Maksimova Y - Search Results

1

Ankyrin-linked hereditary spherocytosis in an African-American kindred.

Sangerman J, Maksimova Y, Edelman EJ, Morrow JS, Forget BG, Gallagher PG. Sangerman J, et al. Among authors: maksimova y. Am J Hematol. 2008 Oct;83(10):789-94. doi: 10.1002/ajh.21254. Am J Hematol. 2008. PMID: 18704959 Free PMC article.

2

A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis.

Edelman EJ, Maksimova Y, Duru F, Altay C, Gallagher PG. Edelman EJ, et al. Among authors: maksimova y. Blood. 2007 Jun 15;109(12):5491-3. doi: 10.1182/blood-2006-09-046573. Epub 2007 Feb 27. Blood. 2007. PMID: 17327413 Free PMC article.

3

Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus.

Bogardus H, Schulz VP, Maksimova Y, Miller BA, Li P, Forget BG, Gallagher PG. Bogardus H, et al. Among authors: maksimova y. Haematologica. 2014 Sep;99(9):e168-70. doi: 10.3324/haematol.2014.110312. Epub 2014 Jun 3. Haematologica. 2014. PMID: 24895341 Free PMC article. No abstract available.

4

A de novo band 3 mutation in hereditary spherocytosis.

Bogardus HH, Maksimova YD, Forget BG, Gallagher PG. Bogardus HH, et al. Pediatr Blood Cancer. 2012 Jun;58(6):1004. doi: 10.1002/pbc.23400. Epub 2011 Dec 13. Pediatr Blood Cancer. 2012. PMID: 22170767 No abstract available.

5

Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis.

Glogowska E, Lezon-Geyda K, Maksimova Y, Schulz VP, Gallagher PG. Glogowska E, et al. Among authors: maksimova y. Blood. 2015 Sep 10;126(11):1281-4. doi: 10.1182/blood-2015-07-657957. Epub 2015 Jul 21. Blood. 2015. PMID: 26198474 Free PMC article.

6

Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype.

Gallagher PG, Maksimova Y, Schulz VP, Forget BG. Gallagher PG, et al. Among authors: maksimova y. Hemoglobin. 2016 Sep;40(5):361-364. doi: 10.1080/03630269.2016.1214921. Epub 2016 Sep 22. Hemoglobin. 2016. PMID: 27821015

7

An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cells.

Gallagher PG, Nilson DG, Steiner LA, Maksimova YD, Lin JY, Bodine DM. Gallagher PG, et al. Among authors: maksimova yd. Blood. 2009 Feb 12;113(7):1547-54. doi: 10.1182/blood-2008-06-164954. Epub 2008 Nov 13. Blood. 2009. PMID: 19008453 Free PMC article.

8

Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genes.

Steiner LA, Maksimova Y, Schulz V, Wong C, Raha D, Mahajan MC, Weissman SM, Gallagher PG. Steiner LA, et al. Among authors: maksimova y. Mol Cell Biol. 2009 Oct;29(20):5399-412. doi: 10.1128/MCB.00777-09. Epub 2009 Aug 17. Mol Cell Biol. 2009. PMID: 19687298 Free PMC article.

9

Patterns of histone H3 lysine 27 monomethylation and erythroid cell type-specific gene expression.

Steiner LA, Schulz VP, Maksimova Y, Wong C, Gallagher PG. Steiner LA, et al. Among authors: maksimova y. J Biol Chem. 2011 Nov 11;286(45):39457-65. doi: 10.1074/jbc.M111.243006. Epub 2011 Sep 21. J Biol Chem. 2011. PMID: 21937433 Free PMC article.

10

Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.

Glogowska E, Schneider ER, Maksimova Y, Schulz VP, Lezon-Geyda K, Wu J, Radhakrishnan K, Keel SB, Mahoney D, Freidmann AM, Altura RA, Gracheva EO, Bagriantsev SN, Kalfa TA, Gallagher PG. Glogowska E, et al. Among authors: maksimova y. Blood. 2017 Oct 19;130(16):1845-1856. doi: 10.1182/blood-2017-05-786004. Epub 2017 Jul 17. Blood. 2017. PMID: 28716860 Free PMC article.

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