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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 study
Emmi Myllymäki, Kaisa Heikinheimo, Auli Suominen, et al.
Developmental Biology
|
February 16, 2010
The essential requirement for Runx1 in the development of the sternum
Anna 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 model
Mohammad 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 Targets
Lotta 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 diseases
Kirika Karppinen, Hanna M Ollila, Kanwal Batool, et al.
Human Molecular Genetics
|
August 9, 2011
Noggin null allele mice exhibit a microform of holoprosencephaly
Eva 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 shelves
Kesinee 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 axes
Jacqueline 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 syndrome
Giustina Ferone, Helen A Thomason, Dario Antonini, et al.
Nature Communications
|
July 23, 2025
Genome-wide association study of pulpal and apical diseases
Aino Salminen, Kati Hyvärinen, Jarmo Ritari, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 46) with videos related to
Sort By:
Page
of 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 study
Emmi Myllymäki, Kaisa Heikinheimo, Auli Suominen, et al.
Developmental Biology
|
February 16, 2010
The essential requirement for Runx1 in the development of the sternum
Anna 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 model
Mohammad 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 Targets
Lotta 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 diseases
Kirika Karppinen, Hanna M Ollila, Kanwal Batool, et al.
Human Molecular Genetics
|
August 9, 2011
Noggin null allele mice exhibit a microform of holoprosencephaly
Eva 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 shelves
Kesinee 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 axes
Jacqueline 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 syndrome
Giustina Ferone, Helen A Thomason, Dario Antonini, et al.
Nature Communications
|
July 23, 2025
Genome-wide association study of pulpal and apical diseases
Aino Salminen, Kati Hyvärinen, Jarmo Ritari, et al.
Page
of 5