M. Narla

发表

New Views of Sickle Cell Disease Pathophysiology and Treatment.

M. Steinberg, W. Rosse, M. Narla, 2000, Hematology. American Society of Hematology. Education Program.

In vivo delayed clearance of Plasmodium falciparum malaria independent of kelch13 polymorphisms and with escalating malaria in Bangladesh.

R. Haque, K. Haldar, R. Ware, 2021, medRxiv.

Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency.

C. Hillyer, X. An, Lixiang Chen, 2021, Blood.

Therapeutic Hemoglobin Levels after Gene Transfer in β-Thalassemia Mice and in Hematopoietic Cells of β-Thalassemia and Sickle Cells Disease Patients

S. Rivella, L. Cartegni, R. Gambari, 2012, PloS one.

membrane-associated ICAM-4 interactions Novel secreted isoform of adhesion molecule ICAM-4: potential regulator of

M. Koury, D. Anstee, L. Peters, 2013 .

Rheologic properties of senescent erythrocytes: loss of surface area and volume with red blood cell age.

T Suzuki, R. Waugh, T. Suzuki, 1992, Blood.

skeleton protein levels and spectrin incorporation into the red blood cell membrane-spectrin gene alter spectrin mRNA and α Mutations in the murine erythroid

D. Bodine, N. Wandersee, C. Birkenmeier, 2002 .

Identification of binding domains on red blood cell glycophorins for Babesia divergens

J. R. Cursino-Santos, G. Halverson, M. Narla, 2014, Transfusion.

A Mouse Model for Diamond-Blackfan Anemia Demonstrates a Dominant Negative Effect of a Point Mutation in the RPS19 Gene

D. Bodine, M. Narla, E. Devlin, 2008 .

Faculty Opinions recommendation of Ribosome levels selectively regulate translation and lineage commitment in human hematopoiesis.

M. Narla, 2018, Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature.

Single Particle Electron Microscopy Analysis of the Bovine Anion Exchanger 1 Reveals a Flexible Linker Connecting the Cytoplasmic and Membrane Domains

Z. Zhou, P. Ge, I. Atanasov, 2013, PloS one.

Faculty Opinions recommendation of Functional selectivity in cytokine signaling revealed through a pathogenic EPO mutation.

M. Narla, 2018, Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature.

The Pyruvate Kinase Activator Mitapivat Ameliorates Anemia and Prevents Iron Overload in a Mouse Model of Hereditary Spherocytosis

C. Kung, L. Dang, C. Brugnara, 2020 .

Use of Jak2 Inhibitors to Limit Ineffective Erythropoiesis and Iron Absorption in Mice Affected by β-Thalassemia and Other Disorders of Red Cell Production.

S. Rivella, X. An, L. Melchiori, 2009 .

Hepcidin as a Therapeutic Tool to Limit Iron Overload and Improve Anemia In β-Thalassemia

S. Rivella, N. Andrews, X. An, 2010 .

Fyn is Involved in Erythropoietin Signaling Pathway and Interfaces Oxidation to Regulate Erythropoiesis

A. Iolascon, L. De Franceschi, L. De Falco, 2018, bioRxiv.

A Dynamic Alternative Splicing Program Regulates Gene Expression In A Differentiation Stage-Specific Manner During Terminal Erythropoiesis

L. Pachter, J. Conboy, S. Gee, 2013 .

Malaria and the erythrocyte

R. Coppel, B. Cooke, M. Narla, 1998, Current opinion in hematology.

Characterisation of the Laminin 10/11 Binding Site on the Lutheran Glycoprotein Suggests a Novel Type of Protein-Protein Interaction.

N. Burton, R. L. Brady, D. Anstee, 2006 .

Regulation of RNA Polymerase II Activity is Essential for Terminal Erythroid Maturation.

K. Lezon-Geyda, P. Gallagher, M. Narla, 2021, Blood.