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Journal Articles

Concurrent transcriptional deregulation of AML1/RUNX1 and GATA factors by the AML1-TRPS1 chimeric gene in t(8;21)(q24;q22) acute myeloid leukemia

Norio Asou, Masatoshi Yanagida, Liqun Huang, Masayuki Yamamoto, Katsuya Shigesada, Hiroaki Mitsuya, Yoshiaki Ito, Motomi Osato

Blood (2007) 109 (9): 4023–4027.

https://doi.org/10.1182/blood-2006-01-031781

Published: 2007

Includes: Supplemental data

Journal Articles

Identification of Cooperating Genetic Alterations in RUNX Leukemia Using the Mouse Model for the Human Familial Leukemia, FPD/AML.

Motomi Osato, MD, Namiko Yamashita, Masatoshi Yanagida, Liqun Huang, Scott Kogan, MD, Masayuki Iwasaki, PhD, Takuro Nakamura, MD, Katsuya Shigesada, PhD, Norio Asou, MD, PhD, Yoshiaki Ito, MD

Blood (2004) 104 (11): 3383.

https://doi.org/10.1182/blood.V104.11.3383.3383

Published: 2004

Journal Articles

Molecular basis for a dominant inactivation of RUNX1/AML1 by the leukemogenic inversion 16 chimera

Gang Huang, Katsuya Shigesada, Hee-Jun Wee, P. Paul Liu, Motomi Osato, Yoshiaki Ito

Blood (2004) 103 (8): 3200–3207.

https://doi.org/10.1182/blood-2003-07-2188

Published: 2004

Journal Articles

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

Joëlle Michaud, Feng Wu, Motomi Osato, Gregory M. Cottles, Masatoshi Yanagida, Norio Asou, Katsuya Shigesada, Yoshiaki Ito, Kathleen F. Benson, Wendy H. Raskind, Colette Rossier, Stylianos E. Antonarakis, Sara Israels, Archie McNicol, Harvey Weiss, Marshall Horwitz, Hamish S. Scott

Blood (2002) 99 (4): 1364–1372.

https://doi.org/10.1182/blood.V99.4.1364

Published: 2002

Journal Articles

Biallelic and Heterozygous Point Mutations in the Runt Domain of the AML1/PEBP2B Gene Associated With Myeloblastic Leukemias

Motomi Osato, Norio Asou, Essam Abdalla, Koyu Hoshino, Hiroshi Yamasaki, Toshiya Okubo, Hitoshi Suzushima, Kiyoshi Takatsuki, Tomohiko Kanno, Katsuya Shigesada, Yoshiaki Ito

Blood (1999) 93 (6): 1817–1824.

https://doi.org/10.1182/blood.V93.6.1817.406k36_1817_1824

Published: 1999

NARROW

Concurrent transcriptional deregulation of AML1/RUNX1 and GATA factors by the AML1-TRPS1 chimeric gene in t(8;21)(q24;q22) acute myeloid leukemia

Identification of Cooperating Genetic Alterations in RUNX Leukemia Using the Mouse Model for the Human Familial Leukemia, FPD/AML.

Molecular basis for a dominant inactivation of RUNX1/AML1 by the leukemogenic inversion 16 chimera

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

Biallelic and Heterozygous Point Mutations in the Runt Domain of the AML1/PEBP2B Gene Associated With Myeloblastic Leukemias

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ASH Publications

American Society of Hematology

Concurrent transcriptional deregulation of AML1/RUNX1 and GATA factors by the AML1-TRPS1 chimeric gene in t(8;21)(q24;q22) acute myeloid leukemia

Identification of Cooperating Genetic Alterations in RUNX Leukemia Using the Mouse Model for the Human Familial Leukemia, FPD/AML.

Molecular basis for a dominant inactivation of RUNX1/AML1 by the leukemogenic inversion 16 chimera

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

Biallelic and Heterozygous Point Mutations in the Runt Domain of the AML1/PEBP2B Gene Associated With Myeloblastic Leukemias

Email alerts

ASH Publications

American Society of Hematology

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