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Journal Articles

A novel homozygous variant of the thrombomodulin gene causes a hereditary bleeding disorder

Makoto Osada, Keiko Maruyama, Koichi Kokame, Ryunosuke Denda, Kohei Yamazaki, Hisako Kunieda, Maki Hirao, Seiji Madoiwa, Nobuo Okumura, Mitsuru Murata, Yasuo Ikeda, Kentaro Watanabe, Yuiko Tsukada, Takahide Kikuchi
Journal: Blood Advances
Blood Adv (2021) 5 (19): 3830–3838.
https://doi.org/10.1182/bloodadvances.2020003814
Published: 2021
Journal Articles

Single- and double-hit events in genes encoding immune targets before and after T cell–engaging antibody therapy in MM

Marietta S. Truger, Johannes Duell, Xiang Zhou, Larissa Heimeshoff, Anna Ruckdeschel, Mara John, Angela Riedel, Sebastian Hüper, Jessica Peter, Wencke Walter, Larissa Haertle, Manja Meggendorfer, Max S. Topp, Andreas Rosenwald, Matteo Claudio Da Via, Niccolo Bolli, Niels Weinhold, Hermann Einsele, Claudia Haferlach, K. Martin Kortüm, Leo Rasche
Journal: Blood Advances
Blood Adv (2021) 5 (19): 3794–3798.
https://doi.org/10.1182/bloodadvances.2021004418
Published: 2021
Includes: Supplemental data
Journal Articles

Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms

Ashley Cartwright, Simon J. Webster, Annika de Jong, Richard J. Dirven, Lisa D. S. Bloomer, Ahlam M. AL-Buhairan, Ulrich Budde, Christer Halldén, David Habart, Jenny Goudemand, Ian R. Peake, Jeroen C. J. Eikenboom, Anne C. Goodeve, Daniel J. Hampshire
Journal: Blood Advances
Blood Adv (2020) 4 (13): 2979–2990.
https://doi.org/10.1182/bloodadvances.2018027813
Published: 2020
Includes: Supplemental data
Journal Articles

Thrombus stability explains the factor V Leiden paradox: a mouse model

S. A. Shaya, R. J. Westrick, P. L. Gross
Journal: Blood Advances
Blood Adv (2019) 3 (21): 3375–3378.
https://doi.org/10.1182/bloodadvances.2019031112
Published: 2019
Journal Articles

Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis

Angela C. Weyand, Steve J. Grzegorski, Megan S. Rost, Kari I. Lavik, Allison C. Ferguson, Marzia Menegatti, Catherine E. Richter, Rosanna Asselta, Stefano Duga, Flora Peyvandi, Jordan A. Shavit
Journal: Blood Advances
Blood Adv (2019) 3 (11): 1670–1680.
https://doi.org/10.1182/bloodadvances.2018029066
Published: 2019
Journal Articles

Gfi1aa and Gfi1b set the pace for primitive erythroblast differentiation from hemangioblasts in the zebrafish embryo

Chris Moore, Joanna L. Richens, Yasmin Hough, Deniz Ucanok, Sunir Malla, Fei Sang, Yan Chen, Stone Elworthy, Robert N. Wilkinson, Martin Gering
Journal: Blood Advances
Blood Adv (2018) 2 (20): 2589–2606.
https://doi.org/10.1182/bloodadvances.2018020156
Published: 2018
Includes: Supplemental data
Journal Articles

Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea

Clinical Trials & Observations Global Advances
Françoise Bernaudin, Cécile Arnaud, Annie Kamdem, Isabelle Hau, Françoise Lelong, Ralph Epaud, Corinne Pondarré, Serge Pissard
Journal: Blood Advances
Blood Adv (2018) 2 (6): 626–637.
https://doi.org/10.1182/bloodadvances.2017014555
Published: 2018
Journal Articles

Low fetal hemoglobin percentage is associated with silent brain lesions in adults with homozygous sickle cell disease

Clinical Trials & Observations
David Calvet, Titien Tuilier, Nicolas Mélé, Guillaume Turc, Anoosha Habibi, Nassim Ait Abdallah, Loubna Majhadi, François Hemery, Myriam Edjlali, Frédéric Galacteros, Pablo Bartolucci
Journal: Blood Advances
Blood Adv (2017) 1 (26): 2503–2509.
https://doi.org/10.1182/bloodadvances.2017005504
Published: 2017
Journal Articles

Disease severity and slower psychomotor speed in adults with sickle cell disease

Clinical Trials & Observations
Dana R. Jorgensen, Andrea Metti, Meryl A. Butters, Joseph M. Mettenburg, Caterina Rosano, Enrico M. Novelli
Journal: Blood Advances
Blood Adv (2017) 1 (21): 1790–1795.
https://doi.org/10.1182/bloodadvances.2017008219
Published: 2017
Includes: Supplemental data
Journal Articles

Gene correction of HAX1 reversed Kostmann disease phenotype in patient-specific induced pluripotent stem cells

Erik Pittermann, Nico Lachmann, Glenn MacLean, Stephan Emmrich, Mania Ackermann, Gudrun Göhring, Brigitte Schlegelberger, Karl Welte, Axel Schambach, Dirk Heckl, Stuart H. Orkin, Tobias Cantz, Jan-Henning Klusmann
Journal: Blood Advances
Blood Adv (2017) 1 (14): 903–914.
https://doi.org/10.1182/bloodadvances.2016003798
Published: 2017
Includes: Supplemental data
Journal Articles

Gene-edited pseudogene resurrection corrects p47 phox -deficient chronic granulomatous disease

Randall K. Merling, Douglas B. Kuhns, Colin L. Sweeney, Xiaolin Wu, Sandra Burkett, Jessica Chu, Janet Lee, Sherry Koontz, Giovanni Di Pasquale, Sandra A. Afione, John A. Chiorini, Elizabeth M. Kang, Uimook Choi, Suk See De Ravin, Harry L. Malech
Journal: Blood Advances
Blood Adv (2016) 1 (4): 270–278.
https://doi.org/10.1182/bloodadvances.2016001214
Published: 2016
Includes: Supplemental data