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1.

Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system.

Volume 88 , No of Volumes: 6 (2006)
T Haitina , J Lindblom , T Renstrom
2.

Diseases caused by defects of mitochondrial carriers: a review.

(2008)
F Palmieri
3.

The mitochondrial transporter family SLC identification, properties and physiopathology.

Volume 25 (2012)
F Palmieri
4.

Mitochondrial transporters of the SLC25 family and associated diseases: a review.

Volume 37 , No of Volumes: 4 (2014)
F Palmieri
5.

A novel member of solute carrier family 25 (SLC25A42) is a transporter of coenzyme A and adenosine 3',5'-diphosphate in human mitochondria.

Volume 284 , No of Volumes: 27 (2009)
G Fiermonte , E Paradies , S Todisco
6.

Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter.

Volume 22 , No of Volumes: 2 (1999)
JA Camacho , C Obie , B Biery
7.

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.

Volume 41 , No of Volumes: 6 (2009)
DL Guernsey , H Jiang , DR Campagna
8.

Mutant deoxynucleotide carrier is associated with congenital microcephaly.

Volume 32 , No of Volumes: 1 (2002)
MJ Rosenberg , R Agarwala , G Bouffard
9.

Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter.

Volume 50 , No of Volumes: 4 (2012)
S Edvardson , V Porcelli , C Jalas , J
10.

Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria.

Volume 92 , No of Volumes: 4 (2013)
B Nota , EA Struys , A Pop , J