Papers

With Tag: Medicinal Chemistry

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Novel Zn 2+ Modulated GPR39 Receptor Agonists Do Not Drive Acute Insulin Secretion in Rodents

PLOS ONE | 2015 | 10.1371/journal.pone.0145849

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Angiotensin Type 2 Receptor Stimulation Ameliorates Left Ventricular Fibrosis and Dysfunction via Regulation of Tissue Inhibitor of Matrix Metalloproteinase 1/Matrix Metalloproteinase 9 Axis and Transforming Growth Factor β1 in the Rat Heart

Christa Thonereineke, Bjorn Dahlof, Dilyara Lauer, Anders Hallberg, Elena Kaschina, Yuliya Sharkovska, Ulrich Kintscher, Svetlana Slavic, Manuela Sommerfeld, Thomas Unger, Ulrike Muscha Steckelings
Hypertension | 2014 | 10.1161/HYPERTENSIONAHA.113.02522

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Prospects for Inhibitors of Protein Tyrosine Phosphatase 1B as Antidiabetic Drugs.

Cheminform | 2004 | 10.1002/chin.200443228

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Designer drugs: a medicinal chemistry perspective

Annals of the New York Academy of Sciences | 2012 | 10.1111/j.1749-6632.2011.06199.x

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Synthesis, Antimycobacterial Activity and 3‐D QSAR Studies of Some New Derivatives of p‐Hydroxybenzohydrazide

Kishore P Bhusari, Ritesh P Bhole
Qsar & Combinatorial Science | 2009 | 10.1002/qsar.200960064

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Multi‐Objective Feature Selection in QSAR Using a Machine Learning Approach

Axel J Soto, Ignacio Ponzoni, Gustavo E Vazquez, Rocio L Cecchini
Qsar & Combinatorial Science | 2009 | 10.1002/qsar.200960053

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Lability Landscape and Protease Resistance of Human Insulin Amyloid: A New Insight into Its Molecular Properties

Journal of Molecular Biology | 2010 | 10.1016/j.jmb.2009.11.012

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Effects of glucosamine sulfate on intracellular UDP-hexosamine and UDP-glucuronic acid levels in bovine primary chondrocytes

Osteoarthritis and Cartilage | 2007 | 10.1016/j.joca.2007.01.010

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Mortality associated with neurofibromatosis type 1: A study based on Italian death certificates (1995-2006)

Orphanet Journal of Rare Diseases | 2011 | 10.1186/1750-1172-6-11

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Mutation spectrum of MLL2 in a cohort of kabuki syndrome patients

Orphanet Journal of Rare Diseases | 2011 | 10.1186/1750-1172-6-38

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Phenylketonuria: reduced tyrosine brain influx relates to reduced cerebral protein synthesis

Orphanet Journal of Rare Diseases | 2013 | 10.1186/1750-1172-8-133

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Cri du Chat syndrome

Orphanet Journal of Rare Diseases | 2006 | 10.1186/1750-1172-1-33

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Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

Orphanet Journal of Rare Diseases | 2014

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