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Allison Piovesan

Showing results (21-30 of 45) with videos related to

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Genome Research|September 3, 2015
Corrigendum: Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cellsJennifer Y Tan, Tamara Sirey, Frantisek Honti, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 8, 2014
Improving mRNA 5' coding sequence determination in the mouse genomeAllison Piovesan, Maria Caracausi, Maria Chiara Pelleri, et al.
Genome Research|March 21, 2015
Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cellsJennifer Y Tan, Tamara Sirey, Frantisek Honti, et al.
Human Molecular Genetics|April 24, 2016
Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotypeMaria Chiara Pelleri, Elena Cicchini, Chiara Locatelli, et al.
Molecular Genetics & Genomic Medicine|March 15, 2019
MTHFR C677T polymorphism analysis: A simple, effective restriction enzyme-based method improving previous protocolsFrancesca Antonaros, Giulia Olivucci, Elena Cicchini, et al.
Heliyon|October 9, 2023
Machine learning based analysis for intellectual disability in Down syndromeFederico Baldo, Allison Piovesan, Marijana Rakvin, et al.
Molecular Biology Reports|July 2, 2014
Characterization of human gene locus CYYR1: a complex multi-transcript systemRaffaella Casadei, Maria Chiara Pelleri, Lorenza Vitale, et al.
Biofactors (Oxford, England)|February 14, 2024
The functional roles of S-adenosyl-methionine and S-adenosyl-homocysteine and their involvement in trisomy 21Maria Caracausi, Giuseppe Ramacieri, Francesca Catapano, et al.
Genomics|June 27, 2017
Genotype-phenotype correlation for congenital heart disease in Down syndrome through analysis of partial trisomy 21 casesMaria Chiara Pelleri, Elena Gennari, Chiara Locatelli, et al.
Annals of Human Biology|July 9, 2013
An estimation of the number of cells in the human bodyEva Bianconi, Allison Piovesan, Federica Facchin, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Genome Research|September 3, 2015
Corrigendum: Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cellsJennifer Y Tan, Tamara Sirey, Frantisek Honti, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 8, 2014
Improving mRNA 5' coding sequence determination in the mouse genomeAllison Piovesan, Maria Caracausi, Maria Chiara Pelleri, et al.
Genome Research|March 21, 2015
Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cellsJennifer Y Tan, Tamara Sirey, Frantisek Honti, et al.
Human Molecular Genetics|April 24, 2016
Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotypeMaria Chiara Pelleri, Elena Cicchini, Chiara Locatelli, et al.
Molecular Genetics & Genomic Medicine|March 15, 2019
MTHFR C677T polymorphism analysis: A simple, effective restriction enzyme-based method improving previous protocolsFrancesca Antonaros, Giulia Olivucci, Elena Cicchini, et al.
Heliyon|October 9, 2023
Machine learning based analysis for intellectual disability in Down syndromeFederico Baldo, Allison Piovesan, Marijana Rakvin, et al.
Molecular Biology Reports|July 2, 2014
Characterization of human gene locus CYYR1: a complex multi-transcript systemRaffaella Casadei, Maria Chiara Pelleri, Lorenza Vitale, et al.
Biofactors (Oxford, England)|February 14, 2024
The functional roles of S-adenosyl-methionine and S-adenosyl-homocysteine and their involvement in trisomy 21Maria Caracausi, Giuseppe Ramacieri, Francesca Catapano, et al.
Genomics|June 27, 2017
Genotype-phenotype correlation for congenital heart disease in Down syndrome through analysis of partial trisomy 21 casesMaria Chiara Pelleri, Elena Gennari, Chiara Locatelli, et al.
Annals of Human Biology|July 9, 2013
An estimation of the number of cells in the human bodyEva Bianconi, Allison Piovesan, Federica Facchin, et al.
Pageof 5