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Journal Articles

Altered Splicing from a Mutated Alternate Branch Point Is Common in Severe Alpha-Spectrin Linked Inherited Anemia

Kimberly Lezon-Geyda, PhD, Vincent P Schulz, PhD, Yelena Maksimova, MS, Patrick G. Gallagher, MD

Blood (2018) 132 (Supplement 1): 503.

https://doi.org/10.1182/blood-2018-99-117752

Published: 2018

Journal Articles

Exteriorisation of Mannoses on Human Erythrocyte Membrane Skeleton Provides 'Eat Me' Signals for Oxidatively Damaged Cells to be Cleared By Macrophages: A Pathway Mediating Hemolysis in Sickle Cell Disease

Mark A Vickers, MD MA, MBBChir, Robert N Barker, Bsc BVSc PhD, Huan Cao, MA PhD, Heather J Wassall, BSc PhD, Megan A Forrester, MA PhD, Lindsay S Hall, BSc PhD, Michael Moss, Bsc PhD, Sadie Henderson, BSc, Gabriela Konieczny, BSc, Minter Beverly, BSc PhD, Jenna Shepherd, B MDSci, Stuart M Haslam, BSc PhD, David C Rees, MA, MBBS, FRCP, Heather M Wilson, BSc PhD, Dimitrios Tampakis, BSc, Maria-Louise Williams, BSc

Blood (2017) 130 (Supplement 1): 919.

https://doi.org/10.1182/blood.V130.Suppl_1.919.919

Published: 2017

Journal Articles

Intron Retention Mechanisms That Regulate SF3B1 and Mitoferrin Gene Expression during Late Erythropoiesis

Marilyn Parra, Gene Yeo, PhD, John G. Conboy, PhD

Blood (2016) 128 (22): 1200.

https://doi.org/10.1182/blood.V128.22.1200.1200

Published: 2016

Journal Articles

The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis

Satheesh Chonat, MD, Mary Risinger, Neha Dagaonkar, Tamara Maghathe, Jennifer Rothman, MD, Jessica Connor, Karen Kalinyak, MD, Amber H Begtrup, PhD, Kejian Zhang, MD MBA, Theodosia A. Kalfa, MD PhD

Blood (2015) 126 (23): 941.

https://doi.org/10.1182/blood.V126.23.941.941

Published: 2015

Journal Articles

The Erythroid Intron Retention Program Encompasses Developmentally Stable and Dynamic Networks and Regulates Diverse Gene Classes

Harold Pimentel, MA, BS, Marilyn Parra, Sherry Gee, Narla Mohandas, D.Sc., Lior Pachter, John G. Conboy, PhD

Blood (2015) 126 (23): 3331.

https://doi.org/10.1182/blood.V126.23.3331.3331

Published: 2015

Journal Articles

Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis

Kimberly Lezon-Geyda, PhD, Yelena Maksimova, MS, Vincent P Schulz, PhD, Bernard G Forget, MD, Patrick G Gallagher, MD

Blood (2014) 124 (21): 4011.

https://doi.org/10.1182/blood.V124.21.4011.4011

Published: 2014

Journal Articles

A Novel Alpha Specrtin Mutation Causing Severe Innefective Erythropoiesis

Theodora Vatopoulou, BSc (Hons), MBChB,MRCP, Barnaby Clarke, PhD, Josu de la Fuente, MRCP, MRCPCH, FRCPath, Anil Dhawan, Sanjay Tewari, MBBS, MRCP, David Rees, FRCPath

Blood (2014) 124 (21): 4002.

https://doi.org/10.1182/blood.V124.21.4002.4002

Published: 2014

Journal Articles

The Patient With Transfusion-Dependent Anemia: Diagnosis and Directed Management With Targeted Next Generation Sequencing and Copy Number Analysis

Vincent P Schulz, PhD, Yelena Maksimova, MS, Kimberly Lezon-Geyda, PhD, Patrick G Gallagher, MD

Blood (2013) 122 (21): 3419.

https://doi.org/10.1182/blood.V122.21.3419.3419

Published: 2013

Journal Articles

Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental Disomy

Hannah Bogardus, Vincent P Schulz, Yelena Maksimova, Barbara A Miller, Bernard G. Forget, MD, Patrick G. Gallagher, MD

Blood (2011) 118 (21): 1030.

https://doi.org/10.1182/blood.V118.21.1030.1030

Published: 2011

Journal Articles

Insulator Elements in Erythrocyte Membrane Genes

Laurie A Steiner, Yelena Maksimova, Jolinta Lin, Ashley Nicole Owen, Vincent Schulz, David M. Bodine, PhD, Patrick G. Gallagher, MD

Blood (2008) 112 (11): 3584.

https://doi.org/10.1182/blood.V112.11.3584.3584

Published: 2008

Journal Articles

Novel Exon 2 Alpha Spectrin Mutation in a Caucasian Family with Pyropoikilocytosis, Elliptocytosis, and Normal Morphology: Three Phenotypes Due to Decreased Spectrin mRNA and Intragenic Crossover

Neeraj Agarwal, MD#, Sabina Swierczek#, PhD, Filipe R. Lorenzo, MD, PhD, Kubendran Naidoo, BScHons, Archana M. Agarwal, MD, Roberto H Nussenzveig, PhD, Jonathan Whisenant, MD, Theresa L. Coetzer, MD, Josef T. Prchal, MD

Blood (2008) 112 (11): 3840.

https://doi.org/10.1182/blood.V112.11.3840.3840

Published: 2008

Journal Articles

Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site

Massimiliano Gaetani, Sara Mootien, Sandra Harper, Patrick G. Gallagher, David W. Speicher

Blood (2008) 111 (12): 5712–5720.

https://doi.org/10.1182/blood-2007-11-122457

Published: 2008

Includes: Supplemental data

Journal Articles

FANCF Co-Localizes with Nonerythroid Alpha Spectrin in Nuclear Foci and Shows Enhanced Binding to It in Normal but Not Fanconi Anemia, Group A, Cells after Damage with a DNA Interstrand Cross-Linking Agent.

Deepa M. Sridharan, PhD, Laura W. McMahon, PhD, Muriel W. Lambert, PhD

Blood (2007) 110 (11): 838.

https://doi.org/10.1182/blood.V110.11.838.838

Published: 2007

Journal Articles

Vascular Dysfunction in Murine Models of Hemolytic Anemia.

Nancy J. Wandersee, PhD, Anne C. Frei, Sandra L. Holzhauer, J. Paul Scott, MD, Kirkwood A. Pritchard, PhD, Karen A. Fagan, MD, Neil Hogg, PhD, Cheryl A. Hillery, MD

Blood (2007) 110 (11): 846.

https://doi.org/10.1182/blood.V110.11.846.846

Published: 2007

Journal Articles

Marked Elliptocytosis in Myelodysplastic Syndromes (MDS) Is Associated to Deletion of Chromosome 20q.

Mansoina Baweja, MD, Alvaro Moreno-Aspitia, MD, David M. Menke, MD, Vivek Roy, MD, Abba Zubair, MD

Blood (2005) 106 (11): 4927.

https://doi.org/10.1182/blood.V106.11.4927.4927

Published: 2005

Journal Articles

The C-Terminus of Alpha Spectrin Binds Protein 4.2 and Is Necessary for Optimal Spectrin-Actin Binding.

Catherine Korsgren, Connie S. Birkenmeier, Jane E. Barker, Luanne L. Peters, Samuel E. Lux

Blood (2005) 106 (11): 810.

https://doi.org/10.1182/blood.V106.11.810.810

Published: 2005

Journal Articles

The SH3 Domain of Alpha Spectrin Binds to Galectin-1 during Erythroid Differentiation.

Paulo R.M. Lima, PhD, Mariana O. Baratti, BSc, Daniela S. Basseres, PhD, Adriana S.S. Duarte, MSc, Fernando F. Costa, PhD, Sara T.O. Saad, PhD

Blood (2005) 106 (11): 1666.

https://doi.org/10.1182/blood.V106.11.1666.1666

Published: 2005

Journal Articles

GFI-1B Is Increased during Erythroid Differentiation and Appears to Regulate Beta Globin Expression and Differentiation.

Stephen Sawyer, Ph.D., Jingchun Chen, MD/Ph.D., Sarah Jacobs-Helber, Ph.D., Randolph Abutin

Blood (2004) 104 (11): 1623.

https://doi.org/10.1182/blood.V104.11.1623.1623

Published: 2004

Journal Articles

Nuclear magnetic resonance studies of mutations at the tetramerization region of human alpha spectrin

Sunghyouk Park, Michael E. Johnson, Leslie W.-M. Fung

Blood (2002) 100 (1): 283–288.

https://doi.org/10.1182/blood.V100.1.283

Published: 2002

Journal Articles

Cloning and nucleotide sequence of a mouse erythrocyte beta-spectrin cDNA

L Cioe, P Laurila, P Meo, K Krebs, S Goodman, PJ Curtis

Blood (1987) 70 (4): 915–920.

https://doi.org/10.1182/blood.V70.4.915.915

Published: 1987

NARROW

Altered Splicing from a Mutated Alternate Branch Point Is Common in Severe Alpha-Spectrin Linked Inherited Anemia

Exteriorisation of Mannoses on Human Erythrocyte Membrane Skeleton Provides 'Eat Me' Signals for Oxidatively Damaged Cells to be Cleared By Macrophages: A Pathway Mediating Hemolysis in Sickle Cell Disease

Intron Retention Mechanisms That Regulate SF3B1 and Mitoferrin Gene Expression during Late Erythropoiesis

The Spectrum of Alpha-Spectrin Associated Hereditary Spherocytosis

The Erythroid Intron Retention Program Encompasses Developmentally Stable and Dynamic Networks and Regulates Diverse Gene Classes

Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis

A Novel Alpha Specrtin Mutation Causing Severe Innefective Erythropoiesis

The Patient With Transfusion-Dependent Anemia: Diagnosis and Directed Management With Targeted Next Generation Sequencing and Copy Number Analysis

Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental Disomy

Insulator Elements in Erythrocyte Membrane Genes

Novel Exon 2 Alpha Spectrin Mutation in a Caucasian Family with Pyropoikilocytosis, Elliptocytosis, and Normal Morphology: Three Phenotypes Due to Decreased Spectrin mRNA and Intragenic Crossover

Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site

FANCF Co-Localizes with Nonerythroid Alpha Spectrin in Nuclear Foci and Shows Enhanced Binding to It in Normal but Not Fanconi Anemia, Group A, Cells after Damage with a DNA Interstrand Cross-Linking Agent.

Vascular Dysfunction in Murine Models of Hemolytic Anemia.

Marked Elliptocytosis in Myelodysplastic Syndromes (MDS) Is Associated to Deletion of Chromosome 20q.

The C-Terminus of Alpha Spectrin Binds Protein 4.2 and Is Necessary for Optimal Spectrin-Actin Binding.

The SH3 Domain of Alpha Spectrin Binds to Galectin-1 during Erythroid Differentiation.

GFI-1B Is Increased during Erythroid Differentiation and Appears to Regulate Beta Globin Expression and Differentiation.

Nuclear magnetic resonance studies of mutations at the tetramerization region of human alpha spectrin

Cloning and nucleotide sequence of a mouse erythrocyte beta-spectrin cDNA

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American Society of Hematology

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American Society of Hematology

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