Chris A. Fisher - Publications

Applicability, safety, and biological activity of regulatory T cell therapy in liver transplantation.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Published: October 03, 2019

Hb Penang [β78(EF2)Leu→Pro, HBB: c.236T>C]: a Novel β-Globin Variant.

Journal: Hemoglobin

Published: October 18, 2018

Phenotypic and molecular characterization of a serum-free miniature erythroid differentiation system suitable for high-throughput screening and single-cell assays.

Journal: Experimental hematology

Published: November 20, 2017

Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia.

Journal: Nature communications

Published: April 05, 2017

Hepcidin detects iron deficiency in Sri Lankan adolescents with a high burden of hemoglobinopathy: A diagnostic test accuracy study.

Journal: American journal of hematology

Published: October 17, 2016

Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis.

Journal: British journal of haematology

Published: July 30, 2016

The chromatin remodelling factor ATRX suppresses R-loops in transcribed telomeric repeats.

Journal: EMBO reports

Published: July 20, 2016

The evolutionary and clinical implications of the uneven distribution of the frequency of the inherited haemoglobin variants over short geographical distances.

Journal: British journal of haematology

Published: May 09, 2016

Transcription factors LRF and BCL11A independently repress expression of fetal hemoglobin.

Journal: Science (New York, N.Y.)

Published: January 28, 2016

Haemoglobin Variant Screening in Jamaica: Meeting Student's Request.

Journal: British journal of haematology

Published: July 01, 2015

Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.

Journal: Blood

Published: December 19, 2014

Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression.

Journal: Blood

Published: January 21, 2014