Identification and characterization of AFG3L2, a novel paraplegin-related gene (Q22010227)

GOA release 2020-03-11

unfolded protein binding

1 reference

GOA release 2020-03-11

8

B Franco

B

Franco

1 reference

7 February 2023

S Banfi

1

S

Banfi

1 reference

7 February 2023

M T Bassi

2

M T

Bassi

1 reference

7 February 2023

G Andolfi

3

G

Andolfi

1 reference

7 February 2023

A Marchitiello

4

A

Marchitiello

1 reference

7 February 2023

S Zanotta

5

S

Zanotta

1 reference

7 February 2023

A Ballabio

6

A

Ballabio

1 reference

7 February 2023

G Casari

7

G

Casari

1 reference

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

7 February 2023

language of work or name

English

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publication date

1 July 1999

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published in

Genomics

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volume

59

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issue

1

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page(s)

51-8

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cites work

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

HSP100/Clp proteins: a common mechanism explains diverse functions

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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.1999.5818

7 January 2021

Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

A radiation hybrid map of the human genome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

Advances in hereditary spastic paraplegia

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

Computational method to predict mitochondrially imported proteins and their targeting sequences

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

Genetic aspects of autosomal dominant late onset cerebellar ataxia

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021

Pure hereditary spastic paraplegia.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5818

7 January 2021