Impaired prosaposin lysosomal trafficking in frontotemporal lobar degeneration due to progranulin mutations (Q33815765)

29 July 2017

Impaired prosaposin lysosomal trafficking in frontotemporal lobar degeneration due to progranulin mutations (English)

1 reference

29 July 2017

1 reference

Prosaposin

1 reference

Sortilin 1

1 reference

Granulin

1 reference

Prosaposin

1 reference

frontotemporal lobar degeneration

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10

William W Seeley

1 reference

29 July 2017

Ji Whae Choi

4

0 references

Alissa Nana Li

object named as

Alissa L Nana

6

0 references

Oliver Bracko

object named as

Oliver Bracko

3

0 references

Nozomi Nishimura

object named as

Nozomi Nishimura

9

0 references

author name string

Xiaolai Zhou

1

1 reference

29 July 2017

Lirong Sun

2

1 reference

29 July 2017

Yan Jia

5

1 reference

29 July 2017

Owen Adam Brady

7

1 reference

29 July 2017

Jean C Cruz Hernandez

8

1 reference

29 July 2017

Fenghua Hu

11

1 reference

29 July 2017

language of work or name

English

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publication date

25 May 2017

1 reference

29 July 2017

Nature Communications

1 reference

29 July 2017

8

1 reference

29 July 2017

15277

1 reference

Creative Commons Attribution 4.0 International

29 July 2017

start time

25 May 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC5477518/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

exact match

https://scigraph.springernature.com/pub.10.1038/ncomms15277

0 references

cites work

Prosaposin is a regulator of progranulin levels and oligomerization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation

4 July 2018

1 reference

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Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation

4 July 2018

1 reference

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Genetics of FTLD: overview and what else we can expect from genetic studies

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Prosaposin facilitates sortilin-independent lysosomal trafficking of progranulin

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Glucocerebrosidase and Parkinson disease: Recent advances

4 July 2018

1 reference

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Possible involvement of lysosomal dysfunction in pathological changes of the brain in aged progranulin-deficient mice

4 July 2018

1 reference

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Neuronal ceroid lipofuscinosis: impact of recent genetic advances and expansion of the clinicopathologic spectrum

4 July 2018

1 reference

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Dissociation of frontotemporal dementia-related deficits and neuroinflammation in progranulin haploinsufficient mice

4 July 2018

1 reference

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Mouse models of frontotemporal dementia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Progranulin: a proteolytically processed protein at the crossroads of inflammation and neurodegeneration

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Progranulin axis and recent developments in frontotemporal lobar degeneration

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease

4 July 2018

1 reference

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Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses

4 July 2018

1 reference

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Transcriptional gene network inference from a massive dataset elucidates transcriptome organization and gene function.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

C-terminus of progranulin interacts with the beta-propeller region of sortilin to regulate progranulin trafficking

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

A harmonized classification system for FTLD-TDP pathology

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Sortilin-mediated endocytosis determines levels of the frontotemporal dementia protein, progranulin.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Accelerated lipofuscinosis and ubiquitination in granulin knockout mice suggest a role for progranulin in successful aging

4 July 2018

1 reference

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Pathophysiology of neuropathic lysosomal storage disorders

4 July 2018

1 reference

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Exaggerated inflammation, impaired host defense, and neuropathology in progranulin-deficient mice

4 July 2018

1 reference

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The granulin gene family: from cancer to dementia

4 July 2018

1 reference

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ESCRT, autophagy, and frontotemporal dementia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

The function of sphingolipids in the nervous system: lessons learnt from mouse models of specific sphingolipid activator protein deficiencies

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Progranulin in frontotemporal lobar degeneration and neuroinflammation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Lysosomal system pathways: genes to neurodegeneration in Alzheimer's disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Glatiramer acetate fights against Alzheimer's disease by inducing dendritic-like microglia expressing insulin-like growth factor 1

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

4 July 2018

1 reference

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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Use of polyethyleneimine polymer in cell culture as attachment factor and lipofection enhancer

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Sortilin is essential for proNGF-induced neuronal cell death

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

The lysosomal trafficking of sphingolipid activator proteins (SAPs) is mediated by sortilin

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Molecular and cell biology of acid beta-glucosidase and prosaposin

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Cellular uptake of saposin (SAP) precursor and lysosomal delivery by the low density lipoprotein receptor-related protein (LRP).

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

The carboxy-terminal domain of the receptor-associated protein binds to the Vps10p domain of sortilin

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Biosynthesis, processing, and targeting of sphingolipid activator protein (SAP )precursor in cultured human fibroblasts. Mannose 6-phosphate receptor-independent endocytosis of SAP precursor

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Proteolytic processing patterns of prosaposin in insect and mammalian cells

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Saposin proteins: structure, function, and role in human lysosomal storage disorders

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Biosynthesis of lysosomal enzymes in cells of the End3 complementation group conditionally defective in endosomal acidification

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Prosaposin: threshold rescue and analysis of the "neuritogenic" region in transgenic mice

4 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS15277

Gaucher disease mouse models: point mutations at the acid beta-glucosidase locus combined with low-level prosaposin expression lead to disease variants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS15277

Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS15277

Culturing pyramidal neurons from the early postnatal mouse hippocampus and cortex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS15277

Involvement of Gaucher Disease Mutations in Parkinson Disease.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5477518

Proteomics analysis of serum from mutant mice reveals lysosomal proteins selectively transported by each of the two mannose 6-phosphate receptors

30 October 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS15277

inferred from DOI database lookup

7 January 2021

based on heuristic

Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28541286

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NCOMMS15277

1 reference

Dimensions Publication ID

29 July 2017

0 references

0 references

1 reference

29 July 2017

1 reference