खोज परिणाम - Yong‐hui Jiang
- प्रदर्शित 1 - 20 परिणाम 78
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1
Modeling Autism by SHANK Gene Mutations in Mice द्वारा Yong‐hui Jiang, Michael Ehlers
प्रकाशित 2013Revisão -
2
DNA Methylation and Susceptibility to Autism Spectrum Disorder द्वारा Martine Tremblay, Yong‐hui Jiang
प्रकाशित 2019Revisão -
3
Overview of Mouse Models of Autism Spectrum Disorders द्वारा Alexandra L. Bey, Yong‐hui Jiang
प्रकाशित 2014Revisão -
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Modeling autism in non‐human primates: Opportunities and challenges द्वारा Hui Zhao, Yong‐hui Jiang, Yongqing Zhang
प्रकाशित 2018Revisão -
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EPIGENETICS AND HUMAN DISEASE द्वारा Yong-hui Jiang, Jan Bressler, Arthur L. Beaudet
प्रकाशित 2004Revisão -
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Epigenetic therapy of Prader–Willi syndrome द्वारा Yuna Kim, Sung Eun Wang, Yong‐hui Jiang
प्रकाशित 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 द्वारा Xiaoming Wang, Qiong Xu, Alexandra L. Bey, Yoonji Lee, Yong‐hui Jiang
प्रकाशित 2014Artigo -
10
Genetics of Angelman Syndrome द्वारा Yong-hui Jiang, Efrat Lev-Lehman, Jan Bressler, Ting‐Fen Tsai, Arthur L. Beaudet
प्रकाशित 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 द्वारा Elie Abdelnour, William Gallentine, Timothy J. McDonald, Monisha Sachdev, Yong‐hui Jiang, Mohamad A. Mikati
प्रकाशित 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 द्वारा Lara J. Duffney, Purnima Valdez, Martine Tremblay, Xinyu Cao, Sarah Montgomery, Allyn McConkie‐Rosell, Yong‐hui Jiang
प्रकाशित 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 द्वारा Stamatina Tzanoulinou, Stefano Musardo, Alessandro Contestabile, Sebastiano Bariselli, Giulia Casarotto, Elia Magrinelli, Yong‐hui Jiang, Denis Jabaudon, Camilla Bellone
प्रकाशित 2022Artigo -
17
Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation द्वारा Yong‐hui Jiang, Dawna Armstrong, Urs Albrecht, Coleen M. Atkins, Jeffrey L. Noebels, Gregor Eichele, J. David Sweatt, Arthur L. Beaudet
प्रकाशित 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 द्वारा C. Smith, Darryll G. DeVera, Dolores J. Lamb, Zafar Nawaz, Yong‐hui Jiang, Arthur L. Beaudet, Bert W. O’Malley
प्रकाशित 2002Artigo -
19
Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing द्वारा Yimin Wang, Xiaonan Du, Bin Rao, Shanshan Yu, Zhezhi Xia, Zheng Guo, Jianmin Zhong, Yunjian Zhang, Yong‐hui Jiang, Yi Wang
प्रकाशित 2017Artigo -
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खोज साधन:
संबंधित विषय
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