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Guocan Yang
Observed names:
G J Yang,
G Yang,
GUO-CAN YANG,
Guo-Can YANG,
Guo-Can Yang,
Guo-can Yang,
Guo‐Can Yang
show all 7
Institution:
Shaoxing People's Hospital
Observed institutions:
Shaoxing University,
Chinese Academy of Medical Sciences & Peking Union Medical College,
Cancer Hospital of Chinese Academy of Medical Sciences,
Shaoxing People's Hospital,
Zhejiang University
ORCID:
0000-0001-8513-876X
Observed ORCID:
0000-0001-8513-876X
OpenAlex ID:
A5110668168
Function and Role of Regulatory T Cells in Rheumatoid Arthritis
2021
·
Qi Jiang
, Guocan Yang
, et al.
·
Frontiers in Immunology
·
257
PDF
Role of Th22 Cells in the Pathogenesis of Autoimmune Diseases
2021
·
Qi Jiang
, Guocan Yang
, et al.
·
Frontiers in Immunology
·
146
PDF
Inflammasome and Its Therapeutic Targeting in Rheumatoid Arthritis
2022
·
Qi Jiang
, Xin Wang
, et al.
·
Frontiers in Immunology
·
55
PDF
Exosomes as Crucial Players in Pathogenesis of Systemic Lupus Erythematosus
2022
·
Yue Fei
, Qi Liu
, et al.
·
Journal of Immunology Research
·
21
PDF
Inflammasomes in rheumatoid arthritis: a pilot study
2023
·
Qi Jiang
, Xin Wang
, et al.
·
BMC Rheumatology
·
19
PDF
Association between rs4938723 functional polymorphism in the promoter region of miR-34b/c gene and cancer risk
2014
·
Qi Liu
, Guocan Yang
, et al.
·
Clinics and Research in Hepatology and Gastroenterology
·
8
Mitochondrial A3243G mutation causes mitochondrial encephalomyopathy in a Chinese patient
2019
·
Xiao-Qun Liu
, Shao-Qing Shen
, et al.
·
Medicine
·
5
Mitochondrial COI/tRNASer(UCN) G7444A mutation may be associated with aminoglycoside-induced and non-syndromic hearing impairment
2012
·
QI LIU
, PING LIU
, et al.
·
Molecular Medicine Reports
·
5
PDF
[The research status and development trend of EGFR gene exon 20 insertion mutant non-small cell lung cancer].
2020
·
G J Yang
, Y Wang
·
PubMed
·
3
A novel compound heterozygous mutation of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome
2019
·
Xin Wang
, Yu Ding
, et al.
·
Endocrine
·
3
A Novel Mutation in the Myosin Binding Protein C Gene in a Prader-Willi Syndrome Pedigree
2021
·
Xiao-qun Liu
, Man Luo
, et al.
·
Reproductive Sciences
·
2
One single-tube PCR assay to detect both CD17 (A>T) and IVS-II nt-654 (C>T) homozygous mutations of β-thalassemia
2013
·
Qi LIU
, Jun-Li WANG
, et al.
·
TURKISH JOURNAL OF MEDICAL SCIENCES
·
2
PDF
Identification of a novel mutation in the BMPR2 gene in a pulmonary arterial hypertension patient using next‐generation sequencing
2021
·
Xiao Xu
, Xin Wang
, et al.
·
Journal of Clinical Laboratory Analysis
[The role of P53 gene in the development of oral squamous cell carcinoma: study of P53 gene mutation by silver staining polymerase chain reaction-single strand conformation polymorphism].
1996
·
Q Chen
, J Fu
, et al.
·
PubMed
[Detection of point mutation of p53 gene by silver staining PCR-SSCP in paraffin-embedded malignant fibrous histiocytoma].
1996
·
J Li
, G Yang
, et al.
·
PubMed
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Works count:
15
Citation count:
526
H-index:
6
I10-index:
5
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