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Items: 5

1.

Association study of polymorphisms in the autosomal mitochondrial complex I subunit gene, NADH dehydrogenase (ubiquinone) flavoprotein 2, and bipolar disorder.

Doyle GA, Dahl JP, Bloch PJ, Weller AE, Lohoff FW, Ferraro TN, Berrettini WH.

Psychiatr Genet. 2011 Feb;21(1):51-2. doi: 10.1097/YPG.0b013e328341333f. No abstract available.

2.

Mitochondrial complex I deficiency of nuclear origin I. Structural genes.

Pagniez-Mammeri H, Loublier S, Legrand A, Bénit P, Rustin P, Slama A.

Mol Genet Metab. 2012 Feb;105(2):163-72. doi: 10.1016/j.ymgme.2011.11.188. Review.

PMID:
22142868
3.

Cellular and animal models for mitochondrial complex I deficiency: a focus on the NDUFS4 subunit.

Breuer ME, Willems PH, Smeitink JA, Koopman WJ, Nooteboom M.

IUBMB Life. 2013 Mar;65(3):202-8. doi: 10.1002/iub.1127. Review.

4.

Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases.

Papa S, Rasmo DD, Technikova-Dobrova Z, Panelli D, Signorile A, Scacco S, Petruzzella V, Papa F, Palmisano G, Gnoni A, Micelli L, Sardanelli AM.

FEBS Lett. 2012 Mar 9;586(5):568-77. doi: 10.1016/j.febslet.2011.09.019. Review.

5.

Association studies of bipolar disorder.

Craddock N, Davé S, Greening J.

Bipolar Disord. 2001 Dec;3(6):284-98. Review.

PMID:
11843779

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