Galina Y. Miasnikova

Cheboksary, CU, Russian Federation

Last Updated: 09/26/2026

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Found 12 publications

VHL, transferrin, and erythropoietin in the regulation of hepcidin.

VHL, transferrin, and erythropoietin in the regulation of hepcidin.

Journal: HemaSphere
Published: September 11, 2025

Increased transferrin protects from thrombosis in Chuvash erythrocytosis.

Increased transferrin protects from thrombosis in Chuvash erythrocytosis.

Journal: American journal of hematology
Published: June 13, 2023

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

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

Journal: British journal of haematology
Published: February 13, 2020

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

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

Journal: Haematologica
Published: July 11, 2019

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

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

Journal: Haematologica
Published: January 21, 2017

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

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

Journal: Human molecular genetics
Published: April 28, 2016

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

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

Journal: Human genetics
Published: March 13, 2015

Complications in children and adolescents with Chuvash polycythemia.

Complications in children and adolescents with Chuvash polycythemia.

Journal: Blood
Published: January 10, 2015

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

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

Journal: Blood
Published: October 26, 2013

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

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

Journal: Haematologica
Published: February 14, 2013

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

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

Journal: Journal of molecular medicine (Berlin, Germany)
Published: June 27, 2012

Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHL(R200W) mutation (Chuvash polycythemia).

Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHL(R200W) mutation (Chuvash polycythemia).

Journal: Haematologica
Published: October 14, 2011
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Last Updated: 09/26/2026