Fleming MD - Search Results

1

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.

2

The G185R mutation disrupts function of the iron transporter Nramp2.

Su MA, Trenor CC, Fleming JC, Fleming MD, Andrews NC. Su MA, et al. Among authors: fleming md, fleming jc. Blood. 1998 Sep 15;92(6):2157-63. Blood. 1998. PMID: 9731075 Free article.

3

The C282Y mutation causing hereditary hemochromatosis does not produce a null allele.

Levy JE, Montross LK, Cohen DE, Fleming MD, Andrews NC. Levy JE, et al. Among authors: fleming md. Blood. 1999 Jul 1;94(1):9-11. Blood. 1999. PMID: 10381492 Free article.

4

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.

5

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.

6

Characterization of a murine high-affinity thiamine transporter, Slc19a2.

Fleming JC, Steinkamp MP, Kawatsuji R, Tartaglini E, Pinkus JL, Pinkus GS, Fleming MD, Neufeld EJ. Fleming JC, et al. Among authors: fleming md. Mol Genet Metab. 2001 Sep-Oct;74(1-2):273-80. doi: 10.1006/mgme.2001.3241. Mol Genet Metab. 2001. PMID: 11592824

7

Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2.

Fleming JC, Tartaglini E, Kawatsuji R, Yao D, Fujiwara Y, Bednarski JJ, Fleming MD, Neufeld EJ. Fleming JC, et al. Among authors: fleming md. Mol Genet Metab. 2003 Sep-Oct;80(1-2):234-41. doi: 10.1016/s1096-7192(03)00141-0. Mol Genet Metab. 2003. PMID: 14567973

8

Identification of a novel mutation (C321X) in HJV.

Huang FW, Rubio-Aliaga I, Kushner JP, Andrews NC, Fleming MD. Huang FW, et al. Among authors: fleming md. Blood. 2004 Oct 1;104(7):2176-7. doi: 10.1182/blood-2004-01-0400. Epub 2004 May 11. Blood. 2004. PMID: 15138164 Free article.

9

Cybrd1 (duodenal cytochrome b) is not necessary for dietary iron absorption in mice.

Gunshin H, Starr CN, Direnzo C, Fleming MD, Jin J, Greer EL, Sellers VM, Galica SM, Andrews NC. Gunshin H, et al. Among authors: fleming md. Blood. 2005 Oct 15;106(8):2879-83. doi: 10.1182/blood-2005-02-0716. Epub 2005 Jun 16. Blood. 2005. PMID: 15961514 Free PMC article.

10

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.

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