Table S1. Mutational status of pancreatic cell lines used.

Aug 14, 2014

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Table S1. Mutational status of pancreatic cell lines used.

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Table S1. Mutational status of pancreatic cell lines used.

Mutational analysis of 35 bladder cancer cell lines using RNA-seq

Mutational analysis of 35 bladder cancer cell lines using RNA-seq. RNA-seq. Cell lines. Genes. Frequently mutated networks in bladder cancer cell lines. Mutations in CBP/p300 network. Fusion. Missense . Nonsense. Mutations in chromatin remodelling genes. Fusion. Missense . Nonsense.

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Table S1

Table S1. Table S1. The primer list used in the present study.

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Supplemental Table S1

Supplemental Table S1. For Site Directed Mutagenesis and cloning of constructs P9GF: 5’ GAC GCT ACT TCA CTA TAG ATA GGA AGT TCA TTT C 3’ P9GR: 5’ GAA ATG AAC TTC CTA TCT ATA GTG AAG TAG CGT C 3’ LAP9GF: 5’ CCC GGA TCC ATC ACT ATA GAT AGG AAG TTC ATT TCA TTT G 3’

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Table S1. Primers used for semiquantitative RT-PCR

Table S1. Primers used for semiquantitative RT-PCR. 4. 4. 10. 10. 3. 3. 10. 10. 93.4. 96.6. 2. 2. 10. 10. 1. 1. 10. 10. 0. 0. 10. 10. 0. 1. 2. 3. 4. 0. 1. 2. 3. 4. 10. 10. 10. 10. 10. 10. 10. 10. 10. 10.

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(Table S1)

(Table S1). B. A. B. E. F. anterior. C. E. posterior. F. (Figure S1). ON. lCa. lCa. m. lo. SOG. PB. C. D. E. D. lCa. CC. Pe. CC. 1.E+02. 1.E+01. 1.E+00. 1.E-01. Relative Kakugo content. 1.E-02. 1.E-03. 1.E-04. days. 0. 1. 4. 6. 9. 14. (4). (3). (3).

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Supplementary Table S1

Relationship between the miRNA-21 in plasma and primary ESCC tissues. Supplementary Table S1. Relationship between the miRNA-375 in plasma and primary ESCC tissues. Supplementary Table S2. 1.0. 1.0. 0.8. 0.8. 0.6. 0.6. 0.4. 0.4. 0.2. 0.2. miR-21 AUC=0.618. miR-375 AUC=0.807. 0. 0.

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Supplemental Table S1

Supplemental Table S1. Table S1. Quantitative real-time RT-PCR primer sequences for genes used in the publication. All sequences are listed in the 5’ – 3’ direction. Supplemental Fig. S1. Induced by E2 and IGF-I. 3hr. 24hr. Repressed by E2 and IGF-I. 3hr. 24hr.

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Table S1. Organisms used for lytA specificity studies

Table S1. Organisms used for lytA specificity studies. lytA 173bp PCR product. Organism. Strain. Streptococcus pneumoniae. ATCC 49619. positive. Streptococcus pneumoniae. ATCC 6303. positive. Streptococcus pneumoniae. positive. ATCC 6305. Streptococcus pneumoniae. positive.

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TABLE S1

TABLE S1.

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Table. S1

Table. S1.

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Table S1

0.023. 0.023. 0.23. 0.23. 2.3. 2.3. 23 c. 23. 5.5. 24.9. 65.07. 4.7. 44.9. 171.3. 1.2. 1.5. 2.3. 1.1. 1.1. 2.1. Table S1. 5-Me-Tetrahydrofolate (5-MeTHF). Folic acid (FA). Tetrahydrofolate (THF). IC 50 s (nM) in physiological folate (FA 0.023 µM).

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Supplementary Table S1.

Supplementary Table S1. Primer sequences used for PCR amplification of DDAH1, DDAH2 and tubulin message. Supplementary Figures. s1A. s1B. s1C. s1D.

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Supplementary Table S1

Supplementary Table S1.

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Table S1

Table S1.

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Supplementary Table S1 . Summary of cell lines used.

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Table S1: Parameters used for collection of the switchgrass internodes.

Table S1: Parameters used for collection of the switchgrass internodes. Values are means ± SE (n=30).

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Supplementary Table S1

Supplementary Table S1. Clinicopathological features of 3 GC patients analysed on miRNA microarray.

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Supplemental Table S1

Supplemental Table S1. Complete list of LC-MS myc interating protiens in the MCF7 cells, proteins highlighted in red are those differentially expressed from the LCC1 and LCC1 EGF treated cells. Supplemental Table S2.

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Table S1 . (Continued)

Table S1 . List of primers used for the amplification of DNA fragments that were used as probes for Northern blot analysis. Table S1 . (Continued).

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Supplemental Table S1

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