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Cesar P Canales

Showing results (1-10 of 20) with videos related to

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EMBO Molecular Medicine|January 5, 2011
Copy number variation and susceptibility to complex traitsCesar P Canales, Katherina Walz
Journal of Visualized Experiments : Jove|September 2, 2016
CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin PreparationsHuazheng Liang, Bassem Akladios, Cesar P Canales, et al.
Plos One|October 3, 2012
RAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis SyndromePaulina Carmona-Mora, Cesar P Canales, Lei Cao, et al.
European Journal of Human Genetics : EJHG|September 25, 2014
The role of GTF2IRD1 in the auditory pathology of Williams-Beuren SyndromeCesar P Canales, Ann C Y Wong, Peter W Gunning, et al.
BMC Molecular Biology|August 27, 2010
Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis SyndromePaulina Carmona-Mora, Carolina A Encina, Cesar P Canales, et al.
BMC Genomics|June 15, 2016
RNA-Seq analysis of Gtf2ird1 knockout epidermal tissue provides potential insights into molecular mechanisms underpinning Williams-Beuren syndromeSusan M Corley, Cesar P Canales, Paulina Carmona-Mora, et al.
British Journal of Medicine and Medical Research|May 20, 2021
Characterization of a Trpc6 Transgenic Mouse Associated with Early Onset FSGSCesar P Canales, Paola Krall, Pamela Kairath, et al.
Human Genetics|August 16, 2015
The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulationPaulina Carmona-Mora, Jocelyn Widagdo, Florence Tomasetig, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 3, 2020
CRL5-dependent regulation of the small GTPases ARL4C and ARF6 controls hippocampal morphogenesisJisoo S Han, Keiko Hino, Wenzhe Li, et al.
Translational Psychiatry|October 2, 2024
Hyperexcitability and translational phenotypes in a preclinical mouse model of SYNGAP1-related intellectual disabilityTimothy A Fenton, Olivia Y Haouchine, Elizabeth B Hallam, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
EMBO Molecular Medicine|January 5, 2011
Copy number variation and susceptibility to complex traitsCesar P Canales, Katherina Walz
Journal of Visualized Experiments : Jove|September 2, 2016
CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin PreparationsHuazheng Liang, Bassem Akladios, Cesar P Canales, et al.
Plos One|October 3, 2012
RAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis SyndromePaulina Carmona-Mora, Cesar P Canales, Lei Cao, et al.
European Journal of Human Genetics : EJHG|September 25, 2014
The role of GTF2IRD1 in the auditory pathology of Williams-Beuren SyndromeCesar P Canales, Ann C Y Wong, Peter W Gunning, et al.
BMC Molecular Biology|August 27, 2010
Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis SyndromePaulina Carmona-Mora, Carolina A Encina, Cesar P Canales, et al.
BMC Genomics|June 15, 2016
RNA-Seq analysis of Gtf2ird1 knockout epidermal tissue provides potential insights into molecular mechanisms underpinning Williams-Beuren syndromeSusan M Corley, Cesar P Canales, Paulina Carmona-Mora, et al.
British Journal of Medicine and Medical Research|May 20, 2021
Characterization of a Trpc6 Transgenic Mouse Associated with Early Onset FSGSCesar P Canales, Paola Krall, Pamela Kairath, et al.
Human Genetics|August 16, 2015
The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulationPaulina Carmona-Mora, Jocelyn Widagdo, Florence Tomasetig, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 3, 2020
CRL5-dependent regulation of the small GTPases ARL4C and ARF6 controls hippocampal morphogenesisJisoo S Han, Keiko Hino, Wenzhe Li, et al.
Translational Psychiatry|October 2, 2024
Hyperexcitability and translational phenotypes in a preclinical mouse model of SYNGAP1-related intellectual disabilityTimothy A Fenton, Olivia Y Haouchine, Elizabeth B Hallam, et al.
Pageof 2