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1. Li jia da yuan
by Li, Jun and Fan, Yongfu
2010, Di 1 ban., ISBN 7501029687, 163 pages
Historic buildings | Vernacular architecture | Yuncheng (Shanxi Sheng, China) History | Architecture, Domestic
Book
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2. Guo jia da shi
: zhan lue ke xue jia Jiang Xinsong sheng si jing shi lu
by Li, Mingsheng, 1956
1999, Di 1 ban., ISBN 9787506316248, 2, 313 p., [2] p. of plates
Scientists | Jiang, Xinsong, 1931-1997
Book
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3. Tong jia da zi dian
: Tong jia da zi dian
by Zhang, Heng and Xu, Menglin
1993, Di 1 ban., ISBN 7207011385, 3, 5, 34, 1032
Homonyms | Chinese language
Book
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4. Zhongguo xian dai zuo jia da ci dian
Zhongguo xian dai wen xue guan
1992, ISBN 7800051404, 16, 693
Biography | Chinese literature | Authors, Chinese
Book
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5. Zhongguo wen xue jia da ci dian
: Song dai juan
by Zeng, Zaozhuang and Li, Wenze and Wu, Hongze, 1963
2004, Di 1 ban., ISBN 7101037895, 1, 3, 6, 2, 29, 1130
Chinese literature | Chinese | History and criticism | Authors, Chinese
Book
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6. Full Text Use of three points to determine the accuracy of guided implantation
by Liang, Ye and Yuan, ShanShan and Huan, JingJing and Wang, HuiXin and Zhang, YiYi and Fang, ChangYun and Li, Jia-Da
PLOS ONE, ISSN 1932-6203, 12/2019, Volume 14, Issue 12, p. e0225823
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7. Full Text Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism
by Men, Meichao and Wu, Jiayu and Zhao, Yaguang and Xing, Xiaoliang and Jiang, Fang and Zheng, Ruizhi and Li, Jia-Da
Fertility and Sterility, ISSN 0015-0282, 11/2019
Journal Article
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8. Full Text PROKR2 mutations in idiopathic hypogonadotropic hypogonadism: selective disruption of the binding to a Gα-protein leads to biased signaling
by Zhao, Yaguang and Wu, Jiayu and Jia, Hong and Wang, Xinying and Zheng, Ruizhi and Jiang, Fang and Chen, Dan-Na and Chen, Zhiheng and Li, Jia-Da
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, ISSN 0892-6638, 03/2019, Volume 33, Issue 3, pp. 4538 - 4546
Idiopathic hypogonadotropic hypogonadism (IHH) is a rare disorder caused by the deficient production, secretion, or action of gonadotropin-releasing hormone.... 
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9. Full Text Identification of a Novel CNV at 8q13 in a Family With Branchio-Oto-Renal Syndrome and Epilepsy
by Men, Meichao and Li, Wu and Chen, Hongsheng and Wu, Jiayu and Feng, Yong and Guo, Hui and Li, Jia-Da
Laryngoscope, ISSN 0023-852X, 2019
Branchio-oto-renal (BOR) syndrome is characterized by branchial defects, hearing loss, preauricular pits, and renal anomalies, whereas patients with all... 
epilepsy | branchio-oto-renal syndrome | CNV | hearing loss | EYA1
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10. Full Text Phenotypic spectrum of idiopathic hypogonadotropic hypogonadism patients with CHD7 variants from a large Chinese cohort
by Wu, Jiayu and Zhao, Yaguang and Wang, Xinying and Jiang, Fang and Hou, Qiao and Chen, Dan-Na and Zheng, Ruizhi and Yu, Renhe and Zhou, Wei and Li, Jia-Da and Men, Meichao
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 11/2019
Abstract Purpose Idiopathic hypogonadotropic hypogonadism (IHH) and CHARGE syndrome are two distinct developmental disorders sharing features of hypogonadism... 
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11. Full Text The Roles of Post-translational Modifications on α-Synuclein in the Pathogenesis of Parkinson’s Diseases
by Zhang, Jiaming and Li, Xiaoping and Li, Jia-Da
Frontiers in Neuroscience, ISSN 1662-453X, 04/2019, Volume 13
Parkinson’s disease is the second most common neurodegenerative disorder. Although the pathogenesis of Parkinson’s disease is not entirely clear, the aberrant... 
Nitration | Translation | Phosphorylation | Parkinson's disease | Disease | Neurodegenerative diseases | Laboratories | Pathogenesis | Cytotoxicity | Synuclein | Risk factors | Proteins | Ubiquitination | Neurodegeneration | Proteomics | Post-translation | Biomarkers | Physiology | Diabetes | Mutation | Movement disorders | Dementia | toxicity | aggregation | post-translational modifications | Parkinson’s disease | α-synuclein
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12. Full Text Potentiation of acid-sensing ion channel activity by the activation of 5-HT 2 receptors in rat dorsal root ganglion neurons
by Qiu, Fang and Qiu, Chun-Yu and Liu, Yu-Qiang and Wu, Dan and Li, Jia-Da and Hu, Wang-Ping
Neuropharmacology, ISSN 0028-3908, 09/2012, Volume 63, Issue 3, pp. 494 - 500
Acid-sensing ion channels (ASICs), as key sensors for extracellular protons, are expressed in nociceptive sensory neurons and contribute to signalling pain... 
receptor | Proton-gated current | Acid-sensing ion channel | Dorsal root ganglion neuron | 5-HT | Neuronal excitability
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13. Full Text Neuroscience: Dependence of olfactory bulb neurogenesis on prokineticin 2 signaling
by Ng, Kwan L and Li, Jia-Da and Cheng, Michelle Y and Leslie, Frances M and Lee, Alex C and Zhou, Qun-Yong
Science, ISSN 0036-8075, 06/2005, Volume 308, Issue 5730, pp. 1923 - 1927
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14. Full Text Astragalus polysaccharides exerts anti-infective activity by inducing human cathelicidin antimicrobial peptide LL-37 in respiratory epithelial cells
: Astragalus polysaccharides enhances LL-37 induction
by Zhao, Lin and Tan, Shuai and Zhang, Hai and Liu, Peng and Tan, Yu-Zhu and Li, Jia-Chuan and Jia, Da and Shen, Xiao-Fei
Phytotherapy Research, ISSN 0951-418X, 08/2018, Volume 32, Issue 8, pp. 1521 - 1529
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15. Full Text DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA
by Bestor, Timothy H and Ooi, Steen K. T and Yang, Zhe and Lin, Shau-Ping and Bernstein, Emily and Li, Keqin and Tempst, Paul and Allis, C. David and Cheng, Xiaodong and Qiu, Chen and Jia, Da and Erdjument-Bromage, Hediye
Nature, ISSN 0028-0836, 08/2007, Volume 448, Issue 7154, pp. 714 - 717
Mammals use DNA methylation for the heritable silencing of retrotransposons and imprinted genes and for the inactivation of the X chromosome in females. The... 
CELLS | MULTIDISCIPLINARY SCIENCES | METHYLTRANSFERASE | Protein Structure, Tertiary | Cell Line | Embryonic Stem Cells - metabolism | Histones - chemistry | Humans | Crystallography, X-Ray | Structure-Activity Relationship | DNA - metabolism | DNA (Cytosine-5-)-Methyltransferases - chemistry | DNA (Cytosine-5-)-Methyltransferases - metabolism | DNA (Cytosine-5-)-Methyltransferases - genetics | DNA Methylation | Animals | Protein Binding | Lysine - metabolism | Mice | Histones - metabolism | Proteins | Deoxyribonucleic acid | DNA | Genetics | Biochemistry | Chromosomes | Crystallography
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16. Full Text Enzymatic O-GlcNAcylation of [alpha]-synuclein reduces aggregation and increases SDS-resistant soluble oligomers
by Zhang, Jiaming and Lei, Haozhi and Chen, Yubei and Ma, Yan-Tao and Jiang, Fang and Tan, Jieqiong and Zhang, Yi and Li, Jia-Da
Neuroscience Letters, ISSN 0304-3940, 08/2017, Volume 655, p. 90
Neurodegenerative diseases including dementia with Lewy bodies, Lewy body variant of Alzheimer's disease, and Parkinson's disease are associated with the... 
Oligomers | Enzymes | Analysis | Bacteria | Alzheimer's disease
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17. The design and implementation of image query system based on color feature
by Yao, Xu-Dong and Jia, Da-Chun and Lin, Li
Proceedings of SPIE - The International Society for Optical Engineering, ISSN 0277-786X, 2013, Volume 8878
ASP.NET technology was used to construct the B/S mode image query system. The theory and technology of database design, color feature extraction from image,... 
database design | ASPNET | B/S | Image retrieval Based on Color Feature | Design engineering | Construction | Databases | Query processing | Images | Color | Feature extraction | Architecture (computers)
Conference Proceeding
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18. Full Text Functional rescue of Kallmann syndrome-associated prokineticin receptor 2 (PKR2) mutants deficient in trafficking
by Chen, Dan-Na and Ma, Yan-Tao and Liu, Huadie and Zhou, Qun-Yong and Li, Jia-Da
Journal of Biological Chemistry, ISSN 0021-9258, 05/2014, Volume 289, Issue 22, pp. 15518 - 15526
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19. Full Text Endosomal sorting of notch receptors through COM MD9-dependent pathways modulates notch signaling
by Li, Haiying and Koo, Yeon and Mao, Xicheng and Sifuentes-Dominguez, Luis and Morris, Lindsey L and Jia, Da and Miyata, Naoteru and Faulkner, Rebecca A and van Deursen, Jan M and Vooijs, Marc and Billadeau, Daniel D and Van de Sluis, Bart and Cleaver, Ondine and Burstein, Ezra
Journal of Cell Biology, ISSN 0021-9525, 11/2015, Volume 211, Issue 3, pp. 605 - 617
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20. Full Text Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias
by Wang, Jun-Ling and Cao, Li and Li, Xun-Hua and Hu, Zheng-Mao and Li, Jia-Da and Zhang, Jian-Guo and Liang, Yu and San-A and Li, Nan and Chen, Su-Qin and Guo, Ji-Feng and Jiang, Hong and Shen, Lu and Zheng, Lan and Mao, Xiao and Yan, Wei-Qian and Zhou, Ying and Shi, Yu-Ting and Ai, San-Xi and Dai, Mei-Zhi and Zhang, Peng and Xia, Kun and Chen, Sheng-Di and Tang, Bei-Sha
Brain, ISSN 0006-8950, 12/2011, Volume 134, Issue 12, pp. 3490 - 3498
Paroxysmal kinesigenic dyskinesias is a paroxysmal movement disorder characterized by recurrent, brief attacks of abnormal involuntary movements induced by... 
paroxysmal kinesigenic dyskinesias | proline-rich transmembrane protein 2 | linkage analysis | whole-exome sequencing | CLASSIFICATION | CLINICAL-FEATURES | LOCUS | NEUROSCIENCES | HUMAN-CHROMOSOME 16 | CLINICAL NEUROLOGY | PERICENTROMERIC REGION | MAPS | ALIGNMENT | CHOREOATHETOSIS | INFANTILE CONVULSIONS | LINKAGE | Haplotypes | Genetic Association Studies | Membrane Proteins - genetics | Humans | Middle Aged | Genotype | Male | Chromosome Mapping | Genetic Loci | Nerve Tissue Proteins - genetics | Pedigree | Adolescent | Adult | Female | Aged | Mutation | Chorea - genetics | Child | Genetic Linkage | Original
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