History of PPAR Discovery

Author:

Youssef Jihan A.,Badr Mostafa Z.

Publisher

Humana Press

Reference33 articles.

1. Afzelius BA (1965) The occurrence and structure of microbodies: a comparative study. J Cell Biol 26:835–843

2. Baes M, Aubourg P (2009) Peroxisomes, myelination and axonal integrity in the CNS. Neuroscientist 15:367–379

3. Braverman NE, Moser AB, Steinberg SJ (2010) Rhizomelic chondrodysplasia punctata type 1. In: Pagon RA, Bird TC, Dolan CR, Stephens K, eds

4. Coulter-Mackie MB, White CT, Hurley RM, Chew BH, Lange D (2011) Primary hyperoxaluria type 1. In: Pagon RA, Bird TD, Dolan CR, Stephens K, Adam MP (eds) GeneReviews™ [Internet]. University of Washington, Seattle, WA, 1993–2002. Jun 19 [updated 2011 Nov 17]

5. Ferdinandusse S, Denis S, Clayton PT, Graham A, Rees JE, Allen JT, McLean BN, Brown AY, Vreken P, Waterham HR, Wanders RJ (2000) Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy. Nat Genet 24:188–191

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