Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein (Q24291666)

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English	Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein	scientific article

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11 November 2019

Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11549317%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

SPG7 matrix AAA peptidase subunit, paraplegin

1 reference

GOA release 2020-03-11

metalloendopeptidase activity

1 reference

GOA release 2020-03-11

AFG3-like AAA ATPase 1

1 reference

GOA release 2020-03-11

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11549317%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

David F. Callen

6

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11 November 2019

Grant R Sutherland

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G R Sutherland

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11 November 2019

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G Kremmidiotis

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11 November 2019

A E Gardner

2

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11 November 2019

C Settasatian

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11 November 2019

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1 August 2001

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11 November 2019

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11 November 2019

76

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11 November 2019

1-3

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11 November 2019

58-65

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11 November 2019

Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2001.6560

7 January 2021

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Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2001.6560

7 January 2021

based on heuristic

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Identification and characterization of AFG3L2, a novel paraplegin-related gene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2001.6560

7 January 2021

based on heuristic

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Identification and characterization of YME1L1, a novel paraplegin-related gene

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2001.6560

7 January 2021

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Hereditary spastic paraplegia: mitochondrial metalloproteases of yeast

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7 January 2021

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Genomic structure and expression analysis of the spastic paraplegia gene, SPG7.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2001.6560

7 January 2021

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Molecular genetics of familial spastic paraplegia: a multitude of responsible genes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2001.6560

7 January 2021

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

1 reference

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7 January 2021

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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

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2001.6560

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.2001.6560

7 January 2021

based on heuristic

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A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3

1 reference

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7 January 2021

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A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.

1 reference

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7 January 2021

based on heuristic

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Biochemical and functional analysis of the YME1 gene product, an ATP and zinc-dependent mitochondrial protease from S. cerevisiae

1 reference

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7 January 2021

based on heuristic

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Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study

1 reference

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7 January 2021

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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

based on heuristic

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

1 reference

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7 January 2021

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

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Advances in hereditary spastic paraplegia

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Base-calling of automated sequencer traces using phred. I. Accuracy assessment

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The role of mitochondria in the pathogenesis of neurodegenerative diseases

1 reference

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Pure hereditary spastic paraplegia.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.

1 reference

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Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.

1 reference

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Identifiers

10.1006/GENO.2001.6560

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11549317%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11549317%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

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