Qian Lu

Changsha, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 9 publications

PKD1 Splice and PKD2 Nonsense Variants Identified in Two Chinese Families With Autosomal Dominant Polycystic Kidney Disease.

PKD1 Splice and PKD2 Nonsense Variants Identified in Two Chinese Families With Autosomal Dominant Polycystic Kidney Disease.

Journal: Nephrology (Carlton, Vic.)

Published: October 17, 2024

Identification of an ND4 Mutation in Leber Hereditary Optic Neuropathy.

Identification of an ND4 Mutation in Leber Hereditary Optic Neuropathy.

Journal: Optometry and vision science : official publication of the American Academy of Optometry

Published: November 09, 2017

SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease.

SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease.

Journal: Neuroscience letters

Published: May 19, 2016

Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2.

Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2.

Journal: Molecular pain

Published: April 13, 2016

Mutation analysis of the CHCHD2 gene in Chinese Han patients with Parkinson's disease.

Mutation analysis of the CHCHD2 gene in Chinese Han patients with Parkinson's disease.

Journal: Parkinsonism & related disorders

Published: January 13, 2016

Identification of a missense mutation in the tyrosinase gene in a Chinese family with oculocutaneous albinism type 1.

Identification of a missense mutation in the tyrosinase gene in a Chinese family with oculocutaneous albinism type 1.

Journal: Molecular medicine reports

Published: December 08, 2015

Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing.

Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing.

Journal: PloS one

Published: November 09, 2015

Tertiary-butylhydroquinone upregulates expression of ATP-binding cassette transporter A1 via nuclear factor E2-related factor 2/heme oxygenase-1 signaling in THP-1 macrophage-derived foam cells.

Tertiary-butylhydroquinone upregulates expression of ATP-binding cassette transporter A1 via nuclear factor E2-related factor 2/heme oxygenase-1 signaling in THP-1 macrophage-derived foam cells.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: June 07, 2013

Antagonism of betulinic acid on LPS-mediated inhibition of ABCA1 and cholesterol efflux through inhibiting nuclear factor-kappaB signaling pathway and miR-33 expression.

Antagonism of betulinic acid on LPS-mediated inhibition of ABCA1 and cholesterol efflux through inhibiting nuclear factor-kappaB signaling pathway and miR-33 expression.

Journal: PloS one

Published: March 08, 2013

Showing 1-9 of 9

Last Updated: 09/26/2026