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David P Rice

Showing results (31-40 of 46) with videos related to

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Journal of Oral Rehabilitation|April 27, 2023
Longitudinal trends in temporomandibular joint disorder symptoms, the impact of malocclusion and orthodontic treatment: A 20-year prospective studyEmmi Myllymäki, Kaisa Heikinheimo, Auli Suominen, et al.
Developmental Biology|February 16, 2010
The essential requirement for Runx1 in the development of the sternumAnna Liakhovitskaia, Eva Lana-Elola, Evangelos Stamateris, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 6, 2008
Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse modelMohammad K Hajihosseini, Raquel Duarte, Jean Pegrum, et al.
Frontiers in Physiology|January 10, 2018
Regulation of Calvarial Osteogenesis by Concomitant De-repression of GLI3 and Activation of IHH TargetsLotta K Veistinen, Tuija Mustonen, Md Rakibul Hasan, et al.
HGG Advances|June 18, 2026
Genetic architecture of 67 oral diseases and their links to systemic diseasesKirika Karppinen, Hanna M Ollila, Kanwal Batool, et al.
Human Molecular Genetics|August 9, 2011
Noggin null allele mice exhibit a microform of holoprosencephalyEva Lana-Elola, Przemko Tylzanowski, Maarit Takatalo, et al.
Developmental Biology|November 13, 2008
Runx1 is involved in the fusion of the primary and the secondary palatal shelvesKesinee Charoenchaikorn, Tomomasa Yokomizo, David P Rice, et al.
Development (Cambridge, England)|May 25, 2006
Gli3-mediated somitic Fgf10 expression gradients are required for the induction and patterning of mammary epithelium along the embryonic axesJacqueline M Veltmaat, Frédéric Relaix, Lendy T Le, et al.
EMBO Molecular Medicine|January 17, 2012
Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndromeGiustina Ferone, Helen A Thomason, Dario Antonini, et al.
Nature Communications|July 23, 2025
Genome-wide association study of pulpal and apical diseasesAino Salminen, Kati Hyvärinen, Jarmo Ritari, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Journal of Oral Rehabilitation|April 27, 2023
Longitudinal trends in temporomandibular joint disorder symptoms, the impact of malocclusion and orthodontic treatment: A 20-year prospective studyEmmi Myllymäki, Kaisa Heikinheimo, Auli Suominen, et al.
Developmental Biology|February 16, 2010
The essential requirement for Runx1 in the development of the sternumAnna Liakhovitskaia, Eva Lana-Elola, Evangelos Stamateris, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 6, 2008
Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse modelMohammad K Hajihosseini, Raquel Duarte, Jean Pegrum, et al.
Frontiers in Physiology|January 10, 2018
Regulation of Calvarial Osteogenesis by Concomitant De-repression of GLI3 and Activation of IHH TargetsLotta K Veistinen, Tuija Mustonen, Md Rakibul Hasan, et al.
HGG Advances|June 18, 2026
Genetic architecture of 67 oral diseases and their links to systemic diseasesKirika Karppinen, Hanna M Ollila, Kanwal Batool, et al.
Human Molecular Genetics|August 9, 2011
Noggin null allele mice exhibit a microform of holoprosencephalyEva Lana-Elola, Przemko Tylzanowski, Maarit Takatalo, et al.
Developmental Biology|November 13, 2008
Runx1 is involved in the fusion of the primary and the secondary palatal shelvesKesinee Charoenchaikorn, Tomomasa Yokomizo, David P Rice, et al.
Development (Cambridge, England)|May 25, 2006
Gli3-mediated somitic Fgf10 expression gradients are required for the induction and patterning of mammary epithelium along the embryonic axesJacqueline M Veltmaat, Frédéric Relaix, Lendy T Le, et al.
EMBO Molecular Medicine|January 17, 2012
Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndromeGiustina Ferone, Helen A Thomason, Dario Antonini, et al.
Nature Communications|July 23, 2025
Genome-wide association study of pulpal and apical diseasesAino Salminen, Kati Hyvärinen, Jarmo Ritari, et al.
Pageof 5