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Malte Spielmann

Showing results (81-90 of 137) with videos related to

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Science (New York, N.Y.)|July 2, 2021
Embryo-scale, single-cell spatial transcriptomicsSanjay R Srivatsan, Mary C Regier, Eliza Barkan, et al.
Scientific Reports|July 15, 2024
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndromeJelena Pozojevic, Radhika Sivaprasad, Joshua Laß, et al.
American Journal of Human Genetics|August 25, 2021
Position effects at the FGF8 locus are associated with femoral hypoplasiaMagdalena Socha, Anna Sowińska-Seidler, Uirá Souto Melo, et al.
European Journal of Human Genetics : EJHG|October 9, 2014
Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patientDenise Emmerich, Tomasz Zemojtel, Jochen Hecht, et al.
Human Molecular Genetics|February 22, 2015
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)Elisa Giorgio, Daniel Robyr, Malte Spielmann, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|July 6, 2026
A 3D Human Bone and Bone Marrow-on-a-Chip Model for In Vitro Bone Remodeling and Immune Cell MaintenanceNina Stelzer, Melanie-Jasmin Ort, Kristian Händler, et al.
American Journal of Human Genetics|August 30, 2016
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian DiseaseDamian Smedley, Max Schubach, Julius O B Jacobsen, et al.
American Journal of Human Genetics|October 2, 2012
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locusMalte Spielmann, Francesco Brancati, Peter M Krawitz, et al.
Elife|April 23, 2025
Diet modulates the therapeutic effects of dimethyl fumarate mediated by the immunometabolic neutrophil receptor HCAR2Joanna Kosinska, Julian C Assmann, Julica Inderhees, et al.
HGG Advances|May 22, 2023
A complex structural variant near <i>SOX3</i> causes X-linked split-hand/foot malformationElke de Boer, Carlo Marcelis, Kornelia Neveling, et al.
Pageof 14

Showing results (81-90 of 137) with videos related to

Sort By:
Pageof 14
Science (New York, N.Y.)|July 2, 2021
Embryo-scale, single-cell spatial transcriptomicsSanjay R Srivatsan, Mary C Regier, Eliza Barkan, et al.
Scientific Reports|July 15, 2024
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndromeJelena Pozojevic, Radhika Sivaprasad, Joshua Laß, et al.
American Journal of Human Genetics|August 25, 2021
Position effects at the FGF8 locus are associated with femoral hypoplasiaMagdalena Socha, Anna Sowińska-Seidler, Uirá Souto Melo, et al.
European Journal of Human Genetics : EJHG|October 9, 2014
Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patientDenise Emmerich, Tomasz Zemojtel, Jochen Hecht, et al.
Human Molecular Genetics|February 22, 2015
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)Elisa Giorgio, Daniel Robyr, Malte Spielmann, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|July 6, 2026
A 3D Human Bone and Bone Marrow-on-a-Chip Model for In Vitro Bone Remodeling and Immune Cell MaintenanceNina Stelzer, Melanie-Jasmin Ort, Kristian Händler, et al.
American Journal of Human Genetics|August 30, 2016
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian DiseaseDamian Smedley, Max Schubach, Julius O B Jacobsen, et al.
American Journal of Human Genetics|October 2, 2012
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locusMalte Spielmann, Francesco Brancati, Peter M Krawitz, et al.
Elife|April 23, 2025
Diet modulates the therapeutic effects of dimethyl fumarate mediated by the immunometabolic neutrophil receptor HCAR2Joanna Kosinska, Julian C Assmann, Julica Inderhees, et al.
HGG Advances|May 22, 2023
A complex structural variant near <i>SOX3</i> causes X-linked split-hand/foot malformationElke de Boer, Carlo Marcelis, Kornelia Neveling, et al.
Pageof 14