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STATA Corporation multivariate
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Mixed-effects model coefficients and p-values for univariate and multivariate linear regressions of ictal duration and postictal suppression index. Significance: p <0.05*, p <0.01**, p <0.001***. Univar coef = Univariate mixed model coefficients; Selective Multivar coef = multivariate model coefficients including age, sex, and significant univariate variables; Complete Multivar coef = multivariate model coefficients including all <t> univariate model variables. </t>
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Mixed-effects model coefficients and p-values for univariate and multivariate linear regressions of ictal duration and postictal suppression index. Significance: p <0.05*, p <0.01**, p <0.001***. Univar coef = Univariate mixed model coefficients; Selective Multivar coef = multivariate model coefficients including age, sex, and significant univariate variables; Complete Multivar coef = multivariate model coefficients including all <t> univariate model variables. </t>
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SLIT2 LTD alterations of slit2 and robo1
Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of <t>ROBO1/2</t> and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.
Alterations Of Slit2 And Robo1, supplied by SLIT2 LTD, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of <t>ROBO1/2</t> and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.
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RStudio nonparametric multivariate cramer test
Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of <t>ROBO1/2</t> and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.
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Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of <t>ROBO1/2</t> and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.
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Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of <t>ROBO1/2</t> and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.
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Statistik Georg Ferber statistik multivariate
Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of <t>ROBO1/2</t> and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.
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Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of <t>ROBO1/2</t> and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.
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Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of <t>ROBO1/2</t> and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.
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Mixed-effects model coefficients and p-values for univariate and multivariate linear regressions of ictal duration and postictal suppression index. Significance: p <0.05*, p <0.01**, p <0.001***. Univar coef = Univariate mixed model coefficients; Selective Multivar coef = multivariate model coefficients including age, sex, and significant univariate variables; Complete Multivar coef = multivariate model coefficients including all  univariate model variables.

Journal: AMIA Summits on Translational Science Proceedings

Article Title: Factors Affecting Electroconvulsive Therapy Ictal Outcomes: Duration and Postictal Suppression

doi:

Figure Lengend Snippet: Mixed-effects model coefficients and p-values for univariate and multivariate linear regressions of ictal duration and postictal suppression index. Significance: p <0.05*, p <0.01**, p <0.001***. Univar coef = Univariate mixed model coefficients; Selective Multivar coef = multivariate model coefficients including age, sex, and significant univariate variables; Complete Multivar coef = multivariate model coefficients including all univariate model variables.

Article Snippet: Univar coef = Univariate mixed model coefficients; Selective Multivar coef = multivariate model coefficients including age, sex, and significant univariate variables; Complete Multivar coef = multivariate model coefficients including all univariate model variables.

Techniques:

Restricted Maximum Likelihood (REML) of univariate and multivariate mixed-effects models for (A) ictal duration, and (B) postictal suppression, rank ordered. REML is the unbiased estimate of variance and covariance parameters for mixed-effects models, with lower REML relating to better fit of the data.

Journal: AMIA Summits on Translational Science Proceedings

Article Title: Factors Affecting Electroconvulsive Therapy Ictal Outcomes: Duration and Postictal Suppression

doi:

Figure Lengend Snippet: Restricted Maximum Likelihood (REML) of univariate and multivariate mixed-effects models for (A) ictal duration, and (B) postictal suppression, rank ordered. REML is the unbiased estimate of variance and covariance parameters for mixed-effects models, with lower REML relating to better fit of the data.

Article Snippet: Univar coef = Univariate mixed model coefficients; Selective Multivar coef = multivariate model coefficients including age, sex, and significant univariate variables; Complete Multivar coef = multivariate model coefficients including all univariate model variables.

Techniques:

Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of ROBO1/2 and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.

Journal: PLoS ONE

Article Title: Inactivation of SLIT2-ROBO1/2 Pathway in Premalignant Lesions of Uterine Cervix: Clinical and Prognostic Significances

doi: 10.1371/journal.pone.0038342

Figure Lengend Snippet: Bars represented the gene expression normalized to β2- microglobulin and relative to a pool of normal cervical tissues, using the -ddCt method. Bars 22 and 23 represent the SiHa and HeLa cell lines, respectively. Analysis of promoter methylation of ROBO1/2 and SLIT2 by MSRA and validation by MSP. ( C1 ) Schematic representation of promoter regions of candidate genes revealing distribution of Hpa II/ Msp I (CCGG: arrowhead) restriction sites. →: location of methylation primers. +1 : transcription start site. ( C2 ) Representative tumor samples (#3920T, #3229T, #4025T) showing methylated status at different genes, normal cervical tissue were unmethylated. M and H : Msp I and Hpa II digested DNA respectively. U: Undigested DNA. K1 and K2 : Controls for DNA digestion and integrity respectively, T: Tumor DNA, N: DNA from corresponding normal tissue. ( C3 ) Representative tumor samples showing methylation status of candidate genes by MSP. U: amplicon obtained with primer for bisulphite modified unmethylated DNA, M: amplicon obtained with primer for bisulphite modified methylated DNA, T: Tumor DNA, N: DNA from corresponding normal tissue. ( D ) Reactivation of RNA expression of ROBO1 and the ncRNAs in SiHa and HeLa cells. Reactivated RNA expression of the ligand-receptor genes in SiHa ( E ) and HeLa ( F ) cell lines in presence of 5 µM, 10 µM and 20 µM 5-aza dC. The bars represent increased gene expression in 5-aza dC treated cells compared to untreated control.

Article Snippet: Moreover Cox multivariate analysis revealed alterations of SLIT2 and ROBO1 , in combination with advanced tumor stage (III/IV), multiparity (≥5) and early sexual debut (<19 years) as determinants of worse prognosis.

Techniques: Gene Expression, Methylation, Biomarker Discovery, Amplification, Modification, RNA Expression, Control

(i) LOH: loss of heterozygosity, (ii) MA-1: microsatellite size alteration of one allele. (iii) LOH + MA: loss of one allele and microsatellite size alteration of the other. (iv) Hemizygous (HE) deletion of ROBO2 locus as shown by D3S2515. (v) & (vi) HE deletion as shown by exonic markers (EM) from ROBO1 and ROBO2 respectively, SST used as control. The sample numbers and marker loci are indicated above and below the figure respectively. →: allelic loss, “*”: allelic size alteration. Deletion of ROBO1/2 and SLIT2 analyzed by microsatellite and exonic markers in ( B ) CIN and ( C ) CACX. T: Tumor DNA, N: DNA from normal cervix/PBL. ( D ) Pattern of deletion and methylation of ROBO1/2 and SLIT2 during disease progression. Asterisk denotes statistical significance (P<0.05). ( E ) Overall alteration patterns of the individual genes, SLIT2-ROBO1 and SLIT2-ROBO2 ligand-receptor pairs, during disease progression. Asterisk denotes statistical significance (P<0.05).

Journal: PLoS ONE

Article Title: Inactivation of SLIT2-ROBO1/2 Pathway in Premalignant Lesions of Uterine Cervix: Clinical and Prognostic Significances

doi: 10.1371/journal.pone.0038342

Figure Lengend Snippet: (i) LOH: loss of heterozygosity, (ii) MA-1: microsatellite size alteration of one allele. (iii) LOH + MA: loss of one allele and microsatellite size alteration of the other. (iv) Hemizygous (HE) deletion of ROBO2 locus as shown by D3S2515. (v) & (vi) HE deletion as shown by exonic markers (EM) from ROBO1 and ROBO2 respectively, SST used as control. The sample numbers and marker loci are indicated above and below the figure respectively. →: allelic loss, “*”: allelic size alteration. Deletion of ROBO1/2 and SLIT2 analyzed by microsatellite and exonic markers in ( B ) CIN and ( C ) CACX. T: Tumor DNA, N: DNA from normal cervix/PBL. ( D ) Pattern of deletion and methylation of ROBO1/2 and SLIT2 during disease progression. Asterisk denotes statistical significance (P<0.05). ( E ) Overall alteration patterns of the individual genes, SLIT2-ROBO1 and SLIT2-ROBO2 ligand-receptor pairs, during disease progression. Asterisk denotes statistical significance (P<0.05).

Article Snippet: Moreover Cox multivariate analysis revealed alterations of SLIT2 and ROBO1 , in combination with advanced tumor stage (III/IV), multiparity (≥5) and early sexual debut (<19 years) as determinants of worse prognosis.

Techniques: Control, Marker, Methylation, Biomarker Discovery

Correlation between deletion/methylation and reduced expression (RNA/protein) of  ROBO1/2  and SLIT2 in CIN/CACX.

Journal: PLoS ONE

Article Title: Inactivation of SLIT2-ROBO1/2 Pathway in Premalignant Lesions of Uterine Cervix: Clinical and Prognostic Significances

doi: 10.1371/journal.pone.0038342

Figure Lengend Snippet: Correlation between deletion/methylation and reduced expression (RNA/protein) of ROBO1/2 and SLIT2 in CIN/CACX.

Article Snippet: Moreover Cox multivariate analysis revealed alterations of SLIT2 and ROBO1 , in combination with advanced tumor stage (III/IV), multiparity (≥5) and early sexual debut (<19 years) as determinants of worse prognosis.

Techniques: Expressing

( A ) In normal cervical epithelium the basal and parabasal layer stained intensely for all the three proteins, whereas the intensity and frequency of stained cells reduced with further differentiation in the spinous layer. ( B ) In primary CACX expression pattern of these proteins were concordant with respective molecular alterations. ( C ) In SiHa cells ROBO1 and ROBO2 were membrane localized, whereas SLIT2 was present mostly in the cytoplasm. T: primary CACX sample; scale bars for both 20X and 40X is 50 µm; original magnifications are indicated in parenthesis. Magnification of panel C is 40X.

Journal: PLoS ONE

Article Title: Inactivation of SLIT2-ROBO1/2 Pathway in Premalignant Lesions of Uterine Cervix: Clinical and Prognostic Significances

doi: 10.1371/journal.pone.0038342

Figure Lengend Snippet: ( A ) In normal cervical epithelium the basal and parabasal layer stained intensely for all the three proteins, whereas the intensity and frequency of stained cells reduced with further differentiation in the spinous layer. ( B ) In primary CACX expression pattern of these proteins were concordant with respective molecular alterations. ( C ) In SiHa cells ROBO1 and ROBO2 were membrane localized, whereas SLIT2 was present mostly in the cytoplasm. T: primary CACX sample; scale bars for both 20X and 40X is 50 µm; original magnifications are indicated in parenthesis. Magnification of panel C is 40X.

Article Snippet: Moreover Cox multivariate analysis revealed alterations of SLIT2 and ROBO1 , in combination with advanced tumor stage (III/IV), multiparity (≥5) and early sexual debut (<19 years) as determinants of worse prognosis.

Techniques: Staining, Expressing, Membrane

Alterations of ( A ) SLIT2 and/or ROBO1 and ( B ) SLIT2 and/or ROBO2 ligand-receptor pairs were significantly associated with poor patient outcome [OS]. ( C ) Representation of Cox Multivariate analyses of genetic, clinical and etiological parameters in predicting outcome of CACX patients. N: total number of samples and P<0.05 denotes statistical significance.

Journal: PLoS ONE

Article Title: Inactivation of SLIT2-ROBO1/2 Pathway in Premalignant Lesions of Uterine Cervix: Clinical and Prognostic Significances

doi: 10.1371/journal.pone.0038342

Figure Lengend Snippet: Alterations of ( A ) SLIT2 and/or ROBO1 and ( B ) SLIT2 and/or ROBO2 ligand-receptor pairs were significantly associated with poor patient outcome [OS]. ( C ) Representation of Cox Multivariate analyses of genetic, clinical and etiological parameters in predicting outcome of CACX patients. N: total number of samples and P<0.05 denotes statistical significance.

Article Snippet: Moreover Cox multivariate analysis revealed alterations of SLIT2 and ROBO1 , in combination with advanced tumor stage (III/IV), multiparity (≥5) and early sexual debut (<19 years) as determinants of worse prognosis.

Techniques: