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Selina Chen-Kiang

Selina Chen-Kiang

D-Index & Metrics

Molecular Biology

D-Index
56
Citations
12483
World Ranking
2199
National Ranking
1092

Overview

Selina Chen-Kiang is affiliated with Cornell University in the United States. Their research spans several fields within medicine and biochemistry, genetics, and molecular biology, with a particular focus on oncology and pathology.

The scientist's work encompasses key subfields such as molecular biology, pathology and forensic medicine, oncology, genetics, and pulmonary and respiratory medicine. This multidisciplinary approach supports a broad investigation into disease mechanisms and therapeutic strategies.

Among the main topics covered in their research are lymphoma diagnosis and treatment, cancer-related gene regulation, chronic lymphocytic leukemia research, CAR-T cell therapy, advanced breast cancer therapies, protein degradation and inhibitors, and cancer mechanisms and therapy.

Selina Chen-Kiang has published extensively in various scientific venues. Frequent publication platforms include Blood, Blood Advances, UNC Libraries, Cancer Research, and Hematological Oncology.

Notable recent papers by the scientist include:

  • Immunomodulation by anticancer cell cycle inhibitors, 2020, Nature Reviews Immunology
  • Radiotherapy Delivered before CDK4/6 Inhibitors Mediates Superior Therapeutic Effects in ER+ Breast Cancer, 2021, Clinical Cancer Research
  • Dysregulation of PRMT5 in chronic lymphocytic leukemia promotes progression with high risk of Richter's transformation, 2023, Nature Communications
  • CDK inhibitors p18(INK4c) and p27(Kip1) mediate two separate pathways to collaboratively suppress pituitary tumorigenesis, 2020, UNC Libraries
  • PRMT5 supports multiple oncogenic pathways in mantle cell lymphoma, 2023, Blood

The scientist collaborates regularly with a group of frequent co-authors including Maurizio Di Liberto, Olivier Elemento, Robert A. Baiocchi, Lapo Alinari, and Xiangao Huang.

Best Publications

  • International Myeloma Working Group molecular classification of multiple myeloma: spotlight review.

    R Fonseca;P L Bergsagel;J Drach;J Shaughnessy

  • Requirement of serine phosphorylation for formation of STAT-promoter complexes

    Xiaokui Zhang;John Blenis;Heng Chun Li;Chris Schindler

  • AID Is Required for c-myc/IgH Chromosome Translocations In Vivo

    Almudena R. Ramiro;Mila Jankovic;Thomas Eisenreich;Thomas Eisenreich;Simone Difilippantonio

  • CDK inhibitors p18(INK4c) and p27(Kip1) mediate two separate pathways to collaboratively suppress pituitary tumorigenesis.

    David S. Franklin;Virginia L. Godfrey;Hayyoung Lee;Grigoriy I. Kovalev

  • Coordinated Silencing of MYC-Mediated miR-29 by HDAC3 and EZH2 as a Therapeutic Target of Histone Modification in Aggressive B-Cell Lymphomas

    Xinwei Zhang;Xinwei Zhang;Xiaohong Zhao;Warren C Fiskus;Jianhong Lin

  • Cell-Cycle Reprogramming for PI3K Inhibition Overrides a Relapse-Specific C481S BTK Mutation Revealed by Longitudinal Functional Genomics in Mantle Cell Lymphoma

    David Chiron;Maurizio Di Liberto;Peter Martin;Xiangao Huang

  • Retinoblastoma protein directly interacts with and activates the transcription factor NF-IL6.

    Phang Lang Chen;Daniel J. Riley;Selina Chen-Kiang;Wen Hwa Lee

  • A Novel Orally Active Small Molecule Potently Induces G1 Arrest in Primary Myeloma Cells and Prevents Tumor Growth by Specific Inhibition of Cyclin-Dependent Kinase 4/6

    Linda B. Baughn;Maurizio Di Liberto;Kaida Wu;Peter L. Toogood

  • Fos and Jun repress transcription activation by NF-IL6 through association at the basic zipper region.

    Wei Hsu;T. K. Kerppola;Phang-Lang Chen;T. Curran

  • The cancer-testis antigens CT7 (MAGE-C1) and MAGE-A3/6 are commonly expressed in multiple myeloma and correlate with plasma-cell proliferation.

    Achim A. Jungbluth;Scott Ely;Maurizio DiLiberto;Ruben Niesvizky

  • Therapeutic Targeting of the Cyclin D3:CDK4/6 Complex in T Cell Leukemia

    Catherine M. Sawai;Jacquelyn Freund;Philmo Oh;Delphine Ndiaye-Lobry

  • Induction of cell cycle arrest and B cell terminal differentiation by CDK inhibitor p18(INK4c) and IL-6.

    Unknown

  • The addition of 5′ cap structures occurs early in hnRNA synthesis and prematurely terminated molecules are capped

    M. Salditt-Georgieff;M. Harpold;S. Chen-Kiang;J.E. Darnell

  • NF-κB1 p50 is required for BLyS attenuation of apoptosis but dispensable for processing of NF-κB2 p100 to p52 in quiescent mature B cells

    Eunice N. Hatada;Richard K.G. Do;Amos Orlofsky;Hsiou Chi Liou

  • N-6-methyl-adenosine in adenovirus type 2 nuclear RNA is conserved in the formation of messenger RNA☆

    Selina Chen-Kiang;Joseph R. Nevins;James E. Darnell

  • Selective inhibition of protein arginine methyltransferase 5 blocks initiation and maintenance of B-cell transformation.

    Lapo Alinari;Kiran V. Mahasenan;Fengting Yan;Vrajesh Karkhanis

  • Deletions of CDKN2C in Multiple Myeloma : Biological and Clinical Implications

    Paola E. Leone;Brian A. Walker;Matthew W. Jenner;Laura Chiecchio

  • Mechanism of BLyS action in B cell immunity.

    Unknown

  • CDK Inhibitor p18INK4c Is Required for the Generation of Functional Plasma Cells

    Michelle R. Tourigny;Josie Ursini-Siegel;Hayyoung Lee;Kai Michael Toellner

  • Telomerase inhibition with an oligonucleotide telomerase template antagonist: in vitro and in vivo studies in multiple myeloma and lymphoma

    Eunice S. Wang;Eunice S. Wang;Eunice S. Wang;Kaida Wu;Kaida Wu;Kaida Wu;Allison C. Chin;Allison C. Chin;Allison C. Chin;Selina Chen-Kiang;Selina Chen-Kiang;Selina Chen-Kiang

Frequent Co-Authors

John P. Leonard
John P. Leonard Cornell University
Morton Coleman
Morton Coleman Cornell University
Olivier Elemento
Olivier Elemento Cornell University
Christopher E. Mason
Christopher E. Mason Cornell University
Malcolm A.S. Moore
Malcolm A.S. Moore Memorial Sloan Kettering Cancer Center
Paul J. Christos
Paul J. Christos Cornell University
Richard R. Furman
Richard R. Furman NewYork–Presbyterian Hospital
Lloyd J. Old
Lloyd J. Old Ludwig Cancer Research
Daniel M. Knowles
Daniel M. Knowles Cornell University
Nina Bhardwaj
Nina Bhardwaj Icahn School of Medicine at Mount Sinai

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