Segui
Desheng Liang
Desheng Liang
State Key Laboratory of Medical Genetics, Central South University
Email verificata su sklmg.edu.cn - Home page
Titolo
Citata da
Citata da
Anno
A SNP in the ABCC11 gene is the determinant of human earwax type
K Yoshiura, A Kinoshita, T Ishida, A Ninokata, T Ishikawa, T Kaname, ...
Nature genetics 38 (3), 324-330, 2006
3502006
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes
D Liang, DS Cram, HU Tan, S Linpeng, Y Liu, H Sun, Y Zhang, F Tian, ...
Genetics in Medicine 21 (9), 1998-2006, 2019
2012019
Pregnancy-related complications and adverse pregnancy outcomes in multiple pregnancies resulting from assisted reproductive technology: a meta-analysis of cohort studies
J Qin, H Wang, X Sheng, D Liang, H Tan, J Xia
Fertility and sterility 103 (6), 1492-1508. e7, 2015
1732015
Non‐invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing
D Liang, W Lv, H Wang, L Xu, J Liu, H Li, L Hu, Y Peng, L Wu
Prenatal diagnosis 33 (5), 409-415, 2013
1672013
Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes
D Liang, Y Peng, W Lv, L Deng, Y Zhang, H Li, P Yang, J Zhang, Z Song, ...
The Journal of Molecular Diagnostics 16 (5), 519-526, 2014
1362014
Common genetic variants on 1p13. 2 associate with risk of autism
K Xia, H Guo, Z Hu, G Xun, L Zuo, Y Peng, K Wang, Y He, Z Xiong, L Sun, ...
Molecular psychiatry 19 (11), 1212-1219, 2014
1132014
MicroRNAs expression in ox-LDL treated HUVECs: MiR-365 modulates apoptosis and Bcl-2 expression
B Qin, B Xiao, D Liang, J Xia, Y Li, H Yang
Biochemical and biophysical research communications 410 (1), 127-133, 2011
1112011
Assisted reproductive technology and risk of congenital malformations: a meta-analysis based on cohort studies
J Qin, X Sheng, H Wang, D Liang, H Tan, J Xia
Archives of gynecology and obstetrics 292, 777-798, 2015
1102015
Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART)
W Lv, X Wei, R Guo, Q Liu, Y Zheng, J Chang, T Bai, H Li, J Zhang, ...
Clinical Chemistry 61 (1), 172-181, 2015
1082015
SNP Cutter: a comprehensive tool for SNP PCR–RFLP assay design
R Zhang, Z Zhu, H Zhu, T Nguyen, F Yao, K Xia, D Liang, C Liu
Nucleic acids research 33 (suppl_2), W489-W492, 2005
882005
Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific …
M Zhou, Z Hu, L Qiu, T Zhou, M Feng, Q Hu, B Zeng, Z Li, Q Sun, Y Wu, ...
Human gene therapy 29 (11), 1252-1263, 2018
632018
MicroRNA let-7c inhibits Bcl-xl expression and regulates ox-LDL-induced endothelial apoptosis
B Qin, B Xiao, D Liang, Y Li, T Jiang, H Yang
BMB reports 45 (8), 464-469, 2012
632012
XRCC2 mutation causes meiotic arrest, azoospermia and infertility
Y Yang, J Guo, L Dai, Y Zhu, H Hu, L Tan, W Chen, D Liang, J He, M Tu, ...
Journal of medical genetics 55 (9), 628-636, 2018
612018
Mutation in PITX2 is associated with ring dermoid of the cornea
K Xia, L Wu, X Liu, X Xi, D Liang, D Zheng, F Cai, Q Pan, Z Long, H Dai, ...
Journal of medical genetics 41 (12), e129-e129, 2004
592004
In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCs
Y Wu, Z Hu, Z Li, J Pang, M Feng, X Hu, X Wang, S Lin-Peng, B Liu, ...
Scientific reports 6 (1), 18865, 2016
572016
TALE nickase mediates high efficient targeted transgene integration at the human multi-copy ribosomal DNA locus
Y Wu, T Gao, X Wang, Y Hu, X Hu, Z Hu, J Pang, Z Li, J Xue, M Feng, ...
Biochemical and biophysical research communications 446 (1), 261-266, 2014
562014
Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum
H Hu, L Wu, Y Feng, Q Pan, Z Long, J Li, H Dai, K Xia, D Liang, N Niikawa, ...
Journal of Human Genetics 52 (6), 492-497, 2007
552007
DMD mutation spectrum analysis in 613 Chinese patients with dystrophinopathy
R Guo, G Zhu, H Zhu, R Ma, Y Peng, D Liang, L Wu
Journal of human genetics 60 (8), 435-442, 2015
542015
A novel de novo POGZ mutation in a patient with intellectual disability
BO Tan, Y Zou, Y Zhang, R Zhang, J Ou, Y Shen, J Zhao, X Luo, J Guo, ...
Journal of human genetics 61 (4), 357-359, 2016
502016
A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemia
L Kang, Y Liu, M Shen, YI Liu, R He, J Song, Y Jin, M Li, Y Zhang, H Dong, ...
Journal of inherited metabolic disease 43 (3), 409-423, 2020
482020
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