Genomic abnormalities of the murine model of Fabry disease after disease-related perturbation, a systems biology approach (Q35768834)

10 August 2017

Genomic abnormalities of the murine model of Fabry disease after disease-related perturbation, a systems biology approach (English)

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10 August 2017

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Monique P Gelderman

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10 August 2017

David F Moore

1

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10 August 2017

Paulo A Ferreira

3

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10 August 2017

Steven R Fuhrmann

4

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10 August 2017

Haiqing Yi

5

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10 August 2017

Abdel Elkahloun

6

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10 August 2017

Lisa M Lix

7

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10 August 2017

Roscoe O Brady

8

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10 August 2017

Raphael Schiffmann

9

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10 August 2017

Ehud Goldin

10

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10 August 2017

language of work or name

English

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publication date

30 April 2007

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

10 August 2017

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10 August 2017

104

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10 August 2017

19

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10 August 2017

8065-8070

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Proteomics of specific treatment-related alterations in Fabry disease: a strategy to identify biological abnormalities.

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Insights into X-linked retinitis pigmentosa type 3, allied diseases and underlying pathomechanisms

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Antiplasmin: the forgotten serpin?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Identification of novel murine- and human-specific RPGRIP1 splice variants with distinct expression profiles and subcellular localization

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Limited proteolysis differentially modulates the stability and subcellular localization of domains of RPGRIP1 that are distinctly affected by mutations in Leber's congenital amaurosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Alpha-galactosidase A deficiency accelerates atherosclerosis in mice with apolipoprotein E deficiency

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Vascular protection: superoxide dismutase isoforms in the vessel wall

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Neuroserpin: a selective inhibitor of tissue-type plasminogen activator in the central nervous system

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

The human DDX and DHX gene families of putative RNA helicases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Deubiquitination of p53 by HAUSP is an important pathway for p53 stabilization

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Regional cerebral hyperperfusion and nitric oxide pathway dysregulation in Fabry disease: reversal by enzyme replacement therapy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Enzyme replacement therapy in Fabry disease: a randomized controlled trial

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

A family of mammalian F-box proteins

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Aging accentuates and bone marrow transplantation ameliorates metabolic defects in Fabry disease mice

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Roles of ubiquitin-mediated proteolysis in cell cycle control

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

alpha-Galactosidase A deficient mice: a model of Fabry disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Cerebrovascular complications of Fabry's disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Asymptotically distribution-free methods for the analysis of covariance structures.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

More powerful procedures for multiple significance testing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Reporting structural equation modeling results in Psychology and Aging: Some proposed guidelines

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Elevated cerebral blood flow velocities in Fabry disease with reversal after enzyme replacement.

12 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701991104

Ascorbate decreases Fabry cerebral hyperperfusion suggesting a reactive oxygen species abnormality: an arterial spin tagging study

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701991104

Fabry disease in mice is associated with age-dependent susceptibility to vascular thrombosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701991104

RPGRIP1s with distinct neuronal localization and biochemical properties associate selectively with RanBP2 in amacrine neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701991104

Principles and practice in reporting structural equation analyses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0701991104

Increased signal intensity in the pulvinar on T1-weighted images: a pathognomonic MR imaging sign of Fabry disease.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1859990

Enzymatic Defect in Fabry's Disease

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17470787

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Alpha-galactosidase A deficiency leads to increased tissue fibrin deposition and thrombosis in mice homozygous for the factor V Leiden mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17470787

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0701991104

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10 August 2017

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10 August 2017

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