SQSTM1 mutations--bridging Paget disease of bone and ALS/FTLD. (Q38184230)

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7 March 2020

title

SQSTM1 mutations--bridging Paget disease of bone and ALS/FTLD (English)

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amyotrophic lateral sclerosis

7 March 2020

main subject

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1

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7 March 2020

Mark S. Searle

series ordinal

3

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7 March 2020

Robert Layfield

series ordinal

4

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7 March 2020

author name string

Veronika Majcher

series ordinal

2

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7 March 2020

language of work or name

English

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publication date

30 January 2014

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Experimental Cell Research

7 March 2020

published in

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7 March 2020

volume

325

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7 March 2020

page(s)

27-37

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7 March 2020

issue

1

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Optineurin suppression causes neuronal cell death via NF-κB pathway.

7 March 2020

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A SQSTM1/p62 mutation linked to Paget's disease increases the osteoclastogenic potential of the bone microenvironment

7 January 2021

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Structural basis for sorting mechanism of p62 in selective autophagy

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Phosphorylation of p62 activates the Keap1-Nrf2 pathway during selective autophagy

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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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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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