The color loci of mice--a genetic century.

No abstract is available for this paper.

• Publication year

  2003

• Venue

  Pigment Cell Research

• Publication date

  2003-08-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1034/J.1600-0749.2003.00067.XPMID 12859616
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Incontinentia Pigmenti

  2011cited by this paper
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  2003cited by this paper
• A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation

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• Spongiform Degeneration in mahoganoid Mutant Mice

  2003cited by this paper
• Genetics of dark skin in mice.

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  2003cited by this paper
• The biology of melanocytes.

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  2002cited by this paper
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  2002influential reference
• Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice

  2002cited by this paper
• SLUG (SNAI2) deletions in patients with Waardenburg disease.

  2002cited by this paper
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• KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential.

  2002cited by this paper
• The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome.

  2002cited by this paper
• Chediak-Higashi Syndrome: a rare disorder of lysosomes and lysosome related organelles.

  2002influential reference
• Agouti: from mouse to man, from skin to fat.

  2002influential reference
• Rab27a is an essential component of melanosome receptor for myosin Va.

  2002cited by this paper
• Pink-eyed dilution protein modulates arsenic sensitivity and intracellular glutathione metabolism.

  2002influential reference
• The leaden Gene Product Is Required with Rab27a to Recruit Myosin Va to Melanosomes in Melanocytes

  2002cited by this paper
• Mutation of melanosome protein RAB38 in chocolate mice

  2002cited by this paper
• Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice

  2002influential reference
• Zinc-finger transcription factor Slug contributes to the function of the stem cell factor c-kit signaling pathway.

  2002cited by this paper
• Ocular albinism type 1: more than meets the eye.

  2001cited by this paper
• The melanosome: membrane dynamics in black and white

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• The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene.

  2001cited by this paper
• How the zebrafish gets its stripes.

  2001cited by this paper
• Pmel17 initiates premelanosome morphogenesis within multivesicular bodies.

  2001cited by this paper
• A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice.

  2001cited by this paper
• Tyrp1 and oculocutaneous albinism type 3.

  2001cited by this paper
• Signaling and transcriptional regulation in the neural crest-derived melanocyte lineage: interactions between KIT and MITF.

  2000cited by this paper
• Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti

  2000cited by this paper
• The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS

  2000cited by this paper
• NEMO/IKK gamma-deficient mice model incontinentia pigmenti.

  2000cited by this paper
• The inbred mouse in pigmentation research: significance of a congenic developmental system.

  2000cited by this paper
• Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice

  2000cited by this paper
• Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.

  2000cited by this paper
• Mitf from neural crest to melanoma: signal transduction and transcription in the melanocyte lineage.

  2000cited by this paper
• NEMO/IKKγ-Deficient Mice Model Incontinentia Pigmenti

  2000cited by this paper
• From Agouti to Pomc—100 years of fat blonde mice

  1999influential reference
• Biochemical control of melanogenesis and melanosomal organization.

  1999cited by this paper
• Obesity in the mouse model of pro-opiomelanocortin deficiency responds to peripheral melanocortin

  1999cited by this paper
• The mouse silver locus encodes a single transcript truncated by the silver mutation

  1999cited by this paper
• Strain-specific white-spotting patterns in laboratory mice.

  1999cited by this paper
• The pigmentary system : physiology and pathophysiology

  1998cited by this paper
• The murine misty mutation: phenotypic effects on melanocytes, platelets and brown fat.

  1998cited by this paper
• A di‐leucine‐based motif in the cytoplasmic tail of LIMP‐II and tyrosinase mediates selective binding of AP‐3

  1998cited by this paper
• An essential role for ectodomain shedding in mammalian development.

  1998influential reference
• MAP kinase links the transcription factor Microphthalmia to c-Kit signalling in melanocytes

  1998cited by this paper
• The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

  1997cited by this paper
• Polymerization of 5,6-dihydroxyindole-2-carboxylic acid to melanin by the pmel 17/silver locus protein.

  1996cited by this paper
• bcl‐2 Protein Expression in Cutaneous Malignant Melanoma and Benign Melanocytic Nevi

  1995cited by this paper
• Online Mendelian Inheritance in Man.

  1995cited by this paper
• Tyrosinase related protein 1 (TRP1) functions as a DHICA oxidase in melanin biosynthesis.

  1994cited by this paper
• Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes.

  1994cited by this paper
• Identification of a human melanoma antigen recognized by tumor-infiltrating lymphocytes associated with in vivo tumor rejection.

  1994cited by this paper
• Genetics, development, and malignancy of melanocytes.

  1993cited by this paper
• Effects of the developmental colour mutations silver and recessive spotting on proliferation of diploid and immortal mouse melanocytes in culture.

  1992cited by this paper
• Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism.

  1991cited by this paper
• A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.

  1990cited by this paper
• Identification of the albino mutation of mouse tyrosinase by analysis of an in vitro revertant.

  1990cited by this paper
• Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene.

  1989cited by this paper
• Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus.

  1987cited by this paper
• Cloning and sequencing of mouse tyrosinase cDNA.

  1987cited by this paper
• Cloning and expression of cDNA encoding mouse tyrosinase.

  1986cited by this paper
• The Coat Colors of Mice

  1979influential reference
• Mendelian inheritance in man

  1971cited by this paper

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  2025cites this paper
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  2025cites this paper
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  2025cites this paper
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  2023cites this paper
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  2023cites this paper
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  2022cites this paper
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  2022cites this paper
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  2022cites this paper
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  2022cites this paper
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  2022cites this paper
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  2022cites this paper
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  2018cites this paper
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  2018cites this paper
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