(Q37238886)

19 August 2017

Lethal phenotype in conditional late-onset arginase 1 deficiency in the mouse (English)

1 reference

19 August 2017

Jennifer Kasten

1

1 reference

19 August 2017

Chuhong Hu

2

1 reference

19 August 2017

Ragini Bhargava

3

1 reference

19 August 2017

Hana Park

4

1 reference

19 August 2017

Denise Tai

5

1 reference

19 August 2017

James A Byrne

6

1 reference

19 August 2017

Bart Marescau

7

1 reference

19 August 2017

Peter P De Deyn

8

1 reference

19 August 2017

Lisa Schlichting

9

1 reference

19 August 2017

Wayne W Grody

10

1 reference

19 August 2017

Stephen D Cederbaum

11

1 reference

19 August 2017

Gerald S Lipshutz

12

1 reference

19 August 2017

language of work or name

1 reference

6 July 2013

1 reference

Molecular Genetics and Metabolism

19 August 2017

1 reference

19 August 2017

110

1 reference

19 August 2017

3

1 reference

19 August 2017

222-230

1 reference

AAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouse

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Fibronectin-α4β1 interactions in hepatic cold ischemia and reperfusion injury: regulation of MMP-9 and MT1-MMP via the p38 MAPK pathway

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Long-term survival of the juvenile lethal arginase-deficient mouse with AAV gene therapy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Tamoxifen induces rapid, reversible atrophy, and metaplasia in mouse stomach

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Arginase I deficiency: severe infantile presentation with hyperammonemia: more common than reported?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

RH10 provides superior transgene expression in mice when compared with natural AAV serotypes for neonatal gene therapy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Diffusion tensor imaging in arginase deficiency reveals damage to corticospinal tracts

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Short-term correction of arginase deficiency in a neonatal murine model with a helper-dependent adenoviral vector.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Toll-like receptor-induced arginase 1 in macrophages thwarts effective immunity against intracellular pathogens

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Arginases I and II: do their functions overlap?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Mouse model for human arginase deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

The human arginases and arginase deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Molecular basis of phenotypic variation in patients with argininemia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Molecular genetic study of human arginase deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Three novel mutations in the liver-type arginase gene in three unrelated Japanese patients with argininemia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Argininemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: case reports and literature review

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Cloning and characterization of the human type II arginase gene.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Analysis of novel ARG1 mutations causing hyperargininemia and correlation with arginase I activity in erythrocytes

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Long-term neurodevelopmental effects of early detection and treatment in a 6-year-old patient with argininaemia diagnosed by newborn screening

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Overexpression of ornithine aminotransferase: consequences on amino acid homeostasis.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Spontaneous ectopic recombination in cell-type-specific Cre mice removes loxP-flanked marker cassettes in vivo.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edema

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3800271

Argininemia presenting with progressive spastic diplegia

3 September 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.020

Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.020

Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.020

Supporting conditional mouse mutagenesis with a comprehensive cre characterization resource

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.020

Ornithine uptake by isolated hepatocytes and distribution within the cell

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.020

10.1016/J.YMGME.2013.06.020

7 January 2021

Identifiers

DOI

1 reference

19 August 2017

1 reference

19 August 2017

1 reference