Yaqing Cao

No. 24 Fu Kang Road
Tianjin, 300192, China

Last Updated: 09/26/2026

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Found 13 publications

Functional analysis of 11 CYP21A2 variants reveals greater loss of enzyme activity in cis variants and improves genotype-phenotype correlation in 21-hydroxylase deficiency.

Functional analysis of 11 CYP21A2 variants reveals greater loss of enzyme activity in cis variants and improves genotype-phenotype correlation in 21-hydroxylase deficiency.

Journal: Journal of endocrinological investigation
Published: April 14, 2026

Novel CYP17A1 variants and functional validation in a large Chinese cohort of complete 17α-hydroxylase deficiency.

Novel CYP17A1 variants and functional validation in a large Chinese cohort of complete 17α-hydroxylase deficiency.

Journal: The Journal of clinical endocrinology and metabolism
Published: November 20, 2025

MYRF Variants in Patients With 46,XY Differences/Disorders of Sex Development and Literature Review.

MYRF Variants in Patients With 46,XY Differences/Disorders of Sex Development and Literature Review.

Journal: American journal of medical genetics. Part A
Published: October 09, 2024

Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency Detected by Long-Read Sequencing and Phenotypes Correlation.

Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency Detected by Long-Read Sequencing and Phenotypes Correlation.

Journal: The Journal of clinical endocrinology and metabolism
Published: September 04, 2024

Novel NUP160 mutations related to simultaneous congenital nephropathy and ovarian insufficiency.

Novel NUP160 mutations related to simultaneous congenital nephropathy and ovarian insufficiency.

Journal: Clinical kidney journal
Published: August 08, 2024

CYP17A1 Pathogenic Variants in 26 Chinese Patients With 17α-Hydroxylase Deficiency by Targeted Long-Read Sequencing.

CYP17A1 Pathogenic Variants in 26 Chinese Patients With 17α-Hydroxylase Deficiency by Targeted Long-Read Sequencing.

Journal: The Journal of clinical endocrinology and metabolism
Published: December 08, 2023

The genetic spectrum of a Chinese series of patients with 46, XY disorders of the sex development.

The genetic spectrum of a Chinese series of patients with 46, XY disorders of the sex development.

Journal: Andrology
Published: December 19, 2022

Corrigendum: Targeting Bcl-2 Proteins in Acute Myeloid Leukemia.

Corrigendum: Targeting Bcl-2 Proteins in Acute Myeloid Leukemia.

Journal: Frontiers in oncology
Published: November 24, 2020

Targeting Bcl-2 Proteins in Acute Myeloid Leukemia.

Targeting Bcl-2 Proteins in Acute Myeloid Leukemia.

Journal: Frontiers in oncology
Published: July 19, 2020

CD19 CAR-T cell treatment conferred sustained remission in B-ALL patients with minimal residual disease.

CD19 CAR-T cell treatment conferred sustained remission in B-ALL patients with minimal residual disease.

Journal: Cancer immunology, immunotherapy : CII
Published: April 20, 2020

Umbilical cord blood-derived mesenchymal stromal cells promote myeloid-derived suppressor cell proliferation by secreting HLA-G to reduce acute graft-versus-host disease after hematopoietic stem cell transplantation.

Umbilical cord blood-derived mesenchymal stromal cells promote myeloid-derived suppressor cell proliferation by secreting HLA-G to reduce acute graft-versus-host disease after hematopoietic stem cell transplantation.

Journal: Cytotherapy
Published: April 13, 2020

HLA-matched and HLA-haploidentical allogeneic CD19-directed chimeric antigen receptor T-cell infusions are feasible in relapsed or refractory B-cell acute lymphoblastic leukemia before hematopoietic stem cell transplantation.

HLA-matched and HLA-haploidentical allogeneic CD19-directed chimeric antigen receptor T-cell infusions are feasible in relapsed or refractory B-cell acute lymphoblastic leukemia before hematopoietic stem cell transplantation.

Journal: Leukemia
Published: May 15, 2019
Showing 1-12 of 13

Last Updated: 09/26/2026