Search Results - Lucy R. Osborne
- Showing 1 - 20 results of 27
- Go to Next Page
-
1
Animal models of Williams syndrome by Lucy R. Osborne
Published 2010Revisão -
2
-
3
-
4
-
5
Williams syndrome by Beth A. Kozel, Boaz Barak, Chong Ae Kim, Carolyn Β. Mervis, Lucy R. Osborne, Melanie Porter, Barbara R. Pober
Published 2021Revisão -
6
-
7
-
8
Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome by Shahryar Khattak, Elise Brimble, Wenbo Zhang, Kirill Zaslavsky, Emma Strong, P. Joel Ross, Jason A. Hendry, Seema Mital, Michael W. Salter, Lucy R. Osborne, James Ellis
Published 2015Artigo -
9
-
10
A Predictive Metabolic Signature for the Transition From Gestational Diabetes Mellitus to Type 2 Diabetes by Amina Allalou, Amarnadh Nalla, Kacey J. Prentice, Ying Liu, Ming Zhang, Feihan F. Dai, Xian Ning, Lucy R. Osborne, Brian Cox, Erica P. Gunderson, Michael B. Wheeler
Published 2016Artigo -
11
-
12
Reduced fear and aggression and altered serotonin metabolism in <i>Gtf2ird1</i>‐targeted mice by Edwin J. Young, Tatiana V. Lipina, Elaine Tam, Ariane Mandel, Steven J. Clapcote, Allison R. Bechard, John Chambers, Howard T.J. Mount, Paul Fletcher, John Roder, Lucy R. Osborne
Published 2007Artigo -
13
7q11.23 Duplication syndrome: Physical characteristics and natural history by Colleen A. Morris, Carolyn Β. Mervis, Alex P. Paciorkowski, Omar Abdul‐Rahman, Sarah Dugan, Alan F. Rope, Patricia I. Bader, Laura G. Hendon, Shelley L. Velleman, Bonnie Klein-Tasman, Lucy R. Osborne
Published 2015Artigo -
14
Identification of Genes from a 500-kb Region at 7q11.23 That Is Commonly Deleted in Williams Syndrome Patients by Lucy R. Osborne, Duane W. Martindale, Stephen W. Scherer, Xiaomei Shi, Jack J. Huizenga, Henry H.Q. Heng, Teresa Costa, Barbara R. Pober, Lorelei Lew, Jacquelyn Brinkman, Johanna M. Rommens, Ben F. Koop, Lap‐Chee Tsui
Published 1996Artigo -
15
Severe Expressive-Language Delay Related to Duplication of the Williams–Beuren Locus by Martin J. Somerville, Carolyn Β. Mervis, Edwin J. Young, Eul‐Ju Seo, Miguel Del Campo, Stephen Bamforth, Ella Peregrine, Wayne Loo, Margaret Lilley, Luis A. Pérez‐Jurado, Colleen A. Morris, Stephen W. Scherer, Lucy R. Osborne
Published 2005Artigo -
16
The Sweet Pee Model for Sglt2 Mutation by Joseph Ly, Tuncer Onay, Karen Sison, Gavasker A. Sivaskandarajah, Venkata Sabbisetti, Lingli Li, Joseph V. Bonventre, Ann M. Flenniken, Neal Paragas, Jon M. Barasch, S. Lee Adamson, Lucy R. Osborne, Janet Rossant, Jürgen Schnermann, Susan E. Quaggin
Published 2011Artigo -
17
First Mouse Model for Combined Osteogenesis Imperfecta and Ehlers-Danlos Syndrome by Frieda Chen, Ruolin Guo, Shousaku Itoh, Luisa Moreno, Esther Rosenthal, Tanya Zappitelli, Ralph Zirngibl, Ann M. Flenniken, William G. Cole, Marc D. Grynpas, Lucy R. Osborne, Wolfgang F. Vogel, Lee K. Adamson, Janet Rossant, Jane E. Aubin
Published 2014Artigo -
18
<i>GTF2I</i> dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders by Alejandro Tobon, Reinald Shyti, Carlo Emanuele Villa, Cristina Cheroni, Patricio Fuentes, Sebastiano Trattaro, Nicolò Caporale, Flavia Troglio, Erika Tenderini, Marija Mihailovich, Adrianos Skaros, William T. Gibson, Alessandro Cuomo, Tiziana Bonaldi, Ciro Mercurio, Mario Varasi, Lucy R. Osborne, Giuseppe Testa
Published 2023Artigo -
19
Elastin: mutational spectrum in supravalvular aortic stenosis by Kay Metcalfe, Agnes K Rucka, Leslie Smoot, Guenter Hofstadler, Gerald Tuzler, Pascal McKeown, Victoria Mok Siu, Anita Rauch, John Dean, N R Dennis, Ian O. Ellis, William Reardon, Cheryl Cytrynbaum, Lucy R. Osborne, John R.W. Yates, Andrew Read, Dian Donnai, Mayada Tassabehji
Published 2000Artigo -
20
Essential Role of Fkbp6 in Male Fertility and Homologous Chromosome Pairing in Meiosis by Michael A. Crackower, Nadine K. Kolas, Junko Noguchi, Renu Sarao, Kazuhiro Kikuchi, Hiroyuki Kaneko, Eiji Kobayashi, Yasuhiro Kawai, I. Kozieradzki, Rushin Landers, Rong Mo, Chi-chung Hui, Edward Nieves, Paula E. Cohen, Lucy R. Osborne, Teiji Wada, Tetsuo Kunieda, Peter B. Møens, Josef Penninger
Published 2003Artigo
Search Tools:
Related Subjects
Biology
Genetics
Gene
Medicine
Neuroscience
Psychology
Chromosome
Cognition
Phenotype
Williams syndrome
Autism
Computational biology
Internal medicine
Psychiatry
Chemistry
Developmental psychology
Gene duplication
Mutation
Anxiety
Cell biology
Endocrinology
Haploinsufficiency
Karyotype
Locus (genetics)
Missense mutation
Mutant
Autism spectrum disorder
Biochemistry
Breakpoint
Chromosomal inversion