(Q80127407)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

title

A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

hereditary spastic paraplegia

28 December 2019

main subject

1 reference

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

author name string

Jakob Hansen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Kirsten Svenstrup

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Debbie Ang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Marit N Nielsen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Jane H Christensen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Niels Gregersen

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Jørgen E Nielsen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Costa Georgopoulos

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

publication date

10 April 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

volume

254

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

page(s)

897-900

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17420924%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00415-006-0470-y

28 December 2019

exact match

0 references

cites work

Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene

1 reference

12 December 2020

Hereditary spastic paraplegia caused by mutations in the SPG4 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular chaperones as essential mediators of mitochondrial biogenesis

1 reference

12 December 2020

The importance of a mobile loop in regulating chaperonin/ co-chaperonin interaction: humans versus Escherichia coli

1 reference

12 December 2020

Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases

1 reference

12 December 2020

Rapid detection of the factor V Leiden mutation by real-time PCR with TaqMan minor groove binder probes

1 reference

12 December 2020

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

1 reference

12 December 2020

The extent of axonal loss in the long tracts in hereditary spastic paraplegia

1 reference

12 December 2020

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12

1 reference

12 December 2020

Hereditary spastic paraplegia

1 reference

12 December 2020

Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter

1 reference

12 December 2020

Identification of in vivo substrates of the yeast mitochondrial chaperonins reveals overlapping but non-identical requirement for hsp60 and hsp10.

1 reference

12 December 2020

A single ring is sufficient for productive chaperonin-mediated folding in vivo

1 reference

12 December 2020