Identification of Zyklopen, a New Member of the Vertebrate Multicopper Ferroxidase Family, and Characterization in Rodents and Human Cells1–3

Autor: Chen, Huijun, Attieh, Zouhair K., Syed, Basharut A., Kuo, Yien-Ming, Stevens, Valerie, Fuqua, Brie K., Andersen, Henriette S., Naylor, Claire E., Evans, Robert W., Gambling, Lorraine, Danzeisen, Ruth, Bacouri-Haidar, Mhenia, Usta, Julnar, Vulpe, Chris D. ^*, McArdle, Harry J.

Publikováno v: In The Journal of Nutrition October 2010 140(10):1728-1735

Maternal Iron Deficiency Identifies Critical Windows for Growth and Cardiovascular Development in the Rat Postimplantation Embryo 1

Autor: Andersen, Henriette S ^*, Gambling, Lorraine ^*, Holtrop, Grietje ^†, McArdle, Harry J ^*

Publikováno v: In The Journal of Nutrition May 2006 136(5):1171-1177

Iron and Copper Interactions in Development and the Effect on Pregnancy Outcome

Autor: Gambling, Lorraine, Danzeisen, Ruth, Fosset, Cedric, Andersen, Henriette S., Dunford, Susan, Srai, S. Kaila S. ^*, McArdle, Harry J. ³

Publikováno v: In The Journal of Nutrition May 2003 133(5):1554S-1556S

The ETFDH c.158A>G Variation Disrupts the Balanced Binding of ESE and ESS Proteins Causing Missplicing and Multiple acyl-CoA Dehydrogenation Deficiency

Autor: Olsen, Rikke K J, Brøner, Sabrina, Sabaratnam, Rugivan, Doktor, Thomas K, Andersen, Henriette S, Bruun, Gitte H, Gahrn, Birthe, Stenbroen, Vibeke, Olpin, Simon E, Dobbie, Angus, Gregersen, Niels, Andresen, Brage S

Publikováno v: Olsen, R K J, Brøner, S, Sabaratnam, R, Doktor, T K, Andersen, H S, Bruun, G H, Gahrn, B, Stenbroen, V, Olpin, S E, Dobbie, A, Gregersen, N & Andresen, B S 2013, ' The ETFDH c.158A >G Variation Disrupts the Balanced Binding of ESE and ESS Proteins Causing Missplicing and Multiple acyl-CoA Dehydrogenation Deficiency ', Human Mutation . https://doi.org/10.1002/humu.22455

Multiple acyl-CoA dehydrogenation deficiency (MADD) is a disorder of fatty acid and amino acid oxidation caused by defects of electron transfer flavoprotein (ETF) or its dehydrogenase (ETFDH). A clear relationship between genotype and phenotype makes

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https://pure.au.dk/portal/da/publications/the-etfdh-c158ag-variation-disrupts-the-balanced-binding-of-ese-and-ess-proteins-causing-missplicing-and-multiple-acylcoa-dehydrogenation-deficiency(3a0a3d78-d47f-480b-a75b-25f44f07be65).html

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