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ArticlesPeer ReviewedFull Text
Age-Related Decrease of Meiotic Cohesins in Human Oocytes
Author / Creator:Tsutsumi, Makiko ; Fujiwara, Reiko ; Nishizawa, Haruki ; Ito, Mayuko ; Kogo, Hiroshi ; Inagaki, Hidehito ; Ohye, Tamae ; Kato, Takema ; Fujii, Takuma ; Kurahashi, Hiroki
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-05, Vol.9 (5), p.e96710-e96710
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Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes
Author / Creator:Mariya, Tasuku ; Kato, Takema ; Sugimoto, Takeshi ; Miyai, Syunsuke ; Inagaki, Hidehito ; Ohye, Tamae ; Sugihara, Eiji ; Muramatsu, Yukako ; Mizuno, Seiji ; Kurahashi, Hiroki
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2022-06, Vol.67 (6), p.363-368
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A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia
Author / Creator:Kawamura, Rie ; Kato, Takema ; Miyai, Shunsuke ; Suzuki, Fumihiko ; Naru, Yuki ; Kato, Maki ; Tanaka, Keiko ; Nagasaka, Miwako ; Tsutsumi, Makiko ; Inagaki, Hidehito ; Ioroi, Tomoaki ; Yoshida, Makiko ; Nao, Tomoya ; Conlin, Laura K. ; Iijima, Kazumoto ; Kurahashi, Hiroki ; Taniguchi-Ikeda, Mariko
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2020-08, Vol.65 (8), p.705-709
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Incontinentia pigmenti inherited from a father with a low level atypical IKBKG deletion mosaicism: a case report
Author / Creator:Kawai, Miki ; Sugimoto, Atsuya ; Ishihara, Yasunori ; Kato, Takema ; Kurahashi, Hiroki
Publisher:London: BioMed Central Ltd
Journal title:BMC pediatrics, 2022-06, Vol.22 (1), p.1-378, Article 378
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Emergence and Characterization of Unusual DS-1-Like G1P[8] Rotavirus Strains in Children with Diarrhea in Thailand
Author / Creator:Komoto, Satoshi ; Tacharoenmuang, Ratana ; Guntapong, Ratigorn ; Ide, Tomihiko ; Haga, Kei ; Katayama, Kazuhiko ; Kato, Takema ; Ouchi, Yuya ; Kurahashi, Hiroki ; Tsuji, Takao ; Sangkitporn, Somchai ; Taniguchi, Koki
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-11, Vol.10 (11), p.e0141739-e0141739
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Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction
Author / Creator:Nishizawa, Haruki ; Ota, Sayuri ; Suzuki, Machiko ; Kato, Takema ; Sekiya, Takao ; Kurahashi, Hiroki ; Udagawa, Yasuhiro
Publisher:England: BioMed Central Ltd
Journal title:Reproductive biology and endocrinology, 2011-08, Vol.9 (1), p.107-107
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Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures
Author / Creator:Inagaki, Hidehito ; Ota, Sayuri ; Nishizawa, Haruki ; Miyamura, Hironori ; Nakahira, Kumiko ; Suzuki, Machiko ; Nishiyama, Sachie ; Kato, Takema ; Yanagihara, Itaru ; Kurahashi, Hiroki
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2019-05, Vol.64 (5), p.459-466
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Impact of DPYD, DPYS, and UPB1 gene variations on severe drug‐related toxicity in patients with cancer
Author / Creator:Yokoi, Katsuyuki ; Nakajima, Yoko ; Matsuoka, Hiroshi ; Shinkai, Yasuko ; Ishihara, Takuma ; Maeda, Yasuhiro ; Kato, Takema ; Katsuno, Hidetoshi ; Masumori, Koji ; Kawada, Kenji ; Yoshikawa, Tetsushi ; Ito, Tetsuya ; Kurahashi, Hiroki
Publisher:Tokyo: John Wiley & Sons, Inc
Journal title:Cancer science, 2020-09, Vol.111 (9), p.3359-3366
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An aggressive systemic mastocytosis preceded by ovarian dysgerminoma
Author / Creator:Tsutsumi, Makiko ; Miura, Hiroki ; Inagaki, Hidehito ; Shinkai, Yasuko ; Kato, Asuka ; Kato, Takema ; Hamada-Tsutsumi, Susumu ; Tanaka, Makito ; Kudo, Kazuko ; Yoshikawa, Tetsushi ; Kurahashi, Hiroki
Publisher:England: BioMed Central Ltd
Journal title:BMC cancer, 2020-11, Vol.20 (1), p.1162-1162, Article 1162
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Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex
Author / Creator:Muto, Yoshinari ; Sasaki, Hitomi ; Sumitomo, Makoto ; Inagaki, Hidehito ; Kato, Maki ; Kato, Takema ; Miyai, Shunsuke ; Kurahashi, Hiroki ; Shiroki, Ryoichi
Publisher:London: Nature Publishing Group UK
Journal title:Human genome variation, 2022-02, Vol.9 (1), p.5-5, Article 5
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Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations
Author / Creator:Inagaki, Hidehito ; Ohye, Tamae ; Kogo, Hiroshi ; Tsutsumi, Makiko ; Kato, Takema ; Tong, Maoqing ; Emanuel, Beverly S. ; Kurahashi, Hiroki
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2013-03, Vol.4 (1), p.1592, Article 1592
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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
Author / Creator:Tacharoenmuang, Ratana ; Komoto, Satoshi ; Guntapong, Ratigorn ; Ide, Tomihiko ; Haga, Kei ; Katayama, Kazuhiko ; Kato, Takema ; Ouchi, Yuya ; Kurahashi, Hiroki ; Tsuji, Takao ; Sangkitporn, Somchai ; Taniguchi, Koki
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-09, Vol.10 (9), p.e0139381-e0139381
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ArticlesPeer ReviewedFull Text
Usefulness of combined NGS and QF‐PCR analysis for product of conception karyotyping
Author / Creator:Kato, Takema ; Miyai, Shunsuke ; Suzuki, Hideki ; Murase, Yuuri ; Ota, Shiyo ; Yamauchi, Hiroko ; Ammae, Michiko ; Nakano, Tatsuya ; Nakaoka, Yoshiharu ; Inoue, Tomoko ; Morimoto, Yoshiharu ; Fukuda, Aisaku ; Utsunomiya, Takafumi ; Nishizawa, Haruki ; Kurahashi, Hiroki
Publisher:Japan: John Wiley & Sons, Inc
Journal title:Reproductive medicine and biology, 2022-01, Vol.21 (1), p.e12449-n/a
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ArticlesPeer ReviewedFull Text
Molecular analysis of low‐level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti
Author / Creator:Kawai, Miki ; Kato, Takema ; Tsutsumi, Makiko ; Shinkai, Yasuko ; Inagaki, Hidehito ; Kurahashi, Hiroki
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2020-12, Vol.8 (12), p.e1531-n/a
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Potential role for nectin-4 in the pathogenesis of pre-eclampsia: a molecular genetic study
Author / Creator:Ito, Mayuko ; Nishizawa, Haruki ; Tsutsumi, Makiko ; Kato, Asuka ; Sakabe, Yoshiko ; Noda, Yoshiteru ; Ohwaki, Akiko ; Miyazaki, Jun ; Kato, Takema ; Shiogama, Kazuya ; Sekiya, Takao ; Kurahashi, Hiroki ; Fujii, Takuma
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2018-09, Vol.19 (1), p.166-166, Article 166
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A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report
Author / Creator:Tsutsumi, Makiko ; Hattori, Hiroyoshi ; Akita, Nobuhiro ; Maeda, Naoko ; Kubota, Toshinobu ; Horibe, Keizo ; Fujita, Naoko ; Kawai, Miki ; Shinkai, Yasuko ; Kato, Maki ; Kato, Takema ; Kawamura, Rie ; Suzuki, Fumihiko ; Kurahashi, Hiroki
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2019-12, Vol.12 (1), p.182-182, Article 182
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Recent advance in our understanding of the molecular nature of chromosomal abnormalities
Author / Creator:Kurahashi, Hiroki ; Bolor, Hasbaira ; Kato, Takema ; Kogo, Hiroshi ; Tsutsumi, Makiko ; Inagaki, Hidehito ; Ohye, Tamae
Publisher:London: Nature Publishing Group UK
Journal title:Journal of human genetics, 2009-05, Vol.54 (5), p.253-260
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PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene
Author / Creator:Kato, Maki ; Kato, Takema ; Hosoba, Eriko ; Ohashi, Masanao ; Fujisaki, Midori ; Ozaki, Mamoru ; Yamaguchi, Masatoshi ; Sameshima, Hiroshi ; Kurahashi, Hiroki
Publisher:London: Nature Publishing Group UK
Journal title:Human genome variation, 2017-06, Vol.4 (1), p.17021-17021, Article 17021
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Placental Genetic Variants in the Upstream Region of the FLT1 Gene in Pre-eclampsia
Author / Creator:Ohwaki, Akiko ; Nishizawa, Haruki ; Kato, Asuka ; Kato, Takema ; Miyazaki, Jun ; Yoshizawa, Hikari ; Noda, Yoshiteru ; Sakabe, Yoshiko ; Ichikawa, Ryoko ; Sekiya, Takao ; Fujii, Takuma ; Kurahashi, Hiroki
Publisher:Tehran: Office for Scientific Journals
Journal title:Journal of reproduction & infertility, 2020-10, Vol.21 (4), p.240-246
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Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease
Author / Creator:Miyazaki, Jun ; Ito, Mayuko ; Nishizawa, Haruki ; Kato, Takema ; Minami, Yukito ; Inagaki, Hidehito ; Ohye, Tamae ; Miyata, Masafumi ; Boda, Hiroko ; Kiriyama, Yuka ; Kuroda, Makoto ; Sekiya, Takao ; Kurahashi, Hiroki ; Fujii, Takuma
Publisher:London: BioMed Central
Journal title:BMC medical genetics, 2015-10, Vol.16 (1), Article 98
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Showing 1 to 20 of 39 results

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Age-Related Decrease of Meiotic Cohesins in Human Oocytes

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Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes

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

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Incontinentia pigmenti inherited from a father with a low level atypical IKBKG deletion mosaicism: a case report

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

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

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

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

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An aggressive systemic mastocytosis preceded by ovarian dysgerminoma

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Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex

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

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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

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Usefulness of combined NGS and QF‐PCR analysis for product of conception karyotyping

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

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

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

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

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

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

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Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

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