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Michael Wegner

Showing results (121-130 of 187) with videos related to

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Human Molecular Genetics|January 24, 2018
Analysis of the human SOX10 mutation Q377X in mice and its implications for genotype-phenotype correlation in SOX10-related human diseaseKathrin Truch, Juliane Arter, Tanja Turnescu, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2006
Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cellsYasuhiro Ito, Stefan Wiese, Natalja Funk, et al.
The Journal of Biological Chemistry|August 29, 2003
A tissue-restricted cAMP transcriptional response: SOX10 modulates alpha-melanocyte-stimulating hormone-triggered expression of microphthalmia-associated transcription factor in melanocytesWade E Huber, E Roydon Price, Hans R Widlund, et al.
Human Mutation|June 1, 2010
Heterozygous SOX9 mutations allowing for residual DNA-binding and transcriptional activation lead to the acampomelic variant of campomelic dysplasiaAlex Staffler, Markus Hammel, Mandy Wahlbuhl, et al.
Brain : a Journal of Neurology|January 8, 2015
Gain of Olig2 function in oligodendrocyte progenitors promotes remyelinationAmélie Wegener, Cyrille Deboux, Corinne Bachelin, et al.
Cancer Research|March 15, 2008
SOX9 is expressed in human fetal prostate epithelium and enhances prostate cancer invasionHongyun Wang, Irwin Leav, Soichiro Ibaragi, et al.
Nature Communications|July 3, 2010
Organogenesis relies on SoxC transcription factors for the survival of neural and mesenchymal progenitorsPallavi Bhattaram, Alfredo Penzo-Méndez, Elisabeth Sock, et al.
Journal of Neurochemistry|July 15, 2010
Glial but not neuronal development in the cochleo-vestibular ganglion requires Sox10Ingrid Breuskin, Morgan Bodson, Nicolas Thelen, et al.
Journal of Clinical Lipidology|February 5, 2011
Effects of lifestyle counseling and combination lipid-modifying therapy on lipoprotein-associated phospholipase A2 mass concentrationKota J Reddy, Manmeet Singh, Richard R Batsell, et al.
Nature Communications|May 31, 2019
Ep400 deficiency in Schwann cells causes persistent expression of early developmental regulators and peripheral neuropathyFranziska Fröb, Elisabeth Sock, Ernst R Tamm, et al.
Pageof 19

Showing results (121-130 of 187) with videos related to

Sort By:
Pageof 19
Human Molecular Genetics|January 24, 2018
Analysis of the human SOX10 mutation Q377X in mice and its implications for genotype-phenotype correlation in SOX10-related human diseaseKathrin Truch, Juliane Arter, Tanja Turnescu, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2006
Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cellsYasuhiro Ito, Stefan Wiese, Natalja Funk, et al.
The Journal of Biological Chemistry|August 29, 2003
A tissue-restricted cAMP transcriptional response: SOX10 modulates alpha-melanocyte-stimulating hormone-triggered expression of microphthalmia-associated transcription factor in melanocytesWade E Huber, E Roydon Price, Hans R Widlund, et al.
Human Mutation|June 1, 2010
Heterozygous SOX9 mutations allowing for residual DNA-binding and transcriptional activation lead to the acampomelic variant of campomelic dysplasiaAlex Staffler, Markus Hammel, Mandy Wahlbuhl, et al.
Brain : a Journal of Neurology|January 8, 2015
Gain of Olig2 function in oligodendrocyte progenitors promotes remyelinationAmélie Wegener, Cyrille Deboux, Corinne Bachelin, et al.
Cancer Research|March 15, 2008
SOX9 is expressed in human fetal prostate epithelium and enhances prostate cancer invasionHongyun Wang, Irwin Leav, Soichiro Ibaragi, et al.
Nature Communications|July 3, 2010
Organogenesis relies on SoxC transcription factors for the survival of neural and mesenchymal progenitorsPallavi Bhattaram, Alfredo Penzo-Méndez, Elisabeth Sock, et al.
Journal of Neurochemistry|July 15, 2010
Glial but not neuronal development in the cochleo-vestibular ganglion requires Sox10Ingrid Breuskin, Morgan Bodson, Nicolas Thelen, et al.
Journal of Clinical Lipidology|February 5, 2011
Effects of lifestyle counseling and combination lipid-modifying therapy on lipoprotein-associated phospholipase A2 mass concentrationKota J Reddy, Manmeet Singh, Richard R Batsell, et al.
Nature Communications|May 31, 2019
Ep400 deficiency in Schwann cells causes persistent expression of early developmental regulators and peripheral neuropathyFranziska Fröb, Elisabeth Sock, Ernst R Tamm, et al.
Pageof 19