Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Christopher, Lemoine"'
Publikováno v:
JPRAS Open, Vol 39, Iss , Pp 75-80 (2024)
Breast augmentation is considered one of the most commonly performed procedures by aesthetic plastic surgeons, representing 16 % of all global plastic surgery procedures in 2020. Given the fact that thoracic trauma comprises over 20 % of trauma world
Externí odkaz:
https://doaj.org/article/40fe129ac11b4676bc86356b8ea45543
Publikováno v:
Development
Disruption of the minor spliceosome due to mutations in RNU4ATAC is linked to primordial dwarfism in microcephalic osteodysplastic primordial dwarfism type 1, Roifman syndrome, and Lowry-Wood syndrome. Similarly, primordial dwarfism in domesticated a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e198541fab5b3446752df08befd2d88
https://europepmc.org/articles/PMC7438004/
https://europepmc.org/articles/PMC7438004/
Disruption of the minor spliceosome causes primordial dwarfism in microcephalic osteodysplastic primordial dwarfism type 1. Similarly, primordial dwarfism in domesticated animals is linked to positive selection in minor spliceosome components. Despit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e657ff7f8fff0be420df1ab09d02b5e1
https://doi.org/10.1101/2020.03.16.994384
https://doi.org/10.1101/2020.03.16.994384
Autor:
Nikita Sturrock, Rahul N. Kanadia, Nhut Nguyen, Marybeth Baumgartner, Katery C. Hyatt, Gabriela S. Aquino, Sahar Al Seesi, Anouk M. Olthof, Christopher Lemoine, Kyle D. Drake
Mutation in minor spliceosome components is linked to the developmental disorder microcephalic osteodysplastic primordial dwarfism type 1 (MOPD1). Here, we inactivated the minor spliceosome in the developing mouse cortex (pallium) by ablating Rnu11,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e38a3e7eff8607ffefff0b8f8c8cbf06
https://europepmc.org/articles/PMC6141777/
https://europepmc.org/articles/PMC6141777/
Autor:
Rahul N. Kanadia, Ashley M Kilcollins, Abdul Rouf Banday, Sahar Al Seesi, Marybeth Baumgartner, Nikita Sturrock, Devi Krishna Priya Karunakaran, Ion I. Mandoiu, Christopher Lemoine
Publikováno v:
Developmental Neurobiology. 75:895-907
In eukaryotes, gene expression requires splicing, which starts with the identification of exon-intron boundaries by the small, nuclear RNA (snRNAs) of the spliceosome, aided by associated proteins. In the mammalian genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfc5b9a5bf9b888e961908110f515f39
https://doi.org/10.1002/dneu.22257
https://doi.org/10.1002/dneu.22257
Autor:
Christopher Lemoine, Marybeth Baumgartner, Nhut Nguyen, Katery C. Hyatt, Kyle D. Drake, Rahul N. Kanadia, Sahar Al Seesi, Anouk M. Olthof, Nikita Sturrock
Inactivation of the minor spliceosome has been linked to microcephalic osteodysplastic primordial dwarfism type 1 (MOPD1). To interrogate how minor intron splicing regulates cortical development, we employed Emx1-Cre to ablate Rnu11, which encodes th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd1c261444b0d27b877121407a9f1fd
Autor:
Marybeth Baumgartner, Claudio Punzo, Ion I. Mandoiu, Aditya Venkatesh, Sahar Al Seesi, Rahul N. Kanadia, Ashley M Kilcollins, Sean Congdon, Abdul Rouf Banday, Christopher Lemoine, Devi Krishna Priya Karunakaran
Publikováno v:
Cell Cycle. 13:2526-2541
In the mammalian genome, each histone family contains multiple replication-dependent paralogs, which are found in clusters where their transcription is thought to be coupled to the cell cycle. Here, we wanted to interrogate the transcriptional regula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5832f2165faf2f0e8005d15a60989f1a
https://doi.org/10.4161/15384101.2015.941757
https://doi.org/10.4161/15384101.2015.941757
Autor:
Christopher Lemoine, Devi Krishna Priya Karunakaran, Abdul Rouf Banday, Ion I. Mandoiu, Sahar Al Seesi, Marybeth Baumgartner, Anouk M. Olthof, Rahul N. Kanadia
Publikováno v:
BMC Genomics
Background The retina as a model system with extensive information on genes involved in development/maintenance is of great value for investigations employing deep sequencing to capture transcriptome change over time. This in turn could enable us to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60f357ad4db0102226ae0cded8d021de
https://pubmed.ncbi.nlm.nih.gov/27586787
https://pubmed.ncbi.nlm.nih.gov/27586787
Autor:
Nisarg Chhaya, Amye Black, Christopher Lemoine, Sean Congdon, Devi Krishna Priya Karunakaran, Rahul N. Kanadia
Publikováno v:
Investigative ophthalmologyvisual science. 56(2)
Purpose To understand how loss of citron kinase (CitK) affects retinal progenitor cells (RPCs) in the developing rat retina. Methods We compared knockout (KO) and wild-type (WT) retinae by immunohistochemistry. The TdT-mediated dUTP terminal nick-end
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bb9c90aa098b8c46b9949ac5fdceb4f
https://pubmed.ncbi.nlm.nih.gov/25593024
https://pubmed.ncbi.nlm.nih.gov/25593024
Autor:
Marybeth, Baumgartner, Christopher, Lemoine, Sahar, Al Seesi, Devi Krishna Priya, Karunakaran, Nikita, Sturrock, Abdul Rouf, Banday, Ashley M, Kilcollins, Ion, Mandoiu, Rahul N, Kanadia
Publikováno v:
Developmental neurobiology. 75(9)
In eukaryotes, gene expression requires splicing, which starts with the identification of exon-intron boundaries by the small, nuclear RNA (snRNAs) of the spliceosome, aided by associated proteins. In the mammalian genome,1% of introns lack canonical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0db01e3381dafa81cb6731e2fca798bb
https://pubmed.ncbi.nlm.nih.gov/25492806
https://pubmed.ncbi.nlm.nih.gov/25492806