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Giovanni Levi

Showing results (31-40 of 59) with videos related to

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Developmental Biology|July 27, 2002
The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathwayGiorgio R Merlo, Laura Paleari, Stefano Mantero, et al.
Molecular and Cellular Neurosciences|February 28, 2002
Preferential transfection of adult mouse neural stem cells and their immediate progeny in vivo with polyethylenimineGregory F Lemkine, Stefano Mantero, Carole Migné, et al.
Molecular and Cellular Neurosciences|May 3, 2003
The Dlx5 homeodomain gene is essential for olfactory development and connectivity in the mouseGiovanni Levi, Adam C Puche, Stefano Mantero, et al.
Human Molecular Genetics|November 23, 2014
Etiology of craniofacial malformations in mouse models of blepharophimosis, ptosis and epicanthus inversus syndromeÉglantine Heude, Brice Bellessort, Anastasia Fontaine, et al.
Genesis (New York, N.Y. : 2000)|July 12, 2002
Mouse model of split hand/foot malformation type IGiorgio R Merlo, Laura Paleari, Stefano Mantero, et al.
Human Molecular Genetics|April 21, 2011
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiencyKamal Bouhali, Aurélie Dipietromaria, Anastasia Fontaine, et al.
Mechanisms of Development|December 7, 2005
Msx1 and Dlx5 act independently in development of craniofacial skeleton, but converge on the regulation of Bmp signaling in palate formationGiovanni Levi, Stefano Mantero, Ottavia Barbieri, et al.
Developmental Biology|March 22, 2003
Galphaq and Galpha11 proteins mediate endothelin-1 signaling in neural crest-derived pharyngeal arch mesenchymeKathryn Ivey, Brandi Tyson, Pallavi Ukidwe, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2008
An endothelin-1 switch specifies maxillomandibular identityTakahiro Sato, Yukiko Kurihara, Rieko Asai, et al.
Neurobiology of Disease|June 23, 2004
Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A diseaseLucilla Nobbio, Tiziana Vigo, Michele Abbruzzese, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Developmental Biology|July 27, 2002
The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathwayGiorgio R Merlo, Laura Paleari, Stefano Mantero, et al.
Molecular and Cellular Neurosciences|February 28, 2002
Preferential transfection of adult mouse neural stem cells and their immediate progeny in vivo with polyethylenimineGregory F Lemkine, Stefano Mantero, Carole Migné, et al.
Molecular and Cellular Neurosciences|May 3, 2003
The Dlx5 homeodomain gene is essential for olfactory development and connectivity in the mouseGiovanni Levi, Adam C Puche, Stefano Mantero, et al.
Human Molecular Genetics|November 23, 2014
Etiology of craniofacial malformations in mouse models of blepharophimosis, ptosis and epicanthus inversus syndromeÉglantine Heude, Brice Bellessort, Anastasia Fontaine, et al.
Genesis (New York, N.Y. : 2000)|July 12, 2002
Mouse model of split hand/foot malformation type IGiorgio R Merlo, Laura Paleari, Stefano Mantero, et al.
Human Molecular Genetics|April 21, 2011
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiencyKamal Bouhali, Aurélie Dipietromaria, Anastasia Fontaine, et al.
Mechanisms of Development|December 7, 2005
Msx1 and Dlx5 act independently in development of craniofacial skeleton, but converge on the regulation of Bmp signaling in palate formationGiovanni Levi, Stefano Mantero, Ottavia Barbieri, et al.
Developmental Biology|March 22, 2003
Galphaq and Galpha11 proteins mediate endothelin-1 signaling in neural crest-derived pharyngeal arch mesenchymeKathryn Ivey, Brandi Tyson, Pallavi Ukidwe, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2008
An endothelin-1 switch specifies maxillomandibular identityTakahiro Sato, Yukiko Kurihara, Rieko Asai, et al.
Neurobiology of Disease|June 23, 2004
Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A diseaseLucilla Nobbio, Tiziana Vigo, Michele Abbruzzese, et al.
Pageof 6