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S M Sirchia

Showing results (1-10 of 16) with videos related to

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Molecular and Cellular Probes|April 1, 1996
Characterization of four microsatellites in an Italian population and their application to paternity testingS M Sirchia, I Garagiola, C De Andreis, et al.
Prenatal Diagnosis|April 29, 1998
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicismS M Sirchia, I Garagiola, G Colucci, et al.
Oncogene|March 29, 2000
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta2 promoter in breast cancer cellsS M Sirchia, A T Ferguson, E Sironi, et al.
Journal of Medical Screening|January 1, 1996
Molecular screening of families affected by familial adenomatous polyposis (FAP)I Gazzoli, C De Andreis, S M Sirchia, et al.
Journal of Hematotherapy|March 4, 1998
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent methodF Poli, S M Sirchia, M Scalamogna, et al.
Human Genetics|October 1, 1994
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotypeS M Sirchia, C De Andreis, S Pariani, et al.
Epilepsia|September 16, 1999
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome: a clinical, EEG, and molecular genetic studyU Aguglia, E Le Piane, A Gambardella, et al.
Journal of Bioluminescence and Chemiluminescence|December 5, 1998
Highly sensitive chemiluminescent method for the detection of cell contaminationS M Sirchia, I Garagiola, C De Andreis, et al.
Cancer Genetics and Cytogenetics|April 1, 1997
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinomaS M Sirchia, S Pariani, F Rossella, et al.
Atherosclerosis|December 4, 2001
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteriesF R Grati, G Ghilardi, S M Sirchia, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Molecular and Cellular Probes|April 1, 1996
Characterization of four microsatellites in an Italian population and their application to paternity testingS M Sirchia, I Garagiola, C De Andreis, et al.
Prenatal Diagnosis|April 29, 1998
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicismS M Sirchia, I Garagiola, G Colucci, et al.
Oncogene|March 29, 2000
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta2 promoter in breast cancer cellsS M Sirchia, A T Ferguson, E Sironi, et al.
Journal of Medical Screening|January 1, 1996
Molecular screening of families affected by familial adenomatous polyposis (FAP)I Gazzoli, C De Andreis, S M Sirchia, et al.
Journal of Hematotherapy|March 4, 1998
Detection of maternal DNA in human cord blood stored for allotransplantation by a highly sensitive chemiluminescent methodF Poli, S M Sirchia, M Scalamogna, et al.
Human Genetics|October 1, 1994
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotypeS M Sirchia, C De Andreis, S Pariani, et al.
Epilepsia|September 16, 1999
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome: a clinical, EEG, and molecular genetic studyU Aguglia, E Le Piane, A Gambardella, et al.
Journal of Bioluminescence and Chemiluminescence|December 5, 1998
Highly sensitive chemiluminescent method for the detection of cell contaminationS M Sirchia, I Garagiola, C De Andreis, et al.
Cancer Genetics and Cytogenetics|April 1, 1997
Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinomaS M Sirchia, S Pariani, F Rossella, et al.
Atherosclerosis|December 4, 2001
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteriesF R Grati, G Ghilardi, S M Sirchia, et al.
Pageof 2