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Malte Spielmann

Showing results (101-110 of 137) with videos related to

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Cell|May 12, 2015
Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactionsDarío G Lupiáñez, Katerina Kraft, Verena Heinrich, et al.
Human Genetics|August 26, 2021
Complete lung agenesis caused by complex genomic rearrangements with neo-TAD formation at the SHH locusUirá Souto Melo, Juliette Piard, Björn Fischer-Zirnsak, et al.
Genome Research|January 13, 2016
Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and miceMalte Spielmann, Naseebullah Kakar, Naeimeh Tayebi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 23, 2022
Parkin Deficiency Impairs Mitochondrial DNA Dynamics and Propagates InflammationKobi Wasner, Semra Smajic, Jenny Ghelfi, et al.
Nature Genetics|September 29, 2018
Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesisBjørt K Kragesteen, Malte Spielmann, Christina Paliou, et al.
JID Innovations : Skin Science From Molecules to Population Health|February 5, 2025
Meeting Report on "10th Anniversary Symposium on Inflammatory Skin Disease"Shirin Emtenani, John F Baines, Katja Bieber, et al.
Annals of Neurology|July 30, 2024
Structural Variants at the LMNB1 Locus: Deciphering Pathomechanisms in Autosomal Dominant Adult-Onset Demyelinating LeukodystrophyPaola Dimartino, Mariia Zadorozhna, Verónica Yumiceba, et al.
Science Translational Medicine|September 5, 2014
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genomeTomasz Zemojtel, Sebastian Köhler, Luisa Mackenroth, et al.
Clinical Genetics|May 16, 2019
Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genesLorenzo Sinibaldi, Valentina Parisi, Silvia Lanciotti, et al.
American Journal of Human Genetics|May 30, 2020
Hi-C Identifies Complex Genomic Rearrangements and TAD-Shuffling in Developmental DiseasesUirá Souto Melo, Robert Schöpflin, Rocio Acuna-Hidalgo, et al.
Pageof 14

Showing results (101-110 of 137) with videos related to

Sort By:
Pageof 14
Cell|May 12, 2015
Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactionsDarío G Lupiáñez, Katerina Kraft, Verena Heinrich, et al.
Human Genetics|August 26, 2021
Complete lung agenesis caused by complex genomic rearrangements with neo-TAD formation at the SHH locusUirá Souto Melo, Juliette Piard, Björn Fischer-Zirnsak, et al.
Genome Research|January 13, 2016
Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and miceMalte Spielmann, Naseebullah Kakar, Naeimeh Tayebi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 23, 2022
Parkin Deficiency Impairs Mitochondrial DNA Dynamics and Propagates InflammationKobi Wasner, Semra Smajic, Jenny Ghelfi, et al.
Nature Genetics|September 29, 2018
Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesisBjørt K Kragesteen, Malte Spielmann, Christina Paliou, et al.
JID Innovations : Skin Science From Molecules to Population Health|February 5, 2025
Meeting Report on "10th Anniversary Symposium on Inflammatory Skin Disease"Shirin Emtenani, John F Baines, Katja Bieber, et al.
Annals of Neurology|July 30, 2024
Structural Variants at the LMNB1 Locus: Deciphering Pathomechanisms in Autosomal Dominant Adult-Onset Demyelinating LeukodystrophyPaola Dimartino, Mariia Zadorozhna, Verónica Yumiceba, et al.
Science Translational Medicine|September 5, 2014
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genomeTomasz Zemojtel, Sebastian Köhler, Luisa Mackenroth, et al.
Clinical Genetics|May 16, 2019
Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genesLorenzo Sinibaldi, Valentina Parisi, Silvia Lanciotti, et al.
American Journal of Human Genetics|May 30, 2020
Hi-C Identifies Complex Genomic Rearrangements and TAD-Shuffling in Developmental DiseasesUirá Souto Melo, Robert Schöpflin, Rocio Acuna-Hidalgo, et al.
Pageof 14