Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Fiona M. La"'
Autor:
Fiona M. La, Michael C. Phillips, Angel X. Xiao, Duyen Quach, Chongren Tang, Daniel J. Rader, Cecilia Vitali, Nicholas N. Lyssenko, John S. Millar
Publikováno v:
Biochimica et biophysica acta. 1861(12 Pt)
ATP-binding cassette transporter A1 (ABCA1) mediates formation of disc-shaped high-density lipoprotein (HDL) from cell lipid and lipid-free apolipoprotein A-I (apo A-I). Discoidal HDL particles are heterogeneous in physicochemical characteristics for
Autor:
Fiona M. Landells, BSc, Michelle E. Pratt, MD, DABD, Sarah E. Finch, MD, Kathryn P. Whelan, MD
Publikováno v:
JAAD Case Reports, Vol 29, Iss , Pp 80-82 (2022)
Externí odkaz:
https://doaj.org/article/24bc061441be49afb894bfdc02b3048b
Autor:
Paola Bernabò, Toma Tebaldi, Ewout J.N. Groen, Fiona M. Lane, Elena Perenthaler, Francesca Mattedi, Helen J. Newbery, Haiyan Zhou, Paola Zuccotti, Valentina Potrich, Hannah K. Shorrock, Francesco Muntoni, Alessandro Quattrone, Thomas H. Gillingwater, Gabriella Viero
Publikováno v:
Cell Reports, Vol 21, Iss 4, Pp 953-965 (2017)
Summary: Genetic alterations impacting ubiquitously expressed proteins involved in RNA metabolism often result in neurodegenerative conditions, with increasing evidence suggesting that translation defects can contribute to disease. Spinal muscular at
Externí odkaz:
https://doaj.org/article/ef460108741d4a5f91aba22cf6b8a65f
Autor:
Jayanth S. Chandran, Xian Lin, Agustin Zapata, Ahmet Höke, Mika Shimoji, Shonagh O'Leary Moore, Matthew P. Galloway, Fiona M. Laird, Philip C. Wong, Donald L. Price, Kathleen R. Bailey, Jacqueline N. Crawley, Toni Shippenberg, Huaibin Cai
Publikováno v:
Neurobiology of Disease, Vol 29, Iss 3, Pp 505-514 (2008)
Loss-of-function mutations in the DJ-1 gene account for an autosomal recessive form of Parkinson's disease (PD). To investigate the physiological functions of DJ-1 in vivo, we generated DJ-1 knockout (DJ-1−/−) mice. Younger (
Externí odkaz:
https://doaj.org/article/df399a00a978488ebc81c32f71b401bb