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Thomas Arbogast

Showing results (1-10 of 11) with videos related to

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Angewandte Chemie (International Ed. in English)|October 7, 2011
Condensation approach to aliphatic oligourea foldamers: helices with N-(pyrrolidin-2-ylmethyl)ureido junctionsJuliette Fremaux, Lucile Fischer, Thomas Arbogast, et al.
Disease Models & Mechanisms|June 3, 2015
Deletion of the App-Runx1 region in mice models human partial monosomy 21Thomas Arbogast, Matthieu Raveau, Claire Chevalier, et al.
Human Molecular Genetics|April 21, 2020
Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomaliesTamar Harel, John N Griffin, Thomas Arbogast, et al.
Plos Genetics|February 13, 2016
Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication SyndromesThomas Arbogast, Abdel-Mouttalib Ouagazzal, Claire Chevalier, et al.
American Journal of Human Genetics|October 3, 2017
The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVsMaria Nicla Loviglio, Thomas Arbogast, Aia Elise Jønch, et al.
Human Molecular Genetics|December 28, 2018
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactionsThomas Arbogast, Parisa Razaz, Jacob Ellegood, et al.
American Journal of Human Genetics|May 28, 2019
Germline-Activating RRAS2 Mutations Cause Noonan SyndromeTetsuya Niihori, Koki Nagai, Atsushi Fujita, et al.
Cell Reports|September 26, 2019
Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial DevelopmentYuqi Qiu, Thomas Arbogast, Sandra Martin Lorenzo, et al.
Plos Genetics|July 14, 2017
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognitionThomas Arbogast, Giovanni Iacono, Claire Chevalier, et al.
Science Advances|October 17, 2025
CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathiesKamal Khan, Erika Tavares, Katherine Bishara, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Angewandte Chemie (International Ed. in English)|October 7, 2011
Condensation approach to aliphatic oligourea foldamers: helices with N-(pyrrolidin-2-ylmethyl)ureido junctionsJuliette Fremaux, Lucile Fischer, Thomas Arbogast, et al.
Disease Models & Mechanisms|June 3, 2015
Deletion of the App-Runx1 region in mice models human partial monosomy 21Thomas Arbogast, Matthieu Raveau, Claire Chevalier, et al.
Human Molecular Genetics|April 21, 2020
Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomaliesTamar Harel, John N Griffin, Thomas Arbogast, et al.
Plos Genetics|February 13, 2016
Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication SyndromesThomas Arbogast, Abdel-Mouttalib Ouagazzal, Claire Chevalier, et al.
American Journal of Human Genetics|October 3, 2017
The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVsMaria Nicla Loviglio, Thomas Arbogast, Aia Elise Jønch, et al.
Human Molecular Genetics|December 28, 2018
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactionsThomas Arbogast, Parisa Razaz, Jacob Ellegood, et al.
American Journal of Human Genetics|May 28, 2019
Germline-Activating RRAS2 Mutations Cause Noonan SyndromeTetsuya Niihori, Koki Nagai, Atsushi Fujita, et al.
Cell Reports|September 26, 2019
Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial DevelopmentYuqi Qiu, Thomas Arbogast, Sandra Martin Lorenzo, et al.
Plos Genetics|July 14, 2017
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognitionThomas Arbogast, Giovanni Iacono, Claire Chevalier, et al.
Science Advances|October 17, 2025
CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathiesKamal Khan, Erika Tavares, Katherine Bishara, et al.
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