نتائج البحث - "Lu, Ying-qian"

المساهمون: National Natural Science Foundation of China, Innovation of Science and Technology of Fujian Province, National Science and Technology major project, Shanghai City Committee of Science and Technology project

المصدر: National Science Review ; volume 7, issue 1, page 92-101 ; ISSN 2095-5138 2053-714X

الاتاحة: http://dx.doi.org/10.1093/nsr/nwz131
http://academic.oup.com/nsr/advance-article-pdf/doi/10.1093/nsr/nwz131/31773952/nwz131.pdf
http://academic.oup.com/nsr/article-pdf/7/1/92/39623564/nwz131.pdf

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7

Academic Journal

Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)

المؤلفون: Lu, Ying-qian, Dong, En-lin, Yang, Wei-qi, Lai, Lu-lu, Lin, Xiao-hong, Ma, Li-xiang, Chen, Wan-jin, Wang, Ning, Lin, Xiang

المساهمون: National Natural Science Foundation of China, Fujian Medical University, Joint Funds for the Innovation of Science and Technology, National Key Clinical Specialty Discipline Construction Program, Key Clinical Specialty Discipline Construction Program

المصدر: Stem Cell Research ; volume 34, page 101354 ; ISSN 1873-5061

الاتاحة: http://dx.doi.org/10.1016/j.scr.2018.11.015
https://api.elsevier.com/content/article/PII:S1873506118302848?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1873506118302848?httpAccept=text/plain

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8

Academic Journal

Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China

المؤلفون: Dong, En-Lin, Wang, Chong, Wu, Shuang, Lu, Ying-Qian, Lin, Xiao-Hong, Su, Hui-Zhen, Zhao, Miao, He, Jin, Ma, Li-Xiang, Wang, Ning, Chen, Wan-Jin, Lin, Xiang

المساهمون: National Natural Science Foundation of China, Program for New Century Excellent Talents in University, Startup Fund for scientific research, Fujian Medical University, National Key Clinical Specialty Discipline Construction Program, Key Clinical Specialty Discipline Construction Program of Fujian

المصدر: Molecular Neurodegeneration ; volume 13, issue 1 ; ISSN 1750-1326

الاتاحة: http://dx.doi.org/10.1186/s13024-018-0269-1
http://link.springer.com/content/pdf/10.1186/s13024-018-0269-1.pdf
http://link.springer.com/article/10.1186/s13024-018-0269-1/fulltext.html

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9

Academic Journal

Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification

المساهمون: National Natural Science Foundation of China (NSFC), CAS, MOST, Clinical Specialty Discipline Construction Program, Key Clinical Specialty Discipline Construction Program of Fujian, Joint Funds for the Innovation of Science and Technology of Fujian Province

المصدر: Neuron ; volume 98, issue 6, page 1116-1123.e5 ; ISSN 0896-6273

الاتاحة: http://dx.doi.org/10.1016/j.neuron.2018.05.037
https://api.elsevier.com/content/article/PII:S0896627318304355?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0896627318304355?httpAccept=text/plain

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10

Academic Journal

Identification of SLC20A2 deletions in patients with primary familial brain calcification

المؤلفون: Guo, Xin‐Xin, Su, Hui‐Zhen, Zou, Xiao‐Huan, Lai, Lu‐Lu, Lu, Ying‐Qian, Wang, Chong, Li, Yun‐Lu, Hong, Jing‐Mei, Zhao, Miao, Lin, Kun‐Xin, Lin, Jie, Zeng, Yi‐Heng, Yao, Xiang‐Ping, Wang, Ning, Chen, Wan‐Jin

المساهمون: National Natural Science Foundation of China

المصدر: Clinical Genetics ; volume 96, issue 1, page 53-60 ; ISSN 0009-9163 1399-0004

الاتاحة: http://dx.doi.org/10.1111/cge.13540
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcge.13540
https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13540
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/cge.13540

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11

Academic Journal

c.835-5T>G Variant in SMN1 Gene Causes Transcript Exclusion of Exon 7 and Spinal Muscular Atrophy

المؤلفون: Wu, Shuang, Li, Yun-Lu, Cheng, Ning-Yi, Wang, Chong, Dong, En-Lin, Lu, Ying-Qian, Li, Jin-Jing, Guo, Xin-Xin, Lin, Xiang, Lai, Lu-Lu, Liu, Zhi-Wei, Wang, Ning, Chen, Wan-Jin

المساهمون: National Natural Science Foundation of China

المصدر: Journal of Molecular Neuroscience ; volume 65, issue 2, page 196-202 ; ISSN 0895-8696 1559-1166

الاتاحة: http://dx.doi.org/10.1007/s12031-018-1079-1
http://link.springer.com/article/10.1007/s12031-018-1079-1/fulltext.html
http://link.springer.com/content/pdf/10.1007/s12031-018-1079-1.pdf

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12

Additional file 2: of Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China

المؤلفون: En-Lin Dong, Wang, Chong, Wu, Shuang, Lu, Ying-Qian, Lin, Xiao-Hong, Su, Hui-Zhen, Zhao, Miao, He, Jin, Ma, Li-Xiang, Wang, Ning, Wan-Jin Chen, Lin, Xiang

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::862415a741c2a140c2a2db8b2e1f7ee1

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13

Academic Journal

Mutation screening of PDGFB gene in Chinese population with primary familial brain calcification

المؤلفون: Yao, Xiang-Ping, Wang, Chong, Su, Hui-Zhen, Guo, Xin-Xin, Lu, Ying-qian, Zhao, Miao, Liu, Yao-Bin, Lai, Jing-Hui, Chen, Hai-Ting, Wang, Ning, Chen, Wan-Jin

المساهمون: National Natural Science Foundation of China, Program for New Century Excellent Talents in University, National Key Clinical Specialty Discipline Construction Program, Key Clinical Specialty Discipline Construction Program of Fujian

المصدر: Gene ; volume 597, page 17-22 ; ISSN 0378-1119

الاتاحة: http://dx.doi.org/10.1016/j.gene.2016.10.037
https://api.elsevier.com/content/article/PII:S0378111916308265?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0378111916308265?httpAccept=text/plain

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