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Anne De Paepe

Showing results (11-20 of 236) with videos related to

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Methods in Molecular Medicine|August 26, 2006
Mutation analysis of the FBN1 gene in patients with Marfan syndromePaul Coucke, Petra Van Acker, Anne De Paepe
Nucleic Acids Research|January 10, 2003
RTPrimerDB: the real-time PCR primer and probe databaseFilip Pattyn, Frank Speleman, Anne De Paepe, et al.
FEBS Letters|July 4, 2002
Quantification of NF1 transcripts reveals novel highly expressed splice variantsIna Vandenbroucke, Jo Vandesompele, Anne De Paepe, et al.
Frontiers in Genetics|October 19, 2013
The ABCC6 transporter: what lessons can be learnt from other ATP-binding cassette transporters?Olivier M Vanakker, Mohammad J Hosen, Anne De Paepe
Best Practice & Research. Clinical Rheumatology|March 11, 2008
Ehlers-Danlos syndromes and Marfan syndromeBert Callewaert, Fransiska Malfait, Bart Loeys, et al.
BMC Genomics|June 12, 2002
Complex splicing pattern generates great diversity in human NF1 transcriptsIna Vandenbroucke, Tom Callens, Anne De Paepe, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|April 9, 2005
Oral health in prevalent types of Ehlers-Danlos syndromesPeter J De Coster, Luc C Martens, Anne De Paepe
Pediatric Dentistry|January 14, 2005
Orofacial manifestations of congenital fibrillin deficiency: pathogenesis and clinical diagnosticsPeter J De Coster, Luc C Martens, Anne De Paepe
The Journal of Biological Chemistry|February 19, 2004
Human fibroblasts with mutations in COL5A1 and COL3A1 genes do not organize collagens and fibronectin in the extracellular matrix, down-regulate alpha2beta1 integrin, and recruit alphavbeta3 Instead of alpha5beta1 integrinNicoletta Zoppi, Rita Gardella, Anne De Paepe, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
Discordance between phenotypic appearance and genotypic findings in a familial case of classical Ehlers-Danlos syndromeRosanna Pallotta, Tamara Ehresmann, Paola Fusilli, et al.
Pageof 24

Showing results (11-20 of 236) with videos related to

Sort By:
Pageof 24
Methods in Molecular Medicine|August 26, 2006
Mutation analysis of the FBN1 gene in patients with Marfan syndromePaul Coucke, Petra Van Acker, Anne De Paepe
Nucleic Acids Research|January 10, 2003
RTPrimerDB: the real-time PCR primer and probe databaseFilip Pattyn, Frank Speleman, Anne De Paepe, et al.
FEBS Letters|July 4, 2002
Quantification of NF1 transcripts reveals novel highly expressed splice variantsIna Vandenbroucke, Jo Vandesompele, Anne De Paepe, et al.
Frontiers in Genetics|October 19, 2013
The ABCC6 transporter: what lessons can be learnt from other ATP-binding cassette transporters?Olivier M Vanakker, Mohammad J Hosen, Anne De Paepe
Best Practice & Research. Clinical Rheumatology|March 11, 2008
Ehlers-Danlos syndromes and Marfan syndromeBert Callewaert, Fransiska Malfait, Bart Loeys, et al.
BMC Genomics|June 12, 2002
Complex splicing pattern generates great diversity in human NF1 transcriptsIna Vandenbroucke, Tom Callens, Anne De Paepe, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|April 9, 2005
Oral health in prevalent types of Ehlers-Danlos syndromesPeter J De Coster, Luc C Martens, Anne De Paepe
Pediatric Dentistry|January 14, 2005
Orofacial manifestations of congenital fibrillin deficiency: pathogenesis and clinical diagnosticsPeter J De Coster, Luc C Martens, Anne De Paepe
The Journal of Biological Chemistry|February 19, 2004
Human fibroblasts with mutations in COL5A1 and COL3A1 genes do not organize collagens and fibronectin in the extracellular matrix, down-regulate alpha2beta1 integrin, and recruit alphavbeta3 Instead of alpha5beta1 integrinNicoletta Zoppi, Rita Gardella, Anne De Paepe, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
Discordance between phenotypic appearance and genotypic findings in a familial case of classical Ehlers-Danlos syndromeRosanna Pallotta, Tamara Ehresmann, Paola Fusilli, et al.
Pageof 24