Gerson S. Kobayashi

Sao Paulo, SP, Brazil

Last Updated: 09/26/2026

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Found 30 publications

Identifying biomarkers and trajectories of executive functions and language development in the first 3 years of life: Design, methods, and findings of the Germina cohort study.

Identifying biomarkers and trajectories of executive functions and language development in the first 3 years of life: Design, methods, and findings of the Germina cohort study.

Journal: Development and psychopathology
Published: March 05, 2025

"SHANK3 deficiency alters early progenitor dynamics and reveals shared pathways with neurodegeneration".

"SHANK3 deficiency alters early progenitor dynamics and reveals shared pathways with neurodegeneration".

Journal: Molecular psychiatry
Published: December 11, 2024

Van der Woude syndrome and amniotic band sequence: A clue to a common genetic etiology? A case report.

Van der Woude syndrome and amniotic band sequence: A clue to a common genetic etiology? A case report.

Journal: Genetics and molecular biology
Published: June 24, 2024

GJB2 c.35del variant up-regulates GJA1 gene expression and affects differentiation of human stem cells.

GJB2 c.35del variant up-regulates GJA1 gene expression and affects differentiation of human stem cells.

Journal: Genetics and molecular biology
Published: June 02, 2023

Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A).

Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A).

Journal: Stem cell research
Published: April 25, 2023

Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: Models for Xia-Gibbs syndrome.

Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: Models for Xia-Gibbs syndrome.

Journal: Gene
Published: December 12, 2022

mir152 hypomethylation as a mechanism for non-syndromic cleft lip and palate.

mir152 hypomethylation as a mechanism for non-syndromic cleft lip and palate.

Journal: Epigenetics
Published: September 01, 2022

DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ.

DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ.

Journal: Biochimica et biophysica acta. Gene regulatory mechanisms
Published: August 05, 2022

Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene-environment interaction.

Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene-environment interaction.

Journal: Nature communications
Published: August 03, 2022

Modeling Early Neural Crest Development via Induction from hiPSC-Derived Neural Plate Border-like Cells.

Modeling Early Neural Crest Development via Induction from hiPSC-Derived Neural Plate Border-like Cells.

Journal: Methods in molecular biology (Clifton, N.J.)
Published: March 31, 2022

Neuroprogenitor Cells From Patients With TBCK Encephalopathy Suggest Deregulation of Early Secretory Vesicle Transport.

Neuroprogenitor Cells From Patients With TBCK Encephalopathy Suggest Deregulation of Early Secretory Vesicle Transport.

Journal: Frontiers in cellular neuroscience
Published: October 27, 2021

A Novel Saliva RT-LAMP Workflow for Rapid Identification of COVID-19 Cases and Restraining Viral Spread.

A Novel Saliva RT-LAMP Workflow for Rapid Identification of COVID-19 Cases and Restraining Viral Spread.

Journal: Diagnostics (Basel, Switzerland)
Published: June 08, 2021
Showing 1-12 of 30

Last Updated: 09/26/2026