Karine Triboult-Giraud

Corbeil-essonnes, France

Last Updated: 09/26/2026

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Found 18 publications

Generation and characterization of three human induced pluripotent stem cell lines from patients with Duchenne muscular dystrophy.

Generation and characterization of three human induced pluripotent stem cell lines from patients with Duchenne muscular dystrophy.

Journal: Stem cell research
Published: April 02, 2026

Generation of two iPSC lines each carrying a stop codon mutation, c.366T > A (p.Y122X) and c.1657C > T (p.R553X), in the CFTR gene from the parental line PCIi033-A using CRISPR/Cas9.

Generation of two iPSC lines each carrying a stop codon mutation, c.366T > A (p.Y122X) and c.1657C > T (p.R553X), in the CFTR gene from the parental line PCIi033-A using CRISPR/Cas9.

Journal: Stem cell research
Published: March 18, 2026

Generation of two iPSC lines carrying two cystic fibrosis rare intronic mutations c.1585-1G>A and c.1680-886A>G in the CFTR gene of the parental line PCIi033-A using CRISPR/Cas tools.

Generation of two iPSC lines carrying two cystic fibrosis rare intronic mutations c.1585-1G>A and c.1680-886A>G in the CFTR gene of the parental line PCIi033-A using CRISPR/Cas tools.

Journal: Stem cell research
Published: March 18, 2026

Generation of six hiPSC lines from patients with WDR45-related neurodegenerative disease (Beta-propeller Protein-Associated Neurodegeneration, BPAN).

Generation of six hiPSC lines from patients with WDR45-related neurodegenerative disease (Beta-propeller Protein-Associated Neurodegeneration, BPAN).

Journal: Stem cell research
Published: February 17, 2026

Generation and characterization of two human induced pluripotent stem cell lines from patients with Danon disease.

Generation and characterization of two human induced pluripotent stem cell lines from patients with Danon disease.

Journal: Stem cell research
Published: February 06, 2026

CRISPR-Cas9 genome editing in the parental iPSC line PCIi033-A to introduce the homozygous mutation p.F508del (c.1521_1523del) in the CFTR gene.

CRISPR-Cas9 genome editing in the parental iPSC line PCIi033-A to introduce the homozygous mutation p.F508del (c.1521_1523del) in the CFTR gene.

Journal: Stem cell research
Published: October 07, 2025

Knock-out of specific DMD gene isoforms in the parental hESC line SA001 using CRISPR/Cas9.

Knock-out of specific DMD gene isoforms in the parental hESC line SA001 using CRISPR/Cas9.

Journal: Stem cell research
Published: August 12, 2025

Generation and characterization of three human induced pluripotent stem cell lines from patients with glycogen storage disease type II.

Generation and characterization of three human induced pluripotent stem cell lines from patients with glycogen storage disease type II.

Journal: Stem cell research
Published: June 24, 2025

Generation of three iPSC lines from patients with CACNA1S related congenital myopathy.

Generation of three iPSC lines from patients with CACNA1S related congenital myopathy.

Journal: Stem cell research
Published: February 21, 2025

Establishment of heterozygous and homozygous SHANK3 knockout clonal pluripotent stem cells from the parental hESC line SA001 using CRISPR/Cas9.

Establishment of heterozygous and homozygous SHANK3 knockout clonal pluripotent stem cells from the parental hESC line SA001 using CRISPR/Cas9.

Journal: Stem cell research
Published: May 09, 2023

CRISPR/Cas9-mediated generation of human embryonic stem cell sub-lines with HPRT1 gene knockout to model Lesch Nyhan disease.

CRISPR/Cas9-mediated generation of human embryonic stem cell sub-lines with HPRT1 gene knockout to model Lesch Nyhan disease.

Journal: Stem cell research
Published: May 04, 2023

Pathological modeling of glycogen storage disease type III with CRISPR/Cas9 edited human pluripotent stem cells.

Pathological modeling of glycogen storage disease type III with CRISPR/Cas9 edited human pluripotent stem cells.

Journal: Frontiers in cell and developmental biology
Published: February 10, 2023
Showing 1-12 of 18

Last Updated: 09/26/2026