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Epigenetics Volume 7, 2012 - Issue 10
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Research Paper

Paternal uniparental disomy 14 and related disorders

Placental gene expression analyses and histological examinations

Masayo Kagami Department of Molecular Endocrinology; National Research Institute for Child Health and Development; Tokyo, Japan
,
Kentaro Matsuoka Departments of Pathology; National Center for Child Health and Development; Tokyo, Japan
,
Toshiro Nagai Department of Pediatrics; Dokkyo University School of Medicine; Koshigaya, Japan
,
Michiko Yamanaka Department of Integrated Women's Health; St. Luke's International Hospital; Tokyo, Japan
,
Kenji Kurosawa Division of Medical Genetics; Kanagawa Children’s Medical Center; Yokohama, Japan
,
Nobuhiro Suzumori Department of Obstetrics and Gynecology; Nagoya City University Graduate School of Medicine; Nagoya, Japan
,
Yoichi Sekita Department of Pathology; Graduate School of Medicine; Osaka University, Osaka, Japan
,
Mami Miyado Department of Molecular Endocrinology; National Research Institute for Child Health and Development; Tokyo, Japan
,
Keiko Matsubara Department of Molecular Endocrinology; National Research Institute for Child Health and Development; Tokyo, Japan
,
Tomoko Fuke Department of Molecular Endocrinology; National Research Institute for Child Health and Development; Tokyo, Japan
,
Fumiko Kato Department of Molecular Endocrinology; National Research Institute for Child Health and Development; Tokyo, Japan; Department of Pediatrics; Hamamatsu University School of Medicine; Hamamatsu, Japan
,
Maki Fukami Department of Molecular Endocrinology; National Research Institute for Child Health and Development; Tokyo, Japan
&
Tsutomu Ogata Department of Molecular Endocrinology; National Research Institute for Child Health and Development; Tokyo, Japan; Department of Pediatrics; Hamamatsu University School of Medicine; Hamamatsu, JapanCorrespondence[email protected]
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Pages 1142-1150 | Published online: 23 Aug 2012

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Line Hjort, Boris Novakovic, Silvija Cvitic, Richard Saffery, Peter Damm & Gernot Desoye. (2022) Placental DNA methylation in pregnancies complicated by maternal diabetes and/or obesity: State of the art and research gaps. Epigenetics 17:13, pages 2188-2208.
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Arturo Hernandez, M Elena Martinez, Lily Ng & Douglas Forrest. (2021) Thyroid Hormone Deiodinases: Dynamic Switches in Developmental Transitions. Endocrinology 162:8.
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Jessica Omark, Yohei Masunaga, Mark Hannibal, Brandon Shaw, Maki Fukami, Fumiko Kato, Hirotomo Saitsu, Masayo Kagami & Tsutomu Ogata. (2020) Kagami–Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG3. Journal of Human Genetics 66:4, pages 439-443.
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Hou-Sung Jung, Stephanie E. Vallee, Mary Beth Dinulos, Gregory J. Tsongalis & Joel A. Lefferts. (2018) Maternally inherited 133kb deletion of 14q32 causing Kagami–Ogata syndrome. Journal of Human Genetics 63:12, pages 1231-1239.
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Arturo Hernandez & J. Stohn. (2018) The Type 3 Deiodinase: Epigenetic Control of Brain Thyroid Hormone Action and Neurological Function. International Journal of Molecular Sciences 19:6, pages 1804.
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Xie Yingjun, Hu Zhiyang, Lin Linhua, Su Fangming, Huang Linhuan, Tan Jinfeng, Pang Qianying & Sun Xiaofang. (2017) Chromosomal uniparental disomy 16 and fetal intrauterine growth restriction. European Journal of Obstetrics & Gynecology and Reproductive Biology 211, pages 1-7.
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Maria Elena Martinez, David F Cox, Brian P Youth & Arturo Hernandez. (2016) Genomic imprinting of DIO3, a candidate gene for the syndrome associated with human uniparental disomy of chromosome 14. European Journal of Human Genetics 24:11, pages 1617-1621.
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Natalia Pervjakova, Silva Kasela, Andrew P Morris, Mart Kals, Andres Metspalu, Cecilia M Lindgren, Andres Salumets & Reedik Mägi. (2016) Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues. Epigenomics 8:6, pages 789-799.
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Makiko Tachibana, Masahiro Nakayama & Yoko Miyoshi. (2016) Placental examination. Current Opinion in Obstetrics & Gynecology 28:2, pages 95-100.
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Tsutomu Ogata & Masayo Kagami. (2015) Kagami–Ogata syndrome: a clinically recognizable upd(14)pat and related disorder affecting the chromosome 14q32.2 imprinted region. Journal of Human Genetics 61:2, pages 87-94.
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Haiming Yuan, Yingjun Xie, Qian Li, Xizi Hu, Xinwei Li, Xiaofang Sun & Weiwei Zhao. (2016) Paternal Uniparental Disomy of Chromosome 14 with Hypospadias. Cytogenetic and Genome Research 148:4, pages 256-261.
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Yang Yu, Qian Gao, Hong-cui Zhao, Rong Li, Jiang-man Gao, Ting Ding, Si-yu Bao, Yue Zhao, Xiao-fang Sun, Yong Fan & Jie Qiao. (2015) Ascorbic acid improves pluripotency of human parthenogenetic embryonic stem cells through modifying imprinted gene expression in the Dlk1-Dio3 region. Stem Cell Research & Therapy 6:1.
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Yuping Wang. 2015. Human Placental Trophoblasts. Human Placental Trophoblasts 391 410 .
Masayo Kagami, Kenji Kurosawa, Osamu Miyazaki, Fumitoshi Ishino, Kentaro Matsuoka & Tsutomu Ogata. (2015) Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami–Ogata syndrome). European Journal of Human Genetics 23:11, pages 1488-1498.
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Diana Darcy, Paldeep Singh Atwal, Cathy Angell, Inder Gadi & Robert Wallerstein. (2015) Mosaic paternal genome-wide uniparental isodisomy with down syndrome. American Journal of Medical Genetics Part A 167:10, pages 2463-2469.
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Mark Howard & Marika Charalambous. (2015) Molecular basis of imprinting disorders affecting chromosome 14: lessons from murine models. REPRODUCTION 149:5, pages R237-R249.
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Jill A. Rosenfeld, Joyce E. Fox, Maria Descartes, Fallon Brewer, Tracy Stroud, Jerome L. Gorski, Sheila J. Upton, John B. Moeschler, Berrin Monteleone, Nicholas J. Neill, Allen N. Lamb, Blake C. Ballif, Lisa G. Shaffer & J. Britt Ravnan. (2015) Clinical features associated with copy number variations of the 14q32 imprinted gene cluster. American Journal of Medical Genetics Part A 167:2, pages 345-353.
Crossref
K M Sargar, T E Herman & M J Siegel. (2014) Paternal uniparental disomy of chromosome 14. Journal of Perinatology 34:9, pages 723-725.
Crossref
Jo Peters. (2014) The role of genomic imprinting in biology and disease: an expanding view. Nature Reviews Genetics 15:8, pages 517-530.
Crossref
Naveed Hussain. 2014. Molecular mechanisms and physiology of disease. Molecular mechanisms and physiology of disease 1 62 .
Rebecca C. Rancourt, Holly R. Harris, Ludovic Barault & Karin B. Michels. (2013) The prevalence of loss of imprinting of H19 and IGF2 at birth . The FASEB Journal 27:8, pages 3335-3343.
Crossref
B. Meister, M. Perez‐Manso & T. Daraio. (2013) Delta‐like 1 Homologue is a Hypothalamus‐Enriched Protein that is Present in Orexin‐Containing Neurones of the Lateral Hypothalamic Area. Journal of Neuroendocrinology 25:7, pages 617-625.
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