(Q28272595)

1

0 references

Sophie Rutschmann

4

object named as

Sophie Rutschmann

0 references

Eliezer Masliah

5

object named as

Eliezer Masliah

0 references

author name string

Justin T Cruite

2

0 references

Xin Du

3

0 references

Michael B A Oldstone

Proceedings of the National Academy of Sciences of the United States of America

7

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language of work or name

English

0 references

publication date

21 August 2012

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published in

0 references

volume

109

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issue

34

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page(s)

13733-8

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describes a project that uses

ImageQuant

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3427069/fullTextXML

inferred from PubMed Central ID database lookup

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

A method and server for predicting damaging missense mutations

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Biology, structure and mechanism of P-type ATPases

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Isolation of a partial candidate gene for Menkes disease by positional cloning

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Diverse mutations in patients with Menkes disease often lead to exon skipping

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

ZBTB1 is a determinant of lymphoid development

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Early onset prion disease from octarepeat expansion correlates with copper binding properties

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Induction of cellular prion protein gene expression by copper in neurons

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Gene action in the X-chromosome of the mouse (Mus musculus L.)

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Gene expression profiling in chronic copper overload reveals upregulation of Prnp and App.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Copper binding to PrPC may inhibit prion disease propagation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Copper(II)-induced conformational changes and protease resistance in recombinant and cellular PrP. Effect of protein age and deamidation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Normal prion protein has an activity like that of superoxide dismutase.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

The cellular prion protein binds copper in vivo

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Copper(II)-induced secondary structure changes and reduced folding stability of the prion protein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Proteinase K-sensitive disease-associated ovine prion protein revealed by conformation-dependent immunoassay

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Preferential Cu2+ coordination by His96 and His111 induces beta-sheet formation in the unstructured amyloidogenic region of the prion protein

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Identification of the Cu2+ binding sites in the N-terminal domain of the prion protein by EPR and CD spectroscopy

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Reversibility of scrapie inactivation is enhanced by copper

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Menkes syndrome and animal models.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Copper(II) ion binding to cellular prion protein.

2 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

Cellular prion protein acquires resistance to proteolytic degradation following copper ion binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

Copper converts the cellular prion protein into a protease-resistant species that is distinct from the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

Copper (II) ions potently inhibit purified PrPres amplification

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

Copper chelation delays the onset of prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

Role of copper and manganese in prion disease progression

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

Isolation and characterization of a proteinase K-sensitive PrPSc fraction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

21 January 2018

ENU mutagenesis in mice

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1211499109

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3427069

Copper binding to the N-terminal tandem repeat region of mammalian and avian prion protein: structural studies using synthetic peptides

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22869751

12 December 2020

inferred from PubMed ID database lookup

Metal-dependent alpha-helix formation promoted by the glycine-rich octapeptide region of prion protein

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22869751

12 December 2020

inferred from PubMed ID database lookup

Variably protease-sensitive prionopathy: a novel disease of the prion protein

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22869751

12 December 2020