Melanie Proven

Old Road, Headington
Oxford, ENG OX37LE, United Kingdom

Last Updated: 09/26/2026

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Found 16 publications

Using Patient Feedback to Improve Treatment Outcomes for Patients with Congenital Dyserythropoietic Anaemia Type I Receiving Interferon Therapy.

Using Patient Feedback to Improve Treatment Outcomes for Patients with Congenital Dyserythropoietic Anaemia Type I Receiving Interferon Therapy.

Journal: Journal of clinical medicine

Published: November 25, 2025

RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation.

RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation.

Journal: medRxiv : the preprint server for health sciences

Published: March 22, 2023

RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation.

RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation.

Journal: Developmental cell

Published: March 14, 2023

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

Journal: British journal of haematology

Published: December 09, 2022

The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper.

The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper.

Journal: HemaSphere

Published: June 10, 2022

The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper.

The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper.

Journal: British journal of haematology

Published: February 24, 2022

Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype.

Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype.

Journal: Hemoglobin

Published: July 27, 2021

Single-cell O2 exchange imaging shows that cytoplasmic diffusion is a dominant barrier to efficient gas transport in red blood cells.

Single-cell O2 exchange imaging shows that cytoplasmic diffusion is a dominant barrier to efficient gas transport in red blood cells.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: April 24, 2020

Genetic and functional insights into CDA-I prevalence and pathogenesis.

Genetic and functional insights into CDA-I prevalence and pathogenesis.

Journal: Journal of medical genetics

Published: January 22, 2020

Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinra.

Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinra.

Journal: Rheumatology (Oxford, England)

Published: July 02, 2019

Severe Drug-Induced Hemolysis in a Patient with Compound Heterozygosity for Hb Peterborough (HBB: c.334G>T) and Hb Lepore-Boston-Washington (NG_000007.3: g.63632_71046del).

Severe Drug-Induced Hemolysis in a Patient with Compound Heterozygosity for Hb Peterborough (HBB: c.334G>T) and Hb Lepore-Boston-Washington (NG_000007.3: g.63632_71046del).

Journal: Hemoglobin

Published: May 08, 2019

A Novel Deletion in the RPL5 Gene in a Lebanese Child With Diamond Blackfan Anemia Unresponsive to Steroid Treatment.

A Novel Deletion in the RPL5 Gene in a Lebanese Child With Diamond Blackfan Anemia Unresponsive to Steroid Treatment.

Journal: Journal of pediatric hematology/oncology

Published: April 02, 2019

Showing 1-12 of 16

Last Updated: 09/26/2026