Takema Kato

Takema Kato

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Takema Kato

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

Cancer Sci 2020 Jul 3. Epub 2020 Jul 3.

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

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http://dx.doi.org/10.1111/cas.14553DOI Listing
July 2020

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

J Dermatol 2020 Jun 18;47(6):669-672. Epub 2020 Mar 18.

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

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http://dx.doi.org/10.1111/1346-8138.15313DOI Listing
June 2020

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

Hum Genet 2020 Jun 2. Epub 2020 Jun 2.

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/10.1007/s00439-020-02186-8DOI Listing
June 2020

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

BMC Med Genomics 2019 12 5;12(1):182. Epub 2019 Dec 5.

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/10.1186/s12920-019-0640-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896736PMC
December 2019

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

Eur J Med Genet 2019 Nov 8;62(11):103570. Epub 2018 Nov 8.

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

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https://linkinghub.elsevier.com/retrieve/pii/S17697212183040
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http://dx.doi.org/10.1016/j.ejmg.2018.11.004DOI Listing
November 2019

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

Case Rep Obstet Gynecol 2019 2;2019:6753184. Epub 2019 Oct 2.

Department of Maternal and Fetal Medicine, Miyagi Children's Hospital, Miyagi, Japan.

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http://dx.doi.org/10.1155/2019/6753184DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791227PMC
October 2019

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

Congenit Anom (Kyoto) 2019 May 6;59(3):88-92. Epub 2018 Jul 6.

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

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http://dx.doi.org/10.1111/cga.12302DOI Listing
May 2019

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

J Hum Genet 2019 May 22;64(5):459-466. Epub 2019 Feb 22.

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

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http://dx.doi.org/10.1038/s10038-019-0578-4DOI Listing
May 2019

A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysis.

Brain Dev 2019 Mar 29;41(3):280-284. Epub 2018 Oct 29.

Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan; Department of Child Neurology, Okayama University Hospital, Okayama, Japan.

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https://linkinghub.elsevier.com/retrieve/pii/S03877604183038
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http://dx.doi.org/10.1016/j.braindev.2018.10.005DOI Listing
March 2019

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

Congenit Anom (Kyoto) 2019 Jan 15;59(1):4-10. Epub 2018 Apr 15.

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

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http://doi.wiley.com/10.1111/cga.12278
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http://dx.doi.org/10.1111/cga.12278DOI Listing
January 2019

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

BMC Med Genet 2018 09 14;19(1):166. Epub 2018 Sep 14.

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

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https://bmcmedgenet.biomedcentral.com/articles/10.1186/s1288
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http://dx.doi.org/10.1186/s12881-018-0681-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137934PMC
September 2018

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

J Obstet Gynaecol Res 2018 Jul 19;44(7):1313-1317. Epub 2018 Apr 19.

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

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http://dx.doi.org/10.1111/jog.13647DOI Listing
July 2018

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

Am J Med Genet A 2018 05;176(5):1245-1248

Genetic Counseling Room, Kagoshima University Hospital, Kagoshima, Japan.

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http://dx.doi.org/10.1002/ajmg.a.38681DOI Listing
May 2018

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

Cytogenet Genome Res 2017 27;153(1):1-9. Epub 2017 Oct 27.

Division of Molecular Genetics, Institute for Comprehensive Medical Science (ICMS), and Genome and Transcriptome Analysis Center, Fujita Health University, Toyoake, Department of Pediatrics, Central Hospital, Aichi Human Service Center, Kasugai, Department of Pediatrics, Toyota Kosei Hospital, Toyota, Department of Obstetrics and Gynecology, Faculty of Medicine, Kagoshima University, and Takeuchi Ladies Clinic/Infertility Center, Kagoshima, and Education Center, Asahikawa Medical University, Hokkaido, Japan.

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http://dx.doi.org/10.1159/000481586DOI Listing
January 2018

PCS/MVA syndrome caused by an insertion in the gene.

Hum Genome Var 2017 8;4:17021. Epub 2017 Jun 8.

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

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http://dx.doi.org/10.1038/hgv.2017.21DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462940PMC
June 2017

A Japanese case of β-ureidopropionase deficiency with dysmorphic features.

Brain Dev 2017 Jan 21;39(1):58-61. Epub 2016 Aug 21.

Department of Child Neurology, Okayama University Hospital, Okayama, Okayama, Japan; Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Okayama, Japan.

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http://dx.doi.org/10.1016/j.braindev.2016.08.001DOI Listing
January 2017

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

Placenta 2016 12 5;48:20-25. Epub 2016 Oct 5.

Department of Obstetrics and Gynecology, Fujita Health University School of Medicine, Toyoake, Japan.

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http://dx.doi.org/10.1016/j.placenta.2016.10.002DOI Listing
December 2016

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

Preimplantation genetic diagnosis/screening by comprehensive molecular testing.

Reprod Med Biol 2016 01 14;15(1):13-19. Epub 2015 Jul 14.

Department of Obstetrics and Gynecology Fujita Health University School of Medicine 470-1192 Toyoake Aichi Japan.

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http://dx.doi.org/10.1007/s12522-015-0216-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715840PMC
January 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

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

Mol Cytogenet 2014 13;7:55. Epub 2014 Aug 13.

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

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http://dx.doi.org/10.1186/s13039-014-0055-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255720PMC
December 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

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

Cancer Genet 2014 Apr 18;207(4):133-40. Epub 2014 Mar 18.

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Pediatrics, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA. Electronic address:

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http://www.medicinno.com/wp-content/uploads/2014/06/Analysis
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http://linkinghub.elsevier.com/retrieve/pii/S221077621400059
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http://dx.doi.org/10.1016/j.cancergen.2014.03.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102306PMC
April 2014

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

Chromosomal translocations and palindromic AT-rich repeats.

Curr Opin Genet Dev 2012 Jun 6;22(3):221-8. Epub 2012 Mar 6.

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.1016/j.gde.2012.02.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378763PMC
June 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

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

Reprod Biol Endocrinol 2011 Aug 2;9:107. Epub 2011 Aug 2.

Department of Obstetrics and Gynecology, Fujita Health University School of Medicine, Fujita Health University, Toyoake, Japan.

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http://dx.doi.org/10.1186/1477-7827-9-107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199758PMC
August 2011

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

Mol Hum Reprod 2011 Jul 2;17(7):447-52. Epub 2011 Feb 2.

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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https://academic.oup.com/molehr/article-lookup/doi/10.1093/m
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http://dx.doi.org/10.1093/molehr/gar008DOI 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

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

Am J Reprod Immunol 2010 Jul 28;64(1):68-76. Epub 2010 Feb 28.

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.1600-0897.2010.00820.xDOI Listing
July 2010

CD9 gene variations are not associated with female infertility in humans.

Gynecol Obstet Invest 2010 2;69(2):116-21. Epub 2009 Dec 2.

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

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http://dx.doi.org/10.1159/000262451DOI Listing
June 2010

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

Gynecol Obstet Invest 2009 17;68(4):239-47. Epub 2009 Sep 17.

Department of Obstetrics and Gynecology, Fujita Health University, Toyoake, Japan.

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http://dx.doi.org/10.1159/000238381DOI Listing
February 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

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

Mol Hum Reprod 2008 Oct 18;14(10):595-602. Epub 2008 Sep 18.

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

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http://dx.doi.org/10.1093/molehr/gan054DOI Listing
October 2008

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

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

J Obstet Gynaecol Res 2008 Feb;34(1):1-6

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.1447-0756.2007.00679.xDOI Listing
February 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

The etiological role of allogeneic fetal rejection in pre-eclampsia.

Am J Reprod Immunol 2007 Jul;58(1):11-20

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.1600-0897.2007.00484.xDOI Listing
July 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