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Journal Articles

Discovering Regulatory SNPs by Genome-Wide Analysis of Differential Scl/TAL-1 Occupancy in Human Primary Erythroid Cells,

Marco De Gobbi, Jim R. Hughes, Karen M. Lower, Chris J. Derry, Emanuele Marchi, Jacqueline Sloane-Stanley, BSc, Nigel Roberts, BSc, Stephen Taylor, Catherine Porcher, Richard J. Gibbons, Douglas R. Higgs, DSc

Blood (2011) 118 (21): 3381.

https://doi.org/10.1182/blood.V118.21.3381.3381

Published: 2011

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

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

Switching Genes On and Off During Hematopoiesis.

Douglas R. Higgs, DSc

Blood (2008) 112 (11): sci-17.

https://doi.org/10.1182/blood.V112.11.sci-17.sci-17

Published: 2008

Journal Articles

Somatic Point Mutations in RUNX1/CBFA2/AML1 Are Common in High-Risk Myelodysplastic Syndrome, but Not in Myelofibrosis with Myeloid Metaplasia.

David P. Steensma, MD, Richard J. Gibbons, MA DPhil FRCP, Ruben A. Mesa, MD, Ayalew Tefferi, MD, Douglas R. Higgs, DSc(Med) FRCP

Blood (2004) 104 (11): 2438.

https://doi.org/10.1182/blood.V104.11.2438.2438

Published: 2004

Journal Articles

A Novel Splicing Mutation in the Gene Encoding the Chromatin-Associated Factor ATRX Associated with Acquired Hemoglobin H Disease in Myelodysplastic Syndrome (ATMDS).

David P. Steensma, MD, Steven L. Allen, MD, Richard J. Gibbons, MA DPhil FRCP, Chris A. Fisher, DPhil, Douglas R. Higgs, DSc(Med) FRCP

Blood (2004) 104 (11): 3606.

https://doi.org/10.1182/blood.V104.11.3606.3606

Published: 2004

NARROW

Discovering Regulatory SNPs by Genome-Wide Analysis of Differential Scl/TAL-1 Occupancy in Human Primary Erythroid Cells,

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

A Transgenic Mouse Model for Congenital Dyserythropoietic Anemia Type I

Switching Genes On and Off During Hematopoiesis.

Somatic Point Mutations in RUNX1/CBFA2/AML1 Are Common in High-Risk Myelodysplastic Syndrome, but Not in Myelofibrosis with Myeloid Metaplasia.

A Novel Splicing Mutation in the Gene Encoding the Chromatin-Associated Factor ATRX Associated with Acquired Hemoglobin H Disease in Myelodysplastic Syndrome (ATMDS).

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ASH Publications

American Society of Hematology

Discovering Regulatory SNPs by Genome-Wide Analysis of Differential Scl/TAL-1 Occupancy in Human Primary Erythroid Cells,

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

A Transgenic Mouse Model for Congenital Dyserythropoietic Anemia Type I

Switching Genes On and Off During Hematopoiesis.

Somatic Point Mutations in RUNX1/CBFA2/AML1 Are Common in High-Risk Myelodysplastic Syndrome, but Not in Myelofibrosis with Myeloid Metaplasia.

A Novel Splicing Mutation in the Gene Encoding the Chromatin-Associated Factor ATRX Associated with Acquired Hemoglobin H Disease in Myelodysplastic Syndrome (ATMDS).

Email alerts

ASH Publications

American Society of Hematology

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