Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins

By Braiterman L.T.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 239-247

Oxford University Press

Access to resources Recommend Favorite

Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage

By Ferrer Isidre   Kapfhammer Josef P.   Hindelang Colette   Kemp Stephan   Troffer-Charlier Nathalie   Broccoli Vania   Callyzot Noëlle   Mooyer Petra   Selhorst Jacqueline   Vreken Peter   Wanders Ronald J.A.   Mandel Jean Louis   Pujol Aurora  

Human Molecular Genetics, Vol. 14, Iss. 23, 2005-12 ,pp. : 3565-3577

Oxford University Press

Access to resources Recommend Favorite

Mutations in the canalicular multispecific organic anion transporter ( cMOAT ) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin–Johnson syndrome

By Adachi Y.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 203-207

Oxford University Press

Access to resources Recommend Favorite

Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures

By Shimozawa Nobuyuki   Suzuki Yasuyuki   Zhang Zhongyi   Imamura Atsushi   Ghaedi Kamran   Fujiki Yukio   Kondo Naomi  

Human Molecular Genetics, Vol. 9, Iss. 13, 2000-08 ,pp. : 1995-1999

Oxford University Press

Access to resources Recommend Favorite

Sub-cellular Localisation of the White/Scarlet ABC Transporter to Pigment Granule Membranes Within the Compound Eye of Drosophila Melanogaster

By Mackenzie S.M.   Howells A.J.   Cox G.B.   Ewart G.D.  

Genetica, Vol. 108, Iss. 3, 2000-03 ,pp. : 239-252

Springer Publishing Company

Access to resources Recommend Favorite