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List of works by Takema Kato

A Japanese case of β-ureidopropionase deficiency with dysmorphic features

scientific article published on 20 August 2016

A Palindrome-Mediated Recurrent Translocation with 3:1 Meiotic Nondisjunction: The t(8;22)(q24.13;q11.21) ⬇️

scientific article published on July 30, 2010

A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia

scientific article published on 10 April 2020

A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysis

scientific article published on 29 October 2018

A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report

scientific article published on 05 December 2019

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 aggressive systemic mastocytosis preceded by ovarian dysgerminoma

scientific article published on 27 November 2020

Analysis of nitric oxide metabolism as a placental or maternal factor underlying the etiology of pre-eclampsia

scientific article published on 17 September 2009

Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases

scientific article published on 04 April 2020

Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation

scientific article

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation

scientific article

CD9 gene variations are not associated with female infertility in humans

scientific article published on 2 December 2009

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 and palindromic AT-rich repeats ⬇️

scientific article published on March 6, 2012

Chromosomal translocations mediated by palindromic DNA.

scientific article

Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction ⬇️

scientific article published on August 2, 2011

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

scientific article published on 30 January 2007

DNA methylation accumulation in gastric mucosa adjacent to cancer after Helicobacter pylori eradication

scientific article published on 12 November 2018

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

scientific article

Emergence and Characterization of Unusual DS-1-Like G1P[8] Rotavirus Strains in Children with Diarrhea in Thailand

scientific article published on 5 November 2015

Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome

scientific article published on 02 October 2019

FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency

article

Genetic variation affects de novo translocation frequency.

scientific article published on February 2006

Genetic variation in the indoleamine 2,3-dioxygenase gene in pre-eclampsia

scientific article published on 28 February 2010

Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying Chromothripsis

scientific article

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

scientific article published on 12 February 2015

Impact of DPYD, DPYS and UPB1 gene variations on severe drug-related toxicity in cancer patients

scientific article published on 03 July 2020

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

scientific article published on 11 June 2009

Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patients.

scientific article

Increased levels of soluble corin in pre-eclampsia and fetal growth restriction

scientific article published on 5 October 2016

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

scientific article published on 26 October 2015

Lethal persistent pulmonary hypertension of the newborn in Bohring-Opitz syndrome

scientific article published on 01 May 2018

Molecular analysis of low-level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti

scientific article published on 21 October 2020

Molecular cloning of a translocation breakpoint hotspot in 22q11.

scientific article published on 31 January 2007

Mouse model for allogeneic immune reaction against fetus recapitulates human pre-eclampsia

scientific article published in February 2008

Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders.

scientific article published on 14 March 2018

Mutations of the SYCP3 gene in women with recurrent pregnancy loss

scientific article published on 24 December 2008

Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation

scientific article published on 18 March 2020

Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures

scientific article published on 22 February 2019

PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene

scientific article

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

scientific article

Palindrome-mediated chromosomal translocations in humans

scientific article

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

scientific article

Placental Genetic Variants in the Upstream Region of the FLT1 Gene in Pre-eclampsia

scientific article published on 01 October 2020

Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss ⬇️

scientific article published on February 2, 2011

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

scientific article

Potential role for nectin-4 in the pathogenesis of pre-eclampsia: a molecular genetic study

scientific article published on 14 September 2018

Potentially effective method for fetal gender determination by noninvasive prenatal testing for X-linked disease

scientific article published on 06 July 2018

Preimplantation genetic diagnosis/screening by comprehensive molecular testing

scientific article published on 14 July 2015

Preimplantation genetic testing for aneuploidy: a comparison of live birth rates in patients with recurrent pregnancy loss due to embryonic aneuploidy or recurrent implantation failure

scientific article published on 01 December 2019

Preimplantation genetic testing for aneuploidy: a comparison of live birth rates in patients with recurrent pregnancy loss due to embryonic aneuploidy or recurrent implantation failure

scientific article published on 01 January 2020

Prenatal diagnosis of premature chromatid separation/mosaic variegated aneuploidy (PCS/MVA) syndrome

scientific article published on 19 April 2018

Prevalence of Emanuel syndrome: theoretical frequency and surveillance result

scientific article published on 01 August 2014

Prostate Stem Cell Antigen Gene Polymorphism Is Associated with H. pylori-related Promoter DNA Methylation in Nonneoplastic Gastric Epithelium

scientific article published on 18 June 2019

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

scientific article published on 17 April 2009

Remote intracranial recurrence of IDH mutant gliomas is associated with TP53 mutations and an 8q gain

scientific article published on 15 September 2017

The etiological role of allogeneic fetal rejection in pre-eclampsia

scientific article published in July 2007

The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications

scientific article published on 02 June 2020

Twin pregnancy with chromosomal abnormalities mimicking a gestational trophoblastic disorder and coexistent foetus on ultrasound

scientific article published on 09 March 2018

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

Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach

scientific article published on 22 May 2020

Whole Genomic Analysis of an Unusual Human G6P[14] Rotavirus Strain Isolated from a Child with Diarrhea in Thailand: Evidence for Bovine-To-Human Interspecies Transmission and Reassortment Events

scientific article published on 30 September 2015

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