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Journal Articles

Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1

Blood (2022) 139 (16): 2534–2546.

https://doi.org/10.1182/blood.2021013753

Published: 2022

Includes: Supplemental data

Journal Articles

Efficient Screening Tests and Gene Mutation Spectrum for Hereditary Stomatocytosis in Japan

Erina Nakahara, Keiko Yamamoto, Takako Aoki, Hiromi Ogura, Taiju Utsugisawa, Hiroyuki Akagawa, Toshiyuki Yamamoto, Yoshiro Maru, Fumihiko Nakamura, Hiroshi Yagasaki, Etsuro Ito, Shouichi Ohga, Hitoshi Kanno

Blood (2021) 138 (Supplement 1): 1996.

https://doi.org/10.1182/blood-2021-152599

Published: 2021

Journal Articles

The Flow Cytometric Osmotic Fragility Test Is an Effective Screening Method for Dehydrated Hereditary Stomatocytosis

Taiju Utsugisawa, MD PhD, Takuya Iwasaki, MLS, Takako Aoki, MLS, Yoshio Okamoto, MLS, Takahiro Kawakami, MD PhD, Hiromi Ogura, MD PhD, Hitoshi Kanno, MDPhD

Blood (2017) 130 (Supplement 1): 929.

https://doi.org/10.1182/blood.V130.Suppl_1.929.929

Published: 2017

Journal Articles

Dysregulated Transcriptional Upregulation of Cell-Cycle Regulators By KLF1 Mutation E325K Induces Cell-Cycle Arrest in Erythroid Cells Differentiated from the Congenital Dyserythropoietic Anemia (CDA)-Patient Specific Induced Pluripotent Stem Cells

Hiroshi Kohara, PhD, Taiju Utsugisawa, MD PhD, Hiromi Ogura, MD PhD, Ai Sugawara, B.Sc., Ogawa Yoshie, M.Sc., Chika Sakamoto, M.Sc., Hitoshi Kanno, MDPhD, Kenzaburo Tani, MD PhD

Blood (2017) 130 (Supplement 1): 2197.

https://doi.org/10.1182/blood.V130.Suppl_1.2197.2197

Published: 2017

Journal Articles

The Novel Missense Mutation of GATA1 Caused Red Cell Adenosine Deaminase Overproduction Associated with Congenital Hemolytic Anemia

Hiromi Ogura, MD PhD, Toshiyuki Yamamoto, MD PhD, Taiju Utsugisawa, MD PhD, Takako Aoki, MLS, Takuya Iwasaki, MLS, Yumiko Ondo, MLS, Takahiro Kawakami, MD PhD, Shinichiro Nakagawa, MD PhD, Shuichi Ozono, MD PhD, Hiroko Inada, MD PhD, Hitoshi Kanno, MD PhD

Blood (2016) 128 (22): 400.

https://doi.org/10.1182/blood.V128.22.400.400

Published: 2016

Journal Articles

COL4A1 is a Novel Causative Gene Responsible for Congenital Hemolytic Anemia, Representing Characteristic Clinical Course in Infants

Hiromi Ogura, MD PhD, Shouichi Ohga, MD PhD, Takako Aoki, MLS, Taiju Utsugisawa, MDPhD, Hidehiro Takahashi, MDPhD, Asayuki Iwai, Kenichiro Watanabe, MD PhD, Yusuke Okuno, MD PhD, Kenichi Yoshida, MD PhD, Satoru Miyano, MD PhD, Seishi Ogawa, MD PhD, Seiji Kojima, MD PhD, Hitoshi Kanno, MD PhD

Blood (2015) 126 (23): 934.

https://doi.org/10.1182/blood.V126.23.934.934

Published: 2015

Journal Articles

ATP11C Encodes a Major Flippase in Human Erythrocyte and Its Genetic Defect Causes Congenital Non-Spherocytic Hemolytic Anemia

Nobuto Arashiki, PhD, Yuichi Takakuwa, MD PhD, Hiromi Ogura, MD PhD, Taiju Utsugisawa, MDPhD, Satoru Miyano, MD PhD, Seishi Ogawa, MD PhD, Seiji Kojima, MD PhD, Shouichi Ohga, MD PhD, Narla Mohandas, DSc, Hitoshi Kanno, MD PhD

Blood (2015) 126 (23): 2131.

https://doi.org/10.1182/blood.V126.23.2131.2131

Published: 2015

Journal Articles

Elevated Red Cell Reduced Glutathione Is a Novel Biomarker of Diamond-Blackfan Anemia

Taiju Utsugisawa, MDPhD, Toshitaka Uchiyama, PhD, Hiromi Ogura, MDPhD, Takako Aoki, Isao Hamaguchi, MD PhD, Akira Ishiguro, MD PhD, Akira Ohara, MD PhD, Seiji Kojima, MD PhD, Shouichi Ohga, MDPhD, Etsuro Ito, MDPhD, Hitoshi Kanno, MDPhD

Blood (2014) 124 (21): 1342.

https://doi.org/10.1182/blood.V124.21.1342.1342

Published: 2014

Journal Articles

Smad7 promotes self-renewal of hematopoietic stem cells

Ulrika Blank, Goran Karlsson, Jennifer L. Moody, Taiju Utsugisawa, Mattias Magnusson, Sofie Singbrant, Jonas Larsson, Stefan Karlsson

Blood (2006) 108 (13): 4246–4254.

https://doi.org/10.1182/blood-2006-02-005611

Published: 2006

Journal Articles

Deficient Ribosomal Protein S19 in Diamond-Blackfan Anemia Causes a Reduction in bcl-2 and Bad and Leads to Apoptosis in Erythroid Progenitor Cells.

Koichi Miyake, MD, PhD, Taiju Utsugisawa, MD, PhD, Johan Flygare, Thomas Kiefer, MD, Isao Hamaguchi, MD, PhD, Johan Richter, MD, PhD, Stefan Karlsson, MD, PhD

Blood (2005) 106 (11): 131.

https://doi.org/10.1182/blood.V106.11.131.131

Published: 2005

Journal Articles

Deficiency of ribosomal protein S19 in CD34 + cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemia

Johan Flygare, Thomas Kiefer, Koichi Miyake, Taiju Utsugisawa, Isao Hamaguchi, Lydie Da Costa, Johan Richter, Edward J. Davey, Hans Matsson, Niklas Dahl, Maciej Wiznerowicz, Didier Trono, Stefan Karlsson

Blood (2005) 105 (12): 4627–4634.

https://doi.org/10.1182/blood-2004-08-3115

Published: 2005

Journal Articles

Hematopoietic Mechanism in Diamond-Blackfan Anemia: Late Erythroid Development Is Not Affected by Ribosomal Protein S19 Deficiency.

Blood (2004) 104 (11): 719.

https://doi.org/10.1182/blood.V104.11.719.719

Published: 2004

Journal Articles

Hematopoietic Stem Cells Overexpressing Smad7 Exhibit Increased Self-Renewal and Regeneration Capacity in Vivo.

Ulrika Blank, Jonas Larsson, Taiju Utsugisawa, Mattias Magnusson, Jenny Klintman, Stefan Karlsson

Blood (2004) 104 (11): 561.

https://doi.org/10.1182/blood.V104.11.561.561

Published: 2004

Journal Articles

Apoptotic Change Is a Major Reason for Defect in Early Erythroid Development in Cell Line Models for Ribosomal Protein (RP) S19 Deficient Diamond-Blackfan Anemia.

Koichi Miyake, MD, PhD, Taiju Utsugisawa, MD, PhD, Johan Flygare, Thomas Kiefer, MD, Johan Richter, MD, PhD, Maciej Wiznerowicz, MD, PhD, Didier Trono, MD, PhD, Stefan Karlsson, MD, PhD

Blood (2004) 104 (11): 2840.

https://doi.org/10.1182/blood.V104.11.2840.2840

Published: 2004

NARROW

Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1

Efficient Screening Tests and Gene Mutation Spectrum for Hereditary Stomatocytosis in Japan

The Flow Cytometric Osmotic Fragility Test Is an Effective Screening Method for Dehydrated Hereditary Stomatocytosis

Dysregulated Transcriptional Upregulation of Cell-Cycle Regulators By KLF1 Mutation E325K Induces Cell-Cycle Arrest in Erythroid Cells Differentiated from the Congenital Dyserythropoietic Anemia (CDA)-Patient Specific Induced Pluripotent Stem Cells

The Novel Missense Mutation of GATA1 Caused Red Cell Adenosine Deaminase Overproduction Associated with Congenital Hemolytic Anemia

COL4A1 is a Novel Causative Gene Responsible for Congenital Hemolytic Anemia, Representing Characteristic Clinical Course in Infants

ATP11C Encodes a Major Flippase in Human Erythrocyte and Its Genetic Defect Causes Congenital Non-Spherocytic Hemolytic Anemia

Elevated Red Cell Reduced Glutathione Is a Novel Biomarker of Diamond-Blackfan Anemia

Smad7 promotes self-renewal of hematopoietic stem cells

Deficient Ribosomal Protein S19 in Diamond-Blackfan Anemia Causes a Reduction in bcl-2 and Bad and Leads to Apoptosis in Erythroid Progenitor Cells.

Deficiency of ribosomal protein S19 in CD34 + cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemia

Hematopoietic Mechanism in Diamond-Blackfan Anemia: Late Erythroid Development Is Not Affected by Ribosomal Protein S19 Deficiency.

Hematopoietic Stem Cells Overexpressing Smad7 Exhibit Increased Self-Renewal and Regeneration Capacity in Vivo.

Apoptotic Change Is a Major Reason for Defect in Early Erythroid Development in Cell Line Models for Ribosomal Protein (RP) S19 Deficient Diamond-Blackfan Anemia.

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American Society of Hematology

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American Society of Hematology

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