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Year | Number of Results |
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2012 | 2 |
2013 | 2 |
2014 | 2 |
2015 | 1 |
2024 | 0 |
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6 results
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Page 1
Iron deficiency modifies gene expression variation induced by augmented hypoxia sensing.
Blood Cells Mol Dis. 2014 Jan;52(1):35-45. doi: 10.1016/j.bcmd.2013.07.016. Epub 2013 Aug 28.
Blood Cells Mol Dis. 2014.
PMID: 23993337
Free PMC article.
Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease.
Zhang X, Zhang W, Saraf SL, Nouraie M, Han J, Gowhari M, Hassan J, Miasnikova G, Sergueeva A, Nekhai S, Kittles R, Machado RF, Garcia JG, Gladwin MT, Steinberg MH, Sebastiani P, McClain DA, Gordeuk VR.
Zhang X, et al.
Hum Genet. 2015 Aug;134(8):895-904. doi: 10.1007/s00439-015-1572-3. Epub 2015 May 30.
Hum Genet. 2015.
PMID: 26025476
Free PMC article.
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Hypoxic response contributes to altered gene expression and precapillary pulmonary hypertension in patients with sickle cell disease.
Zhang X, Zhang W, Ma SF, Desai AA, Saraf S, Miasniakova G, Sergueeva A, Ammosova T, Xu M, Nekhai S, Abbasi T, Casanova NG, Steinberg MH, Baldwin CT, Sebastiani P, Prchal JT, Kittles R, Garcia JG, Machado RF, Gordeuk VR.
Zhang X, et al.
Circulation. 2014 Apr 22;129(16):1650-8. doi: 10.1161/CIRCULATIONAHA.113.005296. Epub 2014 Feb 10.
Circulation. 2014.
PMID: 24515990
Free PMC article.
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Sickle cell disease is associated with decreased HIV but higher HBV and HCV comorbidities in U.S. hospital discharge records: a cross-sectional study.
Nouraie M, Nekhai S, Gordeuk VR.
Nouraie M, et al.
Sex Transm Infect. 2012 Nov;88(7):528-33. doi: 10.1136/sextrans-2011-050459. Epub 2012 May 24.
Sex Transm Infect. 2012.
PMID: 22628662
Free PMC article.
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Adenoviral E4 gene stimulates secretion of pigmental epithelium derived factor (PEDF) that maintains long-term survival of human glomerulus-derived endothelial cells.
Jerebtsova M, Kumari N, Obuhkov Y, Nekhai S.
Jerebtsova M, et al.
Mol Cell Proteomics. 2012 Nov;11(11):1378-88. doi: 10.1074/mcp.M112.020313. Epub 2012 Aug 21.
Mol Cell Proteomics. 2012.
PMID: 22915824
Free PMC article.
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The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W).
Tomasic NL, Piterkova L, Huff C, Bilic E, Yoon D, Miasnikova GY, Sergueeva AI, Niu X, Nekhai S, Gordeuk V, Prchal JT.
Tomasic NL, et al.
Haematologica. 2013 Apr;98(4):560-7. doi: 10.3324/haematol.2012.070508. Epub 2013 Feb 12.
Haematologica. 2013.
PMID: 23403324
Free PMC article.
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