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Horsthemke

Showing results (171-180 of 368) with videos related to

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European Journal of Human Genetics : EJHG|April 6, 2006
Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15Corinna Zogel, Stefan Böhringer, Stephanie Gross, et al.
Genomics|March 6, 2007
C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brainKarin Buiting, Hülya Nazlican, Danuta Galetzka, et al.
European Journal of Human Genetics : EJHG|March 11, 2020
Common genetic variation in the Angelman syndrome imprinting centre affects the imprinting of chromosome 15Jasmin Beygo, Christian Grosser, Sabine Kaya, et al.
Angewandte Chemie (International Ed. in English)|February 4, 2020
Clarification of Decomposition Pathways in a State-of-the-Art Lithium Ion Battery Electrolyte through <sup>13</sup> C-Labeling of Electrolyte ComponentsJonas Henschel, Christoph Peschel, Sven Klein, et al.
Sensors (Basel, Switzerland)|February 11, 2023
Edge-Machine-Learning-Assisted Robust Magnetometer Based on Randomly Oriented NV-Ensembles in DiamondJonas Homrighausen, Ludwig Horsthemke, Jens Pogorzelski, et al.
Human Molecular Genetics|December 1, 2001
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3AM Runte, A Hüttenhofer, S Gross, et al.
Human Genetics|January 27, 2000
The EIF3S3 gene encoding the p40 subunit of the translation initiation factor eIF3 has eight exons and maps to the Langer-Giedion syndrome chromosome region on 8q24, but is not the TRPS1 geneO Schmidt, D von Holtum, S Gross, et al.
Plos One|November 3, 2010
Aging of Xenopus tropicalis eggs leads to deadenylation of a specific set of maternal mRNAs and loss of developmental potentialAnna Kosubek, Ludger Klein-Hitpass, Katrin Rademacher, et al.
Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft|October 15, 2019
In vitro postovulatory oocyte aging affects H3K9 trimethylation in two-cell embryos after IVFTheresa Petri, Debora Dankert, Hannah Demond, et al.
Journal of Medical Genetics|June 1, 1995
Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastomaI Szijan, D R Lohmann, D L Parma, et al.
Pageof 37

Showing results (171-180 of 368) with videos related to

Sort By:
Pageof 37
European Journal of Human Genetics : EJHG|April 6, 2006
Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15Corinna Zogel, Stefan Böhringer, Stephanie Gross, et al.
Genomics|March 6, 2007
C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brainKarin Buiting, Hülya Nazlican, Danuta Galetzka, et al.
European Journal of Human Genetics : EJHG|March 11, 2020
Common genetic variation in the Angelman syndrome imprinting centre affects the imprinting of chromosome 15Jasmin Beygo, Christian Grosser, Sabine Kaya, et al.
Angewandte Chemie (International Ed. in English)|February 4, 2020
Clarification of Decomposition Pathways in a State-of-the-Art Lithium Ion Battery Electrolyte through <sup>13</sup> C-Labeling of Electrolyte ComponentsJonas Henschel, Christoph Peschel, Sven Klein, et al.
Sensors (Basel, Switzerland)|February 11, 2023
Edge-Machine-Learning-Assisted Robust Magnetometer Based on Randomly Oriented NV-Ensembles in DiamondJonas Homrighausen, Ludwig Horsthemke, Jens Pogorzelski, et al.
Human Molecular Genetics|December 1, 2001
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3AM Runte, A Hüttenhofer, S Gross, et al.
Human Genetics|January 27, 2000
The EIF3S3 gene encoding the p40 subunit of the translation initiation factor eIF3 has eight exons and maps to the Langer-Giedion syndrome chromosome region on 8q24, but is not the TRPS1 geneO Schmidt, D von Holtum, S Gross, et al.
Plos One|November 3, 2010
Aging of Xenopus tropicalis eggs leads to deadenylation of a specific set of maternal mRNAs and loss of developmental potentialAnna Kosubek, Ludger Klein-Hitpass, Katrin Rademacher, et al.
Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft|October 15, 2019
In vitro postovulatory oocyte aging affects H3K9 trimethylation in two-cell embryos after IVFTheresa Petri, Debora Dankert, Hannah Demond, et al.
Journal of Medical Genetics|June 1, 1995
Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastomaI Szijan, D R Lohmann, D L Parma, et al.
Pageof 37