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Erina Suzuki

Showing results (11-20 of 48) with videos related to

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American Journal of Clinical Pathology|August 16, 2015
Distinct β-catenin and PIK3CA mutation profiles in endometriosis-associated ovarian endometrioid and clear cell carcinomasToshihide Matsumoto, Masaaki Yamazaki, Hiroyuki Takahashi, et al.
Frontiers in Endocrinology|July 3, 2025
<i>De novo</i> retrotransposon insertion into the <i>FGFR1</i> gene in a boy with congenital hypogonadotropic hypogonadism: a case reportKentaro Sawano, Keisuke Nagasaki, Erina Suzuki, et al.
Reproductive Medicine and Biology|April 11, 2020
Copy-number analysis of Y-linked loci in young men with non-obstructive azoospermia: Implications for the rarity of early onset mosaic loss of chromosome YErina Suzuki, Yoshitomo Kobori, Momori Katsumi, et al.
Heliyon|September 23, 2024
DNA methylation changes in the genome of patients with hypogonadotropic hypogonadismErina Suzuki, Kazuhiko Nakabayashi, Saki Aoto, et al.
Case Reports in Endocrinology|July 11, 2025
De Novo Splice Site Variant of TCF12 in a Boy With Isolated Kallmann SyndromeErina Suzuki, Hirohito Shima, Aki Ueda, 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.
Cytogenetic and Genome Research|January 11, 2018
A de novo 50-bp GNAS Intragenic Duplication in a Patient with Pseudohypoparathyroidism Type 1aErina Suzuki, Ryosuke Bo, Kaori Sue, et al.
Hormone Research in Paediatrics|August 1, 2015
Loss-of-Function SOX10 Mutation in a Patient with Kallmann Syndrome, Hearing Loss, and Iris HypopigmentationErina Suzuki, Yoko Izumi, Yuta Chiba, et al.
Human Pathology|April 27, 2013
Transcriptional regulation of the alpha-1 type II collagen gene by nuclear factor B/p65 and Sox9 in the chondrocytic phenotype of uterine carcinosarcomasTsutomu Yoshida, Miki Hashimura, Takeshi Kuwata, et al.
BMC Pregnancy and Childbirth|March 31, 2021
Labor dystocia and risk of histological chorioamnionitis and funisitis: a study from a single tertiary referral centerHyo Kyozuka, Tuyoshi Murata, Toma Fukuda, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
American Journal of Clinical Pathology|August 16, 2015
Distinct β-catenin and PIK3CA mutation profiles in endometriosis-associated ovarian endometrioid and clear cell carcinomasToshihide Matsumoto, Masaaki Yamazaki, Hiroyuki Takahashi, et al.
Frontiers in Endocrinology|July 3, 2025
<i>De novo</i> retrotransposon insertion into the <i>FGFR1</i> gene in a boy with congenital hypogonadotropic hypogonadism: a case reportKentaro Sawano, Keisuke Nagasaki, Erina Suzuki, et al.
Reproductive Medicine and Biology|April 11, 2020
Copy-number analysis of Y-linked loci in young men with non-obstructive azoospermia: Implications for the rarity of early onset mosaic loss of chromosome YErina Suzuki, Yoshitomo Kobori, Momori Katsumi, et al.
Heliyon|September 23, 2024
DNA methylation changes in the genome of patients with hypogonadotropic hypogonadismErina Suzuki, Kazuhiko Nakabayashi, Saki Aoto, et al.
Case Reports in Endocrinology|July 11, 2025
De Novo Splice Site Variant of TCF12 in a Boy With Isolated Kallmann SyndromeErina Suzuki, Hirohito Shima, Aki Ueda, 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.
Cytogenetic and Genome Research|January 11, 2018
A de novo 50-bp GNAS Intragenic Duplication in a Patient with Pseudohypoparathyroidism Type 1aErina Suzuki, Ryosuke Bo, Kaori Sue, et al.
Hormone Research in Paediatrics|August 1, 2015
Loss-of-Function SOX10 Mutation in a Patient with Kallmann Syndrome, Hearing Loss, and Iris HypopigmentationErina Suzuki, Yoko Izumi, Yuta Chiba, et al.
Human Pathology|April 27, 2013
Transcriptional regulation of the alpha-1 type II collagen gene by nuclear factor B/p65 and Sox9 in the chondrocytic phenotype of uterine carcinosarcomasTsutomu Yoshida, Miki Hashimura, Takeshi Kuwata, et al.
BMC Pregnancy and Childbirth|March 31, 2021
Labor dystocia and risk of histological chorioamnionitis and funisitis: a study from a single tertiary referral centerHyo Kyozuka, Tuyoshi Murata, Toma Fukuda, et al.
Pageof 5