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SINR loss and user selection in massive MU‐MISO systems with ZFBF

ETRI Journal, 2019, 41(5), , pp.637-647

2019

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SINR loss and user selection in massive MU-MISO systems with ZFBF

ETRI journal, 2019-10, Vol.41 (5), p.637-647

2019

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A size-shrinkable matrix metallopeptidase-2-sensitive delivery nanosystem improves the penetration of human programmed death-ligand 1 siRNA into lung-tumor spheroids

Drug delivery, 2021-01, Vol.28 (1), p.1055-1066

2021

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A Universal Predictive Mobility Management Scheme for Urban Ultra-Dense Networks With Control/Data Plane Separation

IEEE access, 2017, Vol.5, p.6015-6026

2017

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Molecular dynamics simulations of the conformational plasticity in the active pocket of salt-inducible kinase 2 (SIK2) multi-state binding with bosutinib

Computational and structural biotechnology journal, 2022-01, Vol.20, p.2574-2586

2022

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P1009: SKLB054, A NOVEL JAK2 INHIBITOR, POTENTLY TREATS MYELOPROLIFERATIVE NEOPLASM WITH JAK2V617F MUTATION

HemaSphere, 2023-08, Vol.7 (S3), p.e2500587-n/a

2023

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Flonoltinib, a Novel JAK2/FLT3 Inhibitor, Potently Treats Hemophagocytic Lymphohistiocytosis and Increases Sensitivity to Dexamethasone

Blood, 2022-11, Vol.140 (Supplement 1), p.2624-2625

2022

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CNN-Based LOS/NLOS Identification in 3-D Massive MIMO Systems

IEEE communications letters, 2018-12, Vol.22 (12), p.2491-2494

2018

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Toward Higher Performance for Channel Estimation With Complex DnCNN

IEEE communications letters, 2020-01, Vol.24 (1), p.198-201

2020

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Discovery of Potent and Orally Effective Dual Janus Kinase 2/FLT3 Inhibitors for the Treatment of Acute Myelogenous Leukemia and Myeloproliferative Neoplasms

Journal of medicinal chemistry, 2019-11, Vol.62 (22), p.10305-10320

2019

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Low-complexity user selection method in 3D MU-MIMO systems

Electronics letters, 2018-10, Vol.54 (20), p.1176-1178

2018

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Discovery of novel β-carboline/acylhydrazone hybrids as potent antitumor agents and overcome drug resistance

European journal of medicinal chemistry, 2018-05, Vol.152, p.516-526

2018

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Discovery of 1,2,4-oxadiazole-Containing hydroxamic acid derivatives as histone deacetylase inhibitors potential application in cancer therapy

European journal of medicinal chemistry, 2019-09, Vol.178, p.116-130

2019

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N‑(Pyrimidin-2-yl)-1,2,3,4-tetrahydroisoquinolin-6-amine Derivatives as Selective Janus Kinase 2 Inhibitors for the Treatment of Myeloproliferative Neoplasms

Journal of medicinal chemistry, 2020-12, Vol.63 (23), p.14921-14936

2020

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The compound millepachine and its derivatives inhibit tubulin polymerization by irreversibly binding to the colchicine-binding site in β-tubulin

The Journal of biological chemistry, 2018-06, Vol.293 (24), p.9461-9472

2018

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Correction to “N‑(Pyrimidin-2-yl)-1,2,3,4-tetrahydroisoquinolin-6-amine Derivatives as Selective Janus Kinase 2 Inhibitors for the Treatment of Myeloproliferative Neoplasms”

Journal of medicinal chemistry, 2021-02, Vol.64 (4), p.2310-2310

2021

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Correction to “Discovery of Potent and Orally Effective Dual Janus Kinase 2/FLT3 Inhibitors for the Treatment of Acute Myelogenous Leukemia and Myeloproliferative Neoplasms”

Journal of medicinal chemistry, 2020-02, Vol.63 (3), p.1441-1442

2020

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Correction to: Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2V617F-induced myeloproliferative neoplasms

Blood cancer journal (New York), 2024-06, Vol.14 (1), p.104, Article 104

2024

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Synthesis and biological evaluation of 6-(pyrimidin-4-yl)-1H-pyrazolo[4,3-b]pyridine derivatives as novel dual FLT3/CDK4 inhibitors

Bioorganic chemistry, 2022-04, Vol.121, p.105669-105669, Article 105669

2022

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An Overview on IEEE 802.11bf: WLAN Sensing

IEEE Communications surveys and tutorials, 2024-06, p.1-1

2024

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Packet-Size Based Overlapping User Grouping in MU-MIMO Systems

2019 IEEE Wireless Communications and Networking Conference (WCNC), 2019, p.1-6

2019

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Correction to: Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2 V617F -induced myeloproliferative neoplasms

Blood cancer journal (New York), 2024-06, Vol.14 (1), p.104

2024

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Correction to: Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2 V617F-induced myeloproliferative neoplasms

Blood cancer journal (New York), 2024-06, Vol.14 (1), p.1-4

2024

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User grouping with adaptive group number for massive MIMO downlink systems

2017 20th International Symposium on Wireless Personal Multimedia Communications (WPMC), 2017, p.459-464

2017

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Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2V617F-induced myeloproliferative neoplasms

Blood cancer journal (New York), 2022-03, Vol.12 (3), p.37, Article 37

2022

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SINR loss and user selection in massive MU‐MISO systems with ZFBF

SINR loss and user selection in massive MU-MISO systems with ZFBF

A size-shrinkable matrix metallopeptidase-2-sensitive delivery nanosystem improves the penetration of human programmed death-ligand 1 siRNA into lung-tumor spheroids

A Universal Predictive Mobility Management Scheme for Urban Ultra-Dense Networks With Control/Data Plane Separation

Molecular dynamics simulations of the conformational plasticity in the active pocket of salt-inducible kinase 2 (SIK2) multi-state binding with bosutinib

P1009: SKLB054, A NOVEL JAK2 INHIBITOR, POTENTLY TREATS MYELOPROLIFERATIVE NEOPLASM WITH JAK2V617F MUTATION

Flonoltinib, a Novel JAK2/FLT3 Inhibitor, Potently Treats Hemophagocytic Lymphohistiocytosis and Increases Sensitivity to Dexamethasone

CNN-Based LOS/NLOS Identification in 3-D Massive MIMO Systems

Toward Higher Performance for Channel Estimation With Complex DnCNN

Discovery of Potent and Orally Effective Dual Janus Kinase 2/FLT3 Inhibitors for the Treatment of Acute Myelogenous Leukemia and Myeloproliferative Neoplasms

Low-complexity user selection method in 3D MU-MIMO systems

Discovery of novel β-carboline/acylhydrazone hybrids as potent antitumor agents and overcome drug resistance

Discovery of 1,2,4-oxadiazole-Containing hydroxamic acid derivatives as histone deacetylase inhibitors potential application in cancer therapy

N‑(Pyrimidin-2-yl)-1,2,3,4-tetrahydroisoquinolin-6-amine Derivatives as Selective Janus Kinase 2 Inhibitors for the Treatment of Myeloproliferative Neoplasms

The compound millepachine and its derivatives inhibit tubulin polymerization by irreversibly binding to the colchicine-binding site in β-tubulin

Correction to “N‑(Pyrimidin-2-yl)-1,2,3,4-tetrahydroisoquinolin-6-amine Derivatives as Selective Janus Kinase 2 Inhibitors for the Treatment of Myeloproliferative Neoplasms”

Correction to “Discovery of Potent and Orally Effective Dual Janus Kinase 2/FLT3 Inhibitors for the Treatment of Acute Myelogenous Leukemia and Myeloproliferative Neoplasms”

Correction to: Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2V617F-induced myeloproliferative neoplasms

Synthesis and biological evaluation of 6-(pyrimidin-4-yl)-1H-pyrazolo[4,3-b]pyridine derivatives as novel dual FLT3/CDK4 inhibitors

An Overview on IEEE 802.11bf: WLAN Sensing

Packet-Size Based Overlapping User Grouping in MU-MIMO Systems

Correction to: Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2 V617F -induced myeloproliferative neoplasms

Correction to: Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2 V617F-induced myeloproliferative neoplasms

User grouping with adaptive group number for massive MIMO downlink systems

Preclinical studies of Flonoltinib Maleate, a novel JAK2/FLT3 inhibitor, in treatment of JAK2V617F-induced myeloproliferative neoplasms

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