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P F Pignatti

Showing results (21-30 of 117) with videos related to

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Human Molecular Genetics|April 1, 1995
Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasisP F Pignatti, C Bombieri, C Marigo, et al.
Prenatal Diagnosis|May 1, 1989
First-trimester prenatal diagnosis of cystic fibrosis using the polymerase chain reaction: report of eight casesP Gasparini, G Novelli, A Savoia, et al.
American Journal of Respiratory Cell and Molecular Biology|March 1, 1990
The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary diseaseP Gasparini, A Savoia, M Luisetti, et al.
Microbiologica|July 1, 1986
Resistance of HSV-1 growth to aphidicolin in two aphidicolin resistant cell linesG Rappazzo, A Grillo, O Biondi, et al.
Human Heredity|January 1, 1990
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian populationP Gasparini, E Trabetti, A Savoia, et al.
Molecular and Cellular Probes|April 1, 1997
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA)S Rossetti, S Englisch, E Bresin, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1996
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 geneA E Turco, M Clementi, S Rossetti, et al.
Molecular and Cellular Probes|June 1, 1995
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genesS Rossetti, S Corrà, M O Biasi, et al.
American Journal of Respiratory and Critical Care Medicine|May 1, 1996
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic childrenL C Martinati, E Trabetti, A Casartelli, et al.
Prenatal Diagnosis|June 1, 1992
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reactionA Turco, B Peissel, P Quaia, et al.
Pageof 12

Showing results (21-30 of 117) with videos related to

Sort By:
Pageof 12
Human Molecular Genetics|April 1, 1995
Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasisP F Pignatti, C Bombieri, C Marigo, et al.
Prenatal Diagnosis|May 1, 1989
First-trimester prenatal diagnosis of cystic fibrosis using the polymerase chain reaction: report of eight casesP Gasparini, G Novelli, A Savoia, et al.
American Journal of Respiratory Cell and Molecular Biology|March 1, 1990
The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary diseaseP Gasparini, A Savoia, M Luisetti, et al.
Microbiologica|July 1, 1986
Resistance of HSV-1 growth to aphidicolin in two aphidicolin resistant cell linesG Rappazzo, A Grillo, O Biondi, et al.
Human Heredity|January 1, 1990
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian populationP Gasparini, E Trabetti, A Savoia, et al.
Molecular and Cellular Probes|April 1, 1997
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA)S Rossetti, S Englisch, E Bresin, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1996
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 geneA E Turco, M Clementi, S Rossetti, et al.
Molecular and Cellular Probes|June 1, 1995
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genesS Rossetti, S Corrà, M O Biasi, et al.
American Journal of Respiratory and Critical Care Medicine|May 1, 1996
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic childrenL C Martinati, E Trabetti, A Casartelli, et al.
Prenatal Diagnosis|June 1, 1992
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reactionA Turco, B Peissel, P Quaia, et al.
Pageof 12