Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients. - Test2 - elhamkhani - TriplyDB

Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients.

Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients.

http://www.wikidata.org/entity/Q35140340

about

Differential expression of the nuclear-encoded mitochondrial transcriptome in pediatric septic shock Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss Degenerative Ataxias: challenges in clinical research.The expression characteristics of mt-ND2 gene in chicken.Frataxin deficiency impairs mitochondrial biogenesis in cells, mice and humans.Early cerebellar deficits in mitochondrial biogenesis and respiratory chain complexes in the KIKO mouse model of Friedreich ataxia.Gene Expression Profile in Peripheral Blood Cells of Friedreich Ataxia Patients.

P2860

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P2860

Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients.

http://www.wikidata.org/entity/Q35140340

description

2014 nî lūn-bûn

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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի ապրիլին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Gene expression profiling of m ...... dreich ataxia (FRDA) patients.

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Gene expression profiling of m ...... dreich ataxia (FRDA) patients.

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type

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Gene expression profiling of m ...... dreich ataxia (FRDA) patients.

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Gene expression profiling of m ...... dreich ataxia (FRDA) patients.

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Gene expression profiling of m ...... dreich ataxia (FRDA) patients.

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Gene expression profiling of m ...... dreich ataxia (FRDA) patients.

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JOURNAL.PONE.0094069

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Gene expression profiling of m ...... edreich ataxia (FRDA) patients

@en

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Behnam Kamalidehghan

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Goh Yong Meng

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Majid Sadeghizadeh

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Massoud Houshmand

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Mohammad Hossein Salehi

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Omid Aryani

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P2860

NDUFA4 is a subunit of complex IV of the mammalian electron transport chain

In vivo maturation of human frataxin

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

The role of mitochondria in cellular iron-sulfur protein biogenesis and iron metabolism

Frataxin acts as an iron chaperone protein to modulate mitochondrial aconitase activity.

Mitochondrial iron detoxification is a primary function of frataxin that limits oxidative damage and preserves cell longevity.

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

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e94069

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scholarly article

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10.1371/JOURNAL.PONE.0094069

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4

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9

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Shahriar Nafissi

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261408589

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phosphorylation

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