Zhuang L - Search Results

1

Nondeletional α-thalassemia (α2- IVS-1-116, A>G HBA2): an α2 gene point mutation detected in an African-American female for the first time.

Dainer P, Patel N, Zhuang L, Carmichael H, Kutlar F. Dainer P, et al. Among authors: zhuang l. Acta Haematol. 2014;132(1):22-3. doi: 10.1159/000355426. Epub 2013 Dec 13. Acta Haematol. 2014. PMID: 24356242 No abstract available.

2

Hb Fulton-Georgia [α20(B1)His→Pro; HBA1: c.62A>C]: a new α-globin variant coinherited with α-thalassemia-2 (3.7 kb deletion) and Hb SC disease.

Zhuang L, Patel N, Bryant S, Kutlar A, Kutlar F, Young AN. Zhuang L, et al. Hemoglobin. 2013;37(5):481-5. doi: 10.3109/03630269.2013.810640. Epub 2013 Jul 3. Hemoglobin. 2013. PMID: 24006930

3

Two new hemoglobin variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A].

Kutlar F, Unguru Y, Dixon N, Patel N, Bailey L, Zhuang L, Carmichael H, Kutlar A. Kutlar F, et al. Among authors: zhuang l. Hemoglobin. 2014;38(3):207-10. doi: 10.3109/03630269.2014.881371. Epub 2014 Jan 29. Hemoglobin. 2014. PMID: 24471829

4

Two new γ chain variants: Hb F-Augusta GA [(G)γ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [(A)γ125(H3)Glu → Ala; HBG1: c.377A > C].

Kutlar F, Ameri A, Patel NH, Zhuang L, Johnson LE, Cheng ML, Kutlar A. Kutlar F, et al. Among authors: zhuang l. Hemoglobin. 2014;38(5):376-80. doi: 10.3109/03630269.2014.960526. Hemoglobin. 2014. PMID: 25271994

5

Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia.

Yee ME, Quarmyne MO, Segbefia C, Young AN, Zhuang L, Kutlar F. Yee ME, et al. Among authors: zhuang l. J Pediatr Hematol Oncol. 2016 Jan;38(1):e32-4. doi: 10.1097/MPH.0000000000000477. J Pediatr Hematol Oncol. 2016. PMID: 26583619

6

Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.

Kutlar F, Hilliard LM, Zhuang L, Patel N, Eroglu B, Meiler SE, Carmichael H, Russell RB, Kutlar A. Kutlar F, et al. Among authors: zhuang l. Blood Cells Mol Dis. 2009 Nov-Dec;43(3):235-8. doi: 10.1016/j.bcmd.2009.08.006. Epub 2009 Sep 15. Blood Cells Mol Dis. 2009. PMID: 19758826

7

Neonatal cyanosis due to a novel fetal hemoglobin: Hb F-Circleville [Ggamma63(E7)His-->Leu, CAT>CTT].

Dainer E, Shell R, Miller R, Atkin JF, Pastore M, Kutlar A, Zhuang L, Holley L, Davis DH, Kutlar F. Dainer E, et al. Among authors: zhuang l. Hemoglobin. 2008;32(6):596-600. doi: 10.1080/03630260802507915. Hemoglobin. 2008. PMID: 19065339

8

Thalassemia-like phenotype in a novel complex hemoglobinopathy with α, β, δ globin chain abnormalities.

Sabio H, Dixon N, Patel N, Obiaga C, Zhuang L, Meiler SE, Kutlar A, Kutlar F. Sabio H, et al. Among authors: zhuang l. J Pediatr Hematol Oncol. 2011 Dec;33(8):589-91. doi: 10.1097/MPH.0b013e318228255c. J Pediatr Hematol Oncol. 2011. PMID: 22042275

9

Diclofenac-induced stimulation of SMCT1 (SLC5A8) in a heterologous expression system: a RPE specific phenomenon.

Ananth S, Zhuang L, Gopal E, Itagaki S, Ellappan B, Smith SB, Ganapathy V, Martin P. Ananth S, et al. Among authors: zhuang l. Biochem Biophys Res Commun. 2010 Mar 26;394(1):75-80. doi: 10.1016/j.bbrc.2010.02.109. Epub 2010 Feb 21. Biochem Biophys Res Commun. 2010. PMID: 20178774 Free PMC article.

10

Sodium-coupled and electrogenic transport of B-complex vitamin nicotinic acid by slc5a8, a member of the Na/glucose co-transporter gene family.

Gopal E, Fei YJ, Miyauchi S, Zhuang L, Prasad PD, Ganapathy V. Gopal E, et al. Among authors: zhuang l. Biochem J. 2005 May 15;388(Pt 1):309-16. doi: 10.1042/BJ20041916. Biochem J. 2005. PMID: 15651982 Free PMC article.

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