Citations for
1FAR1, FAR2
Fatty acyl-CoA reductases of birds.
Hellenbrand J, Biester EM, Gruber J, Hamberg M, Frentzen M.
BMC Biochem 12:64. doi: 10.1186/1471-2091-12-64. 2011
2CBR4, DHRS1, DHRS1, DHRS11, DHRS12, DHRS7C, DHRSX, FAR1, FAR2, HSD17B11, HSD17B13, HSD17B14, HSD17B2, HSD17B3, HSD17B4, HSD17B6, HSD17B7P2, HSD17B8, HSD17BP1, HSD3B7, HSDL1, QDPR, RDH10, RDH12, RDH13, SDR16C6, SDR39U1, SDR42E1, TDH, TGDS, UXS1
The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative.
Persson B, Kallberg Y, Bray JE, Bruford E, Dellaporta SL, Favia AD, Duarte RG, Jörnvall H, Kavanagh KL, Kedishvili N, Kisiela M, Maser E, Mindnich R, Orchard S, Penning TM, Thornton JM, Adamski J, Oppermann U.
Chem Biol Interact 178(1-3):94-8. Epub 2008 Nov 5. 2009
3FAR2
Underdiagnosed amyloidosis: amyloidosis of lysozyme variant.
Granel B, Serratrice J, Disdier P, Weiller PJ, Valleix S, Grateau G, Droz D.
Am J Med 118(3):321-2. No abstract available. 2005
4FAR1, FAR2
Mammalian wax biosynthesis. I. Identification of two fatty acyl-Coenzyme A reductases with different substrate specificities and tissue distributions.
Cheng JB, Russell DW.
J Biol Chem 279(36):37789-97. Epub 2004 Jun 27. 2004
5FAR2, LYZ
Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis.
Booth DR, et al.
Nature 385 : 787-793. 1997
6FAR2, LYZ
Human lysozyme gene mutations cause hereditary systemic amyloidosis.
Pepys MB, et al.
Nature 362 : 553-557. 1993