Literature DB >> 28816024

Continuous hypomethylation of the KCNQ1OT1:TSS-DMR in monochorionic twins discordant for Beckwith-Wiedemann syndrome.

Takanobu Inoue1,2, Akie Nakamura1, Keiko Matsubara1, Hiromi Nyuzuki3, Keisuke Nagasaki3, Akira Oka2, Maki Fukami1, Masayo Kagami1.   

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Year:  2017        PMID： 28816024     DOI： 10.1002/ajmg.a.38419

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  3 in total

1.  Overexpression of long non-coding RNA KCNQ1OT1 is related to good prognosis via inhibiting cell proliferation in non-small cell lung cancer.

Authors:  Xiao Sun; Yanlu Xin; Maolong Wang; Shicheng Li; Shuncheng Miao; Yunpeng Xuan; Yuanyong Wang; Tong Lu; Jia Liu; Wenjie Jiao
Journal:  Thorac Cancer       Date:  2018-03-05       Impact factor: 3.500

2.  (Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith-Wiedemann syndrome.

Authors:  Laura Fontana; Maria F Bedeschi; Giulia A Cagnoli; Jole Costanza; Nicola Persico; Silvana Gangi; Matteo Porro; Paola F Ajmone; Patrizia Colapietro; Carlo Santaniello; Milena Crippa; Silvia M Sirchia; Monica Miozzo; Silvia Tabano
Journal:  Mol Genet Genomic Med       Date:  2020-07-06       Impact factor: 2.183

Review 3.  Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance.

Authors:  Laura Fontana; Silvia Tabano; Silvia Maitz; Patrizia Colapietro; Emanuele Garzia; Alberto Giovanni Gerli; Silvia Maria Sirchia; Monica Miozzo
Journal:  Int J Mol Sci       Date:  2021-03-26       Impact factor: 5.923
  3 in total

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