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Scientific Reports
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July 2, 2016
Stimulated emission of Cooper pairs in a high-temperature cuprate superconductor
Wentao Zhang, Tristan Miller, Christopher L Smallwood, et al.
European Journal of Pediatrics
|
September 7, 2005
Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy
Maja von der Hagen, Angela M Kaindl, Kathrin Koehler, et al.
Nutrients
|
June 24, 2022
Selenium Status in Paediatric Patients with Neurodevelopmental Diseases
Christian L Görlich, Qian Sun, Viola Roggenkamp, et al.
Journal of Child Neurology
|
February 12, 2008
Spinal muscular atrophy with respiratory distress type 1 (SMARD1)
Angela M Kaindl, Ulf-Peter Guenther, Sabine Rudnik-Schöneborn, et al.
Leukemia
|
November 19, 2013
Blocking ETV6/RUNX1-induced MDM2 overexpression by Nutlin-3 reactivates p53 signaling in childhood leukemia
U Kaindl, M Morak, C Portsmouth, et al.
Journal of Child Neurology
|
August 12, 2006
Selenoprotein N muscular dystrophy: differential diagnosis for early-onset limited mobility of the spine
Stefanie Sponholz, Maja von der Hagen, Gabriele Hahn, et al.
Physical Review. B, Condensed Matter
|
February 1, 1993
Orbital character of states at the Fermi level in La2-xSrxCuO4 and R2-xCexCuO4 (R=Nd,Sm)
Pellegrin, Nücker, Fink, et al.
Annals of Neurology
|
December 11, 2008
Erythropoietin protects the developing brain from hyperoxia-induced cell death and proteome changes
Angela M Kaindl, Marco Sifringer, Andrea Koppelstaetter, et al.
Developmental Neuroscience
|
August 13, 2009
Erythropoietin attenuates hyperoxia-induced cell death by modulation of inflammatory mediators and matrix metalloproteinases
Marco Sifringer, Kerstin Genz, Daniela Brait, et al.
Molecular Neurobiology
|
August 22, 2016
Early Changes in Hippocampal Neurogenesis in Transgenic Mouse Models for Alzheimer's Disease
M S Unger, J Marschallinger, J Kaindl, et al.
Page
of 55
Search research articles
Search
Showing results (351-360 of 543) with videos related to
Sort By:
Page
of 55
Scientific Reports
|
July 2, 2016
Stimulated emission of Cooper pairs in a high-temperature cuprate superconductor
Wentao Zhang, Tristan Miller, Christopher L Smallwood, et al.
European Journal of Pediatrics
|
September 7, 2005
Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy
Maja von der Hagen, Angela M Kaindl, Kathrin Koehler, et al.
Nutrients
|
June 24, 2022
Selenium Status in Paediatric Patients with Neurodevelopmental Diseases
Christian L Görlich, Qian Sun, Viola Roggenkamp, et al.
Journal of Child Neurology
|
February 12, 2008
Spinal muscular atrophy with respiratory distress type 1 (SMARD1)
Angela M Kaindl, Ulf-Peter Guenther, Sabine Rudnik-Schöneborn, et al.
Leukemia
|
November 19, 2013
Blocking ETV6/RUNX1-induced MDM2 overexpression by Nutlin-3 reactivates p53 signaling in childhood leukemia
U Kaindl, M Morak, C Portsmouth, et al.
Journal of Child Neurology
|
August 12, 2006
Selenoprotein N muscular dystrophy: differential diagnosis for early-onset limited mobility of the spine
Stefanie Sponholz, Maja von der Hagen, Gabriele Hahn, et al.
Physical Review. B, Condensed Matter
|
February 1, 1993
Orbital character of states at the Fermi level in La2-xSrxCuO4 and R2-xCexCuO4 (R=Nd,Sm)
Pellegrin, Nücker, Fink, et al.
Annals of Neurology
|
December 11, 2008
Erythropoietin protects the developing brain from hyperoxia-induced cell death and proteome changes
Angela M Kaindl, Marco Sifringer, Andrea Koppelstaetter, et al.
Developmental Neuroscience
|
August 13, 2009
Erythropoietin attenuates hyperoxia-induced cell death by modulation of inflammatory mediators and matrix metalloproteinases
Marco Sifringer, Kerstin Genz, Daniela Brait, et al.
Molecular Neurobiology
|
August 22, 2016
Early Changes in Hippocampal Neurogenesis in Transgenic Mouse Models for Alzheimer's Disease
M S Unger, J Marschallinger, J Kaindl, et al.
Page
of 55