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Malte Spielmann

Showing results (121-130 of 137) with videos related to

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Nature Communications|October 30, 2022
Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomesRobert Schöpflin, Uirá Souto Melo, Hossein Moeinzadeh, et al.
Nature Genetics|April 29, 2024
A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagyKarla P Figueroa, Caspar Gross, Elena Buena-Atienza, et al.
Nature Communications|October 9, 2023
Author Correction: Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformationUirá Souto Melo, Jerome Jatzlau, Cesar A Prada-Medina, et al.
Nature Communications|April 11, 2023
Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformationUirá Souto Melo, Jerome Jatzlau, Cesar A Prada-Medina, et al.
Human Genetics|June 23, 2021
Genome sequencing in families with congenital limb malformationsJonas Elsner, Martin A Mensah, Manuel Holtgrewe, et al.
Human Mutation|July 5, 2022
WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephalyNina Bögershausen, Hannah E Krawczyk, Rami A Jamra, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 7, 2022
Alternative splicing of BUD13 determines the severity of a developmental disorder with lipodystrophy and progeroid featuresUwe Kornak, Namrata Saha, Boris Keren, et al.
Nature|February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulatorLila Allou, Sara Balzano, Andreas Magg, et al.
Nature Medicine|October 15, 2025
Germany's national genomDE strategyAndreas Till, Roman A Siddiqui, Christian Altbürger, et al.
Nature|November 15, 2023
Single-cell, whole-embryo phenotyping of mammalian developmental disordersXingfan Huang, Jana Henck, Chengxiang Qiu, et al.
Pageof 14

Showing results (121-130 of 137) with videos related to

Sort By:
Pageof 14
Nature Communications|October 30, 2022
Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomesRobert Schöpflin, Uirá Souto Melo, Hossein Moeinzadeh, et al.
Nature Genetics|April 29, 2024
A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagyKarla P Figueroa, Caspar Gross, Elena Buena-Atienza, et al.
Nature Communications|October 9, 2023
Author Correction: Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformationUirá Souto Melo, Jerome Jatzlau, Cesar A Prada-Medina, et al.
Nature Communications|April 11, 2023
Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformationUirá Souto Melo, Jerome Jatzlau, Cesar A Prada-Medina, et al.
Human Genetics|June 23, 2021
Genome sequencing in families with congenital limb malformationsJonas Elsner, Martin A Mensah, Manuel Holtgrewe, et al.
Human Mutation|July 5, 2022
WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephalyNina Bögershausen, Hannah E Krawczyk, Rami A Jamra, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 7, 2022
Alternative splicing of BUD13 determines the severity of a developmental disorder with lipodystrophy and progeroid featuresUwe Kornak, Namrata Saha, Boris Keren, et al.
Nature|February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulatorLila Allou, Sara Balzano, Andreas Magg, et al.
Nature Medicine|October 15, 2025
Germany's national genomDE strategyAndreas Till, Roman A Siddiqui, Christian Altbürger, et al.
Nature|November 15, 2023
Single-cell, whole-embryo phenotyping of mammalian developmental disordersXingfan Huang, Jana Henck, Chengxiang Qiu, et al.
Pageof 14