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Hidehito Inagaki

Showing results (11-20 of 98) with videos related to

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Molecular Genetics & Genomic Medicine|October 21, 2020
Molecular analysis of low-level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia PigmentiMiki Kawai, Takema Kato, Makiko Tsutsumi, et al.
Frontiers in Genetics|July 28, 2016
Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal RearrangementsHidehito Inagaki, Takema Kato, Makiko Tsutsumi, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|October 9, 2012
HORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activityHiroshi Kogo, Makiko Tsutsumi, Hidehito Inagaki, et al.
BMC Medical Genetics|December 14, 2018
Exonic duplication of the OTC gene by a complex rearrangement that likely occurred via a replication-based mechanism: a case reportKatsuyuki Yokoi, Yoko Nakajima, Hidehito Inagaki, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Lethal persistent pulmonary hypertension of the newborn in Bohring-Opitz syndromeMasaya Kibe, Satoshi Ibara, Hidehito Inagaki, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|October 2, 2002
Generation of human artificial chromosomes expressing naturally controlled guanosine triphosphate cyclohydrolase I geneMasashi Ikeno, Hidehito Inagaki, Keiko Nagata, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 26, 2012
HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytesHiroshi Kogo, Makiko Tsutsumi, Tamae Ohye, et al.
Congenital Anomalies|February 22, 2012
Molecular basis of maternal age-related increase in oocyte aneuploidyHiroki Kurahashi, Makiko Tsutsumi, Sachie Nishiyama, et al.
Molecular Cytogenetics|July 9, 2021
A Turner syndrome case associated with dic(Y;22)Rie Kawamura, Hidehito Inagaki, Midori Yamada, et al.
Pigment Cell Research|March 16, 2004
The tyrosinase gene of the i(b) albino mutant of the medaka fish carries a transposable element insertion in the promoter regionAtsuo Iida, Hidehito Inagaki, Miho Suzuki, et al.
Pageof 10

Showing results (11-20 of 98) with videos related to

Sort By:
Pageof 10
Molecular Genetics & Genomic Medicine|October 21, 2020
Molecular analysis of low-level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia PigmentiMiki Kawai, Takema Kato, Makiko Tsutsumi, et al.
Frontiers in Genetics|July 28, 2016
Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal RearrangementsHidehito Inagaki, Takema Kato, Makiko Tsutsumi, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|October 9, 2012
HORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activityHiroshi Kogo, Makiko Tsutsumi, Hidehito Inagaki, et al.
BMC Medical Genetics|December 14, 2018
Exonic duplication of the OTC gene by a complex rearrangement that likely occurred via a replication-based mechanism: a case reportKatsuyuki Yokoi, Yoko Nakajima, Hidehito Inagaki, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Lethal persistent pulmonary hypertension of the newborn in Bohring-Opitz syndromeMasaya Kibe, Satoshi Ibara, Hidehito Inagaki, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|October 2, 2002
Generation of human artificial chromosomes expressing naturally controlled guanosine triphosphate cyclohydrolase I geneMasashi Ikeno, Hidehito Inagaki, Keiko Nagata, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 26, 2012
HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytesHiroshi Kogo, Makiko Tsutsumi, Tamae Ohye, et al.
Congenital Anomalies|February 22, 2012
Molecular basis of maternal age-related increase in oocyte aneuploidyHiroki Kurahashi, Makiko Tsutsumi, Sachie Nishiyama, et al.
Molecular Cytogenetics|July 9, 2021
A Turner syndrome case associated with dic(Y;22)Rie Kawamura, Hidehito Inagaki, Midori Yamada, et al.
Pigment Cell Research|March 16, 2004
The tyrosinase gene of the i(b) albino mutant of the medaka fish carries a transposable element insertion in the promoter regionAtsuo Iida, Hidehito Inagaki, Miho Suzuki, et al.
Pageof 10