1,815,413 Works

Additional file 8: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S6. Tertiary structure of protein. (PNG 9 kb)

Additional file 5: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S3. Signal peptide of CsMAPEG coding protein. (PNG 9 kb)

Additional file 7: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S5. Secondary protein structure of CsMAPEG. (PNG 1 kb)

Additional file 6: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S4. The transmembrane region of CsMAPEG coding protein. (PNG 5 kb)

Additional file 5: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S3. Signal peptide of CsMAPEG coding protein. (PNG 9 kb)

Additional file 6: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S4. The transmembrane region of CsMAPEG coding protein. (PNG 5 kb)

Additional file 3: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S1. The conserved domain of CsMAPEG coding protein. (PNG 2 kb)

Additional file 8: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S6. Tertiary structure of protein. (PNG 9 kb)

Additional file 4: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S2. Protein hydrophobicity prediction of CsMAPEG. (GIF 10 kb)

Additional file 10: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S8. pCXSN-CsMAPEG genetic transformation of cucumber. A:cucumber seed; B:co-culture; C:screening culture; D:plant regeneration; E:rooting culture of resistant seedlings; F:regeneration of resistant seedlings; G:seed of transgenic plants. (PNG 720 kb)

Additional file 3: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S1. The conserved domain of CsMAPEG coding protein. (PNG 2 kb)

Additional file 4: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S2. Protein hydrophobicity prediction of CsMAPEG. (GIF 10 kb)

Additional file 10: of Expression and functional analysis of the propamocarb-related gene CsMAPEG in cucumber

Fan Zhang, Zhiwei Qin, Xiuyan Zhou, Ming Xin, Shengnan Li & Jie Luan
Figure S8. pCXSN-CsMAPEG genetic transformation of cucumber. A:cucumber seed; B:co-culture; C:screening culture; D:plant regeneration; E:rooting culture of resistant seedlings; F:regeneration of resistant seedlings; G:seed of transgenic plants. (PNG 720 kb)

Additional file 3: of The reduction of XIAP is associated with inflammasome activation in RPE: implications for AMD pathogenesis

Jiangyuan Gao, Jing Cui, Aikun Wang, Hao Chen, Alison Fong & Joanne Matsubara
Figure S3. XIAP siRNA knockdown enhances caspase-1 cleavage in murine macrophage cell line RAW264.7. The murine macrophage RAW264.7 cell line was used as a positive control cell type to study the relationship between caspase-1 cleavage and XIAP protein level. Under the same LPS/ATP combined stimulation, RAW264.7 cells pretreated with 10 nM XIAP siRNA showed enhanced cleavage of full-length pro-caspase-1 (45 kD) into cleaved caspase-1 bands (20 kD). (EPS 2163 kb)

Additional file 3: of The reduction of XIAP is associated with inflammasome activation in RPE: implications for AMD pathogenesis

Jiangyuan Gao, Jing Cui, Aikun Wang, Hao Chen, Alison Fong & Joanne Matsubara
Figure S3. XIAP siRNA knockdown enhances caspase-1 cleavage in murine macrophage cell line RAW264.7. The murine macrophage RAW264.7 cell line was used as a positive control cell type to study the relationship between caspase-1 cleavage and XIAP protein level. Under the same LPS/ATP combined stimulation, RAW264.7 cells pretreated with 10 nM XIAP siRNA showed enhanced cleavage of full-length pro-caspase-1 (45 kD) into cleaved caspase-1 bands (20 kD). (EPS 2163 kb)

Additional file 1: of The reduction of XIAP is associated with inflammasome activation in RPE: implications for AMD pathogenesis

Jiangyuan Gao, Jing Cui, Aikun Wang, Hao Chen, Alison Fong & Joanne Matsubara
Figure S1. Control siRNA transfection does not affect the level of XIAP mRNA. A series of non-targeting control siRNA concentrations as shown was tested. No significant changes in XIAP mRNA level were observed compared to the non-transfected naĂŻve cells. (EPS 80 kb)

Additional file 1: of The reduction of XIAP is associated with inflammasome activation in RPE: implications for AMD pathogenesis

Jiangyuan Gao, Jing Cui, Aikun Wang, Hao Chen, Alison Fong & Joanne Matsubara
Figure S1. Control siRNA transfection does not affect the level of XIAP mRNA. A series of non-targeting control siRNA concentrations as shown was tested. No significant changes in XIAP mRNA level were observed compared to the non-transfected naĂŻve cells. (EPS 80 kb)

Additional file 2: of The reduction of XIAP is associated with inflammasome activation in RPE: implications for AMD pathogenesis

Jiangyuan Gao, Jing Cui, Aikun Wang, Hao Chen, Alison Fong & Joanne Matsubara
Figure S2. XIAP siRNA transfection on primary human fetal RPE cells. At 2.5 nM concentration, the XIAP targeting siRNAs reduced the XIAP mRNA level to less than 50% of untreated controls, as early as 24 h post-transfection. A higher siRNA concentration (5.0 nM) or longer transfection incubation (48 h) did not further reduce XIAP mRNA levels, suggesting the 2.5 nM siRNA concentration and the 24 h incubation period was already effective (* p<0.05, one-way ANOVA)....

Additional file 2: of The reduction of XIAP is associated with inflammasome activation in RPE: implications for AMD pathogenesis

Jiangyuan Gao, Jing Cui, Aikun Wang, Hao Chen, Alison Fong & Joanne Matsubara
Figure S2. XIAP siRNA transfection on primary human fetal RPE cells. At 2.5 nM concentration, the XIAP targeting siRNAs reduced the XIAP mRNA level to less than 50% of untreated controls, as early as 24 h post-transfection. A higher siRNA concentration (5.0 nM) or longer transfection incubation (48 h) did not further reduce XIAP mRNA levels, suggesting the 2.5 nM siRNA concentration and the 24 h incubation period was already effective (* p<0.05, one-way ANOVA)....

Additional file 7: of Arm-less mitochondrial tRNAs conserved for over 30 millions of years in spiders

Joan Pons, Pere Bover, Leticia Bidegaray-Batista & Miquel Arnedo
Figure S5. Photography of long PCR fragments analyzed by agaroge gel electrophoresis after ethidium bromide staining and UV exposition. Parachtes teruelis (103), P. riberai (105), P. romandiolae (352), P. limbarae (475), P. ignavus (479), and Harpactocrates apennicola (350). S refers to short PCR fragment and L to large one. (TIF 981 kb)

Additional file 7: of Arm-less mitochondrial tRNAs conserved for over 30 millions of years in spiders

Joan Pons, Pere Bover, Leticia Bidegaray-Batista & Miquel Arnedo
Figure S5. Photography of long PCR fragments analyzed by agaroge gel electrophoresis after ethidium bromide staining and UV exposition. Parachtes teruelis (103), P. riberai (105), P. romandiolae (352), P. limbarae (475), P. ignavus (479), and Harpactocrates apennicola (350). S refers to short PCR fragment and L to large one. (TIF 981 kb)

Additional file 7: of WTAP facilitates progression of hepatocellular carcinoma via m6A-HuR-dependent epigenetic silencing of ETS1

Yunhao Chen, Chuanhui Peng, Junru Chen, Diyu Chen, Beng Yang, Bin He, Wendi Hu, Yanpeng Zhang, Hua Liu, Longfei Dai, Haiyang Xie, Lin Zhou, Jian Wu & Shusen Zheng
Figure S1. Expression of WTAP in cell lines and functional investigations of WTAP. a Expression and survival analysis of WTAP in HCC (data from TCGA, analyzed with UALACN, http://ualcan.path.uab.edu/analysis.html ); b, c mRNA (b) and protein (c) level of WTAP in an immortalized hepatic cell line (QSG-7701) and nine HCC cell lines; d, e Negative control vector or Flag-WTAP was transfected into HCCLM3 (d) or SMMC-7721 (e) with the overexpression efficiency determined. Proliferation capacities were...

Additional file 9: of WTAP facilitates progression of hepatocellular carcinoma via m6A-HuR-dependent epigenetic silencing of ETS1

Yunhao Chen, Chuanhui Peng, Junru Chen, Diyu Chen, Beng Yang, Bin He, Wendi Hu, Yanpeng Zhang, Hua Liu, Longfei Dai, Haiyang Xie, Lin Zhou, Jian Wu & Shusen Zheng
Figure S3. Mechanisms of WTAP-mediated modulation on ETS1. a Representative immunofluorescence images of Huh7 cells with the deficiency of WTAP to determine the subcellular distribution and expression of WTAP and ETS1 (scale bar, 30 μm). WTAP mainly localized in nucleus while ETS1 mainly in cytoplasm. However, fluorescence intensity of ETS1 significantly augmented in either cytosolic or nuclear regions (especially in nuclear membrane); b Cytosolic and nuclear separation analysis was conducted to examine the expression of...

Additional file 9: of WTAP facilitates progression of hepatocellular carcinoma via m6A-HuR-dependent epigenetic silencing of ETS1

Yunhao Chen, Chuanhui Peng, Junru Chen, Diyu Chen, Beng Yang, Bin He, Wendi Hu, Yanpeng Zhang, Hua Liu, Longfei Dai, Haiyang Xie, Lin Zhou, Jian Wu & Shusen Zheng
Figure S3. Mechanisms of WTAP-mediated modulation on ETS1. a Representative immunofluorescence images of Huh7 cells with the deficiency of WTAP to determine the subcellular distribution and expression of WTAP and ETS1 (scale bar, 30 μm). WTAP mainly localized in nucleus while ETS1 mainly in cytoplasm. However, fluorescence intensity of ETS1 significantly augmented in either cytosolic or nuclear regions (especially in nuclear membrane); b Cytosolic and nuclear separation analysis was conducted to examine the expression of...

Additional file 8: of WTAP facilitates progression of hepatocellular carcinoma via m6A-HuR-dependent epigenetic silencing of ETS1

Yunhao Chen, Chuanhui Peng, Junru Chen, Diyu Chen, Beng Yang, Bin He, Wendi Hu, Yanpeng Zhang, Hua Liu, Longfei Dai, Haiyang Xie, Lin Zhou, Jian Wu & Shusen Zheng
Figure S2. The impact of WTAP in vivo. a The level of WTAP and Ki67 in xenograft tumor tissues was detected by IHC (scale bar, 50â Îźm; magnification, 400X); b-d Tumor growth curve (c) of SMMC7721 with stable WTAP epitopic expression cells in a xenograft mouse model was based on the tumor sizes. And the photography (b) and tumor weights (d) were recorded to exhibit the growth difference within the influence of WTAP. (TIF 4248...

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