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Single-Cell Transcriptomic Analysis of Tumor-Derived Fibroblasts and Normal Tissue-Resident Fibroblasts Reveals Fibroblast Heterogeneity in Breast Cancer

Cancers, 2020-05, Vol.12 (5), p.1307

2020

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Synthetic antibacterial minerals: harnessing a natural geochemical reaction to combat antibiotic resistance

Scientific reports, 2022-01, Vol.12 (1), p.1218-1218, Article 1218

2022

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Single-cell RNA-Seq reveals changes in immune landscape in post-traumatic osteoarthritis

Frontiers in immunology, 2022-07, Vol.13, p.938075-938075

2022

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Methionine Adenosyltransferase 1a (MAT1A) Enhances Cell Survival During Chemotherapy Treatment and is Associated with Drug Resistance in Bladder Cancer PDX Mice

International journal of molecular sciences, 2019-10, Vol.20 (20), p.4983

2019

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Loss of Cadherin-11 in pancreatic ductal adenocarcinoma alters tumor-immune microenvironment

Frontiers in oncology, 2023-10, Vol.13, p.1286861-1286861

2023

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IL-17A Increases Doxorubicin Efficacy in Triple Negative Breast Cancer

Frontiers in oncology, 2022-07, Vol.12, p.928474-928474

2022

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Comparative Molecular Analysis of Cancer Behavior Cultured In Vitro, In Vivo, and Ex Vivo

Cancers, 2020-03, Vol.12 (3), p.690

2020

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Curcumin Nanodiscs Improve Solubility and Serve as Radiological Protectants against Ionizing Radiation Exposures in a Cell-Cycle Dependent Manner

Nanomaterials (Basel, Switzerland), 2022-10, Vol.12 (20), p.3619

2022

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Immediate effects of acute Mars mission equivalent doses of SEP and GCR radiation on the murine gastrointestinal system-protective effects of curcumin-loaded nanolipoprotein particles (cNLPs)

Frontiers in astronomy and space sciences, 2023, Vol.10

2023

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Tracking Tumor Colonization in Xenograft Mouse Models Using Accelerator Mass Spectrometry

Scientific reports, 2018-10, Vol.8 (1), p.15013-10, Article 15013

2018

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Discovery of potent and orally bioavailable heterocycle-based β3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2007-09, Vol.17 (18), p.5245-5250

2007

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Discovery of Potent, Nonsteroidal, and Highly Selective Glucocorticoid Receptor Antagonists

Journal of medicinal chemistry, 2002-06, Vol.45 (12), p.2417-2424

2002

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Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (22), p.6797-6801

2010

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Potent and selective, sulfamide-based human β3-adrenergic receptor agonists

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (12), p.3235-3240

2004

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In Vitro and in Vivo Characterization of 3-{2-[6-(2-tert-Butoxyethoxy)pyridin-3-yl]-1H-imidazol-4-yl}benzonitrile Hydrochloride Salt, a Potent and Selective NPY5 Receptor Antagonist

Journal of medicinal chemistry, 2003-02, Vol.46 (5), p.670-673

2003

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Methionine Adenosyltransferase 1a (MAT1A) Enhances Cell Survival During Chemotherapy Treatment and is Associated with Drug Resistance in Bladder Cancer PDX Mice

International journal of molecular sciences, 2019-10, Vol.20 (20)

2019

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Abstract PO065: Single cell transcriptomics of triple negative breast cancer allografts following chemotherapy treatment reveals increased T cell abundance in doxorubicin-sensitive tumors

Cancer immunology research, 2021-02, Vol.9 (2_Supplement), p.PO065-PO065

2021

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Missed Appointment Rates and the Implication on Primary Care Practice

Martin, Kelly A

2020

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Slaves as criminal informers in ancient Rome

International journal of comparative and applied criminal justice, 1999-09, Vol.23 (2), p.307-312

Kelly, Martin A.

1999

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Jesus and police brutality

International journal of comparative and applied criminal justice, 1999-04, Vol.23 (1), p.137-140

Kelly, Martin A.

1999

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Executive security in imperial Rome

International journal of comparative and applied criminal justice, 1998-09, Vol.22 (2), p.341-350

Kelly, Martin A.

1998

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Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl -4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6- y l]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (22), p.6797-6801

2010

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Discovery of potent and orally bioavailable heterocycle-based beta3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2007-09, Vol.17 (18), p.5245-5250

2007

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Discovery of potent and orally bioavailable heterocycle-based β 3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2007, Vol.17 (18), p.5245-5250

2007

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In vitro and in vivo characterization of 3-[2-[6-(2-tert-butoxyethoxy)pyridin-3-yl]-1H-imidazol-4-yl]benzonitrile hydrochloride salt, a potent and selective NPY5 receptor antagonist

Journal of medicinal chemistry, 2003-02, Vol.46 (5), p.670-673

2003

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Single-Cell Transcriptomic Analysis of Tumor-Derived Fibroblasts and Normal Tissue-Resident Fibroblasts Reveals Fibroblast Heterogeneity in Breast Cancer

Synthetic antibacterial minerals: harnessing a natural geochemical reaction to combat antibiotic resistance

Single-cell RNA-Seq reveals changes in immune landscape in post-traumatic osteoarthritis

Methionine Adenosyltransferase 1a (MAT1A) Enhances Cell Survival During Chemotherapy Treatment and is Associated with Drug Resistance in Bladder Cancer PDX Mice

Loss of Cadherin-11 in pancreatic ductal adenocarcinoma alters tumor-immune microenvironment

IL-17A Increases Doxorubicin Efficacy in Triple Negative Breast Cancer

Comparative Molecular Analysis of Cancer Behavior Cultured In Vitro, In Vivo, and Ex Vivo

Curcumin Nanodiscs Improve Solubility and Serve as Radiological Protectants against Ionizing Radiation Exposures in a Cell-Cycle Dependent Manner

Immediate effects of acute Mars mission equivalent doses of SEP and GCR radiation on the murine gastrointestinal system-protective effects of curcumin-loaded nanolipoprotein particles (cNLPs)

Tracking Tumor Colonization in Xenograft Mouse Models Using Accelerator Mass Spectrometry

Discovery of potent and orally bioavailable heterocycle-based β3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Discovery of Potent, Nonsteroidal, and Highly Selective Glucocorticoid Receptor Antagonists

Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

Potent and selective, sulfamide-based human β3-adrenergic receptor agonists

In Vitro and in Vivo Characterization of 3-{2-[6-(2-tert-Butoxyethoxy)pyridin-3-yl]-1H-imidazol-4-yl}benzonitrile Hydrochloride Salt, a Potent and Selective NPY5 Receptor Antagonist

Methionine Adenosyltransferase 1a (MAT1A) Enhances Cell Survival During Chemotherapy Treatment and is Associated with Drug Resistance in Bladder Cancer PDX Mice

Abstract PO065: Single cell transcriptomics of triple negative breast cancer allografts following chemotherapy treatment reveals increased T cell abundance in doxorubicin-sensitive tumors

Missed Appointment Rates and the Implication on Primary Care Practice

Slaves as criminal informers in ancient Rome

Jesus and police brutality

Executive security in imperial Rome

Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl -4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6- y l]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

Discovery of potent and orally bioavailable heterocycle-based beta3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Discovery of potent and orally bioavailable heterocycle-based β 3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

In vitro and in vivo characterization of 3-[2-[6-(2-tert-butoxyethoxy)pyridin-3-yl]-1H-imidazol-4-yl]benzonitrile hydrochloride salt, a potent and selective NPY5 receptor antagonist

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