11 research outputs found

    Example of X chromosome inactivation status in 5 samples.

    No full text
    <p>Polymerase chain reaction products from the androgen receptor (<i>AR</i>) methylation assay shows random X chromosome inactivation (50–79%) in samples A and C, and skewed X chromosome inactivation (80–89%) in sample E. Samples B and D have a non-informative status. For each sample, DNA was either undigested (−) or digested (+) with the methylation-sensitive restriction enzyme <i>HpaII</i>. Marker (331-bp and 242-bp) fragments are visible.</p

    Degrees of X chromosome inactivation (XCI) in healthy women (HW), women with rheumatoid arthritis (RA), and women with systemic sclerosis (SSc) in the French cohort (Fr).

    No full text
    <p>Upper part: Proportional analysis with respect to the three categories of XCI: Extreme skewing (90:10 → 100:0), Medium skewing (80:20 → 89:11), and Random (50:50 → 79:21). <i>P</i> values were from <i>Χ</i><sup>2</sup> with Yates’ correction. Lower part: Scatter plots showing a difference of the distribution of XCI patterns in women with RA and SSc compared to HW (<i>P</i> = 0.013 and 0.009 respectively, Kolmogorov–Smirnov).</p

    Autoantibodies against A) EphB2 and B) THEX1 analyzed in patients with scleroderma.

    No full text
    <p>Sera reactivity against A) EphB2 or B) THEX1 is given by Absorbance (Abs) value for patients with systemic sclerosis (SSc), patients with SSc positive for anti-topoisomerase antibody (ATA<sup>pos</sup>), positive for anti-centromere antibody (ACA<sup>pos</sup>) or negative for both (ACA/ATA<sup>neg</sup>), and compared to all controls (CTLS) including healthy controls (HC) and controls with other Rheumatic diseases (RD), with a total of n = 166 with 85 HC and 81 RD for EphB2 and n = 180 with 99 HC and 81 RD for THEX1. Sera were tested at dilution 1/100 and defined as positive when Abs≄0 (on or above the dotted blue line). Red bars represent medians with interquartile ranges. Percentage of individuals positive for anti-EphB2 or THEX1 antibodies are indicated in the upper part of the graph. All P values are calculated using Mann Whitney test by comparing Abs results from patients with SSc as a whole group or in SSc subgroups to all controls (CTLS).</p

    Autoantibodies against peptide 7 (P7 from EphB2 protein) analyzed in patients with scleroderma (SSc), lupus (SLE), Rheumatoid Arthritis (RA) and healthy controls (HC).

    No full text
    <p>Sera reactivity against the peptide 7 (P7 at 10ÎŒg/well) is given by Absorbance (Abs) values for all patients and controls. Sera were tested at dilution 1/100 and defined as positive when Abs≄0 (on or above the dotted blue line). Red bars represent medians with interquartile ranges. Percentage of individuals positive for anti-P7 antibodies are indicated in the upper part of the graph. One data point for SLE is outside the Y axis limit (-0,41) and not represented here but counted for statistics. P value is calculated using Mann Whitney test by comparing patients with SLE to all controls (SSc, RA and HC, n = 157).</p

    Autoantibodies against A) EphB2 and B) THEX1 analyzed in subgroups of patients with lupus.

    No full text
    <p>Sera reactivity against EphB2 or THEX1 is given by Absorbance (Abs) value for patients with Systemic Lupus Erythematosus (SLE), positive for anti-dsDNA antibodies (dsDNA<sup>pos</sup>) or negative (dsDNA<sup>neg</sup>) and compared to all controls (CTLS) including healthy controls (HC) and controls with other Rheumatic diseases (RD), with a total of n = 166 with 85 HC and 81 RD for EphB2 and n = 180 with 99 HC and 81 RD for THEX1. Sera were tested at dilution 1/100 and defined as positive when Abs≄0 (on or above the dotted blue line). Red bars represent medians with interquartile ranges. Percentage of individuals positive for anti-EphB2 or THEX1 antibodies are indicated in the upper part of the graph. All P values are calculated using Mann Whitney test by comparing Abs results from patients with SLE as a whole group or in SLE subgroups to all controls (CTLS).</p
    corecore