Display Order by Show
Library » authors: Koenig M
Items 1 - 7 of 7.
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays.
Drmanac R, Sparks AB, Callow MJ, Halpern AL, Burns NL, Kermani BG, Carnevali P, Nazarenko I, Ni...
Science (2010) 327: 78-81.
Category: genomics, methods ¤ Added: Jan 11th, 2010 ¤ Rating: ◊◊
¤ PubMed ¤ Publisher Website
Disabled early recruitment of antioxidant defenses in Friedreich's ataxia.
Chantrel-Groussard K, Geromel V, Puccio H, Koenig M, Munnich A, Rotig A, Rustin P
Human Molecular Genetics (2001)
Category: mitochondrial diseases ¤ Added: Jan 26th, 2004 ¤ Rating: ◊◊
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
Puccio H, Simon D, Cossee M, Criqui-Filipe P, Tiziano F, Melki J, Hindelang C, Matyas R, Rustin...
Nature Genetics (2001)
Category: mitochondrial diseases ¤ Added: Jan 16th, 2004 ¤ Rating: ◊◊
Clinical and genetic abnormalities in patients with Friedreich's ataxia.
Durr A, Cossee M, Agid Y, Campuzano V, Mignard C, Penet C, Mandel JL, Brice A, Koenig M
New England Journal of Medicine (1996)
Category: mitochondrial diseases ¤ Added: Jan 15th, 2004 ¤ Rating: ◊◊
Friedreich ataxia: a paradigm for mitochondrial diseases.
Puccio H, Koenig M
Current Opinion in Genetics and Development (2002)
Category: mitochondrial diseases ¤ Added: Jun 26th, 2002 ¤ Rating: ◊◊
Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis.
Pook MA, Al-Mahdawi S, Carroll CJ, Cossee M, Puccio H, Lawrence L, Clark P, Lowrie MB, Bradley ...
Neurogenetics (2001)
Category: mitochondrial diseases ¤ Added: May 23rd, 2002 ¤ Rating: ◊
Frataxin knockin mouse.
Miranda CJ, Santos MM, Ohshima K, Smith J, Li L, Bunting M, Cossee M, Koenig M, Sequeiros J, Ka...
FEBS Letters (2002)
Category: mitochondrial diseases ¤ Added: May 22nd, 2002 ¤ Rating: ◊◊