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A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder.
Szot JO, Cuny H, Martin EM, Sheng DZ, Iyer K, Portelli S, Nguyen V, Gereis JM, Alankarage D, Chitayat D, Chong K, Wentzensen IM, Vincent-Delormé C, Lermine A, Burkitt-Wright E, Ji W, Jeffries L, Pais LS, Tan TY, Pitt J, Wise CA, Wright H, Andrews ID, Pruniski B, Grebe TA, Corsten-Janssen N, Bouman K, Poulton C, Prakash S, Keren B, Brown NJ, Hunter MF, Heath O, Lakhani SA, McDermott JH, Ascher DB, Chapman G, Bozon K, Dunwoodie SL. Szot JO, et al. Among authors: heath o. J Clin Invest. 2024 Feb 15;134(4):e174824. doi: 10.1172/JCI174824. J Clin Invest. 2024. PMID: 38357931 Free PMC article.
Palladium-Catalyzed Cross-Coupling of Alkenyl Carboxylates.
Becica J, Heath ORJ, Zheng CHM, Leitch DC. Becica J, et al. Among authors: heath orj. Angew Chem Int Ed Engl. 2020 Sep 21;59(39):17277-17281. doi: 10.1002/anie.202006586. Epub 2020 Jul 28. Angew Chem Int Ed Engl. 2020. PMID: 32578315
Institutional Performance and Vote Buying in India.
Heath O, Tillin L. Heath O, et al. Stud Comp Int Dev. 2018;53(1):90-110. doi: 10.1007/s12116-017-9254-x. Epub 2017 Nov 7. Stud Comp Int Dev. 2018. PMID: 31983779 Free PMC article.
Histologically atypical case of Gaucher disease type 1.
Sabljak J, Heath O, Halligan R, Cheng DR. Sabljak J, et al. Among authors: heath o. BMJ Case Rep. 2023 Sep 29;16(9):e256368. doi: 10.1136/bcr-2023-256368. BMJ Case Rep. 2023. PMID: 37775277
Biallelic Variants in PYROXD2 Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial Function.
Van Bergen NJ, Hock DH, Spencer L, Massey S, Stait T, Stark Z, Lunke S, Roesley A, Peters H, Lee JY, Le Fevre A, Heath O, Mignone C, Yang JY, Ryan MM, D'Arcy C, Nash M, Smith S, Caruana NJ, Thorburn DR, Stroud DA, White SM, Christodoulou J, Brown NJ. Van Bergen NJ, et al. Among authors: heath o. Int J Mol Sci. 2022 Jan 17;23(2):986. doi: 10.3390/ijms23020986. Int J Mol Sci. 2022. PMID: 35055180 Free PMC article.