Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Virginie Laugel-Haushalter

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
BMC Research Notes|March 28, 2013
Molars and incisors: show your microarray IDsVirginie Laugel-Haushalter, Marie Paschaki, Christelle Thibault-Carpentier, et al.
Frontiers in Physiology|January 24, 2017
Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel DefectsSupawich Morkmued, Virginie Laugel-Haushalter, Eric Mathieu, et al.
Scientific Reports|July 1, 2015
Phenotypic and evolutionary implications of modulating the ERK-MAPK cascade using the dentition as a modelPauline Marangoni, Cyril Charles, Paul Tafforeau, et al.
European Journal of Oral Sciences|January 14, 2017
Enamel and dental anomalies in latent-transforming growth factor beta-binding protein 3 mutant miceSupawich Morkmued, Joseph Hemmerle, Eric Mathieu, et al.
Molecular Syndromology|January 8, 2015
A Novel Mutation in the ROGDI Gene in a Patient with Kohlschütter-Tönz SyndromeMathilde Huckert, Helen Mecili, Virginie Laugel-Haushalter, et al.
Frontiers in Physiology|October 16, 2018
Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root PatterningVirginie Laugel-Haushalter, Supawich Morkmued, Corinne Stoetzel, et al.
Frontiers in Genetics|June 14, 2019
A New <i>SLC10A7</i> Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis ImperfectaVirginie Laugel-Haushalter, Séverine Bär, Elise Schaefer, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 7, 2019
Protocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental InvolvementTristan Rey, Julien Tarabeux, Bénédicte Gerard, et al.
Plos One|January 14, 2014
RSK2 is a modulator of craniofacial developmentVirginie Laugel-Haushalter, Marie Paschaki, Pauline Marangoni, et al.
Journal of Medical Genetics|March 8, 2024
Biallelic variants in Plexin B2 (<i>PLXNB2</i>) cause amelogenesis imperfecta, hearing loss and intellectual disabilityClaire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
BMC Research Notes|March 28, 2013
Molars and incisors: show your microarray IDsVirginie Laugel-Haushalter, Marie Paschaki, Christelle Thibault-Carpentier, et al.
Frontiers in Physiology|January 24, 2017
Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel DefectsSupawich Morkmued, Virginie Laugel-Haushalter, Eric Mathieu, et al.
Scientific Reports|July 1, 2015
Phenotypic and evolutionary implications of modulating the ERK-MAPK cascade using the dentition as a modelPauline Marangoni, Cyril Charles, Paul Tafforeau, et al.
European Journal of Oral Sciences|January 14, 2017
Enamel and dental anomalies in latent-transforming growth factor beta-binding protein 3 mutant miceSupawich Morkmued, Joseph Hemmerle, Eric Mathieu, et al.
Molecular Syndromology|January 8, 2015
A Novel Mutation in the ROGDI Gene in a Patient with Kohlschütter-Tönz SyndromeMathilde Huckert, Helen Mecili, Virginie Laugel-Haushalter, et al.
Frontiers in Physiology|October 16, 2018
Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root PatterningVirginie Laugel-Haushalter, Supawich Morkmued, Corinne Stoetzel, et al.
Frontiers in Genetics|June 14, 2019
A New <i>SLC10A7</i> Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis ImperfectaVirginie Laugel-Haushalter, Séverine Bär, Elise Schaefer, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 7, 2019
Protocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental InvolvementTristan Rey, Julien Tarabeux, Bénédicte Gerard, et al.
Plos One|January 14, 2014
RSK2 is a modulator of craniofacial developmentVirginie Laugel-Haushalter, Marie Paschaki, Pauline Marangoni, et al.
Journal of Medical Genetics|March 8, 2024
Biallelic variants in Plexin B2 (<i>PLXNB2</i>) cause amelogenesis imperfecta, hearing loss and intellectual disabilityClaire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, et al.
Pageof 2