Page 1 | Search Results | Blood | American Society of Hematology

1-11 of 11

Sort by

Sort Order Select

Journal Articles

Comparative Clinical and Gene Expression Analysis of Sickle Cell Anemia and Hemoglobin SC Disease

Kathleen Vaughan, BA, Lena Diaw, PhD, Wang Zhengyuan, PhD, Chia-Hao Liu, PhD, Marci Barr, BS, Deepika Darbari, MD, Kimberley A. Woodhouse, MS, Darlene Allen, MT(ASCP), Meghan Quinn, BS, Catherine Seamon, RN, Elizabeth S. Klings, MD, Nalini Raghavachari, PhD, James G. Taylor VI, MD

Blood (2014) 124 (21): 4059.

https://doi.org/10.1182/blood.V124.21.4059.4059

Published: 2014

Journal Articles

Iron, Expression of the Pattern Recognition Receptor-Inflammasome System, and Early Death in Adults with Sickle Cell Disease

Eduard J. van Beers, MD PhD, Yanqin Yang, MS, Nalini Raghavachari, PhD, Xin Tian, PhD, Darlene Allen, MT(ASCP), James S. Nichols, RN, Laurel Mendelsohn, BS, Sergei A. Nekhai, PhD, Victor R. Gordeuk, MD, James G. Taylor VI, MD, Gregory J. Kato, MD

Blood (2014) 124 (21): 2702.

https://doi.org/10.1182/blood.V124.21.2702.2702

Published: 2014

Journal Articles

Apoliprotein A-I Mimetic Peptide and Sickle Vasculopathy: Mouse Model Study of Acute Administration.

Lewis L. Hsu, MD, PhD, Valeriani Bead, MD, Lita A. Freeman, Ph.D., Gregory J. Kato, MD, James G Taylor, VI, MD, Katherine C Wood, Ph.D., Biljana Musicki, PhD, Constance Tom Noguchi, PhD, Dan Berkowitz, MD, Alan T Remaley, MD, PhD, Marcelo Amar, MD

Blood (2009) 114 (22): 1521.

https://doi.org/10.1182/blood.V114.22.1521.1521

Published: 2009

Journal Articles

Liver Hypoxia and Tissue Injury Are Specific to Sickle Cell Mice in An Experimental Model of Sickle Cell Vaso-Occlusion.

Lewis L. Hsu, MD, PhD, Audrey C Noguchi, Constance Noguchi, PhD, Katherine C Wood, Ph.D., James G Taylor, VI, MD, Gregory J. Kato, MD, Mark Gladwin, MD, Bhalchandra Diwan, PhD

Blood (2009) 114 (22): 2569.

https://doi.org/10.1182/blood.V114.22.2569.2569

Published: 2009

Journal Articles

Sickle Cell Leg Ulcers Are Associated with Hyperuricemia, Hemolysis, Pulmonary Hypertension and Death.

Caterina P. Minniti, MD, Mariana Hildesheim, Vandana Sachdev, MD, Darlene Allen, Oswaldo Castro, MD, James G Taylor, VI, MD, Gregory J. Kato, MD

Blood (2009) 114 (22): 2583.

https://doi.org/10.1182/blood.V114.22.2583.2583

Published: 2009

Journal Articles

A GCH1 Haplotype Associated with Susceptibility to Vasoocclusive Pain and Impaired Vascular Function in Sickle Cell Anemia.

James G Taylor, VI, MD, Inna Belfer, MD, PhD, Krupa Desai, BS, Victoria Youngblood, BS, Lita A. Freeman, Ph.D., Deepika S. Darbari, MD, Gregory J. Kato, MD, Jacqueline N. Milton, BS, Stephen W Hartley, Martin H Steinberg, MD, David Goldman, MD, Mitchell B Max, MD, Deceased

Blood (2009) 114 (22): 575.

https://doi.org/10.1182/blood.V114.22.575.575

Published: 2009

Journal Articles

Arginine Metabolite Profiling in Sickle Cell Disease: Abnormal Levels and Correlations with Pulmonary Hypertension, Desaturation, Hemolysis and Organ Dysfunction.

Gregory J. Kato, MD, Wang Zeneng, PhD, James G. Taylor, VI, MD, Roberto F. Machado, MD, William C. Blackwelder, PhD, Mark T. Gladwin, MD, Stanley L. Hazen, MD, PhD

Blood (2006) 108 (11): 1205.

https://doi.org/10.1182/blood.V108.11.1205.1205

Published: 2006

Journal Articles

Mutations and Polymorphisms Influencing Hemolysis in Hemoglobin Genes and Risk of Pulmonary Hypertension in Sickle Cell Disease: Effect of Hemoglobin SC.

James G. Taylor, VI, MD, Diana Ackah, BS, Crystal Cobb, BS, Oswaldo Castro, MD, Gregory J. Kato, MD, Stephen Jacob Chanock, MD, Mark Gladwin, MD

Blood (2006) 108 (11): 1206.

https://doi.org/10.1182/blood.V108.11.1206.1206

Published: 2006

Journal Articles

vRare VCAM1 Promoter Haplotypes Prevalent in African Americans Are Hyperinducible.

James G. Taylor, VI, MD, Gila Idelman, PhD, Ron Tongbai, PhD, Renee A. Chen, MS, Cynthia M. Haggerty, MS, Stephen Jacob Chanock, MD, Kevin Gardner, MD, PhD

Blood (2006) 108 (11): 1813.

https://doi.org/10.1182/blood.V108.11.1813.1813

Published: 2006

Journal Articles

Severity of Sickle Cell Disease: Modeling Interrelationships among Hemolysis, Pulmonary Hypertension and Risk of Death.

Paola Sebastiani, PhD, Vikki G. Nolan, MPH, Clinton T. Baldwin, PhD, Maria M. Abad-Grau, PhD, Ling Wang, MS, Adeboye H. Adewoye, MD, Lillian C. McMahon, MD, Lindsay A. Farrer, PhD, James G. Taylor, VI, MD, Gregory J. Kato, MD, Mark T. Gladwin, MD, Martin H. Steinberg, MD

Blood (2006) 108 (11): 786.

https://doi.org/10.1182/blood.V108.11.786.786

Published: 2006

Journal Articles

The Hyperhemolysis Phenotype in Sickle Cell Anemia: Increased Risk of Leg Ulcers, Priapism, Pulmonary Hypertension and Death with Decreased Risk of Vasoocclusive Events.

James G. Taylor, VI, MD, Vikki G. Nolan, MPH, Gregory J. Kato, MD, Mark Gladwin, MD, Martin H. Steinberg, MD

Blood (2006) 108 (11): 787.

https://doi.org/10.1182/blood.V108.11.787.787

Published: 2006

NARROW

Comparative Clinical and Gene Expression Analysis of Sickle Cell Anemia and Hemoglobin SC Disease

Iron, Expression of the Pattern Recognition Receptor-Inflammasome System, and Early Death in Adults with Sickle Cell Disease

Apoliprotein A-I Mimetic Peptide and Sickle Vasculopathy: Mouse Model Study of Acute Administration.

Liver Hypoxia and Tissue Injury Are Specific to Sickle Cell Mice in An Experimental Model of Sickle Cell Vaso-Occlusion.

Sickle Cell Leg Ulcers Are Associated with Hyperuricemia, Hemolysis, Pulmonary Hypertension and Death.

A GCH1 Haplotype Associated with Susceptibility to Vasoocclusive Pain and Impaired Vascular Function in Sickle Cell Anemia.

Arginine Metabolite Profiling in Sickle Cell Disease: Abnormal Levels and Correlations with Pulmonary Hypertension, Desaturation, Hemolysis and Organ Dysfunction.

Mutations and Polymorphisms Influencing Hemolysis in Hemoglobin Genes and Risk of Pulmonary Hypertension in Sickle Cell Disease: Effect of Hemoglobin SC.

vRare VCAM1 Promoter Haplotypes Prevalent in African Americans Are Hyperinducible.

Severity of Sickle Cell Disease: Modeling Interrelationships among Hemolysis, Pulmonary Hypertension and Risk of Death.

The Hyperhemolysis Phenotype in Sickle Cell Anemia: Increased Risk of Leg Ulcers, Priapism, Pulmonary Hypertension and Death with Decreased Risk of Vasoocclusive Events.

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only