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R Brouns

Showing results (41-50 of 46) with videos related to

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Oral Diseases|November 8, 2023
The value of regular follow-up of oral leukoplakia for early detection of malignant transformationIlkay Evren, Ahmad M Najim, Jos B Poell, et al.
Acta Neurologica Belgica|February 3, 2010
Organisation of inhospital acute stroke care and minimum criteria for stroke care units. Recommendations of the Belgian Stroke Council, V Thijs, A Peeters, et al.
Experimental Dermatology|March 24, 2018
A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell deathJennifer A Easton, Ahmad K Albuloushi, Miriam A F Kamps, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 29, 2005
Toward positional cloning of the curly tail geneMadeleine R Brouns, Marian C E Peeters, Jan M Geurts, et al.
Cells|April 26, 2024
Genomic Engineering of Oral Keratinocytes to Establish In Vitro Oral Potentially Malignant Disease Models as a Platform for Treatment InvestigationLeon J Wils, Marijke Buijze, Marijke Stigter-van Walsum, et al.
Human Molecular Genetics|January 26, 2011
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouseMadeleine R Brouns, Sandra C P De Castro, Els A Terwindt-Rouwenhorst, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Oral Diseases|November 8, 2023
The value of regular follow-up of oral leukoplakia for early detection of malignant transformationIlkay Evren, Ahmad M Najim, Jos B Poell, et al.
Acta Neurologica Belgica|February 3, 2010
Organisation of inhospital acute stroke care and minimum criteria for stroke care units. Recommendations of the Belgian Stroke Council, V Thijs, A Peeters, et al.
Experimental Dermatology|March 24, 2018
A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell deathJennifer A Easton, Ahmad K Albuloushi, Miriam A F Kamps, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 29, 2005
Toward positional cloning of the curly tail geneMadeleine R Brouns, Marian C E Peeters, Jan M Geurts, et al.
Cells|April 26, 2024
Genomic Engineering of Oral Keratinocytes to Establish In Vitro Oral Potentially Malignant Disease Models as a Platform for Treatment InvestigationLeon J Wils, Marijke Buijze, Marijke Stigter-van Walsum, et al.
Human Molecular Genetics|January 26, 2011
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouseMadeleine R Brouns, Sandra C P De Castro, Els A Terwindt-Rouwenhorst, et al.
Pageof 5