欧美人妻中文字幕天天弄_久久最新获取地址日韩精品_国内精品久久久精品电影院_999色视频在线观看

上海天昊生物客戶發(fā)表論文匯總

Mutations in epigenetic regulators are involved in acute lymphoblastic leukemia relapse following allogeneic hematopoietic stem cell transplantation.
Xiao H,et al.
Oncotarget. 2016 Jan 19; 7(3): 2696–2708.
 
 
The complete chloroplast genome sequence of Dioscorea zingiberensis (Dioscoreceae).
Zhou W,et al.
Mitochondrial DNA A DNA MappSeq Anal. 2016 Jul;27(4):2730-1.
 
 
The complete chloroplast genome sequence of medicinal plant Pinellia ternata.
Han L,et al.
Mitochondrial DNA A DNA MappSeq Anal. 2016 Jul;27(4):2921-2.
 
 
Association between WT1 polymorphisms and susceptibility to breast cancer: results from a case-control studyin a southwestern Chinese population.
Qi XW,et al.
Am J Cancer Res. 2015 Feb 15;5(3):1234-50.
 
 
Shared and discrepant susceptibility for carotid artery and aortic arch calcification: A genetic association study.
Zhang Y,et al.
Atherosclerosis. 2015 Aug;241(2):371-5.
 
 
Assessment of functional tag single nucleotide polymorphisms within the DRD2 gene as risk factors for post-traumatic stress disorder in the Han Chinese population.
Duan Z,et al.
J Affect Disord. 2015 Dec 1;188:210-7.
 
 
Association Study of IL-12B Polymorphisms Susceptibility with Ankylosing Spondylitis in Mainland Han Population.
Zhang L,et al.
PLoS One. 2015 Jun 23;10(6):e0130982.
 
 
Analysis of single nucleotide polymorphisms within ADAM12 and risk of knee osteoarthritis in a Chinese Han population.
Wang L,et al.
Biomed Res Int. 2015;2015:518643.
 
 
First Analysis of the Association Between CYP3A4/5, ABCB1 Genetic Polymorphisms and Oxcarbazepine Metabolism and Transport in Chinese Epileptic Patients with Oxcarbazepine Monotherapy and Bitherapy.
Wang P,et al.
J Pharm Pharm Sci. 2015;18(3):256-65.
 
 
Effects of CYP3A4/5 and ABCB1 genetic polymorphisms on carbamazepine metabolism and transport in Chinese patients with epilepsy treated with carbamazepine in monotherapy and bitherapy.
Wang P,et al.
Epilepsy Res. 2015 Nov;117:52-7.
 
 
Association of polymorphisms in the MAFB gene and the risk of coronary artery disease and ischemic stroke: a case-control study.
Yang Q,et al.
Lipids Health Dis. 2015 Jul 25;14:79.
 
 
An ADAM10 promoter polymorphism is a functional variant in severe sepsis patients and confers susceptibility to the development of sepsis.
Cui L,et al.
Crit Care. 2015 Mar 5;19:73.
 
 
Low-frequency coding variants at 6p21.33 and 20q11.21 are associated with lung cancer risk in Chinese populations.
Jin G,et al.
Am J Hum Genet. 2015 May 7;96(5):832-40.
 
 
Epstein-Barr virus-induced gene 3 (EBI3) polymorphisms and expression are associated with susceptibility to pulmonary tuberculosis.
Zheng R,et al.
Tuberculosis (Edinb). 2015 Jul;95(4):497-504.
 
 
Affection of single-nucleotide polymorphisms in miR-27a, miR-124a, and miR-146a on susceptibility to type 2 diabetes mellitus in Chinese Han people.
Wang TT,et al.
Chin Med J (Engl). 2015 Feb 20;128(4):533-9.
 
 
Lack of Association between the TSPAN18 Gene and Schizophrenia Based on New Data from Han Chinese and a Meta-Analysis.
Zhang B,et al.
Int J Mol Sci. 2015 May 26;16(6):11864-72.
 
 
Association between UBE2E2 variant rs7612463 and type 2 diabetes mellitus in a Chinese Han Population.
Kazakova EV,et al.
Acta Biochim Pol. 2015;62(2):241-5.
 
 
Interleukin 12B rs3212227 T > G polymorphism was associated with an increased risk of gastric cardiac adenocarcinoma in a Chinese population.
Yin J,et al.
Dis Esophagus. 2015 Apr;28(3):291-8.
 
 
Association between polymorphisms of interleukin 12 and rheumatoid arthritis associated biomarkers in a Chinese population.
Shen L,et al.
Cytokine. 2015 Dec;76(2):363-7.
 
 
A genome-wide association study of mitochondrial DNA in Chinese men identifies two risk single nucleotide substitutions for idiopathic oligoasthenospermia.
Lu C,et al.
Mitochondrion. 2015 Sep;24:87-92.
 
 
IL1B gene polymorphisms, age and the risk of non-small cell lung cancer in a Chinese population.
Li Y,et al.
Lung Cancer. 2015 Sep;89(3):232-7.
 
 
SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.
Li H,et al.
Genomics. 2015 Aug;106(2):83-7.
 
 
Association of DRD3, COMT, and SLC6A4 Gene Polymorphisms with Type 2 Diabetes in Southern Chinese: A Hospital-Based Case–Control Study.
Xiu L,et al.
Diabetes Technol Ther. 2015 Aug;17(8):580-6.
 
 
Variant TP53BP1 rs560191 G>C is associated with risk of gastric cardia adenocarcinoma in a Chinese Han population.
Zhang S,et al.
Chin J Cancer Res. 2015 Apr;27(2):156-62.
 
 
Association of the VRK2 gene rs3732136 polymorphism with schizophrenia in a Northwest Chinese Han population.
Zhang B,et al.
Genet Mol Res. 2015 Aug 14;14(3):9404-11.
 
 
Genetic Variations of IL17F and IL23A Show Associations with Behçet’s Disease and Vogt-Koyanagi-Harada Syndrome.
Hou S,et al.
Ophthalmology. 2015 Mar;122(3):518-23.
 
 
Up-regulation of long noncoding RNA MALAT1 contributes to proliferation and metastasis in esophageal squamous cell carcinoma.
Hu L,et al.
J Exp Clin Cancer Res. 2015 Jan 22;34:7.
 
 
UAssociation of Tag SNPs and Rare CNVs of the MIR155HG/miR-155 Gene with Epilepsy in the Chinese Han Population.
Tao H,et al.
Biomed Res Int. 2015;2015:837213.
 
 
Interactions between Obesity-Related Copy Number Variants and Dietary Behaviors in Childhood Obesity.
Zhang D,et al.
Nutrients. 2015 Apr 22;7(4):3054-66.
 
 
Association between DEFB103 gene copy number variation and ankylosing spondylitis: a case-control study.
Cai G,et al.
Tissue Antigens. 2015 Sep;86(3):195-8.
 
 
A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
Zhang X,et al.
BMC Genomics. 2015 May 8;16:364.
 
 
     
 
Mitochondrial DNA haplogroups and short-term neurological outcomes of ischemic stroke.
Cai B,et al.
SCIENTIFIC REPORTS. 2015 May;5:9864.
 
 
Whole-exome and targeted sequencing identify ROBO1 and ROBO2 mutations as progression-related drivers in myelodysplastic syndromes.
Xu F,et al.
Nat Commun. 2015 Nov 26;6:8806.
 
 
Epigenetic deregulated miR-375 contributes to the constitutive activation of JAK2/STAT signaling in myeloproliferative neoplasm.
Yin LH,et al.
Leuk Res. 2015 Apr;39(4):471-8.
 
 
Genomic variations of the mevalonate pathway in porokeratosis.
Zhang Z,et al.
Elife. 2015 Jul 23;4:e06322.
 
 
Identification and validation of the methylation biomarkers of non-small cell lung cancer (NSCLC).
Guo S,et al.
Clin Epigenetics. 2015 Jan 22;7(1):3.
 
 
Correlation of PCSK9 gene polymorphism with cerebral ischemic stroke in Xinjiang Han and Uygur populations
Han D,et al.
Med Sci Monit. 2014 Sep 30;20:1758-67. doi:10.12659/MSM.892091.
 
 
A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss
Du W, et al.
Genomics. 2014 Aug 19. pii: S0888-7543(14)00124-4.
 
 
Genetic variation in BIN1 gene and Alzheimer’s disease risk in Han Chinese individuals
Tan MS, et al.
Neurobiol Aging, 2014, 35(7):1781.e1-8.
 
 
PRPF4 mutations cause autosomal dominant retinitis pigmentosa
Chen X, et al.
Hum Mol Genet, 2014, 23(11):2926-39.
 
 
Clinical relevance of tag single nucleotide polymorphisms within the CAT gene in patients with PTSD in the Chongqing Han population
Duan ZX, et al.
Int J Clin Exp Pathol, 2014, 7(4):1724-32.
 
 
The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population
Han Y, et al.
J Oral Pathol Med, 2014, 43(7):554-60.
 
 
Gene copy number alterations in the azoospermia-associated AZFc region and their effect on spermatogenic impairment
Lu C, et al.
Mol Hum Reprod, 2014 online.
 
 
Impacts of COX-1 gene polymorphisms on vascular outcomes in atients with ischemic stroke and treated with aspirin
Cao L, et al.
Gene, 2014, 546(2):172-6.
 
 
Pathogenic variants screening in five non-obstructive azoospermiaassociated genes
Lu C, et al.
Mol Hum Reprod, 2014, 20(2):178-83.
 
 
Single nucleotide polymorphisms of the interleukin-33 (IL-33) gene are associated with ankylosing spondylitis in Chinese individuals: a case–control pilot study
Fan D, et al.
Scand J Rheumatol, 2014, 14:1-22.
 
 
Lack of Association Between TESPA1 Gene Polymorphisms (rs1801876, rs2171497, rs4758994, and rs997173) and Ankylosing Spondylitis in a Chinese Population
Liu S, et al.
Inflammation, 2014 online.
 
 
Association between Copy Number Variations HLA-DQA1 and Ankylosing Spondylitis in Chinese Han population
Wang J, et al.
Genes Immun, 2013, 14(8):500-3.
 
 
A1180V of Cardiac Sodium Channel Gene (SCN5A): Is It a Risk Factor for Dilated Cardiomyopathy or Just a Common Variant in Han Chinese?
Shen C, et al.
Dis Markers, 2013, 35(5):531-5.
 
 
ADAM33 polymorphisms are associated with asthma and a distinctive palm dermatoglyphic pattern
Xue W, et al.
Mol Med Rep, 2013, 8(6):1795-800.
 
 
Association between microRNA polymorphisms and humoral immunity to hepatitis B vaccine
Xiong Y, et al.
Hum Vaccin Immunother, 2013, 9(8):1673-8.
 
 
Association of GWAS-linked loci with late-onset Alzheimer’s disease in a northern Han Chinese population
Tan L, et al.
Alzheimers Dement, 2013, 9(5):546-53.
 
 
Haplotype analysis of eight genes of the monoubiquitinated FANCD2–DNA damage–repair pathway in breast cancer patients
Tang LL, et al.
Cancer Epidemiol, 2013, 37(3):311-7.
 
 
HLA-DQA1基因拷貝數(shù)目多態(tài)性與中國漢族人群類風(fēng)濕關(guān)節(jié)炎易感性的研究
陳潔君等
風(fēng)濕病與關(guān)節(jié)炎,2013,(08):7-10.
 
 
Interleukin 10 rs1800872 T>G Polymorphism was Associated with an Increased Risk of Esophageal Cancer in a Chinese Population
Sun JM, et al.
Asian Pac J Cancer Prev, 2013, 14(6):3443-7.
 
 
Interleukin 17A rs4711998 A>G polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population
Yin J, et al.
Dis Esophagus, 2014, 27(1):87-92.
 
 
Interleukin 1B rs16944 G > A polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population
Zheng L, et al.
"Clin Biochem, 2013, 46(15):1469-73.
 
 
Lack of association between COMT Val158Met polymorphism and late-onset Alzheimer’s disease in Han Chinese
Zhou J, et al.
Neurosci Lett, 2013, 554:162-6.
 
 
NLRP3 polymorphisms are associated with late-onset Alzheimer's disease in Han Chinese
Tan MS, et al.
J Neuroimmunol, 2013, 265(1-2):91-5.
 
 
SIRT2 polymorphism rs10410544 is associated with Alzheimer's disease in a Han Chinese population
Xia M, et al.
J Neurol Sci, 2014, 336(1-2):48-51.
 
 
The relationship between single nucleotide polymorphisms of the NTRK2 gene and sporadic Alzheimer’s disease in the Chinese Han population
Zeng F, et al.
Neurosci Lett, 2013, 550:55-9.
 
 
TMEM106B and APOE polymorphisms interact to confer risk for late-onset Alzheimer’s disease in Han Chinese
Lu RC, et al.
J Neural Transm, 2014, 121(3):283-7.
 
 
Toll-like receptor 9 promoter polymorphism is associated with decreased risk of Alzheimer’s disease in Han Chinese
Wang YL, et al.
J Neuroinflammation, 2013, 10(1):101.
 
 
Association of TOMM40 Polymorphisms with Late-Onset Alzheimer’s Disease in a Northern Han Chinese Population
Ma XY, et al.
Neuromolecular Med, 2013, 15(2):279-87.
 
 
Clinical Significance of MYT1L Gene Polymorphisms in Chinese Patients with Gastric Cancer
Zhang Y, et al.
PLoS One, 2013, 8(8):e71979.
 
 
Silencing of DLGAP5 by siRNA Significantly Inhibits the Proliferation and Invasion of Hepatocellular Carcinoma Cells
Liao W, et al.
PLoS One, 2013, 8(12):e80789.
 
 
Detecting Genetic Association of Common Human Facial Morphological Variation Using High Density 3D Image Registration
Peng S, et al.
PLoS Comput Biol, 2013, 9(12):e1003375.
 
 
Genetic variation in Clusterin gene and Alzheimer’s disease risk in Han Chinese
Yu JT, et al.
Neurobiol Aging, 2013, 34(7):1921.e17-23.
 
 
Lack of Association between NLGN3, NLGN4, SHANK2 and SHANK3 Gene Variants and Autism Spectrum Disorder in a Chinese Population
Liu Y, et al.
PLoS One, 2013, 8(2):e56639.
 
 
分子人類學(xué)中的單核苷酸突變檢測方法的研究進(jìn)展
胡抗等
生命科學(xué), 2013, 25(1):119-125
 
 
A functional copy number variation in the WWOX gene is associated with lung cancer risk in Chinese
Yang L, et al.
Hum Mol Genet, 2013, 22(9):1886-94.
 
 
Characterization of large deletions in the F8 gene using multiple competitive amplification and genome walking technique
You GL, et al.
J Thromb Haemost, 2013, 11(6):1103-10.
 
 
Impacts and interactions of PDGFRB, MMP-3, TIMP-2, and RNF213 polymorphisms on the risk of Moyamoya disease in Han Chinese human subjects
Wang X, et al.
Gene, 2013, 526(2):437-42.
 
 
MiR-196a2 rs11614913 T > C polymorphism and risk of esophageal cancer in a Chinese population
Wei J, et al.
Hum Immunol, 2013, 74(9):1199-205.
 
 
Polymorphism rs7214723 in CAMKK1 and lung cancer risk in Chinese population
Zhang YH, et al.
Tumour Biol, 2013, 34(5):3147-52.
 
 
SLC26A4 gene polymorphism and late-onset Alzheimer’s disease in a Han Chinese population from Qingdao, China
Jifang Zhang, et al.
Neural regeneration research,2013,8(8):754-759.
 
 
The -144C/A Polymorphism in the Promoter of HSP90beta Is Associated with Multiple Organ Dysfunction Scores
Zhao Y, et al.
PLoS One, 2013, 8(3):e58646.
 
 
No association of SORT1 gene polymorphism with sporadic Alzheimer’s disease in the Chinese Han population
Zeng F, et al.
Neuroreport, 2013, 24(9):464-8.
 
 
Association and Cumulative Effects of GWAS-Identified Genetic Variants for Nonsyndromic Orofacial Clefts in a Chinese Population
Pan Y, et al.
Environ Mol Mutagen, 2013, 54(4):261-7.
 
 
An Association Study on ADAM10 Promoter Polymorphisms and Atherosclerotic Cerebral Infarction in a Chinese Population
Li Y, et al.
CNS Neurosci Ther, 2013, 19(10):785-94.
 
 
The CRHR1 Gene Contributes to Genetic Susceptibility of Aggressive Behavior Towards Others in Chinese Southwest Han Population
Chen B, et al.
J Mol Neurosci, 2014, 52(4):481-6.
 
 
Evaluation of Five Candidate Genes from GWAS for Association with Oligozoospermia in a Han Chinese Population
Xu M, et al.
PLoS One, 2013, 8(11):e80374.
 
 
Impact of endothelial nitric oxide synthase gene polymorphism on severity of enterovirus 71-infection in Chinese children
Li JA, et al.
Clin Biochem, 2013, 46(18):1842-7.
 
 
The effect of functional MAPKAPK2 copy number variation CNV-30450 on elevating nasopharyngeal carcinoma risk is modulated by EBV infection
Yang L, et al.
Carcinogenesis, 2014, 35(1):46-52.
 
 
Missense variants in CR1 are associated with increased risk of Alzheimer’ disease in Han Chinese
Ma XY, et al.
Neurobiol Aging, 2014, 35(2):443.e17-21.
 
 
Genetic variation in PICALM and Alzheimer’s disease risk in Han Chinese
Jiang T, et al.
Neurobiol Aging, 2014, 35(4):934.e1-3.
 
 
Molecular defects identified by whole exome sequencing in a child with Fanconi anemia
Zheng Z, et al.
Gene, 2013, 530(2):295-300.
 
 
Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy
Zhang Z, et al.
Am J Hum Genet, 2012, 90(1):125-32.
 
 
Combined Erlotinib and Cetuximab overcome the acquired resistance to epidermal growth factor receptors tyrosine kinase inhibitor in non-small-cell lung cancer
Wang M, et al.
J Cancer Res Clin Oncol, 2012, 138(12):2069-77.
 
 
孤獨(dú)癥的臨床特征及相關(guān)拷貝數(shù)變異的研究
張穎等
復(fù)旦大學(xué)碩士學(xué)位論文
 
 
廣西壯族女性堿性成纖維生長因子基因單核苷酸多態(tài)性與骨質(zhì)疏松
林朝文等
中國組織工程研究, 2012, 16(50):9443-9447.
 
 
A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections
Xu X, et al.
BMC Med Genet, 2012, 13:75.
 
 
Absence of gene mutations in KIT-positive carcinoma showing thymus-like elements of the thyroid
Pan Y, et al.
Hum Pathol, 2012, 43(3):350-5.
 
 
BAT3 基因多態(tài)性與漢族人群肺癌易感性的相關(guān)性 ［BAT3 gene polymorphisms and susceptibility to lung cancer in Han Chinese］
王彬等
現(xiàn)代人類學(xué)通訊,6(28):165-173
 
 
Characterisation and validation of a novel panel of the six short tandem repeats for genetic counselling in Chinese haemophilia A pedigrees
Ding QL, et al.
Haemophilia, 2012, 18(4):621-5.
 
 
Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease
Chen X, et al.
J Thromb Haemost, 2012, 10(8):1508-14.
 
 
Physical activity modifies the association between CYBA gene polymorphisms and small artery elasticity in a Chinese population
Zhu Z, et al.
Hypertens Res, 2012, 35(7):739-44.
 
 
Replication of the MTHFD1 L Gene Association with Late-Onset Alzheimer’s Disease in a Northern Han Chinese Population
Ma XY, et al.
J Alzheimers Dis, 2012, 29(3):521-5.
 
 
染色體15q11.2和15q13.3區(qū)域的微缺失與中國兒童失神癲癇的相關(guān)性
張平平等
實(shí)用兒科臨床雜志,2012,27(7):522-525
 
 
Thirteen Chinese patients with sporadic Paget’s disease of bone: clinical features, SQSTM1 mutation identification, and functional analysis
Gu JM, et al.
J Bone Miner Metab, 2012, 30(5):525-33.
 
 
Clinical Significance of SOD2 and GSTP1 Gene Polymorphisms in Chinese Patients With Gastric Cancer
Xu Z, et al.
Cancer, 2012, 118(22):5489-96.
 
 
A Functional Copy-Number Variation in MAPKAPK2 Predicts Risk and Prognosis of Lung Cancer
Liu B, et al.
Am J Hum Genet, 2012, 91(2):384-90.
 
 
Association of Fcγ receptor IIB polymorphism with cryptococcal meningitis in HIV-uninfected Chinese patients
Hu XP, et al.
PLoS One, 2012, 7(8):e42439.
 
 
A miRNA Binding Site Single-Nucleotide Polymorphism in the 39-UTR Region of the IL23R Gene Is Associated with Breast Cancer
Wang L, et al.
PLoS One, 2012, 7(12):e49823.
 
 
B-cell Lymphoma 2 rs17757541 C>G Polymorphism was Associated with an Increased Risk of Gastric Cardiac Adenocarcinoma in a Chinese Population
Li Q, et al.
Asian Pac J Cancer Prev, 2013, 14(7):4301-6.
 
 
廣西百色地區(qū)壯族婦女脂聯(lián)素基因單核苷酸多態(tài)性與骨密度的關(guān)系
王金花等
解剖學(xué)報(bào),2012,43(1):109-113
 
 
SORCS1 and APOE polymorphisms interact to confer risk for late-onset Alzheimer's disease in a Northern Han Chinese population
Wang HF, et al.
Brain Res, 2012, 1448:111-6.
 
 
FTO基因單核苷酸多態(tài)性與中國漢族兒童/青少年肥胖的關(guān)聯(lián)性研究
許玉洋等
浙江大學(xué)碩士學(xué)位論文
 
 
Catechol-O-methyltransferase polymorphisms do not play a significant role in pain perception in male Chinese Han population
Xiang X, et al.
Physiol Genomics, 2012, 44(5):318-28.
 
 
HLA-B*58:01 allele is associated with augmented risk for both mild and severe cutaneous adverse reactions induced by allopurinol in Han Chinese
Cao ZH, et al.
Pharmacogenomics, 2012, 13(10):1193-201.
 
 
Association of FCRL4 polymorphisms on disease susceptibility and severity of ankylosing spondylitis in Chinese Han population
Zeng Z, et al.
Clin Rheumatol, 2012, 31(10):1449-54.
 
 
Genetic variations in T-cell activation and effector pathways modulate alloimmune responses after allogeneic hematopoietic stem cell transplantation in patients with hematologic malignancies
Xiao H, et al.
Haematologica, 2012, 97(12):1804-12.
 
 
Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification
Du R, et al.
J Hum Genet, 2012, 57(8):545-51.
 
 
Genetic Association of SLC2A14 Polymorphism with Alzheimer’s Disease in a Han Chinese Population
Wang W, et al.
J Mol Neurosci, 2012, 47(3):481-4.
 
 
Association Analysis of IL-17A and IL-17F Polymorphisms in Chinese Han Women with Breast Cancer
Wang L, et al.
PLoS One, 2012, 7(3):e34400.
 
 
The FCGR2B rs10917661 polymorphism may confer susceptibility to ankylosing spondylitis in Han Chinese: a case-control study
Duan ZH, et al.
Scand J Rheumatol, 2012, 41(3):219-22.
 
 
Genetically elevated levels of circulating triglycerides and brachial-ankle pulse wave velocity in a Chinese population
Yao WM, et al.
"J Hum Hypertens, 2013, 27(4):265-70.
 
 
人類 Y 染色體 36 個(gè)新 STR 位點(diǎn)的篩選與鑒定
彭冬鉑等
遺傳,2012, 34(11):1409-1416
 
 
人類細(xì)胞系基因表達(dá)中校正因子的選擇
孫斯平等
國際遺傳學(xué)雜志, 2012,35(5):262-267.
 
 
An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer’s disease
Liu QY, et al.
Neurobiol Aging, 2013, 34(5):1519.e13-7.
 
 
廣西百色地區(qū)壯族男性人群骨密度與脂聯(lián)素基因單核苷酸多態(tài)性的關(guān)系
王金花等
中國組織工程研究與臨床康復(fù), 2011,15(33):6252-6256.
 
 
Immunosuppressive cytokine gene polymorphisms and outcome after related and unrelated hematopoietic cell transplantation in Chinese population
Xiao H,et al.
Biol Blood Marrow Transplant, 2011, 17(4):542-9.
 
 
Two novel mutations in the Spastin gene of Chinese patients with hereditary spastic paraplegia
Fei QZ,et al.
Eur J Neurol, 2011, 18(9):1194-6.
 
 
人染色體 8p11(CHRNB3-CHRNA6)區(qū)域基因多態(tài)性與中國漢族人群肺癌易感性的相關(guān)性
張曉博等
遺傳, 2011,33(8):886-894.
 
 
新疆維吾爾族健康人中 Tim-3基因結(jié)構(gòu)分析
王燕等
山東大學(xué)學(xué)報(bào), 2011,49(2):88-92.
 
 
Familial Nonsyndromic Patent Ductus Arteriosus Caused by Mutations in TFAP2B
Chen YW,et al.
Pediatr Cardiol, 2011, 32(7):958-65.
 
 
First report of multiple CEBPA mutations contributing to donor origin of leukemia relapse after allogeneic hematopoietic stem cell transplantation
Xiao H,et al.
Blood, 2011, 117(19):5257-60.
 
 
X-linked recessive combined pituitary hormone deficiency is mapped to Xp22.3–Xp11 in a Chinese family
Wang CL,et al.
Genomics, 2011, 98(6):440-4.
 
 
非小細(xì)胞肺癌中EGFR和K-ras基因突變與蛋白表達(dá)相關(guān)性的研究
欒煥玲等
中國癌癥雜志, 2010, 20(7):486-491.
 
 
Rapid method for identification of six common species of mycobacteria based on multiplex SNP analysis
Wang H,et al.
J Clin Microbiol, 2010, 48(1):247-50.
 
 
The prevalence of factor VIII inhibitors and genetic aspects of inhibitor development in Chinese patients with haemophilia A
Wang XF,et al.
Haemophilia, 2010, 16(4):632-9.
 
 
Relationship between TNFA, TNFB and TNFRII gene polymorphisms and outcome after unrelated hematopoietic cell transplantation in a Chinese population
Xiao HW,et al.
Bone Marrow Transplant, 2011, 46(3):400-7.
 
 
Association of TGF-beta1 gene polymorphisms in exon1 and blood levels with essential hypertension
He F,et al.
Blood Press, 2010, 19(4):225-33.
 
 
Analysis of the association between BTNL2 polymorphism and tuberculosis in Chinese Han population
Lian Y,et al.
Infect Genet Evol, 2010, 10(4):517-21.
 
 
VANGL2 Mutations in Human Cranial Neural-Tube Defects
Lei YP,et al.
N Engl J Med, 2010, 362(23):2232-5.
 
 
K-ras Mutations in the Plasma of Colorecta Cancer Patients
Shen YQ,et al.
LabMedicine, 2010, 41(3):156-158.
 
 
Association between NMDA receptor subunit 2b gene polymorphism and Alzheimer's disease in Chinese Han population in Shanghai
Chen C,et al.
Neurosci Bull, 2010, 26(5):395-400.
 
 
Association between VDR and ESR1 gene polymorphisms with bone and obesity phenotypes in Chinese male nuclear families
Gu JM,et al.
Acta Pharmacol Sin, 2009, 30(12):1634-42.
 
 
Association study between C7673T polymorphism in apolipoprotein B gene and cerebral infarction with family history in a Chinese population
Zhang L,et al.
Neurol India, 2009, 57(5):584-8.
 
 
Early onset Paget's disease of bone caused by a novel mutation (78dup27) of the TNFRSF11A gene in a Chinese family
Ke YH,et al.
Acta Pharmacol Sin, 2009, 30(8):1204-10.
 
 
Haemophilia A in two unrelated females due to F8 gene inversions combined with skewed inactivation of X chromosome
Wang X,et al.
Thromb Haemost, 2009, 101(4):775-8.
 
 
Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia
Yue H, et al.
Bone, 2009, 44(4):547-54.
 
 
載脂蛋白B基因C7673T多態(tài)與有家族聚集現(xiàn)象腦出血的關(guān)系
張樂等
中華醫(yī)學(xué)遺傳學(xué)雜志, 2008,25(2):145-149
 
 
MMP2 promoter polymorphism (C-1306T) and risk of recurrence in patients with hepatocellular carcinoma after transplantation
Wu LM, et al.
Clin Genet, 2008, 73(3):273-8.
 
 
Polymorphisms in cytokine genes and their association with acute rejection and recurrence of hepatitis B in Chinese liver transplant recipients
Xie HY, et al.
Arch Med Res, 2008, 39(4):420-8.
 
 
Novel BSCL2 gene mutation E189X in Chinese congenital generalized lipodystrophy child with early onset diabetes mellitus
Jin J, et al.
Eur J Endocrinol, 2007, 157(6):783-7.
 
 
Recipient cytotoxic T lymphocyte antigen-4 +49 G/G genotype is associated with reduced incidence of hepatitis B virus recurrence after liver transplantation among Chinese patients
Jiang Z, et al.
Liver Int, 2007, 27(9):1202-8.
 
 

------分隔線----------------------------