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Journal Articles

CRISPR/dCas9 (D10A) -Mediated Hb CS Gene Editing and Identification of Genetically Modified Fibroblasts

Lian Yu, Wei Hao Wu, WANG Shunqing, Ken H. Young, Funeng Jiang, PhD

Blood (2019) 134 (Supplement_1): 5754.

https://doi.org/10.1182/blood-2019-129931

Published: 2019

Journal Articles

Effects of Voxelotor (GBT440) Therapy on Laboratory Testing of Sickle Cell Patients

Michelle E. Savedra, MT(ASCP), Jessica L. Szuberski, MLS ASCP, Tavanna R. Porter, MS, LCGC, Molly S. Hein, Phuong L. Nguyen, MD, Min Shi, MD PhD, Aruna Rangan, MD, James D. Hoyer, MD, Jennifer L. Oliveira, MD

Blood (2019) 134 (Supplement_1): 1011.

https://doi.org/10.1182/blood-2019-131125

Published: 2019

Journal Articles

Molecular Analysis in Patients with Idiopathic Erythrocytosis

Katarzyna Aleksandra Jalowiec, Naomi A. Porret, PhD, Raphael Joncourt, Alicia Rovo

Blood (2019) 134 (Supplement_1): 2230.

https://doi.org/10.1182/blood-2019-128169

Published: 2019

Journal Articles

The Optimal Cut-Off Level for Hemoglobin A2 to Differentiate between Sickle Cell Disease Genotypes

Fayiz Al Shueili, MD, Murtadha K. Al-Khabori, BSc,MD FRCPC, MSc, Salam Al-Kindi, Yasser Wali, MD, Shoaib Al-Zadjali, PhD

Blood (2018) 132 (Supplement 1): 2391.

https://doi.org/10.1182/blood-2018-99-118697

Published: 2018

Journal Articles

KLF1 Mutations Are Not Common in Israel but Can Explain Occasional Cases of Elevated HbA2 or Very Elevated Fetal Hemoglobin

Deborah Rund, MD, Dvora Filon, PhD, Natalie Bloch Isenberg, MD, Neta Goldschmidt, MD

Blood (2018) 132 (Supplement 1): 3640.

https://doi.org/10.1182/blood-2018-99-113903

Published: 2018

Journal Articles

Precision Medicine for Sickle Cell Disease through Whole Genome Sequencing

Blood (2018) 132 (Supplement 1): 3641.

https://doi.org/10.1182/blood-2018-99-117606

Published: 2018

Journal Articles

Engineered Human Umbilical Cord Derived Erythroid Progenitor Cells (HUDEP2) with Sickle or β-Thalassemia Mutation: An in-Vitro System for Testing Pharmacological Induction of Fetal Hemoglobin

So Hyun Park, BS, Ciaran M Lee, PhD, Yankai Zhang, PhD, Alicia Chang, MD, Vivien A Sheehan, MD PhD, Gang Bao, PhD

Blood (2018) 132 (Supplement 1): 3478.

https://doi.org/10.1182/blood-2018-99-114241

Published: 2018

Journal Articles

A Novel Recombinant Eklf-GATA1 Fusion Protein Reduces Sickling of Cultured Mouse Erythrocytes

Jianqiong Zhu, MD, Hongzhen Li, MD PhD, Wulin Aerbajinai, MD PhD, Chutima Kumkhaek, PhD, Kyung Chin, Griffin Rodgers, MD

Blood (2018) 132 (Supplement 1): 3479.

https://doi.org/10.1182/blood-2018-99-115209

Published: 2018

Journal Articles

Next-Generation Sequencing (NGS) in Childhood Myeloproliferative Diseases (MPD)

Michelina Santopietro, MD, Giovanna Palumbo, MD, Maria Luisa Moleti, MD, Anna Maria Testi, MD, Luisa Cardarelli, MD, Nicola Monaco, MDcal Student, Francesco Malaspina, MD, Camilla Presicce, MDcal Student, Sonia Maria Orlando, Alessandro Pancrazzi, PhD, Annalisa Pacilli, PhD, Giada Rotunno, PhD, Alessandro M. Vannucchi, MD, Robin Foà, MD, Fiorina Giona, MD

Blood (2018) 132 (Supplement 1): 3049.

https://doi.org/10.1182/blood-2018-99-118102

Published: 2018

Journal Articles

Phenotypes of Hb Okayama Mutation

Rudra Ray, PhD MSc, Ankita Biswas, Msc, Sunistha Bhattacharjee, Msc, Maitreyee Bhattacharyya, DM

Blood (2018) 132 (Supplement 1): 4898.

https://doi.org/10.1182/blood-2018-99-118079

Published: 2018

Journal Articles

First Report of α-Thalassemia Genotypes from Transcaucasia

Gunay Aliyeva, Chingiz Asadov, Tahira Mammadova, Zaur Mammadbayov, Eldar Abdulalimov, Surmaya Gafarova

Blood (2018) 132 (Supplement 1): 4899.

https://doi.org/10.1182/blood-2018-99-110285

Published: 2018

Journal Articles

Symptomatic Hemoglobin New Mexico and a Case of Therapeutic Benefit with Acetazolamide

Ahmed Ayad, MD, Sara Nofal, MD, Crystal Jobson, MD, Yuval Raizen, MD, Mona Lisa Alattar, MD

Blood (2018) 132 (Supplement 1): 4918.

https://doi.org/10.1182/blood-2018-99-119250

Published: 2018

Journal Articles

Familial Polycythemia Likely Due to Novel Hemoglobin Variant Hemoglobin Hyden

Sandhya Kolagatla, Nagabhishek Moka, MD, Samuel D. Bailey, MD

Blood (2018) 132 (Supplement 1): 4925.

https://doi.org/10.1182/blood-2018-99-119590

Published: 2018

Journal Articles

Single Cell Transcriptome Analysis Reveals Changing Levels and Distributions of Stemness across Disease States in Pediatric AML

Lisa Wei, BS, Diane Trinh, Soheil Meshinchi, MD PhD, Marco A. Marra, PhD

Blood (2017) 130 (Supplement 1): 3953.

https://doi.org/10.1182/blood.V130.Suppl_1.3953.3953

Published: 2017

Journal Articles

Retrospective Analysis of the HB A2 Value in Sickle Cell Positive Population in Central Gujarat, India

Seema S. Bhatwadekar, MD, Parth Shah, MD, Sandip Shah, MD, Harsukh Toprani, MD, Bijal Shah, MBBS,DCP, Devenkumar Desai, MBBS DCP, Bhagvanji B Zanzarukiya, MD, Tejas S Patel, MD, Tushar Toprani, MD

Blood (2017) 130 (Supplement 1): 4789.

https://doi.org/10.1182/blood.V130.Suppl_1.4789.4789

Published: 2017

Journal Articles

Microcytic Anemia and Celiac Disease Preceding Pulmonary Symptoms in Lane-Hamilton Syndrome

Robert Szulawski, DO, Catherine D Quinn, MD, Eric Safyan, MD

Blood (2017) 130 (Supplement 1): 4753.

https://doi.org/10.1182/blood.V130.Suppl_1.4753.4753

Published: 2017

Journal Articles

Longer Term Follow-up on the First Patients with Severe Hemoglobinopathies Treated with Lentiglobin Gene Therapy

Blood (2017) 130 (Supplement 1): 4609.

https://doi.org/10.1182/blood.V130.Suppl_1.4609.4609

Published: 2017

Journal Articles

Genome Editing Strategies to Treat Beta-Hemoglobinopathies

Mitchell J Weiss, MD PhD

Blood (2017) 130 (Supplement 1): SCI-16.

https://doi.org/10.1182/blood.V130.Suppl_1.SCI-16.SCI-16

Published: 2017

Journal Articles

Insights into Hematopoiesis in GATA2 Deficiency Using Single-Cell Transcriptomics

Elina A.M. Hirvonen, MSc, Inari Natri, MB, Mattila Pirkko, PhD, Jenni Lahtela, PhD, Pitkänen Esa, PhD, Ulla Wartiovaara-Kautto, MD PhD, Outi Kilpivaara, PhD

Blood (2017) 130 (Supplement 1): 2478.

https://doi.org/10.1182/blood.V130.Suppl_1.2478.2478

Published: 2017

Journal Articles

GWAS of Osmotic Hemolysis in 12,352 Healthy Blood Donors Identifies Red Cell Genetic Variants Associated with Steady State Hemolysis in Patients with Sickle Cell Disease

Grier Page, PhD BS, MS, Tamir Kanias, PhD, Marion C. Lanteri, PhD, Yuelong Guo, PhD, Alan E. Mast, MDPhD, Richard G. Cable, MD, Bryan R Spencer, MPH, Joseph Kiss, MD, Stacey Endres, MPH, Donald Brambilla, PhD, Seyed Mehdi Nouraie, PhD MD, Victor R. Gordeuk, MD, Steven Kleinman, MD, Mark T Gladwin, MD, Michael Paul Busch, MD PhD

Blood (2017) 130 (Supplement 1): 1117.

https://doi.org/10.1182/blood.V130.Suppl_1.1117.1117

Published: 2017

NARROW

CRISPR/dCas9 (D10A) -Mediated Hb CS Gene Editing and Identification of Genetically Modified Fibroblasts

Effects of Voxelotor (GBT440) Therapy on Laboratory Testing of Sickle Cell Patients

Molecular Analysis in Patients with Idiopathic Erythrocytosis

The Optimal Cut-Off Level for Hemoglobin A2 to Differentiate between Sickle Cell Disease Genotypes

KLF1 Mutations Are Not Common in Israel but Can Explain Occasional Cases of Elevated HbA2 or Very Elevated Fetal Hemoglobin

Precision Medicine for Sickle Cell Disease through Whole Genome Sequencing

Engineered Human Umbilical Cord Derived Erythroid Progenitor Cells (HUDEP2) with Sickle or β-Thalassemia Mutation: An in-Vitro System for Testing Pharmacological Induction of Fetal Hemoglobin

A Novel Recombinant Eklf-GATA1 Fusion Protein Reduces Sickling of Cultured Mouse Erythrocytes

Next-Generation Sequencing (NGS) in Childhood Myeloproliferative Diseases (MPD)

Phenotypes of Hb Okayama Mutation

First Report of α-Thalassemia Genotypes from Transcaucasia

Symptomatic Hemoglobin New Mexico and a Case of Therapeutic Benefit with Acetazolamide

Familial Polycythemia Likely Due to Novel Hemoglobin Variant Hemoglobin Hyden

Single Cell Transcriptome Analysis Reveals Changing Levels and Distributions of Stemness across Disease States in Pediatric AML

Retrospective Analysis of the HB A2 Value in Sickle Cell Positive Population in Central Gujarat, India

Microcytic Anemia and Celiac Disease Preceding Pulmonary Symptoms in Lane-Hamilton Syndrome

Longer Term Follow-up on the First Patients with Severe Hemoglobinopathies Treated with Lentiglobin Gene Therapy

Genome Editing Strategies to Treat Beta-Hemoglobinopathies

Insights into Hematopoiesis in GATA2 Deficiency Using Single-Cell Transcriptomics

GWAS of Osmotic Hemolysis in 12,352 Healthy Blood Donors Identifies Red Cell Genetic Variants Associated with Steady State Hemolysis in Patients with Sickle Cell Disease

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American Society of Hematology

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American Society of Hematology

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