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Ludwine Messiaen

Showing results (1-10 of 88) with videos related to

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JAMA|June 24, 2010
Error in a study of the clinical and mutational spectrum of neurofibromatosis type 1-like syndromeLudwine Messiaen, Eric Legius
Human Genetics|April 17, 2003
Interphase FISH, the structure of reciprocal translocation chromosomes and physical mapping studies rule out the duplication of the NF1 gene at 17q11.2. A replyHildegard Kehrer-Sawatzki, Ludwine Messiaen
Plos Genetics|November 30, 2011
The NF1 gene contains hotspots for L1 endonuclease-dependent de novo insertionKatharina Wimmer, Tom Callens, Annekatrin Wernstedt, 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.
FEBS Letters|July 4, 2002
Quantification of NF1 transcripts reveals novel highly expressed splice variantsIna Vandenbroucke, Jo Vandesompele, Anne De Paepe, et al.
Analytical Biochemistry|September 12, 2006
Real-time quantitative allele discrimination assay using 3' locked nucleic acid primers for detection of low-percentage mosaic mutationsOphélia Maertens, Eric Legius, Frank Speleman, et al.
FEBS Letters|February 28, 2004
Neurofibromin is actively transported to the nucleusIna Vandenbroucke, Patrick Van Oostveldt, Elisabeth Coene, et al.
Human Mutation|August 10, 2004
The human FOXL2 mutation databaseDiane Beysen, Jo Vandesompele, Ludwine Messiaen, et al.
Pigment Cell Research|January 15, 2005
Pigment cell-related manifestations in neurofibromatosis type 1: an overviewSofie De Schepper, Joachim Boucneau, Jo Lambert, et al.
Genetic Testing and Molecular Biomarkers|June 26, 2010
Identification of PKHD1 multiexon deletions using multiplex ligation-dependent probe amplification and quantitative polymerase chain reactionVal Zvereff, Suxia Yao, Julia Ramsey, et al.
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
JAMA|June 24, 2010
Error in a study of the clinical and mutational spectrum of neurofibromatosis type 1-like syndromeLudwine Messiaen, Eric Legius
Human Genetics|April 17, 2003
Interphase FISH, the structure of reciprocal translocation chromosomes and physical mapping studies rule out the duplication of the NF1 gene at 17q11.2. A replyHildegard Kehrer-Sawatzki, Ludwine Messiaen
Plos Genetics|November 30, 2011
The NF1 gene contains hotspots for L1 endonuclease-dependent de novo insertionKatharina Wimmer, Tom Callens, Annekatrin Wernstedt, 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.
FEBS Letters|July 4, 2002
Quantification of NF1 transcripts reveals novel highly expressed splice variantsIna Vandenbroucke, Jo Vandesompele, Anne De Paepe, et al.
Analytical Biochemistry|September 12, 2006
Real-time quantitative allele discrimination assay using 3' locked nucleic acid primers for detection of low-percentage mosaic mutationsOphélia Maertens, Eric Legius, Frank Speleman, et al.
FEBS Letters|February 28, 2004
Neurofibromin is actively transported to the nucleusIna Vandenbroucke, Patrick Van Oostveldt, Elisabeth Coene, et al.
Human Mutation|August 10, 2004
The human FOXL2 mutation databaseDiane Beysen, Jo Vandesompele, Ludwine Messiaen, et al.
Pigment Cell Research|January 15, 2005
Pigment cell-related manifestations in neurofibromatosis type 1: an overviewSofie De Schepper, Joachim Boucneau, Jo Lambert, et al.
Genetic Testing and Molecular Biomarkers|June 26, 2010
Identification of PKHD1 multiexon deletions using multiplex ligation-dependent probe amplification and quantitative polymerase chain reactionVal Zvereff, Suxia Yao, Julia Ramsey, et al.
Pageof 9