |
| Q37750938 | Shades of meaning: the pigment-type switching system as a tool for discovery |
| Q26739678 | Signaling Pathways in Melanogenesis |
| Q34943036 | Signaling from the human melanocortin 1 receptor to ERK1 and ERK2 mitogen-activated protein kinases involves transactivation of cKIT. |
| Q33913618 | Signaling pathways in melanosome biogenesis and pathology |
| Q34603456 | Signatures of positive selection in genes associated with human skin pigmentation as revealed from analyses of single nucleotide polymorphisms. |
| Q59339812 | Signatures of selection and environmental adaptation across the goat genome post-domestication |
| Q92636095 | Significance of 5-S-Cysteinyldopa as a Marker for Melanoma |
| Q29031362 | Silver Hair Syndromes: Chediak-Higashi Syndrome (CHS) and Griscelli Syndromes (GS) |
| Q38495233 | Silymarin inhibits melanin synthesis in melanocyte cells |
| Q47867774 | Simple chronic colitis model using hypopigmented mice with a Hermansky-Pudlak syndrome 5 gene mutation |
| Q46974664 | Single base-pair deletion in ASIP exon 3 associated with recessive black phenotype in impala (Aepyceros melampus). |
| Q91069571 | Skin transcriptome profiles associated with black- and white-coated regions in Boer and Macheng black crossbred goats |
| Q34768426 | Skin transcriptome profiles associated with coat color in sheep |
| Q27301355 | Skipping of exons by premature termination of transcription and alternative splicing within intron-5 of the sheep SCF gene: a novel splice variant |
| Q33901756 | Slc7a11 gene controls production of pheomelanin pigment and proliferation of cultured cells |
| Q34494222 | Spectral analysis by XANES reveals that GPNMB influences the chemical composition of intact melanosomes |
| Q35771686 | Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders |
| Q37314646 | Stripes and belly-spots -- a review of pigment cell morphogenesis in vertebrates. |
| Q34397495 | Systematic review of treatment modalities for gingival depigmentation: a random-effects poisson regression analysis |
| Q26776085 | The Genetics of Deafness in Domestic Animals |
| Q34669802 | The Roles of ADAMs Family Proteinases in Skin Diseases |
| Q36257261 | The Silver locus product Pmel17/gp100/Silv/ME20: controversial in name and in function |
| Q47310453 | The Tyr (albino) locus of the laboratory mouse |
| Q38180693 | The biology of melanocyte and melanocyte stem cell |
| Q37477461 | The causes of repeated genetic evolution |
| Q35579764 | The functional basis of wing patterning in Heliconius butterflies: the molecules behind mimicry |
| Q39956143 | The genetic basis of recessive self-colour pattern in a wild sheep population |
| Q34113992 | The genetics of adaptive coat color in gophers: coding variation at Mc1r is not responsible for dorsal color differences |
| Q24534055 | The genetics of sun sensitivity in humans |
| Q41255342 | The integrated analysis of RNA-seq and microRNA-seq depicts miRNA-mRNA networks involved in Japanese flounder (Paralichthys olivaceus) albinism |
| Q36970638 | The many faces of Notch signaling in skin-derived cells |
| Q24681659 | The new mutation theory of phenotypic evolution |
| Q37903418 | The pleiotropic roles of autophagy regulators in melanogenesis |
| Q28573030 | The rat Ruby ( R) locus is Rab38: identical mutations in Fawn-hooded and Tester-Moriyama rats derived from an ancestral Long Evans rat sub-strain |
| Q34652201 | The regulation of skin pigmentation |
| Q35996973 | The role of isoforms in the evolution of cryptic coloration in Peromyscus mice |
| Q64121062 | Transcriptomic Analysis of Coding Genes and Non-Coding RNAs Reveals Complex Regulatory Networks Underlying the Black Back and White Belly Coat Phenotype in Chinese Wuzhishan Pigs |
| Q33226924 | Triazine-based tyrosinase inhibitors identified by chemical genetic screening |
| Q58322248 | Tyrosinase Degradation in Amelanotic Melanoma Cells is Mediated by Cytoplasmic Factors in Addition to Proteasome-Mediated Mechanism |
| Q38009396 | Unraveling the thread of nature's tapestry: the genetics of diversity and convergence in animal pigmentation |
| Q47614021 | Unusual leucophore-like cells specifically appear in the lineage of melanophores in the periodic albino mutant of Xenopus laevis |
| Q64101774 | Variation in pigmentation gene expression is associated with distinct aposematic color morphs in the poison frog Dendrobates auratus |
| Q42498524 | Vitiligo - The story from within: A transmission electron microscopic study before and after narrow-band ultraviolet B. |
| Q21092842 | What Controls Variation in Human Skin Color? |
| Q38344566 | Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects |
| Q33355991 | Zebrafish endzone regulates neural crest-derived chromatophore differentiation and morphology |
| Q24616650 | cis-Regulatory changes in Kit ligand expression and parallel evolution of pigmentation in sticklebacks and humans |
| Q38295495 | colgate/hdac1 Repression of foxd3 expression is required to permit mitfa-dependent melanogenesis |
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