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Kensaku Sasaki

Showing results (1-10 of 11) with videos related to

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Gene|November 1, 2012
Uniparental disomy analysis in trios using genome-wide SNP array and whole-genome sequencing data imply segmental uniparental isodisomy in general populationsKensaku Sasaki, Hiroyuki Mishima, Kiyonori Miura, et al.
BMC Research Notes|September 9, 2011
Agile parallel bioinformatics workflow management using PwrakeHiroyuki Mishima, Kensaku Sasaki, Masahiro Tanaka, et al.
Journal of Human Genetics|April 28, 2017
Fetiform teratoma was a parthenogenetic tumor arising from a mature ovumKiyonori Miura, Takumi Kurabayashi, Chisei Satoh, et al.
Seikagaku. the Journal of Japanese Biochemical Society|May 2, 2013
[Molecular cloning and characterisation of UVSSA, the responsible gene for UV-sensitive syndrome]Tomoo Ogi, Yuka Nakazawa, Kensaku Sasaki, et al.
European Journal of Human Genetics : EJHG|August 19, 2007
Japanese and North American/European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterationsKensaku Sasaki, Hidenobu Soejima, Ken Higashimoto, et al.
American Journal of Medical Genetics. Part A|July 22, 2008
Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12DHideo Kuniba, Ritsuko K Pooh, Kensaku Sasaki, et al.
Plos One|May 5, 2012
Copy number alteration and uniparental disomy analysis categorizes Japanese papillary thyroid carcinomas into distinct groupsMichiko Matsuse, Kensaku Sasaki, Eijun Nishihara, et al.
Journal of Human Genetics|March 8, 2013
Copy number variation of the antimicrobial-gene, defensin beta 4, is associated with susceptibility to cervical cancerShuhei Abe, Kiyonori Miura, Akira Kinoshita, et al.
European Journal of Human Genetics : EJHG|March 15, 2013
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndromeKen Higashimoto, Toshiyuki Maeda, Junichiro Okada, et al.
Nature Genetics|April 3, 2012
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repairYuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Gene|November 1, 2012
Uniparental disomy analysis in trios using genome-wide SNP array and whole-genome sequencing data imply segmental uniparental isodisomy in general populationsKensaku Sasaki, Hiroyuki Mishima, Kiyonori Miura, et al.
BMC Research Notes|September 9, 2011
Agile parallel bioinformatics workflow management using PwrakeHiroyuki Mishima, Kensaku Sasaki, Masahiro Tanaka, et al.
Journal of Human Genetics|April 28, 2017
Fetiform teratoma was a parthenogenetic tumor arising from a mature ovumKiyonori Miura, Takumi Kurabayashi, Chisei Satoh, et al.
Seikagaku. the Journal of Japanese Biochemical Society|May 2, 2013
[Molecular cloning and characterisation of UVSSA, the responsible gene for UV-sensitive syndrome]Tomoo Ogi, Yuka Nakazawa, Kensaku Sasaki, et al.
European Journal of Human Genetics : EJHG|August 19, 2007
Japanese and North American/European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterationsKensaku Sasaki, Hidenobu Soejima, Ken Higashimoto, et al.
American Journal of Medical Genetics. Part A|July 22, 2008
Prenatal diagnosis of Costello syndrome using 3D ultrasonography amniocentesis confirmation of the rare HRAS mutation G12DHideo Kuniba, Ritsuko K Pooh, Kensaku Sasaki, et al.
Plos One|May 5, 2012
Copy number alteration and uniparental disomy analysis categorizes Japanese papillary thyroid carcinomas into distinct groupsMichiko Matsuse, Kensaku Sasaki, Eijun Nishihara, et al.
Journal of Human Genetics|March 8, 2013
Copy number variation of the antimicrobial-gene, defensin beta 4, is associated with susceptibility to cervical cancerShuhei Abe, Kiyonori Miura, Akira Kinoshita, et al.
European Journal of Human Genetics : EJHG|March 15, 2013
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndromeKen Higashimoto, Toshiyuki Maeda, Junichiro Okada, et al.
Nature Genetics|April 3, 2012
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repairYuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, et al.
Pageof 2