about
Prognostic value of serum nicotinamide phosphoribosyltransferase in patients with bladder cancer.Polymorphisms and plasma levels of IL-27: impact on genetic susceptibility and clinical outcome of bladder cancer.A Functional Polymorphism in the Promoter of MiR-143/145 Is Associated With the Risk of Cervical Squamous Cell Carcinoma in Chinese Women: A Case-Control Study.Pri-Mir-34b/C and Tp-53 Polymorphisms are Associated With The Susceptibility of Papillary Thyroid Carcinoma: A Case-Control Study.Association Between Genetic Polymorphisms in the Promoter Regions of Let-7 and Risk of Papillary Thyroid Carcinoma: A Case-Control StudyA polymorphism rs4705341 in the flanking region of miR-143/145 predicts risk and prognosis of colorectal cancer.Association between polymorphisms in IL-27 gene and pre-eclampsia.Genetic variants in NAMPT predict bladder cancer risk and prognosis in individuals from southwest Chinese Han group.Association of an insertion/deletion polymorphism in IL1A 3'-UTR with risk for cervical carcinoma in Chinese Han Women.The variations in the IL1RL1 gene and susceptibility to preeclampsia.Fatal liver cyst rupture in polycystic liver disease complicated with autosomal dominant polycystic kidney disease: A case report.Genetic association of polymorphisms in AXIN1 gene with clear cell renal cell carcinoma in a Chinese population.Genetic Association of Interleukin-31 Gene Polymorphisms with Epithelial Ovarian Cancer in Chinese Population.Association of genetic variations in RTN4 3'-UTR with risk for clear cell renal cell carcinoma.Association between IL-27 gene polymorphisms and risk of papillary thyroid carcinoma.Association between polymorphisms in IL21 gene and risk for sepsis.Combined analysis of pri-miR-34b/c rs4938723 and TP53 Arg72Pro with cervical cancer risk.Association between polymorphisms in IL27 gene and renal cell carcinoma.Association between polymorphisms in AXIN1 gene and atrial septal defect.Associations of TIM-1 Genetic Polymorphisms with Asthma: A Meta-analysis.The variations in the AXIN1 gene and susceptibility to cryptorchidism.Genome-wide association study identifies loci and candidate genes for non-idiopathic pulmonary hypertension in Eastern Chinese Han populationAssociation between a Single Nucleotide Polymorphism in the 3'-UTR of and the Risk of Nonidiopathic Pulmonary Arterial Hypertension in Chinese PopulationIdentifying novel microhaplotypes for ancestry inferenceAssociation between two single nucleotide polymorphisms of interleukin-27 gene and increased cryptorchidism riskInsertion/deletion polymorphism inIL1A3′-UTR is associated with susceptibility to endometrial cancer in Chinese Han womenAn insertion–deletion polymorphism ininterleukin-1αgene associated with susceptibility to preeclampsiaAssociation between a functional insertion/deletion polymorphism in IL1A gene and risk of papillary thyroid carcinomaAssociation between a functional polymorphism rs712 within let-7-binding site and risk of papillary thyroid cancerEvaluation of the microhaplotype markers in kinship analysis
P50
Q34492819-5251C1D1-DE37-493D-B5D9-B69D892D1950Q35654119-06743F1F-A15C-4694-87D0-17ECE98309B7Q36194694-A7D31092-241E-41DC-AF53-6C2E1B5BDBF2Q36255905-B194E39D-71EF-4D0B-A2C1-2CE49D71440AQ37176320-8E5BD17D-0919-485B-B249-380A4C4D3207Q37641734-7D7007BA-8A5D-418F-8AD4-80931F2084DBQ40225405-A4A20BDA-363B-430F-B1F4-4DFA0446DA14Q43794221-35A310AC-911A-42C6-92AC-69628DE80E16Q44728369-F248B081-DA79-4797-A5F0-E640477F4CC2Q46317388-06915C02-109C-4290-A8D0-C4AC632BA799Q47625769-908CB6DC-71F9-48D1-A858-FE334C1067EDQ50101417-75FE70CE-95F6-4291-9968-D08A25EDA73DQ50351497-E8EB3E7D-AB5B-4CAB-A1EB-DCAC3D98925DQ50540987-CE064485-9C36-4C49-B77C-FC01C6E13992Q51279715-6733235E-3A5A-4EDE-8D3D-7E347778A9E4Q51705602-C0B1BF66-F89C-4C49-A02B-53B7AA4D9116Q52899617-28DEA599-8B23-470E-BF26-B8DD68E94191Q53216723-8499FF81-6DC6-4701-9907-1C5778B79323Q54186984-6DAFB2CB-7A4B-4B08-A824-D74BE89D6C05Q54401556-D9BF5EDD-BDC8-458F-AA0B-3A74CDB970C6Q55058962-B6525016-B3A8-4F2A-AE79-7F04C5C2D49AQ57021251-072EDDDA-9841-48BA-9FFA-6DC51E36D3D6Q58567359-E4C666FD-29E1-49E5-B297-BFDD25E73EEAQ58856502-EA1FAB64-CD90-428B-A0E4-63ADB477F385Q58856526-FF5B8848-C31B-4BBF-BFB3-9F617D0BE9C5Q58856534-B4718B91-53E7-4DB0-A885-6851DEBEA3A5Q58856548-4F5E9F61-F679-4920-AE96-34112C0EC997Q58856552-A4033BB1-FC66-4F52-8B0A-92E8C355E88CQ58856556-925943A0-07CF-4DF5-8BBC-130649E17D6DQ90585115-0C23976B-975B-4B82-AAEF-C7086A0D8001
P50
description
researcher ORCID: 0000-0001-8462-2875
@en
name
Peng Chen
@ast
Peng Chen
@en
Peng Chen
@es
Peng Chen
@nl
type
label
Peng Chen
@ast
Peng Chen
@en
Peng Chen
@es
Peng Chen
@nl
prefLabel
Peng Chen
@ast
Peng Chen
@en
Peng Chen
@es
Peng Chen
@nl
P106
P1153
57199131947
P31
P496
0000-0001-8462-2875