Literature DB >> 18619672

Placentomegaly in paternal uniparental disomy for human chromosome 14.

M Kagami, K Yamazawa, K Matsubara, N Matsuo, T Ogata.   

Abstract

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Year:  2008        PMID： 18619672     DOI： 10.1016/j.placenta.2008.06.001

Source DB:  PubMed          Journal:  Placenta        ISSN： 0143-4004            Impact factor:   3.481


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  8 in total

1.  Assessing the effect of the CLPG mutation on the microRNA catalog of skeletal muscle using high-throughput sequencing.

Authors:  Florian Caiment; Carole Charlier; Tracy Hadfield; Noelle Cockett; Michel Georges; Denis Baurain
Journal:  Genome Res       Date:  2010-10-13       Impact factor: 9.043

2.  The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers.

Authors:  Masayo Kagami; Maureen J O'Sullivan; Andrew J Green; Yoshiyuki Watabe; Osamu Arisaka; Nobuhide Masawa; Kentarou Matsuoka; Maki Fukami; Keiko Matsubara; Fumiko Kato; Anne C Ferguson-Smith; Tsutomu Ogata
Journal:  PLoS Genet       Date:  2010-06-17       Impact factor: 5.917

3.  Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype.

Authors:  Masayo Kagami; Fumiko Kato; Keiko Matsubara; Tomoko Sato; Gen Nishimura; Tsutomu Ogata
Journal:  Eur J Hum Genet       Date:  2012-02-22       Impact factor: 4.246

4.  Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome).

Authors:  Masayo Kagami; Kenji Kurosawa; Osamu Miyazaki; Fumitoshi Ishino; Kentaro Matsuoka; Tsutomu Ogata
Journal:  Eur J Hum Genet       Date:  2015-02-18       Impact factor: 4.246

Review 5.  Molecular mechanisms leading to the phenotypic development in paternal and maternal uniparental disomy for chromosome 14.

Authors:  Tsutomu Ogata; Masayo Kagami
Journal:  Clin Pediatr Endocrinol       Date:  2008-11-08

6.  Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patients.

Authors:  Masayo Kagami; Keisuke Nagasaki; Rika Kosaki; Reiko Horikawa; Yasuhiro Naiki; Shinji Saitoh; Toshihiro Tajima; Tohru Yorifuji; Chikahiko Numakura; Seiji Mizuno; Akie Nakamura; Keiko Matsubara; Maki Fukami; Tsutomu Ogata
Journal:  Genet Med       Date:  2017-05-31       Impact factor: 8.822

7.  Paternal uniparental disomy 14 and related disorders: placental gene expression analyses and histological examinations.

Authors:  Masayo Kagami; Kentaro Matsuoka; Toshiro Nagai; Michiko Yamanaka; Kenji Kurosawa; Nobuhiro Suzumori; Yoichi Sekita; Mami Miyado; Keiko Matsubara; Tomoko Fuke; Fumiko Kato; Maki Fukami; Tsutomu Ogata
Journal:  Epigenetics       Date:  2012-08-23       Impact factor: 4.528

8.  Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome.

Authors:  Tomoko Fuke; Seiji Mizuno; Toshiro Nagai; Tomonobu Hasegawa; Reiko Horikawa; Yoko Miyoshi; Koji Muroya; Tatsuro Kondoh; Chikahiko Numakura; Seiji Sato; Kazuhiko Nakabayashi; Chiharu Tayama; Kenichiro Hata; Shinichiro Sano; Keiko Matsubara; Masayo Kagami; Kazuki Yamazawa; Tsutomu Ogata
Journal:  PLoS One       Date:  2013-03-22       Impact factor: 3.240
  8 in total

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