Resultados da busca - Yong‐hui Jiang
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1
Modeling Autism by SHANK Gene Mutations in Mice por Yong‐hui Jiang, Michael Ehlers
Publicado em 2013Revisão -
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DNA Methylation and Susceptibility to Autism Spectrum Disorder por Martine Tremblay, Yong‐hui Jiang
Publicado em 2019Revisão -
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Overview of Mouse Models of Autism Spectrum Disorders por Alexandra L. Bey, Yong‐hui Jiang
Publicado em 2014Revisão -
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Modeling autism in non‐human primates: Opportunities and challenges por Hui Zhao, Yong‐hui Jiang, Yongqing Zhang
Publicado em 2018Revisão -
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EPIGENETICS AND HUMAN DISEASE por Yong-hui Jiang, Jan Bressler, Arthur L. Beaudet
Publicado em 2004Revisão -
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Epigenetic therapy of Prader–Willi syndrome por Yuna Kim, Sung Eun Wang, Yong‐hui Jiang
Publicado em 2019Revisão -
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Transcriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant mice por Xiaoming Wang, Qiong Xu, Alexandra L. Bey, Yoonji Lee, Yong‐hui Jiang
Publicado em 2014Artigo -
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Genetics of Angelman Syndrome por Yong-hui Jiang, Efrat Lev-Lehman, Jan Bressler, Ting‐Fen Tsai, Arthur L. Beaudet
Publicado em 1999Revisão -
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Does age affect response to quinidine in patients with KCNT1 mutations? Report of three new cases and review of the literature por Elie Abdelnour, William Gallentine, Timothy J. McDonald, Monisha Sachdev, Yong‐hui Jiang, Mohamad A. Mikati
Publicado em 2017Revisão -
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Epigenetics and autism spectrum disorder: A report of an autism case with mutation in H1 linker histone <i>HIST1H1E</i> and literature review por Lara J. Duffney, Purnima Valdez, Martine Tremblay, Xinyu Cao, Sarah Montgomery, Allyn McConkie‐Rosell, Yong‐hui Jiang
Publicado em 2018Revisão -
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Inhibition of Trpv4 rescues circuit and social deficits unmasked by acute inflammatory response in a Shank3 mouse model of Autism por Stamatina Tzanoulinou, Stefano Musardo, Alessandro Contestabile, Sebastiano Bariselli, Giulia Casarotto, Elia Magrinelli, Yong‐hui Jiang, Denis Jabaudon, Camilla Bellone
Publicado em 2022Artigo -
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Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation por Yong‐hui Jiang, Dawna Armstrong, Urs Albrecht, Coleen M. Atkins, Jeffrey L. Noebels, Gregor Eichele, J. David Sweatt, Arthur L. Beaudet
Publicado em 1998Artigo -
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Genetic Ablation of the Steroid Receptor Coactivator-Ubiquitin Ligase, E6-AP, Results in Tissue-Selective Steroid Hormone Resistance and Defects in Reproduction por C. Smith, Darryll G. DeVera, Dolores J. Lamb, Zafar Nawaz, Yong‐hui Jiang, Arthur L. Beaudet, Bert W. O’Malley
Publicado em 2002Artigo -
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Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing por Yimin Wang, Xiaonan Du, Bin Rao, Shanshan Yu, Zhezhi Xia, Zheng Guo, Jianmin Zhong, Yunjian Zhang, Yong‐hui Jiang, Yi Wang
Publicado em 2017Artigo -
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Assuntos relacionados
Biology
Gene
Genetics
Medicine
Neuroscience
Psychology
Autism
Phenotype
Psychiatry
Cell biology
Mutation
Autism spectrum disorder
Internal medicine
Ubiquitin
Ubiquitin ligase
Computational biology
Gene expression
Exome sequencing
DNA methylation
Developmental psychology
Epigenetics
Receptor
UBE3A
Angelman syndrome
Bioinformatics
Disease
Pathology
Pediatrics
Endocrinology
Epilepsy