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Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.
Vathipadiekal V, Alsultan A, Baltrusaitis K, Farrell JJ, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Suliman A, Patra PK, Milton JN, Farrer LA, Chui DH, Al-Ali AK, Sebastiani P, Steinberg MH. Vathipadiekal V, et al. Among authors: naserullah z. Am J Hematol. 2016 Jun;91(6):E308-11. doi: 10.1002/ajh.24368. Epub 2016 Apr 28. Am J Hematol. 2016. PMID: 27185208 Free PMC article. No abstract available.
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.
Sebastiani P, Farrell JJ, Alsultan A, Wang S, Edward HL, Shappell H, Bae H, Milton JN, Baldwin CT, Al-Rubaish AM, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra PK, Farrer LA, Ngo D, Vathipadiekal V, Chui DH, Al-Ali AK, Steinberg MH. Sebastiani P, et al. Among authors: naserullah z. Blood Cells Mol Dis. 2015 Mar;54(3):224-30. doi: 10.1016/j.bcmd.2015.01.001. Epub 2015 Jan 30. Blood Cells Mol Dis. 2015. PMID: 25703683 Free PMC article.
Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia.
Shaikho EM, Habara AH, Alsultan A, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Patra PK, Sebastiani P, Baltrusaitis K, Farrell JJ, Jiang Z, Luo HY, Chui DH, Al-Ali AK, Steinberg MH. Shaikho EM, et al. Among authors: naserullah z. Blood Cells Mol Dis. 2016 Jul;59:49-51. doi: 10.1016/j.bcmd.2016.04.001. Epub 2016 Apr 13. Blood Cells Mol Dis. 2016. PMID: 27282567 Free PMC article. No abstract available.
A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.
Vathipadiekal V, Farrell JJ, Wang S, Edward HL, Shappell H, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Simkin I, Farrer LA, Jiang Z, Luo HY, Huang S, Mostoslavsky G, Murphy GJ, Patra PK, Chui DH, Alsultan A, Al-Ali AK, Sebastiani P, Steinberg MH. Vathipadiekal V, et al. Among authors: naserullah z. Am J Hematol. 2016 Nov;91(11):1118-1122. doi: 10.1002/ajh.24527. Epub 2016 Aug 22. Am J Hematol. 2016. PMID: 27501013 Free PMC article.
Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.
Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, Luo HY, Chui DH, Farrell JJ, Al-Ali AK, Alsultan A. Ngo D, et al. Among authors: naserullah z. Blood Cells Mol Dis. 2013 Jun;51(1):22-6. doi: 10.1016/j.bcmd.2012.12.005. Epub 2013 Mar 7. Blood Cells Mol Dis. 2013. PMID: 23465615 Free PMC article.
Mutations in the β-globin gene from a Saudi population: an update.
Borgio JF, AbdulAzeez S, Naserullah ZA, Al-Jarrash S, Al-Ali RA, Al-Madan MS, Al-Muhanna F, Al-Suliman AM, Al-Nafie A, Steinberg MH, Al-Ali AK. Borgio JF, et al. Among authors: naserullah za. Int J Lab Hematol. 2016 Apr;38(2):e38-40. doi: 10.1111/ijlh.12463. Epub 2016 Jan 29. Int J Lab Hematol. 2016. PMID: 26822801 No abstract available.
The ‑α3.7 deletion in α‑globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population.
Borgio JF, Abdulazeez S, Almandil NB, Naserullah ZA, Al-Jarrash S, Al-Suliman AM, Elfakharay HI, Qaw FS, Alabdrabalnabi FI, Alkhalifah MA, Shakil Akhtar M, Qutub H, Al-Ali AK. Borgio JF, et al. Among authors: naserullah za. Mol Med Rep. 2018 Jan;17(1):1879-1884. doi: 10.3892/mmr.2017.8033. Epub 2017 Nov 13. Mol Med Rep. 2018. PMID: 29138844
Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT).
Al-Amodi AM, Ghanem NZ, Aldakeel SA, Ibrahim Al Asoom L, Rafique Ahmed N, Almandil NB, Naserullah ZA, Al-Jarrash S, Shakil Akhtar M, AbdulAzeez S, Al-Ali AK, Borgio JF. Al-Amodi AM, et al. Among authors: naserullah za. Curr Med Res Opin. 2018 May;34(5):945-951. doi: 10.1080/03007995.2018.1435520. Epub 2018 Feb 15. Curr Med Res Opin. 2018. PMID: 29383950
20 results