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John J Greer

Showing results (61-70 of 72) with videos related to

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American Journal of Respiratory Cell and Molecular Biology|January 9, 2015
Stimulation of Respiratory Motor Output and Ventilation in a Murine Model of Pompe Disease by AmpakinesMai K ElMallah, Silvia Pagliardini, Sara M Turner, et al.
Experimental Lung Research|May 15, 2003
Expression and activity of matrix metallo proteinases 2 and 9 and their inhibitors in rat lungs during the perinatal period and in diaphragmatic herniaRobert P Lemke, Wei Zhang, Denis Balcerazak, et al.
Human Molecular Genetics|March 7, 2008
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndromeRodney C Samaco, John D Fryer, Jun Ren, et al.
The Journal of Biological Chemistry|February 13, 2003
Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apneaGerard T Berry, Shuang Wu, Roberto Buccafusca, et al.
Human Molecular Genetics|July 21, 2016
Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromesAin A Kamaludin, Christa Smolarchuk, Jocelyn M Bischof, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|August 21, 2007
Mechanisms of action of the congenital diaphragmatic hernia-inducing teratogen nitrofenB Rhiannon Noble, Randal P Babiuk, Robin D Clugston, et al.
Pediatrics|September 15, 2010
Retinol status of newborn infants is associated with congenital diaphragmatic herniaLeonardus W J E Beurskens, Dick Tibboel, Jan Lindemans, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|May 16, 2019
Regulation of breathing pattern by IL-10Charoula Eleni Giannakopoulou, Adamantia Sotiriou, Maria Dettoraki, et al.
Molecular Genetics and Metabolism|August 5, 2008
Characterization of the null murine sodium/myo-inositol cotransporter 1 (Smit1 or Slc5a3) phenotype: myo-inositol rescue is independent of expression of its cognate mitochondrial ribosomal protein subunit 6 (Mrps6) gene and of phosphatidylinositol levels in neonatal brainRoberto Buccafusca, Charles P Venditti, Lawrence C Kenyon, et al.
Plos Genetics|August 17, 2005
Fog2 is required for normal diaphragm and lung development in mice and humansKate G Ackerman, Bruce J Herron, Sara O Vargas, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
American Journal of Respiratory Cell and Molecular Biology|January 9, 2015
Stimulation of Respiratory Motor Output and Ventilation in a Murine Model of Pompe Disease by AmpakinesMai K ElMallah, Silvia Pagliardini, Sara M Turner, et al.
Experimental Lung Research|May 15, 2003
Expression and activity of matrix metallo proteinases 2 and 9 and their inhibitors in rat lungs during the perinatal period and in diaphragmatic herniaRobert P Lemke, Wei Zhang, Denis Balcerazak, et al.
Human Molecular Genetics|March 7, 2008
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndromeRodney C Samaco, John D Fryer, Jun Ren, et al.
The Journal of Biological Chemistry|February 13, 2003
Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apneaGerard T Berry, Shuang Wu, Roberto Buccafusca, et al.
Human Molecular Genetics|July 21, 2016
Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromesAin A Kamaludin, Christa Smolarchuk, Jocelyn M Bischof, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|August 21, 2007
Mechanisms of action of the congenital diaphragmatic hernia-inducing teratogen nitrofenB Rhiannon Noble, Randal P Babiuk, Robin D Clugston, et al.
Pediatrics|September 15, 2010
Retinol status of newborn infants is associated with congenital diaphragmatic herniaLeonardus W J E Beurskens, Dick Tibboel, Jan Lindemans, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|May 16, 2019
Regulation of breathing pattern by IL-10Charoula Eleni Giannakopoulou, Adamantia Sotiriou, Maria Dettoraki, et al.
Molecular Genetics and Metabolism|August 5, 2008
Characterization of the null murine sodium/myo-inositol cotransporter 1 (Smit1 or Slc5a3) phenotype: myo-inositol rescue is independent of expression of its cognate mitochondrial ribosomal protein subunit 6 (Mrps6) gene and of phosphatidylinositol levels in neonatal brainRoberto Buccafusca, Charles P Venditti, Lawrence C Kenyon, et al.
Plos Genetics|August 17, 2005
Fog2 is required for normal diaphragm and lung development in mice and humansKate G Ackerman, Bruce J Herron, Sara O Vargas, et al.
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