Roper D - Search Results

1

IFN-gamma enhances production of nitric oxide from macrophages via a mechanism that depends on nucleotide oligomerization domain-2.

Tötemeyer S, Sheppard M, Lloyd A, Roper D, Dowson C, Underhill D, Murray P, Maskell D, Bryant C. Tötemeyer S, et al. Among authors: roper d. J Immunol. 2006 Apr 15;176(8):4804-10. doi: 10.4049/jimmunol.176.8.4804. J Immunol. 2006. PMID: 16585574

2

Transcriptional and epigenetic basis for restoration of G6PD enzymatic activity in human G6PD-deficient cells.

Makarona K, Caputo VS, Costa JR, Liu B, O'Connor D, Iskander D, Roper D, Robertson L, Bhatnagar N, Terpos E, Georgiou E, Papaioannou M, Layton DM, Luzzatto L, Roberts I, Karadimitris A. Makarona K, et al. Among authors: roper d. Blood. 2014 Jul 3;124(1):134-41. doi: 10.1182/blood-2014-02-553792. Epub 2014 May 7. Blood. 2014. PMID: 24805191 Free article.

3

Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcome.

Clarke JL, Vulliamy TJ, Roper D, Mesbah-Namin SA, Wild BJ, Walker JI, Will AM, Bolton-Maggs PH, Mason PJ, Layton DM. Clarke JL, et al. Among authors: roper d. Blood Cells Mol Dis. 2003 May-Jun;30(3):258-63. doi: 10.1016/s1079-9796(03)00027-5. Blood Cells Mol Dis. 2003. PMID: 12737943

4

Severe hemolytic anemia associated with the homozygous state for an unstable hemoglobin variant (Hb Bushwick).

Srivastava P, Kaeda JS, Roper D, Vulliamy TJ, Buckley M, Luzzatto L. Srivastava P, et al. Among authors: roper d. Blood. 1995 Sep 1;86(5):1977-82. Blood. 1995. PMID: 7655024 Free article.

5

Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia.

Vulliamy TJ, Kaeda JS, Ait-Chafa D, Mangerini R, Roper D, Barbot J, Mehta AB, Athanassiou-Metaxa M, Luzzatto L, Mason PJ. Vulliamy TJ, et al. Among authors: roper d. Br J Haematol. 1998 Jun;101(4):670-5. doi: 10.1046/j.1365-2141.1998.00763.x. Br J Haematol. 1998. PMID: 9674740 Free article.

6

Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infant.

Percy MJ, Crowley LJ, Roper D, Vulliamy TJ, Layton DM, Barber MJ. Percy MJ, et al. Among authors: roper d. Blood Cells Mol Dis. 2006 Jan-Feb;36(1):81-90. doi: 10.1016/j.bcmd.2005.10.001. Epub 2005 Nov 28. Blood Cells Mol Dis. 2006. PMID: 16310381

7

Splenic infarction in a patient with sickle cell trait and hereditary spherocytosis.

Tso AC, Roper DR, Wong CL, Bain B, Layton DM. Tso AC, et al. Am J Hematol. 2011 Aug;86(8):695-6. doi: 10.1002/ajh.22015. Epub 2011 Apr 20. Am J Hematol. 2011. PMID: 21509796 Free article. No abstract available.

8

Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians.

Sirdah M, Reading NS, Vankayalapati H, Perkins SL, Shubair ME, Aboud L, Roper D, Prchal JT. Sirdah M, et al. Among authors: roper d. Blood Cells Mol Dis. 2012 Oct 15-Dec 15;49(3-4):152-8. doi: 10.1016/j.bcmd.2012.06.003. Epub 2012 Jul 5. Blood Cells Mol Dis. 2012. PMID: 22770933

9

Laboratory diagnosis of G6PD deficiency. A British Society for Haematology Guideline.

Roper D, Layton M, Rees D, Lambert C, Vulliamy T, De la Salle B, D'Souza C; British Society for Haematology. Roper D, et al. Among authors: d souza c. Br J Haematol. 2020 Apr;189(1):24-38. doi: 10.1111/bjh.16366. Epub 2020 Jan 28. Br J Haematol. 2020. PMID: 31991476 Free article. No abstract available.

10

Abrogation of red blood cell G6PD enzyme activity through Heat treatment: development of survey material for the UK NEQAS G6PD scheme.

Roper DR, De la Salle B, Soni V, Fletcher K, Green JA. Roper DR, et al. Int J Lab Hematol. 2017 Jun;39(3):308-316. doi: 10.1111/ijlh.12627. Epub 2017 Mar 20. Int J Lab Hematol. 2017. PMID: 28318100 Clinical Trial.

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