Product References
A novel hypoxia-driven gene signature that can predict the prognosis of hepatocellular carcinoma.
Bioengineered
Zeng Z,Lei S,Wang J,Yang Y,Lan J,Tian Q,Chen T,Hao X
Sun May 01 00:00:00 UTC 2022
A novel hypoxia-driven gene signature that can predict the prognosis of hepatocellular carcinoma.
Bioengineered
Zeng Z,Lei S,Wang J,Yang Y,Lan J,Tian Q,Chen T,Hao X
Sun May 01 00:00:00 UTC 2022
Complement factor H‑related 3 overexpression affects hepatocellular carcinoma proliferation and apoptosis.
Molecular medicine reports
Liu H,Zhang L,Wang P
Sun Sep 01 00:00:00 UTC 2019
Quantitative analysis of hydroxyapatite-binding plasma proteins in genotyped individuals with late-stage age-related macular degeneration.
Experimental eye research
Arya S,Emri E,Synowsky SA,Shirran SL,Barzegar-Befroei N,Peto T,Botting CH,Lengyel I,Stewart AJ
Sun Jul 01 00:00:00 UTC 2018
Quantitative analysis of hydroxyapatite-binding plasma proteins in genotyped individuals with late-stage age-related macular degeneration.
Experimental eye research
Arya S,Emri E,Synowsky SA,Shirran SL,Barzegar-Befroei N,Peto T,Botting CH,Lengyel I,Stewart AJ
Sun Jul 01 00:00:00 UTC 2018
Complement-Regulatory Proteins CFHR1 and CFHR3 and Patient Response to Anti-CD20 Monoclonal Antibody Therapy.
Clinical cancer research : an official journal of the American Association for Cancer Research
Rogers LM,Mott SL,Smith BJ,Link BK,Sahin D,Weiner GJ
Wed Feb 15 00:00:00 UTC 2017
Complement-Regulatory Proteins CFHR1 and CFHR3 and Patient Response to Anti-CD20 Monoclonal Antibody Therapy.
Clinical cancer research : an official journal of the American Association for Cancer Research
Rogers LM,Mott SL,Smith BJ,Link BK,Sahin D,Weiner GJ
Wed Feb 15 00:00:00 UTC 2017
A haplotype in CFH family genes confers high risk of rare glomerular nephropathies.
Scientific reports
Ding Y,Zhao W,Zhang T,Qiang H,Lu J,Su X,Wen S,Xu F,Zhang M,Zhang H,Zeng C,Liu Z,Chen H
Thu Jul 20 00:00:00 UTC 2017
A haplotype in CFH family genes confers high risk of rare glomerular nephropathies.
Scientific reports
Ding Y,Zhao W,Zhang T,Qiang H,Lu J,Su X,Wen S,Xu F,Zhang M,Zhang H,Zeng C,Liu Z,Chen H
Thu Jul 20 00:00:00 UTC 2017
A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan.
PloS one
Yoshida Y,Miyata T,Matsumoto M,Shirotani-Ikejima H,Uchida Y,Ohyama Y,Kokubo T,Fujimura Y
Mon Feb 29 00:00:00 UTC 2016
A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan.
PloS one
Yoshida Y,Miyata T,Matsumoto M,Shirotani-Ikejima H,Uchida Y,Ohyama Y,Kokubo T,Fujimura Y
Mon Feb 29 00:00:00 UTC 2016