MelanocyteAmelanism: Amelanism (also known as amelanosis) is a pigmentation abnormality characterized by the lack of pigments called melanins, commonly associated with a genetic loss of tyrosinase function. Amelanism can affect fish, amphibians, reptiles, birds, and mammals including humans.Vitiligo Research FoundationMelanosome: A melanosome is an organelle found in animal cells, and is the cellular site of synthesis, storage and transport of melanin, the most common light-absorbing pigment found in the animal kingdom. These melanosomes are responsible for color and photoprotection in animal tissues.List of Bratz charactersMicrophthalmia-associated transcription factor: Microphthalmia-associated transcription factor also known as class E basic helix-loop-helix protein 32 or bHLHe32 is a protein that in humans is encoded by the MITF gene.James A. Schlipmann Melanoma Cancer Foundation: The James A. Schlipmann Melanoma Cancer Foundation is a US-based non-profit organization with a mission to fund clinical trials and research studies, and to advance education, awareness, screenings and treatment to eventually eradicate melanoma.Acromelanism: Acromelanism is a genetically determined, temperature-dependent pigmentation pattern, with full expression only occurring on legs, ears, tail and face. Seen in Siamese and Himalayan cats, rats, and rabbits.Human hair color: Hair color is the pigmentation of hair follicles due to two types of melanin: eumelanin and pheomelanin. Generally, if more eumelanin is present, the colour of the hair is darker; if less eumelanin is present, the hair is lighter.Nevus: Naevius|Nevis|Nevius}}Progressive macular hypomelanosis: Progressive macular hypomelanosis is a common skin condition, a disorder, observed more frequently in young women with darkly pigmented skin who originate from or reside in tropical climates.Dermal equivalent: The dermal equivalent is an in vitro model of the dermal layer of skin. It is constructed by seeding dermal fibroblasts into a collagen gel.Prostacyclin synthaseKeratinocyte: A keratinocyte is the predominant cell type in the epidermis, the outermost layer of the skin, constituting 90% of the cells found there.Idiopathic eruptive macular pigmentation: Idiopathic eruptive macular pigmentation is a skin condition developing in young persons, with an average age of 11, characterized by asymptomatic widespread brown to gray macules of up to several centimeters in diameter on the neck, trunk, and proximal extremities.Dyschromatosis symmetrica hereditaria: Dyschromatosis symmetrica hereditaria (also known as "Reticulate acropigmentation of Dohi," and "Symmetrical dyschromatosis of the extremities") is a rare autosomally inherited dermatosis. It is characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities.Melanocortin 1 receptor: The melanocortin 1 receptor (MC1R), also known as melanocyte-stimulating hormone receptor (MSHR), melanin-activating peptide receptor, or melanotropin receptor, is a G protein–coupled receptor that binds to a class of pituitary peptide hormones known as the melanocortins, which include adrenocorticotropic hormone (ACTH) and the different forms of melanocyte-stimulating hormone (MSH). MC1R is one of the key proteins involved in regulating mammalian skin and hair color.Agouti gene: The Agouti gene is responsible for determining whether a mammal's coat is banded (agouti) or of a solid color (non-agouti). The chief product of the Agouti gene is Agouti signalling peptide (ASP), but there are a number of alternative splice products.Uveoparotitis: Uveoparotitis is a symptom of sarcoidosis. It describes a chronic inflammation of the parotid gland and uvea.Truncal neural crest: The truncal neural crest or trunk neural crest is a form of neural crest.MotesanibBenign melanocytic nevus: A benign melanocytic nevus (also known as a "Banal nevus," "Common acquired melanocytic nevus," "Mole," "Nevocellular nevus," and "Nevocytic nevus") is a cutaneous condition characterised by well-circumscribed, round or ovoid lesions, generally measuring from 2 to 6 mm in diameter.UVB-induced apoptosis: UVB-induced apoptosis is the programmed cell death of cells that become damaged by ultraviolet rays. This is notable in skin cells, to prevent melanoma.Hair follicle nevus: Hair follicle nevus (also known as a "Vellus hamartoma") is a cutaneous condition that presents as a small papule from which fine hairs protrude evenly from the surface.PhenylthiocarbamideAncestimIdioteuthis cordiformis: Idioteuthis cordiformis is a species of whip-lash squid found in tropical regions of the west Pacific Ocean. The species is commonly known as the 'love-heart squid' because the species name cordiformis is Latin for 'heart shaped'.Polyphenol oxidase: Polyphenol oxidase (PPO or monophenol monooxygenase or Polyphenol oxidase I, chloroplastic) is a tetramer that contains four atoms of copper per molecule, and binding sites for two aromatic compounds and oxygen. The enzyme catalyses the o-hydroxylation of monophenol molecules in which the benzene ring contains a single hydroxyl substituent to o-diphenols (phenol molecules containing two hydroxyl substituents).Griscelli syndrome type 2: Griscelli syndrome type 2 (also known as "Partial albinism with immunodeficiency") is a rare autosomal recessive syndrome characterized by variable pigmentary dilution, hair with silvery metallic sheen, frequent pyogenic infections, neutropenia, and thrombocytopenia.James, William; Berger, Timothy; Elston, Dirk (2005).AlsactideErythromelanosis follicularis faciei et colli: Erythromelanosis follicularis faciei et colli is an erythematous pigmentary disease involving the follicles, characterized by a reddish-brown, sharply demarcated, symmetrical discoloration involving the preauricular and maxillary regions.James, William; Berger, Timothy; Elston, Dirk (2005).ACTH receptor: The adrenocorticotropic hormone receptor or ACTH receptor also known as the melanocortin receptor 2 or MC2 receptor is a type of melanocortin receptor (type 2) which is specific for ACTH.Oculocutaneous albinism type I: Oculocutaneous Albinism Type I or –Type 1A (OCA1A) is an autosomal recessive skin disease associated with albinism. This type of albinism is caused when the gene OCA1 does not function properly.Glucose-methanol-choline oxidoreductase family: In molecular biology, the glucose-methanol-choline oxidoreductase family (GMC oxidoreductase) is a family of enzymes with oxidoreductase activity.Melanoma-associated antigen: C:230-239 C:271-279Renal stem cell: Renal stem cells are self-renewing, multipotent stem cells which are able to give rise to all the cell types of the kidney. It is involved in the homeostasis and repair of the kidney, and holds therapeutic potential for treatment of kidney failure.