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Takema Kato

Showing results (21-30 of 75) with videos related to

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Molecular Human Reproduction|September 23, 2008
Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patientsHaruki Nishizawa, Kanako Pryor-Koishi, Machiko Suzuki, et al.
Gynecologic and Obstetric Investigation|September 25, 2009
Analysis of nitric oxide metabolism as a placental or maternal factor underlying the etiology of pre-eclampsiaHaruki Nishizawa, Kanako Pryor-Koishi, Machiko Suzuki, et al.
Nature Communications|March 14, 2013
Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocationsHidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|June 15, 2007
The etiological role of allogeneic fetal rejection in pre-eclampsiaHaruki Nishizawa, Kiyoshi Hasegawa, Machiko Suzuki, et al.
Cytogenetic and Genome Research|October 27, 2017
Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying ChromothripsisTakema Kato, Yuya Ouchi, Hidehito Inagaki, et al.
Human Genome Variation|February 11, 2022
Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complexYoshinari Muto, Hitomi Sasaki, Makoto Sumitomo, et al.
Human Genome Variation|June 15, 2017
PCS/MVA syndrome caused by an <i>Alu</i> insertion in the <i>BUB1B</i> geneMaki Kato, Takema Kato, Eriko Hosoba, et al.
The Tohoku Journal of Experimental Medicine|September 7, 2022
An Infant Case of Streptococcus Pneumoniae-Associated Thrombotic Microangiopathy with Heterozygous CFI Mutation and CFHR3-CFHR1 DeletionYuji Matsumoto, Yohei Ikezumi, Tomomi Kondoh, et al.
Brain Tumor Pathology|July 27, 2025
Integrated analysis of MYC expression, 8q24.21 copy number, and recurrence patterns in astrocytoma, IDH-mutantMasanobu Kumon, Shunsuke Nakae, Shigeo Ohba, et al.
Molecular Cytogenetics|September 9, 2011
DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocationTakema Kato, Hidehito Inagaki, Maoqing Tong, et al.
Pageof 8

Showing results (21-30 of 75) with videos related to

Sort By:
Pageof 8
Molecular Human Reproduction|September 23, 2008
Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patientsHaruki Nishizawa, Kanako Pryor-Koishi, Machiko Suzuki, et al.
Gynecologic and Obstetric Investigation|September 25, 2009
Analysis of nitric oxide metabolism as a placental or maternal factor underlying the etiology of pre-eclampsiaHaruki Nishizawa, Kanako Pryor-Koishi, Machiko Suzuki, et al.
Nature Communications|March 14, 2013
Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocationsHidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|June 15, 2007
The etiological role of allogeneic fetal rejection in pre-eclampsiaHaruki Nishizawa, Kiyoshi Hasegawa, Machiko Suzuki, et al.
Cytogenetic and Genome Research|October 27, 2017
Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying ChromothripsisTakema Kato, Yuya Ouchi, Hidehito Inagaki, et al.
Human Genome Variation|February 11, 2022
Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complexYoshinari Muto, Hitomi Sasaki, Makoto Sumitomo, et al.
Human Genome Variation|June 15, 2017
PCS/MVA syndrome caused by an <i>Alu</i> insertion in the <i>BUB1B</i> geneMaki Kato, Takema Kato, Eriko Hosoba, et al.
The Tohoku Journal of Experimental Medicine|September 7, 2022
An Infant Case of Streptococcus Pneumoniae-Associated Thrombotic Microangiopathy with Heterozygous CFI Mutation and CFHR3-CFHR1 DeletionYuji Matsumoto, Yohei Ikezumi, Tomomi Kondoh, et al.
Brain Tumor Pathology|July 27, 2025
Integrated analysis of MYC expression, 8q24.21 copy number, and recurrence patterns in astrocytoma, IDH-mutantMasanobu Kumon, Shunsuke Nakae, Shigeo Ohba, et al.
Molecular Cytogenetics|September 9, 2011
DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocationTakema Kato, Hidehito Inagaki, Maoqing Tong, et al.
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