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

1-5 of 5

Sort by

Sort Order Select

Journal Articles

Cryo-EM structure of the human native plasma coagulation factor XIII complex

Sneha Singh, Gregor Hagelueken, Deniz Ugurlar, Samhitha Urs Ramaraje Urs, Amit Sharma, Manoranjan Mahapatra, Friedel Drepper, Diana Imhof, Pitter F Huesgen, Johannes Oldenburg, Matthias Geyer, Arijit Biswas

Blood blood.2024025369.

https://doi.org/10.1182/blood.2024025369

Published: 2024

Includes: Supplemental data

Journal Articles

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5′ splice site

Hamideh Yadegari, Arijit Biswas, Mohammad Suhail Akhter, Julia Driesen, Vytautas Ivaskevicius, Natascha Marquardt, Johannes Oldenburg

Blood (2016) 128 (17): 2144–2152.

https://doi.org/10.1182/blood-2016-02-699686

Published: 2016

Includes: Supplemental data

Journal Articles

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine–based ER retention motif

Katrin J. Czogalla, Arijit Biswas, Simone Rost, Matthias Watzka, Johannes Oldenburg

Blood (2014) 124 (8): 1354–1362.

https://doi.org/10.1182/blood-2013-12-545988

Published: 2014

Includes: Supplemental data

Journal Articles

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces

Katrin J. Czogalla, Arijit Biswas, Ann-Christin Wendeln, Philipp Westhofen, Clemens R. Müller, Matthias Watzka, Johannes Oldenburg

Blood (2013) 122 (15): 2743–2750.

https://doi.org/10.1182/blood-2013-05-501692

Published: 2013

Includes: Supplemental data

Journal Articles

Genetic Background in Patients with Severe Factor XIII A-Subunit Deficiency Treated with Recombinant FXIII

Vytautas Ivaskevicius, MD, Arijit Biswas, MD, Anne Thomas, MD, Ramin Tehranchi, M.D., Ph.D., Johannes Oldenburg, MD

Blood (2012) 120 (21): 1125.

https://doi.org/10.1182/blood.V120.21.1125.1125

Published: 2012

NARROW

Cryo-EM structure of the human native plasma coagulation factor XIII complex

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5′ splice site

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine–based ER retention motif

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces

Genetic Background in Patients with Severe Factor XIII A-Subunit Deficiency Treated with Recombinant FXIII

Email alerts

ASH Publications

American Society of Hematology

Cryo-EM structure of the human native plasma coagulation factor XIII complex

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5′ splice site

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine–based ER retention motif

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces

Genetic Background in Patients with Severe Factor XIII A-Subunit Deficiency Treated with Recombinant FXIII

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only