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The Journal of the Acoustical Society of America
|
November 15, 2018
Prediction of three articulatory categories in vocal sound imitations using models for auditory receptive fields
Anders Friberg, Tony Lindeberg, Martin Hellwagner, et al.
ACS Omega
|
June 18, 2020
Structural Evidence for Isoform-Selective Allosteric Inhibition of Lactate Dehydrogenase A
Anders Friberg, Hartmut Rehwinkel, Duy Nguyen, et al.
Reviews in Endocrine & Metabolic Disorders
|
February 23, 2011
Hedonic and incentive signals for body weight control
Emil Egecioglu, Karolina P Skibicka, Caroline Hansson, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
February 2, 2006
Nuclear progesterone receptor A and B isoforms in mouse fallopian tube and uterus: implications for expression, regulation, and cellular function
Ruijin Shao, Birgitta Weijdegård, Karin Ljungström, et al.
Biology of Reproduction
|
September 24, 2004
Progesterone-receptor antagonists and statins decrease de novo cholesterol synthesis and increase apoptosis in rat and human periovulatory granulosa cells in vitro
Emilia Rung, P Anders Friberg, Ruijin Shao, et al.
Journal of Medicinal Chemistry
|
December 19, 2012
Discovery of potent myeloid cell leukemia 1 (Mcl-1) inhibitors using fragment-based methods and structure-based design
Anders Friberg, Dominico Vigil, Bin Zhao, et al.
Chemmedchem
|
April 3, 2020
Computationally Empowered Workflow Identifies Novel Covalent Allosteric Binders for KRAS<sup>G12C</sup>
Jérémie Mortier, Anders Friberg, Volker Badock, et al.
Journal of Medicinal Chemistry
|
May 19, 2026
Identification of the Piperidyl Urea Derivative BAY-439 as a Potent and Selective Inhibitor of Human Phospholipase A<sub>2</sub> Group V (hPLA<sub>2</sub>-G5) for the Treatment of Inflammatory Pain
Gernot Langer, Nico Bräuer, Daryl Walter, et al.
Journal of Medicinal Chemistry
|
April 7, 2015
Discovery of tricyclic indoles that potently inhibit Mcl-1 using fragment-based methods and structure-based design
Jason P Burke, Zhiguo Bian, Subrata Shaw, et al.
Journal of Medicinal Chemistry
|
September 27, 2024
Discovery of BAY-405: An Azaindole-Based MAP4K1 Inhibitor for the Enhancement of T-Cell Immunity against Cancer
Jeffrey Mowat, Rafael Carretero, Gabriele Leder, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
The Journal of the Acoustical Society of America
|
November 15, 2018
Prediction of three articulatory categories in vocal sound imitations using models for auditory receptive fields
Anders Friberg, Tony Lindeberg, Martin Hellwagner, et al.
ACS Omega
|
June 18, 2020
Structural Evidence for Isoform-Selective Allosteric Inhibition of Lactate Dehydrogenase A
Anders Friberg, Hartmut Rehwinkel, Duy Nguyen, et al.
Reviews in Endocrine & Metabolic Disorders
|
February 23, 2011
Hedonic and incentive signals for body weight control
Emil Egecioglu, Karolina P Skibicka, Caroline Hansson, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
February 2, 2006
Nuclear progesterone receptor A and B isoforms in mouse fallopian tube and uterus: implications for expression, regulation, and cellular function
Ruijin Shao, Birgitta Weijdegård, Karin Ljungström, et al.
Biology of Reproduction
|
September 24, 2004
Progesterone-receptor antagonists and statins decrease de novo cholesterol synthesis and increase apoptosis in rat and human periovulatory granulosa cells in vitro
Emilia Rung, P Anders Friberg, Ruijin Shao, et al.
Journal of Medicinal Chemistry
|
December 19, 2012
Discovery of potent myeloid cell leukemia 1 (Mcl-1) inhibitors using fragment-based methods and structure-based design
Anders Friberg, Dominico Vigil, Bin Zhao, et al.
Chemmedchem
|
April 3, 2020
Computationally Empowered Workflow Identifies Novel Covalent Allosteric Binders for KRAS<sup>G12C</sup>
Jérémie Mortier, Anders Friberg, Volker Badock, et al.
Journal of Medicinal Chemistry
|
May 19, 2026
Identification of the Piperidyl Urea Derivative BAY-439 as a Potent and Selective Inhibitor of Human Phospholipase A<sub>2</sub> Group V (hPLA<sub>2</sub>-G5) for the Treatment of Inflammatory Pain
Gernot Langer, Nico Bräuer, Daryl Walter, et al.
Journal of Medicinal Chemistry
|
April 7, 2015
Discovery of tricyclic indoles that potently inhibit Mcl-1 using fragment-based methods and structure-based design
Jason P Burke, Zhiguo Bian, Subrata Shaw, et al.
Journal of Medicinal Chemistry
|
September 27, 2024
Discovery of BAY-405: An Azaindole-Based MAP4K1 Inhibitor for the Enhancement of T-Cell Immunity against Cancer
Jeffrey Mowat, Rafael Carretero, Gabriele Leder, et al.
Page
of 5