Chutima Chanprasert

Bangkok, Thailand

Last Updated: 09/26/2026

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Found 9 publications

An induced pluripotent stem cell line (MUSIi019-A) generated from a patient with distal renal tubular acidosis carrying a compound heterozygous mutation in solute carrier family 4 member 1 (SLC4A1) gene.

An induced pluripotent stem cell line (MUSIi019-A) generated from a patient with distal renal tubular acidosis carrying a compound heterozygous mutation in solute carrier family 4 member 1 (SLC4A1) gene.

Journal: Stem cell research

Published: December 15, 2022

Generation of an induced pluripotent stem cell line (MUSIi015-A) from a diabetic patient carrying mutations in ZYG11A (p.L475P) and GATA6 (p.E51K).

Generation of an induced pluripotent stem cell line (MUSIi015-A) from a diabetic patient carrying mutations in ZYG11A (p.L475P) and GATA6 (p.E51K).

Journal: Stem cell research

Published: August 19, 2021

Generation of an induced pluripotent stem cell line (MUSIi014-A) from an affected member of a family with autosomal dominant diabetes carrying p.L475P mutation in ZYG11A gene associated with a cell cycle arrest in beta-cell.

Generation of an induced pluripotent stem cell line (MUSIi014-A) from an affected member of a family with autosomal dominant diabetes carrying p.L475P mutation in ZYG11A gene associated with a cell cycle arrest in beta-cell.

Journal: Stem cell research

Published: August 18, 2021

Vitamin D pathway gene polymorphisms, vitamin D level, and cytokines in children with type 1 diabetes.

Vitamin D pathway gene polymorphisms, vitamin D level, and cytokines in children with type 1 diabetes.

Journal: Gene

Published: January 07, 2021

Autosomal dominant diabetes associated with a novel ZYG11A mutation resulting in cell cycle arrest in beta-cells.

Autosomal dominant diabetes associated with a novel ZYG11A mutation resulting in cell cycle arrest in beta-cells.

Journal: Molecular and cellular endocrinology

Published: September 18, 2020

Defective functions of HNF1A variants on BCL2L1 transactivation and beta-cell growth.

Defective functions of HNF1A variants on BCL2L1 transactivation and beta-cell growth.

Journal: Biochemical and biophysical research communications

Published: May 08, 2020

DNAJC3 mutation in Thai familial type 2 diabetes mellitus.

DNAJC3 mutation in Thai familial type 2 diabetes mellitus.

Journal: International journal of molecular medicine

Published: December 01, 2017

Impact of KCNQ1, CDKN2A/2B, CDKAL1, HHEX, MTNR1B, SLC30A8, TCF7L2, and UBE2E2 on risk of developing type 2 diabetes in Thai population.

Impact of KCNQ1, CDKN2A/2B, CDKAL1, HHEX, MTNR1B, SLC30A8, TCF7L2, and UBE2E2 on risk of developing type 2 diabetes in Thai population.

Journal: BMC medical genetics

Published: August 07, 2017

Loss-of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes.

Loss-of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes.

Journal: Diabetes

Published: July 12, 2017

Showing 1-9 of 9

Last Updated: 09/26/2026