Cagrı Gulec

Istanbul, Turkey

Last Updated: 09/26/2026

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Found 13 publications

Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinism.

Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinism.

Journal: Endocrine

Published: September 11, 2024

Methylation of the ESR1 promoters in visceral adipose tissue and its relationship with obesity.

Methylation of the ESR1 promoters in visceral adipose tissue and its relationship with obesity.

Journal: Molecular biology reports

Published: September 02, 2024

Investigation of oral health findings and genotype correlations in osteogenesis imperfecta.

Investigation of oral health findings and genotype correlations in osteogenesis imperfecta.

Journal: Odontology

Published: August 03, 2024

A Novel RNPC3 Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy.

A Novel RNPC3 Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy.

Journal: Hormone research in paediatrics

Published: February 24, 2023

Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants.

Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants.

Journal: Bone

Published: September 14, 2021

Antenatal diagnostic dilemma in a pseudodominant pedigree with lamin-B receptor (LBR)-related regressive spondylometaphyseal dysplasia.

Antenatal diagnostic dilemma in a pseudodominant pedigree with lamin-B receptor (LBR)-related regressive spondylometaphyseal dysplasia.

Journal: American journal of medical genetics. Part A

Published: January 22, 2021

LEF1 Induces DHRS2 Gene Expression in Human Acute Leukemia Jurkat T-Cells

LEF1 Induces DHRS2 Gene Expression in Human Acute Leukemia Jurkat T-Cells

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: June 27, 2020

Precocious or early puberty in patients with combined pituitary hormone deficiency due to POU1F1 gene mutation: case report and review of possible mechanisms.

Precocious or early puberty in patients with combined pituitary hormone deficiency due to POU1F1 gene mutation: case report and review of possible mechanisms.

Journal: Hormones (Athens, Greece)

Published: July 12, 2018

Role of simvastatin and RORα activity in the macrophage apoptotic pathway.

Role of simvastatin and RORα activity in the macrophage apoptotic pathway.

Journal: Anatolian journal of cardiology

Published: June 15, 2017

Low dose monoethyl phthalate (MEP) exposure triggers proliferation by activating PDX-1 at 1.1B4 human pancreatic beta cells.

Low dose monoethyl phthalate (MEP) exposure triggers proliferation by activating PDX-1 at 1.1B4 human pancreatic beta cells.

Journal: Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association

Published: March 19, 2016

High MN1 expression increases the in vitro clonogenic activity of primary mouse B-cells.

High MN1 expression increases the in vitro clonogenic activity of primary mouse B-cells.

Journal: Leukemia research

Published: December 05, 2014

Association between non-coding polymorphisms of HOPX gene and syncope in hypertrophic cardiomyopathy.

Association between non-coding polymorphisms of HOPX gene and syncope in hypertrophic cardiomyopathy.

Journal: Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology

Published: July 19, 2014

Showing 1-12 of 13

Last Updated: 09/26/2026