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Human Molecular Genetics
|
December 22, 2018
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in mice
Roberto Silva-Rojas, Susan Treves, Hugues Jacobs, et al.
In Vivo (Athens, Greece)
|
February 2, 2011
Cell death after high-LET irradiation in orthotopic human hepatocellular carcinoma in vivo
Anaïs Altmeyer, Mihaela Ignat, Jean-Marc Denis, et al.
International Journal of Nanomedicine
|
July 16, 2011
Microencapsulation of nanoemulsions: novel Trojan particles for bioactive lipid molecule delivery
Xiang Li, Nicolas Anton, Thi Minh Chau Ta, et al.
Diabetes
|
July 13, 2022
PATAS, a First-in-Class Therapeutic Peptide Biologic, Improves Whole-Body Insulin Resistance and Associated Comorbidities In Vivo
Edwige Schreyer, Cathy Obringer, Nadia Messaddeq, et al.
Circulation
|
June 18, 2003
Overexpression of the serotonin 5-HT2B receptor in heart leads to abnormal mitochondrial function and cardiac hypertrophy
Canan G Nebigil, Fabrice Jaffré, Nadia Messaddeq, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
December 22, 2009
Divergent roles of prokineticin receptors in the endothelial cells: angiogenesis and fenestration
Célia Guilini, Kyoji Urayama, Gulen Turkeri, et al.
Developmental Biology
|
July 26, 2005
TAF10 is required for the establishment of skin barrier function in foetal, but not in adult mouse epidermis
Arup Kumar Indra, William S Mohan, Mattia Frontini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 23, 2013
Lack of myotubularin (MTM1) leads to muscle hypotrophy through unbalanced regulation of the autophagy and ubiquitin-proteasome pathways
Lama Al-Qusairi, Ivana Prokic, Leonela Amoasii, et al.
Biochimica Et Biophysica Acta
|
December 17, 2008
Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasia
Stéphanie Pannier, Vincent Couloigner, Nadia Messaddeq, et al.
Cardiovascular Research
|
September 23, 2008
Transgenic myocardial overexpression of prokineticin receptor-2 (GPR73b) induces hypertrophy and capillary vessel leakage
Kyoji Urayama, Deniz B Dedeoglu, Célia Guilini, et al.
Page
of 11
Search research articles
Search
Showing results (11-20 of 108) with videos related to
Sort By:
Page
of 11
Human Molecular Genetics
|
December 22, 2018
STIM1 over-activation generates a multi-systemic phenotype affecting the skeletal muscle, spleen, eye, skin, bones and immune system in mice
Roberto Silva-Rojas, Susan Treves, Hugues Jacobs, et al.
In Vivo (Athens, Greece)
|
February 2, 2011
Cell death after high-LET irradiation in orthotopic human hepatocellular carcinoma in vivo
Anaïs Altmeyer, Mihaela Ignat, Jean-Marc Denis, et al.
International Journal of Nanomedicine
|
July 16, 2011
Microencapsulation of nanoemulsions: novel Trojan particles for bioactive lipid molecule delivery
Xiang Li, Nicolas Anton, Thi Minh Chau Ta, et al.
Diabetes
|
July 13, 2022
PATAS, a First-in-Class Therapeutic Peptide Biologic, Improves Whole-Body Insulin Resistance and Associated Comorbidities In Vivo
Edwige Schreyer, Cathy Obringer, Nadia Messaddeq, et al.
Circulation
|
June 18, 2003
Overexpression of the serotonin 5-HT2B receptor in heart leads to abnormal mitochondrial function and cardiac hypertrophy
Canan G Nebigil, Fabrice Jaffré, Nadia Messaddeq, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
December 22, 2009
Divergent roles of prokineticin receptors in the endothelial cells: angiogenesis and fenestration
Célia Guilini, Kyoji Urayama, Gulen Turkeri, et al.
Developmental Biology
|
July 26, 2005
TAF10 is required for the establishment of skin barrier function in foetal, but not in adult mouse epidermis
Arup Kumar Indra, William S Mohan, Mattia Frontini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 23, 2013
Lack of myotubularin (MTM1) leads to muscle hypotrophy through unbalanced regulation of the autophagy and ubiquitin-proteasome pathways
Lama Al-Qusairi, Ivana Prokic, Leonela Amoasii, et al.
Biochimica Et Biophysica Acta
|
December 17, 2008
Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasia
Stéphanie Pannier, Vincent Couloigner, Nadia Messaddeq, et al.
Cardiovascular Research
|
September 23, 2008
Transgenic myocardial overexpression of prokineticin receptor-2 (GPR73b) induces hypertrophy and capillary vessel leakage
Kyoji Urayama, Deniz B Dedeoglu, Célia Guilini, et al.
Page
of 11