(Q24295115)

https://api.crossref.org/works/10.1074/JBC.M306702200

13 March 2024

1 reference

GOA release 2020-03-11

protein homooligomerization

1 reference

hereditary spastic paraplegia

GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

hereditary spastic paraplegia 3A

1 reference

1 reference

https://api.crossref.org/works/10.1074/JBC.M306702200

13 March 2024

1 reference

https://api.crossref.org/works/10.1074/JBC.M306702200

13 March 2024

author name string

Peng-Peng Zhu

1

0 references

Andrew Patterson

2

0 references

Brigitte Lavoie

3

0 references

Julia Stadler

4

0 references

Marwa Shoeb

5

0 references

Rakesh Patel

6

0 references

Craig Blackstone

7

0 references

language of work or name

English

0 references

publication date

5 December 2003

0 references

23 September 2003

1 reference

Europe PubMed Central

PubMed publication ID

14506257

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14506257

full work available at URL

13 March 2024

http://www.jbc.org/article/S0021925820756772/pdf

1 reference

Europe PubMed Central

PubMed publication ID

14506257

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14506257

https://api.elsevier.com/content/article/PII:S0021925820756772?httpAccept=text/xml

13 March 2024

1 reference

https://api.crossref.org/works/10.1074/JBC.M306702200

https://api.elsevier.com/content/article/PII:S0021925820756772?httpAccept=text/plain

13 March 2024

1 reference

https://api.crossref.org/works/10.1074/JBC.M306702200

https://syndication.highwire.org/content/doi/10.1074/jbc.M306702200

13 March 2024

1 reference

https://api.crossref.org/works/10.1074/JBC.M306702200

Journal of Biological Chemistry

13 March 2024

published in

0 references

volume

278

0 references

issue

49

0 references

page(s)

49063-71

0 references

cites work

Recent advances in hereditary spastic paraplegia

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Is the transportation highway the right road for hereditary spastic paraplegia?

21 January 2018

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Hereditary spastic paraplegia

21 January 2018

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Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias

21 January 2018

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A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

21 January 2018

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Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

21 January 2018

1 reference

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The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia

21 January 2018

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Structure of human guanylate-binding protein 1 representing a unique class of GTP-binding proteins

21 January 2018

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Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

21 January 2018

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SPG3A: An additional family carrying a new atlastin mutation

21 January 2018

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Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation

21 January 2018

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

21 January 2018

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SOSUI: classification and secondary structure prediction system for membrane proteins

21 January 2018

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CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

21 January 2018

1 reference

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Interaction of the deafness-dystonia protein DDP/TIMM8a with the signal transduction adaptor molecule STAM1

21 January 2018

1 reference

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OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M306702200

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

21 January 2018

1 reference

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Phosphorylation of the head domain of neurofilament protein (NF-M): a factor regulating topographic phosphorylation of NF-M tail domain KSP sites in neurons

21 January 2018

1 reference

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Biochemical characterization and localization of a non-N-methyl-D-aspartate glutamate receptor in rat brain

21 January 2018

1 reference

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Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells

21 January 2018

1 reference

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Torsin A and its torsion dystonia-associated mutant forms are lumenal glycoproteins that exhibit distinct subcellular localizations

21 January 2018

1 reference

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Domains mediating intramolecular folding and oligomerization of MxA GTPase.

21 January 2018

1 reference

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Intramolecular backfolding of the carboxyl-terminal end of MxA protein is a prerequisite for its oligomerization

21 January 2018

1 reference

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Three-dimensional reconstruction of dynamin in the constricted state

21 January 2018

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A novel GTP-binding protein hGBP3 interacts with NIK/HGK

21 January 2018

1 reference

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The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype

21 January 2018

1 reference

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Connection of the mitochondrial outer and inner membranes by Fzo1 is critical for organellar fusion

21 January 2018

1 reference

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Interferon-induced mx proteins: dynamin-like GTPases with antiviral activity

21 January 2018

1 reference

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A novel ADP-ribosylation like factor (ARL-6), interacts with the protein-conducting channel SEC61beta subunit

21 January 2018

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Dissection of COPI and Arf1 dynamics in vivo and role in Golgi membrane transport

21 January 2018

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Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

21 January 2018

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Mutant dynactin in motor neuron disease.

21 January 2018

1 reference

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Hereditary spastic paraplegia: the pace quickens

21 January 2018

1 reference

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Hereditary (familial) spastic paraplegia; further clinical and pathologic observations.

21 January 2018

1 reference

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Intermolecular and interdomain interactions of a dynamin-related GTP-binding protein, Dnm1p/Vps1p-like protein

21 January 2018

1 reference

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Membrane traffic: Arl GTPases get a GRIP on the Golgi

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M306702200

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M306702200

inferred from DOI database lookup

7 January 2021

based on heuristic

Inhibition of Axonal Growth by Brefeldin A in Hippocampal Neurons in Culture

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M306702200

inferred from DOI database lookup

7 January 2021

based on heuristic

Classification of the hereditary ataxias and paraplegias

7

1 reference

https://api.crossref.org/works/10.1074/JBC.M306702200

Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia

13 March 2024

14

1 reference

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Phase separation of integral membrane proteins in Triton X-114 solution

13 March 2024

24

1 reference

https://api.crossref.org/works/10.1074/JBC.M306702200

13 March 2024

Identifiers

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

14506257

1 reference

Consolidated OpenCitations Corpus – April 2017