Search research articles
Contact Us
Filters
Showing results (1-10 of 20) with videos related to
Page
of 2
Sort By:
EMBO Molecular Medicine
|
January 5, 2011
Copy number variation and susceptibility to complex traits
Cesar 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 Preparations
Huazheng 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 Syndrome
Paulina 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 Syndrome
Cesar 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 Syndrome
Paulina 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 syndrome
Susan 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 FSGS
Cesar 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 regulation
Paulina 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 morphogenesis
Jisoo 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 disability
Timothy A Fenton, Olivia Y Haouchine, Elizabeth B Hallam, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
EMBO Molecular Medicine
|
January 5, 2011
Copy number variation and susceptibility to complex traits
Cesar 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 Preparations
Huazheng 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 Syndrome
Paulina 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 Syndrome
Cesar 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 Syndrome
Paulina 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 syndrome
Susan 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 FSGS
Cesar 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 regulation
Paulina 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 morphogenesis
Jisoo 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 disability
Timothy A Fenton, Olivia Y Haouchine, Elizabeth B Hallam, et al.
Page
of 2