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Reproductive Medicine and Biology
|
September 25, 2024
Compound heterozygous <i>KCTD19</i> variants in a man with isolated nonobstructive azoospermia
Yuki Muranishi, Yuko Katoh-Fukui, Atsushi Hattori, et al.
BMC Medical Genomics
|
May 30, 2019
Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells
Atsushi Hattori, Kohji Okamura, Yumiko Terada, et al.
Human Molecular Genetics
|
April 18, 2023
Chromosomal microdeletion leading to pituitary gigantism through hormone-gene overexpression
Yuko Katoh-Fukui, Atsushi Hattori, Ruogu Zhang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 30, 2007
Cadherin-8 is required for the first relay synapses to receive functional inputs from primary sensory afferents for cold sensation
Sachihiro C Suzuki, Hidemasa Furue, Kohei Koga, et al.
Human Genome Variation
|
March 14, 2018
An unclassified variant of <i>CHD7</i> activates a cryptic splice site in a patient with CHARGE syndrome
Yuko Katoh-Fukui, Shuichi Yatsuga, Hirohito Shima, et al.
Journal of the Endocrine Society
|
March 10, 2022
Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse
Yasuko Fujisawa, Hiroyuki Ono, Alu Konno, et al.
Development (Cambridge, England)
|
November 28, 2008
A critical time window of Sry action in gonadal sex determination in mice
Ryuji Hiramatsu, Shogo Matoba, Masami Kanai-Azuma, et al.
Bone
|
November 4, 2018
Mouse polycomb group gene Cbx2 promotes osteoblastic but suppresses adipogenic differentiation in postnatal long bones
Yuko Katoh-Fukui, Takashi Baba, Tetsuya Sato, et al.
European Journal of Medical Genetics
|
February 4, 2019
WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome
Akito Sutani, Hirohito Shima, Atsushi Hijikata, et al.
Human Genome Variation
|
September 7, 2025
DHX37 variants in patients with 46,XY disorders or differences of sex development
Yuko Katoh-Fukui, Daisuke Saito, Hiroko Narumi, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 5
Reproductive Medicine and Biology
|
September 25, 2024
Compound heterozygous <i>KCTD19</i> variants in a man with isolated nonobstructive azoospermia
Yuki Muranishi, Yuko Katoh-Fukui, Atsushi Hattori, et al.
BMC Medical Genomics
|
May 30, 2019
Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells
Atsushi Hattori, Kohji Okamura, Yumiko Terada, et al.
Human Molecular Genetics
|
April 18, 2023
Chromosomal microdeletion leading to pituitary gigantism through hormone-gene overexpression
Yuko Katoh-Fukui, Atsushi Hattori, Ruogu Zhang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 30, 2007
Cadherin-8 is required for the first relay synapses to receive functional inputs from primary sensory afferents for cold sensation
Sachihiro C Suzuki, Hidemasa Furue, Kohei Koga, et al.
Human Genome Variation
|
March 14, 2018
An unclassified variant of <i>CHD7</i> activates a cryptic splice site in a patient with CHARGE syndrome
Yuko Katoh-Fukui, Shuichi Yatsuga, Hirohito Shima, et al.
Journal of the Endocrine Society
|
March 10, 2022
Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse
Yasuko Fujisawa, Hiroyuki Ono, Alu Konno, et al.
Development (Cambridge, England)
|
November 28, 2008
A critical time window of Sry action in gonadal sex determination in mice
Ryuji Hiramatsu, Shogo Matoba, Masami Kanai-Azuma, et al.
Bone
|
November 4, 2018
Mouse polycomb group gene Cbx2 promotes osteoblastic but suppresses adipogenic differentiation in postnatal long bones
Yuko Katoh-Fukui, Takashi Baba, Tetsuya Sato, et al.
European Journal of Medical Genetics
|
February 4, 2019
WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome
Akito Sutani, Hirohito Shima, Atsushi Hijikata, et al.
Human Genome Variation
|
September 7, 2025
DHX37 variants in patients with 46,XY disorders or differences of sex development
Yuko Katoh-Fukui, Daisuke Saito, Hiroko Narumi, et al.
Page
of 5