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Items: 1 to 50 of 256

1.

An Unusual Case of Low Hemoglobin Oxygen Saturation.

Homsy E, Alghothani L, Chui DHK, Sood N.

Ann Am Thorac Soc. 2019 Jun;16(6):756-759. doi: 10.1513/AnnalsATS.201811-829CC. No abstract available.

PMID:
31149860
2.

Inhibition of LSD1 by small molecule inhibitors stimulates fetal hemoglobin synthesis.

Le CQ, Myers G, Habara A, Jearawiriyapaisarn N, Murphy GJ, Chui DHK, Steinberg MH, Engel JD, Cui S.

Blood. 2019 May 30;133(22):2455-2459. doi: 10.1182/blood.2018892737. Epub 2019 Apr 16. No abstract available.

PMID:
30992270
3.

Editing aberrant splice sites efficiently restores β-globin expression in β-thalassemia.

Xu S, Luk K, Yao Q, Shen AH, Zeng J, Wu Y, Luo HY, Brendel C, Pinello L, Chui DHK, Wolfe SA, Bauer DE.

Blood. 2019 May 23;133(21):2255-2262. doi: 10.1182/blood-2019-01-895094. Epub 2019 Jan 31.

PMID:
30704988
4.

The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease.

Al-Allawi N, Qadir SMA, Puehringer H, Chui DHK, Farrell JJ, Oberkanins C.

Int J Lab Hematol. 2019 Feb;41(1):87-93. doi: 10.1111/ijlh.12927. Epub 2018 Sep 14.

PMID:
30216683
5.

Induced pluripotent stem cell-based mapping of β-globin expression throughout human erythropoietic development.

Vanuytsel K, Matte T, Leung A, Naing ZH, Morrison T, Chui DHK, Steinberg MH, Murphy GJ.

Blood Adv. 2018 Aug 14;2(15):1998-2011. doi: 10.1182/bloodadvances.2018020560.

6.

Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation.

Singh SA, Sarangi S, Appiah-Kubi A, Hsu P, Smith WB, Gallagher PG, Glader B, Chui DHK.

Pediatr Blood Cancer. 2018 Sep;65(9):e27220. doi: 10.1002/pbc.27220. Epub 2018 May 11.

PMID:
29749692
7.

Notch and Aryl Hydrocarbon Receptor Signaling Impact Definitive Hematopoiesis from Human Pluripotent Stem Cells.

Leung A, Zulick E, Skvir N, Vanuytsel K, Morrison TA, Naing ZH, Wang Z, Dai Y, Chui DHK, Steinberg MH, Sherr DH, Murphy GJ.

Stem Cells. 2018 Jul;36(7):1004-1019. doi: 10.1002/stem.2822. Epub 2018 Apr 1.

8.

A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy.

Akinbami AO, Sobota AE, Luo HY, Chui DHK, Steinberg MH.

J Pediatr Hematol Oncol. 2018 Apr;40(3):e145-e147. doi: 10.1097/MPH.0000000000001068.

PMID:
29309373
9.

A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression.

Morrison TA, Wilcox I, Luo HY, Farrell JJ, Kurita R, Nakamura Y, Murphy GJ, Cui S, Steinberg MH, Chui DHK.

Blood Cells Mol Dis. 2018 Mar;69:1-9. doi: 10.1016/j.bcmd.2017.11.003. Epub 2017 Nov 29.

10.

A phased SNP-based classification of sickle cell anemia HBB haplotypes.

Shaikho EM, Farrell JJ, Alsultan A, Qutub H, Al-Ali AK, Figueiredo MS, Chui DHK, Farrer LA, Murphy GJ, Mostoslavsky G, Sebastiani P, Steinberg MH.

BMC Genomics. 2017 Aug 11;18(1):608. doi: 10.1186/s12864-017-4013-y.

11.

The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia.

Cancio MI, Aygun B, Chui DHK, Rothman JA, Scott JP, Estepp JH, Hankins JS.

Pediatr Blood Cancer. 2017 Nov;64(11). doi: 10.1002/pbc.26596. Epub 2017 Apr 28.

12.

Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family.

Pernudy-Ubau A, Salinas-Molina J, Requenez Y, Ortiz-Lopez M, Puller AC, García-Rosales K, Rodríguez-Estrada A, Rodríguez-Romero W, Mejía-Baltodano G, Luo HY, Chui DHK.

Hemoglobin. 2017 Jan;41(1):50-52. doi: 10.1080/03630269.2017.1302949. Epub 2017 Apr 11.

PMID:
28395541
13.

A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0 -thalassaemia homozygotes.

Jiang Z, Luo HY, Farrell JJ, Zhang Z, Schulz VP, Albarawi D, Steinberg MH, Al-Allawi NAS, Gallagher PG, Forget BG, Chui DHK.

Br J Haematol. 2018 Mar;180(5):755-757. doi: 10.1111/bjh.14445. Epub 2017 Feb 27. No abstract available.

PMID:
28240767
14.

A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells.

Park S, Gianotti-Sommer A, Molina-Estevez FJ, Vanuytsel K, Skvir N, Leung A, Rozelle SS, Shaikho EM, Weir I, Jiang Z, Luo HY, Chui DHK, Figueiredo MS, Alsultan A, Al-Ali A, Sebastiani P, Steinberg MH, Mostoslavsky G, Murphy GJ.

Stem Cell Reports. 2017 Apr 11;8(4):1076-1085. doi: 10.1016/j.stemcr.2016.12.017. Epub 2017 Jan 19.

15.

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.

Am J Hematol. 2016 Nov;91(11):1118-1122. doi: 10.1002/ajh.24527. Epub 2016 Aug 22.

16.

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.

Blood Cells Mol Dis. 2016 Jul;59:49-51. doi: 10.1016/j.bcmd.2016.04.001. Epub 2016 Apr 13. No abstract available.

PMID:
27282567
17.

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.

Am J Hematol. 2016 Jun;91(6):E308-11. doi: 10.1002/ajh.24368. Epub 2016 Apr 28. No abstract available.

18.

Diverse hematological phenotypes of β-thalassemia carriers.

Luo HY, Chui DH.

Ann N Y Acad Sci. 2016 Mar;1368(1):49-55. doi: 10.1111/nyas.13056. Epub 2016 Apr 28. Review.

PMID:
27123947
19.

Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A).

Boucher MO, Chui DH, Woda BA, Newburger PE.

Hemoglobin. 2016 Jun;40(3):208-9. doi: 10.3109/03630269.2016.1165245.

PMID:
27117572
20.

The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes.

Jiang Z, Luo HY, Huang S, Farrell JJ, Davis L, Théberge R, Benson KA, Riolueang S, Viprakasit V, Al-Allawi NA, Ünal S, Gümrük F, Akar N, Başak AN, Osorio L, Badens C, Pissard S, Joly P, Campbell AD, Gallagher PG, Steinberg MH, Forget BG, Chui DH.

Br J Haematol. 2016 Mar;172(6):958-65. doi: 10.1111/bjh.13909. Epub 2016 Jan 13.

21.

Therapeutic fetal-globin inducers reduce transcriptional repression in hemoglobinopathy erythroid progenitors through distinct mechanisms.

Dai Y, Sangerman J, Luo HY, Fucharoen S, Chui DH, Faller DV, Perrine SP.

Blood Cells Mol Dis. 2016 Jan;56(1):62-9. doi: 10.1016/j.bcmd.2015.10.004. Epub 2015 Oct 27.

22.

Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.

Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH.

Hemoglobin. 2016;40(1):64-5. doi: 10.3109/03630269.2015.1080725. Epub 2015 Sep 15.

PMID:
26372199
23.

Duration-dependent regulation of autophagy by isoflurane exposure in aged rats.

Li ZQ, Li LX, Mo N, Cao YY, Kuerban B, Liang YX, Fan DS, Chui DH, Guo XY.

Neurosci Bull. 2015 Aug;31(4):505-13. doi: 10.1007/s12264-015-1549-1. Epub 2015 Aug 8.

24.

Autophagy is involved in oral rAAV/Aβ vaccine-induced Aβ clearance in APP/PS1 transgenic mice.

Wang HC, Zhang T, Kuerban B, Jin YL, Le W, Hara H, Fan DS, Wang YJ, Tabira T, Chui DH.

Neurosci Bull. 2015 Aug;31(4):491-504. doi: 10.1007/s12264-015-1546-4. Epub 2015 Aug 8.

25.

MALDI-ISD Mass Spectrometry Analysis of Hemoglobin Variants: a Top-Down Approach to the Characterization of Hemoglobinopathies.

Théberge R, Dikler S, Heckendorf C, Chui DH, Costello CE, McComb ME.

J Am Soc Mass Spectrom. 2015 Aug;26(8):1299-310. doi: 10.1007/s13361-015-1164-4. Epub 2015 May 22.

26.

Fanconi's Anemia Effect or Sickle Cell Anemia Effect: That is the Question.

Unal S, Chui DH, Gumruk F.

Hemoglobin. 2015;39(4):287-9. doi: 10.3109/03630269.2015.1041036. Epub 2015 May 15.

PMID:
25976779
27.

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.

Blood Cells Mol Dis. 2015 Mar;54(3):224-30. doi: 10.1016/j.bcmd.2015.01.001. Epub 2015 Jan 30.

28.

Surgical stress induces brain-derived neurotrophic factor reduction and postoperative cognitive dysfunction via glucocorticoid receptor phosphorylation in aged mice.

Tian XS, Tong YW, Li ZQ, Li LX, Zhang T, Ren TY, Zhou T, Wang HC, Zhan R, Sun Y, Yan Z, Wang QD, Fan DS, Kong FJ, Guo XY, Xiao WZ, Chui DH.

CNS Neurosci Ther. 2015 May;21(5):398-409. doi: 10.1111/cns.12368. Epub 2015 Jan 22.

29.

A double-blind, rct testing beneficial modulation of BDNF in middle-aged, life style-stressed subjects: a clue to brain protection?

Chui DH, Marcellino M, Marotta F, Sweed H, Solimene U, Vignali AI, Xiao W, Ayala A, Cagnuolo U, Zerbinati N.

J Clin Diagn Res. 2014 Nov;8(11):MC01-6. doi: 10.7860/JCDR/2014/10301.5141. Epub 2014 Nov 20.

30.

The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patient.

Unal S, Chui DH, Luo HY, Okur H, Oymak Y, Gumruk F.

Hemoglobin. 2015;39(1):66-8. doi: 10.3109/03630269.2014.982255. Epub 2015 Jan 9.

PMID:
25572182
31.

Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.

Edward HL, Pisani LA, Rodriguez-Romero WE, Chaves-Villalobos J, Garcia-Quesada J, Harris NS, Luo HY, Steinberg MH, Forget BG, Chui DH.

Hemoglobin. 2014;38(6):381-4. doi: 10.3109/03630269.2014.971960. Epub 2014 Oct 27.

PMID:
25347256
32.

The genetics of hemoglobin A2 regulation in sickle cell anemia.

Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH.

Am J Hematol. 2014 Nov;89(11):1019-23. doi: 10.1002/ajh.23811. Epub 2014 Aug 4.

33.

A phase 2 trial of HQK-1001 in HbE-β thalassemia demonstrates HbF induction and reduced anemia.

Patthamalai P, Fuchareon S, Chaneiam N, Ghalie RG, Chui DH, Boosalis MS, Perrine SP.

Blood. 2014 Mar 20;123(12):1956-7. doi: 10.1182/blood-2013-11-538470. No abstract available.

34.

HbC disorders.

Steinberg MH, Chui DH.

Blood. 2013 Nov 21;122(22):3698. doi: 10.1182/blood-2013-09-526764. No abstract available.

35.

Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.

Alsultan A, Alabdulaali MK, Griffin PJ, Alsuliman AM, Ghabbour HA, Sebastiani P, Albuali WH, Al-Ali AK, Chui DH, Steinberg MH.

Br J Haematol. 2014 Feb;164(4):597-604. doi: 10.1111/bjh.12650. Epub 2013 Nov 13.

36.

A phase 2 study of HQK-1001, an oral fetal haemoglobin inducer, in β-thalassaemia intermedia.

Inati A, Kahale M, Perrine SP, Chui DH, Taher AT, Koussa S, Abi Nasr T, Abbas HA, Ghalie RG.

Br J Haematol. 2014 Feb;164(3):456-8. doi: 10.1111/bjh.12635. Epub 2013 Nov 13. No abstract available.

37.

Fetal hemoglobin in sickle cell anemia: a glass half full?

Steinberg MH, Chui DH, Dover GJ, Sebastiani P, Alsultan A.

Blood. 2014 Jan 23;123(4):481-5. doi: 10.1182/blood-2013-09-528067. Epub 2013 Nov 12.

38.

The profiling and identification of the metabolites of (+)-catechin and study on their distribution in rats by HPLC-DAD-ESI-IT-TOF-MS(n) technique.

Liang J, Xu F, Zhang YZ, Zang XY, Wang D, Shang MY, Wang X, Chui DH, Cai SQ.

Biomed Chromatogr. 2014 Mar;28(3):401-11. doi: 10.1002/bmc.3034. Epub 2013 Sep 16.

PMID:
24105958
39.

Activation of the canonical nuclear factor-κB pathway is involved in isoflurane-induced hippocampal interleukin-1β elevation and the resultant cognitive deficits in aged rats.

Li ZQ, Rong XY, Liu YJ, Ni C, Tian XS, Mo N, Chui DH, Guo XY.

Biochem Biophys Res Commun. 2013 Sep 6;438(4):628-34. doi: 10.1016/j.bbrc.2013.08.003. Epub 2013 Aug 9.

PMID:
23933318
40.

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

Croteau SE, Luo HY, Lehmann LE, Chui DH, Neufeld EJ.

Pediatr Blood Cancer. 2013 Oct;60(10):E131-4. doi: 10.1002/pbc.24611. Epub 2013 Jun 15.

PMID:
23776097
41.

The aryl hydrocarbon receptor directs hematopoietic progenitor cell expansion and differentiation.

Smith BW, Rozelle SS, Leung A, Ubellacker J, Parks A, Nah SK, French D, Gadue P, Monti S, Chui DH, Steinberg MH, Frelinger AL, Michelson AD, Theberge R, McComb ME, Costello CE, Kotton DN, Mostoslavsky G, Sherr DH, Murphy GJ.

Blood. 2013 Jul 18;122(3):376-85. doi: 10.1182/blood-2012-11-466722. Epub 2013 May 30.

42.

Upregulation of P2X3 receptors by neuronal calcium sensor protein VILIP-1 in dorsal root ganglions contributes to the bone cancer pain in rats.

Liu M, Yang H, Fang D, Yang JJ, Cai J, Wan Y, Chui DH, Han JS, Xing GG.

Pain. 2013 Sep;154(9):1551-68. doi: 10.1016/j.pain.2013.04.022. Epub 2013 Apr 26.

PMID:
23707265
43.

Gigantic splenomegaly in a 27-year-old male of South-East Asian descent with concurrent diagnosis of myeloproliferative neoplasm and hemoglobin H disease.

Shi Y, Kulbacki E, Chui DH, Wang E.

Eur J Haematol. 2013 Sep;91(3):284-5. doi: 10.1111/ejh.12137. Epub 2013 Jun 28. No abstract available.

PMID:
23672282
44.

Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia.

Alsultan A, Ngo D, Bae H, Sebastiani P, Baldwin CT, Melista E, Suliman AM, Albuali WH, Nasserullah Z, Luo HY, Chui DH, Steinberg MH, Al-Ali AK.

Am J Hematol. 2013 Jun;88(6):531-2. doi: 10.1002/ajh.23434. Epub 2013 May 2. No abstract available.

45.

Identification of the first mutation in a BRE motif of the β-globin gene and its inheritance with two other α-globin gene mutations in a Lebanese family.

Inati A, Abbas HA, Al-Danaf J, Souaid M, Kahale M, Koussa S, Abou Nasr T, Davis L, Luo HY, Chui DH.

Hemoglobin. 2013;37(2):171-5. doi: 10.3109/03630269.2013.772523.

PMID:
23470150
46.

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.

Blood Cells Mol Dis. 2013 Jun;51(1):22-6. doi: 10.1016/j.bcmd.2012.12.005. Epub 2013 Mar 7.

47.

Hemoglobin Shady Grove: a novel fetal methemoglobin variant.

Marks A, Luo HY, Chui DH, Greenberg J.

Pediatr Blood Cancer. 2013 Aug;60(8):E55-6. doi: 10.1002/pbc.24503. Epub 2013 Mar 4.

PMID:
23460588
48.

Massive splenic infarction in an adolescent with hemoglobin S-HPFH.

Whyte D, Forget B, Chui DH, Luo HY, Pashankar F.

Pediatr Blood Cancer. 2013 Jul;60(7):E49-51. doi: 10.1002/pbc.24444. Epub 2012 Dec 31.

PMID:
23281181
49.

Pulse oximetry screening for critical congenital heart defects.

Verhovsek MM, Chui DH.

Lancet. 2012 Oct 13;380(9850):1305-6; author reply 1306. doi: 10.1016/S0140-6736(12)61754-1. No abstract available.

PMID:
23063278
50.

Effective properties of a sturgeon-based bioactive compound on stress-induced hippocampal degeneration and on in vitro neurogenesis.

Marotta F, Chui DH, Yadav H, Lorenzetti A, Celep G, Jain S, Bomba A, Polimeni A, Zhong K, Allegri F.

J Biol Regul Homeost Agents. 2012 Jul-Sep;26(3):327-35.

PMID:
23034252

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