中国科学院机构知识库网格系统: 检索

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	Absence of PNET formation and normal longevity in a mouse model of Mahvash disease 期刊论文 OAI收割 HELIYON, 2024, 卷号: 10, 期号: 15, 页码: 13 作者: Xu, Yingna; Liu, Qiaofeng; Chen, Chuan-Wei; Wang, Qiuying; Du, Tianyuan \| 收藏 \| 浏览/下载：22/0 \| 提交时间：2024/09/26 Glucagon Glucagon receptor Amino acid Metabolism Mahvash disease
	The nicotinamide nucleotide transhydrogenase gene could impair blood glucose level stability and increase basal metabolism 期刊论文 iSwitch采集 Pakistan journal of agricultural sciences, 2018, 卷号: 55, 期号: 3, 页码: 603-609 作者: Soudy, Fathia; Asif, Akhtar Rasool; Miao, Yuanxin; Jing, Lu; Luan, Yu 收藏 \| 浏览/下载：89/0 \| 提交时间：2019/05/08 Nnt Blood glucose Familial glucocorticoid deficiency Glucose metabolism Autosomal recessive disorder Feed conversion ratio Mice
	Development of the Swimbladder Surfactant System and Biogenesis of Lysosome-Related Organelles Is Regulated by BLOS1 in Zebrafish 期刊论文 OAI收割 GENETICS, 2018, 卷号: 208, 期号: 3, 页码: 1131-1146 作者: Chen, Tianbing; Song, Guili; Yang, Huihui; Mao, Lin; Cui, Zongbin \| 收藏 \| 浏览/下载：51/0 \| 提交时间：2019/07/03 lysosome-related organelles Hermansky-Pudlak syndrome surfactant system swimbladder
	Molecular defects in the factor X gene caused by novel heterozygous mutations IVS5+1G > A and Asp409del 期刊论文 OAI收割 HAEMOPHILIA, 2013, 卷号: 19, 期号: 1, 页码: 94-99 作者: Zhou, J. W.; Liang, Q.; Chen, Q.; Xie, Y.; Ding, Q. L. \| 收藏 \| 浏览/下载：37/0 \| 提交时间：2019/01/08 bleeding disorder factor X deficiency molecular modelling splice-site mutation type II deficiency
	Multimeric BLM is dissociated upon ATP hydrolysis and functions as monomers in resolving DNA structures 期刊论文 OAI收割 NUCLEIC ACIDS RESEARCH, 2012, 卷号: 40, 期号: 19, 页码: 9802 Xu, YN; Bazeille, N; Ding, XY; Lu, XM; Wang, PY; Bugnard, E; Grondin, V; Dou, SX; Xi, XG 收藏 \| 浏览/下载：24/0 \| 提交时间：2013/09/18 BLOOMS-SYNDROME HELICASE SYNDROME GENE-PRODUCT WERNER-SYNDROME PROTEIN SINGLE-STRANDED-DNA RECQ HELICASES HEXAMERIC HELICASES TOPOISOMERASE III REPLICATION FORK ARGININE FINGER UVRD HELICASE
	Recent progress in neurodegenerative disorder research in China 期刊论文 OAI收割 SCIENCE CHINA-LIFE SCIENCES, 2010, 卷号: 53, 期号: 3, 页码: 348-355 作者: Zhou JiaWei 收藏 \| 浏览/下载：23/0 \| 提交时间：2012/07/13 neurodegenerative disorders pathogenesis diagnosis neuroprotection Alzheimer's disease Parkinson's disease ALZHEIMERS-DISEASE PARKINSONS-DISEASE RAT-BRAIN PROTEIN PHOSPHATASE-2A UNDERLYING MECHANISMS INDUCED NEUROTOXICITY DOPAMINERGIC-NEURONS TAU-PHOSPHORYLATION CEREBROSPINAL-FLUID NEUROTROPHIC FACTOR
	Kinetic Mechanism of DNA Unwinding by the BLM Helicase Core and Molecular Basis for Its Low Processivity 期刊论文 OAI收割 BIOCHEMISTRY, 2010, 卷号: 49, 期号: 4, 页码: 656 Yang, Y; Dou, SX; Xu, YN; Bazeille, N; Wang, PY; Rigolet, P; Xu, HQ; Xi, XG 收藏 \| 浏览/下载：30/0 \| 提交时间：2013/09/18 SINGLE-STRANDED-DNA ESCHERICHIA-COLI RECQ BLOOMS-SYNDROME HELICASE SYNDROME GENE-PRODUCT C VIRUS HELICASE SYNDROME PROTEIN STEP-SIZE HOMOLOGOUS RECOMBINATION MONOMERIC HELICASE HEXAMERIC HELICASE
	Self-Q-switched and mode-locked Nd,Cr : YAG laser with 6.52-W average output power 期刊论文 OAI收割 OPTICS COMMUNICATIONS, 2007, 卷号: 277, 期号: 1, 页码: 130 Wang, SM; Li, QN; Du, SF; Zhang, QL; Shi, YX; Xing, H; Zhang, DX; Feng, BH; Zhang, ZG; Zhang, SW 收藏 \| 浏览/下载：15/0 \| 提交时间：2013/09/24
	Structural and functional analyses of disease-causing missense mutations in Bloom syndrome protein 期刊论文 OAI收割 NUCLEIC ACIDS RESEARCH, 2007, 卷号: 35, 期号: 18, 页码: 6297 Guo, RB; Rigolet, P; Ren, H; Zhang, B; Zhang, XD; Dou, SX; Wang, PY; Amor-Gueret, M; Xi, XG 收藏 \| 浏览/下载：19/0 \| 提交时间：2013/09/24