Extra-renal locations of the a4 subunit of H(+)ATPase

por Golder, Zoe J., Karet Frankl, Fiona E.
Publicado 2016

Renal peroxiredoxin 6 interacts with anion exchanger 1 and plays a novel role in pH homeostasis

por Sorrell, Sara L., Golder, Zoe J., Johnstone, Duncan B., Frankl, Fiona E. Karet
Publicado 2016

Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissues

por Bicci, Iacopo, Calabrese, Claudia, Golder, Zoe J, Gomez-Duran, Aurora, Chinnery, Patrick F
Publicado 2021

Heteroplasmic mitochondrial DNA mutations in frontotemporal lobar degeneration

por Nie, Yu, Murley, Alexander, Golder, Zoe, Rowe, James B., Allinson, Kieren, Chinnery, Patrick F.
Publicado 2022

Mice deficient in H(+)-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear

por Lorente-Cánovas, Beatriz, Ingham, Neil, Norgett, Elizabeth E., Golder, Zoe J., Karet Frankl, Fiona E., Steel, Karen P.
Publicado 2013

High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob Disease

por Murley, Alexander G., Nie, Yu, Golder, Zoe, Keogh, Michael John, Smith, Colin, Ironside, James W., Chinnery, Patrick F.
Publicado 2023

Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family

por Kullar, Peter J, Gomez-Duran, Aurora, Gammage, Payam A, Garone, Caterina, Minczuk, Michal, Golder, Zoe, Wilson, Janet, Montoya, Julio, Häkli, Sanna, Kärppä, Mikko, Horvath, Rita, Majamaa, Kari, Chinnery, Patrick F
Publicado 2018

Frequency and signature of somatic variants in 1461 human brain exomes

por Wei, Wei, Keogh, Michael J., Aryaman, Juvid, Golder, Zoe, Kullar, Peter J., Wilson, Ian, Talbot, Kevin, Turner, Martin R., McKenzie, Chris-Anne, Troakes, Claire, Attems, Johannes, Smith, Colin, Sarraj, Safa Al, Morris, Chris M., Ansorge, Olaf, Jones, Nick S., Ironside, James W., Chinnery, Patrick F.
Publicado 2018