(Q47732172)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28472853%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

title

Genetic Rescue of Mitochondrial and Skeletal Muscle Impairment in an Induced Pluripotent Stem Cells Model of Coenzyme Q10 Deficiency (English)

1 reference

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19 March 2020

0 references

4

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19 March 2020

Josep M. Canals

16

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19 March 2020

Damià Romero-Moya

1

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19 March 2020

José A. Rodriguez-Gomez

5

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19 March 2020

Cristina Prieto

11

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19 March 2020

Rafael Artuch

23

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19 March 2020

Pablo Menendez

25

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19 March 2020

22

Pura Muñoz-Cánoves

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19 March 2020

9

Alessandra Giorgetti

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19 March 2020

21

Francesc Cardellach

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19 March 2020

author name string

Carlos Santos-Ocaña

2

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19 March 2020

Julio Castaño

3

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19 March 2020

Vanesa Ruiz-Bonilla

6

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19 March 2020

Clara Bueno

7

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19 March 2020

Patricia González-Rodríguez

8

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19 March 2020

Eusebio Perdiguero

10

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19 March 2020

Constanza Moren-Nuñez

12

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19 March 2020

Daniel J Fernández-Ayala

13

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19 March 2020

Maria Victoria Cascajo

14

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19 March 2020

Iván Velasco

15

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19 March 2020

Raquel Montero

17

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19 March 2020

Delia Yubero

18

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19 March 2020

Cristina Jou

19

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19 March 2020

José López-Barneo

20

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19 March 2020

Plácido Navas

24

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19 March 2020

publication date

23 May 2017

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19 March 2020

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19 March 2020

volume

35

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19 March 2020

issue

7

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19 March 2020

page(s)

1687-1703

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Metabolism and function of coenzyme Q.

19 March 2020

cites work

1 reference

Is coenzyme Q a key factor in aging?

21 January 2018

1 reference

Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency

21 January 2018

1 reference

Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition.

21 January 2018

1 reference

Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis

21 January 2018

1 reference

Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders

21 January 2018

1 reference

Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency

21 January 2018

1 reference

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

21 January 2018

1 reference

CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures

21 January 2018

1 reference

ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency

21 January 2018

1 reference

ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption

21 January 2018

1 reference

A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease

21 January 2018

1 reference

Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

21 January 2018

1 reference

Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations

21 January 2018

1 reference

Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid.

21 January 2018

1 reference

Coenzyme Q deficiency in muscle

21 January 2018

1 reference

The yeast Coq4 polypeptide organizes a mitochondrial protein complex essential for coenzyme Q biosynthesis

21 January 2018

1 reference

Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesis.

21 January 2018

1 reference

Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency.

21 January 2018

1 reference

COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency

21 January 2018

1 reference

Mutations in COQ4, an essential component of coenzyme Q biosynthesis, cause lethal neonatal mitochondrial encephalomyopathy.

21 January 2018

1 reference

Primary and secondary CoQ(10) deficiencies in humans

21 January 2018

1 reference

Coenzyme Q10 deficiencies in neuromuscular diseases

21 January 2018

1 reference

Coenzyme Q biosynthesis in health and disease

21 January 2018

1 reference

Clinical, biochemical and molecular aspects of cerebellar ataxia and Coenzyme Q10 deficiency.

21 January 2018

1 reference

Heterogeneity of coenzyme Q10 deficiency: patient study and literature review

21 January 2018

1 reference

Harnessing the potential of induced pluripotent stem cells for regenerative medicine

21 January 2018

1 reference

ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering

21 January 2018

1 reference

Induction of pluripotent stem cells from fibroblast cultures.

21 January 2018

1 reference

Reprogramming human B cells into induced pluripotent stem cells and its enhancement by C/EBPα.

21 January 2018

1 reference

Feeder-free derivation of induced pluripotent stem cells from adult human adipose stem cells

21 January 2018

1 reference

Human ES- and iPS-derived myogenic progenitors restore DYSTROPHIN and improve contractility upon transplantation in dystrophic mice.

21 January 2018

1 reference

Cellular Ontogeny and Hierarchy Influence the Reprogramming Efficiency of Human B Cells into Induced Pluripotent Stem Cells.

21 January 2018

1 reference

Human ESCs predisposition to karyotypic instability: Is a matter of culture adaptation or differential vulnerability among hESC lines due to inherent properties?

21 January 2018

1 reference

Human induced pluripotent stem cells develop teratoma more efficiently and faster than human embryonic stem cells regardless the site of injection

21 January 2018

1 reference

Genome engineering using the CRISPR-Cas9 system

21 January 2018

1 reference

Accelerated high-yield generation of limb-innervating motor neurons from human stem cells

21 January 2018

1 reference

Characterization of CoQ₁₀ biosynthesis in fibroblasts of patients with primary and secondary CoQ₁₀ deficiency

21 January 2018

1 reference

Analysis of coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes

21 January 2018

1 reference

Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells.

21 January 2018

1 reference

Cord blood-derived CD34+ hematopoietic cells with low mitochondrial mass are enriched in hematopoietic repopulating stem cell function.

21 January 2018

1 reference

Protocols to detect senescence-associated beta-galactosidase (SA-betagal) activity, a biomarker of senescent cells in culture and in vivo

21 January 2018

1 reference

Non-cell-autonomous effect of human SOD1 G37R astrocytes on motor neurons derived from human embryonic stem cells

21 January 2018

1 reference

Ligand-independent FLT3 activation does not cooperate with MLL-AF4 to immortalize/transform cord blood CD34+ cells

21 January 2018

1 reference

Bone environment is essential for osteosarcoma development from transformed mesenchymal stem cells

21 January 2018

1 reference

Mitofusin 2 in POMC neurons connects ER stress with leptin resistance and energy imbalance.

21 January 2018

1 reference

Loss of PINK1 function promotes mitophagy through effects on oxidative stress and mitochondrial fission

21 January 2018

1 reference

Brief report: efficient generation of hematopoietic precursors and progenitors from human pluripotent stem cell lines

21 January 2018

1 reference

Neural differentiation of human induced pluripotent stem cells follows developmental principles but with variable potency

21 January 2018

1 reference

A cellular model for sporadic ALS using patient-derived induced pluripotent stem cells

21 January 2018

1 reference

Epigenetic control of adult skeletal muscle stem cell functions.

21 January 2018

1 reference

Inhibition of complex I of the electron transport chain causes O2-. -mediated mitochondrial outgrowth.

21 January 2018

1 reference

Molecular diagnosis of coenzyme Q10 deficiency.

21 January 2018

1 reference

Coenzyme Q and mitochondrial disease

21 January 2018

1 reference

Mitochondrial disorders in the nervous system

21 January 2018

1 reference

Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease

21 January 2018

1 reference

Coenzyme Q biosynthesis: Coq6 is required for the C5-hydroxylation reaction and substrate analogs rescue Coq6 deficiency

21 January 2018

1 reference

Coq10, a mitochondrial coenzyme Q binding protein, is required for proper respiration in Schizosaccharomyces pombe

21 January 2018

1 reference

Cerebellar ataxia with coenzyme Q10 deficiency: Diagnosis and follow-up after coenzyme Q10 supplementation

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/STEM.2634

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28472853%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

1 reference