Center-Authored Papers

Filters: Author is Shimamura, Akiko  [Clear All Filters]
2008
Austin KM, Gupta ML, Coats SA, Tulpule A, Mostoslavsky G, Balazs AB, Mulligan RC, Daley G, Pellman D, Shimamura A.  2008.  Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome.. The Journal of clinical investigation. 118(4):1511-8. Abstract
Kayed H, Bekasi S, Keleg S, Welsch T, Esposito I, Shimamura A, Michalski CW, Friess H, Kleeff J.  2008.  Expression of the Shwachman-Bodian-Diamond syndrome (SBDS) protein in human pancreatic cancer and chronic pancreatitis.. Histology and histopathology. 23(7):819-26. Abstract
Ganapathi KA, Shimamura A.  2008.  Ribosomal dysfunction and inherited marrow failure.. British journal of haematology. 141(3):376-87. Abstract
Vlachos A, Ball S, Dahl N, Alter BP, Sheth S, Ramenghi U, Meerpohl J, Karlsson S, Liu JM, Leblanc T et al..  2008.  Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.. British journal of haematology. 142(6):859-76. Abstract
Shimamura A.  2008.  Diamond-Blackfan anemia: a new facet.. Blood. 112(5):1552-3.
Park I-H, Arora N, Huo H, Maherali N, Ahfeldt T, Shimamura A, Lensch WM, Cowan C, Hochedlinger K, Daley GQ.  2008.  Disease-specific induced pluripotent stem cells.. Cell. 134(5):877-86. Abstract
2009
Shimamura A.  2009.  Clinical approach to marrow failure.. Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program. :329-37. Abstract
Burroughs LM, Woolfrey AE, Shimamura A.  2009.  Shwachman-Diamond syndrome: a review of the clinical presentation, molecular pathogenesis, diagnosis, and treatment.. Hematology/oncology clinics of North America. 23(2):233-48. Abstract
Du H-Y, Pumbo E, Ivanovich J, An P, Maziarz RT, Reiss UM, Chirnomas D, Shimamura A, Vlachos A, Lipton JM et al..  2009.  TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.. Blood. 113(2):309-16. Abstract
2010
Tulpule A, Lensch WM, Miller JD, Austin K, D'andrea A, Schlaeger TM, Shimamura A, Daley GQ.  2010.  Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage.. Blood. 115(17):3453-62. Abstract
Sakamoto KM, Shimamura A, Davies SM.  2010.  Congenital disorders of ribosome biogenesis and bone marrow failure.. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 16(1 Suppl):S12-7. Abstract
Parmar K, Kim J, Sykes SM, Shimamura A, Stuckert P, Zhu K, Hamilton A, Deloach MK, Kutok JL, Akashi K et al..  2010.  Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1.. Stem cells (Dayton, Ohio). 28(7):1186-95. Abstract
Rosenberg PS, Zeidler C, Bolyard AA, Alter BP, Bonilla MA, Boxer LA, Dror Y, Kinsey S, Link DC, Newburger PE et al..  2010.  Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.. British journal of haematology. 150(2):196-9. Abstract
Shimamura A, Alter BP.  2010.  Pathophysiology and management of inherited bone marrow failure syndromes.. Blood reviews. 24(3):101-22. Abstract
Becker PS, Taylor JA, Trobridge GD, Zhao X, Beard BC, Chien S, Adair J, Kohn DB, Wagner JE, Shimamura A et al..  2010.  Preclinical correction of human Fanconi anemia complementation group A bone marrow cells using a safety-modified lentiviral vector.. Gene therapy. 17(10):1244-52. Abstract
Wong TE, Calicchio ML, Fleming MD, Shimamura A, Harris MH.  2010.  SBDS protein expression patterns in the bone marrow.. Pediatric blood & cancer. 55(3):546-9. Abstract
2011
Burwick N, Shimamura A, Liu JM.  2011.  Non-Diamond Blackfan anemia disorders of ribosome function: Shwachman Diamond syndrome and 5q- syndrome.. Seminars in hematology. 48(2):136-43. Abstract
Dror Y, Donadieu J, Koglmeier J, Dodge J, Toiviainen-Salo S, Makitie O, Kerr E, Zeidler C, Shimamura A, Shah N et al..  2011.  Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome.. Annals of the New York Academy of Sciences. 1242(1):40-55. Abstract
Huang JN, Shimamura A.  2011.  Clinical spectrum and molecular pathophysiology of Shwachman-Diamond syndrome.. Current opinion in hematology. 18(1):30-35. Abstract
Click ES, Cox B, Olson SB, Grompe M, Akkari Y, Moreau LA, Shimamura A, Sternen DL, Liu YJ, Leppig KA et al..  2011.  Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene.. American journal of medical genetics. Part A. 155A(7):1673-9. Abstract
Marro K, Otto R, Kolokythas O, Shimamura A, Sanders JE, McDonald GB, Friedman SD.  2011.  A simulation-based comparison of two methods for determining relaxation rates from relaxometry images.. Magnetic resonance imaging. 29(4):497-506. Abstract
2012
Kazenwadel J, Secker GA, Liu YJ, Rosenfeld JA, Wildin RS, Cuellar-Rodriguez J, Hsu AP, Dyack S, Fernandez CV, Chong C-E et al..  2012.  Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature.. Blood. 119(5):1283-1291. Abstract
Singh SA, Vlachos A, Morgenstern NJ, Ouansafi I, Ip W, Rommens JM, Durie P, Shimamura A, Lipton JM.  2012.  Breast cancer in a case of Shwachman Diamond syndrome.. Pediatric blood & cancer. 59(5):945-6. Abstract
Burwick N, Coats SA, Nakamura T, Shimamura A.  2012.  Impaired ribosomal subunit association in Shwachman-Diamond syndrome.. Blood. Abstract
2013
Myers KC, Davies SM, Shimamura A.  2013.  Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update.. Hematology/oncology clinics of North America. 27(1):117-28,ix. Abstract