Basis of lethality in C. elegans lacking CUP-5, the Mucolipidosis Type IV orthologue (Q46985990)

27 December 2017

title

Basis of lethality in C. elegans lacking CUP-5, the Mucolipidosis Type IV orthologue (English)

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27 December 2017

main subject

Caenorhabditis elegans

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mucolipidosis type IV

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Lara Schaheen

1

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27 December 2017

Hope Dang

series ordinal

2

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27 December 2017

Hanna Fares

series ordinal

3

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27 December 2017

language of work or name

English

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publication date

1 May 2006

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27 December 2017

published in

Developmental Biology

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27 December 2017

volume

293

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27 December 2017

page(s)

382-391

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27 December 2017

issue

2

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27 December 2017

The neurogenetics of mucolipidosis type IV

cites work

1 reference

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Cloning of the gene encoding a novel integral membrane protein, mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IV

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The apical disposition of the Caenorhabditis elegans intestinal terminal web is maintained by LET-413.

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Cathepsin L protease (CPL-1) is essential for yolk processing during embryogenesis in Caenorhabditis elegans.

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Receptor-mediated endocytosis in the Caenorhabditis elegans oocyte.

7 January 2021

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Evidence that RME-1, a conserved C. elegans EH-domain protein, functions in endocytic recycling.

7 January 2021

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The Caenorhabditis elegans mucolipin-like gene cup-5 is essential for viability and regulates lysosomes in multiple cell types

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Hrs mediates downregulation of multiple signalling receptors in Drosophila

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Identification and characterization of the single channel function of human mucolipin-1 implicated in mucolipidosis type IV, a disorder affecting the lysosomal pathway

7 January 2021

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Hrs regulates endosome membrane invagination and tyrosine kinase receptor signaling in Drosophila

7 January 2021

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Growth factor regulation of autophagy and cell survival in the absence of apoptosis

7 January 2021

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Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse

7 January 2021

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Autophagy genes are essential for dauer development and life-span extension in C. elegans

7 January 2021

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Apg9p/Cvt7p is an integral membrane protein required for transport vesicle formation in the Cvt and autophagy pathways

7 January 2021

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WIPI-1alpha (WIPI49), a member of the novel 7-bladed WIPI protein family, is aberrantly expressed in human cancer and is linked to starvation-induced autophagy

7 January 2021

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The coronin-like protein POD-1 is required for anterior-posterior axis formation and cellular architecture in the nematode caenorhabditis elegans

7 January 2021

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7 January 2021

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The Atg1-Atg13 complex regulates Atg9 and Atg23 retrieval transport from the pre-autophagosomal structure

7 January 2021

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

7 January 2021

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Inactivation of the autophagy gene bec-1 triggers apoptotic cell death in C. elegans

7 January 2021

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Specific interference by ingested dsRNA

7 January 2021

1 reference

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Caenorhabditis elegans functional orthologue of human protein h-mucolipin-1 is required for lysosome biogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2006.02.008

Lysosomal storage disorders

7 January 2021

1 reference

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Mechanisms of AIF-mediated apoptotic DNA degradation in Caenorhabditis elegans.

7 January 2021

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Cell cycle-dependent modulation of telomerase activity in tumor cells.

7 January 2021

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7 January 2021

Identifiers

DOI

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27 December 2017

PubMed ID

16530747

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27 December 2017