Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes-Reference-Cited by-同舟云学术

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes

Published:2008-01-06 Issue:2 Volume:40 Page:237-242
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Kagami Masayo,Sekita Yoichi,Nishimura Gen,Irie Masahito,Kato Fumiko,Okada Michiyo,Yamamori Shunji,Kishimoto Hiroshi,Nakayama Masahiro,Tanaka Yukichi,Matsuoka Kentarou,Takahashi Tsutomu,Noguchi Mika,Tanaka Yoko,Masumoto Kouji,Utsunomiya Takeshi,Kouzan Hiroko,Komatsu Yumiko,Ohashi Hirofumi,Kurosawa Kenji,Kosaki Kenjirou,Ferguson-Smith Anne C,Ishino Fumitoshi,Ogata Tsutomu

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2007.56.pdf

Reference28 articles.

1. Cavaille, J., Seitz, H., Paulsen, M., Ferguson-Smith, A.C. & Bachellerie, J.P. Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region. Hum. Mol. Genet. 11, 1527–1538 (2002).

2. Charlier, C. et al. Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8. Genome Res. 11, 850–862 (2001).

3. Paulsen, M. et al. Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2–H19 region. Genome Res. 11, 2085–2094 (2001).

4. Lin, S.P. et al. Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. Nat. Genet. 35, 97–102 (2003).

5. Murphy, S.K. et al. Epigenetic detection of human chromosome 14 uniparental disomy. Hum. Mutat. 22, 92–97 (2003).

Cited by 267 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prenatal diagnosis of recurrent Kagami–Ogata syndrome inherited from a mother affected by Temple syndrome: a case report and literature review;BMC Medical Genomics;2024-08-29

2. Targeting of retrovirus-derivedRtl8a/8breduces social response and increases apathy-like behavior associated with GABRB2 reduction;2024-08-02

3. Identification of the sequences responsible for maternalH19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth in mice;2024-07-10

4. Epigenetic Regulation of DLK1-DIO3 Region in Thyroid Carcinoma;Cells;2024-06-08

5. Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndrome;Clinical Epigenetics;2024-05-07