(Q34214082)

31 July 2017

1 reference

title

The color loci of mice--a genetic century (English)

1 reference

31 July 2017

Dorothy C Bennett

1

1 reference

PubMed ID

12859616

31 July 2017

M Lynn Lamoreux

series ordinal

2

1 reference

31 July 2017

1 August 2003

1 reference

Pigment Cell & Melanoma Research

31 July 2017

1 reference

31 July 2017

16

1 reference

31 July 2017

333-344

1 reference

31 July 2017

4

1 reference

Genetics of dark skin in mice

31 July 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

How the zebrafish gets its stripes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Human and mouse disorders of pigmentation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Genetics, development, and malignancy of melanocytes.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Strain-specific white-spotting patterns in laboratory mice.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

SLUG (SNAI2) deletions in patients with Waardenburg disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

An essential role for ectodomain shedding in mammalian development

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

NEMO/IKK gamma-deficient mice model incontinentia pigmenti.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

MAP kinase links the transcription factor Microphthalmia to c-Kit signalling in melanocytes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Cloning and expression of cDNA encoding mouse tyrosinase

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Identification of the albino mutation of mouse tyrosinase by analysis of an in vitro revertant

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Tyrp1 and oculocutaneous albinism type 3

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Biochemical control of melanogenesis and melanosomal organization

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

The mouse silver locus encodes a single transcript truncated by the silver mutation.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Identification of a human melanoma antigen recognized by tumor-infiltrating lymphocytes associated with in vivo tumor rejection

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Pmel17 initiates premelanosome morphogenesis within multivesicular bodies

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Polymerization of 5,6-dihydroxyindole-2-carboxylic acid to melanin by the pmel 17/silver locus protein

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

A di-leucine-based motif in the cytoplasmic tail of LIMP-II and tyrosinase mediates selective binding of AP-3.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

The melanosome: membrane dynamics in black and white

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Hermansky-Pudlak syndrome: vesicle formation from yeast to man.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Mutation of melanosome protein RAB38 in chocolate mice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Ocular albinism type 1: more than meets the eye.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Melanophilin, the product of the leaden locus, is required for targeting of myosin-Va to melanosomes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Rab27a is an essential component of melanosome receptor for myosin Va

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

The leaden gene product is required with Rab27a to recruit myosin Va to melanosomes in melanocytes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

From Agouti to Pomc--100 years of fat blonde mice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Agouti: from mouse to man, from skin to fat.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Spongiform degeneration in mahoganoid mutant mice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

bcl-2 protein expression in cutaneous malignant melanoma and benign melanocytic nevi.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

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/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

The inbred mouse in pigmentation research: significance of a congenic developmental system

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0749.2003.00067.X

7 January 2021

10.1034/J.1600-0749.2003.00067.X

Identifiers

DOI

1 reference

release_gawykyq7lnf6rnnmosgikz6n7u

31 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/gawykyq7lnf6rnnmosgikz6n7u

24 November 2022

mapped directly with Wikidata item

PubMed ID

12859616

1 reference

PubMed ID

12859616