Original language | English (US) |
---|---|
Pages (from-to) | e5-e9 |
Journal | Haematologica |
Volume | 103 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2018 |
ASJC Scopus subject areas
- Hematology
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Hsp90 inhibition disrupts JAK-STAT signaling and leads to reductions in splenomegaly in patients with myeloproliferative neoplasms. / Hobbs, Gabriela S.; Hanasoge Somasundara, Amritha Varshini; Kleppe, Maria et al.
In: Haematologica, Vol. 103, No. 1, 01.2018, p. e5-e9.Research output: Contribution to journal › Letter › peer-review
TY - JOUR
T1 - Hsp90 inhibition disrupts JAK-STAT signaling and leads to reductions in splenomegaly in patients with myeloproliferative neoplasms
AU - Hobbs, Gabriela S.
AU - Hanasoge Somasundara, Amritha Varshini
AU - Kleppe, Maria
AU - Litvin, Rivka
AU - Arcila, Maria
AU - Ahn, Jihae
AU - McKenney, Anna Sophia
AU - Knapp, Kristina
AU - Ptashkin, Ryan
AU - Weinstein, Howard
AU - Heinemann, Murk Hein
AU - Francis, Jasmine
AU - Chanel, Suzanne
AU - Berman, Ellin
AU - Mauro, Michael
AU - Tallman, Martin S.
AU - Heaney, Mark L.
AU - Levine, Ross L.
AU - Rampal, Raajit K.
N1 - Funding Information: 1Division of Hematology/Oncology, Massachusetts General Hospital, Harvard Medical School;2Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center; 3Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center;4Department of Pathology, Memorial Sloan Kettering Cancer Center;5Driskill Graduate Program in Life Sciences, Feinberg School of Medicine, Northwestern University;6Gerstner Sloan Kettering Graduate School of Biomedical Sciences, and Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program;7Center for Epigenetics Research Memorial Sloan Kettering Center;8Cardiology Service, Department of Medicine Memorial Sloan Kettering Cancer Center;9Department of Surgery, Memorial Sloan Kettering Cancer Center and 10Department of Medicine, Columbia University Medical Center, USA Funding: this work was supported by funding from Novartis Pharmaceuticals; Cancer Center Support Grant/Core Grant to Memorial Sloan Kettering Cancer Center (P30 CA008748); NCI 1K08CA188529-01 (RKR); KK12CA087723-14 (GSH); NCI R01CA173636 (RLL); K99 HL122503-01A1 (MK); NIH National Institute of General Medical Sciences Grant T32 GM007739 and NCI F30CA18349 (ASM). Correspondence: rampalr@mskcc.org doi:10.3324/haematol.2017.177600 Information on authorship, contributions, and financial & other disclosures was provided by the authors and is available with the online version of this article at www.haematologica.org. Funding Information: Funding: this work was supported by funding from Novartis Pharmaceuticals; Cancer Center Support Grant/Core Grant to Memorial Sloan Kettering Cancer Center(P30 CA008748); NCI 1K08CA188529-01 (RKR); KK12CA087723-14 (GSH); NCI R01CA173636 (RLL); K99 HL122503-01A1 (MK); NIH National Institute of General Medical Sciences Grant T32 GM007739 and NCI F30CA18349 (ASM).
PY - 2018/1
Y1 - 2018/1
UR - http://www.scopus.com/inward/record.url?scp=85040079612&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85040079612&partnerID=8YFLogxK
U2 - 10.3324/haematol.2017.177600
DO - 10.3324/haematol.2017.177600
M3 - Letter
C2 - 29051283
AN - SCOPUS:85040079612
VL - 103
SP - e5-e9
JO - Haematologica
JF - Haematologica
SN - 0390-6078
IS - 1
ER -