Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR019391-01
Application #
6973661
Study Section
Special Emphasis Panel (ZRG1-CDF-4 (31))
Project Start
2004-04-15
Project End
2005-04-14
Budget Start
2004-04-15
Budget End
2005-04-14
Support Year
1
Fiscal Year
2004
Total Cost
$203,393
Indirect Cost
Name
University of Louisville
Department
Pediatrics
Type
Schools of Medicine
DUNS #
057588857
City
Louisville
State
KY
Country
United States
Zip Code
40292
Hosono, Naoko; Makishima, Hideki; Mahfouz, Reda et al. (2017) Recurrent genetic defects on chromosome 5q in myeloid neoplasms. Oncotarget 8:6483-6495
Yoshizato, Tetsuichi; Nannya, Yasuhito; Atsuta, Yoshiko et al. (2017) Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation. Blood 129:2347-2358
Jobe, F; Patel, B; Kuzmanovic, T et al. (2017) Deletion of Ptpn1 induces myeloproliferative neoplasm. Leukemia 31:1229-1234
Molenaar, R J; Thota, S; Nagata, Y et al. (2015) Clinical and biological implications of ancestral and non-ancestral IDH1 and IDH2 mutations in myeloid neoplasms. Leukemia 29:2134-42
Ruffalo, Matthew; Husseinzadeh, Holleh; Makishima, Hideki et al. (2015) Whole-exome sequencing enhances prognostic classification of myeloid malignancies. J Biomed Inform 58:104-113
Shen, Wenyi; Clemente, Michael J; Hosono, Naoko et al. (2014) Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria. J Clin Invest 124:4529-38
Hosono, N; Makishima, H; Jerez, A et al. (2014) Recurrent genetic defects on chromosome 7q in myeloid neoplasms. Leukemia 28:1348-51
Clemente, Michael J; Przychodzen, Bartlomiej; Jerez, Andres et al. (2013) Deep sequencing of the T-cell receptor repertoire in CD8+ T-large granular lymphocyte leukemia identifies signature landscapes. Blood 122:4077-85
Gómez-Seguí, I; Makishima, H; Jerez, A et al. (2013) Novel recurrent mutations in the RAS-like GTP-binding gene RIT1 in myeloid malignancies. Leukemia 27:1943-6
Kar, Sarah Abu; Jankowska, Anna; Makishima, Hideki et al. (2013) Spliceosomal gene mutations are frequent events in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia. Haematologica 98:107-13

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