Srinivas Aluri, Ph.D.

Medicine

Phone718-430-7967
Emailsrinivas.aluri@einsteinmed.org

Source: Scopus
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118 Citations
6 h-Index
16 Article
2 Review article

A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformation
Zhan, H. Q., Najmi, M., Lin, K., Aluri, S., Fiser, A., David Goldman, I. & Zhao, R., Nov 13 2020, In: Journal of Biological Chemistry. 295, 46, p. 15650-15661 12 p.
Research output: Contribution to journal › Article › peer-review

Open Access
Biological basis for efficacy of activin receptor ligand traps in myelodysplastic syndromes
Verma, A., Suragani, R. N. V. S., Aluri, S., Shah, N., Bhagat, T. D., Alexander, M. J., Komrokji, R. & Kumar, R., Feb 3 2020, In: Journal of Clinical Investigation. 130, 2, p. 582-589 8 p.
Research output: Contribution to journal › Review article › peer-review
9 Scopus citations
The thrombopoietin mimetic JNJ-26366821 increases megakaryopoiesis without affecting malignant myeloid proliferation
Adrianzen-Herrera, D., Choudhary, G., Gordon-Mitchell, S., Ramachandra, N., Bhagat, T., Zhang, H., Aluri, S., Shastri, A., Steidl, U., Will, B., Yang, W. L., Mahler, M., Eichenbaum, G., Guha, C. & Verma, A., Aug 23 2020, In: Leukemia and Lymphoma. 61, 10, p. 2453-2465 13 p.
Research output: Contribution to journal › Article › peer-review
1 Scopus citations
Lactate-mediated epigenetic reprogramming regulates formation of human pancreatic cancer-associated fibroblasts
Bhagat, T. D., Von Ahgrens, D., Dawlaty, M., Zou, Y., Baddour, J., Achreja, A., Zhao, H., Yang, L., Patel, B., Kwak, C., Choudhary, G. S., Gordon-Mitchell, S., Alluri, S., Bhattacharyya, S., Sahu, S., Yu, Y., Bartenstein, M., Giricz, O., Suzuki, M., Sohal, D. & 12 others, Gupta, S., Guerrero, P., Batra, S., Goggins, M., Steidl, U., Greally, J., Agarwal, B., Pradhan, K., Banerjee, D., Nagrath, D., Maitra, A. & Verma, A., Oct 2019, In: eLife. 8, e50663.
Research output: Contribution to journal › Article › peer-review

Open Access
18 Scopus citations
Stem cell mutations can be detected in myeloma patients years before onset of secondary leukemias
Sridharan, A., Schinke, C. D., Georgiev, G., da Silva Ferreira, M., Thiruthuvanathan, V., MacArthur, I., Bhagat, T. D., Choudhary, G. S., Aluri, S., Chen, J., Pradhan, K., Xia, Y., Panjikaran, M., Sims, G., Bhagat, C. K., Bender, R., Keeler, L., Graber, A., Heuck, C., Fletcher, F. A. & 10 others, Alapat, D., Weinhold, N., Johnson, S. K., Wickrema, A., Barlogie, B., Morgan, G. J., Shastri, A., Steidl, U., Will, B. & Verma, A., 2019, In: Blood Advances. 3, 23, p. 3962-3967 6 p.
Research output: Contribution to journal › Article › peer-review

Open Access
1 Scopus citations

A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformation

Biological basis for efficacy of activin receptor ligand traps in myelodysplastic syndromes

The thrombopoietin mimetic JNJ-26366821 increases megakaryopoiesis without affecting malignant myeloid proliferation

Lactate-mediated epigenetic reprogramming regulates formation of human pancreatic cancer-associated fibroblasts

Stem cell mutations can be detected in myeloma patients years before onset of secondary leukemias