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N Resta

Showing results (11-20 of 37) with videos related to

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Journal of Medical Genetics|June 3, 2004
Site directed mutagenesis of hMLH1 exonic splicing enhancers does not correlate with splicing disruptionP Lastella, N Resta, I Miccolis, et al.
Human Mutation|January 29, 2003
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patientsJ Boudeau, A Kieloch, D R Alessi, et al.
Human Molecular Genetics|December 23, 1999
Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesisG Guanti, N Resta, C Simone, et al.
Forensic Science International. Genetics|November 7, 2012
Allele frequencies of the new European Standard Set (ESS) loci in a population of Apulia (Southern Italy)M Piglionica, S Lonero Baldassarra, E Giardina, et al.
Gut|January 13, 2006
Cancer risks in LKB1 germline mutation carriersH Mehenni, N Resta, J-G Park, et al.
American Journal of Human Genetics|November 1, 1993
Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)A Stella, N Resta, M Gentile, et al.
Minerva Anestesiologica|March 1, 1976
[Diagnostic and therapeutic difficulties in tetanus]A Gullo, C Melloni, E Romano, et al.
Clinical Genetics|June 6, 2003
Endoglin gene mutations and polymorphisms in Italian patients with hereditary haemorrhagic telangiectasiaP Lastella, C Sabbà, G M Lenato, et al.
Journal of Forensic Sciences|July 29, 2000
Distribution of HumvWA31, HumFESFPS, HumTH01, HumTPOX, HumCD4, HumCSF1PO alleles in a Southern Italian population sampleN Di Nunno, S L Baldassarra, M Carbonara, et al.
Journal of Medical Genetics|January 5, 2002
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP familyM Montera, F Piaggio, C Marchese, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|June 3, 2004
Site directed mutagenesis of hMLH1 exonic splicing enhancers does not correlate with splicing disruptionP Lastella, N Resta, I Miccolis, et al.
Human Mutation|January 29, 2003
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patientsJ Boudeau, A Kieloch, D R Alessi, et al.
Human Molecular Genetics|December 23, 1999
Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesisG Guanti, N Resta, C Simone, et al.
Forensic Science International. Genetics|November 7, 2012
Allele frequencies of the new European Standard Set (ESS) loci in a population of Apulia (Southern Italy)M Piglionica, S Lonero Baldassarra, E Giardina, et al.
Gut|January 13, 2006
Cancer risks in LKB1 germline mutation carriersH Mehenni, N Resta, J-G Park, et al.
American Journal of Human Genetics|November 1, 1993
Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)A Stella, N Resta, M Gentile, et al.
Minerva Anestesiologica|March 1, 1976
[Diagnostic and therapeutic difficulties in tetanus]A Gullo, C Melloni, E Romano, et al.
Clinical Genetics|June 6, 2003
Endoglin gene mutations and polymorphisms in Italian patients with hereditary haemorrhagic telangiectasiaP Lastella, C Sabbà, G M Lenato, et al.
Journal of Forensic Sciences|July 29, 2000
Distribution of HumvWA31, HumFESFPS, HumTH01, HumTPOX, HumCD4, HumCSF1PO alleles in a Southern Italian population sampleN Di Nunno, S L Baldassarra, M Carbonara, et al.
Journal of Medical Genetics|January 5, 2002
A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP familyM Montera, F Piaggio, C Marchese, et al.
Pageof 4