AP-3 mediates tyrosinase but not TRP-1 trafficking in human melanocytes (Q24291443)

GOA release 2020-03-11

melanosome organization

1 reference

GOA release 2020-03-11

author name string

M Huizing

1

0 references

R Sarangarajan

2

0 references

E Strovel

3

0 references

Y Zhao

4

0 references

W A Gahl

5

0 references

R E Boissy

Molecular Biology of the Cell

6

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language of work or name

English

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publication date

July 2001

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published in

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volume

12

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issue

7

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page(s)

2075-85

0 references

cites work

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The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness

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

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Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouse

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A cytoplasmic sequence in human tyrosinase defines a second class of di-leucine-based sorting signals for late endosomal and lysosomal delivery

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The mammalian AP-3 adaptor-like complex mediates the intracellular transport of lysosomal membrane glycoproteins.

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27 September 2017

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27 September 2017

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Melanosomes are specialized members of the lysosomal lineage of organelles.

27 September 2017

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Lysosomal acid phosphatase is transported to lysosomes via the cell surface

27 September 2017

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27 September 2017

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27 September 2017

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On the analysis of the pathophysiology of Chediak-Higashi syndrome. Defects expressed by cultured melanocytes.

27 September 2017

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Distinguishing between the catalytic potential and apparent expression of tyrosinase activities

27 September 2017

1 reference

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Melanogenic regulatory factors in coated vesicles from melanoma cells

27 September 2017

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Defective expression of the mu3 subunit of the AP-3 adaptor complex in the Drosophila pigmentation mutant carmine

30 May 2018

1 reference

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Ceroid pigment deposition in circulating blood monocytes and T lymphocytes in Hermansky-Pudlak syndrome: an ultrastructural study

29 November 2018

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12 December 2020

Misrouting of tyrosinase with a truncated cytoplasmic tail as a result of the murine platinum (cp) mutation

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12 December 2020

Dense core lysosomes can fuse with late endosomes and are re-formed from the resultant hybrid organelles

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12 December 2020

Reliability of absent platelet dense bodies as a diagnostic criterion for Hermansky-Pudlak syndrome

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12 December 2020

Lysosome-associated membrane protein-1 (LAMP-1) is the melanocyte vesicular membrane glycoprotein band II

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12 December 2020

A new variant of Hermansky-Pudlak syndrome due to mutations in a gene responsible for vesicle formation

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12 December 2020

Golgi-melanosome relationship in human melanoma in vitro

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12 December 2020

Altered protein localization in melanocytes from Hermansky-Pudlak syndrome: support for the role of the HPS gene product in intracellular trafficking

1 reference

12 December 2020

Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome)

1 reference

12 December 2020

Mouse models of Hermansky Pudlak syndrome: a review

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12 December 2020

Ultrastructural and cytochemical observations on B-16 and Harding-Passey mouse melanomas. The origin of premelanosomes and compound melanosomes

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12 December 2020

Hermansky-Pudlak syndrome: models for intracellular vesicle formation

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12 December 2020