(Q28564688)

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Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene

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31 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12874111%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene (English)

2 references

PubMed publication ID

31 January 2017

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12874111%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1

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6 November 2019

Mustafa A. Salih

8

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6 November 2019

Emilio Di Maria

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6 November 2019

Nicholas W. Wood

14

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6 November 2019

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Mary M Reilly

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6 November 2019

Michaela Auer-Grumbach

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Michaela Auer-Grumbach

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6 November 2019

Mary G. Sweeney

4

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Mary G Sweeney

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6 November 2019

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Shu-Fang An

6

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PubMed publication ID

31 January 2017

Europe PubMed Central

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6 November 2019

Peter de Jonghe

10

2 references

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31 January 2017

Europe PubMed Central

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6 November 2019

Francesco Scaravilli

13

2 references

PubMed publication ID

31 January 2017

Europe PubMed Central

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6 November 2019

Dennis A Stephenson

2

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6 November 2019

Michael J Groves

3

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6 November 2019

Mary B Davis

5

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6 November 2019

Henry Houlden

7

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6 November 2019

Vincent Timmerman

9

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6 November 2019

publication date

1 August 2003

2 references

PubMed publication ID

31 January 2017

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6 November 2019

Human Molecular Genetics

2 references

PubMed publication ID

31 January 2017

Europe PubMed Central

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6 November 2019

12

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PubMed publication ID

31 January 2017

Europe PubMed Central

PubMed publication ID

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6 November 2019

15

2 references

PubMed publication ID

31 January 2017

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12874111%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1917-1925

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12874111%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Familial dysautonomia is caused by mutations of the IKAP gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

The development and pathogenesis of the sensory neuropathy in the mutant rat mf.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

A linkage map of the rat genome derived from three F2 crosses

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Overview of QTL mapping software and introduction to map manager QT.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

NF-kappaB is involved in the survival of cerebellar granule neurons: association of IkappaBbeta [correction of Ikappabeta] phosphorylation with cell survival.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Cytosolic chaperonin-containing t-complex polypeptide 1 changes the content of a particular subunit species concomitant with substrate binding and folding activities during the cell cycle

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Identification of six Tcp-1-related genes encoding divergent subunits of the TCP-1-containing chaperonin

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Structures and co-regulated expression of the genes encoding mouse cytosolic chaperonin CCT subunits

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

The 'sequential allosteric ring' mechanism in the eukaryotic chaperonin-assisted folding of actin and tubulin

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Association of actin filaments with axonal microtubule tracts

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Involvement of T-complex protein-1delta in dopamine triggered apoptosis in chick embryo sympathetic neurons

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG198

21 January 2018

Identifiers

10.1093/HMG/DDG198

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12874111%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12874111%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

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