Mouse coat color mutations: from fancy mice to functional genomics (Q36476144)

14 August 2017

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title

Mouse coat color mutations: from fancy mice to functional genomics (English)

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14 August 2017

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2

Neal G Copeland

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14 August 2017

3

Nancy A Jenkins

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14 August 2017

Eiríkur Steingrímsson

series ordinal

1

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14 August 2017

1 September 2006

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14 August 2017

Developmental Dynamics

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14 August 2017

235

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14 August 2017

9

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14 August 2017

2401-2411

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MGF (KIT Ligand) Is a Chemokinetic Factor for Melanoblast Migration into Hair Follicles

14 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

The melanocortin-1 receptor: red hair and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

Melanosomal pH controls rate of melanogenesis, eumelanin/phaeomelanin ratio and melanosome maturation in melanocytes and melanoma cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The melanosome as a model to study organelle motility in mammals

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Mitf expression is sufficient to direct differentiation of medaka blastula derived stem cells to melanocytes

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The color loci of mice--a genetic century

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The 8818G allele of the agouti signaling protein (ASIP) gene is ancestral and is associated with darker skin color in African Americans.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Degenerative disorders caused by Bcl-2 deficiency prevented by loss of its BH3-only antagonist Bim

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The transcription factor Sox10 is a key regulator of peripheral glial development.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Genetics of dark skin in mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Lineage-specific requirements of beta-catenin in neural crest development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

A biochemical function for attractin in agouti-induced pigmentation and obesity

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Accessory proteins for melanocortin signaling: attractin and mahogunin

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Checks and balancers: balancer chromosomes to facilitate genome annotation

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

MART-1 is required for the function of the melanosomal matrix protein PMEL17/GP100 and the maturation of melanosomes

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Pax3 functions at a nodal point in melanocyte stem cell differentiation

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Indispensable role of Bcl2 in the development of the melanocyte stem cell

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Worldwide polymorphism at the MC1R locus and normal pigmentation variation in humans

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The migratory pathway of neural crest cells into the skin of mouse embryos

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

EDNRB/EDN3 and Hirschsprung disease type II.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Novel myosin heavy chain encoded by murine dilute coat colour locus

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Dilute suppressor dsu acts semidominantly to suppress the coat color phenotype of a deletion mutation, dl20J, of the murine dilute locus

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Dominant role of the niche in melanocyte stem-cell fate determination

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Mechanisms of hair graying: incomplete melanocyte stem cell maintenance in the niche

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Molecular characterization of melanocyte stem cells in their niche.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

dsu functions in a MYO5A-independent pathway to suppress the coat color of dilute mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Distinct protein sorting and localization to premelanosomes, melanosomes, and lysosomes in pigmented melanocytic cells

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

SLUG (SNAI2) deletions in patients with Waardenburg disease

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Chediak-Higashi Syndrome: a rare disorder of lysosomes and lysosome related organelles

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The temporal requirement for endothelin receptor-B signalling during neural crest development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Preservation of eumelanin hair pigmentation in proopiomelanocortin-deficient mice on a nonagouti (a/a) genetic background

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Pink-eyed dilution protein modulates arsenic sensitivity and intracellular glutathione metabolism.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Melanocytes and the microphthalmia transcription factor network

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Melanocyte stem cell maintenance and hair graying

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Dilute suppressor, a new suppressor gene in the house mouse

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The Silver locus product Pmel17/gp100/Silv/ME20: controversial in name and in function

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Genetics of pigmentary disorders

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

The etiology of oculocutaneous albinism (OCA) type II: the pink protein modulates the processing and transport of tyrosinase

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Effects of G-protein mutations on skin color

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Tyrosinase maturation through the mammalian secretory pathway: bringing color to life

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Simple and highly efficient BAC recombineering using galK selection

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

A mutation in Rab27a causes the vesicle transport defects observed in ashen mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Regulation of yellow pigment formation in mice: a historical perspective

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Visualization of melanosome dynamics within wild-type and dilute melanocytes suggests a paradigm for myosin V function In vivo

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Identification of an organelle receptor for myosin-Va

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Obesity in the mouse model of pro-opiomelanocortin deficiency responds to peripheral melanocortin

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Engineering a mouse balancer chromosome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20840

7 January 2021

Identifiers

DOI

10.1002/DVDY.20840

1 reference

14 August 2017

1 reference

PubMed ID

16691561