Zobrazeno 1 - 10
of 136
pro vyhledávání: '"Lisa Stubbs"'
Autor:
P. Anne Weisner, Chih-Ying Chen, Younguk Sun, Jennifer Yoo, Wei-Chun Kao, Huimin Zhang, Emily T. Baltz, Joseph M. Troy, Lisa Stubbs
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 9, Iss 11, Pp 3891-3906 (2019)
AUTS2 was originally discovered as the gene disrupted by a translocation in human twins with Autism spectrum disorder, intellectual disability, and epilepsy. Since that initial finding, AUTS2-linked mutations and variants have been associated with a
Externí odkaz:
https://doaj.org/article/3508d13688684926bf63c96fc9c20563
Publikováno v:
PLoS ONE, Vol 14, Iss 10, p e0224287 (2019)
The parental allele specificity of mammalian imprinted genes has been evolutionarily well conserved, although its functional constraints and associated mechanisms are not fully understood. In the current study, we generated a mouse mutant with switch
Externí odkaz:
https://doaj.org/article/d9ef7bb89b9f4676876ce3a162e53c2f
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 22, p 8861 (2020)
Core histone variants, such as H2A.X and H3.3, serve specialized roles in chromatin processes that depend on the genomic distributions and amino acid sequence differences of the variant proteins. Modifications of these variants alter interactions wit
Externí odkaz:
https://doaj.org/article/5621a4284d0f4985a235eb1aaee7cef6
Autor:
Syed Abbas Bukhari, Michael C Saul, Christopher H Seward, Huimin Zhang, Miles Bensky, Noelle James, Sihai Dave Zhao, Sriram Chandrasekaran, Lisa Stubbs, Alison M Bell
Publikováno v:
PLoS Genetics, Vol 13, Iss 7, p e1006840 (2017)
Animals exhibit dramatic immediate behavioral plasticity in response to social interactions, and brief social interactions can shape the future social landscape. However, the molecular mechanisms contributing to behavioral plasticity are unclear. Her
Externí odkaz:
https://doaj.org/article/de66b683e0454c7b982deac17db72951
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187611 (2017)
The application of complex network modeling to analyze large co-expression data sets has gained traction during the last decade. In particular, the use of the weighted gene co-expression network analysis framework has allowed an unbiased and systems-
Externí odkaz:
https://doaj.org/article/6afaa5f9766a49cbad4fc8feec7ab001
Autor:
Licia Selleri, Marisa S Bartolomei, Wendy A Bickmore, Lin He, Lisa Stubbs, Wolf Reik, Gregory S Barsh
Publikováno v:
PLoS Genetics, Vol 12, Iss 12, p e1006485 (2016)
Externí odkaz:
https://doaj.org/article/daabc09d1a304f2fb1ade70f0946421b
Autor:
C Chase Bolt, Soumya Negi, Nuno Guimarães-Camboa, Huimin Zhang, Joseph M Troy, Xiaochen Lu, Andreas Kispert, Sylvia M Evans, Lisa Stubbs
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0154413 (2016)
The T-box transcription factor TBX18 is essential to mesenchymal cell differentiation in several tissues and Tbx18 loss-of-function results in dramatic organ malformations and perinatal lethality. Here we demonstrate for the first time that Tbx18 is
Externí odkaz:
https://doaj.org/article/f6ba77bcb90240929d6c94aa02deef55
Autor:
Katja Nowick, Christopher Fields, Tim Gernat, Derek Caetano-Anolles, Nadezda Kholina, Lisa Stubbs
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e21553 (2011)
The molecular changes underlying major phenotypic differences between humans and other primates are not well understood, but alterations in gene regulation are likely to play a major role. Here we performed a thorough evolutionary analysis of the lar
Externí odkaz:
https://doaj.org/article/394883d3c5734e92b6150b4a079cfa2d
Autor:
Yunshu Song, Christopher H. Seward, Chih-Ying Chen, Amber LeBlanc, Analise M. Leddy, Lisa Stubbs
Publikováno v:
bioRxiv
Rearrangements within theAUTS2region are associated with a rare syndromic disorder with intellectual disability, developmental delay and behavioral abnormalities as core features. In addition, smaller regional variants are linked to wide range of neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a220a2037b1cd2a9a4cb7898d85e6d95
https://europepmc.org/articles/PMC10187298/
https://europepmc.org/articles/PMC10187298/
Autor:
Joseph M. Troy, Wei-Chun Kao, Lisa Stubbs, Jennifer Yoo, Emily T Baltz, P Anne Weisner, Chih-Ying Chen, Huimin Zhang, Younguk Sun
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 9, Iss 11, Pp 3891-3906 (2019)
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics
AUTS2 was originally discovered as the gene disrupted by a translocation in human twins with Autism spectrum disorder, intellectual disability, and epilepsy. Since that initial finding, AUTS2-linked mutations and variants have been associated with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::425e03165a5fdfc213d55595ec9f59ed
http://g3journal.org/lookup/doi/10.1534/g3.119.400723
http://g3journal.org/lookup/doi/10.1534/g3.119.400723