Sayaka Ohta
Tokyo, Japan
Last Updated: 09/26/2026
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Found 10 publications
Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2.
Journal: Stem cell research
Published: February 25, 2021
Whole genome sequencing of 45 Japanese patients with intellectual disability.
Journal: American journal of medical genetics. Part A
Published: September 28, 2020
Activin/Nodal/TGF-β Pathway Inhibitor Accelerates BMP4-Induced Cochlear Gap Junction Formation During in vitro Differentiation of Embryonic Stem Cells.
Journal: Frontiers in cell and developmental biology
Published: September 02, 2020
Modeling gap junction beta 2 gene-related deafness with human iPSC.
Journal: Human molecular genetics
Published: August 21, 2020
Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss.
Journal: Stem cell research
Published: March 19, 2020
Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation.
Journal: Stem cell research
Published: October 04, 2019
A Japanese patient with RAD51-associated Fanconi anemia.
Journal: American journal of medical genetics. Part A
Published: November 26, 2018
Partial monosomy of 10p and duplication of another chromosome in two patients.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: November 28, 2015
Nationwide survey of Cockayne syndrome in Japan: Incidence, clinical course and prognosis.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: October 14, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026