Jie Qing - Publications

Dexmedetomidine alleviates myocardial ischemia-reperfusion injury by down-regulating miR-34b-3p to activate the Jagged1/Notch signaling pathway.

Journal: International immunopharmacology

Published: November 23, 2022

Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice.

Journal: Frontiers of medicine

Published: November 15, 2022

Salvianolic acid B alleviates comorbid pain in depression induced by chronic restraint stress through inhibiting GABAergic neuron excitation via an ERK-CREB-BDNF axis-dependent mechanism.

Journal: Journal of psychiatric research

Published: August 29, 2021

Lung adenocarcinoma misdiagnosed as IgG4-related lung disease: A case report and literature review.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: August 12, 2021

Case Report: Identification of a Novel ODAD3 Variant in a Patient With Primary Ciliary Dyskinesia.

Journal: Frontiers in genetics

Published: January 12, 2021

Blood and Bronchoalveolar Lavage Fluid Metagenomic Next-Generation Sequencing in Pneumonia.

Journal: The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale

Published: February 29, 2020

Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach.

Journal: PloS one

Published: August 02, 2016

The role of transcription factors of neurosensory cells in non-syndromic sensorineural hearing loss with or without inner ear malformation.

Journal: Acta oto-laryngologica

Published: December 05, 2015

Posterior spinal transpedicular wedge osteotomy for kyphosis due to delayed osteoporotic vertebral fracture in elderly

Journal: Zhongguo gu shang = China journal of orthopaedics and traumatology

Published: October 28, 2015

The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.

Journal: Genetic testing and molecular biomarkers

Published: July 18, 2015

Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.

Journal: Genetic testing and molecular biomarkers

Published: December 11, 2014

Mutation screening in taperin gene in Chinese with prelingual nonsyndromic hearing impairment

Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery

Published: August 19, 2014