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Pyrosequencing Inc methylation analysis using
Methylation Analysis Using, supplied by Pyrosequencing Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/methylation+analysis+using/methylation+analysis/pm40490796-5-3-6
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methylation analysis using - by Bioz Stars, 2026-11
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Methylation:

Article Title: Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith-Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted region.
Article Snippet: .. Results We conducted methylation analysis using pyrosequencing in 77 patients showing the BWS-phenotype without molecular defects in the 11p15.5 imprinted region. ..

Article Title: Accelerated neurodegeneration through chaperone-mediated oligomerization of tau
Article Snippet: .. To see whether this was the mechanism leading to the significantly increased FKBP51 expression found in the aged brain, methylation analysis using pyrosequencing was performed on DNA from PCG brain tissue of aging nondemented samples ( n = 6) on multiple CpG sites in functional glucocorticoid response elements in intron 7, intron 2, and the promoter (Figure ) of FKBP5 ( 54 ). ..

Article Title: Abstracts
Article Snippet: .. Method: To detect genetic causes of these patients, we first performed methylation analysis using pyrosequencing for the PLAGL1-, PEG1/MEST-, PEG10-, H19-, Kv-, DLK1-MEG3 intergenic-, MEG3-, SNRPN-, ZNF597-, and GNAS A/B-DMRs. ..

Expressing:

Article Title: Accelerated neurodegeneration through chaperone-mediated oligomerization of tau
Article Snippet: .. To see whether this was the mechanism leading to the significantly increased FKBP51 expression found in the aged brain, methylation analysis using pyrosequencing was performed on DNA from PCG brain tissue of aging nondemented samples ( n = 6) on multiple CpG sites in functional glucocorticoid response elements in intron 7, intron 2, and the promoter (Figure ) of FKBP5 ( 54 ). ..

Functional Assay:

Article Title: Accelerated neurodegeneration through chaperone-mediated oligomerization of tau
Article Snippet: .. To see whether this was the mechanism leading to the significantly increased FKBP51 expression found in the aged brain, methylation analysis using pyrosequencing was performed on DNA from PCG brain tissue of aging nondemented samples ( n = 6) on multiple CpG sites in functional glucocorticoid response elements in intron 7, intron 2, and the promoter (Figure ) of FKBP5 ( 54 ). ..



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Heatmap of <t>array-based</t> <t>methylation</t> analysis using analysis method 1 . The heatmap indicates 56 aberrant <t>DMRs</t> out of 78 examined DMRs. Each row represents a DMR; each column represents a patient. Germline DMRs are shown on a gray background, secondary DMRs on a light green background, and unclassifiable DMRs on a white background. Methylation disturbances of DMRs are classified into seven categories based on the degree. B, Beckwith-Wiedemann syndrome; P, pseudohypoparathyroidism type 1B; O, overgrowth; S, Silver-Russell syndrome; TS, Temple syndrome; TN, transient neonatal diabetes mellitus; W, Prader-Willi syndrome; SG, small for gestational age; N, neurodevelopmental delay and/or intellectual developmental disorder; A, assisted reproductive technology; T, monozygotic monochorionic diamniotic twins; V, variants of uncertain significance; L, likely pathogenic; DMR, differential methylated region; Chr, chromosome; MML, median methylation level of CpG sites in the DMR; SD, standard deviation; mean, mean MML of 16 healthy controls
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Image Search Results


Heatmap of array-based methylation analysis using analysis method 1 . The heatmap indicates 56 aberrant DMRs out of 78 examined DMRs. Each row represents a DMR; each column represents a patient. Germline DMRs are shown on a gray background, secondary DMRs on a light green background, and unclassifiable DMRs on a white background. Methylation disturbances of DMRs are classified into seven categories based on the degree. B, Beckwith-Wiedemann syndrome; P, pseudohypoparathyroidism type 1B; O, overgrowth; S, Silver-Russell syndrome; TS, Temple syndrome; TN, transient neonatal diabetes mellitus; W, Prader-Willi syndrome; SG, small for gestational age; N, neurodevelopmental delay and/or intellectual developmental disorder; A, assisted reproductive technology; T, monozygotic monochorionic diamniotic twins; V, variants of uncertain significance; L, likely pathogenic; DMR, differential methylated region; Chr, chromosome; MML, median methylation level of CpG sites in the DMR; SD, standard deviation; mean, mean MML of 16 healthy controls

Journal: Clinical Epigenetics

Article Title: Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance

doi: 10.1186/s13148-024-01744-5

Figure Lengend Snippet: Heatmap of array-based methylation analysis using analysis method 1 . The heatmap indicates 56 aberrant DMRs out of 78 examined DMRs. Each row represents a DMR; each column represents a patient. Germline DMRs are shown on a gray background, secondary DMRs on a light green background, and unclassifiable DMRs on a white background. Methylation disturbances of DMRs are classified into seven categories based on the degree. B, Beckwith-Wiedemann syndrome; P, pseudohypoparathyroidism type 1B; O, overgrowth; S, Silver-Russell syndrome; TS, Temple syndrome; TN, transient neonatal diabetes mellitus; W, Prader-Willi syndrome; SG, small for gestational age; N, neurodevelopmental delay and/or intellectual developmental disorder; A, assisted reproductive technology; T, monozygotic monochorionic diamniotic twins; V, variants of uncertain significance; L, likely pathogenic; DMR, differential methylated region; Chr, chromosome; MML, median methylation level of CpG sites in the DMR; SD, standard deviation; mean, mean MML of 16 healthy controls

Article Snippet: Consequently, we identified MLID in 29 patients with epimutation confirmed by methylation analysis for multiple ID-associated DMRs using pyrosequencing and/or methylation-specific multiple ligation-dependent probe amplification.

Techniques: Methylation, Standard Deviation