(Q30412384)

22 September 2017

Insights into the mutation-induced HHH syndrome from modeling human mitochondrial ornithine transporter-1. (English)

1 reference

22 September 2017

1

Jing-Fang Wang

1 reference

22 September 2017

2

Kuo-Chen Chou

1 reference

PMC publication ID

3266937

22 September 2017

language of work or name

English

0 references

publication date

26 January 2012

1 reference

22 September 2017

1 reference

22 September 2017

7

1 reference

22 September 2017

1

1 reference

22 September 2017

e31048

1 reference

Creative Commons Attribution 4.0 International

22 September 2017

start time

26 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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20 June 2018

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Mitochondrial carriers in the cytoplasmic state have a common substrate binding site

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Structural basis for lipid-mediated interactions between mitochondrial ADP/ATP carrier monomers

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The role and structure of mitochondrial carriers

20 June 2018

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20 June 2018

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20 June 2018

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The mitochondrial ornithine transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms

20 June 2018

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20 June 2018

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Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

20 June 2018

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20 June 2018

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Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter

20 June 2018

1 reference

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20 June 2018

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Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)

20 June 2018

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Knowledge-based prediction of protein structures and the design of novel molecules

20 June 2018

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Hyperornithinemia, hyperammonemia, homocitrullinuria (HHH) syndrome: presentation as acute liver disease with coagulopathy

20 June 2018

1 reference

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Basic charge clusters and predictions of membrane protein topology.

20 June 2018

1 reference

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Single-body residue-level knowledge-based energy score combined with sequence-profile and secondary structure information for fold recognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Molecular modeling of two CYP2C19 SNPs and its implications for personalized drug design

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Q-SiteFinder: an energy-based method for the prediction of protein-ligand binding sites.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Insights from studying the mutation-induced allostery in the M2 proton channel by molecular dynamics

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Insight into the molecular switch mechanism of human Rab5a from molecular dynamics simulations

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Receptor independent and receptor dependent CoMSA modeling with IVE-PLS: application to CBG benchmark steroids and reductase activators

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Molecular dynamics studies on the interactions of PTP1B with inhibitors: from the first phosphate-binding site to the second one.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Molecular dynamics studies on T1 lipase: insight into a double-flap mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Insights from investigating the interactions of adamantane-based drugs with the M2 proton channel from the H1N1 swine virus

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

PROCHECK: a program to check the stereochemical quality of protein structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Seven novel mutations in the ORNT1 gene (SLC25A15) in patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

A novel mutation, P126R, in a Japanese patient with HHH syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031048

Protein threading using PROSPECT: design and evaluation.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266937

Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3266937

Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia

26 November 2018

1 reference

12 December 2020

Anesthesia for a patient with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome

1 reference

12 December 2020

Abnormal urinary excretion of polyamines in HHH syndrome (hyperornithinemia associated with hyperammonemia and homocitrullinuria)

1 reference

12 December 2020

A case of hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome with spastic paraparesis and severe distal muscle atrophy of lower limbs

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12 December 2020

HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation

1 reference

12 December 2020

3D structure modeling of cytochrome P450 2C19 and its implication for personalized drug design

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12 December 2020

A negative cooperativity mechanism of human CYP2E1 inferred from molecular dynamics simulations and free energy calculations

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12 December 2020

Exploration of conformational transition in the aryl-binding site of human FXa using molecular dynamics simulations

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12 December 2020

10.1371/JOURNAL.PONE.0031048

Identifiers

DOI

1 reference

22 September 2017

0 references

1 reference

PMC publication ID

3266937

22 September 2017

PubMed publication ID

22292090

1 reference

PMC publication ID

3266937