1. CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10. (4th October 2018) Authors: Huang, Xiaoping; Wu, Beverly P; Nguyen, Diana; Liu, Yi-Ting; Marani, Melika; Hench, Jürgen; Bénit, Paule; Kozjak-Pavlovic, Vera; Rustin, Pierre; Frank, Stephan; Narendra, Derek P Journal: Human molecular genetics Issue: Volume 28:Number 2(2019) Page Start: 349 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. From Nf1 to Sdhb knockout: Successes and failures in the quest for animal models of pheochromocytoma. (5th February 2016) Authors: Lepoutre-Lussey, Charlotte; Thibault, Constance; Buffet, Alexandre; Morin, Aurélie; Badoual, Cécile; Bénit, Paule; Rustin, Pierre; Ottolenghi, Chris; Janin, Maxime; Castro-Vega, Luis-Jaime; Trapman, Jan; Gimenez-Roqueplo, Anne-Paule; Favier, Judith Journal: Molecular and cellular endocrinology Issue: Volume 421(2016) Page Start: 40 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Mitochondrial DNA inheritance in patients with deleted mtDNA. Issue 9 (1st September 2001) Authors: Quintana-Murci, Lluis; Rötig, Agnes; Munnich, Arnold; Rustin, Pierre; Bourgeron, Thomas Journal: Journal of medical genetics Issue: Volume 38:Issue 9(2001) Page Start: e28 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Lipin1 deficiency causes sarcoplasmic reticulum stress and chaperone‐responsive myopathy. (12th November 2018) Authors: Rashid, Talha; Nemazanyy, Ivan; Paolini, Cecilia; Tatsuta, Takashi; Crespin, Paul; de Villeneuve, Delphine; Brodesser, Susanne; Benit, Paule; Rustin, Pierre; Baraibar, Martin A; Agbulut, Onnik; Olivier, Anne; Protasi, Feliciano; Langer, Thomas; Chrast, Roman; de Lonlay, Pascale; de Foucauld, Hele... Journal: EMBO journal Issue: Volume 38:Number 1(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Friedreich's Ataxia, Frataxin, PIP5K1B: Echo of a Distant Fracas. (30th September 2013) Authors: Bayot, Aurélien; Rustin, Pierre Other Names: Santos Renata Academic Editor. Journal: Oxidative medicine and cellular longevity Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. Issue 4 (12th March 2011) Authors: Gardie, Betty; Remenieras, Audrey; Kattygnarath, Darouna; Bombled, Johny; Lefèvre, Sandrine; Perrier-Trudova, Victoria; Rustin, Pierre; Barrois, Michel; Slama, Abdelhamid; Avril, Marie-Françoise; Bessis, Didier; Caron, Olivier; Caux, Frédéric; Collignon, Patrick; Coupier, Isabelle; Cremin, Carol;... Journal: Journal of medical genetics Issue: Volume 48:Issue 4(2011) Page Start: 226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Supernumerary subunits NDUFA3, NDUFA5 and NDUFA12 are required for the formation of the extramembrane arm of human mitochondrial complex I. Issue 9 (6th April 2014) Authors: Rak, Malgorzata; Rustin, Pierre Journal: FEBS letters Issue: Volume 588:Issue 9(2014) Page Start: 1832 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 43 Maple syrup urine disease metabolites induce apoptosis in neural cells without cytochrome c release or changes in mitochondrial membrane potential. (November 1998) Authors: Jouvet, Philippe; Rustin, Pierre; Felderhoff, Ursula; Pocock, Jennifer; Joashi, Umesh; Mazarakis, Nicholas D.; Sarraf, Catherine; Edwards, A. David; Mehmet, Huseyin Journal: Biochemical Society transactions Issue: Volume 26:Number 4(1998) Page Start: S341 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. ACO2 mutations: A novel phenotype associating severe optic atrophy and spastic paraplegia. (April 2018) Authors: Marelli, Cecilia; Hamel, Christian; Quiles, Melanie; Carlander, Bertrand; Larrieu, Lise; Delettre, Cecile; Sarzi, Emmanuelle; Chretien, Dominique; Rustin, Pierre; Koenig, Michel; Guissart, Claire Journal: Neurology Issue: Volume 4:Number 2(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Drug development for mitochondrial disease: recent progress, current challenges, and future prospects. (2nd January 2016) Authors: Bénit, Paule; Schiff, Manuel; Cwerman-Thibault, Hélène; Corral-Debrinski, Marisol; Rustin, Pierre Journal: Expert opinion on orphan drugs Issue: Volume 4:Number 1(2016:Jan.) Page Start: 83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗