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L Villard

Showing results (71-80 of 99) with videos related to

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American Journal of Medical Genetics|October 26, 2000
Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three familiesA M Lossi, L Colleaux, P Chiaroni, et al.
Journal of Clinical Microbiology|January 16, 1999
Pulsed-field gel electrophoresis is more efficient than ribotyping and random amplified polymorphic DNA analysis in discrimination of Pasteurella haemolytica strainsA Kodjo, L Villard, C Bizet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 21, 2020
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature reviewM-V André, P Cacciagli, A Cano, et al.
Genomics|March 1, 1995
Construction of a YAC contig spanning the Xq13.3 subbandL Villard, J Gecz, L Colleaux, et al.
Journal of Pharmaceutical and Biomedical Analysis|June 30, 2006
Diastereoisomeric resolution of a pronucleotide using solid phase extraction and high performance liquid chromatography: application to a stereoselective decomposition kinetic in cell extractsC Foulon, C Vaccher, A-L Villard, et al.
Biomedical Chromatography : BMC|July 23, 2005
Column selection and method development for the separation of nucleoside phosphotriester diastereoisomers, new potential anti-viral drugs. Application to cellular extract analysisJ F Goossens, C Foulon, A-L Villard, et al.
Letters in Applied Microbiology|April 4, 2000
Detection of Escherichia coli O157:H7 in heifers' faecal samples using an automated immunoconcentration systemC Vernozy-Rozand, P Feng, M P Montet, et al.
Journal of Medical Genetics|October 7, 2004
Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded malesV Cantagrel, A-M Lossi, S Boulanger, et al.
Journal of Medical Genetics|February 12, 2002
Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardationA M Lossi, F Laugier-Anfossi, D Depetris, et al.
American Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1M Raynaud, C Gendrot, B Dessay, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics|October 26, 2000
Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three familiesA M Lossi, L Colleaux, P Chiaroni, et al.
Journal of Clinical Microbiology|January 16, 1999
Pulsed-field gel electrophoresis is more efficient than ribotyping and random amplified polymorphic DNA analysis in discrimination of Pasteurella haemolytica strainsA Kodjo, L Villard, C Bizet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 21, 2020
The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature reviewM-V André, P Cacciagli, A Cano, et al.
Genomics|March 1, 1995
Construction of a YAC contig spanning the Xq13.3 subbandL Villard, J Gecz, L Colleaux, et al.
Journal of Pharmaceutical and Biomedical Analysis|June 30, 2006
Diastereoisomeric resolution of a pronucleotide using solid phase extraction and high performance liquid chromatography: application to a stereoselective decomposition kinetic in cell extractsC Foulon, C Vaccher, A-L Villard, et al.
Biomedical Chromatography : BMC|July 23, 2005
Column selection and method development for the separation of nucleoside phosphotriester diastereoisomers, new potential anti-viral drugs. Application to cellular extract analysisJ F Goossens, C Foulon, A-L Villard, et al.
Letters in Applied Microbiology|April 4, 2000
Detection of Escherichia coli O157:H7 in heifers' faecal samples using an automated immunoconcentration systemC Vernozy-Rozand, P Feng, M P Montet, et al.
Journal of Medical Genetics|October 7, 2004
Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded malesV Cantagrel, A-M Lossi, S Boulanger, et al.
Journal of Medical Genetics|February 12, 2002
Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardationA M Lossi, F Laugier-Anfossi, D Depetris, et al.
American Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1M Raynaud, C Gendrot, B Dessay, et al.
Pageof 10