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Maria J Barrero

Showing results (21-30 of 29) with videos related to

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Nature Biotechnology|October 22, 2008
Efficient and rapid generation of induced pluripotent stem cells from human keratinocytesTrond Aasen, Angel Raya, Maria J Barrero, et al.
Molecular Oncology|January 8, 2025
CRISPR targeting of FOXL2 c.402C>G mutation reduces malignant phenotype in granulosa tumor cells and identifies anti-tumoral compoundsSandra Amarilla-Quintana, Paloma Navarro, Iván Hernández, et al.
Molecular Neurobiology|December 15, 2024
EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental SyndromeLaura Machado Lara Carvalho, Jessica Rzasa, Jennifer Kerkhof, et al.
Frontiers in Genetics|July 11, 2026
A role for <i>EHMT2</i> in a novel autosomal recessive neurodevelopmental syndrome? A case reportDmitrijs Rots, Beatriz Cristina de Oliveira, Laura Machado Lara Carvalho, et al.
International Journal of Molecular Sciences|August 26, 2022
Differences in Expression of <i>IQSEC2</i> Transcript Isoforms in Male and Female Cases with Loss of Function Variants and Neurodevelopmental DisorderBeatriz Baladron, Lidia M Mielu, Estrella López-Martín, et al.
Cell Stem Cell|January 8, 2011
Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in cultureLouise C Laurent, Igor Ulitsky, Ileana Slavin, et al.
Human Genomics|March 26, 2026
Translating multi-omics into healthcare: requisites for scalable and equitable implementationBirute Tumiene, David R Adams, Robert Allaway, et al.
Genome Medicine|May 12, 2026
Unprocessed U1 snRNAs as a biomarker of INTS11- and BRAT1-related neurodevelopmental disordersBeatrice Valtorta, Zuzana Polackova, Reza Maroofian, et al.
Nature Communications|July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activityAleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Nature Biotechnology|October 22, 2008
Efficient and rapid generation of induced pluripotent stem cells from human keratinocytesTrond Aasen, Angel Raya, Maria J Barrero, et al.
Molecular Oncology|January 8, 2025
CRISPR targeting of FOXL2 c.402C>G mutation reduces malignant phenotype in granulosa tumor cells and identifies anti-tumoral compoundsSandra Amarilla-Quintana, Paloma Navarro, Iván Hernández, et al.
Molecular Neurobiology|December 15, 2024
EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental SyndromeLaura Machado Lara Carvalho, Jessica Rzasa, Jennifer Kerkhof, et al.
Frontiers in Genetics|July 11, 2026
A role for <i>EHMT2</i> in a novel autosomal recessive neurodevelopmental syndrome? A case reportDmitrijs Rots, Beatriz Cristina de Oliveira, Laura Machado Lara Carvalho, et al.
International Journal of Molecular Sciences|August 26, 2022
Differences in Expression of <i>IQSEC2</i> Transcript Isoforms in Male and Female Cases with Loss of Function Variants and Neurodevelopmental DisorderBeatriz Baladron, Lidia M Mielu, Estrella López-Martín, et al.
Cell Stem Cell|January 8, 2011
Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in cultureLouise C Laurent, Igor Ulitsky, Ileana Slavin, et al.
Human Genomics|March 26, 2026
Translating multi-omics into healthcare: requisites for scalable and equitable implementationBirute Tumiene, David R Adams, Robert Allaway, et al.
Genome Medicine|May 12, 2026
Unprocessed U1 snRNAs as a biomarker of INTS11- and BRAT1-related neurodevelopmental disordersBeatrice Valtorta, Zuzana Polackova, Reza Maroofian, et al.
Nature Communications|July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activityAleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
Pageof 3