Adelina I. Sergueeva

发表

Endothelin-1, vascular endothelial growth factor and systolic pulmonary artery pressure in patients with Chuvash polycythemia.

S. Nekhai, O. Castro, J. Prchal, 2006, Haematologica.

Thrombotic risk in congenital erythrocytosis due to up-regulated hypoxia sensing is not associated with elevated hematocrit

D. Stockton, J. Prchal, F. Lorenzo, 2019, Haematologica.

downregulation of hepcidin expression mutation is associated with R200W VHL Chuvash polycythemia

Tatiana Ammosova, S. Nekhai, T. Ganz, 2012 .

Chuvash polycythemia VHLR200W mutation is associated with down-regulation of hepcidin expression.

Tatiana Ammosova, S. Nekhai, T. Ganz, 2011, Blood.

Altered cytokine profiles in patients with Chuvash polycythemia

Tatiana Ammosova, S. Nekhai, V. Gordeuk, 2009, American journal of hematology.

Elevated homocysteine, glutathione and cysteinylglycine concentrations in patients homozygous for the Chuvash polycythemia VHL mutation

Tatiana Ammosova, S. Nekhai, J. Prchal, 2008, Haematologica.

Decreased serum glucose and glycosylated hemoglobin levels in patients with Chuvash polycythemia: a role for HIF in glucose metabolism

J. Prchal, D. McClain, V. Gordeuk, 2012, Journal of Molecular Medicine.

Endemic polycythemia in Russia: mutation in the VHL gene.

D. Stockton, R. Kralovics, J. Prchal, 2002, Blood cells, molecules & diseases.

abnormalities but not tumors Chuvash polycythemia VHL mutation with thrombosis and vascular Congenital disorder of oxygen sensing: association of the homozygous

P. Choyke, J. Butman, J. Prchal, 2013 .

Effect of congenital upregulation of hypoxia inducible factors on percentage of fetal hemoglobin in the blood.

S. Nekhai, V. Gordeuk, Galina Y. Miasnikova, 2013, Blood.

Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHLR200W mutation (Chuvash polycythemia)

M. Gladwin, A. Remaley, G. Kato, 2012, Haematologica.

The heterozygote advantage of the Chuvash polycythemia VHLR200W mutation may be protection against anemia

T. Ganz, J. Prchal, V. Gordeuk, 2011, Haematologica.

Increased size of solid organs in patients with Chuvash polycythemia and in mice with altered expression of HIF-1α and HIF-2α

G. Semenza, J. Prchal, V. Gordeuk, 2010, Journal of Molecular Medicine.

Peripheral blood mononuclear cells show prominent gene expression by erythroid progenitors in diseases characterized by heightened erythropoiesis

S. Nekhai, J. Prchal, V. Gordeuk, 2020, British journal of haematology.

Prospective Assessment of Pulmonary Hypertension in Children with Chuvash Polycythemia.

V. Gordeuk, C. Sable, N. Dham, 2007 .

Phlebotomy-Induced Iron Deficiency Increases the Expression of Prothrombotic Genes

J. Prchal, T. Tashi, V. Gordeuk, 2020 .

Hypoxic Response Contributes to Altered Gene Expression and Precapillary Pulmonary Hypertension in Patients With Sickle Cell Disease

P. Sebastiani, Wei Zhang, R. Kittles, 2014, Circulation.

Congenital disorder of oxygen sensing: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors.

P. Choyke, J. Butman, J. Prchal, 2004, Blood.

The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W)

S. Nekhai, C. Huff, J. Prchal, 2013, Haematologica.

Complications in children and adolescents with Chuvash polycythemia.

J. Prchal, V. Gordeuk, M. Nouraie, 2015, Blood.

A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in sickle cell disease.

M. Gladwin, Wei Zhang, Tatiana Ammosova, 2016, Human molecular genetics.

Prospective study of thrombosis and thrombospondin-1 expression in Chuvash polycythemia

Tatiana Ammosova, S. Nekhai, J. Prchal, 2017, Haematologica.

Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease

M. Gladwin, P. Sebastiani, Wei Zhang, 2015, Human Genetics.

Decreased serum glucose and glycosylated hemoglobin levels in patients with Chuvash polycythemia: a role for HIF in glucose metabolism

J. Prchal, D. McClain, V. Gordeuk, 2012, Journal of Molecular Medicine.

Iron deficiency modifies gene expression variation induced by augmented hypoxia sensing.

Wei Zhang, Tatiana Ammosova, S. Nekhai, 2014, Blood cells, molecules & diseases.

Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia

David Mole, Kiichi Hirota, Enli Liu, 2002, Nature Genetics.

Gene expression changes in sickle cell reticulocytes and their clinical associations

M. Gladwin, S. Nekhai, J. Prchal, 2023, Scientific reports.