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Stephen Archacki

Showing results (11-20 of 15) with videos related to

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Cellular Signalling|August 23, 2015
pVHL interacts with Ceramide kinase like (CERKL) protein and ubiquitinates it for oxygen dependent proteasomal degradationJiaxiang Chen, Fei Liu, Hui Li, et al.
Biochimica Et Biophysica Acta|May 17, 2012
HSF4 is involved in DNA damage repair through regulation of Rad51Xiukun Cui, Jing Zhang, Rong Du, et al.
Molecular Vision|April 16, 2016
Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosaMeng Gao, Su Zhang, Chunjie Liu, et al.
Human Genetics|September 23, 2018
Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophyShanshan Han, Xiliang Liu, Shanglun Xie, et al.
The Journal of Investigative Dermatology|March 23, 2013
Mutations in ABCB6 cause dyschromatosis universalis hereditariaCaie Zhang, Duanzhuo Li, Jianguo Zhang, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Cellular Signalling|August 23, 2015
pVHL interacts with Ceramide kinase like (CERKL) protein and ubiquitinates it for oxygen dependent proteasomal degradationJiaxiang Chen, Fei Liu, Hui Li, et al.
Biochimica Et Biophysica Acta|May 17, 2012
HSF4 is involved in DNA damage repair through regulation of Rad51Xiukun Cui, Jing Zhang, Rong Du, et al.
Molecular Vision|April 16, 2016
Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosaMeng Gao, Su Zhang, Chunjie Liu, et al.
Human Genetics|September 23, 2018
Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophyShanshan Han, Xiliang Liu, Shanglun Xie, et al.
The Journal of Investigative Dermatology|March 23, 2013
Mutations in ABCB6 cause dyschromatosis universalis hereditariaCaie Zhang, Duanzhuo Li, Jianguo Zhang, et al.
Pageof 2