Global Analysis of Gene Expression in the Developing Brain of Gtf2ird1 Knockout Mice

por O'Leary, Jennifer, Osborne, Lucy R.
Publicado 2011

Frequency of the 7q11.23 inversion polymorphism in transmitting parents of children with Williams syndrome and in the general population does not differ between North America and E...

por Morris, Colleen A, Mervis, Carolyn B, Osborne, Lucy R
Publicado 2011

Enhanced prefrontal serotonin 5-HT(1A) currents in a mouse model of Williams-Beuren syndrome with low innate anxiety

por Proulx, Éliane, Young, Edwin J., Osborne, Lucy R., Lambe, Evelyn K.
Publicado 2010

DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number

por Strong, Emma, Mervis, Carolyn B., Tam, Elaine, Morris, Colleen A., Klein-Tasman, Bonita P., Velleman, Shelley L., Osborne, Lucy R.
Publicado 2023

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype

por Qaiser, Farah, Yin, Yue, Mervis, Carolyn B., Morris, Colleen A., Klein-Tasman, Bonita P., Tam, Elaine, Osborne, Lucy R., Yuen, Ryan K. C.
Publicado 2021

Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome

por Khattak, Shahryar, Brimble, Elise, Zhang, Wenbo, Zaslavsky, Kirill, Strong, Emma, Ross, P. Joel, Hendry, Jason, Mital, Seema, Salter, Michael W., Osborne, Lucy R., Ellis, James
Publicado 2015

A Predictive Metabolic Signature for the Transition From Gestational Diabetes Mellitus to Type 2 Diabetes

por Allalou, Amina, Nalla, Amarnadh, Prentice, Kacey J., Liu, Ying, Zhang, Ming, Dai, Feihan F., Ning, Xian, Osborne, Lucy R., Cox, Brian J., Gunderson, Erica P., Wheeler, Michael B.
Publicado 2016

Transcription Factor 2I Regulates Neuronal Development via TRPC3 in 7q11.23 Disorder Models

por Deurloo, Marielle H. S., Turlova, Ekaterina, Chen, Wen-Liang, Lin, You Wei, Tam, Elaine, Tassew, Nardos G., Wu, Michael, Huang, Ya-Chi, Crawley, Jacqueline N., Monnier, Philippe P., Groffen, Alexander J. A., Sun, Hong-Shuo, Osborne, Lucy R., Feng, Zhong-Ping
Publicado 2018

Enu Mutagenesis Identifies a Novel Platelet Phenotype in a Loss-Of-Function Jak2 Allele

por Anderson, Nicole M., Javadi, Mojib, Berndl, Elizabeth, Berberovic, Zorana, Bailey, Monica L., Huang, Kai, Flenniken, Ann M., Osborne, Lucy R., Adamson, S. Lee, Rossant, Janet, Carter-Su, Christin, Wang, Chen, McNagny, Kelly M., Paulson, Robert F., Minden, Mark D., Stanford, William L., Barber, Dwayne L.
Publicado 2013