(Q50645963)

17 March 2018

title

Lysosomal exocytosis is impaired in mucolipidosis type IV. (English)

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17 March 2018

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Janice M LaPlante

1

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17 March 2018

Mei Sun

2

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17 March 2018

John Falardeau

3

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17 March 2018

Daisy Dai

4

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17 March 2018

Edward M Brown

5

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17 March 2018

Susan A Slaugenhaupt

6

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17 March 2018

Peter M Vassilev

7

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17 March 2018

publication date

17 August 2006

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17 March 2018

Molecular Genetics and Metabolism

published in

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17 March 2018

volume

89

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17 March 2018

issue

4

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17 March 2018

page(s)

339-348

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17 March 2018

Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel

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Congenital corneal clouding with abnormal systemic storage bodies: A new variant of mucolipidosis

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The molecular basis of mucolipidosis type IV.

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Mucolipidosis IV consists of one complementation group

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Mucolipidosis type IV: abnormal transport of lipids to lysosomes

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Abnormal transport along the lysosomal pathway in mucolipidosis, type IV disease

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Purification and characterization of an N-acetyl-beta-D-glucosaminidase from cortical granules of Xenopus laevis eggs

7 January 2021

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Noninvasive diagnosis and ophthalmic features of mucolipidosis type IV.

7 January 2021

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Constitutive achlorhydria in mucolipidosis type IV

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Synaptotagmin VII regulates Ca(2+)-dependent exocytosis of lysosomes in fibroblasts

7 January 2021

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7 January 2021

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Synaptotagmin II negatively regulates Ca2+-triggered exocytosis of lysosomes in mast cells

7 January 2021

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7 January 2021

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7 January 2021

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Membrane fusion. Ready...aim...fire!

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Actin filaments and myosin I alpha cooperate with microtubules for the movement of lysosomes

7 January 2021

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10.1016/J.YMGME.2006.05.016

7 January 2021

Identifiers

DOI

1 reference

17 March 2018

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17 March 2018