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Xavier Estivill

Showing results (31-40 of 239) with videos related to

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Plos One|December 17, 2009
Nucleotide, cytogenetic and expression impact of the human chromosome 8p23.1 inversion polymorphismNina Bosch, Marta Morell, Immaculada Ponsa, et al.
Scientific Reports|October 15, 2017
Signatures of positive selection reveal a universal role of chromatin modifiers as cancer driver genesLuis Zapata, Hana Susak, Oliver Drechsel, et al.
Genome Biology|December 6, 2018
miRTrace reveals the organismal origins of microRNA sequencing dataWenjing Kang, Yrin Eldfjell, Bastian Fromm, et al.
BMC Molecular Biology|December 15, 2010
Overexpression of miR-128 specifically inhibits the truncated isoform of NTRK3 and upregulates BCL2 in SH-SY5Y neuroblastoma cellsMonica Guidi, Margarita Muiños-Gimeno, Birgit Kagerbauer, et al.
Genetic Epidemiology|January 30, 2008
Maximizing association statistics over genetic modelsJuan R González, Josep L Carrasco, Frank Dudbridge, et al.
Human Mutation|August 24, 2021
Actionable genomic variants in 6045 participants from the Qatar Genome ProgramAmal Elfatih, Borbala Mifsud, Najeeb Syed, et al.
Epigenomics|October 5, 2019
Epigenetic modification of the pentose phosphate pathway and the IGF-axis in women with gestational diabetes mellitusAngela Steyn, Nigel J Crowther, Shane A Norris, et al.
Human Mutation|April 5, 2002
A common frameshift mutation and other variants in GJB4 (connexin 30.3): Analysis of hearing impairment familiesNúria López-Bigas, Salvatore Melchionda, Paolo Gasparini, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Diagnosis of autosomal dominant polycystic kidney disease using efficient PKD1 and PKD2 targeted next-generation sequencingDaniel Trujillano, Gemma Bullich, Stephan Ossowski, et al.
BMC Bioinformatics|June 9, 2009
Accounting for uncertainty when assessing association between copy number and disease: a latent class modelJuan R González, Isaac Subirana, Geòrgia Escaramís, et al.
Pageof 24

Showing results (31-40 of 239) with videos related to

Sort By:
Pageof 24
Plos One|December 17, 2009
Nucleotide, cytogenetic and expression impact of the human chromosome 8p23.1 inversion polymorphismNina Bosch, Marta Morell, Immaculada Ponsa, et al.
Scientific Reports|October 15, 2017
Signatures of positive selection reveal a universal role of chromatin modifiers as cancer driver genesLuis Zapata, Hana Susak, Oliver Drechsel, et al.
Genome Biology|December 6, 2018
miRTrace reveals the organismal origins of microRNA sequencing dataWenjing Kang, Yrin Eldfjell, Bastian Fromm, et al.
BMC Molecular Biology|December 15, 2010
Overexpression of miR-128 specifically inhibits the truncated isoform of NTRK3 and upregulates BCL2 in SH-SY5Y neuroblastoma cellsMonica Guidi, Margarita Muiños-Gimeno, Birgit Kagerbauer, et al.
Genetic Epidemiology|January 30, 2008
Maximizing association statistics over genetic modelsJuan R González, Josep L Carrasco, Frank Dudbridge, et al.
Human Mutation|August 24, 2021
Actionable genomic variants in 6045 participants from the Qatar Genome ProgramAmal Elfatih, Borbala Mifsud, Najeeb Syed, et al.
Epigenomics|October 5, 2019
Epigenetic modification of the pentose phosphate pathway and the IGF-axis in women with gestational diabetes mellitusAngela Steyn, Nigel J Crowther, Shane A Norris, et al.
Human Mutation|April 5, 2002
A common frameshift mutation and other variants in GJB4 (connexin 30.3): Analysis of hearing impairment familiesNúria López-Bigas, Salvatore Melchionda, Paolo Gasparini, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Diagnosis of autosomal dominant polycystic kidney disease using efficient PKD1 and PKD2 targeted next-generation sequencingDaniel Trujillano, Gemma Bullich, Stephan Ossowski, et al.
BMC Bioinformatics|June 9, 2009
Accounting for uncertainty when assessing association between copy number and disease: a latent class modelJuan R González, Isaac Subirana, Geòrgia Escaramís, et al.
Pageof 24