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Koki Yamada

Showing results (31-40 of 45) with videos related to

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American Journal of Human Genetics|August 19, 2007
CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20qAlan Shiels, Thomas M Bennett, Harry L S Knopf, et al.
The Journal of Reproduction and Development|July 30, 2023
Sex difference in developmental changes in visualized Kiss1 neurons in newly generated Kiss1-Cre ratsKoki Yamada, Mayuko Nagae, Tetsuya Mano, et al.
Endocrinology|June 3, 2026
Central fractalkine-CX3CR1 signaling mediates systemic LPS-induced inhibition of LH pulses in female ratsYuki Otsuka, Shunsaku Kadoi, Shunsuke Seki, et al.
Scientific Reports|May 3, 2024
Raphe glucose-sensing serotonergic neurons stimulate KNDy neurons to enhance LH pulses via 5HT2CR: rat and goat studiesSho Nakamura, Takuya Sasaki, Yoshihisa Uenoyama, et al.
Scientific Reports|November 22, 2023
Conditional Oprk1-dependent Kiss1 deletion in kisspeptin neurons caused estrogen-dependent LH pulse disruption and LH surge attenuation in female ratsMayuko Nagae, Koki Yamada, Yuki Enomoto, et al.
Human Genetics|December 17, 2002
Skewed X-chromosome inactivation causes intra-familial phenotypic variation of an EBP mutation in a family with X-linked dominant chondrodysplasia punctataShuya Shirahama, Akira Miyahara, Hiroshi Kitoh, et al.
American Journal of Human Genetics|October 24, 2002
Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL familyRaidah Al-Baradie, Koki Yamada, Cynthia St Hilaire, et al.
ACG Case Reports Journal|June 4, 2026
Delayed Bile Duct Injury Preceded by Sepsis After Biliary Cooling-Assisted Ablation of Hilar Hepatocellular CarcinomaChihiro Tarumi, Yuki Tokuda, Akira Nishio, et al.
Molecular Vision|November 3, 2010
KIF21A mutations in two Chinese families with congenital fibrosis of the extraocular muscles (CFEOM)Xian Yang, Koki Yamada, Bradley Katz, et al.
BMC Genetics|March 8, 2002
CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIXElizabeth C Engle, Nathalie McIntosh, Koki Yamada, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|August 19, 2007
CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20qAlan Shiels, Thomas M Bennett, Harry L S Knopf, et al.
The Journal of Reproduction and Development|July 30, 2023
Sex difference in developmental changes in visualized Kiss1 neurons in newly generated Kiss1-Cre ratsKoki Yamada, Mayuko Nagae, Tetsuya Mano, et al.
Endocrinology|June 3, 2026
Central fractalkine-CX3CR1 signaling mediates systemic LPS-induced inhibition of LH pulses in female ratsYuki Otsuka, Shunsaku Kadoi, Shunsuke Seki, et al.
Scientific Reports|May 3, 2024
Raphe glucose-sensing serotonergic neurons stimulate KNDy neurons to enhance LH pulses via 5HT2CR: rat and goat studiesSho Nakamura, Takuya Sasaki, Yoshihisa Uenoyama, et al.
Scientific Reports|November 22, 2023
Conditional Oprk1-dependent Kiss1 deletion in kisspeptin neurons caused estrogen-dependent LH pulse disruption and LH surge attenuation in female ratsMayuko Nagae, Koki Yamada, Yuki Enomoto, et al.
Human Genetics|December 17, 2002
Skewed X-chromosome inactivation causes intra-familial phenotypic variation of an EBP mutation in a family with X-linked dominant chondrodysplasia punctataShuya Shirahama, Akira Miyahara, Hiroshi Kitoh, et al.
American Journal of Human Genetics|October 24, 2002
Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL familyRaidah Al-Baradie, Koki Yamada, Cynthia St Hilaire, et al.
ACG Case Reports Journal|June 4, 2026
Delayed Bile Duct Injury Preceded by Sepsis After Biliary Cooling-Assisted Ablation of Hilar Hepatocellular CarcinomaChihiro Tarumi, Yuki Tokuda, Akira Nishio, et al.
Molecular Vision|November 3, 2010
KIF21A mutations in two Chinese families with congenital fibrosis of the extraocular muscles (CFEOM)Xian Yang, Koki Yamada, Bradley Katz, et al.
BMC Genetics|March 8, 2002
CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIXElizabeth C Engle, Nathalie McIntosh, Koki Yamada, et al.
Pageof 5