Samuel M. Cohen

ORCID: 0000-0003-4277-6184
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About
Contact & Profiles
Research Areas
  • Carcinogens and Genotoxicity Assessment
  • Peroxisome Proliferator-Activated Receptors
  • Neuroscience and Neuropharmacology Research
  • Arsenic contamination and mitigation
  • Pharmacogenetics and Drug Metabolism
  • Animal testing and alternatives
  • Genomics, phytochemicals, and oxidative stress
  • Effects and risks of endocrine disrupting chemicals
  • Sulfur Compounds in Biology
  • Hedgehog Signaling Pathway Studies
  • Toxic Organic Pollutants Impact
  • Pesticide Exposure and Toxicity
  • Bladder and Urothelial Cancer Treatments
  • RNA Research and Splicing
  • Potato Plant Research
  • Genetics and Neurodevelopmental Disorders
  • Ubiquitin and proteasome pathways
  • Developmental Biology and Gene Regulation
  • Epigenetics and DNA Methylation
  • Biochemical Analysis and Sensing Techniques
  • Heavy Metal Exposure and Toxicity
  • Environmental Toxicology and Ecotoxicology
  • Cancer, Lipids, and Metabolism
  • Metabolomics and Mass Spectrometry Studies
  • Immunotoxicology and immune responses

University of Nebraska Medical Center
2007-2025

University of Pennsylvania
2024

NYU Langone Health
2012-2023

Stanford University
2021

Harvard University
2013-2020

Dana-Farber Cancer Institute
2013-2020

Second Affiliated Hospital of Zhejiang University
2018

New York University
2014-2018

Nebraska Medical Center
1977-2014

University of British Columbia
2004

The last several years have seen considerable confusion regarding the terms "apoptosis" and "necrosis" in pathology. This situation prompted Society of Toxicologic Pathologists to charter Committee on Nomenclature Cell Death, which was charged with making recommendations about use toxicity studies. recommends term describe findings comprising dead cells histological sections, regardless pathway by died. modifiers "apoptotic" "oncotic" or "mixed apoptotic oncotic" are recommended specify...

10.1177/019262339902700419 article EN Toxicologic Pathology 1999-07-01
Gerald Matchett Irina Gasanova Christina A. Riccio Dawood Nasir Mary Sunna and 95 more Brian J. Bravenec Omaira Azizad Brian Farrell Abu Minhajuddin Jesse W. Stewart Lawrence W. Liang Tiffany S. Moon Pamela E. Fox Callie Ebeling Miakka N. Smith Devin M. Trousdale Babatunde Ogunnaike Anand M. Abraham Robert S. Ackerman Oluwafunmilayo B. Adebayo-Adonis Venkatesh Aiyagari Aditee P. Ambardekar Kelechi B. Anyaehie David M. Bashover Matthew Burke Bourneuf James R. Brann Grace Wilkowski Bryant Matthew P. Bunker Leigh Anne Catoe Catherine Chen Jeffrey S. Chen Joy Lo Chen Gloria Cheng Ivan Nicholas Chew Jeanette Chin Samuel M. Cohen Mary Abigail Cowlishaw Janice Davis Jennifer L. Davis TomMario Alando Davis David G. DePinto Paul E. Dilfer Renee D. Doherty Philip James DuChamp Katherine L. Duncan Colin C. Ehlenbach Ahmad Elsharydah Sonia D. Estes Akil Farishta William Eric Foster David Francis Shannon Garitty Nicholas W. Gill Louise A. Gliga Joseph Arthur Graham Nancy B. Greilich Jessica E. Grundt Allan J. Hamilton Hooman Heravi Douglas C. Huynh Ray K. Hwong Rachel E. Jacobs Syed Jaffery Aveline P. Jerome Suja John Enas Kandil Asif Khan Sarah Khorsand Jennifer Meeyun Kim Elena Koepke Grayson Jeffrey Koval Brian P. Kurtz Xuan T. Langridge Gene W. Lee Simon J. Craddock Lee Matthew Leveno Dawn Lewellen Frederick C. Li Nathaniel Loo Xi Luo Rachelle A. Makinde Anna Martin Evan Z. Mayes Diane E. McCune John McGrimley Jennifer J. McGuire Kyle Meinhardt Akeel Merchant Zahid Merchant David Mercier Brandon Mitchell Andrea J. Murray Shamsideen O. Musa Geoffrey Edward Nelson Seth Nelson L. H. Nguyen Linsey Nohrn Osamudiamen O. Obanor Chinwe C. Ononogbu Mihir Parikh

10.1007/s00134-021-06577-x article EN Intensive Care Medicine 2021-12-14

Four trivalent arsenic species, inorganic arsenite (iAs(III)), monomethylarsonous acid (MMA(III)), dimethylarsinous (DMA(III)), and phenylarsine oxide (PhAs(III)O), have shown increasing binding affinity with the hemoglobin (Hb) of rats humans. The stoichiometry was consistent number reactive cysteine residues in alpha beta chains Hb. Comparing rat Hb human for same 3-16 times stronger than as demonstrated by their apparent constants. Comparative experiments involving incubation red blood...

10.1021/tx049756s article EN Chemical Research in Toxicology 2004-11-26

The two-year rodent bioassay remains the mainstay for carcinogenicity testing, although numerous difficulties have been identified. Fundamentally, a chemical can increase risk of cancer (1) by damaging DNA directly (DNA reactive) or (2) indirectly increasing number replications (non-DNA reactive). Mechanistic research has identified precursor lesions in sequence key events necessary neoplasia development. Based on these concepts, author proposed short-term (thirteen-week) assay screening...

10.1177/0192623310363813 article EN Toxicologic Pathology 2010-03-09

High doses of sodium phenobarbital (NaPB), a constitutive androstane receptor (CAR) activator, have been shown to produce hepatocellular tumors in rodents by mitogenic mode action (MOA) involving CAR activation. The effect 1-week dietary treatment with NaPB on liver weight and histopathology, hepatic CYP2B enzyme activity CYP2B/3A mRNA expression, replicative DNA synthesis selected genes related cell proliferation, functional transcriptomic metabolomic analyses was studied male CD-1 mice,...

10.1093/toxsci/kfu173 article EN Toxicological Sciences 2014-08-21

Learning and memory depend on neuronal plasticity originating at the synapse requiring nuclear gene expression to persist. However, how synapse-to-nucleus communication supports long-term behavior has remained elusive. Among cytonuclear signaling proteins, γCaMKII stands out in its ability rapidly shuttle Ca2+/CaM nucleus thus activate CREB-dependent transcription. Here we show that elimination of prevents activity-dependent key genes (BDNF, c-Fos, Arc), inhibits persistent synaptic...

10.1038/s41467-018-04705-8 article EN cc-by Nature Communications 2018-06-18

Sonic Hedgehog (Shh) signaling is crucial for growth, cell fate determination, and axonal guidance in the developing nervous system. Although receptors Patched (Ptch1) Smoothened (Smo) are required Shh signaling, a number of distinct co-receptors contribute to these critical responses Shh. Several membrane-embedded proteins such as Boc, Cdo, Gas1 bind promote signaling. In addition, heparan sulfate proteoglycans (HSPGs) have also been implicated initiation responses. However, attributes...

10.1074/jbc.m112.438937 article EN cc-by Journal of Biological Chemistry 2013-07-19

Chronic progressive nephropathy (CPN) is a spontaneous renal disease of rats which can be serious confounder in toxicology studies. It with known physiological factors that modify progression, such as high dietary protein. The weight evidence supports an absence counterpart humans. There extensive advanced CPN, particularly end-stage kidney, risk factor for development background incidence atypical tubule hyperplasia and tumors (RTT). likely cause underlying this association neoplasia the...

10.1093/toxsci/kfs305 article EN cc-by-nc Toxicological Sciences 2012-10-26

Abstract Bovine rumen fluid and slurried hamster feces completely reduced millimolar levels of arsenate to arsenite upon incubation under anoxic conditions. This activity was strongly inhibited by autoclaving or aerobic conditions, partially tungstate chloramphenicol. The rate reduction faster in from a population arsenate-watered (100 ppm) hamsters compared control group watered without arsenate. Using radioisotope methods, reductase also detected at very low concentrations added (...

10.1111/j.1574-6941.2002.tb00966.x article EN FEMS Microbiology Ecology 2002-07-01

The present study was conducted to determine whether long-lasting desensitization of bladder afferents could be achieved using a single local application the capsaicin (CAP)-like irritant resiniferatoxin (RTX), and compare effects RTX CAP on behavioral histological endpoints. While rats were anesthetized, vehicle (VEH), (10-100 nmol) or mumol) instilled in (intravesical, i.ves.) via cannula surgically implanted into dome. Beginning 1 week after treatment, once per for 4 weeks, tested...

10.1016/0304-3959(94)00193-i article EN Pain 1995-05-01
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