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Kenichiro Hata

Showing results (191-200 of 266) with videos related to

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Cell Reports|February 2, 2024
Development of sexual dimorphism of skeletal muscles through the adrenal cortex, caused by androgen-induced global gene suppressionFumiya Takahashi, Takashi Baba, Antonius Christianto, et al.
Gene|February 26, 2016
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infantsJanette Mareska Rumbajan, Yuko Yamaguchi, Kazuhiko Nakabayashi, et al.
Biology of Reproduction|February 21, 2009
Abnormal DNA methyltransferase expression in mouse germline stem cells results in spermatogenic defectsSeiji Takashima, Masanori Takehashi, Jiyoung Lee, et al.
Nucleic Acids Research|September 25, 2015
Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactiveStéphanie Maupetit-Méhouas, Bertille Montibus, David Nury, et al.
Clinical Immunology (Orlando, Fla.)|June 17, 2020
X-linked inhibitor of apoptosis protein deficiency complicated with Crohn's disease-like enterocolitis and Takayasu arteritis: A case reportIchiro Takeuchi, Toshinao Kawai, Meika Nambu, et al.
European Journal of Haematology|November 13, 2013
Poor responses to tyrosine kinase inhibitors in a child with precursor B-cell acute lymphoblastic leukemia with SNX2-ABL1 chimeric transcriptAki Masuzawa, Chikako Kiyotani, Tomoo Osumi, et al.
Journal of Medical Genetics|August 30, 2017
<i>CTCF</i> deletion syndrome: clinical features and epigenetic delineationIkumi Hori, Rie Kawamura, Kazuhiko Nakabayashi, et al.
Journal of Human Genetics|May 3, 2014
Compilation of copy number variants identified in phenotypically normal and parous Japanese womenOhsuke Migita, Kayoko Maehara, Hiromi Kamura, et al.
Placenta|September 3, 2021
Diagnostic predictability of miR-4535 and miR-1915-5p expression in amniotic fluid for foetal morbidity of infectionKenichi Yoshikawa, Chihiro Kiyoshima, Toyofumi Hirakawa, et al.
Journal of Medical Genetics|June 25, 2020
Loss of imprinting of the human-specific imprinted gene <i>ZNF597</i> causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndromeKazuki Yamazawa, Takanobu Inoue, Yoshihiro Sakemi, et al.
Pageof 27

Showing results (191-200 of 266) with videos related to

Sort By:
Pageof 27
Cell Reports|February 2, 2024
Development of sexual dimorphism of skeletal muscles through the adrenal cortex, caused by androgen-induced global gene suppressionFumiya Takahashi, Takashi Baba, Antonius Christianto, et al.
Gene|February 26, 2016
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infantsJanette Mareska Rumbajan, Yuko Yamaguchi, Kazuhiko Nakabayashi, et al.
Biology of Reproduction|February 21, 2009
Abnormal DNA methyltransferase expression in mouse germline stem cells results in spermatogenic defectsSeiji Takashima, Masanori Takehashi, Jiyoung Lee, et al.
Nucleic Acids Research|September 25, 2015
Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactiveStéphanie Maupetit-Méhouas, Bertille Montibus, David Nury, et al.
Clinical Immunology (Orlando, Fla.)|June 17, 2020
X-linked inhibitor of apoptosis protein deficiency complicated with Crohn's disease-like enterocolitis and Takayasu arteritis: A case reportIchiro Takeuchi, Toshinao Kawai, Meika Nambu, et al.
European Journal of Haematology|November 13, 2013
Poor responses to tyrosine kinase inhibitors in a child with precursor B-cell acute lymphoblastic leukemia with SNX2-ABL1 chimeric transcriptAki Masuzawa, Chikako Kiyotani, Tomoo Osumi, et al.
Journal of Medical Genetics|August 30, 2017
<i>CTCF</i> deletion syndrome: clinical features and epigenetic delineationIkumi Hori, Rie Kawamura, Kazuhiko Nakabayashi, et al.
Journal of Human Genetics|May 3, 2014
Compilation of copy number variants identified in phenotypically normal and parous Japanese womenOhsuke Migita, Kayoko Maehara, Hiromi Kamura, et al.
Placenta|September 3, 2021
Diagnostic predictability of miR-4535 and miR-1915-5p expression in amniotic fluid for foetal morbidity of infectionKenichi Yoshikawa, Chihiro Kiyoshima, Toyofumi Hirakawa, et al.
Journal of Medical Genetics|June 25, 2020
Loss of imprinting of the human-specific imprinted gene <i>ZNF597</i> causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndromeKazuki Yamazawa, Takanobu Inoue, Yoshihiro Sakemi, et al.
Pageof 27