Sarah Swerdlow

ORCID: 0009-0002-4150-753X
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About
Contact & Profiles
Research Areas
  • Chronic Myeloid Leukemia Treatments
  • Autophagy in Disease and Therapy
  • Bacteriophages and microbial interactions
  • Genomics and Phylogenetic Studies
  • Chronic Lymphocytic Leukemia Research
  • Career Development and Diversity
  • RNA Research and Splicing
  • Genomics and Chromatin Dynamics
  • Protein Degradation and Inhibitors
  • RNA and protein synthesis mechanisms
  • Cell death mechanisms and regulation
  • Biomedical and Engineering Education
  • Immune Cell Function and Interaction
  • Eosinophilic Disorders and Syndromes
  • Herpesvirus Infections and Treatments
  • Higher Education and Employability
  • Fungal Plant Pathogen Control
  • Antibiotic Resistance in Bacteria
  • Galectins and Cancer Biology
  • Experimental Learning in Engineering
  • DNA Repair Mechanisms
  • Plant and Fungal Interactions Research
  • Various Chemistry Research Topics
  • Cancer-related gene regulation
  • Bacterial Genetics and Biotechnology

University of Pittsburgh at Greensburg
2023-2025

California Northstate University
2025

University of Pittsburgh
2024

University of California, Berkeley
2024

Thiel College
2014-2022

National Institute of Environmental Health Sciences
2014

University Hospitals of Cleveland
2007-2011

Case Western Reserve University
2007-2011

Comprehensive Blood & Cancer Center
2008

U-M Rogel Cancer Center
2008

It is generally believed that shutting down the kinase activity of BCR-ABL by imatinib will completely inhibit its functions, leading to inactivation downstream signaling pathways and cure disease. Imatinib highly effective at treating human Philadelphia chromosome-positive (Ph(+)) chronic myeloid leukemia (CML) in phase but not Ph(+) B cell acute lymphoblastic (B-ALL) CML blast crisis. We find SRC kinases activated remain fully active imatinib-treated mouse leukemic cells, suggesting does...

10.1073/pnas.0606509103 article EN Proceedings of the National Academy of Sciences 2006-11-02

Glucocorticoid hormones, including dexamethasone, induce apoptosis in lymphocytes and consequently are used clinically as chemotherapeutic agents many hematologic malignancies. Dexamethasone also induces autophagy lymphocytes, although the mechanism is not fully elucidated. Through gene expression analysis, we found that dexamethasone of a encoding stress response protein variously referred to Dig2, RTP801, or REDD1. This reported inhibit mammalian target rapamycin (mTOR) signaling. Because...

10.1074/jbc.m111.245423 article EN cc-by Journal of Biological Chemistry 2011-07-07

Glucocorticosteroid hormones, including prednisone and dexamethasone (Dex), have been used to treat lymphoid malignancies for many years because they readily induce apoptosis in immature lymphocytes lacking Bcl-2. However, elevated expression of the anti-apoptotic protein Bcl-2 inhibits contributes glucocorticoid resistance. Using Bcl-2-negative WEHI7.2 lymphoma line as an experimental model, we found that Dex not only induces but also autophagy. The caspase inhibitor Z-VAD-fmk inhibited...

10.4161/auto.5920 article EN Autophagy 2008-07-01

A report on research that explicates three models of pedagogical practice underpin and characterize inquiry instruction in a course-based experience.

10.1187/cbe.21-03-0057 article EN CBE—Life Sciences Education 2022-01-03

Alternative transcription start sites can affect transcript isoform diversity and translation levels. In a recently described form of gene regulation, coordinated transcriptional translational interference results in isoform-dependent changes protein expression. Specifically, long undecoded (LUTI) is transcribed from gene-distal promoter, interfering with expression the gene-proximal promoter. Although chromatin features associated LUTI have been described, mechanism underlying LUTI-based...

10.1016/j.molcel.2024.06.029 article EN cc-by-nc Molecular Cell 2024-07-22

Two bacteriophages, BeatusComedenti and Cyan, were isolated using Arthrobacter sp. globiformis , respectively. which contain 100 70 putative genes, are assigned to actinobacteriophage clusters AT AZ1,

10.17912/micropub.biology.001417 article EN PubMed 2025-01-01

e18531 Background: Ponatinib has been well studied in treating Chronic Myeloid Leukemia. However, there are no reviews to date analyzing the efficacy of ponatinib Ph+ Acute Lymphoblastic Leukemia (ALL). is a 3rd generation, broad-spectrum tyrosine kinase inhibitor (TKI) designed suppress mutations conferring resistance earlier generations TKIs including threonine isoleucine mutation at position 315 (T315I) BCR-ABL fusion protein. We aim review clinical studies evaluating ALL populations....

10.1200/jco.2025.43.16_suppl.e18531 article EN Journal of Clinical Oncology 2025-05-28

Bacteria in the Arthrobacter genus belong to phylum Actinobacteria and are primarily soil-dwelling. Over 600 bacteriophages infecting hosts have been isolated sequenced, genomic analyses show these phages be highly diverse with mosaic genome architectures. We describe here a group of 32 grouped Cluster AZ, on four different strains all siphoviral morphologies. The AZ exhibit spectrum diversity can subdivided into subclusters. intracluster was analyzed in-depth at whole level through...

10.1101/2025.05.26.655371 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2025-05-27

10.1016/j.mrfmmm.2014.09.004 article EN Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 2014-09-27
David I. Hanauer Richard M. Alvey Ping An Christa T. Bancroft Kristen Butela and 84 more Sean T. Coleman Kari Clase Patrick Collins Stephanie B. Conant Pamela L. Connerly Bernadette J. Connors Megan K. Dennis Erin Doyle Dustin Edwards Christy Fillman Ann M. Findley Victoria Frost Maria D. Gainey Urszula Golebiewska Nancy Guild Sharon Gusky Allison A. Johnson Kristen Johnson Karen K. Klyczek Julia Y. Lee‐Soety Heather Lindberg Matthew D. Mastropaolo Julie A. Merkle Jon Mitchell Sally D. Molloy Fernando Nieto Jillian C. Nissen Tiara Pérez Morales Nick T. Peters Susanne P. Pfeifer Richard S. Pollenz Mary L. Preuss Germán Rosas-Acosta Margaret S. Saha Amy B. Sprenkle C. Nicole Sunnen Deborah M. Tobiason Sara S. Tolsma Vassie C. Ware Yesmi Patricia Ahumada‐Santos Regina V. Alvarez Justin Anderson Mary A. Ayuk María Elena Báez‐Flores D. Smith Bailey Frederick N. Baliraine Elizabeth Behr Andréa Beyer Suparna Bhalla Laura Cecilia Bono Donald P. Breakwell Christine A. Byrum Iain Duffy Alyssa M. Gleichsner Melinda Harrison Renee Ho Lee E. Hughes Jacob D. Kagey Kathryn P. Kohl Sean P. McClory Alison E. Moyer María Alejandra Mussi Holly Nance Imade Y. Nsa Shallee T. Page Jesús Ricardo Parra Unda Jessica M. Rocheleau Sarah Swerdlow Kara Thoemke Megan S. Valentine Quinn Vega Catherine Ward Daniel C. Williams Ellen Wisner William H. Biederman Steven G. Cresawn Mark Graham Graham F. Hatfull Danielle M. Heller Deborah Jacobs-Sera Denise L. Monti Pushpa Ramakrishna Daniel A. Russell Viknesh Sivanathan

The professional identity of scientists has historically been cultivated to value research over teaching, which can undermine initiatives that aim reform science education. Course-Based Research Experiences (CRE) and the inclusive Education Communities (iREC) are two successful impactful efforts integrate teaching. this study is explicate instructors who implement a CRE within an established iREC explore how contributes success these programs. 97 from Science Alliance (SEA) participated in...

10.3389/feduc.2024.1442306 article EN cc-by Frontiers in Education 2024-10-24

VOLUME 286 (2011) PAGES 30181–30189 The grant information footnote should read as follows. This work was supported, in whole or part, by National Institutes of Health Grants R01 CA42755 and CA85804 (to C. W. D.), AG031903 S. M.), T32 HL007147 J. K. GM007250 M.). “Acknowledgments” Dig2/RTP801 knock-out mice were obtained from Quark Pharmaceuticals, Inc., for whom they exclusively generated at Lexicon. We thank Tamotsu Yoshimori Noboru Mizushima providing LC3 cDNA Mark Jackson suggestions...

10.1074/jbc.a111.245423 article EN cc-by Journal of Biological Chemistry 2011-11-01

Alternative transcription start sites can affect transcript isoform diversity and translation levels. In a recently described form of gene regulation, coordinated transcriptional translational interference results in isoform-dependent changes protein expression. Specifically, long undecoded (LUTI) is transcribed from gene-distal promoter, interfering with expression the gene-proximal promoter. While chromatin features associated LUTI have been described, mechanism underlying LUTI-based not...

10.1101/2023.04.27.538572 preprint EN cc-by-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-04-27

Course-based undergraduate research experiences (CUREs) provide a way for students to gain experience in classroom setting. Few examples of cell culture CUREs or online exist the literature.

10.1128/jmbe.v22i1.2619 article EN cc-by-nc-nd Journal of Microbiology and Biology Education 2021-04-30

BabyYoda and Lynlen are two cluster EB phages that were discovered at Thiel College using

10.1128/mra.01006-23 article EN Microbiology Resource Announcements 2023-12-22
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