Y. Maksimova

发表

Chromatin Architecture and Transcription Factor Binding Regulate Expression of Erythrocyte Membrane Protein Genes

M. Mahajan, S. Weissman, D. Raha, 2009, Molecular and Cellular Biology.

Nonsense mutations of the α-spectrin gene in hereditary pyropoikilocytosis

B. Forget, P. Gallagher, Y. Maksimova, 2008, Haematologica.

Erythrocyte peripheral type benzodiazepine receptor/voltage-dependent anion channels are upregulated by Plasmodium falciparum.

G. Bouyer, P. Gallagher, S. Égée, 2011, Blood.

Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytes.

Mack Y Su, J. Craft, Yaoping Zhang, 2014, Blood.

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

B. Forget, V. Schulz, P. Gallagher, 2014, Haematologica.

The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytes.

D. Vandorpe, S. Alper, P. Gallagher, 2010, American journal of physiology. Cell physiology.

Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity

C. Colangelo, R. Lifton, Dianqing Wu, 2009, Cell.

Late-onset Leclercia adecarboxylata sepsis in a premature neonate

V. Schulz, P. Gallagher, M. Bizzarro, 2013, Journal of Perinatology.

Failure of Terminal Erythroid Differentiation in EKLF-Deficient Mice Is Associated with Cell Cycle Perturbation and Reduced Expression of E2F2

H. Dressman, M. Arcasoy, D. Bodine, 2008, Molecular and Cellular Biology.

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.

Brian E. Smith, D. S. Houston, R. Zarychanski, 2012, Blood.

Ankyrin‐linked hereditary spherocytosis in an African–American kindred

J. Sangerman, B. Forget, P. Gallagher, 2008, American journal of hematology.

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

D. Bodine, P. Gallagher, Laurie A. Steiner, 2009, Blood.

Patterns of Histone H3 Lysine 27 Monomethylation and Erythroid Cell Type-specific Gene Expression*

V. Schulz, P. Gallagher, Vincent P. Schulz, 2011, The Journal of Biological Chemistry.

Aberrant splicing contributes to severe α-spectrin-linked congenital hemolytic anemia.

P. Newburger, D. Speicher, S. Israels, 2019, The Journal of clinical investigation.

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

B. Forget, V. Schulz, P. Gallagher, 2016, Hemoglobin.

Aberrant splicing contributes to severe alpha-spectrin-linked congenital hemolytic anemia

P. Newburger, D. Speicher, S. Israels, 2022 .

Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.

E. R. Schneider, R. Altura, John Wu, 2017, Blood.

RED CELLS , IRON , AND ERYTHROPOIESIS Novel mechanisms of PIEZO 1 dysfunction in hereditary xerocytosis

E. R. Schneider, R. Altura, John Wu, 2017 .

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

V. Schulz, K. Lezon-Geyda, P. Gallagher, 2015, Blood.

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

P. Gallagher, J. Edelman, F. Duru, 2010 .

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

P. Gallagher, F. Duru, E. Edelman, 2007, Blood.

A Comprehensive Model of the Spectrin Divalent Tetramer Binding Region Deduced Using Homology Modeling and Chemical Cross-linking of a Mini-spectrin*

David W Speicher, D. Speicher, Hsin-Yao Tang, 2010, Journal of Biological Chemistry.

A de novo band 3 mutation in hereditary spherocytosis

B. Forget, P. Gallagher, Y. Maksimova, 2012, Pediatric blood & cancer.

Dynamic CO-Localization of GATA1, NFE2, and EKLF and Changes in Gene Expression During Hematopoiesis

M. Mahajan, D. Bodine, V. Schulz, 2010 .

A Fused α-β “Mini-spectrin” Mimics the Intact Erythrocyte Spectrin Head-to-head Tetramer*

D. Speicher, P. Gallagher, S. Harper, 2010, The Journal of Biological Chemistry.

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

D. Bodine, P. Gallagher, Laurie A. Steiner, 2009, Blood.

An insulator with barrier-element activity promotes (cid:1) -spectrin gene expression in erythroid cells

D. Bodine, Laurie A. Steiner, Y. Maksimova, 2009 .

functional analysis cytoplasmic tail of polycystin-1: mutational and Cation channel regulation by COOH-terminal

D. Vandorpe, A. Wandinger-Ness, V. Gattone, 2015 .

A Comprehensive Model of the Spectrin Divalent Tetramer Binding Region Deduced Using Homology Modeling and Chemical Cross-linking of a Mini-spectrin*

D. Speicher, Hsin-Yao Tang, P. Gallagher, 2010, The Journal of Biological Chemistry.

Aberrant splicing contributes to severe α-spectrin-linked congenital hemolytic anemia.

S. Israels, S. Baserga, N. Mittal, 2019, The Journal of clinical investigation.