المؤلفون: Garrett, Lillian, Trümbach, Dietrich, Lee, Donghyung, Mandillo, Silvia, Samaco, Rodney, Flenniken, Ann M, Stewart, Michelle, IMPC Consortium, White, Jacqueline K, McKerlie, Colin, Nutter, Lauryl M.J., Vukobradovic, Igor, Verraragavan, Surabi, Yuva, Lisa, Heaney, Jason D, Dickinson, Mary E, Meziane, Hamid, Hérault, Yann, Wells, Sara, Lloyd, K.C. Kent, Bower, Lynette, Lanaue, Louise, Clary, Dave, Zimprich, Annemarie, Gailus-Durner, Valerie, Fuchs, Helmut, Brown, Steve D.M., Chesler, Elissa J, Wurst, Wolfgang, HrabÄ› de Angelis, Martin, Hölter, Sabine M

المصدر: Faculty Research 2024

مصطلحات موضوعية: JMG

وصف الملف: application/pdf

Relation: https://mouseion.jax.org/stfb2024/202; https://mouseion.jax.org/context/stfb2024/article/1187/viewcontent/1_s2.0_S2772408524001406_main.pdf

الاتاحة: https://mouseion.jax.org/stfb2024/202
https://doi.org/10.1016/j.nsa.2024.104075
https://mouseion.jax.org/context/stfb2024/article/1187/viewcontent/1_s2.0_S2772408524001406_main.pdf

المؤلفون: Veeraragavan, Surabi, Wan, Ying-Wooi, Connolly, Daniel R, Hamilton, Shannon M, Ward, Christopher S, Soriano, Sirena, Pitcher, Meagan R, McGraw, Christopher M, Huang, Sharon G, Green, Jennie R, Yuva, Lisa A, Liang, Agnes J, Neul, Jeffrey L, Yasui, Dag H, LaSalle, Janine M, Liu, Zhandong, Paylor, Richard, Samaco, Rodney C

المصدر: Human Molecular Genetics. 25(15)

مصطلحات موضوعية: Rett Syndrome, Brain Disorders, Neurosciences, Pediatric, Mental Health, Rare Diseases, Genetics, Orphan Drug, Neurodegenerative, Intellectual and Developmental Disabilities (IDD), 5.1 Pharmaceuticals, Development of treatments and therapeutic interventions, Aetiology, 2.1 Biological and endogenous factors, Congenital, Animals, Behavior, Animal, Disease Models, Animal, Female, Humans, Male, Methyl-CpG-Binding Protein 2, Mice, Mutation, Rats, Rats, Sprague-Dawley, Rats, Transgenic, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

URL الوصول: https://escholarship.org/uc/item/129756bx

المؤلفون: Veeraragavan, Surabi, Soriano, Sirena, Ward, Christopher, Connolly, Daniel, de la Haza, Pedro Albelda, Liang, Agnes, Yuva, Lisa, Paylor, Richard, Samaco, Rodney

المصدر: Biological Psychiatry ; volume 81, issue 10, page S64-S65 ; ISSN 0006-3223

الاتاحة: http://dx.doi.org/10.1016/j.biopsych.2017.02.168
https://api.elsevier.com/content/article/PII:S0006322317302883?httpAccept=text/plain
https://api.elsevier.com/content/article/PII:S0006322317302883?httpAccept=text/xml

المؤلفون: Veeraragavan, Surabi, Wan, Ying-Wooi, Connolly, Daniel R, Hamilton, Shannon M, Ward, Christopher S, Soriano, Sirena, Pitcher, Meagan R, McGraw, Christopher M, Huang, Sharon G, Green, Jennie R, Yuva, Lisa A, Liang, Agnes J, Neul, Jeffrey L, Yasui, Dag H, LaSalle, Janine M, Liu, Zhandong, Paylor, Richard, Samaco, Rodney C

المصدر: Veeraragavan, S; Wan, YW; Connolly, DR; Hamilton, SM; Ward, CS; Soriano, S; et al.(2015). Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome. Human Molecular Genetics, 25(15), 3284-3302. doi: 10.1093/hmg/ddw178. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/129756bx
Human molecular genetics, vol 25, iss 15

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Methyl-CpG-Binding Protein 2, Intellectual and Developmental Disabilities (IDD), Neurodegenerative, Medical and Health Sciences, Transgenic, Mice, Congenital, Rare Diseases, Rett Syndrome, Genetics, Animals, Humans, 2.1 Biological and endogenous factors, Aetiology, Pediatric, Genetics & Heredity, Behavior, Animal, Neurosciences, Biological Sciences, Rats, Brain Disorders, Orphan Drug, Mental Health, 5.1 Pharmaceuticals, Disease Models, Mutation, Female, Sprague-Dawley, Development of treatments and therapeutic interventions

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a20592288507ae54d94c0d472c2b1698
http://www.escholarship.org/uc/item/129756bx

المؤلفون: Hamilton, Shannon M., Green, Jennie R., Veeraragavan, Surabi, Yuva, Lisa, McCoy, Aaron, Wu, Yumei, Warren, Joe, Little, Lara, Ji, Diana, Cui, Xiaoxia, Weinstein, Edward, Paylor, Richard

المصدر: Behavioral Neuroscience ; volume 128, issue 2, page 103-109 ; ISSN 1939-0084 0735-7044

الاتاحة: http://dx.doi.org/10.1037/a0035988
http://psycnet.apa.org/journals/bne/128/2/103.pdf

المؤلفون: Paylor, Richard, Baskall-Baldini, Linda, Yuva, Lisa, Wehner, Jeanne M.

المصدر: Behavioral Neuroscience ; volume 110, issue 6, page 1415-1425 ; ISSN 1939-0084 0735-7044

الاتاحة: http://dx.doi.org/10.1037/0735-7044.110.6.1415
http://psycnet.apa.org/journals/bne/110/6/1415.pdf

المؤلفون: Bowers, Barbara J., Christensen, Steven C., Pauley, James R., Paylor, Richard, Yuva, Lisa, Dunbar, Scott E., Wehner, Jeanne M.

المصدر: Journal of Neurochemistry ; volume 64, issue 6, page 2737-2746 ; ISSN 0022-3042 1471-4159

الاتاحة: http://dx.doi.org/10.1046/j.1471-4159.1995.64062737.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1471-4159.1995.64062737.x
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1471-4159.1995.64062737.x

المؤلفون: Veeraragava, Surabi, Ying-Wooi Wan, Connolly, Daniel R., Hamilton, Shannon M., Ward, Christopher S., Soriano, Sirena, Pitcher, Meagan R., McGraw, Christopher M., Huang, Sharon G., Green, Jennie R., Yuva, Lisa A., Liang, Agnes J., Neul, Jeffrey L., Yasui, Dag H., LaSalle, Janine M., Zhandong Liu, Paylor, Richard, Samaco, Rodney C.

المصدر: Human Molecular Genetics; 8/1/2016, Vol. 25 Issue 15, p3284-3302, 19p