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Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity.
Berhe S, Heeney MM, Campagna DR, Thompson JF, White EJ, Ross T, Peake RWA, Hanrahan JD, Rodriguez V, Renaud DL, Patnaik MS, Chang E, Bottomley SS, Fleming MD. Berhe S, et al. Among authors: fleming md. Haematologica. 2018 Dec;103(12):e561-e563. doi: 10.3324/haematol.2018.199109. Epub 2018 Jul 13. Haematologica. 2018. PMID: 30006447 Free PMC article. No abstract available.
The molecular defect in hypotransferrinemic mice.
Trenor CC 3rd, Campagna DR, Sellers VM, Andrews NC, Fleming MD. Trenor CC 3rd, et al. Among authors: fleming md. Blood. 2000 Aug 1;96(3):1113-8. Blood. 2000. PMID: 10910930 Free article.
The Steap proteins are metalloreductases.
Ohgami RS, Campagna DR, McDonald A, Fleming MD. Ohgami RS, et al. Among authors: fleming md. Blood. 2006 Aug 15;108(4):1388-94. doi: 10.1182/blood-2006-02-003681. Epub 2006 Apr 11. Blood. 2006. PMID: 16609065 Free PMC article.
X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation.
Tubman VN, Levine JE, Campagna DR, Monahan-Earley R, Dvorak AM, Neufeld EJ, Fleming MD. Tubman VN, et al. Among authors: fleming md. Blood. 2007 Apr 15;109(8):3297-9. doi: 10.1182/blood-2006-02-004101. Epub 2007 Jan 5. Blood. 2007. PMID: 17209061 Free article.
266 results