Classification and molecular biology of polycythemias (erythrocytoses) and thrombocytosis.

No abstract is available for this paper.

• Publication year

  2003

• Venue

  Hematology/Oncology Clinics of North America

• Publication date

  2003-10-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/S0889-8588(03)00090-XPMID 14560779
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia.

  2003cited by this paper
• Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry.

  2003cited by this paper
• Mutations in the VHL gene in sporadic apparently congenital polycythemia.

  2003cited by this paper
• Biochemical characterization of PRV-1, a novel hematopoietic cell surface receptor, which is overexpressed in polycythemia rubra vera.

  2002cited by this paper
• Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera.

  2002cited by this paper
• Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected *

  2002cited by this paper
• Endemic polycythemia in Russia: mutation in the VHL gene.

  2002cited by this paper
• Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia

  2002cited by this paper
• Mouse model of congenital polycythemia: Homologous replacement of murine gene by mutant human erythropoietin receptor gene.

  2001cited by this paper
• Lack of pathogenic mutations in the 5′‐untranslated region of the thrombopoietin gene in patients with non‐familial essential thrombocythaemia

  2001cited by this paper
• Lessons to better understanding of hypoxia sensing. Acquired and congenital mutations resulting in polycythemia.

  2001cited by this paper
• Genetic heterogeneity of primary familial and congenital polycythemia

  2001cited by this paper
• Familial thrombocytosis as a recessive, possibly X‐linked trait in an Arab family

  2001cited by this paper
• Increased expression of the INK4a/ARF locus in polycythemia vera.

  2001cited by this paper
• Lessons to better understanding of hypoxia sensing

  2001cited by this paper
• Thrombocytosis and thrombocythemia.

  2001cited by this paper
• Hereditary thrombocythaemia is a genetically heterogeneous disorder: exclusion of TPO and MPL in two families with hereditary thrombocythaemia

  2000cited by this paper
• Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia.

  2000cited by this paper
• HIF-1 and human disease: one highly involved factor.

  2000cited by this paper
• The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis

  1999cited by this paper
• A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications.

  1999cited by this paper
• Von Hippel‐Lindau Syndrome

  1999cited by this paper
• An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia

  1998cited by this paper
• Molecular genetics and cytogenetics of myeloproliferative disorders.

  1998cited by this paper
• Impaired expression of the thrombopoietin receptor by platelets from patients with polycythemia vera.

  1998cited by this paper
• Losartan, an angiotensin II type 1 receptor antagonist, lowers hematocrit in posttransplant erythrocytosis.

  1998cited by this paper
• Expression of Bcl-x in erythroid precursors from patients with polycythemia vera.

  1998cited by this paper
• Clonality markers in polycythaemia and primary thrombocythaemia.

  1998cited by this paper
• 5 Clonality markers in polycythaemia and primary thrombocythaemia

  1998cited by this paper
• 7 Molecular genetics and cytogenetics of myeloproliferative disorders

  1998cited by this paper
• Red Cell Enzymopathies

  1998cited by this paper
• Congenital polycythemia in Chuvashia.

  1997cited by this paper
• Anti-erythropoietin (EPO) receptor monoclonal antibodies distinguish EPO-dependent and EPO-independent erythroid progenitors in polycythemia vera.

  1994cited by this paper
• Trends in the incidence of polycythemia vera among olmsted county, Minnesota residents, 1935–1989

  1994cited by this paper
• Occurrence, etiology, and clinical significance of extreme thrombocytosis: a study of 280 cases.

  1994cited by this paper
• Clinical evaluation of erythrocytosis in patients with hepatocellular carcinoma.

  1994cited by this paper
• Autosomal dominant polycythemia.

  1985cited by this paper
• [Diphosphoglyceromutase deficiency: new cases associated with erythrocytosis].

  1984cited by this paper
• Human erythroid colony formation in vitro: Evidence for clonal origin

  1976cited by this paper
• Detection of mutant hemoglobins with altered affinity for oxygen. A simplified technique.

  1976cited by this paper
• Diagnosis and classification of the polycythemias.

  1975cited by this paper
• [Familial erythrocytosis among the residents of the Chuvash ASSR].

  1974cited by this paper
• Letter: Bone-marrow responses in polycythemia vera.

  1974cited by this paper
• Familial erythrocytosis among the residents of the Chuvash ASSR

  1974cited by this paper
• Letter: Bone-marrow responses in polycythemia vera.

  1974cited by this paper

• Novel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TTT>TTG); HBB: c.258T>G]

  2020cites this paper
• Diseases of the Hematopoietic and Hemolymphatic Systems

  2020cites this paper
• Myeloid Neoplasms with an Erythroid Cell Lineage

  2016cites this paper
• Haemoglobin Ypsilanti: an incidental finding in two diabetic patients.

  2014cites this paper
• High concordance rate of HER2 status assessed via silver in situ hybridisation (SISH) between core biopsy and excision specimens: a 4 year retrospective review from a single institution.

  2014cites this paper
• A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paraganglioma

  2012cites this paper
• A Case Report: Cushing's Disease Presenting with Polycythemia and Venous Thromboembolism

  2012cites this paper
• Haematological and immunological effects of repeated dose exposure of rats to integerrimine N-oxide from Senecio brasiliensis.

  2011cites this paper
• Chapter 10 – Polycythemia

  2011cites this paper
• EPO Receptor Gain-of-Function Causes Hereditary Polycythemia, Alters CD34+ Cell Differentiation and Increases Circulating Endothelial Precursors

  2010cites this paper
• Polycythemia vera

  2010cites this paper
• Hematological diseases and stroke.

  2009cites this paper
• Hydroxyurea induced acute elevations in liver function tests

  2008cites this paper
• Hemoglobin Ypsilanti: a high-oxygen-affinity hemoglobin demonstrated by two automated high-pressure liquid chromatography systems.

  2007cites this paper
• Polycythemia Vera and Other Polycythemic Disorders — Biological Aspects

  2007cites this paper
• Secondary Polycythemia Caused by Giant Hydronephrosis due to Ureteropelvic Junction Obstruction

  2007cites this paper
• Molecular basis of the diagnosis and treatment of polycythemia vera and essential thrombocythemia.

  2006cites this paper
• Polycythemia as the first manifestation of Cushing’s disease

  2006cites this paper
• Lymphoma, erythrocytosis, and tumor erythropoietin gene expression in a horse.

  2006cites this paper
• Secondary polycythemia caused by ureteropelvic junction obstruction successfully treated by laparoscopic nephrectomy.

  2006cites this paper
• Clinical presentation of a patient with congenital polycythemia.

  2006cites this paper
• Idiopathic erythrocytosis and other non-clonal polycythemias.

  2006cites this paper
• Geriatric chorea.

  2006cites this paper
• Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patients.

  2005cites this paper
• Classification of myeloid neoplasms: a comparative review.

  2005cites this paper
• Polycythemia vera and other primary polycythemias

  2005cites this paper
• Classification and Molecular Biology of Polycythemias (Erythrocytoses)

  2004cites this paper
• Erythropoietin and erythropoiesis: polycythemias due to disruption of oxygen homeostasis.

  2004cites this paper
• Instability of PRV-1 mRNA: a factor to be considered in PRV-1 quantification for the diagnosis of polycythemia vera.

  2004cites this paper
• Polycythemia and oxygen sensing.

  2004cites this paper
• Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia.

  2003cites this paper
• Polycythemia vera.

  2003cites this paper