A. Bayot

发表

Towards the control of intracellular protein turnover: mitochondrial Lon protease inhibitors versus proteasome inhibitors.

B. Friguet, N. Basse, B. Pirotte, 2008, Biochimie.

Induced pluripotent stem cells-derived neurons from patients with Friedreich ataxia exhibit differential sensitivity to resveratrol and nicotinamide

M. Peschanski, P. Rustin, L. Aubry, 2019, Scientific Reports.

Mitochondrial proteases and cancer.

A. Bulteau, A. Bayot, 2011, Biochimica et biophysica acta.

Dymeclin de fi ciency causes postnatal microcephaly , hypomyelination and reticulum-to-Golgi traf fi cking defects in mice and humans

G. Ball, P. Gressens, F. Perez, 2015 .

The NDUFB6 subunit of the mitochondrial respiratory chain complex I is required for electron transfer activity: a proof of principle study on stable and controlled RNA interference in human cell lines.

P. Bénit, P. Rustin, Malgorzata Rak, 2011, Biochemical and biophysical research communications.

Mitochondrial dysfunction caused by novel ATAD3A mutations.

T. Wai, A. Gelot, N. Dorison, 2020, Molecular genetics and metabolism.

Identification of Novel Oxidized Protein Substrates and Physiological Partners of the Mitochondrial ATP-dependent Lon-like Protease Pim1*

P. Roepstorff, B. Friguet, A. Rogowska-Wrzesińska, 2010, The Journal of Biological Chemistry.

Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia.

P. Rustin, N. Laing, J. Christodoulou, 2013, American journal of human genetics.

Overexpression of the yeast frataxin homolog (Yfh1): contrasting effects on iron-sulfur cluster assembly, heme synthesis and resistance to oxidative stress.

A. Rogowska-Wrzesińska, A. Dancis, J. Camadro, 2009, Mitochondrion.

Cis-silencing of PIP5K1B evidenced in Friedreich's ataxia patient cells results in cytoskeleton anomalies.

P. Rustin, Malgorzata Rak, L. Aubry, 2013, Human molecular genetics.

Friedreich's ataxia: the vicious circle hypothesis revisited

P. Rustin, J. Camadro, A. Bayot, 2011, BMC medicine.

FAST-1 antisense RNA epigenetically alters FXN expression

M. Pook, A. Bayot, S. Al‐Mahdawi, 2018, Scientific Reports.

The TOMM machinery is a molecular switch in PINK1 and PARK2/PARKIN-dependent mitochondrial clearance

F. Waharte, J. Salamero, A. Brice, 2013, Autophagy.

Effect of Lon protease knockdown on mitochondrial function in HeLa cells.

M. Priault, P. Rustin, B. Friguet, 2014, Biochimie.

Dymeclin deficiency causes postnatal microcephaly, hypomyelination and reticulum-to-Golgi trafficking defects in mice and humans.

G. Ball, P. Gressens, F. Perez, 2015, Human molecular genetics.

Deletion of the mitochondrial Pim1/Lon protease in yeast results in accelerated aging and impairment of the proteasome.

B. Friguet, N. Erjavec, A. Bulteau, 2013, Free radical biology & medicine.

Large Interruptions of GAA Repeat Expansion Mutations in Friedreich Ataxia Are Very Rare

F. Cavalcanti, P. Giunti, S. Cavallaro, 2018, Front. Cell. Neurosci..

FAST-1 antisense RNA epigenetically alters FXN expression

M. Pook, A. Bayot, S. Al‐Mahdawi, 2018, Scientific Reports.

Friedreich's Ataxia, Frataxin, PIP5K1B: Echo of a Distant Fracas

P. Rustin, A. Bayot, 2013, Oxidative medicine and cellular longevity.

Deletion of the mitochondrial Pim1/Lon protease in yeast results in accelerated aging and impairment of the proteasome.

B. Friguet, N. Erjavec, A. Bulteau, 2013, Free radical biology & medicine.

Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia.

P. Rustin, N. Laing, J. Christodoulou, 2013, American journal of human genetics.