List of works - Tamae Ohye

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

scientific article published on 22 October 2013

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

scientific article published on 5 November 2015

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

scientific article published on 18 September 2013

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

scientific article

Age-related decrease of meiotic cohesins in human oocytes

scientific article

An immunocompetent child with chromosomally integrated human herpesvirus 6B accidentally identified during the care of Mycoplasma pneumoniae infection

scientific article published on 11 December 2013

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

scientific article

Biopterin metabolism in patients with malignant syndrome

scientific article published in April 2003

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

scientific journal article

Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.

scientific article published on 7 November 2008

Chromosomal translocations mediated by palindromic DNA.

scientific article

Chromosomally integrated human herpesvirus 6 in the Japanese population

scientific article published on 10 July 2018

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

scientific article published on 23 January 2020

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

scientific article

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

scientific article published on 30 January 2007

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

scientific article

Definition and refinement of the 7q36.3 duplication region associated with schizophrenia.

scientific article published on January 2013

Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion.

scientific article

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

scientific article published on 02 April 2014

Failure of homologous synapsis and sex-specific reproduction problems ⬇️

scientific article published on June 18, 2012

Genetic variation affects de novo translocation frequency.

scientific article published on February 2006

HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes

scientific journal article

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

scientific journal article

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

scientific article published on 9 November 2013

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

scientific article published on 12 February 2015

Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.

scientific article published on 11 June 2009

Inherited chromosomally integrated human herpesvirus 6 is a risk factor for spontaneous abortion

scientific article published on 28 September 2020

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

scientific article published on 18 May 2020

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

scientific article published on 26 October 2015

Localization of sepiapterin reductase in the human brain

scientific article published in November 2002

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

scientific article published on 15 December 2011

Molecular and virological evidence of viral activation from chromosomally integrated human herpesvirus 6A in a patient with X-linked severe combined immunodeficiency

scientific article published on 6 May 2014

Molecular basis of maternal age‐related increase in oocyte aneuploidy ⬇️

scientific article published on March 1, 2012

Molecular cloning of a translocation breakpoint hotspot in 22q11.

scientific article published on 31 January 2007

Mutations of the SYCP3 gene in women with recurrent pregnancy loss

scientific article published on 24 December 2008

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

scientific article

Palindrome-mediated chromosomal translocations in humans

scientific article

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

scientific article published on October 2005

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

scientific article

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

scientific article

Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.

scientific article

Prevalence of Emanuel syndrome: theoretical frequency and surveillance result

scientific article published on 01 August 2014

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

scientific article published on 17 April 2009

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

scientific article

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

scientific journal article

Signature of backward replication slippage at the copy number variation junction

scientific article published on 20 March 2014

Transmission of chromosomally integrated human herpesvirus 6 via cord blood transplantation

scientific article published on 16 November 2016

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

scientific article published on 9 January 2008

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

scientific article

List of works by Tamae Ohye

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

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

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

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

Age-related decrease of meiotic cohesins in human oocytes

An immunocompetent child with chromosomally integrated human herpesvirus 6B accidentally identified during the care of Mycoplasma pneumoniae infection

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

Biopterin metabolism in patients with malignant syndrome

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

Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.

Chromosomal translocations mediated by palindromic DNA.

Chromosomally integrated human herpesvirus 6 in the Japanese population

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

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

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

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

Definition and refinement of the 7q36.3 duplication region associated with schizophrenia.

Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion.

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

Failure of homologous synapsis and sex-specific reproduction problems ⬇️

Genetic variation affects de novo translocation frequency.

HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes

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

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

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

Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.

Inherited chromosomally integrated human herpesvirus 6 is a risk factor for spontaneous abortion

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

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

Localization of sepiapterin reductase in the human brain

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

Molecular and virological evidence of viral activation from chromosomally integrated human herpesvirus 6A in a patient with X-linked severe combined immunodeficiency

Molecular basis of maternal age‐related increase in oocyte aneuploidy ⬇️

Molecular cloning of a translocation breakpoint hotspot in 22q11.

Mutations of the SYCP3 gene in women with recurrent pregnancy loss

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

Palindrome-mediated chromosomal translocations in humans

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

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

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

Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.

Prevalence of Emanuel syndrome: theoretical frequency and surveillance result

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

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

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

Signature of backward replication slippage at the copy number variation junction

Transmission of chromosomally integrated human herpesvirus 6 via cord blood transplantation

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

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

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