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Katoh-Fukui, Yuko
182  results:
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1

Systematic molecular analyses for 115 karyotypically normal..:

Muranishi, Yuki ; Kobori, Yoshitomo ; Katoh-Fukui, Yuko...
Human Reproduction.  39 (2024)  5 - p. 1131-1140 , 2024
Link: https://doi.org/10.1093/..
 
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2

PTPN11 and FLNAvariants in a boy with ambiguous genitalia, ..:

Muranishi, Yuki ; Itonaga, Tomoyo ; Ihara, Kenji...
Clinical Pediatric Endocrinology.  33 (2024)  3 - p. 169-173 , 2024
Link: https://doi.org/10.1297/..
 
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3

Expression levels and DNA methylation profiles of the growt..:

Hattori, Atsushi ; Seki, Atsuhito ; Inaba, Naoto...
Scientific Reports.  14 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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4

FRI307 Gigantism Due To Transcriptional Activation Of GHRH:..:

Hattori, Atsushi ; Katoh-Fukui, Yuko ; Zhang, Ruogu...
Journal of the Endocrine Society.  7 (2023)  Supplement_1 - p. , 2023
Link: https://doi.org/10.1210/..
 
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5

Chromosomal microdeletion leading to pituitary gigantism th..:

Katoh-Fukui, Yuko ; Hattori, Atsushi ; Zhang, Ruogu...
Human Molecular Genetics.  32 (2023)  14 - p. 2318-2325 , 2023
Link: https://doi.org/10.1093/..
 
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6

Intrauterine Hyponutrition Reduces Fetal Testosterone Produ..:

Fujisawa, Yasuko ; Ono, Hiroyuki ; Konno, Alu...
Journal of the Endocrine Society.  6 (2022)  4 - p. , 2022
Link: https://doi.org/10.1210/..
 
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7

POU1F1/Pou1f1 c.143-83A > G Variant Disrupts the Branch ..:

Akiba, Kazuhisa ; Hasegawa, Yukihiro ; Katoh-Fukui, Yuko...
Endocrinology.  164 (2022)  2 - p. , 2022
Link: https://doi.org/10.1210/..
 
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8

NDNF variants are rare in patients with congenital hypogona..:

Tamaoka, Satoshi ; Suzuki, Erina ; Hattori, Atsushi...
Human Genome Variation.  8 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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9

Role of Liquid–Liquid Separation in Endocrine and Living Ce..:

Akiba, Kazuhisa ; Katoh-Fukui, Yuko ; Yoshida, Kei...
Journal of the Endocrine Society.  5 (2021)  10 - p. , 2021
Link: https://doi.org/10.1210/..
 
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10

WDR11 is another causative gene for coloboma, cardiac anoma..:

Sutani, Akito ; Shima, Hirohito ; Hijikata, Atsushi...
European Journal of Medical Genetics.  63 (2020)  1 - p. 103626 , 2020
Link: https://doi.org/10.1016/..
 
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11

Mouse polycomb group gene Cbx2 promotes osteoblastic but su..:

Katoh-Fukui, Yuko ; Baba, Takashi ; Sato, Tetsuya...
Bone.  120 (2019)  - p. 219-231 , 2019
Link: https://doi.org/10.1016/..
 
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12

MYRF haploinsufficiency causes 46,XY and 46,XX disorders of..:

Hamanaka, Kohei ; Takata, Atsushi ; Uchiyama, Yuri...
Human Molecular Genetics.  28 (2019)  14 - p. 2319-2329 , 2019
Link: https://doi.org/10.1093/..
 
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13

Transient multifocal genomic crisis creating chromothriptic..:

Hattori, Atsushi ; Okamura, Kohji ; Terada, Yumiko...
BMC Medical Genomics.  12 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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14

An unclassified variant of CHD7 activates a cryptic splice ..:

Katoh-Fukui, Yuko ; Yatsuga, Shuichi ; Shima, Hirohito...
Human Genome Variation.  5 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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15

Next generation sequencing-based mutation screening of 86 p..:

Hattori, Atsushi ; Katoh-Fukui, Yuko ; Nakamura, Akie...
Endocrine Journal.  64 (2017)  10 - p. 947-954 , 2017
Link: https://doi.org/10.1507/..
 
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