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Results of search for 'au:"Yang, Zhenglin"', page 1 of 6
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Authors
Chen, Haoyu
Chen, Yuhong
Gibbs, Daniel
Gong, Bo
Huang, Lulin
Lin, Ying
Liu, Xiaoqi
Lu, Fang
Ma, Shi
Pearson, Erik
Shi, Yi
Tong, Zongzhong
Yang, Jiyun
Yang, Xian
Yang, Zhenglin
Zhang, Dingding
Zhang, Kang
Zhao, Peiquan
Zhao, Yu
Zhu, Xianjun
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1.
[Progress in molecular genetic studies of retinitis pigmentosa].
[electronic resource]
by
Li, Youping
Yang, Zhenglin
Producer:
20150618
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 32
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2.
Expression of wild type and mutant ELOVL4 in cell culture: subcellular localization and cell viability.
[electronic resource]
by
Karan, Goutam
Yang, Zhenglin
Zhang, Kang
Producer:
20040506
In:
Molecular vision
vol. 10
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3.
[Association of PLEKHA7, COL11A1 and PCMTD1-ST18 gene polymorphisms with primary angle closure glaucoma in ethnic Han Chinese from Sichuan].
[electronic resource]
by
Tan, Chang
Huang, Lulin
Yang, Zhenglin
Producer:
20160922
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 33
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4.
Treatment with carbonic anhydrase inhibitors depresses electroretinogram responsiveness in mice.
[electronic resource]
by
Sauvé, Yves
Karan, Goutam
Yang, Zhenglin
Li, Chunmei
Hu, Jianbin
Zhang, Kang
Producer:
20070409
In:
Advances in experimental medicine and biology
vol. 572
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5.
Loss of caveolin-1 promotes endothelial-mesenchymal transition during sepsis: a membrane proteomic study.
[electronic resource]
by
Huang, Xiaobo
Pan, Lingai
Pu, Hong
Wang, Yiping
Zhang, Xiaoqin
Li, Chunling
Yang, Zhenglin
Producer:
20140512
In:
International journal of molecular medicine
vol. 32
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6.
Genetic analysis and molecular mapping of a novel gene for zebra mutation in rice (Oryza sativa L.).
[electronic resource]
by
Wang, Qiushi
Sang, Xianchun
Ling, Yinghua
Zhao, Fangming
Yang, Zhenglin
Li, Yunfeng
He, Guanghua
Producer:
20100125
In:
Journal of genetics and genomics = Yi chuan xue bao
vol. 36
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7.
Clinical features of autosomal dominant retinitis pigmentosa associated with a Rhodopsin mutation.
[electronic resource]
by
Chen, Haoyu
Chen, Yali
Horn, Rachael
Yang, Zhenglin
Wang, Changguan
Turner, Matthew J
Zhang, Kang
Producer:
20070319
In:
Annals of the Academy of Medicine, Singapore
vol. 35
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8.
A family with X-linked optic atrophy linked to the OPA2 locus Xp11.4-Xp11.2.
[electronic resource]
by
Katz, Bradley J
Zhao, Yu
Warner, Judith E A
Tong, Zongzhong
Yang, Zhenglin
Zhang, Kang
Producer:
20061213
In:
American journal of medical genetics. Part A
vol. 140
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9.
Altered intrinsic brain activity in patients with familial cortical myoclonic tremor and epilepsy: an amplitude of low-frequency fluctuation study.
[electronic resource]
by
Wang, Pu
Luo, Cheng
Dong, Li
Bin, Yi
Ma, Shi
Yao, Dezhong
Guo, Fuqiang
Yang, Zhenglin
Producer:
20160112
In:
Journal of the neurological sciences
vol. 351
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10.
Elovl4 mRNA distribution in the developing mouse retina and phylogenetic conservation of Elovl4 genes.
[electronic resource]
by
Zhang, Xian-Mei
Yang, Zhenglin
Karan, Goutam
Hashimoto, Takao
Baehr, Wolfgang
Yang, Xian-Jie
Zhang, Kang
Producer:
20030715
In:
Molecular vision
vol. 9
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11.
Fine mapping of a pistilloid-stamen (PS) gene on the short arm of chromosome 1 in rice.
[electronic resource]
by
Luo, Hongfa
Li, Yunfeng
Yang, Zhenglin
Zhong, Bingqiang
Xie, Rong
Ren, Maozhi
Luo, Da
He, Guanghua
Producer:
20070125
In:
Genome
vol. 49
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12.
Automated design of genetic toggle switches with predetermined bistability.
[electronic resource]
by
Chen, Shuobing
Zhang, Haoqian
Shi, Handuo
Ji, Weiyue
Feng, Jingchen
Gong, Yan
Yang, Zhenglin
Ouyang, Qi
Producer:
20140425
In:
ACS synthetic biology
vol. 1
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13.
Genetic analysis and fine mapping of a dynamic rolled leaf gene, RL10(t), in rice (Oryza sativa L.).
[electronic resource]
by
Luo, Zengke
Yang, Zhenglin
Zhong, Bingqiang
Li, Yunfeng
Xie, Rong
Zhao, Fangming
Ling, Yinghua
He, Guanghua
Producer:
20080115
In:
Genome
vol. 50
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14.
A reappraisal of the clinical spectrum of North Carolina macular dystrophy.
[electronic resource]
by
Khurana, Rahul N
Sun, Xufang
Pearson, Eric
Yang, Zhenglin
Harmon, Jennifer
Goldberg, Morton F
Zhang, Kang
Producer:
20091016
In:
Ophthalmology
vol. 116
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15.
Whole-exome sequencing identifies a novel homozygous frameshift mutation in the PROM1 gene as a causative mutation in two patients with sporadic retinitis pigmentosa.
[electronic resource]
by
Liu, Sanmei
Xie, Lan
Yue, Jun
Ma, Tao
Peng, Chunyan
Qiu, Biyuan
Yang, Zhenglin
Yang, Jiyun
Producer:
20170228
In:
International journal of molecular medicine
vol. 37
Online resources:
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16.
A novel mutation in LMX1B gene causes nail-patella syndrome in a large Chinese family.
[electronic resource]
by
Lin, Ying
Zhao, Juan
Chen, Shipei
Zeng, Xuebin
Du, Qiong
Yang, Yang
Lu, Fang
Pu, Yonghong
Yang, Zhenglin
Producer:
20081113
In:
Bone
vol. 43
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17.
Clinical characterization and genetic mapping of North Carolina macular dystrophy.
[electronic resource]
by
Yang, Zhenglin
Tong, Zongzhong
Chorich, Louis J
Pearson, Erik
Yang, Xian
Moore, Anthony
Hunt, David M
Zhang, Kang
Producer:
20080411
In:
Vision research
vol. 48
Online resources:
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18.
Loss of ER retention and sequestration of the wild-type ELOVL4 by Stargardt disease dominant negative mutants.
[electronic resource]
by
Karan, Goutam
Yang, Zhenglin
Howes, Kimberly
Zhao, Yu
Chen, Yali
Cameron, D Josh
Lin, Yin
Pearson, Erik
Zhang, Kang
Producer:
20060413
In:
Molecular vision
vol. 11
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19.
Mutations in the RPGR gene cause X-linked cone dystrophy.
[electronic resource]
by
Yang, Zhenglin
Peachey, Neal S
Moshfeghi, Darius M
Thirumalaichary, Sukanya
Chorich, Lou
Shugart, Yin Y
Fan, Keke
Zhang, Kang
Producer:
20020909
In:
Human molecular genetics
vol. 11
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20.
Suppression of Rap1 impairs cardiac myofibrils and conduction system in zebrafish.
[electronic resource]
by
Dong, Wei
Yang, Zhenglin
Yang, Fan
Wang, Jialiang
Zhuang, Yan
Xu, Chongren
Zhang, Bo
Tian, Xiao-Li
Liu, Dong
Producer:
20130528
In:
PloS one
vol. 7
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