Fleming MD - Search Results

1

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.

2

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.

3

A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice.

Fleming MD, Campagna DR, Haslett JN, Trenor CC 3rd, Andrews NC. Fleming MD, et al. Genes Dev. 2001 Mar 15;15(6):652-7. doi: 10.1101/gad.873001. Genes Dev. 2001. PMID: 11274051 Free PMC article.

4

nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse.

Ohgami RS, Campagna DR, Antiochos B, Wood EB, Sharp JJ, Barker JE, Fleming MD. Ohgami RS, et al. Among authors: fleming md. Blood. 2005 Nov 15;106(10):3625-31. doi: 10.1182/blood-2005-01-0379. Epub 2005 Jun 30. Blood. 2005. PMID: 15994289 Free PMC article.

5

Identification of a ferrireductase required for efficient transferrin-dependent iron uptake in erythroid cells.

Ohgami RS, Campagna DR, Greer EL, Antiochos B, McDonald A, Chen J, Sharp JJ, Fujiwara Y, Barker JE, Fleming MD. Ohgami RS, et al. Among authors: fleming md. Nat Genet. 2005 Nov;37(11):1264-9. doi: 10.1038/ng1658. Epub 2005 Oct 16. Nat Genet. 2005. PMID: 16227996 Free PMC article.

6

The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron-sulfur cluster biogenesis.

Pondarré C, Antiochos BB, Campagna DR, Clarke SL, Greer EL, Deck KM, McDonald A, Han AP, Medlock A, Kutok JL, Anderson SA, Eisenstein RS, Fleming MD. Pondarré C, et al. Among authors: fleming md. Hum Mol Genet. 2006 Mar 15;15(6):953-64. doi: 10.1093/hmg/ddl012. Epub 2006 Feb 8. Hum Mol Genet. 2006. PMID: 16467350

7

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.

8

Loss of the acyl-CoA binding protein (Acbp) results in fatty acid metabolism abnormalities in mouse hair and skin.

Lee L, DeBono CA, Campagna DR, Young DC, Moody DB, Fleming MD. Lee L, et al. Among authors: fleming md. J Invest Dermatol. 2007 Jan;127(1):16-23. doi: 10.1038/sj.jid.5700511. Epub 2006 Aug 10. J Invest Dermatol. 2007. PMID: 16902415 Free PMC article.

9

Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis.

Pondarre C, Campagna DR, Antiochos B, Sikorski L, Mulhern H, Fleming MD. Pondarre C, et al. Among authors: fleming md. Blood. 2007 Apr 15;109(8):3567-9. doi: 10.1182/blood-2006-04-015768. Epub 2006 Dec 27. Blood. 2007. PMID: 17192398 Free PMC article.

10

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.

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