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Shuji Takada

Showing results (51-60 of 127) with videos related to

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Nucleic Acids Research|November 29, 2019
Exploring trophoblast-specific Tead4 enhancers through chromatin conformation capture assays followed by functional screeningJunko Tomikawa, Shuji Takada, Kohji Okamura, et al.
Biochemical and Biophysical Research Communications|September 11, 2014
In vivo knockdown of ErbB3 in mice inhibits Schwann cell precursor migrationTomohiro Torii, Yuki Miyamoto, Shuji Takada, et al.
Clinical Epigenetics|March 9, 2019
Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMRMasayo Kagami, Atsuhiro Yanagisawa, Miyuki Ota, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|May 1, 2016
Cord blood-derived endothelial colony-forming cell function is disrupted in congenital diaphragmatic herniaHideshi Fujinaga, Hiroko Fujinaga, Nobuyuki Watanabe, et al.
Human Gene Therapy|July 15, 2022
Adeno-Associated Virus-Mediated Gene Therapy for Patients' Fibroblasts, Induced Pluripotent Stem Cells, and a Mouse Model of Congenital Adrenal HyperplasiaYasuhiro Naiki, Mami Miyado, Miyuki Shindo, et al.
Biochemical and Biophysical Research Communications|November 2, 2005
Transforming activity of the lymphotoxin-beta receptor revealed by expression screeningShin-ichiro Fujiwara, Yoshihiro Yamashita, Young Lim Choi, et al.
The Journal of Biological Chemistry|May 2, 2012
L-Sox5 and Sox6 proteins enhance chondrogenic miR-140 microRNA expression by strengthening dimeric Sox9 activitySatoshi Yamashita, Shigeru Miyaki, Yoshio Kato, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 3, 2018
Phenotypic Variation in 46,XX Disorders of Sex Development due to the NR5A1 p.R92W Variant: A Sibling Case Report and Literature ReviewKei Takasawa, Maki Igarashi, Makoto Ono, et al.
Clinical Epigenetics|May 27, 2021
ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbanceMasayo Kagami, Kaori Hara-Isono, Keiko Matsubara, et al.
Frontiers in Endocrinology|April 26, 2021
A Testis-Specific Long Noncoding RNA, <i>Start</i>, Is a Regulator of Steroidogenesis in Mouse Leydig CellsKai Otsuka, Shin Matsubara, Akira Shiraishi, et al.
Pageof 13

Showing results (51-60 of 127) with videos related to

Sort By:
Pageof 13
Nucleic Acids Research|November 29, 2019
Exploring trophoblast-specific Tead4 enhancers through chromatin conformation capture assays followed by functional screeningJunko Tomikawa, Shuji Takada, Kohji Okamura, et al.
Biochemical and Biophysical Research Communications|September 11, 2014
In vivo knockdown of ErbB3 in mice inhibits Schwann cell precursor migrationTomohiro Torii, Yuki Miyamoto, Shuji Takada, et al.
Clinical Epigenetics|March 9, 2019
Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMRMasayo Kagami, Atsuhiro Yanagisawa, Miyuki Ota, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|May 1, 2016
Cord blood-derived endothelial colony-forming cell function is disrupted in congenital diaphragmatic herniaHideshi Fujinaga, Hiroko Fujinaga, Nobuyuki Watanabe, et al.
Human Gene Therapy|July 15, 2022
Adeno-Associated Virus-Mediated Gene Therapy for Patients' Fibroblasts, Induced Pluripotent Stem Cells, and a Mouse Model of Congenital Adrenal HyperplasiaYasuhiro Naiki, Mami Miyado, Miyuki Shindo, et al.
Biochemical and Biophysical Research Communications|November 2, 2005
Transforming activity of the lymphotoxin-beta receptor revealed by expression screeningShin-ichiro Fujiwara, Yoshihiro Yamashita, Young Lim Choi, et al.
The Journal of Biological Chemistry|May 2, 2012
L-Sox5 and Sox6 proteins enhance chondrogenic miR-140 microRNA expression by strengthening dimeric Sox9 activitySatoshi Yamashita, Shigeru Miyaki, Yoshio Kato, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 3, 2018
Phenotypic Variation in 46,XX Disorders of Sex Development due to the NR5A1 p.R92W Variant: A Sibling Case Report and Literature ReviewKei Takasawa, Maki Igarashi, Makoto Ono, et al.
Clinical Epigenetics|May 27, 2021
ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbanceMasayo Kagami, Kaori Hara-Isono, Keiko Matsubara, et al.
Frontiers in Endocrinology|April 26, 2021
A Testis-Specific Long Noncoding RNA, <i>Start</i>, Is a Regulator of Steroidogenesis in Mouse Leydig CellsKai Otsuka, Shin Matsubara, Akira Shiraishi, et al.
Pageof 13