Y. Qiu

YKL-40 siRNA downregulates the expression of eotaxin , IL-5 , GM-CSF in an epithelial cell model of asthma

Yi Wu, Wenhui Li, Yi Yang, 2016 .

Ovalbumin enhances YKL-40, IL-5, GM-CSF, and eotaxin expression simultaneously in primarily cultured mouse tracheal epithelial cells

Yi Wu, S. Ju, Juan Zhou, 2014, In Vitro Cellular & Developmental Biology - Animal.

Cerebral phaeohyphomycosis in an immunocompetent patient.

Su-Qin Ben, Xue-cheng Tong, Y. Qiu, 2020, Medecine et maladies infectieuses.

Compound Heterozygous Mutations in the DUOX2/DUOXA2 Genes Cause Congenital Hypothyroidism

Shao-Gang Ma, Y. Qiu, Man-Li Guo, 2017, Yonsei medical journal.

Two novel TSHR gene mutations (p.R528C and c.392+4del4) associated with congenital hypothyroidism

Shao-Gang Ma, Hong Liu, H. Yue, 2016, Endocrine research.

Novel genetic variants in the TPO gene cause congenital hypothyroidism

Shao-Gang Ma, Hong Zhu, Hong Liu, 2015, Scandinavian journal of clinical and laboratory investigation.

SEPT6_TRIM33 Gene Fusion and Mutated TP53 Pathway Associate With Unfavorable Prognosis in Patients With B-Cell Lymphomas

H. Fu, Hua-rong Zhou, Jianzhen Shen, 2021, Frontiers in Oncology.

Ovalbumin enhances YKL-40, IL-5, GM-CSF, and eotaxin expression simultaneously in primarily cultured mouse tracheal epithelial cells

Yi Wu, S. Ju, Juan Zhou, 2014, In Vitro Cellular & Developmental Biology - Animal.

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

Shao-Gang Ma, Y. Qiu, Man-Li Guo, 2016, Journal of clinical research in pediatric endocrinology.

[Bronchoalveolar lavage fluid was used to diagnose two cases of 2019-nCoV infection].

Y. Qiu, F. Tan, Z. Xu, 2020, Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases.

Mutational spectrum of phenylketonuria in Jiangsu province

Yu Liang, Jia Song, Dong-mei Sun, 2015, European Journal of Pediatrics.

Compound heterozygous mutations (p.T561M and c.2422delT) in the TPO gene associated with congenital hypothyroidism

Shao-Gang Ma, Y. Qiu, Man-Li Guo, 2016, Journal of pediatric endocrinology & metabolism : JPEM.