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Maki Fukami

Showing results (111-120 of 319) with videos related to

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Molecular Reproduction and Development|October 6, 2020
SOX9 is colocalized with paraspeckle protein NONO in cultured murine sertoli cells and features structural characteristics of intrinsically disordered proteinsKazuhisa Akiba, Satoshi Narumi, Riko Nishimura, et al.
Molecular and Cellular Pediatrics|January 25, 2020
Random X chromosome inactivation in patients with Klinefelter syndromeKenichi Kinjo, Tomoko Yoshida, Yoshitomo Kobori, et al.
Micropublication Biology|March 3, 2021
Similar responsiveness between C57BL/6N and C57BL/6J mouse substrains to superovulationMiyuki Shindo, Hideki Tsumura, Kenji Miyado, et al.
Journal of Human Genetics|March 22, 2022
ACAN biallelic variants in a girl with severe idiopathic short statureYohei Masunaga, Yumiko Ohkubo, Gen Nishimura, et al.
Archives of Environmental Contamination and Toxicology|October 29, 2017
Expression of Xenobiotic Biomarkers CYP1 Family in Preputial Tissue of Patients with Hypospadias and Phimosis and Its Association with DNA Methylation Level of SRD5A2 Minimal PromoterSeiichiroh Ohsako, Toshiki Aiba, Mami Miyado, et al.
Journal of Human Genetics|October 25, 2019
De novo ZBTB7A variant in a patient with macrocephaly, intellectual disability, and sleep apnea: implications for the phenotypic development in 19p13.3 microdeletionsAkira Ohishi, Yohei Masunaga, Shigeo Iijima, et al.
The Journal of Clinical Endocrinology and Metabolism|June 23, 2012
PRKAR1A mutation affecting cAMP-mediated G protein-coupled receptor signaling in a patient with acrodysostosis and hormone resistanceKeisuke Nagasaki, Tomoko Iida, Hidetoshi Sato, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 8, 2026
Efficacy and safety of GH treatment in Japanese pediatric patients with <i>SHOX</i> deficiency: an open-label extension studyTsutomu Ogata, Sumito Dateki, Maki Fukami, et al.
Human Genome Variation|May 27, 2017
The first Japanese case of central precocious puberty with a novel <i>MKRN3</i> mutationJunko Nishioka, Hirohito Shima, Maki Fukami, et al.
Clinical Chemistry|January 26, 2012
Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosteroneYuhei Koyama, Keiko Homma, Maki Fukami, et al.
Pageof 32

Showing results (111-120 of 319) with videos related to

Sort By:
Pageof 32
Molecular Reproduction and Development|October 6, 2020
SOX9 is colocalized with paraspeckle protein NONO in cultured murine sertoli cells and features structural characteristics of intrinsically disordered proteinsKazuhisa Akiba, Satoshi Narumi, Riko Nishimura, et al.
Molecular and Cellular Pediatrics|January 25, 2020
Random X chromosome inactivation in patients with Klinefelter syndromeKenichi Kinjo, Tomoko Yoshida, Yoshitomo Kobori, et al.
Micropublication Biology|March 3, 2021
Similar responsiveness between C57BL/6N and C57BL/6J mouse substrains to superovulationMiyuki Shindo, Hideki Tsumura, Kenji Miyado, et al.
Journal of Human Genetics|March 22, 2022
ACAN biallelic variants in a girl with severe idiopathic short statureYohei Masunaga, Yumiko Ohkubo, Gen Nishimura, et al.
Archives of Environmental Contamination and Toxicology|October 29, 2017
Expression of Xenobiotic Biomarkers CYP1 Family in Preputial Tissue of Patients with Hypospadias and Phimosis and Its Association with DNA Methylation Level of SRD5A2 Minimal PromoterSeiichiroh Ohsako, Toshiki Aiba, Mami Miyado, et al.
Journal of Human Genetics|October 25, 2019
De novo ZBTB7A variant in a patient with macrocephaly, intellectual disability, and sleep apnea: implications for the phenotypic development in 19p13.3 microdeletionsAkira Ohishi, Yohei Masunaga, Shigeo Iijima, et al.
The Journal of Clinical Endocrinology and Metabolism|June 23, 2012
PRKAR1A mutation affecting cAMP-mediated G protein-coupled receptor signaling in a patient with acrodysostosis and hormone resistanceKeisuke Nagasaki, Tomoko Iida, Hidetoshi Sato, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 8, 2026
Efficacy and safety of GH treatment in Japanese pediatric patients with <i>SHOX</i> deficiency: an open-label extension studyTsutomu Ogata, Sumito Dateki, Maki Fukami, et al.
Human Genome Variation|May 27, 2017
The first Japanese case of central precocious puberty with a novel <i>MKRN3</i> mutationJunko Nishioka, Hirohito Shima, Maki Fukami, et al.
Clinical Chemistry|January 26, 2012
Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosteroneYuhei Koyama, Keiko Homma, Maki Fukami, et al.
Pageof 32