Homologous recombination between single-stranded DNA and chromosomal genes in Saccharomyces cerevisiae.

Por Simon, J R, Moore, P D
Publicado em 1987

Persistent Mitochondrial Damage by Nitric Oxide and its Derivatives: Neuropathological Implications

Por Bolaños, Juan P., Heales, Simon J. R.
Publicado em 2010

Common induction and regulation of biphenyl, xylene/toluene, and salicylate catabolism in Pseudomonas paucimobilis.

Por Furukawa, K, Simon, J R, Chakrabarty, A M
Publicado em 1983

Biochemical Diagnosis of Coenzyme Q(10) Deficiency

Por Yubero, Delia, Montero, Raquel, Artuch, Rafael, Land, John M., Heales, Simon J.R., Hargreaves, Iain P.
Publicado em 2014

Inhibition of Mitochondrial Complex I Impairs Release of α-Galactosidase by Jurkat Cells

Por Jonathan R. A. Lambert, Steven J. Howe, Ahad A. Rahim, Derek G. Burke, Simon J. R. Heales
Publicado em 2019-09-01

Analysis of rhodamine and fluorescein-labeled F-actin diffusion in vitro by fluorescence photobleaching recovery.

Por Simon, J R, Gough, A, Urbanik, E, Wang, F, Lanni, F, Ware, B R, Taylor, D L
Publicado em 1988

Glucocerebrosidase Deficiency in Substantia Nigra of Parkinson Disease Brains

Por Gegg, Matthew E, Burke, Derek, Heales, Simon J R, Cooper, J Mark, Hardy, John, Wood, Nicholas W, Schapira, Anthony H V
Publicado em 2012

The pleiotropic effects of decanoic acid treatment on mitochondrial function in fibroblasts from patients with complex I deficient Leigh syndrome

Por Kanabus, Marta, Fassone, Elisa, Hughes, Sean David, Bilooei, Sara Farahi, Rutherford, Tricia, Donnell, Maura O’, Heales, Simon J. R., Rahman, Shamima
Publicado no J Inherit Metab Dis (2016)

Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype

Por Bowron, Ann, Honeychurch, Julie, Williams, Maggie, Tsai-Goodman, Beverley, Clayton, Nicol, Jones, Lucy, Shortland, Graham J., Qureshi, Shakeel A., Heales, Simon J. R., Steward, Colin G.
Publicado no J Inherit Metab Dis (2014)

Erratum to: Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype

Por Bowron, Ann, Honeychurch, Julie, Williams, Maggie, Tsai-Goodman, Beverley, Clayton, Nicol, Jones, Lucy, Shortland, Graham J., Qureshi, Shakeel A., Heales, Simon J. R., Steward, Colin G.
Publicado no J Inherit Metab Dis (2015)

Mutations in the Gene Encoding 3-Hydroxyisobutyryl-CoA Hydrolase Results in Progressive Infantile Neurodegeneration

Por Loupatty, Ference J., Clayton, Peter T., Ruiter, Jos P. N., Ofman, Rob, IJlst, Lodewijk, Brown, Garry K., Thorburn, David R., Harris, Robert A., Duran, Marinus, DeSousa, Carlos, Krywawych, Steve, Heales, Simon J. R., Wanders, Ronald J. A.
Publicado em 2007

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia

Por Kurian, Manju A., Zhen, Juan, Cheng, Shu-Yuan, Li, Yan, Mordekar, Santosh R., Jardine, Philip, Morgan, Neil V., Meyer, Esther, Tee, Louise, Pasha, Shanaz, Wassmer, Evangeline, Heales, Simon J.R., Gissen, Paul, Reith, Maarten E.A., Maher, Eamonn R.
Publicado em 2009

An LC–MS/MS-Based Method for the Quantification of Pyridox(am)ine 5′-Phosphate Oxidase Activity in Dried Blood Spots from Patients with Epilepsy

Por Wilson, Matthew P., Footitt, Emma J., Papandreou, Apostolos, Uudelepp, Mari-Liis, Pressler, Ronit, Stevenson, Danielle C., Gabriel, Camila, McSweeney, Mel, Baggot, Matthew, Burke, Derek, Stödberg, Tommy, Riney, Kate, Schiff, Manuel, Heales, Simon J. R., Mills, Kevin A., Gissen, Paul, Clayton, Peter T., Mills, Philippa B.
Publicado no Anal Chem (2017)

Missense dopamine transporter mutations associate with adult parkinsonism and ADHD

Por Hansen, Freja H., Skjørringe, Tina, Yasmeen, Saiqa, Arends, Natascha V., Sahai, Michelle A., Erreger, Kevin, Andreassen, Thorvald F., Holy, Marion, Hamilton, Peter J., Neergheen, Viruna, Karlsborg, Merete, Newman, Amy H., Pope, Simon, Heales, Simon J.R., Friberg, Lars, Law, Ian, Pinborg, Lars H., Sitte, Harald H., Loland, Claus, Shi, Lei, Weinstein, Harel, Galli, Aurelio, Hjermind, Lena E., Møller, Lisbeth B., Gether, Ulrik
Publicado em 2014