Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Komal Vadodaria"'
Autor:
Janani Iyer, Mayanglambam Dhruba Singh, Matthew Jensen, Payal Patel, Lucilla Pizzo, Emily Huber, Haley Koerselman, Alexis T. Weiner, Paola Lepanto, Komal Vadodaria, Alexis Kubina, Qingyu Wang, Abigail Talbert, Sneha Yennawar, Jose Badano, J. Robert Manak, Melissa M. Rolls, Arjun Krishnan, Santhosh Girirajan
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-19 (2018)
The 16p11.2 deletion leads to a range of neurodevelopmental phenotypes, but to date, sequencing studies have not been able to pinpoint individual genes that are causative for the disease on their own. Here, using Drosophila homologs of 14 16p11.2 gen
Externí odkaz:
https://doaj.org/article/d7ac17fe1f8f4fac96fe435cdcaaa18c
Autor:
Santhosh Girirajan, Arjun Krishnan, Sneha Yennawar, Abigail Talbert, Paola Lepanto, Jose L. Badano, J. Robert Manak, Komal Vadodaria, Qingyu Wang, Haley Koerselman, Matthew Jensen, Payal Patel, Janani Iyer, Melissa M. Rolls, Emily Huber, Mayanglambam Dhruba Singh, Alexis Kubina, Lucilla Pizzo, Alexis T. Weiner
Rare CNVs such as the 16p11.2 deletion are associated with extensive phenotypic heterogeneity, complicating disease gene discovery and functional evaluation. We used RNA interference in Drosophila melanogaster to evaluate the phenotype, function, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f54a08d1017c58c90fd5f3be95291f7a
https://doi.org/10.1101/185355
https://doi.org/10.1101/185355
