(Q45972327)

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Fluctuating liver functions in siblings with MPV17 mutations and possible improvement associated with dietary and pharmaceutical treatments targeting respiratory chain complex II.

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Fluctuating liver functions in siblings with MPV17 mutations and possible improvement associated with dietary and pharmaceutical treatments targeting respiratory chain complex II. (English)

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

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Shunsaku Kaji

1

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Kei Murayama

2

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Ikuo Nagata

3

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Hironori Nagasaka

4

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Masaki Takayanagi

5

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Akira Ohtake

6

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Hiroyasu Iwasa

7

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Masahiko Nishiyama

8

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Yasushi Okazaki

9

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Hiroko Harashima

10

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Takahiro Eitoku

11

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Michiko Yamamoto

12

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Hiroaki Matsushita

13

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Koichi Kitamoto

14

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Shinji Sakata

15

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Takeshi Katayama

16

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Shuji Sugimoto

17

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Yoshio Fujimoto

18

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Jun Murakami

19

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Susumu Kanzaki

20

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

Kazuo Shiraki

21

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

publication date

12 May 2009

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Europe PubMed Central

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18 December 2017

http://europepmc.org/abstract/MED/19520594

Molecular Genetics and Metabolism

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

97

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

4

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

292-296

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Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Mitochondrial DNA depletion is a prevalent cause of multiple respiratory chain deficiency in childhood

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Navajo neurohepatopathy is caused by a mutation in the MPV17 gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Glucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Leigh syndrome: clinical features and biochemical and DNA abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Melatonin protects against 6-OHDA-induced neurotoxicity in rats: a role for mitochondrial complex I activity

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Coomassie blue-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for direct visualization of polypeptides during electrophoresis.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Dominant inheritance of premature ovarian failure associated with mutant mitochondrial DNA polymerase gamma.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

ORTHOTOPIC LIVER TRANSPLANTATION FOR MITOCHONDRIAL RESPIRATORY CHAIN DISORDERS: A STUDY OF 5 CHILDREN1

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Genetic control of oxidative phosphorylation and experimental models of defects

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Mitochondrial hepatopathies: advances in genetics and pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.04.014

7 January 2021

Identifiers

10.1016/J.YMGME.2009.04.014

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19520594

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