Hiroki Kurahashi

Hiroki Kurahashi

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Hiroki Kurahashi

Publications by authors named "Hiroki Kurahashi"

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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

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

Clinical and genetic aspects of mild hypophosphatasia in Japanese patients.

Mol Genet Metab Rep 2019 Dec 11;21:100515. Epub 2019 Oct 11.

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

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http://dx.doi.org/10.1016/j.ymgmr.2019.100515DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796780PMC
December 2019

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

Corrigendum to "Frequent intragenic microdeletions of elastin in familial supravalvular aortic stenosis." [Int. J. Cardiol., 274 (2019) 290-295].

Int J Cardiol 2019 Oct 27;292:283. Epub 2019 Jun 27.

Department of Pediatrics, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.ijcard.2019.06.020DOI Listing
October 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

Two siblings with 11qter deletion syndrome that had been rescued in their mother by uniparental disomy.

Eur J Med Genet 2019 Mar 18;62(3):224-228. Epub 2018 Jul 18.

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

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http://dx.doi.org/10.1016/j.ejmg.2018.07.018DOI Listing
March 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

A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant.

Brain Dev 2019 Mar 2;41(3):285-291. Epub 2018 Nov 2.

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

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http://dx.doi.org/10.1016/j.braindev.2018.10.008DOI Listing
March 2019

promoter-associated lncRNA is essential for myogenic differentiation.

EMBO Rep 2019 03 8;20(3). Epub 2019 Jan 8.

Division for Therapies against Intractable Diseases, Institute for Comprehensive Medical Science (ICMS), Fujita Health University, Toyoake, Japan

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http://embor.embopress.org/lookup/doi/10.15252/embr.20184746
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http://dx.doi.org/10.15252/embr.201847468DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399612PMC
March 2019

Clinical Consequences of Chromothripsis and Other Catastrophic Cellular Events.

Methods Mol Biol 2018 ;1769:21-33

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

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http://dx.doi.org/10.1007/978-1-4939-7780-2_2DOI Listing
February 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

Frequent intragenic microdeletions of elastin in familial supravalvular aortic stenosis.

Int J Cardiol 2019 Jan 13;274:290-295. Epub 2018 Sep 13.

Department of Pediatrics, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.ijcard.2018.09.032DOI Listing
January 2019

Exonic duplication of the OTC gene by a complex rearrangement that likely occurred via a replication-based mechanism: a case report.

BMC Med Genet 2018 12 12;19(1):210. Epub 2018 Dec 12.

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/s12881-018-0733-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292170PMC
December 2018

Compound heterozygous RYR1 mutations by whole exome sequencing in a family with three repeated affected fetuses with fetal akinesia.

Eur J Obstet Gynecol Reprod Biol 2018 11 12;230:200-202. Epub 2018 Sep 12.

Department of Obstetrics & Gynecology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

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http://dx.doi.org/10.1016/j.ejogrb.2018.09.013DOI Listing
November 2018

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

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

A constitutional jumping translocation involving the Y and acrocentric chromosomes.

Asian J Androl 2018 Aug 17. Epub 2018 Aug 17.

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

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http://dx.doi.org/10.4103/aja.aja_60_18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337947PMC
August 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

The DNA Damage Checkpoint Eliminates Mouse Oocytes with Chromosome Synapsis Failure.

Mol Cell 2017 Sep 24;67(6):1026-1036.e2. Epub 2017 Aug 24.

Cornell University, Departments of Biomedical Sciences and Molecular Biology and Genetics, Ithaca, NY 14850, USA. Electronic address:

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http://dx.doi.org/10.1016/j.molcel.2017.07.027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621520PMC
September 2017

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

Intragenic deletion detected by whole-genome sequencing in congenital myasthenic syndromes.

Neurol Genet 2017 Jun 3;3(3):e152. Epub 2017 May 3.

Institute of Genetic Medicine (Y.A., A.T., T.E., P.J.L., A.R., H.L.), Newcastle University, UK; Division of Neurology (P.J.L.), Federal University of Parana, Brazil; Leibniz-Institut für Analytische Wissenschaften ISAS e.V. (A.R.), Germany; Department of Neurosciences and Mental Health (P.V.), University of Lisbon, Portugal; and Division of Molecular Genetics (H.I., H.K.), Fujita Health University, Japan.

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http://dx.doi.org/10.1212/NXG.0000000000000152DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415388PMC
June 2017

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

Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations.

Cytogenet Genome Res 2016 19;150(2):86-92. Epub 2017 Jan 19.

Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.

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http://dx.doi.org/10.1159/000455026DOI Listing
February 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

A PDE3A mutation in familial hypertension and brachydactyly syndrome.

J Hum Genet 2016 Aug 7;61(8):701-3. Epub 2016 Apr 7.

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.2016.32DOI Listing
August 2016

Successful living donor liver transplantation for classical maple syrup urine disease.

Pediatr Transplant 2016 Aug 20;20(5):707-710. Epub 2016 Jun 20.

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

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http://dx.doi.org/10.1111/petr.12738DOI Listing
August 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

Annexin A5 haplotype M2 is not a risk factor for recurrent spontaneous abortion in Northern Europe: is there sufficient evidence?

Reprod Biomed Online 2016 May 27;32(5):469-73. Epub 2016 Feb 27.

Institute of Human Genetics, University of Muenster, Vesaliusweg 12-14, 48149 Muenster, Germany.

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http://dx.doi.org/10.1016/j.rbmo.2016.02.004DOI Listing
May 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

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

A unique TBX5 microdeletion with microinsertion detected in patient with Holt-Oram syndrome.

Am J Med Genet A 2015 Dec 28;167A(12):3192-6. Epub 2015 Sep 28.

Department of Human Genetics, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.

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http://dx.doi.org/10.1002/ajmg.a.37359DOI Listing
December 2015

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

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

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

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

Decreased expression of apelin in placentas from severe pre-eclampsia patients.

Hypertens Pregnancy 2013 Nov 11;32(4):410-21. Epub 2013 Jul 11.

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

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http://dx.doi.org/10.3109/10641955.2013.813535DOI Listing
November 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

MTA3 regulates CGB5 and Snail genes in trophoblast.

Biochem Biophys Res Commun 2013 Apr 17;433(4):379-84. Epub 2013 Mar 17.

Department of Obstetrics, Gynecology & Reproductive Biology, Michigan State University, Grand Rapids, MI 49503, USA.

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http://dx.doi.org/10.1016/j.bbrc.2013.02.102DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3761375PMC
April 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

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

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

A functional variation in the hypocretin neuropeptide precursor gene may be associated with obstructive sleep apnea syndrome in Japan.

Laryngoscope 2012 Apr 2;122(4):925-9. Epub 2012 Feb 2.

Department of Otolaryngology, Second Hospital, School of Medicine, Fujita Health University, Toyoake, Aichi, Japan.

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http://dx.doi.org/10.1002/lary.23179DOI Listing
April 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

Impact of indoleamine 2,3-dioxygenase on the antioxidant system in the placentas of severely pre-eclamptic patients.

Syst Biol Reprod Med 2011 Aug 1;57(4):174-8. Epub 2011 Jul 1.

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

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http://dx.doi.org/10.3109/19396368.2011.587590DOI Listing
August 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

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