Kyungjo Jeong

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 8 publications

Integrated mutational landscape analysis of poorly differentiated high-grade neuroendocrine carcinoma of the uterine cervix.

Integrated mutational landscape analysis of poorly differentiated high-grade neuroendocrine carcinoma of the uterine cervix.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 16, 2024

Baseline characteristics of the Korean genetic cohort of inherited cystic kidney disease.

Baseline characteristics of the Korean genetic cohort of inherited cystic kidney disease.

Journal: Kidney research and clinical practice
Published: April 15, 2023

Factors Associated With the Development and Severity of Polycystic Liver in Patients With Autosomal Dominant Polycystic Kidney Disease.

Factors Associated With the Development and Severity of Polycystic Liver in Patients With Autosomal Dominant Polycystic Kidney Disease.

Journal: Journal of Korean medical science
Published: March 17, 2023

FAM120A couples SREBP-dependent transcription and splicing of lipogenesis enzymes downstream of mTORC1.

FAM120A couples SREBP-dependent transcription and splicing of lipogenesis enzymes downstream of mTORC1.

Journal: Molecular cell
Published: July 28, 2022

Homologous recombination deficiency (HRD) signature-3 in ovarian and uterine carcinosarcomas correlates with preclinical sensitivity to Olaparib, a poly (adenosine diphosphate [ADP]- ribose) polymerase (PARP) inhibitor.

Homologous recombination deficiency (HRD) signature-3 in ovarian and uterine carcinosarcomas correlates with preclinical sensitivity to Olaparib, a poly (adenosine diphosphate [ADP]- ribose) polymerase (PARP) inhibitor.

Journal: Gynecologic oncology
Published: March 04, 2022

Integrated mutational landscape analysis of uterine leiomyosarcomas.

Integrated mutational landscape analysis of uterine leiomyosarcomas.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 20, 2021

Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice.

Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice.

Journal: Frontiers in cell and developmental biology
Published: February 01, 2021

Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study.

Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study.

Journal: BMC nephrology
Published: November 27, 2020
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Last Updated: 09/26/2026