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Hidehito Inagaki

Showing results (51-60 of 98) with videos related to

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Journal of Human Genetics|January 14, 2022
Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomesTasuku Mariya, Takema Kato, Takeshi Sugimoto, et al.
Genome Research|November 11, 2008
Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humansHidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
American Journal of Human Genetics|August 16, 2006
Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)Terry Ashley, Ann P Gaeth, Hidehito Inagaki, et al.
JSES International|July 10, 2023
A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndromeYusuke Kawano, Atsuhito Seki, Takashi Kuroiwa, et al.
Journal of Human Genetics|February 26, 2025
Translocation-specific polymerase chain reaction in preimplantation genetic testing for recurrent translocation carrierGen Furukawa, Rie Kawamura, Hidehito Inagaki, et al.
Genes|August 29, 2024
Comparative Analysis of Two NGS-Based Platforms for Product-of-Conception KaryotypingYuri Murase, Yui Shichiri, Hidehito Inagaki, et al.
Journal of Human Genetics|February 24, 2019
Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structuresHidehito Inagaki, Sayuri Ota, Haruki Nishizawa, et al.
Plos One|May 9, 2014
Age-related decrease of meiotic cohesins in human oocytesMakiko Tsutsumi, Reiko Fujiwara, Haruki Nishizawa, et al.
Congenital Anomalies|June 25, 2022
A case of 46,XY disorders of sex development with congenital heart disease caused by a GATA4 variantYui Shichiri, Yoshimi Kato, Hidehito Inagaki, et al.
JIMD Reports|May 13, 2018
Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal InversionKatsuyuki Yokoi, Yoko Nakajima, Tamae Ohye, et al.
Pageof 10

Showing results (51-60 of 98) with videos related to

Sort By:
Pageof 10
Journal of Human Genetics|January 14, 2022
Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomesTasuku Mariya, Takema Kato, Takeshi Sugimoto, et al.
Genome Research|November 11, 2008
Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humansHidehito Inagaki, Tamae Ohye, Hiroshi Kogo, et al.
American Journal of Human Genetics|August 16, 2006
Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)Terry Ashley, Ann P Gaeth, Hidehito Inagaki, et al.
JSES International|July 10, 2023
A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndromeYusuke Kawano, Atsuhito Seki, Takashi Kuroiwa, et al.
Journal of Human Genetics|February 26, 2025
Translocation-specific polymerase chain reaction in preimplantation genetic testing for recurrent translocation carrierGen Furukawa, Rie Kawamura, Hidehito Inagaki, et al.
Genes|August 29, 2024
Comparative Analysis of Two NGS-Based Platforms for Product-of-Conception KaryotypingYuri Murase, Yui Shichiri, Hidehito Inagaki, et al.
Journal of Human Genetics|February 24, 2019
Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structuresHidehito Inagaki, Sayuri Ota, Haruki Nishizawa, et al.
Plos One|May 9, 2014
Age-related decrease of meiotic cohesins in human oocytesMakiko Tsutsumi, Reiko Fujiwara, Haruki Nishizawa, et al.
Congenital Anomalies|June 25, 2022
A case of 46,XY disorders of sex development with congenital heart disease caused by a GATA4 variantYui Shichiri, Yoshimi Kato, Hidehito Inagaki, et al.
JIMD Reports|May 13, 2018
Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal InversionKatsuyuki Yokoi, Yoko Nakajima, Tamae Ohye, et al.
Pageof 10