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

1-11 of 11

Sort by

Sort Order Select

Journal Articles

Tibetan Enriched PKLR Variant Is Beneficial to High Altitude Adaption By Improving Oxygen Delivery

Jihyun Song, PhD, Virginia Abello, MD, Ricardo Amaru, MD, Adelina Sergueeva, MD, Jainagul Isakova, Penelope A. Kosinski, MS, Brigitte A. van Oirschot, Victor R. Gordeuk, MD, Charles Kung, PhD, Richard van Wijk, PhD, Josef T. Prchal, MD

Blood (2018) 132 (Supplement 1): 1027.

https://doi.org/10.1182/blood-2018-99-117389

Published: 2018

Journal Articles

Chuvash Polycythemia Patients from Afghanistan and Southern India Share a Common VHL Gene Haplotype. Support for Its Origin before Asians and Europeans Diverged

Christine Min, Jihyun Song, PhD, Joachim R. Goethert, MD, Soo Jin Kim, MS, Victor R. Gordeuk, MD, Josef T. Prchal, MD, Alan Lubin, MD

Blood (2017) 130 (Supplement 1): 930.

https://doi.org/10.1182/blood.V130.Suppl_1.930.930

Published: 2017

Journal Articles

Deletion Of The Von Hippel-Lindau Gene Interferes With The Development Of Peripheral B-Cell Subsets

Kathrin Händschke, Stefanie Weber, Mandy Necke, Anita Hollenbeck, Bertram Opalka, PhD, Ulrich Dührsen, MD, Joachim Rudolf Göthert, MD

Blood (2013) 122 (21): 3666.

https://doi.org/10.1182/blood.V122.21.3666.3666

Published: 2013

Journal Articles

Expression of the Hypoxia-Inducible Factors In the AML and MDS: Is Not Associated with the Von Hippel-Lindau Gene

Hongyan Tong, Chen Mei, Kongfei Li, Jie Jin

Blood (2010) 116 (21): 5114.

https://doi.org/10.1182/blood.V116.21.5114.5114

Published: 2010

Journal Articles

Zebrafish mutants in the von Hippel-Lindau tumor suppressor display a hypoxic response and recapitulate key aspects of Chuvash polycythemia

Ellen van Rooijen, Emile E. Voest, Ive Logister, Jeroen Korving, Thorsten Schwerte, Stefan Schulte-Merker, Rachel H. Giles, Fredericus J. van Eeden

Blood (2009) 113 (25): 6449–6460.

https://doi.org/10.1182/blood-2008-07-167890

Published: 2009

Includes: Multimedia, Supplemental data

Journal Articles

Familial Erythrocytosis Associated with a Mutation in the HIF Prolyl Hydroxylase, PHD2.

Melanie J. Percy, PhD, Q. Zhao, PhD, A. Flores, PhD, C. N. Harrison, MD, T. R.J. Lappin, PhD, P. H. Maxwell, MD, PhD, M. F. McMullin, MD, F. S. Lee, MD, PhD

Blood (2005) 106 (11): 127.

https://doi.org/10.1182/blood.V106.11.127.127

Published: 2005

Journal Articles

Mutations in the VHL Gene Are the Major Identified Cause of Inherited Erythrocytosis.

Melanie J. Percy, PhD, F. G.C. Jones, MD, T. R.J. Lappin, PhD, M. F. McMullin, MD

Blood (2005) 106 (11): 569.

https://doi.org/10.1182/blood.V106.11.569.569

Published: 2005

Journal Articles

The worldwide distribution of the VHL 598C > T mutation indicates a single founding event

Enli Liu, Melanie J. Percy, Christopher I. Amos, Yongli Guan, Sanjay Shete, David W. Stockton, Mary F. McMullin, Lydia A. Polyakova, Sonny O. Ang, Yves D. Pastore, Katerina Jedlickova, Terry R. J. Lappin, Victor Gordeuk, Josef T. Prchal

Blood (2004) 103 (5): 1937–1940.

https://doi.org/10.1182/blood-2003-07-2550

Published: 2004

Journal Articles

Mutations in the VHL gene in sporadic apparently congenital polycythemia

Yves D. Pastore, Jaroslav Jelinek, Sonny Ang, Yongli Guan, Enli Liu, Katerina Jedlickova, Lakshmanan Krishnamurti, Josef T. Prchal

Blood (2003) 101 (4): 1591–1595.

https://doi.org/10.1182/blood-2002-06-1843

Published: 2003

Journal Articles

Paraneoplastic erythrocytosis associated with an inactivating point mutation of the von Hippel-Lindau gene in a renal cell carcinoma

Michael S. Wiesener, Melchior Seyfarth, Christina Warnecke, Jan Steffen Jürgensen, Christian Rosenberger, Neil V. Morgan, Eamonn R. Maher, Ulrich Frei, Kai-Uwe Eckardt

Blood (2002) 99 (10): 3562–3565.

https://doi.org/10.1182/blood.V99.10.3562

Published: 2002

Journal Articles

Coexpression of Erythropoietin and Vascular Endothelial Growth Factor in Nervous System Tumors Associated With von Hippel-Lindau Tumor Suppressor Gene Loss of Function

Marion Krieg, Hugo H. Marti, Karl H. Plate

Blood (1998) 92 (9): 3388–3393.

https://doi.org/10.1182/blood.V92.9.3388

Published: 1998

NARROW

Tibetan Enriched PKLR Variant Is Beneficial to High Altitude Adaption By Improving Oxygen Delivery

Chuvash Polycythemia Patients from Afghanistan and Southern India Share a Common VHL Gene Haplotype. Support for Its Origin before Asians and Europeans Diverged

Deletion Of The Von Hippel-Lindau Gene Interferes With The Development Of Peripheral B-Cell Subsets

Expression of the Hypoxia-Inducible Factors In the AML and MDS: Is Not Associated with the Von Hippel-Lindau Gene

Zebrafish mutants in the von Hippel-Lindau tumor suppressor display a hypoxic response and recapitulate key aspects of Chuvash polycythemia

Familial Erythrocytosis Associated with a Mutation in the HIF Prolyl Hydroxylase, PHD2.

Mutations in the VHL Gene Are the Major Identified Cause of Inherited Erythrocytosis.

The worldwide distribution of the VHL 598C > T mutation indicates a single founding event

Mutations in the VHL gene in sporadic apparently congenital polycythemia

Paraneoplastic erythrocytosis associated with an inactivating point mutation of the von Hippel-Lindau gene in a renal cell carcinoma

Coexpression of Erythropoietin and Vascular Endothelial Growth Factor in Nervous System Tumors Associated With von Hippel-Lindau Tumor Suppressor Gene Loss of Function

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only