Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ori S. Cohen"'
Publikováno v:
Genes
Pten germline haploinsufficient (Pten+/−) mice, which model macrocephaly/autism syndrome, show social and repetitive behavior deficits, early brain overgrowth, and cortical–subcortical hyperconnectivity. Previous work indicated that altered neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1a2fd874500311d13812b84ace053e50
https://pubmed.ncbi.nlm.nih.gov/34573348
https://pubmed.ncbi.nlm.nih.gov/34573348
Autor:
Damon T. Page, Amy E. Clipperton-Allen, Jason P. Lerch, Jacob Ellegood, Jenna Levy, Ori S. Cohen, Aya Zucca, Massimiliano Aceti
Publikováno v:
Translational Psychiatry
Translational Psychiatry, Vol 9, Iss 1, Pp 1-14 (2019)
Translational Psychiatry, Vol 9, Iss 1, Pp 1-14 (2019)
Haploinsufficiency for PTEN is a cause of autism spectrum disorder and brain overgrowth; however, it is not known if PTEN mutations disrupt scaling across brain areas during development. To address this question, we used magnetic resonance imaging to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c2081427bbff5ed5be8779a66ef0ae5
https://doi.org/10.1038/s41398-019-0656-6
https://doi.org/10.1038/s41398-019-0656-6
Publikováno v:
Genes
Volume 12
Issue 9
Genes, Vol 12, Iss 1366, p 1366 (2021)
Volume 12
Issue 9
Genes, Vol 12, Iss 1366, p 1366 (2021)
Pten germline haploinsufficient (Pten+/−) mice, which model macrocephaly/autism syndrome, show social and repetitive behavior deficits, early brain overgrowth, and cortical–subcortical hyperconnectivity. Previous work indicated that altered neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57ffe732588db91be60b5c6ab4a1cfd3
https://doi.org/10.3390/genes12091366
https://doi.org/10.3390/genes12091366
Autor:
Daniel S. Tylee, Stephen J. Glatt, Jonathan L. Hess, Joshua K. Rim, Ori S. Cohen, Totadri Dhimal, Alfred J. Espinoza, Sarah Y. Mccoy, Muhammad Tahir
Publikováno v:
Autism Research. 10:439-455
Genome-wide expression studies of samples derived from individuals with autism spectrum disorder (ASD) and their unaffected siblings have been widely used to shed light on transcriptomic differences associated with this condition. Females have histor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad7014ac491edb604e8fe6b0fe52c2a2
https://doi.org/10.1002/aur.1679
https://doi.org/10.1002/aur.1679
Autor:
W-H Chang, T. Lu, L. Wang, C-H Chen, Thomas W. Weickert, Cs-J Fann, H-G Hwu, Cynthia Shannon Weickert, D Liu, Dai Zhang, Sarah Y. Mccoy, Y Shen, C-M Liu, Stephen V. Faraone, Yishan Shi, Y-L Liu, Weihua Yue, Xu-Feng Huang, Debora A. Rothmond, C-C Wen, Stephen J. Glatt, Danielle Weinberg, Ori S. Cohen, Musheng Xu, Tetsufumi Kanazawa, Wei Tang, Lin He, Ronglin Che, Cherrie Galletly, J Yan, T M Duncan, C-C Chang, Ming T. Tsuang, Jay L. Hess, L M Paish, Frank A. Middleton, Q Xu
Publikováno v:
Molecular Psychiatry. 21:975-982
The rs1076560 polymorphism of DRD2 (encoding dopamine receptor D2) is associated with alternative splicing and cognitive functioning; however, a mechanistic relationship to schizophrenia has not been shown. Here, we demonstrate that rs1076560(T) impa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00c8f2be3e1803af3f9f2f26542db07c
https://doi.org/10.1038/mp.2015.137
https://doi.org/10.1038/mp.2015.137
Autor:
William Byerley, Marina Myles-Worsley, Ori S. Cohen, Parisa Afshari, Josepha Tiobech, Frank A. Middleton, Stephen V. Faraone
Publikováno v:
Complex Psychiatry. 1:125-144
We have recently described a hemi-deletion on chromosome 9p24.2 at the SLC1A1 gene locus and its co-segregation with schizophrenia in an extended Palauan pedigree. This finding represents a point of convergence for several pathophysiological models o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a50de743e81bb3fb69e9c1cdc4185fa6
https://doi.org/10.1159/000433599
https://doi.org/10.1159/000433599
Autor:
Sean Bialosuknia, Yanli Zhang-James, Ori S. Cohen, Stephen J. Glatt, Stephen V. Faraone, Sarah Y. Mccoy, Lu Liu, Frank A. Middleton, Ming T. Tsuang
Publikováno v:
Schizophrenia Research. 142:188-199
The diverse spatial and temporal expression of alternatively spliced transcript isoforms shapes neurodevelopment and plays a major role in neuronal adaptability. Although alternative splicing is extremely common in the brain, its role in mental illne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ab0b73233ad1eb0385b90256600f7d5
https://doi.org/10.1016/j.schres.2012.09.015
https://doi.org/10.1016/j.schres.2012.09.015
Autor:
Daniel S, Tylee, Alfred J, Espinoza, Jonathan L, Hess, Muhammad A, Tahir, Sarah Y, McCoy, Joshua K, Rim, Totadri, Dhimal, Ori S, Cohen, Stephen J, Glatt
Publikováno v:
Autism research : official journal of the International Society for Autism Research. 10(3)
Genome-wide expression studies of samples derived from individuals with autism spectrum disorder (ASD) and their unaffected siblings have been widely used to shed light on transcriptomic differences associated with this condition. Females have histor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ddf48b67732bb9818af0efef2041f3d8
https://pubmed.ncbi.nlm.nih.gov/27529825
https://pubmed.ncbi.nlm.nih.gov/27529825
Autor:
Parisa, Afshari, Marina, Myles-Worsley, Ori S, Cohen, Josepha, Tiobech, Stephen V, Faraone, William, Byerley, Frank A, Middleton
Publikováno v:
Molecular neuropsychiatry. 1(3)
We have recently described a hemi-deletion on chromosome 9p24.2 at the SLC1A1 gene locus and its co-segregation with schizophrenia in an extended Palauan pedigree. This finding represents a point of convergence for several pathophysiological models o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d14b05cb64dc5231411040aa44a014b6
https://pubmed.ncbi.nlm.nih.gov/26380821
https://pubmed.ncbi.nlm.nih.gov/26380821
Autor:
Richard Bouley, Ori S. Cohen, Dennis Brown, Margaret McLaughlin, Núria M. Pastor-Soler, Sylvie Breton
Publikováno v:
American Journal of Physiology-Renal Physiology. 288:F1103-F1112
Vasopressin-stimulated insertion of the aquaporin 2 (AQP2) water channel into the plasma membrane of kidney collecting duct principal cells is a key event in the urinary concentrating mechanism. The paradigm for vasopressin-receptor signaling involve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e62f74c11cbd32093e6386a41697e104
https://doi.org/10.1152/ajprenal.00337.2004
https://doi.org/10.1152/ajprenal.00337.2004