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Giuseppe Merla

Showing results (91-100 of 129) with videos related to

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Molecular Cancer|January 16, 2016
Deregulated expression of cryptochrome genes in human colorectal cancerGianluigi Mazzoccoli, Tommaso Colangelo, Anna Panza, et al.
Nature Genetics|December 16, 2014
7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineagesAntonio Adamo, Sina Atashpaz, Pierre-Luc Germain, et al.
Clinical Genetics|May 16, 2023
Novel biallelic variants expand the phenotype of NAA20-related syndromeGianluca D'Onofrio, Claudia Cuccurullo, Silje Kathrine Larsen, et al.
European Journal of Human Genetics : EJHG|July 10, 2020
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann-Steiner and Rubinstein-Taybi syndromesElisabetta Di Fede, Valentina Massa, Bartolomeo Augello, et al.
Genes|April 1, 2020
DNA Methylation in the Diagnosis of Monogenic DiseasesFlavia Cerrato, Angela Sparago, Francesca Ariani, et al.
European Journal of Human Genetics : EJHG|March 26, 2024
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicismMarcello Niceta, Andrea Ciolfi, Marco Ferilli, et al.
Leukemia|July 10, 2018
Correction: MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequencesAlberto L'Abbate, Doron Tolomeo, Ingrid Cifola, et al.
Leukemia|February 23, 2018
MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequencesAlberto L Abbate, Doron Tolomeo, Ingrid Cifola, et al.
Genome Research|April 3, 2015
BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomaliesGuntram Borck, Friederike Hög, Maria Lisa Dentici, et al.
Clinical Genetics|July 17, 2023
Congenital heart defects in CTNNB1 syndrome: Raising clinical awarenessLorenzo Sinibaldi, Giacomo Garone, Alessandra Mandarino, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Molecular Cancer|January 16, 2016
Deregulated expression of cryptochrome genes in human colorectal cancerGianluigi Mazzoccoli, Tommaso Colangelo, Anna Panza, et al.
Nature Genetics|December 16, 2014
7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineagesAntonio Adamo, Sina Atashpaz, Pierre-Luc Germain, et al.
Clinical Genetics|May 16, 2023
Novel biallelic variants expand the phenotype of NAA20-related syndromeGianluca D'Onofrio, Claudia Cuccurullo, Silje Kathrine Larsen, et al.
European Journal of Human Genetics : EJHG|July 10, 2020
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann-Steiner and Rubinstein-Taybi syndromesElisabetta Di Fede, Valentina Massa, Bartolomeo Augello, et al.
Genes|April 1, 2020
DNA Methylation in the Diagnosis of Monogenic DiseasesFlavia Cerrato, Angela Sparago, Francesca Ariani, et al.
European Journal of Human Genetics : EJHG|March 26, 2024
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicismMarcello Niceta, Andrea Ciolfi, Marco Ferilli, et al.
Leukemia|July 10, 2018
Correction: MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequencesAlberto L'Abbate, Doron Tolomeo, Ingrid Cifola, et al.
Leukemia|February 23, 2018
MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequencesAlberto L Abbate, Doron Tolomeo, Ingrid Cifola, et al.
Genome Research|April 3, 2015
BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomaliesGuntram Borck, Friederike Hög, Maria Lisa Dentici, et al.
Clinical Genetics|July 17, 2023
Congenital heart defects in CTNNB1 syndrome: Raising clinical awarenessLorenzo Sinibaldi, Giacomo Garone, Alessandra Mandarino, et al.
Pageof 13