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Maki Fukami

Showing results (61-70 of 319) with videos related to

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Endocrine Journal|January 19, 2011
Identification of chromosome 15q26 terminal deletion with telomere sequences and its bearing on genotype-phenotype analysisSumito Dateki, Maki Fukami, Yoko Tanaka, et al.
Hormone Research in Paediatrics|April 17, 2010
Hypothalamic dysfunction in a female with isolated hypogonadotropic hypogonadism and compound heterozygous TACR3 mutations and clinical manifestation in her heterozygous motherMaki Fukami, Tetsuo Maruyama, Sumito Dateki, et al.
Clinical Epigenetics|June 9, 2025
Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith-Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted regionTatsuki Urakawa, Yuri Kanamaru, Naoko Amano, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 12, 2014
Skeletal Deformity Associated with SHOX DeficiencyAtsuhito Seki, Tomoko Jinno, Erina Suzuki, et al.
Journal of Human Genetics|June 10, 2021
Structural and numerical Y chromosomal variations in elderly men identified through multiplex ligation-dependent probe amplificationYasuko Ogiwara, Mami Miyado, Erina Suzuki, et al.
Plos One|May 12, 2011
Mamld1 knockdown reduces testosterone production and Cyp17a1 expression in mouse Leydig tumor cellsMichiko Nakamura, Maki Fukami, Fumihiro Sugawa, et al.
Endocrine Journal|March 11, 2005
Association of micropenis with Pro185Ala polymorphism of the gene for aryl hydrocarbon receptor repressor involved in dioxin signalingShun Soneda, Maki Fukami, Masatoshi Fujimoto, et al.
The Journal of Clinical Endocrinology and Metabolism|May 19, 2005
Association of cryptorchidism with a specific haplotype of the estrogen receptor alpha gene: implication for the susceptibility to estrogenic environmental endocrine disruptorsRie Yoshida, Maki Fukami, Isoji Sasagawa, et al.
Human Reproduction (Oxford, England)|August 31, 2020
Foetal virilisation caused by overproduction of non-aromatisable 11-oxygenated C19 steroids in maternal adrenal tumourKeisuke Nagasaki, Kaoru Takase, Chikahiko Numakura, et al.
Cytogenetic and Genome Research|April 9, 2018
Somatically Acquired Isodicentric Y and Mosaic Loss of Chromosome Y in a Boy with HypospadiasMami Miyado, Koji Muroya, Momori Katsumi, et al.
Pageof 32

Showing results (61-70 of 319) with videos related to

Sort By:
Pageof 32
Endocrine Journal|January 19, 2011
Identification of chromosome 15q26 terminal deletion with telomere sequences and its bearing on genotype-phenotype analysisSumito Dateki, Maki Fukami, Yoko Tanaka, et al.
Hormone Research in Paediatrics|April 17, 2010
Hypothalamic dysfunction in a female with isolated hypogonadotropic hypogonadism and compound heterozygous TACR3 mutations and clinical manifestation in her heterozygous motherMaki Fukami, Tetsuo Maruyama, Sumito Dateki, et al.
Clinical Epigenetics|June 9, 2025
Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith-Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted regionTatsuki Urakawa, Yuri Kanamaru, Naoko Amano, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 12, 2014
Skeletal Deformity Associated with SHOX DeficiencyAtsuhito Seki, Tomoko Jinno, Erina Suzuki, et al.
Journal of Human Genetics|June 10, 2021
Structural and numerical Y chromosomal variations in elderly men identified through multiplex ligation-dependent probe amplificationYasuko Ogiwara, Mami Miyado, Erina Suzuki, et al.
Plos One|May 12, 2011
Mamld1 knockdown reduces testosterone production and Cyp17a1 expression in mouse Leydig tumor cellsMichiko Nakamura, Maki Fukami, Fumihiro Sugawa, et al.
Endocrine Journal|March 11, 2005
Association of micropenis with Pro185Ala polymorphism of the gene for aryl hydrocarbon receptor repressor involved in dioxin signalingShun Soneda, Maki Fukami, Masatoshi Fujimoto, et al.
The Journal of Clinical Endocrinology and Metabolism|May 19, 2005
Association of cryptorchidism with a specific haplotype of the estrogen receptor alpha gene: implication for the susceptibility to estrogenic environmental endocrine disruptorsRie Yoshida, Maki Fukami, Isoji Sasagawa, et al.
Human Reproduction (Oxford, England)|August 31, 2020
Foetal virilisation caused by overproduction of non-aromatisable 11-oxygenated C19 steroids in maternal adrenal tumourKeisuke Nagasaki, Kaoru Takase, Chikahiko Numakura, et al.
Cytogenetic and Genome Research|April 9, 2018
Somatically Acquired Isodicentric Y and Mosaic Loss of Chromosome Y in a Boy with HypospadiasMami Miyado, Koji Muroya, Momori Katsumi, et al.
Pageof 32