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Victor Felix

Showing results (111-120 of 147) with videos related to

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Nucleic Acids Research|December 11, 2020
HMPDACC: a Human Microbiome Project Multi-omic data resourceHeather Huot Creasy, Victor Felix, Jain Aluvathingal, et al.
Human Genetics|July 15, 2018
Phenotypic and genotypic overlap between mosaic NF2 and schwannomatosis in patients with multiple non-intradermal schwannomasHildegard Kehrer-Sawatzki, Lan Kluwe, Reinhard E Friedrich, et al.
Nucleic Acids Research|October 29, 2014
Disease Ontology 2015 update: an expanded and updated database of human diseases for linking biomedical knowledge through disease dataWarren A Kibbe, Cesar Arze, Victor Felix, et al.
Acta Neuropathologica|May 30, 2016
The importance of nerve microenvironment for schwannoma developmentAlexander Schulz, Robert Büttner, Christian Hagel, et al.
Annals of Neurology|July 30, 2016
Multifocal nerve lesions and LZTR1 germline mutations in segmental schwannomatosisSaid Farschtschi, Victor-Felix Mautner, Mirko Pham, et al.
Database : the Journal of Biological Databases and Curation|January 18, 2017
Cryptosporidium hominis gene catalog: a resource for the selection of novel Cryptosporidium vaccine candidatesOlukemi O Ifeonu, Raphael Simon, Sharon M Tennant, et al.
Human Mutation|July 28, 2012
Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorderJulia Vogt, Tanja Mussotter, Kathrin Bengesser, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 15, 2010
Monozygotic twins with neurofibromatosis type 1 (NF1) display differences in methylation of NF1 gene promoter elements, 5' untranslated region, exon and intron 1Anja Harder, Sabrina Titze, Lena Herbst, et al.
BMC Neurology|October 4, 2013
Lovastatin improves impaired synaptic plasticity and phasic alertness in patients with neurofibromatosis type 1Florian Mainberger, Nikolai H Jung, Martin Zenker, et al.
Human Mutation|August 21, 2010
Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletionsAngelika C Roehl, Julia Vogt, Tanja Mussotter, et al.
Pageof 15

Showing results (111-120 of 147) with videos related to

Sort By:
Pageof 15
Nucleic Acids Research|December 11, 2020
HMPDACC: a Human Microbiome Project Multi-omic data resourceHeather Huot Creasy, Victor Felix, Jain Aluvathingal, et al.
Human Genetics|July 15, 2018
Phenotypic and genotypic overlap between mosaic NF2 and schwannomatosis in patients with multiple non-intradermal schwannomasHildegard Kehrer-Sawatzki, Lan Kluwe, Reinhard E Friedrich, et al.
Nucleic Acids Research|October 29, 2014
Disease Ontology 2015 update: an expanded and updated database of human diseases for linking biomedical knowledge through disease dataWarren A Kibbe, Cesar Arze, Victor Felix, et al.
Acta Neuropathologica|May 30, 2016
The importance of nerve microenvironment for schwannoma developmentAlexander Schulz, Robert Büttner, Christian Hagel, et al.
Annals of Neurology|July 30, 2016
Multifocal nerve lesions and LZTR1 germline mutations in segmental schwannomatosisSaid Farschtschi, Victor-Felix Mautner, Mirko Pham, et al.
Database : the Journal of Biological Databases and Curation|January 18, 2017
Cryptosporidium hominis gene catalog: a resource for the selection of novel Cryptosporidium vaccine candidatesOlukemi O Ifeonu, Raphael Simon, Sharon M Tennant, et al.
Human Mutation|July 28, 2012
Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorderJulia Vogt, Tanja Mussotter, Kathrin Bengesser, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 15, 2010
Monozygotic twins with neurofibromatosis type 1 (NF1) display differences in methylation of NF1 gene promoter elements, 5' untranslated region, exon and intron 1Anja Harder, Sabrina Titze, Lena Herbst, et al.
BMC Neurology|October 4, 2013
Lovastatin improves impaired synaptic plasticity and phasic alertness in patients with neurofibromatosis type 1Florian Mainberger, Nikolai H Jung, Martin Zenker, et al.
Human Mutation|August 21, 2010
Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletionsAngelika C Roehl, Julia Vogt, Tanja Mussotter, et al.
Pageof 15