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Claudia Spits

Showing results (31-40 of 52) with videos related to

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Human Molecular Genetics|March 14, 2022
Mitochondrial DNA variants segregate during human preimplantation development into genetically different cell lineages that are maintained postnatallyJoke Mertens, Marius Regin, Neelke De Munck, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cellsFilippo Zambelli, Kim Vancampenhout, Dorien Daneels, et al.
Elife|December 9, 2024
Complex aneuploidy triggers autophagy and p53-mediated apoptosis and impairs the second lineage segregation in human preimplantation embryosMarius Regin, Yingnan Lei, Edouard Couvreu De Deckersberg, et al.
Cell Stem Cell|December 2, 2022
The consequences of recurrent genetic and epigenetic variants in human pluripotent stem cellsPeter W Andrews, Ivana Barbaric, Nissim Benvenisty, et al.
Plos One|November 11, 2014
A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genomeKim Vancampenhout, Ben Caljon, Claudia Spits, et al.
Human Molecular Genetics|November 26, 2020
MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cellsSilvie Franck, Lise Barbé, Simon Ardui, et al.
Nucleic Acids Research|May 16, 2006
Single-cell chromosomal imbalances detection by array CGHCedric Le Caignec, Claudia Spits, Karen Sermon, et al.
Biology Open|January 12, 2022
Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicingSilvie Franck, Edouard Couvreu De Deckersberg, Jodi L Bubenik, et al.
Stem Cell Reports|June 19, 2018
Random Mutagenesis, Clonal Events, and Embryonic or Somatic Origin Determine the mtDNA Variant Type and Load in Human Pluripotent Stem CellsFilippo Zambelli, Joke Mertens, Dominika Dziedzicka, et al.
Human Reproduction Open|January 20, 2025
The interplay between mitochondrial DNA genotypes, female infertility, ovarian response, and mutagenesis in oocytesAnnelore Van Der Kelen, Letizia Li Piani, Joke Mertens, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|March 14, 2022
Mitochondrial DNA variants segregate during human preimplantation development into genetically different cell lineages that are maintained postnatallyJoke Mertens, Marius Regin, Neelke De Munck, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cellsFilippo Zambelli, Kim Vancampenhout, Dorien Daneels, et al.
Elife|December 9, 2024
Complex aneuploidy triggers autophagy and p53-mediated apoptosis and impairs the second lineage segregation in human preimplantation embryosMarius Regin, Yingnan Lei, Edouard Couvreu De Deckersberg, et al.
Cell Stem Cell|December 2, 2022
The consequences of recurrent genetic and epigenetic variants in human pluripotent stem cellsPeter W Andrews, Ivana Barbaric, Nissim Benvenisty, et al.
Plos One|November 11, 2014
A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genomeKim Vancampenhout, Ben Caljon, Claudia Spits, et al.
Human Molecular Genetics|November 26, 2020
MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cellsSilvie Franck, Lise Barbé, Simon Ardui, et al.
Nucleic Acids Research|May 16, 2006
Single-cell chromosomal imbalances detection by array CGHCedric Le Caignec, Claudia Spits, Karen Sermon, et al.
Biology Open|January 12, 2022
Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicingSilvie Franck, Edouard Couvreu De Deckersberg, Jodi L Bubenik, et al.
Stem Cell Reports|June 19, 2018
Random Mutagenesis, Clonal Events, and Embryonic or Somatic Origin Determine the mtDNA Variant Type and Load in Human Pluripotent Stem CellsFilippo Zambelli, Joke Mertens, Dominika Dziedzicka, et al.
Human Reproduction Open|January 20, 2025
The interplay between mitochondrial DNA genotypes, female infertility, ovarian response, and mutagenesis in oocytesAnnelore Van Der Kelen, Letizia Li Piani, Joke Mertens, et al.
Pageof 6