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Naoki Harada

Showing results (251-260 of 261) with videos related to

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Nature Genetics|July 6, 2004
Heterozygous TGFBR2 mutations in Marfan syndromeTakeshi Mizuguchi, Gwenaëlle Collod-Beroud, Takushi Akiyama, et al.
Nature Genetics|March 16, 2002
Haploinsufficiency of NSD1 causes Sotos syndromeNaohiro Kurotaki, Kiyoshi Imaizumi, Naoki Harada, et al.
Cancer Medicine|July 7, 2026
Duocarmycin-Bearing Antibody-Mimetic Drug Conjugate Combined With an ATR Inhibitor Results in Complete Tumor Regression in a KPL-4 Xenograft ModelToshiya Tanaka, Akira Sugiyama, Juri Sakata, et al.
American Journal of Human Genetics|April 11, 2003
Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndromeNoriko Miyake, Naohiro Kurotaki, Hirobumi Sugawara, et al.
American Journal of Medical Genetics. Part A|November 10, 2005
No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patientsNoriko Miyake, Osamu Shimokawa, Naoki Harada, et al.
Nucleic Acids Research|November 28, 2023
Exome-wide benchmark of difficult-to-sequence regions using short-read next-generation DNA sequencingAtsushi Hijikata, Mikita Suyama, Shingo Kikugawa, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypesHaruya Sakai, Remco Visser, Shiro Ikegawa, et al.
Journal of Gastroenterology|July 31, 2015
The impact of an inosine triphosphate pyrophosphatase genotype on bilirubin increase in chronic hepatitis C patients treated with simeprevir, pegylated interferon plus ribavirinYuki Tahata, Naoki Hiramatsu, Tsugiko Oze, et al.
Journal of Gastroenterology|November 12, 2014
Impact of alpha-fetoprotein on hepatocellular carcinoma development during entecavir treatment of chronic hepatitis B virus infectionRyoko Yamada, Naoki Hiramatsu, Tsugiko Oze, et al.
Human Mutation|October 1, 2003
Fifty microdeletions among 112 cases of Sotos syndrome: low copy repeats possibly mediate the common deletionNaohiro Kurotaki, Naoki Harada, Osamu Shimokawa, et al.
Pageof 27

Showing results (251-260 of 261) with videos related to

Sort By:
Pageof 27
Nature Genetics|July 6, 2004
Heterozygous TGFBR2 mutations in Marfan syndromeTakeshi Mizuguchi, Gwenaëlle Collod-Beroud, Takushi Akiyama, et al.
Nature Genetics|March 16, 2002
Haploinsufficiency of NSD1 causes Sotos syndromeNaohiro Kurotaki, Kiyoshi Imaizumi, Naoki Harada, et al.
Cancer Medicine|July 7, 2026
Duocarmycin-Bearing Antibody-Mimetic Drug Conjugate Combined With an ATR Inhibitor Results in Complete Tumor Regression in a KPL-4 Xenograft ModelToshiya Tanaka, Akira Sugiyama, Juri Sakata, et al.
American Journal of Human Genetics|April 11, 2003
Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndromeNoriko Miyake, Naohiro Kurotaki, Hirobumi Sugawara, et al.
American Journal of Medical Genetics. Part A|November 10, 2005
No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patientsNoriko Miyake, Osamu Shimokawa, Naoki Harada, et al.
Nucleic Acids Research|November 28, 2023
Exome-wide benchmark of difficult-to-sequence regions using short-read next-generation DNA sequencingAtsushi Hijikata, Mikita Suyama, Shingo Kikugawa, et al.
American Journal of Medical Genetics. Part A|July 13, 2006
Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypesHaruya Sakai, Remco Visser, Shiro Ikegawa, et al.
Journal of Gastroenterology|July 31, 2015
The impact of an inosine triphosphate pyrophosphatase genotype on bilirubin increase in chronic hepatitis C patients treated with simeprevir, pegylated interferon plus ribavirinYuki Tahata, Naoki Hiramatsu, Tsugiko Oze, et al.
Journal of Gastroenterology|November 12, 2014
Impact of alpha-fetoprotein on hepatocellular carcinoma development during entecavir treatment of chronic hepatitis B virus infectionRyoko Yamada, Naoki Hiramatsu, Tsugiko Oze, et al.
Human Mutation|October 1, 2003
Fifty microdeletions among 112 cases of Sotos syndrome: low copy repeats possibly mediate the common deletionNaohiro Kurotaki, Naoki Harada, Osamu Shimokawa, et al.
Pageof 27