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European Journal of Medical Genetics
|
December 31, 2024
Brain calcification in congenital heart defects and ectodermal dysplasia (CHDED)
Daisuke Watanabe, Yohei Hasebe, Hideaki Yagasaki, et al.
Journal of Human Genetics
|
May 19, 2017
A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate
Koji Kato, Fuyuki Miya, Ikumi Hori, et al.
Scientific Reports
|
August 26, 2024
Biallelic structural variants in three patients with ERCC8-related Cockayne syndrome and a potential pitfall of copy number variation analysis
Daisuke Watanabe, Nobuhiko Okamoto, Yuichi Kobayashi, et al.
Journal of Neurochemistry
|
October 28, 2016
Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability
Nanako Hamada, Yutaka Negishi, Makoto Mizuno, et al.
Nature Communications
|
August 27, 2025
Clonal diversity shapes the tumour microenvironment leading to distinct immunotherapy responses in metastatic urothelial carcinoma
Takashi Kamatani, Kota Umeda, Tomohiro Iwasawa, et al.
Experimental and Therapeutic Medicine
|
September 21, 2012
Identification of a set of genes associated with response to interleukin-2 and interferon-α combination therapy for renal cell carcinoma through genome-wide gene expression profiling
Osamu Mizumori, Hitoshi Zembutsu, Yoichiro Kato, et al.
British Journal of Cancer
|
October 6, 2021
Landscape of prognostic signatures and immunogenomics of the AXL/GAS6 axis in renal cell carcinoma
Kyohei Hakozaki, Nobuyuki Tanaka, Kimiharu Takamatsu, et al.
Plos One
|
September 3, 2011
Hepatitis C virus infection suppresses the interferon response in the liver of the human hepatocyte chimeric mouse
Masataka Tsuge, Yoshifumi Fujimoto, Nobuhiko Hiraga, et al.
European Journal of Medical Genetics
|
June 27, 2023
Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences
Mamiko Yamada, Yohei Nitta, Tomoko Uehara, et al.
Diabetes
|
June 2, 2021
Genotype-Structure-Phenotype Correlations of Disease-Associated IGF1R Variants and Similarities to Those of INSR Variants
Jun Hosoe, Yuki Kawashima-Sonoyama, Fuyuki Miya, et al.
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Search research articles
Search
Showing results (71-80 of 109) with videos related to
Sort By:
Page
of 11
European Journal of Medical Genetics
|
December 31, 2024
Brain calcification in congenital heart defects and ectodermal dysplasia (CHDED)
Daisuke Watanabe, Yohei Hasebe, Hideaki Yagasaki, et al.
Journal of Human Genetics
|
May 19, 2017
A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate
Koji Kato, Fuyuki Miya, Ikumi Hori, et al.
Scientific Reports
|
August 26, 2024
Biallelic structural variants in three patients with ERCC8-related Cockayne syndrome and a potential pitfall of copy number variation analysis
Daisuke Watanabe, Nobuhiko Okamoto, Yuichi Kobayashi, et al.
Journal of Neurochemistry
|
October 28, 2016
Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability
Nanako Hamada, Yutaka Negishi, Makoto Mizuno, et al.
Nature Communications
|
August 27, 2025
Clonal diversity shapes the tumour microenvironment leading to distinct immunotherapy responses in metastatic urothelial carcinoma
Takashi Kamatani, Kota Umeda, Tomohiro Iwasawa, et al.
Experimental and Therapeutic Medicine
|
September 21, 2012
Identification of a set of genes associated with response to interleukin-2 and interferon-α combination therapy for renal cell carcinoma through genome-wide gene expression profiling
Osamu Mizumori, Hitoshi Zembutsu, Yoichiro Kato, et al.
British Journal of Cancer
|
October 6, 2021
Landscape of prognostic signatures and immunogenomics of the AXL/GAS6 axis in renal cell carcinoma
Kyohei Hakozaki, Nobuyuki Tanaka, Kimiharu Takamatsu, et al.
Plos One
|
September 3, 2011
Hepatitis C virus infection suppresses the interferon response in the liver of the human hepatocyte chimeric mouse
Masataka Tsuge, Yoshifumi Fujimoto, Nobuhiko Hiraga, et al.
European Journal of Medical Genetics
|
June 27, 2023
Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences
Mamiko Yamada, Yohei Nitta, Tomoko Uehara, et al.
Diabetes
|
June 2, 2021
Genotype-Structure-Phenotype Correlations of Disease-Associated IGF1R Variants and Similarities to Those of INSR Variants
Jun Hosoe, Yuki Kawashima-Sonoyama, Fuyuki Miya, et al.
Page
of 11