(Q28218945)

inferred from title

author

Gertrude-Emilia Costin

4

object named as

Gertrude-E Costin

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author name string

Kazutomo Toyofuku

1

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Julio C Valencia

2

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Tsuneto Kushimoto

3

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Victoria M Virador

5

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Wilfred D Vieira

6

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Victor J Ferrans

7

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Vincent J Hearing

Pigment Cell & Melanoma Research

8

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language of work or name

English

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publication date

June 2002

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published in

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volume

15

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issue

3

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page(s)

217-24

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cites work

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

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Endoplasmic reticulum retention is a common defect associated with tyrosinase-negative albinism

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A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

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Inverse correlation between pink-eyed dilution protein expression and induction of melanogenesis by bafilomycin A1

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The mouse p (pink-eyed dilution) and human P genes, oculocutaneous albinism type 2 (OCA2), and melanosomal pH

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Production of melanocyte-specific antibodies to human melanosomal proteins: expression patterns in normal human skin and in cutaneous pigmented lesions

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High-molecular-weight forms of tyrosinase and the tyrosinase-related proteins: evidence for a melanogenic complex

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Albinism and skin cancer in Southern Africa.

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Oculocutaneous albinism types 1 and 3 are ER retention diseases: mutation of tyrosinase or Tyrp1 can affect the processing of both mutant and wild-type proteins

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The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes

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African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism

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Inherited disorders of pigmentation

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Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene

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Pink-eyed dilution (p) gene in rodents: Increased pigmentation in tissue culture

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Melanosomal defects in melanocytes from mice lacking expression of the pink-eyed dilution gene: correction by culture in the presence of excess tyrosine

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Melanosomal tyrosine transport in normal and pink-eyed dilution murine melanocytes

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The pinkeyed-dilution protein and the eumelanin/pheomelanin switch: in support of a unifying hypothesis

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Normal tyrosine transport and abnormal tyrosinase routing in pink-eyed dilution melanocytes

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A line of non-tumorigenic mouse melanocytes, syngeneic with the B16 melanoma and requiring a tumour promoter for growth

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Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequences

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Expression and ultrastructural localization of HMB-45 antigen

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Ultrastructural localization of HMB-45 binding sites

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Promotion of tyrosinase folding in COS 7 cells by calnexin

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A model for melanosome biogenesis based on the purification and analysis of early melanosomes

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Pmel17 initiates premelanosome morphogenesis within multivesicular bodies

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A common temperature-sensitive allelic form of human tyrosinase is retained in the endoplasmic reticulum at the nonpermissive temperature.

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Sorting and targeting of melanosomal membrane proteins: signals, pathways, and mechanisms

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Modulation of murine melanocyte function in vitro by agouti signal protein

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