(Q24309083)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

SPG7 matrix AAA peptidase subunit, paraplegin

12 November 2019

main subject

1 reference

GOA release 2020-03-11

unfolded protein binding

1 reference

GOA release 2020-03-11

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Marina Mora

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Andrea Ballabio

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

author name string

M De Fusco

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

S Ciarmatori

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

M Zeviani

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

G De Michele

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

A Filla

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

S Cocozza

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

R Marconi

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

A Dürr

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

B Fontaine

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

P Fernandez

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

language of work or name

English

0 references

publication date

1 June 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

volume

93

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

page(s)

973-983

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

Basic local alignment search tool

12 November 2019

cites work

1 reference

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7 January 2021

The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria

1 reference

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7 January 2021

X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus

1 reference

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7 January 2021

Computational method to predict mitochondrially imported proteins and their targeting sequences

1 reference

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7 January 2021

A 200-amino acid ATPase module in search of a basic function

1 reference

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7 January 2021

Detection of a 4-bp insertion (CACA) functional polymorphism at nucleotide 241 of the cellular adhesion regulatory molecule CMAR (formerly CAR).

1 reference

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7 January 2021

Genomic and cDNA sequence analysis of the cell matrix adhesion regulator gene

1 reference

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7 January 2021

The phenotype of "pure" autosomal dominant spastic paraplegia

1 reference

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7 January 2021

Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product

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7 January 2021

Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy

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7 January 2021

Advances in hereditary spastic paraplegia.

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7 January 2021

Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer

1 reference

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7 January 2021

Spastic paraplegia, epilepsy, and mental retardation in several members of a family: a novel genetic disorder.

1 reference

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7 January 2021

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7 January 2021

Genetic aspects of autosomal dominant late onset cerebellar ataxia

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7 January 2021

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

1 reference

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7 January 2021

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p

1 reference

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7 January 2021

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

1 reference

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7 January 2021

X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene

1 reference

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7 January 2021

The cell adhesion regulator (CAR) gene, TaqI and insertion/deletion polymorphisms, and regional assignment to the peritelomeric region of 16q by linkage analysis

1 reference

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7 January 2021

The scanning model for translation: an update

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7 January 2021

Structural neurology: are seeds at the root of neuronal degeneration?

1 reference

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7 January 2021

Association of late onset spastic paraparesis and dementia: probably an autosomal dominant form of complicated paraplegia

1 reference

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7 January 2021

How do polypeptides cross the mitochondrial membranes?

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981203-9

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

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7 January 2021

Yta10p is required for the ATP-dependent degradation of polypeptides in the inner membrane of mitochondria

1 reference

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7 January 2021

Mutations in RCA1 and AFG3 inhibit F1-ATPase assembly in Saccharomyces cerevisiae

1 reference

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7 January 2021

Motor and somatosensory evoked potentials in hereditary spastic paraplegia

1 reference

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7 January 2021

Hereditary "pure" spastic paraplegia: a study of nine families

1 reference

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7 January 2021

Cloning and characterization of a gene that regulates cell adhesion

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7 January 2021

Pure hereditary spastic paraplegia.

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7 January 2021

Promotion of mitochondrial membrane complex assembly by a proteolytically inactive yeast Lon.

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7 January 2021

Three genes for mitochondrial proteins suppress null-mutations in both Afg3 and Rca1 when over-expressed

1 reference

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7 January 2021

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

1 reference

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7 January 2021

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus

1 reference

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7 January 2021

Central motor conduction studies in hereditary spastic paraplegia

1 reference

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7 January 2021

Identification of a set of yeast genes coding for a novel family of putative ATPases with high similarity to constituents of the 26S protease complex

1 reference

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7 January 2021

Yta10p, a member of a novel ATPase family in yeast, is essential for mitochondrial function

1 reference

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7 January 2021

Multisystem involvement of the central nervous system in Strümpell's disease. A neurophysiological and neuropsychological study

1 reference

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7 January 2021

Cloning of human and rat cDNAs encoding the mitochondrial single-stranded DNA-binding protein (SSB)

1 reference

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7 January 2021

Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags database

1 reference

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7 January 2021

Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

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7 January 2021

A family with hereditary spastic paraparesis and epilepsy.

1 reference

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7 January 2021

Disorders of mitochondria and related metabolism

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7 January 2021

Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene

1 reference

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7 January 2021

10.1016/S0092-8674(00)81203-9

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

2311474

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9635427%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

2311474

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2311474