Caveat mTOR: aberrant signaling disrupts corticogenesis

Bằng Osborne, Lucy R.
Được phát hành 2010

Animal Models of Williams Syndrome

Bằng OSBORNE, LUCY R.
Được phát hành 2010

Rearrangements of the Williams–Beuren syndrome locus: molecular basis and implications for speech and language development

Bằng Osborne, Lucy R., Mervis, Carolyn B.
Được phát hành 2007

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

Bằng O'Leary, Jennifer, Osborne, Lucy R.
Được phát hành 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...

Bằng Mervis Carolyn B, Morris Colleen A, Osborne Lucy R
Được phát hành 2011-02-01

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...

Bằng Morris, Colleen A, Mervis, Carolyn B, Osborne, Lucy R
Được phát hành 2011

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

Bằng Proulx, Éliane, Young, Edwin J., Osborne, Lucy R., Lambe, Evelyn K.
Được phát hành 2010

Refinement of the Genomic Structure of STX1A and Mutation Analysis in Nondeletion Williams Syndrome Patients

Bằng Wu, Yuan-Qing, Bejjani, Bassem A., Tsui, Lap-Chee, Mandel, Ariane, Osborne, Lucy R., Shaffer, Lisa G.
Được phát hành 2002

Observation of a parental inversion variant in a rare Williams–Beuren syndrome family with two affected children

Bằng Scherer, Stephen W., Gripp, Karen W., Lucena, Jaume, Nicholson, Linda, Bonnefont, Jean-Paul, Pérez-Jurado, Luis A., Osborne, Lucy R.
Được phát hành 2005

Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23

Bằng Strong, Emma, Butcher, Darci T., Singhania, Rajat, Mervis, Carolyn B., Morris, Colleen A., De Carvalho, Daniel, Weksberg, Rosanna, Osborne, Lucy R.
Xuất bản năm Am J Hum Genet (2015)

High Prevalence of Diabetes and Pre-Diabetes in Adults With Williams Syndrome

Bằng Pober, Barbara R., Wang, Erica T., Caprio, Sonia, Petersen, Kitt F., Brandt, Cynthia, Stanley, Takara L., Osborne, Lucy R., Dziura, James, Gulanski, Barbara
Được phát hành 2010

The Common Inversion of the Williams–Beuren Syndrome Region at 7q11.23 Does Not Cause Clinical Symptoms

Bằng Tam, Elaine, Young, Edwin J., Morris, Colleen A., Marshall, Christian R., Loo, Wayne, Scherer, Stephen W., Mervis, Carolyn B., Osborne, Lucy R.
Được phát hành 2008

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

Bằng Qaiser, Farah, Yin, Yue, Mervis, Carolyn B., Morris, Colleen A., Klein-Tasman, Bonita P., Tam, Elaine, Osborne, Lucy R., Yuen, Ryan K. C.
Xuất bản năm Orphanet J Rare Dis (2021)

A 1.5 million–base pair inversion polymorphism in families with Williams-Beuren syndrome

Bằng Osborne, Lucy R., Li, Martin, Pober, Barbara, Chitayat, David, Bodurtha, Joann, Mandel, Ariane, Costa, Teresa, Grebe, Theresa, Cox, Sarah, Tsui, Lap-Chee, Scherer, Stephen W.
Được phát hành 2001

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

Bằng 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
Xuất bản năm Mol Brain (2015)

Children with 7q11.23 Duplication Syndrome: Psychological Characteristics

Bằng Mervis, Carolyn B., Klein-Tasman, Bonita P., Huffman, Myra J., Velleman, Shelley L., Pitts, C. Holley, Henderson, Danielle R., Woodruff-Borden, Janet, Morris, Colleen A., Osborne, Lucy R.
Xuất bản năm Am J Med Genet A (2015)

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

Bằng 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.
Xuất bản năm Diabetes (2016)

The Centre for Modeling Human Disease Gene Trap resource

Bằng To, Christine, Epp, Trevor, Reid, Tammy, Lan, Qing, Yu, Mei, Li, Carol Y. J., Ohishi, Minako, Hant, Paula, Tsao, Nora, Casallo, Guillermo, Rossant, Janet, Osborne, Lucy R., Stanford, William L.
Được phát hành 2004

Substrain Differences Reveal Novel Disease-Modifying Gene Candidates That Alter the Clinical Course of a Rodent Model of Multiple Sclerosis

Bằng Summers deLuca, Leslie E., Pikor, Natalia B., O’Leary, Jennifer, Galicia-Rosas, Georgina, Ward, Lesley A., Defreitas, Dustin, Finlay, Trisha M., Ousman, Shalina S., Osborne, Lucy R., Gommerman, Jennifer L.
Được phát hành 2010

Duplication of GTF2I Results in Separation Anxiety in Mice and Humans

Bằng Mervis, Carolyn B., Dida, Joana, Lam, Emily, Crawford-Zelli, Nicole A., Young, Edwin J., Henderson, Danielle R., Onay, Tuncer, Morris, Colleen A., Woodruff-Borden, Janet, Yeomans, John, Osborne, Lucy R.
Được phát hành 2012