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Journal Articles

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts

Raffaele Renella, Nigel A. Roberts, Jill M. Brown, Marco De Gobbi, Louise E. Bird, Tasneem Hassanali, Jacqueline A. Sharpe, Jacqueline Sloane-Stanley, David J. P. Ferguson, Jacqueline Cordell, Veronica J. Buckle, Douglas R. Higgs, William G. Wood

Blood (2011) 117 (25): 6928–6938.

https://doi.org/10.1182/blood-2010-09-308478

Published: 2011

Includes: Supplemental data

Journal Articles

Global gene expression analysis of human erythroid progenitors

Alison T. Merryweather-Clarke, Ann Atzberger, Shamit Soneji, Nicki Gray, Kevin Clark, Craig Waugh, Simon J. McGowan, Stephen Taylor, Asoke K. Nandi, William G. Wood, David J. Roberts, Douglas R. Higgs, Veronica J. Buckle, Kathryn J. H. Robson

Blood (2011) 117 (13): e96–e108.

https://doi.org/10.1182/blood-2010-07-290825

Published: 2011

Includes: Supplemental data

Journal Articles

Regulation of Gata1 Expression by HS + 3.5

Julia E Draper, William G Wood, PhD, Catherine Porcher, Paresh Vyas

Blood (2010) 116 (21): 3864.

https://doi.org/10.1182/blood.V116.21.3864.3864

Published: 2010

Journal Articles

Codanin-1 Mutations In Congenital Dyserythropoietic Anemia Type 1 Affect HP1α Localization In Erythroblasts

Raffaele Renella, MD, PhD, Nigel Roberts, BSc, Jill M Brown, MSc, Marco De Gobbi, MD, PhD, Louise Bird, PhD, Tasneem Hassanali, BSc, Jacqueline Sloane-Stanley, BSc, Jacqueline A Sharpe, PhD, Jacqueline Loelia Cordell, BSc, David J.P. Ferguson, MD, PhD, Veronica Buckle, PhD, Douglas R. Higgs, DSc, William G Wood, PhD

Blood (2010) 116 (21): 1003.

https://doi.org/10.1182/blood.V116.21.1003.1003

Published: 2010

Journal Articles

Does Transcription of Remote α- Globin Regulatory Elements Affect Their Function?.

Monika S Kowalczyk, MD, Jim R Hughes, DPhil, Jacqueline A Sharpe, PhD, Jill M Brown, BSc, Veronica J Buckle, PhD, William G Wood, PhD, Douglas R Higgs, FRS

Blood (2009) 114 (22): 4060.

https://doi.org/10.1182/blood.V114.22.4060.4060

Published: 2009

Journal Articles

Chromosome looping at the human α-globin locus is mediated via the major upstream regulatory element (HS −40)

Douglas Vernimmen, Fatima Marques-Kranc, Jacqueline A. Sharpe, Jacqueline A. Sloane-Stanley, William G. Wood, Helen A. C. Wallace, Andrew J. H. Smith, Douglas R. Higgs

Blood (2009) 114 (19): 4253–4260.

https://doi.org/10.1182/blood-2009-03-213439

Published: 2009

Includes: Supplemental data

Journal Articles

A Transgenic Mouse Model for Congenital Dyserythropoietic Anemia Type I

Raffaele Renella, MD, Nigel A Roberts, BSc, Jacqueline A Sharpe, PhD, Pik-Shan Li, BSc, Jill M Brown, BSc, Christian Babbs, PhD, Cristina Fugazza, PhD, Nicolas Goardon, PhD, Douglas R Higgs, DSc, William G Wood, PhD

Blood (2008) 112 (11): 3455.

https://doi.org/10.1182/blood.V112.11.3455.3455

Published: 2008

Journal Articles

Multiple Site Gfi1b Self-Regulation and GATA1/SCL Pentameric Complex: Shifting the Equilibrium towards Repression

Aurora Hernández, Ana Villegas, MD, PhD, Francisco Iborra, PhD, William G. Wood, PhD, Eduardo Anguita, MD, PhD

Blood (2008) 112 (11): 4766.

https://doi.org/10.1182/blood.V112.11.4766.4766

Published: 2008

Journal Articles

Tissue-specific histone modification and transcription factor binding in α globin gene expression

Marco De Gobbi, Eduardo Anguita, Jim Hughes, Jacqueline A. Sloane-Stanley, Jacqueline A. Sharpe, Christoph M. Koch, Ian Dunham, Richard J. Gibbons, William G. Wood, Douglas R. Higgs

Blood (2007) 110 (13): 4503–4510.

https://doi.org/10.1182/blood-2007-06-097964

Published: 2007

Includes: Supplemental data

Journal Articles

A lack of border guards?

William G. Wood, Douglas R. Higgs

Blood (2006) 108 (4): 1121.

https://doi.org/10.1182/blood-2006-06-026013

Published: 2006

Journal Articles

Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I

Momin R. Ahmed, Aref Chehal, Laila Zahed, Ali Taher, Joud Haidar, Ali Shamseddine, Anne-Marie O'Hea, Nicola Bienz, Orly Dgany, Nili Avidan, Jacqui S. Beckmann, Hannah Tamary, Douglas Higgs, Paresh Vyas, William G. Wood, Sunitha N. Wickramasinghe

Blood (2006) 107 (12): 4968–4969.

https://doi.org/10.1182/blood-2006-01-0081

Published: 2006

Journal Articles

A novel deletion causing α thalassemia clarifies the importance of the major human alpha globin regulatory element

Vip Viprakasit, Cornelis L. Harteveld, Helena Ayyub, Jackie S. Stanley, Piero C. Giordano, William G. Wood, Douglas R. Higgs

Blood (2006) 107 (9): 3811–3812.

https://doi.org/10.1182/blood-2005-12-4834

Published: 2006

Journal Articles

Identification of a Gain-of-Function SNP Causing a New Model of α-Thalassaemia.

Marco De Gobbi, MD, Vip Viprakasit, MD, PhD, Pieter J. de Jong, PhD, Yuko Yoshinaga, PhD, Jan-Fang Cheng, PhD, Jim R. Hughes, PhD, Chris A. Fisher, PhD, William G. Wood, PhD, Donald K. Bowden, PhD, Douglas R. Higgs, MD

Blood (2005) 106 (11): 523.

https://doi.org/10.1182/blood.V106.11.523.523

Published: 2005

Journal Articles

An Entirely Novel Form of α Thalassemia in Patients from the South Pacific Linked to Chromosome 16.

Vip Viprakasit, MD, PhD, Marco De Gobbi, MD, Helena Ayyub, BSc, Ioannis Ragoussis, PhD, William G. Wood, PhD, Donald K. Bowden, MD, Douglas R. Higgs, MD, DSc

Blood (2005) 106 (11): 2688.

https://doi.org/10.1182/blood.V106.11.2688.2688

Published: 2005

Journal Articles

A novel molecular basis for β thalassemia intermedia poses new questions about its pathophysiology

Anuja Premawardhena, Christopher A. Fisher, Nancy F. Olivieri, Shanthimala de Silva, Jackie Sloane-Stanley, William G. Wood, David J. Weatherall

Blood (2005) 106 (9): 3251–3255.

https://doi.org/10.1182/blood-2005-02-0593

Published: 2005

Journal Articles

Deletion of the mouse α-globin regulatory element (HS −26) has an unexpectedly mild phenotype

Eduardo Anguita, Jacqueline A. Sharpe, Jacqueline A. Sloane-Stanley, Cristina Tufarelli, Douglas R. Higgs, William G. Wood

Blood (2002) 100 (10): 3450–3456.

https://doi.org/10.1182/blood-2002-05-1409

Published: 2002

Journal Articles

α-Thalassemia resulting from a negative chromosomal position effect

Virginia M. Barbour, Cristina Tufarelli, Jacqueline A. Sharpe, Zoe E. Smith, Helena Ayyub, Cynthia A. Heinlein, Jacqueline Sloane-Stanley, Karel Indrak, William G. Wood, Douglas R. Higgs

Blood (2000) 96 (3): 800–807.

https://doi.org/10.1182/blood.V96.3.800

Published: 2000

Journal Articles

Unusually Severe Heterozygous β-Thalassemia: Evidence for an Interacting Gene Affecting Globin Translation

P. Joy Ho, Georgina W. Hall, Suzanne Watt, Nicholas C. West, Jennifer W. Wimperis, William G. Wood, Swee Lay Thein

Blood (1998) 92 (9): 3428–3435.

https://doi.org/10.1182/blood.V92.9.3428

Published: 1998

NARROW

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts

Global gene expression analysis of human erythroid progenitors

Regulation of Gata1 Expression by HS + 3.5

Codanin-1 Mutations In Congenital Dyserythropoietic Anemia Type 1 Affect HP1α Localization In Erythroblasts

Does Transcription of Remote α- Globin Regulatory Elements Affect Their Function?.

Chromosome looping at the human α-globin locus is mediated via the major upstream regulatory element (HS −40)

A Transgenic Mouse Model for Congenital Dyserythropoietic Anemia Type I

Multiple Site Gfi1b Self-Regulation and GATA1/SCL Pentameric Complex: Shifting the Equilibrium towards Repression

Tissue-specific histone modification and transcription factor binding in α globin gene expression

A lack of border guards?

Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I

A novel deletion causing α thalassemia clarifies the importance of the major human alpha globin regulatory element

Identification of a Gain-of-Function SNP Causing a New Model of α-Thalassaemia.

An Entirely Novel Form of α Thalassemia in Patients from the South Pacific Linked to Chromosome 16.

A novel molecular basis for β thalassemia intermedia poses new questions about its pathophysiology

Deletion of the mouse α-globin regulatory element (HS −26) has an unexpectedly mild phenotype

α-Thalassemia resulting from a negative chromosomal position effect

Unusually Severe Heterozygous β-Thalassemia: Evidence for an Interacting Gene Affecting Globin Translation

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American Society of Hematology

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American Society of Hematology

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