Hasil Pencarian - W Ted Brown
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NF-κB Signaling in the Brain of Autistic Subjects oleh Mazhar Malik, Zujaja Tauqeer, Ashfaq M. Sheikh, Guang Wen, Amenah Nagori, Kun Yang, W. Ted Brown, Xiaohong Li
Diterbitkan 2011-01-01Dapatkan teks lengkap
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Erratum to “NF-κB Signaling in the Brain of Autistic Subjects” oleh Mazhar Malik, Fujiang Cao, Zujaja Tauqeer, Ashfaq M. Sheikh, Guang Wen, Amenah Nagori, Kun Yang, W. Ted Brown, Xiaohong Li
Diterbitkan 2013-01-01Dapatkan teks lengkap
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Increasing maternal or post-weaning folic acid alters gene expression and moderately changes behavior in the offspring. oleh Subit Barua, Kathryn K Chadman, Salomon Kuizon, Diego Buenaventura, Nathan W Stapley, Felicia Ruocco, Umme Begum, Sara R Guariglia, W Ted Brown, Mohammed A Junaid
Diterbitkan 2014-01-01Dapatkan teks lengkap
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Ubiquitin-Proteasome-Collagen (CUP) Pathway in Preterm Premature Rupture of Fetal Membranes oleh Xinliang Zhao, Xinliang Zhao, Xinliang Zhao, Xiaoyan Dong, Xiucui Luo, Xiucui Luo, Jing Pan, Jing Pan, Weina Ju, Weina Ju, Meijiao Zhang, Peirong Wang, Peirong Wang, Peirong Wang, Mei Zhong, Mei Zhong, Yanhong Yu, Yanhong Yu, W. Ted Brown, W. Ted Brown, Nanbert Zhong, Nanbert Zhong, Nanbert Zhong, Nanbert Zhong, Nanbert Zhong, Nanbert Zhong, Nanbert Zhong
Diterbitkan 2017-06-01Dapatkan teks lengkap
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(Epi)genetic variants of the sarcomere-desmosome are associated with premature utero-contraction in spontaneous preterm labor oleh Jie Wang, Xiucui Luo, Jing Pan, Xiaoyan Dong, Xiujuan Tian, Zhihua Tu, Weina Ju, Meijiao Zhang, Mei Zhong, Charles De Chen, Michael Flory, Yong Wang, W. Ted Brown, Nanbert Zhong
Diterbitkan 2021-03-01Dapatkan teks lengkap
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LncRNA pathway involved in premature preterm rupture of membrane (PPROM): an epigenomic approach to study the pathogenesis of reproductive disorders. oleh Xiucui Luo, Qingxi Shi, Yang Gu, Jing Pan, Maofang Hua, Meilin Liu, Ziqing Dong, Meijiao Zhang, Leilei Wang, Ying Gu, Julia Zhong, Xinliang Zhao, Edmund C Jenkins, W Ted Brown, Nanbert Zhong
Diterbitkan 2013-01-01Dapatkan teks lengkap
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Correction: Mutations in the Gene Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families. oleh Milen Velinov, Natalia Dolzhanskaya, Michael Gonzalez, Eric Powell, Ioanna Konidari, William Hulme, John F. Staropoli, Winnie Xin, Guang Y. Wen, Rosemary Barone, Scott H. Coppel, Katherine Sims, W. Ted Brown, Stephan Züchner
Diterbitkan 2012-01-01Dapatkan teks lengkap
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Mutations in the gene DNAJC5 cause autosomal dominant Kufs disease in a proportion of cases: study of the Parry family and 8 other families. oleh Milen Velinov, Natalia Dolzhanskaya, Michael Gonzalez, Eric Powell, Ioanna Konidari, William Hulme, John F Staropoli, Winnie Xin, Guang Y Wen, Rosemary Barone, Scott H Coppel, Katherine Sims, W Ted Brown, Stephan Züchner
Diterbitkan 2012-01-01Dapatkan teks lengkap
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Fragile X targeted pharmacotherapy: lessons learned and future directions oleh Craig A. Erickson, Matthew H. Davenport, Tori L. Schaefer, Logan K. Wink, Ernest V. Pedapati, John A. Sweeney, Sarah E. Fitzpatrick, W. Ted Brown, Dejan Budimirovic, Randi J. Hagerman, David Hessl, Walter E. Kaufmann, Elizabeth Berry-Kravis
Diterbitkan 2017-06-01Dapatkan teks lengkap
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Abnormal intracellular accumulation and extracellular Aβ deposition in idiopathic and Dup15q11.2-q13 autism spectrum disorders. oleh Jerzy Wegiel, Janusz Frackowiak, Bozena Mazur-Kolecka, N Carolyn Schanen, Edwin H Cook, Marian Sigman, W Ted Brown, Izabela Kuchna, Jarek Wegiel, Krzysztof Nowicki, Humi Imaki, Shuang Yong Ma, Abha Chauhan, Ved Chauhan, David L Miller, Pankaj D Mehta, Michael Flory, Ira L Cohen, Eric London, Barry Reisberg, Mony J de Leon, Thomas Wisniewski
Diterbitkan 2012-01-01Dapatkan teks lengkap
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