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Akiko Shimamura

Showing results (71-80 of 158) with videos related to

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Human Molecular Genetics|September 25, 2018
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)Aaron Seo, Suleyman Gulsuner, Sarah Pierce, et al.
Haematologica|July 16, 2016
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patientsSiobán B Keel, Angela Scott, Marilyn Sanchez-Bonilla, et al.
DNA Repair|April 2, 2018
Targeted mass spectrometry enables robust quantification of FANCD2 mono-ubiquitination in response to DNA damageJeffrey R Whiteaker, Lei Zhao, Richard G Ivey, et al.
Clinical Case Reports|November 29, 2023
Treatment of recurrent pediatric myelodysplastic syndrome post hematopoietic stem cell transplantationFranziska Wachter, Yana Pikman, Jacob Bledsoe, et al.
Transplantation and Cellular Therapy|October 25, 2022
Bringing Patient and Caregivers Voices to the Clinical Trial Chorus: A Report From the BMT CTN Patient and Caregiver Advocacy Task ForceSumithira Vasu, Shernan G Holtan, Akiko Shimamura, et al.
Journal of Pediatric Hematology/Oncology|June 4, 2016
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic AnalysisOrna Steinberg-Shemer, Siobán Keel, Orly Dgany, et al.
Stem Cells (Dayton, Ohio)|May 28, 2010
Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1Kalindi Parmar, Jungmin Kim, Stephen M Sykes, et al.
The Journal of Pediatrics|August 16, 2025
Growth Patterns in Shwachman-Diamond Syndrome: Findings from the North American Shwachman-Diamond Syndrome RegistryLois Schwarz, Leah Cheng, Sarah Steltz, et al.
Haematologica|April 2, 2026
Preemptive hematopoietic stem cell transplantation in <i>RUNX1</i> familial platelet disorder: a shared decision-making frameworkTimothy S Olson, Katrin Ericson, Joseph H Antin, et al.
JCI Insight|May 1, 2019
Therapeutic discovery for marrow failure with MDS predisposition using pluripotent stem cellsMelisa Ruiz-Gutierrez, Özge Vargel Bölükbaşı, Gabriela Alexe, et al.
Pageof 16

Showing results (71-80 of 158) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|September 25, 2018
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)Aaron Seo, Suleyman Gulsuner, Sarah Pierce, et al.
Haematologica|July 16, 2016
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patientsSiobán B Keel, Angela Scott, Marilyn Sanchez-Bonilla, et al.
DNA Repair|April 2, 2018
Targeted mass spectrometry enables robust quantification of FANCD2 mono-ubiquitination in response to DNA damageJeffrey R Whiteaker, Lei Zhao, Richard G Ivey, et al.
Clinical Case Reports|November 29, 2023
Treatment of recurrent pediatric myelodysplastic syndrome post hematopoietic stem cell transplantationFranziska Wachter, Yana Pikman, Jacob Bledsoe, et al.
Transplantation and Cellular Therapy|October 25, 2022
Bringing Patient and Caregivers Voices to the Clinical Trial Chorus: A Report From the BMT CTN Patient and Caregiver Advocacy Task ForceSumithira Vasu, Shernan G Holtan, Akiko Shimamura, et al.
Journal of Pediatric Hematology/Oncology|June 4, 2016
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic AnalysisOrna Steinberg-Shemer, Siobán Keel, Orly Dgany, et al.
Stem Cells (Dayton, Ohio)|May 28, 2010
Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1Kalindi Parmar, Jungmin Kim, Stephen M Sykes, et al.
The Journal of Pediatrics|August 16, 2025
Growth Patterns in Shwachman-Diamond Syndrome: Findings from the North American Shwachman-Diamond Syndrome RegistryLois Schwarz, Leah Cheng, Sarah Steltz, et al.
Haematologica|April 2, 2026
Preemptive hematopoietic stem cell transplantation in <i>RUNX1</i> familial platelet disorder: a shared decision-making frameworkTimothy S Olson, Katrin Ericson, Joseph H Antin, et al.
JCI Insight|May 1, 2019
Therapeutic discovery for marrow failure with MDS predisposition using pluripotent stem cellsMelisa Ruiz-Gutierrez, Özge Vargel Bölükbaşı, Gabriela Alexe, et al.
Pageof 16