Tamae Ohye

Tamae Ohye

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Tamae Ohye

Publications by authors named "Tamae Ohye"

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Inherited chromosomally integrated human herpesvirus-6 in a patient with XIAP deficiency.

Transpl Infect Dis 2020 May 18:e13331. Epub 2020 May 18.

Deprtment of Child Health and Development, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.

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http://dx.doi.org/10.1111/tid.13331DOI Listing
May 2020

Coinfection With Human Herpesvirus (HHV)-6B in Immunocompetent, Healthy Individuals With Chromosomally Integrated HHV-6A.

J Pediatric Infect Dis Soc 2020 Jan 23. Epub 2020 Jan 23.

Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.

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http://dx.doi.org/10.1093/jpids/piaa009DOI Listing
January 2020

Chromosomally integrated human herpesvirus 6 in the Japanese population.

J Med Virol 2018 10 10;90(10):1636-1642. Epub 2018 Jul 10.

Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.

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http://dx.doi.org/10.1002/jmv.25244DOI Listing
October 2018

Analysis of the origin of inherited chromosomally integrated human herpesvirus 6 in the Japanese population.

J Gen Virol 2017 Jul 12;98(7):1823-1830. Epub 2017 Jul 12.

Department of Pediatrics, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1099/jgv.0.000834DOI Listing
July 2017

Transmission of chromosomally integrated human herpesvirus 6 via cord blood transplantation.

Transpl Infect Dis 2017 Feb 25;19(1). Epub 2016 Dec 25.

Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.

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http://dx.doi.org/10.1111/tid.12636DOI Listing
February 2017

Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements.

Front Genet 2016 12;7:125. Epub 2016 Jul 12.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health UniversityToyoake, Japan; Genome and Transcriptome Analysis Center, Fujita Health UniversityToyoake, Japan.

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http://dx.doi.org/10.3389/fgene.2016.00125DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940405PMC
July 2016

Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome.

Hum Genome Var 2015 12;2:15003. Epub 2015 Feb 12.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Aichi, Japan; Genome and Transcriptome Analysis Center, Fujita Health University, Aichi, Japan.

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http://dx.doi.org/10.1038/hgv.2015.3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785586PMC
April 2016

A simple cytogenetic method to detect chromosomally integrated human herpesvirus-6.

J Virol Methods 2016 Feb 6;228:74-8. Epub 2015 Nov 6.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.jviromet.2015.11.001DOI Listing
February 2016

Age-related decrease of meiotic cohesins in human oocytes.

PLoS One 2014 7;9(5):e96710. Epub 2014 May 7.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0096710PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013030PMC
October 2015

Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney disease.

BMC Med Genet 2015 Oct 26;16:98. Epub 2015 Oct 26.

Department of Obstetrics and Gynecology, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.

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http://dx.doi.org/10.1186/s12881-015-0245-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623244PMC
October 2015

Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case.

Surg Today 2014 Nov 22;44(11):2195-200. Epub 2014 Jan 22.

Department of Endocrine Surgery, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan,

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http://dx.doi.org/10.1007/s00595-013-0826-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194010PMC
November 2014

A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis.

Endocr J 2014 22;61(1):19-23. Epub 2013 Oct 22.

Department of Endocrine Surgery, Fujita Health University School of Medicine, Toyoake 470-1192, Japan.

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http://dx.doi.org/10.1507/endocrj.ej13-0335DOI Listing
October 2014

Prevalence of Emanuel syndrome: theoretical frequency and surveillance result.

Pediatr Int 2014 Aug;56(4):462-6

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

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http://doi.wiley.com/10.1111/ped.12437
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http://dx.doi.org/10.1111/ped.12437DOI Listing
August 2014

Signature of backward replication slippage at the copy number variation junction.

J Hum Genet 2014 May 20;59(5):247-50. Epub 2014 Mar 20.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.

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http://dx.doi.org/10.1038/jhg.2014.20DOI Listing
May 2014

Dual roles for the telomeric repeats in chromosomally integrated human herpesvirus-6.

Sci Rep 2014 Apr 2;4:4559. Epub 2014 Apr 2.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1038/srep04559DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972506PMC
April 2014

Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient.

Pediatr Pulmonol 2014 Mar 18;49(3):E52-5. Epub 2013 Sep 18.

Department of Pediatrics, Fujita Health University, Toyoake, Aichi, Japan.

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http://dx.doi.org/10.1002/ppul.22814DOI Listing
March 2014

[Positive and negative aspects of genetic testing for familial cancer].

Nihon Geka Gakkai Zasshi 2014 Jan;115(1):34-8

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.

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January 2014

Identification of an enhancer region for immune activation in the human GTP cyclohydrolase I gene.

Biochem Biophys Res Commun 2013 Dec 9;442(1-2):72-8. Epub 2013 Nov 9.

Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama 226-8501, Japan.

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http://dx.doi.org/10.1016/j.bbrc.2013.11.002DOI Listing
December 2013

Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations.

Nat Commun 2013 ;4:1592

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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http://www.nature.com/articles/ncomms2595
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http://dx.doi.org/10.1038/ncomms2595DOI Listing
June 2013

HORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activity.

Genes Cells 2012 Nov 8;17(11):897-912. Epub 2012 Oct 8.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.

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http://dx.doi.org/10.1111/gtc.12005DOI Listing
November 2012

Failure of homologous synapsis and sex-specific reproduction problems.

Front Genet 2012 18;3:112. Epub 2012 Jun 18.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

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http://dx.doi.org/10.3389/fgene.2012.00112DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376420PMC
October 2012

Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytes.

J Hum Genet 2012 Aug 31;57(8):515-22. Epub 2012 May 31.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Aichi, Japan.

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http://www.nature.com/articles/jhg201261
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http://dx.doi.org/10.1038/jhg.2012.61DOI Listing
August 2012

HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes.

Genes Cells 2012 Jun 25;17(6):439-54. Epub 2012 Apr 25.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1111/j.1365-2443.2012.01600.xDOI Listing
June 2012

Molecular basis of maternal age-related increase in oocyte aneuploidy.

Congenit Anom (Kyoto) 2012 Mar;52(1):8-15

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University Department of Obstetrics and Gynecology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.

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http://dx.doi.org/10.1111/j.1741-4520.2011.00350.xDOI Listing
March 2012

Mechanism of complex gross chromosomal rearrangements: a commentary on concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation.

J Hum Genet 2012 Feb 15;57(2):81-3. Epub 2011 Dec 15.

The Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1038/jhg.2011.143DOI Listing
February 2012

DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation.

Mol Cytogenet 2011 Sep 8;4:18. Epub 2011 Sep 8.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1186/1755-8166-4-18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3197554PMC
September 2011

Characterization of a novel mouse gene encoding an SYCP3-like protein that relocalizes from the XY body to the nucleolus during prophase of male meiosis I.

Biol Reprod 2011 Jul 30;85(1):165-71. Epub 2011 Mar 30.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.

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http://dx.doi.org/10.1095/biolreprod.110.087270DOI Listing
July 2011

Paternal origin of the de novo constitutional t(11;22)(q23;q11).

Eur J Hum Genet 2010 Jul 24;18(7):783-7. Epub 2010 Feb 24.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

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http://dx.doi.org/10.1038/ejhg.2010.20DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987363PMC
July 2010

Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans.

J Hum Genet 2010 May 26;55(5):293-9. Epub 2010 Mar 26.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

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http://www.nature.com/articles/jhg201026
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http://dx.doi.org/10.1038/jhg.2010.26DOI Listing
May 2010

Recent advance in our understanding of the molecular nature of chromosomal abnormalities.

J Hum Genet 2009 May 17;54(5):253-60. Epub 2009 Apr 17.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

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http://dx.doi.org/10.1038/jhg.2009.35DOI Listing
May 2009

Two different forms of palindrome resolution in the human genome: deletion or translocation.

Hum Mol Genet 2008 Apr 9;17(8):1184-91. Epub 2008 Jan 9.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan

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http://dx.doi.org/10.1093/hmg/ddn008DOI Listing
April 2008

Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm.

Fertil Steril 2007 Nov 19;88(5):1446-8. Epub 2007 Apr 19.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.

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http://linkinghub.elsevier.com/retrieve/pii/S001502820700129
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http://dx.doi.org/10.1016/j.fertnstert.2007.01.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810970PMC
November 2007

Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.

Nucleic Acids Res 2007 30;35(4):1198-208. Epub 2007 Jan 30.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/
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http://dx.doi.org/10.1093/nar/gkm036DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1851657PMC
April 2007

Molecular cloning of a translocation breakpoint hotspot in 22q11.

Genome Res 2007 Apr 31;17(4):461-9. Epub 2007 Jan 31.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1101/gr.5769507DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1832093PMC
April 2007

Palindrome-mediated chromosomal translocations in humans.

DNA Repair (Amst) 2006 Sep 10;5(9-10):1136-45. Epub 2006 Jul 10.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1016/j.dnarep.2006.05.035DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824556PMC
September 2006

Chromosomal translocations mediated by palindromic DNA.

Cell Cycle 2006 Jun 15;5(12):1297-303. Epub 2006 Jun 15.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

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http://dx.doi.org/10.4161/cc.5.12.2809DOI Listing
June 2006

Genetic variation affects de novo translocation frequency.

Science 2006 Feb;311(5763):971

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake Aichi 470-1192, Japan [corrected]

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http://dx.doi.org/10.1126/science.1121452DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2818512PMC
February 2006

Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates.

Hum Mutat 2005 Oct;26(4):332-42

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake,Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1002/humu.20228DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2818517PMC
October 2005

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.

J Biol Chem 2004 Aug 20;279(34):35377-83. Epub 2004 Jun 20.

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1074/jbc.M400354200DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810964PMC
August 2004

Biopterin metabolism in patients with malignant syndrome.

Parkinsonism Relat Disord 2003 Apr;9 Suppl 1:S11-4

Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1016/s1353-8020(02)00120-7DOI Listing
April 2003

Localization of sepiapterin reductase in the human brain.

Brain Res 2002 Nov;954(2):237-46

Department of Anatomy, Fujita Health University School of Medicine, Toyoake, Aichi 470-1192, Japan.

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http://dx.doi.org/10.1016/s0006-8993(02)03341-3DOI Listing
November 2002