Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A. (Q34307291)

1 August 2017

Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A. (English)

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hereditary spastic paraplegia

1 August 2017

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Peng-Peng Zhu

1

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1 August 2017

Kyle R Denton

2

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1 August 2017

Tyler Mark Pierson

3

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1 August 2017

Xue-Jun Li

4

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1 August 2017

Craig Blackstone

5

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1 August 2017

6 June 2014

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1 August 2017

Human Molecular Genetics

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1 August 2017

23

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1 August 2017

21

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1 August 2017

5638-5648

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describes a project that uses

1 August 2017

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4189900/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutation

6 July 2018

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Loss of spastin function results in disease-specific axonal defects in human pluripotent stem cell-based models of hereditary spastic paraplegia

6 July 2018

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6 July 2018

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A conserved role for atlastin GTPases in regulating lipid droplet size

6 July 2018

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6 July 2018

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Endoplasmic reticulum structure and interconnections with other organelles

6 July 2018

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Structural basis for conformational switching and GTP loading of the large G protein atlastin

6 July 2018

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A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutations

6 July 2018

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Recapitulation of spinal motor neuron-specific disease phenotypes in a human cell model of spinal muscular atrophy.

6 July 2018

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Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII trafficking

6 July 2018

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NIH Image to ImageJ: 25 years of image analysis

6 July 2018

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Microtubule-targeting drugs rescue axonal swellings in cortical neurons from spastin knockout mice

6 July 2018

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Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance

6 July 2018

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Cellular pathways of hereditary spastic paraplegia

6 July 2018

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The dynamin-like GTPase Sey1p mediates homotypic ER fusion in S. cerevisiae

6 July 2018

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Genetics of hereditary spastic paraplegias

6 July 2018

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Emerging aspects of ER organization in root hair tip growth: lessons from RHD3 and Atlastin

6 July 2018

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Increased axonal mitochondrial mobility does not slow amyotrophic lateral sclerosis (ALS)-like disease in mutant SOD1 mice

6 July 2018

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A more efficient method to generate integration-free human iPS cells

6 July 2018

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Structural basis for the nucleotide-dependent dimerization of the large G protein atlastin-1/SPG3A

6 July 2018

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Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.

6 July 2018

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Hereditary spastic paraplegias: membrane traffic and the motor pathway

6 July 2018

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Molecular motors in neurons: transport mechanisms and roles in brain function, development, and disease.

6 July 2018

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Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway

6 July 2018

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Specification of region-specific neurons including forebrain glutamatergic neurons from human induced pluripotent stem cells

6 July 2018

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Further assembly required: construction and dynamics of the endoplasmic reticulum network

6 July 2018

1 reference

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Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network

6 July 2018

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Coordination of sonic hedgehog and Wnt signaling determines ventral and dorsal telencephalic neuron types from human embryonic stem cells

6 July 2018

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Axonal transport defects in neurodegenerative diseases

6 July 2018

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A class of dynamin-like GTPases involved in the generation of the tubular ER network

6 July 2018

1 reference

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Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin

6 July 2018

1 reference

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Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

6 July 2018

1 reference

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Membrane proteins of the endoplasmic reticulum induce high-curvature tubules

6 July 2018

1 reference

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Quantitative and functional analyses of spastin in the nervous system: implications for hereditary spastic paraplegia

6 July 2018

1 reference

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Atlastin GTPases are required for Golgi apparatus and ER morphogenesis

6 July 2018

1 reference

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Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity

6 July 2018

1 reference

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Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content

6 July 2018

1 reference

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Visualization and quantification of mitochondrial dynamics in living animal cells.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

A class of membrane proteins shaping the tubular endoplasmic reticulum

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Traffic accidents: molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Advances in the hereditary spastic paraplegias

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Evidence for mitochondrial control of neuronal polarity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

The ROOT HAIR DEFECTIVE3 gene encodes an evolutionarily conserved protein with GTP-binding motifs and is required for regulated cell enlargement in Arabidopsis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Arabidopsis RHD3 mediates the generation of the tubular ER network and is required for Golgi distribution and motility in plant cells.

6 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU280

ROOT HAIR DEFECTIVE3 family of dynamin-like GTPases mediates homotypic endoplasmic reticulum fusion and is essential for Arabidopsis development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU280

Drosophila Atlastin regulates the stability of muscle microtubules and is required for synapse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU280

ATL1 and REEP1 mutations in hereditary and sporadic upper motor neuron syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU280

A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU280

Characterization of a novel SPG3A deletion in a French-Canadian family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU280

A novel missense mutation confirms ATL3 as a gene for hereditary sensory neuropathy type 1.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

Response of mitochondrial traffic to axon determination and differential branch growth.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189900

28 October 2018

Identifiers

DOI

10.1093/HMG/DDU280

1 reference

1 August 2017

1 reference

1 August 2017

1 reference