BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 35427809)

  • 1. A boy with overgrowth caused by multi-locus imprinting disturbance including hypomethylation of MEST:alt-TSS-DMR.
    Narusawa H; Sasaki S; Hara-Isono K; Matsubara K; Fukami M; Nagasaki K; Kagami M
    Eur J Med Genet; 2022 Jun; 65(6):104502. PubMed ID: 35427809
    [TBL] [Abstract][Full Text] [Related]  

  • 2. ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance.
    Kagami M; Hara-Isono K; Matsubara K; Nakabayashi K; Narumi S; Fukami M; Ohkubo Y; Saitsu H; Takada S; Ogata T
    Clin Epigenetics; 2021 May; 13(1):119. PubMed ID: 34039421
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR.
    Kagami M; Yanagisawa A; Ota M; Matsuoka K; Nakamura A; Matsubara K; Nakabayashi K; Takada S; Fukami M; Ogata T
    Clin Epigenetics; 2019 Mar; 11(1):42. PubMed ID: 30846001
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Uncovering the phenotypic consequences of multi-locus imprinting disturbances using genome-wide methylation analysis in genomic imprinting disorders.
    Kim HY; Shin CH; Shin CH; Ko JM
    PLoS One; 2023; 18(8):e0290450. PubMed ID: 37594968
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.
    Eggermann T; Yapici E; Bliek J; Pereda A; Begemann M; Russo S; Tannorella P; Calzari L; de Nanclares GP; Lombardi P; Temple IK; Mackay D; Riccio A; Kagami M; Ogata T; Lapunzina P; Monk D; Maher ER; Tümer Z
    Clin Epigenetics; 2022 Mar; 14(1):41. PubMed ID: 35296332
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two infants with mild, atypical clinical features of Kagami-Ogata syndrome caused by epimutation.
    Higashiyama H; Ohsone Y; Takatani R; Futatani T; Kosaki R; Kagami M
    Eur J Med Genet; 2022 Oct; 65(10):104580. PubMed ID: 35953028
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterization of temple syndrome families with 14q32 epimutations.
    Brück J; Begemann M; Dey D; Elbracht M; Eggermann T
    Eur J Med Genet; 2020 Dec; 63(12):104077. PubMed ID: 33010492
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus imprinting disturbance: a female-dominant phenomenon?
    Sano S; Matsubara K; Nagasaki K; Kikuchi T; Nakabayashi K; Hata K; Fukami M; Kagami M; Ogata T
    J Hum Genet; 2016 Aug; 61(8):765-9. PubMed ID: 27121328
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2.
    Yamaguchi Y; Tayama C; Tomikawa J; Akaishi R; Kamura H; Matsuoka K; Wake N; Minakami H; Kato K; Yamada T; Nakabayashi K; Hata K
    Clin Epigenetics; 2019 Aug; 11(1):113. PubMed ID: 31370882
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance.
    Fontana L; Tabano S; Maitz S; Colapietro P; Garzia E; Gerli AG; Sirchia SM; Miozzo M
    Int J Mol Sci; 2021 Mar; 22(7):. PubMed ID: 33810554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57.
    Bak M; Boonen SE; Dahl C; Hahnemann JM; Mackay DJ; Tümer Z; Grønskov K; Temple IK; Guldberg P; Tommerup N
    BMC Med Genet; 2016 Apr; 17():29. PubMed ID: 27075368
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi.
    Paganini L; Carlessi N; Fontana L; Silipigni R; Motta S; Fiori S; Guerneri S; Lalatta F; Cereda A; Sirchia S; Miozzo M; Tabano S
    Epigenetics; 2015; 10(7):643-9. PubMed ID: 26061650
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Placentas from pregnancies conceived by IVF/ICSI have a reduced DNA methylation level at the H19 and MEST differentially methylated regions.
    Nelissen EC; Dumoulin JC; Daunay A; Evers JL; Tost J; van Montfoort AP
    Hum Reprod; 2013 Apr; 28(4):1117-26. PubMed ID: 23343754
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.
    Fontana L; Bedeschi MF; Maitz S; Cereda A; Faré C; Motta S; Seresini A; D'Ursi P; Orro A; Pecile V; Calvello M; Selicorni A; Lalatta F; Milani D; Sirchia SM; Miozzo M; Tabano S
    Epigenetics; 2018; 13(9):897-909. PubMed ID: 30221575
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
    Inoue T; Nakamura A; Iwahashi-Odano M; Tanase-Nakao K; Matsubara K; Nishioka J; Maruo Y; Hasegawa Y; Suzumura H; Sato S; Kobayashi Y; Murakami N; Nakabayashi K; Yamazawa K; Fuke T; Narumi S; Oka A; Ogata T; Fukami M; Kagami M
    Clin Epigenetics; 2020 Jun; 12(1):86. PubMed ID: 32546215
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations.
    Maeda T; Higashimoto K; Jozaki K; Yatsuki H; Nakabayashi K; Makita Y; Tonoki H; Okamoto N; Takada F; Ohashi H; Migita M; Kosaki R; Matsubara K; Ogata T; Matsuo M; Hamasaki Y; Ohtsuka Y; Nishioka K; Joh K; Mukai T; Hata K; Soejima H
    Genet Med; 2014 Dec; 16(12):903-12. PubMed ID: 24810686
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequency and characterization of DNA methylation defects in children born SGA.
    Bens S; Haake A; Richter J; Leohold J; Kolarova J; Vater I; Riepe FG; Buiting K; Eggermann T; Gillessen-Kaesbach G; Platzer K; Prawitt D; Caliebe A; Siebert R
    Eur J Hum Genet; 2013 Aug; 21(8):838-43. PubMed ID: 23232699
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach.
    Bilo L; Ochoa E; Lee S; Dey D; Kurth I; Kraft F; Rodger F; Docquier F; Toribio A; Bottolo L; Binder G; Fekete G; Elbracht M; Maher ER; Begemann M; Eggermann T
    Clin Epigenetics; 2023 Mar; 15(1):35. PubMed ID: 36859312
    [TBL] [Abstract][Full Text] [Related]  

  • 19. In-depth characterization of the placental imprintome reveals novel differentially methylated regions across birth weight categories.
    Deyssenroth MA; Marsit CJ; Chen J; Lambertini L
    Epigenetics; 2020; 15(1-2):47-60. PubMed ID: 31403346
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.