Li Jin - Publications

Affiliations: 
School of Life Sciences, Fudan University 

64 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Yang X, Zhang X, Jiao J, Zhang F, Pan Y, Wang Q, Chen Q, Cai B, Tang S, Zhou Z, Chen S, Yin H, Fu W, Luo Y, Li D, ... ... Jin L, et al. Rare variants in FANCA induce premature ovarian insufficiency. Human Genetics. PMID 31535215 DOI: 10.1007/s00439-019-02059-9  0.44
2019 Shi X, Liu Q, Zhao H, Lu J, Huang Y, Ma Y, Xia J, Liu M, Tu W, Jin L, Wang J, Zhao Y, Wu W. Increased expression of GAB1 promotes inflammation and fibrosis in systemic sclerosis. Experimental Dermatology. PMID 31505074 DOI: 10.1111/exd.14033  0.44
2019 Li W, Wu H, Li F, Tian S, Kherraf ZE, Zhang J, Ni X, Lv M, Liu C, Tan Q, Shen Y, Amiri-Yekta A, Cazin C, Zhang J, Liu W, ... ... Jin L, et al. Biallelic mutations in cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice. Journal of Medical Genetics. PMID 31501240 DOI: 10.1136/jmedgenet-2019-106344  0.44
2019 Wang S, Xiang C, Mou L, Yang Y, Zhong R, Wang L, Sun C, Qin Z, Yang J, Qian J, Zhao Y, Wang Y, Pan X, Qie J, Jiang Y, ... ... Jin L, et al. Trans-acting nonsynonymous variant of FOXA1 predisposes to hepatocellular carcinoma through modulating FOXA1-ERα transcriptional program and may have undergone natural selection. Carcinogenesis. PMID 31400761 DOI: 10.1093/carcin/bgz136  0.36
2019 Wong JYY, Zhang H, Hsiung CA, Shiraishi K, Yu K, Matsuo K, Wong MP, Hong YC, Wang J, Seow WJ, Wang Z, Song M, Kim HN, Chang IS, Chatterjee N, ... ... Jin L, et al. Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women. Genomics. PMID 31306748 DOI: 10.1016/j.ygeno.2019.07.008  0.44
2019 Sun Y, Chen Y, Li Y, Li Z, Li C, Yu T, Xiao L, Yu B, Zhao H, Tao M, Jiang J, Yan J, Wang Y, Zeng H, Shen X, ... ... Jin L, et al. Association of TSR1 Variants and Spontaneous Coronary Artery Dissection. Journal of the American College of Cardiology. 74: 167-176. PMID 31296287 DOI: 10.1016/j.jacc.2019.04.062  0.36
2019 Liu J, Zhu Q, Han J, Zhang H, Li Y, Ma Y, He D, Gu J, Zhou X, Reveille JD, Jin L, Zou H, Ren S, Wang J. IgG Galactosylation status combined with MYOM2-rs2294066 precisely predicts anti-TNF response in ankylosing spondylitis. Molecular Medicine (Cambridge, Mass.). 25: 25. PMID 31195969 DOI: 10.1186/s10020-019-0093-2  0.44
2019 Wen SQ, Yao HB, Du PX, Wei LH, Tong XZ, Wang LX, Wang CC, Zhou BY, Shi MS, Zhabagin M, Wang J, Xu D, Jin L, Li H. Molecular genealogy of Tusi Lu's family reveals their paternal relationship with Jochi, Genghis Khan's eldest son. Journal of Human Genetics. PMID 31164702 DOI: 10.1038/s10038-019-0618-0  0.44
2019 Shen Y, Yang T, Cao X, Zhang Y, Zhao L, Li H, Zhao T, Xu J, Zhang H, Guo Q, Cai J, Gao B, Yu H, Yin S, Song R, ... ... Jin L, et al. Conjugation of DM1 to anti-CD30 antibody has potential antitumor activity in CD30-positive hematological malignancies with lower systemic toxicity. Mabs. 1-13. PMID 31161871 DOI: 10.1080/19420862.2019.1618674  0.44
2019 Liu C, Lv M, He X, Zhu Y, Amiri-Yekta A, Li W, Wu H, Kherraf ZE, Liu W, Zhang J, Tan Q, Tang S, Zhu YJ, Zhong Y, Li C, ... ... Jin L, et al. Homozygous mutations in induce multiple morphological abnormalities of the sperm flagella and male infertility. Journal of Medical Genetics. PMID 31048344 DOI: 10.1136/jmedgenet-2019-106011  0.32
2019 Wang Y, Li Y, Hao M, Liu X, Zhang M, Wang J, Xiong M, Shugart YY, Jin L. Robust Reference Powered Association Test of Genome-Wide Association Studies. Frontiers in Genetics. 10: 319. PMID 31024629 DOI: 10.3389/fgene.2019.00319  0.44
2019 Chen S, Pu W, Guo S, Jin L, He D, Wang J. Genome-Wide DNA Methylation Profiles Reveal Common Epigenetic Patterns of Interferon-Related Genes in Multiple Autoimmune Diseases. Frontiers in Genetics. 10: 223. PMID 31024609 DOI: 10.3389/fgene.2019.00223  0.44
2019 Jiang Y, Wang Y, Yuan Z, Xu K, Zhang K, Zhu Z, Li P, Suo C, Tian W, Fan M, Jin L, Ye W, Dong Q, Cui M, Chen X. Total Cerebral Small Vessel Disease Burden Is Related to Worse Performance on the Mini-Mental State Examination and Incident Dementia: A Prospective 5-Year Follow-Up. Journal of Alzheimer's Disease : Jad. PMID 31006685 DOI: 10.3233/JAD-181135  0.32
2019 Liu W, He X, Yang S, Zouari R, Wang J, Wu H, Kherraf ZE, Liu C, Coutton C, Zhao R, Tang D, Tang S, Lv M, Fang Y, Li W, ... ... Jin L, et al. Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice. American Journal of Human Genetics. PMID 30929735 DOI: 10.1016/j.ajhg.2019.02.020  0.44
2019 Sang Q, Zhang Z, Shi J, Sun X, Li B, Yan Z, Xue S, Ai A, Lyu Q, Li W, Zhang J, Wu L, Mao X, Chen B, Mu J, ... ... Jin L, et al. A pannexin 1 channelopathy causes human oocyte death. Science Translational Medicine. 11. PMID 30918116 DOI: 10.1126/scitranslmed.aav8731  0.32
2019 Wang Y, Jiang Y, Suo C, Yuan Z, Xu K, Yang Q, Tang W, Zhang K, Zhu Z, Tian W, Fan M, Li S, Ye W, Dong Q, Jin L, et al. Deep/mixed cerebral microbleeds are associated with cognitive dysfunction through thalamocortical connectivity disruption: The Taizhou Imaging Study. Neuroimage. Clinical. 22: 101749. PMID 30875641 DOI: 10.1016/j.nicl.2019.101749  0.32
2019 Guo S, Jiang S, Epperla N, Ma Y, Maadooliat M, Ye Z, Olson B, Wang M, Kitchner T, Joyce J, Strenn R, Mazza JJ, Meece JK, Wu W, Jin L, et al. A gene-based recessive diplotype exome scan discovers , a novel hepcidin-regulating iron metabolism gene. Blood. PMID 30814063 DOI: 10.1182/blood-2018-10-879585  0.44
2019 Lyu Q, Jin L, Yang X, Zhang F. LncRNA MINCR activates Wnt/β-catenin signals to promote cell proliferation and migration in oral squamous cell carcinoma. Pathology, Research and Practice. PMID 30777615 DOI: 10.1016/j.prp.2019.01.041  0.32
2019 Li S, Fang F, Cui M, Jiang Y, Wang Y, Kong X, Tian W, Fan M, Yuan Z, Chen J, Yang Q, Xue F, Wang J, Lu M, Wang X, ... ... Jin L, et al. Incidental findings on brain MRI among Chinese at the age of 55-65 years: the Taizhou Imaging Study. Scientific Reports. 9: 464. PMID 30679548 DOI: 10.1038/s41598-018-36893-0  0.44
2019 Zhang X, Jin L, Tian Z, Wang J, Yang Y, Liu J, Chen Y, Hu C, Chen T, Zhao Y, He Y. Nitric oxide inhibits autophagy and promotes apoptosis in hepatocellular carcinoma. Cancer Science. PMID 30657629 DOI: 10.1111/cas.13945  0.44
2019 Li S, Han X, Wang Y, Chen S, Niu J, Qian Z, Li P, Jin L, Xu C. Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysis. Prenatal Diagnosis. PMID 30650192 DOI: 10.1002/pd.5420  0.44
2019 Liu J, Wu N, Yang N, Takeda K, Chen W, Li W, Du R, Liu S, Zhou Y, Zhang L, Liu Z, Zuo Y, Zhao S, Blank R, ... ... Jin L, et al. TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30636772 DOI: 10.1038/s41436-018-0377-x  0.44
2019 Dong S, Wang C, Li X, Shen Q, Fu X, Wu M, Song C, Yang N, Wu Y, Wang H, Jin L, Xu H, Zhang F. Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract. Molecular Genetics and Genomics : Mgg. PMID 30604070 DOI: 10.1007/s00438-018-1522-6  0.32
2018 Liu W, Wu H, Wang L, Yang X, Liu C, He X, Li W, Wang J, Chen Y, Wang H, Gao Y, Tang S, Yang S, Jin L, Zhang F, et al. Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 30745215 DOI: 10.1016/j.jgg.2018.09.006  0.44
2018 Jiang D, He Z, Wang C, Zhou Y, Li F, Pu W, Zhang X, Feng X, Zhang M, Yecheng X, Xu Y, Jin L, Guo S, Wang J, Wang M. Epigenetic silencing of ZNF132 mediated by methylation-sensitive Sp1 binding promotes cancer progression in esophageal squamous cell carcinoma. Cell Death & Disease. 10: 1. PMID 30578410 DOI: 10.1038/s41419-018-1236-z  0.44
2018 Liu J, Pu W, Li Y, Ma Y, Zhu Q, Wan W, Yang C, Wang X, Chen X, Zhou X, Reveille JD, Jin L, Zou H, Wang J. Genetic association of non-MHC region with ankylosing spondylitis in a Chinese population. Annals of the Rheumatic Diseases. PMID 30552171 DOI: 10.1136/annrheumdis-2018-214625  0.44
2018 Liu Q, Lu J, Lin J, Tang Y, Pu W, Shi X, Jiang S, Liu J, Ma Y, Li Y, Xu J, Jin L, Wang J, Wu W. Salvianolic acid B attenuates experimental skin fibrosis of systemic sclerosis. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie. 110: 546-553. PMID 30530290 DOI: 10.1016/j.biopha.2018.12.016  0.44
2018 Chen J, Wang H, Jin L, Wang L, Huang X, Chen W, Yan M, Liu G. Profile analysis of circRNAs induced by porcine endemic diarrhea virus infection in porcine intestinal epithelial cells. Virology. 527: 169-179. PMID 30530223 DOI: 10.1016/j.virol.2018.11.014  0.32
2018 Ding W, Pu W, Jiang S, Ma Y, Liu Q, Wu W, Chu H, Zou H, Jin L, Wang J, Zhou X. Evaluation of the antifibrotic potency by knocking down SPARC, CCR2 and SMAD3. Ebiomedicine. PMID 30470612 DOI: 10.1016/j.ebiom.2018.11.016  0.44
2018 Li Y, Liu X, Ma Y, Wang Y, Zhou W, Hao M, Yuan Z, Liu J, Xiong M, Shugart YY, Wang J, Jin L. knnAUC: an open-source R package for detecting nonlinear dependence between one continuous variable and one binary variable. Bmc Bioinformatics. 19: 448. PMID 30466390 DOI: 10.1186/s12859-018-2427-4  0.44
2018 Jiang Y, Fan Z, Wang Y, Suo C, Cui M, Yuan Z, Tian W, Fan M, Zhang D, Wang X, Jin L, Ye W, Li S, Chen X. Low Bone Mineral Density Is Not Associated with Subclinical Atherosclerosis: A Population-Based Study in Rural China. Cardiology. 141: 78-87. PMID 30423564 DOI: 10.1159/000493166  0.44
2018 He X, Li W, Wu H, Lv M, Liu W, Liu C, Zhu F, Li C, Fang Y, Yang C, Cheng H, Zhang J, Tan J, Chen T, Tang D, ... ... Jin L, et al. Novel homozygous mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella. Journal of Medical Genetics. PMID 30415212 DOI: 10.1136/jmedgenet-2018-105486  0.44
2018 Wang M, Wu Z, Hu Y, Wang Y, Tan Y, Xiang Y, Wang L, Jin L, Huang H. An adapted carrier for the cryopreservation of human testicular spermatozoa. Reproductive Biomedicine Online. PMID 30366839 DOI: 10.1016/j.rbmo.2018.08.021  0.36
2018 Li W, He X, Yang S, Liu C, Wu H, Liu W, Lv M, Tang D, Tan J, Tang S, Chen Y, Wang J, Zhang Z, Wang H, Jin L, et al. Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility. Journal of Human Genetics. PMID 30310178 DOI: 10.1038/s10038-018-0520-1  0.44
2018 Yang N, Wu N, Zhang L, Zhao Y, Liu J, Liang X, Ren X, Li W, Chen W, Dong S, Zhao S, Lin J, Xiang H, Xue H, Chen L, ... ... Jin L, et al. TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice. Human Molecular Genetics. PMID 30307510 DOI: 10.1093/hmg/ddy358  0.32
2018 Liu Q, Shi X, Tang L, Xu W, Jiang S, Ding W, Feng Q, Chu H, Ma Y, Li Y, Lu J, Pu W, Zhou X, Jin L, Wang J, et al. Salvianolic acid B attenuates experimental pulmonary inflammation by protecting endothelial cells against oxidative stress injury. European Journal of Pharmacology. PMID 30273543 DOI: 10.1016/j.ejphar.2018.09.030  0.44
2018 Wu S, Zhang M, Yang X, Peng F, Zhang J, Tan J, Yang Y, Wang L, Hu Y, Peng Q, Li J, Liu Y, Guan Y, Chen C, Hamer MA, ... ... Jin L, et al. Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans. Plos Genetics. 14: e1007640. PMID 30248107 DOI: 10.1371/journal.pgen.1007640  0.32
2018 Ji J, Xu M, Wang R, Wang Y, Qin Y, Li L, Zheng H, Yang S, Li S, Miao D, Jin L, Zhou L, Ling X, Xia Y, Lu C, et al. Human mitochondrial DNA haplogroup M8a influences the penetrance of m.8684C>T in Han Chinese men with non-obstructive azoospermia. Reproductive Biomedicine Online. PMID 30236824 DOI: 10.1016/j.rbmo.2018.08.004  0.36
2018 Wang C, Pu W, Zhao D, Zhou Y, Lu T, Chen S, He Z, Feng X, Wang Y, Li C, Li S, Jin L, Guo S, Wang J, Wang M. Identification of Hyper-Methylated Tumor Suppressor Genes-Based Diagnostic Panel for Esophageal Squamous Cell Carcinoma (ESCC) in a Chinese Han Population. Frontiers in Genetics. 9: 356. PMID 30233644 DOI: 10.3389/fgene.2018.00356  0.44
2018 Jiao R, Lin N, Hu Z, Bennett DA, Jin L, Xiong M. Bivariate Causal Discovery and Its Applications to Gene Expression and Imaging Data Analysis. Frontiers in Genetics. 9: 347. PMID 30233639 DOI: 10.3389/fgene.2018.00347  0.32
2018 Feng W, Guo X, Huang H, Xu C, Li Y, Guo S, Zhao Z, Li Q, Lu D, Jin L, Wang J, Jiang G, Wu J. Polymorphism rs3819102 in thymidylate synthase and environmental factors: effects on lung cancer in Chinese population. Current Problems in Cancer. PMID 30180988 DOI: 10.1016/j.currproblcancer.2018.07.005  0.44
2018 Shi X, Liu Q, Li N, Tu W, Luo R, Mei X, Ma Y, Xu W, Chu H, Jiang S, Du Z, Zhao H, Zhao L, Jin L, Wu W, et al. MiR-3606-3p inhibits systemic sclerosis through targeting TGF-β type II receptor. Cell Cycle (Georgetown, Tex.). PMID 30145936 DOI: 10.1080/15384101.2018.1509621  0.44
2018 Xu XH, Bao Y, Wang X, Yan F, Guo S, Ma Y, Xu D, Jin L, Xu J, Wang J. Hypoxic-stabilized EPAS1 proteins transactivate DNMT1 and cause promoter hypermethylation and transcription inhibition of EPAS1 in non-small cell lung cancer. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201700715. PMID 29920222 DOI: 10.1096/fj.201700715  0.44
2017 Pu W, Wang C, Chen S, Zhao D, Zhou Y, Ma Y, Wang Y, Li C, Huang Z, Jin L, Guo S, Wang J, Wang M. Targeted bisulfite sequencing identified a panel of DNA methylation-based biomarkers for esophageal squamous cell carcinoma (ESCC). Clinical Epigenetics. 9: 129. PMID 29270239 DOI: 10.1186/s13148-017-0430-7  0.44
2017 Ding W, Pu W, Wang L, Jiang S, Zhou X, Tu W, Yu L, Zhang J, Guo S, Liu Q, Ma Y, Chen S, Wu W, Reveille J, Zou H, ... Jin L, et al. Genome-wide DNA methylation analysis in systemic sclerosis reveals hypomethylation of interferon-associated genes in CD4+ and CD8+ T cells. The Journal of Investigative Dermatology. PMID 29248544 DOI: 10.1016/j.jid.2017.12.003  0.44
2017 Fan L, Chen L, Ni X, Guo S, Zhou Y, Wang C, Zheng Y, Shen F, Kolluri VK, Muktiali M, Zhao Z, Wu J, Zhao D, He Z, Feng X, ... ... Jin L, et al. Genetic variant of miR-4293 rs12220909 is associated with susceptibility to non-small cell lung cancer in a Chinese Han population. Plos One. 12: e0175666. PMID 28410417 DOI: 10.1371/journal.pone.0175666  0.44
2016 Guo S, Li Y, Wang Y, Chu H, Chen Y, Liu Q, Guo G, Tu W, Wu W, Zou H, Yang L, Xiao R, Ma Y, Zhang F, Xiong M, ... Jin L, et al. Copy Number Variation of HLA-DQA1 and APOBEC3A/3B Contribute to the Susceptibility of Systemic Sclerosis in the Chinese Han Population. The Journal of Rheumatology. PMID 27036383 DOI: 10.3899/jrheum.150945  0.44
2015 Shen F, Chen J, Guo S, Zhou Y, Zheng Y, Yang Y, Zhang J, Wang X, Wang C, Zhao D, Wang M, Zhu M, Fan L, Xiang J, Xia Y, ... ... Jin L, et al. Genetic variants in miR-196a2 and miR-499 are associated with susceptibility to esophageal squamous cell carcinoma in Chinese Han population. Tumour Biology : the Journal of the International Society For Oncodevelopmental Biology and Medicine. PMID 26518769 DOI: 10.1007/s13277-015-4268-3  0.44
2015 Zhang P, Wang J, Lu T, Wang X, Zheng Y, Guo S, Yang Y, Wang M, Kolluri VK, Qiu L, Shen F, Fan L, Li J, Wang Y, Wei Q, ... Jin L, et al. miR-449b rs10061133 and miR-4293 rs12220909 polymorphisms are associated with decreased esophageal squamous cell carcinoma in a Chinese population. Tumour Biology : the Journal of the International Society For Oncodevelopmental Biology and Medicine. PMID 26055141 DOI: 10.1007/s13277-015-3422-2  0.44
2015 Guo S, Yan F, Xu J, Bao Y, Zhu J, Wang X, Wu J, Li Y, Pu W, Liu Y, Jiang Z, Ma Y, Chen X, Xiong M, Jin L, et al. Identification and validation of the methylation biomarkers of non-small cell lung cancer (NSCLC). Clinical Epigenetics. 7: 3. PMID 25657825 DOI: 10.1186/s13148-014-0035-3  0.44
2015 Dong Z, Guo S, Yang Y, Wu J, Guan M, Zou H, Jin L, Wang J. Association between ABCG2 Q141K polymorphism and gout risk affected by ethnicity and gender: a systematic review and meta-analysis. International Journal of Rheumatic Diseases. 18: 382-91. PMID 25639607 DOI: 10.1111/1756-185X.12519  0.44
2014 He D, Wang J, Yi L, Guo X, Guo S, Guo G, Tu W, Wu W, Yang L, Xiao R, Li Y, Chu H, Lai S, Jin L, Zou H, et al. Association of the HLA-DRB1 with scleroderma in Chinese population. Plos One. 9: e106939. PMID 25184637 DOI: 10.1371/journal.pone.0106939  0.44
2014 Song X, Guo S, Chen Y, Yang C, Ji H, Zhang F, Jiang Z, Ma Y, Li Y, Jin L, Zou H, Zhou X, Wang J. Association between HLA-DQA1 gene copy number polymorphisms and susceptibility to rheumatoid arthritis in Chinese Han population. Journal of Genetics. 93: 215-8. PMID 24840843 DOI: 10.1007/s12041-014-0339-2  0.44
2014 Guo S, Tan L, Pu W, Wu J, Xu K, Wu J, Li Q, Ma Y, Xu J, Jin L, Wang J. Quantitative assessment of the diagnostic role of APC promoter methylation in non-small cell lung cancer. Clinical Epigenetics. 6: 5. PMID 24661338 DOI: 10.1186/1868-7083-6-5  0.44
2014 Guo S, Wang YL, Li Y, Jin L, Xiong M, Ji QH, Wang J. Significant SNPs have limited prediction ability for thyroid cancer. Cancer Medicine. 3: 731-5. PMID 24591304 DOI: 10.1002/cam4.211  0.44
2014 Wu L, Guo S, Yang D, Ma Y, Ji H, Chen Y, Zhang J, Wang Y, Jin L, Wang J, Liu J. Copy number variations of HLA-DRB5 is associated with systemic lupus erythematosus risk in Chinese Han population. Acta Biochimica Et Biophysica Sinica. 46: 155-60. PMID 24366815 DOI: 10.1093/abbs/gmt137  0.44
2013 Wang YL, Feng SH, Guo SC, Wei WJ, Li DS, Wang Y, Wang X, Wang ZY, Ma YY, Jin L, Ji QH, Wang JC. Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population. Journal of Medical Genetics. 50: 689-95. PMID 23847140 DOI: 10.1136/jmedgenet-2013-101687  0.36
2013 Wang X, Wang L, Guo S, Bao Y, Ma Y, Yan F, Xu K, Xu Z, Jin L, Lu D, Xu J, Wang JC. Hypermethylation reduces expression of tumor-suppressor PLZF and regulates proliferation and apoptosis in non-small-cell lung cancers. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 27: 4194-203. PMID 23804241 DOI: 10.1096/fj.13-229070  0.44
2013 Lin S, Pan L, Guo S, Wu J, Jin L, Wang JC, Wang S. Prognostic role of microRNA-181a/b in hematological malignancies: a meta-analysis. Plos One. 8: e59532. PMID 23533632 DOI: 10.1371/journal.pone.0059532  0.44
2012 Wu J, Liu J, Zhou Y, Ying J, Zou H, Guo S, Wang L, Zhao N, Hu J, Lu D, Jin L, Li Q, Wang JC. Predictive value of XRCC1 gene polymorphisms on platinum-based chemotherapy in advanced non-small cell lung cancer patients: a systematic review and meta-analysis. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 18: 3972-81. PMID 22705987 DOI: 10.1158/1078-0432.CCR-11-1531  0.44
2008 Guo A, Jin L, Deng Z, Cai S, Guo S, Lin W. New stemona alkaloids from the roots of Stemona sessilifolia. Chemistry & Biodiversity. 5: 598-605. PMID 18421751 DOI: 10.1002/cbdv.200890056  0.44
2002 Liu S, Xi YZ, Guo SQ, Liu N, Liang F, Jin L, Chen XG, Kong FH. [Expression of alpha subunit for IL-6 receptor at mRNA and protein levels in human leukemic cells]. Zhongguo Shi Yan Xue Ye Xue Za Zhi / Zhongguo Bing Li Sheng Li Xue Hui = Journal of Experimental Hematology / Chinese Association of Pathophysiology. 10: 22-6. PMID 12513831  0.36
2002 Han HX, Kong FH, Xi YZ, Sun YY, Jin L, Liu N, Guo SQ. [Selection of donor in mismatched hematopoietic stem cell transplantation by CREG, residue match and HLA three-dimensional structure]. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 10: 553-6. PMID 12513720  0.36
2001 Han HX, Kong FH, Xi YZ, Jin L, Liu N, Tu M, Guo SQ. [A New Criterion for Donor and Recipient Selection in Hematopoietic Stem Cell Transplantation - the Matching of Three-Dimensional Structure of HLA Molecular Modeling] Zhongguo Shi Yan Xue Ye Xue Za Zhi. 9: 354-358. PMID 12578579  0.36
Show low-probability matches.