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Journal Articles

Functional Complementation between β-Catenin and Hoxa9 Sustains HSC Self-Renewal in a Prmt1-Dependent Manner

Jennifer Lynch, PhD, Clemence Virely, PhD, Priscilla Lau, PhD, Huacheng Luo, PhD, Suming Huang, PhD, Eric Chi Wai So, PhD

Blood (2019) 134 (Supplement_1): 449.

https://doi.org/10.1182/blood-2019-131052

Published: 2019

Journal Articles

Elucidating an Erythroblast Survival Mechanism: Differential Contributions of Exosome Complex Catalytic Subunits

Charu Mehta, MS, Isabela J Fraga de Andrade, Bachelors in Biological Science, Nobuyuki Tanimura, PhD, Gary M Wilson, Erik A. Ranheim, MD PhD, Joshua J Coon, PhD, Emery H Bresnick, PhD

Blood (2019) 134 (Supplement_1): 155.

https://doi.org/10.1182/blood-2019-126917

Published: 2019

Journal Articles

Changing the Natural History of Fanconi Anemia Complementation Group-A with Gene Therapy: Early Results of U.S. Phase I Study of Lentiviral-Mediated Ex-Vivo FANCA Gene Insertion in Human Stem and Progenitor Cells

Agnieszka Czechowicz, MD PhD, Maria Grazia Roncarolo, MD, Brian C Beard, PhD, Ken Law, PhD, Eileen Nicoletti, MD, Paula Río, PhD, Juan A. Bueren, PhD, Jonathan D Schwartz, MD, Sandeep Soni, MBBS

Blood (2019) 134 (Supplement_1): 3350.

https://doi.org/10.1182/blood-2019-127352

Published: 2019

Journal Articles

Hematopoietic Stem and Progenitor Cell Proliferation and Differentiation Requires the Trithorax Protein Ash2l In Vivo

Nicolas Chatain, PhD, Juliane Lüscher-Firzlaff, Chao-Chung Kuo, Agnieszka Bochyńska, Andrea Ullius, Bernd Denecke, Ivan Costa, Steffen Koschmieder, MD, Bernhard Lüscher

Blood (2018) 132 (Supplement 1): 2566.

https://doi.org/10.1182/blood-2018-99-115950

Published: 2018

Journal Articles

Modeling Fanconi Anemia Using Human Induced Pluripotent Stem Cells By Reversible Complementation

R. Grant Rowe, MD PhD, William Marion, Sonya Ruiz-Torres, Edroaldo Lummertz da Rocha, Yosra Girvan, Thorsten Schlaeger, PhD, Trista E. North, PhD, Susanne Wells, George Q. Daley, MD PhD

Blood (2018) 132 (Supplement 1): 3856.

https://doi.org/10.1182/blood-2018-99-111701

Published: 2018

Journal Articles

TGF-β1 Production By Bone Marrow Mesenchymal Stem Cells of FANCD2 Differs from Other Fanconi Anemia Complementation Groups

Ilgın Cagnan, MSc, Aysen Gunel-Ozcan, MD PhD, Fatima Aerts-Kaya, MD PhD, Najim Ameziane, PhD, Baris Kuskonmaz, MD, Josephine Dorsman, PhD, Fatma Gumruk, MD, Duygu Cetinkaya, MD

Blood (2017) 130 (Supplement 1): 2464.

https://doi.org/10.1182/blood.V130.Suppl_1.2464.2464

Published: 2017

Journal Articles

Novel Lineage Depletion and Manufacturing Allows for Unprecedented Preservation of Autologous Blood Stem Cells for Gene Therapy of Fanconi Anemia Complementation Group Α

Jennifer Adair, PhD, Devikha Chandrasekaran, MS, Stefanie Schmuck, BS, Gabriella Sghia-Hughes, BS, Grace Choi, BS, Anne Lee, BS, Kevin G Haworth, BS, PhD, Ann Woolfrey, MD, Lauri S Burroughs, MD, Pamela S. Becker, MD PhD, Hans-Peter Kiem, MD PhD

Blood (2017) 130 (Supplement 1): 2451.

https://doi.org/10.1182/blood.V130.Suppl_1.2451.2451

Published: 2017

Journal Articles

Gene Heterogenicity Diagnosis on Children with Complicated Immunological and Hematological Abnormalities

Chunfu Li, MD, Haixia Guo, MD PhD

Blood (2017) 130 (Supplement 1): 4946.

https://doi.org/10.1182/blood.V130.Suppl_1.4946.4946

Published: 2017

Journal Articles

The C Domain Mediates the Export of FVIII from the Endoplasmic Reticulum By Interacting with MCFD2

Zhigang Liu, PhD, Chunlei Zheng, PhD, Denise E. Sabatino, PhD, Bin Zhang, PhD

Blood (2016) 128 (22): 255.

https://doi.org/10.1182/blood.V128.22.255.255

Published: 2016

Journal Articles

Functional Dissection of Chromosome 7q Loss and Haploinsufficient Gene Discovery Using iPSC Models of MDS

Andriana Kotini, PhD, Jeffrey J Delrow, PhD, Timothy A. Graubert, MD, Stephen Nimer, MD, Eirini P Papapetrou, MD PhD

Blood (2014) 124 (21): 524.

https://doi.org/10.1182/blood.V124.21.524.524

Published: 2014

Journal Articles

Evidence for a Dominant Negative Effect Conferred By the APOL1 G2 Sickle Cell Nephropathy Risk Allele in an in Vivo Model

Blair R. Anderson, Erica E. Davis, PhD, Marilyn J. Telen, MD, Allison E. Ashley-Koch, PhD

Blood (2014) 124 (21): 1374.

https://doi.org/10.1182/blood.V124.21.1374.1374

Published: 2014

Journal Articles

Novel activating mutations lacking cysteine in type I cytokine receptors in acute lymphoblastic leukemia

Chen Shochat, Noa Tal, Vitalina Gryshkova, Yehudit Birger, Obul R. Bandapalli, Giovanni Cazzaniga, Nava Gershman, Andreas E. Kulozik, Andrea Biondi, Marc R. Mansour, Jean-Claude Twizere, Martina U. Muckenthaler, Nir Ben-Tal, Stefan N. Constantinescu, Dani Bercovich, Shai Izraeli

Blood (2014) 124 (1): 106–110.

https://doi.org/10.1182/blood-2013-10-529685

Published: 2014

Includes: Supplemental data

Journal Articles

Acute Lymphoblastic Leukemia Is a Bcl-2 Dependent Disease: Proteomic Profiling and Pre-Clinical Efficacy Of a Selective Bcl-2 Antagonist ABT-199

Blood (2013) 122 (21): 3919.

https://doi.org/10.1182/blood.V122.21.3919.3919

Published: 2013

Journal Articles

Analysis of disease-causing GATA1 mutations in murine gene complementation systems

Amy E. Campbell, Lorna Wilkinson-White, Joel P. Mackay, Jacqueline M. Matthews, Gerd A. Blobel

Blood (2013) 121 (26): 5218–5227.

https://doi.org/10.1182/blood-2013-03-488080

Published: 2013

Includes: Supplemental data

Journal Articles

Dissecting the Molecular Pathways That Underlie Disease-Causing GATA1 Mutations

Amy E Campbell, Lorna Wilkinson-White, PhD, Joel P Mackay, PhD, Jacqueline M Matthews, PhD, Gerd A Blobel, MD, PhD

Blood (2012) 120 (21): 3439.

https://doi.org/10.1182/blood.V120.21.3439.3439

Published: 2012

Journal Articles

GATA-1-Dependent and -Independent Modes of Establishing the Erythroid Cell Genetic Network.

Nathaniel James Pope, Emery H Bresnick, PhD

Blood (2012) 120 (21): 2083.

https://doi.org/10.1182/blood.V120.21.2083.2083

Published: 2012

Journal Articles

Linking Organelle Remodeling with the Erythroid Cell Genetic Network

Yoon-A Kang, Jonathan N Ouellette, Genís Campreciós, PhD, Saghi Ghaffari, MD, PhD, Emery H Bresnick, PhD

Blood (2012) 120 (21): 367.

https://doi.org/10.1182/blood.V120.21.367.367

Published: 2012

Journal Articles

Loss of Ezh2 Promotes the Development of Mutant-RUNX1 Induced MDS

Goro Sashida, MD, PhD, Satomi Tanaka, MD, Makiko Mochizuki-Kashio, PhD, Atsunori Saraya, MS, Tomoya Muto, MD, Atsushi Iwama, MD, PhD

Blood (2012) 120 (21): 402.

https://doi.org/10.1182/blood.V120.21.402.402

Published: 2012

Journal Articles

Overcoming reprogramming resistance of Fanconi anemia cells

Lars U. W. Müller, Michael D. Milsom, Chad E. Harris, Rutesh Vyas, Kristina M. Brumme, Kalindi Parmar, Lisa A. Moreau, Axel Schambach, In-Hyun Park, Wendy B. London, Kelly Strait, Thorsten Schlaeger, Alexander L. DeVine, Elke Grassman, Alan D'Andrea, George Q. Daley, David A. Williams

Blood (2012) 119 (23): 5449–5457.

https://doi.org/10.1182/blood-2012-02-408674

Published: 2012

Includes: Supplemental data

Journal Articles

Linking Transcription Factor Pathways to Disease-Causing GATA1 Mutations

Amy E Campbell, Gerd A. Blobel, MD, PhD

Blood (2011) 118 (21): 2371.

https://doi.org/10.1182/blood.V118.21.2371.2371

Published: 2011

NARROW

Functional Complementation between β-Catenin and Hoxa9 Sustains HSC Self-Renewal in a Prmt1-Dependent Manner

Elucidating an Erythroblast Survival Mechanism: Differential Contributions of Exosome Complex Catalytic Subunits

Changing the Natural History of Fanconi Anemia Complementation Group-A with Gene Therapy: Early Results of U.S. Phase I Study of Lentiviral-Mediated Ex-Vivo FANCA Gene Insertion in Human Stem and Progenitor Cells

Hematopoietic Stem and Progenitor Cell Proliferation and Differentiation Requires the Trithorax Protein Ash2l In Vivo

Modeling Fanconi Anemia Using Human Induced Pluripotent Stem Cells By Reversible Complementation

TGF-β1 Production By Bone Marrow Mesenchymal Stem Cells of FANCD2 Differs from Other Fanconi Anemia Complementation Groups

Novel Lineage Depletion and Manufacturing Allows for Unprecedented Preservation of Autologous Blood Stem Cells for Gene Therapy of Fanconi Anemia Complementation Group Α

Gene Heterogenicity Diagnosis on Children with Complicated Immunological and Hematological Abnormalities

The C Domain Mediates the Export of FVIII from the Endoplasmic Reticulum By Interacting with MCFD2

Functional Dissection of Chromosome 7q Loss and Haploinsufficient Gene Discovery Using iPSC Models of MDS

Evidence for a Dominant Negative Effect Conferred By the APOL1 G2 Sickle Cell Nephropathy Risk Allele in an in Vivo Model

Novel activating mutations lacking cysteine in type I cytokine receptors in acute lymphoblastic leukemia

Acute Lymphoblastic Leukemia Is a Bcl-2 Dependent Disease: Proteomic Profiling and Pre-Clinical Efficacy Of a Selective Bcl-2 Antagonist ABT-199

Analysis of disease-causing GATA1 mutations in murine gene complementation systems

Dissecting the Molecular Pathways That Underlie Disease-Causing GATA1 Mutations

GATA-1-Dependent and -Independent Modes of Establishing the Erythroid Cell Genetic Network.

Linking Organelle Remodeling with the Erythroid Cell Genetic Network

Loss of Ezh2 Promotes the Development of Mutant-RUNX1 Induced MDS

Overcoming reprogramming resistance of Fanconi anemia cells

Linking Transcription Factor Pathways to Disease-Causing GATA1 Mutations

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American Society of Hematology

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American Society of Hematology

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