Tristetraprolin exerts tumor suppressive functions on the tumorigenesis of glioma by targeting IL-13.
International immunopharmacology | 2016-10-01 | PMID 27424080
Zeng Bo, Zhu Danhua, Su Zhipeng and 2 more
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 6987 of 10600
Association of Promoter Polymorphisms of Interleukin-10 and Interferon-Gamma Genes with Tuberculosis in Azeri Population of Iran.
Iranian journal of allergy, asthma, and immunology | 2016-06-01 | PMID 27424131
Asgharzadeh Mohammad, Ghorghanlu Sajjad, Rashedi Jalil and 5 more
Cytotoxic T Lymphocyte Antigen-4 Gene Variants in Type 2 Diabetic Patients with or without Neuropathy.
Iranian journal of allergy, asthma, and immunology | 2016-06-01 | PMID 27424137
Kiani Javad, Khadempar Saedeh, Hajilooi Mehrdad and 3 more
Lack of Association between Interleukin-8 Gene +781 C/T Polymorphism and Henoch-Schönlein Purpura in Childhood.
Iranian journal of allergy, asthma, and immunology | 2016-06-01 | PMID 27424139
Xu Hui, Pan Yan-Xiang, Zhang Junfeng and 3 more
A Bigger Toolbox: Biotechnology in Biodiversity Conservation.
Trends in biotechnology | 2017-01-01 | PMID 27424151
Corlett Richard T
Putative binding mode of Escherichia coli exopolyphosphatase and polyphosphates based on a hybrid in silico/biochemical approach.
Archives of biochemistry and biophysics | 2016-09-15 | PMID 27424154
Boetsch Cristhian, Aguayo-Villegas Daniel R, Gonzalez-Nilo Fernando D and 2 more
Exenatide and metformin express their anti-inflammatory effects on human monocytes/macrophages by the attenuation of MAPKs and NFκB signaling.
Naunyn-Schmiedeberg's archives of pharmacology | 2016-10-01 | PMID 27424158
Bułdak Łukasz, Machnik Grzegorz, Bułdak Rafał Jakub and 3 more
Genes: EBP, TNF
A first-in-human phase I study to evaluate the MEK1/2 inhibitor, cobimetinib, administered daily in patients with advanced solid tumors.
Investigational new drugs | 2016-10-01 | PMID 27424159
Rosen Lee S, LoRusso Patricia, Ma Wen Wee and 10 more
Genes: BRAF
Association between Sirtuin 1 Gene rs10997870 Polymorphism and Suicide Behaviors in Bipolar Disorder.
Neuropsychobiology | 2016-01-01 | PMID 27424200
Nivoli Alessandra, Porcelli Stefano, Albani Diego and 5 more
Genes: SIRT1
A 3'UTR polymorphism marks differential KLRG1 mRNA levels through disruption of a miR-584-5p binding site and associates with pemphigus foliaceus susceptibility.
Biochimica et biophysica acta | 2016-10-01 | PMID 27424220
Cipolla Gabriel A, Park Jong Kook, de Oliveira Liana A and 7 more
Genes: KLRG1, CTLA4, KLRD1, NKG7
Early B-cell factor 1 (EBF1) is critical for transcriptional control of SLAMF1 gene in human B cells.
Biochimica et biophysica acta | 2016-10-01 | PMID 27424222
Schwartz Anton M, Putlyaeva Lidia V, Covich Milica and 9 more
Genes: SLAMF1, EBF1, ELF1, SPI1, STAT6, TCF3
Genetic Diversity Among Historical Olive (Olea europaea L.) Genotypes from Southern Anatolia Based on SSR Markers.
Biochemical genetics | 2016-12-01 | PMID 27424255
Sakar Ebru, Unver Hulya, Ercisli Sezai
Genetic variability of Rickettsia spp. in Ixodes persulcatus ticks from continental and island areas of the Russian Far East.
Ticks and tick-borne diseases | 2016-10-01 | PMID 27424272
Igolkina Y, Bondarenko E, Rar V and 8 more
[Advances of Epigenetic Studies on Mechanisms of Paramutation].
Sheng li ke xue jin zhan [Progress in physiology] | 2016-02-01 | PMID 27424399
Cheng Shan, Wang Xiao-Rong, Ding Wei
[When to refer patients for oncogenetic counseling?].
Revue medicale suisse | 2016-05-18 | PMID 27424422
Viassolo Valeria, Chappuis Pierre O
[BRCA mutations: from Angelina Jolie to specific therapies].
Revue medicale suisse | 2016-05-18 | PMID 27424423
Lopez Veronica Aedo, Stravodimou Athina, Unger Sheila and 2 more
Genes: BRCA1, BRCA2
Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans.
Cancer letters | 2016-10-01 | PMID 27424524
Försti Asta, Frank Christoph, Smolkova Bozena and 11 more
Genes: PTTG1, ZWILCH, ZWINT, BUB3, CENPF, ESPL1, NEK2
Genomics era and complex disorders: Implications of GWAS with special reference to coronary artery disease, type 2 diabetes mellitus, and cancers.
Journal of postgraduate medicine | 2000-01-01 | PMID 27424552
Pranavchand R, Reddy B M
Genes: CAD
Ex vivo expanded regulatory T cells CD4+CD25+FoxP3+CD127Low develop strong immunosuppressive activity in patients with remitting-relapsing multiple sclerosis.
Autoimmunity | 2016-09-01 | PMID 27424664
Lifshitz Gelena V, Zhdanov Dmitry D, Lokhonina Anastasia V and 4 more
Recurrent HOXB13 mutations in the Dutch population do not associate with increased breast cancer risk.
Scientific reports | 2016-07-18 | PMID 27424772
Liu Jingjing, Prager-van der Smissen Wendy J C, Schmidt Marjanka K and 11 more
Genes: HOXB13, BRCA1
Mutation of the key residue for extraribosomal function of ribosomal protein S19 cause increased grooming behaviors in mice.
Neuroscience letters | 2016-08-26 | PMID 27424793
Chen Jun, Kaitsuka Taku, Fujino Rika and 3 more
Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma.
Nature communications | 2016-07-18 | PMID 27424798
Chahal Harvind S, Lin Yuan, Ransohoff Katherine J and 9 more
Genes: AHR, ASIP, BNC2, CADM1, OCA2, TYR
Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology | 2016-09-01 | PMID 27424800
Hauberg Mads Engel, Holm-Nielsen Marie Hebsgaard, Mattheisen Manuel and 4 more
Mutant IDH1 Downregulates ATM and Alters DNA Repair and Sensitivity to DNA Damage Independent of TET2.
Cancer cell | 2016-08-08 | PMID 27424808
Inoue Satoshi, Li Wanda Y, Tseng Alan and 35 more
Genes: IDH1, TET2, ATM
Evolutionary processes and environmental factors underlying the genetic diversity and lifestyles of Bacillus cereus group bacteria.
Research in microbiology | 2017-05-01 | PMID 27424810
Patiño-Navarrete Rafael, Sanchis Vincent
Heterogeneity and antibiotic resistance in Propionibacterium acnes isolates and its therapeutic implications: blurring the lines between commensal and pathogenic phylotypes.
Dermatologic therapy | 2016-11-01 | PMID 27424878
Sadhasivam Suresh, Sinha Mau, Saini Swamini and 5 more
Circular Permutation Probes for Illuminating Phosphorylation of Estrogen Receptor.
Methods in molecular biology (Clifton, N.J.) | 2016-01-01 | PMID 27424903
Kim Sung-Bae, Tao Hiroaki
Imaging Histone Methylations in Living Animals.
Methods in molecular biology (Clifton, N.J.) | 2016-01-01 | PMID 27424907
Sekar Thillai V, Paulmurugan Ramasamy
Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene.
Bone | 2016-10-01 | PMID 27424934
Choi Hyung Jin, Park Hyojung, Zhang Lei and 10 more
Genes: UHMK1, ESR1, KCNH1
Real-time PCR assay with high resolution melting for EGFR and BIM mutation of lung cancer.
European review for medical and pharmacological sciences | 2016-07-01 | PMID 27424979
Xia J-J, Zhao S-F, Xiong L-W and 6 more
Genes: EGFR
Genetic testing in veterinary dermatology.
Veterinary dermatology | 2017-02-01 | PMID 27425028
Leeb Tosso, Müller Eliane J, Roosje Petra and 1 more
CYP4F2 affects phenotypic outcome in adrenoleukodystrophy by modulating the clearance of very long-chain fatty acids.
Biochimica et biophysica acta | 2016-10-01 | PMID 27425035
van Engen Catherine E, Ofman Rob, Dijkstra Inge M E and 8 more
Genes: ABCD1
New insights toward the pathogenesis of ankylosing spondylitis; genetic variations and epigenetic modifications.
Modern rheumatology | 2017-03-01 | PMID 27425039
Mahmoudi Mahdi, Aslani Saeed, Nicknam Mohammad Hossein and 2 more
Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene.
Journal of clinical research in pediatric endocrinology | 2017-03-01 | PMID 27425121
Şahin Sezgin, Hiort Olaf, Thiele Susanne and 2 more
Genes: GNAS
Near fatal asthma: treatment and prevention.
European annals of allergy and clinical immunology | 2016-07-01 | PMID 27425166
D'Amato G, Vitale C, Lanza M and 10 more
Phylogeography and population genetics of Schizothorax o'connori: strong subdivision in the Yarlung Tsangpo River inferred from mtDNA and microsatellite markers.
Scientific reports | 2016-07-18 | PMID 27425185
Guo Xiang-Zhao, Zhang Gui-Rong, Wei Kai-Jian and 5 more
Additive reductions in zebrafish PRPS1 activity result in a spectrum of deficiencies modeling several human PRPS1-associated diseases.
Scientific reports | 2016-07-18 | PMID 27425195
Pei Wuhong, Xu Lisha, Varshney Gaurav K and 11 more
Genes: PRPS1
OaMAX2 of Orobanche aegyptiaca and Arabidopsis AtMAX2 share conserved functions in both development and drought responses.
Biochemical and biophysical research communications | 2016-09-16 | PMID 27425246
Li Weiqiang, Nguyen Kien Huu, Watanabe Yasuko and 2 more
Genes: MAX
Modulation of TRPV4 by diverse mechanisms.
The international journal of biochemistry & cell biology | 2016-09-01 | PMID 27425399
Darby W G, Grace M S, Baratchi S and 1 more
Genes: TRPV4
Prevalence of Hispanic BRCA1 and BRCA2 mutations among hereditary breast and ovarian cancer patients from Brazil reveals differences among Latin American populations.
Cancer genetics | 2016-09-01 | PMID 27425403
Alemar Bárbara, Herzog Josef, Brinckmann Oliveira Netto Cristina and 5 more
Genes: BRCA1, BRCA2
Automated Structure- and Sequence-Based Design of Proteins for High Bacterial Expression and Stability.
Molecular cell | 2016-07-21 | PMID 27425410
Goldenzweig Adi, Goldsmith Moshe, Hill Shannon E and 13 more
The Molecular Basis for Ubiquitin and Ubiquitin-like Specificities in Bacterial Effector Proteases.
Molecular cell | 2016-07-21 | PMID 27425412
Pruneda Jonathan N, Durkin Charlotte H, Geurink Paul P and 4 more
Genes: NEDD8
Interrogating the Molecular Basis for Substrate Recognition in Serotonin and Dopamine Transporters with High-Affinity Substrate-Based Bivalent Ligands.
ACS chemical neuroscience | 2016-10-19 | PMID 27425420
Andersen Jacob, Ladefoged Lucy Kate, Kristensen Trine N Bjerre and 6 more
Mesenchymal Tumors Can Derive from Ng2/Cspg4-Expressing Pericytes with β-Catenin Modulating the Neoplastic Phenotype.
Cell reports | 2016-07-26 | PMID 27425618
Sato Shingo, Tang Yuning J, Wei Qingxia and 10 more
Gene Expression Architecture of Mouse Dorsal and Tail Skin Reveals Functional Differences in Inflammation and Cancer.
Cell reports | 2016-07-26 | PMID 27425619
Quigley David A, Kandyba Eve, Huang Phillips and 9 more
EDN1 Gene Variant is Associated with Neonatal Persistent Pulmonary Hypertension.
Scientific reports | 2016-07-18 | PMID 27425626
Mei Mei, Cheng Guoqiang, Sun Bijun and 4 more
Genes: EDN1, ACE, NOS3, VEGFA
Pancreatic involvement in cystic fibrosis.
Minerva medica | 2016-12-01 | PMID 27425634
Ozen Alahdab Yesim, Duman Deniz G
Roles of Insulin Resistance, Endothelial Dysfunction and Lifestyle Changes in the Development of Cardiovascular Disease in Diabetic Patients.
Current drug targets | 2017-01-01 | PMID 27425648
Sun Dongdong, Man Wanrong, Zhang Lei
Implementation of a Reliable Next-Generation Sequencing Strategy for Molecular Diagnosis of Dystrophinopathies.
The Journal of molecular diagnostics : JMD | 2016-09-01 | PMID 27425820
Alame Melissa, Lacourt Delphine, Zenagui Reda and 5 more
Genes: DMD
Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy.
The Journal of molecular diagnostics : JMD | 2016-09-01 | PMID 27425821
Qu Yu-Jin, Bai Jin-Li, Cao Yan-Yan and 8 more
Genes: SMN1
Developing therapeutically more efficient Neurturin variants for treatment of Parkinson's disease.
Neurobiology of disease | 2016-12-01 | PMID 27425888
Runeberg-Roos Pia, Piccinini Elisa, Penttinen Anna-Maija and 11 more
Genes: NRTN, GDNF
Minute amounts of hamartin wildtype rescue the emergence of tuber-like lesions in conditional Tsc1 ablated mice.
Neurobiology of disease | 2016-11-01 | PMID 27425891
Robens Barbara K, Grote Alexander, Pitsch Julika and 3 more
Genes: TSC1
Discovering potential cancer driver genes by an integrated network-based approach.
Molecular bioSystems | 2016-08-16 | PMID 27426053
Shi Kai, Gao Lin, Wang Bingbo
Enhancement of a high efficient autoinducible expression system in Bacillus subtilis by promoter engineering.
Protein expression and purification | 2016-11-01 | PMID 27426133
Cheng Jintao, Guan Chengran, Cui Wenjing and 4 more
Influence of CYP3A5*3 and ABCB1 C3435T on clinical outcomes and trough plasma concentrations of imatinib in Nigerians with chronic myeloid leukaemia.
Journal of clinical pharmacy and therapeutics | 2016-10-01 | PMID 27426203
Adeagbo B A, Bolaji O O, Olugbade T A and 3 more
Genes: ABCB1, ABCG2
[Current status of EGFR/ErbB inhibitors in non-small cell lung carcinoma].
Medicina clinica | 2016-04-01 | PMID 27426241
Álvarez-Fernández Carlos, Esteban-González Emilio
Genes: EGFR
[Afatinib as first-line therapy in mutation-positive EGFR. Results by type of mutation].
Medicina clinica | 2016-04-01 | PMID 27426243
Vidal Óscar Juan
Genes: EGFR
[Evidence on afatinib in patients progressing on a first-line treatment].
Medicina clinica | 2016-04-01 | PMID 27426244
Artal Cortés Ángel, Gimeno Pelegrín Joaquín, Alejandro María Álvarez
Genes: EGFR
[Afatinib in patients with squamous cell carcinoma of the lung: current context and the option of oral treatment].
Medicina clinica | 2016-04-01 | PMID 27426245
Cobo Manuel, Gutiérrez Vanesa, Rodelo Luis and 3 more
Genes: EGFR
[Toxicity associated with EGRF inhibition: review and key aspects in the management of afatinib].
Medicina clinica | 2016-04-01 | PMID 27426246
Taus Álvaro
Genes: EGFR
Recombinant herpes simplex virus type 1 strains with targeted mutations relevant for aciclovir susceptibility.
Scientific reports | 2016-07-18 | PMID 27426251
Brunnemann Anne-Kathrin, Liermann Kristin, Deinhardt-Emmer Stefanie and 6 more
Parkinson-like phenotype in insulin-resistant PED/PEA-15 transgenic mice.
Scientific reports | 2016-07-18 | PMID 27426254
Perruolo Giuseppe, Viggiano Davide, Fiory Francesca and 6 more
Long-term outcomes of gene therapy for the treatment of Leber's hereditary optic neuropathy.
EBioMedicine | 2016-08-01 | PMID 27426279
Yang Shuo, Ma Si-Qi, Wan Xing and 8 more
Progressive Cerebellar Atrophy and a Novel Homozygous Pathogenic DNAJC19 Variant as a Cause of Dilated Cardiomyopathy Ataxia Syndrome.
Pediatric neurology | 2016-09-01 | PMID 27426421
Al Teneiji Amal, Siriwardena Komudi, George Kristen and 2 more
Genes: DNAJC19
The acquisition of Clostridium tyrobutyricum mutants with improved bioproduction under acidic conditions after two rounds of heavy-ion beam irradiation.
Scientific reports | 2016-07-18 | PMID 27426447
Zhou Xiang, Yang Zhen, Jiang Ting-Ting and 4 more
CLOVES syndrome: review of a PIK3CA-related overgrowth spectrum (PROS).
Clinical genetics | 2017-01-01 | PMID 27426476
Martinez-Lopez A, Blasco-Morente G, Perez-Lopez I and 6 more
Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency.
The Journal of allergy and clinical immunology | 2016-12-01 | PMID 27426521
Tsujita Yuki, Mitsui-Sekinaka Kanako, Imai Kohsuke and 30 more
Genes: PTEN
Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
Clinical genetics | 2017-03-01 | PMID 27426723
Su W, Zhu P, Wang R and 9 more
Genes: GATA4, TBX5
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia.
American journal of human genetics | 2016-08-04 | PMID 27426733
Wade Emma M, Daniel Philip B, Jenkins Zandra A and 27 more
Genes: FLNA, TAB2
Heterozygous Mutations in MAP3K7, Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome.
American journal of human genetics | 2016-08-04 | PMID 27426734
Le Goff Carine, Rogers Curtis, Le Goff Wilfried and 8 more
Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy.
American journal of human genetics | 2016-08-04 | PMID 27426735
Kopajtich Robert, Murayama Kei, Janecke Andreas R and 25 more
Alcohol Suppresses Tonic GABAA Receptor Currents in Cerebellar Granule Cells in the Prairie Vole: A Neural Signature of High-Alcohol-Consuming Genotypes.
Alcoholism, clinical and experimental research | 2016-08-01 | PMID 27426857
Kaplan Joshua S, Mohr Claudia, Hostetler Caroline M and 3 more
Current and emerging approaches for assessing von Willebrand disease in 2016.
International journal of laboratory hematology | 2016-05-01 | PMID 27426859
Federici A B
Genes: VWF
Generation of a LacZ reporter transgenic mouse line for the stereological analysis of oligodendrocyte loss in galactosylceramidase deficiency.
Journal of neuroscience research | 2016-12-01 | PMID 27426866
Zhu Hongling, Ornaghi Francesca, Belin Sophie and 3 more
Genes: MBP
Molecular characterization of species of Cloacina (Strongyloidea: Cloacininae) from the common wallaroo, Macropus robustus (Marsupialia: Macropodidae) in Australia.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2016-10-01 | PMID 27426890
Shuttleworth Mary A, Beveridge Ian, Koehler Anson V and 2 more
Tumour hypoxia promotes melanoma growth and metastasis via High Mobility Group Box-1 and M2-like macrophages.
Scientific reports | 2016-07-18 | PMID 27426915
Huber Roman, Meier Barbara, Otsuka Atsushi and 15 more
Genes: HMGB1
Molecular cloning and functional characterization of porcine E74-like factor 4 (ELF4).
Developmental and comparative immunology | 2016-12-01 | PMID 27426928
Shi Yanling, Wang Dang, Zhu Xinyu and 4 more
Genes: ELF4
Lack of Association between NOD2 rs3135500 and IL12B rs1368439 microRNA Binding Site SNPs and Colorectal Cancer Susceptibility in an Iranian Population.
MicroRNA (Shariqah, United Arab Emirates) | 2016-01-01 | PMID 27426943
Chaleshi Vahid, Tajali Raziye, Savabkar Sanaz and 7 more
Genes: NOD2
Association between STR -794 CATT5-8 and SNP -173 G/C polymorphisms in the MIF gene and Lepromatous Leprosy in Mestizo patients of western Mexico.
Human immunology | 2016-10-01 | PMID 27426952
Martinez-Guzman M A, Alvarado-Navarro A, Pereira-Suarez A L and 2 more
Genes: MIF
The role of vascular endothelial growth factor -634 G/C and its soluble receptor on chronic liver disease and hepatocellular carcinoma.
Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology | 2016-06-01 | PMID 27426958
Ratnasari Neneng, Nurdjanah Siti, Sadewa Ahmad H and 1 more
Genomic Recoding Broadly Obstructs the Propagation of Horizontally Transferred Genetic Elements.
Cell systems | 2016-08-01 | PMID 27426981
Ma Natalie Jing, Isaacs Farren J
GAPO syndrome: a new syndromic cause of premature ovarian insufficiency.
Climacteric : the journal of the International Menopause Society | 2016-12-01 | PMID 27426988
Benetti-Pinto C L, Ferreira V, Andrade L and 2 more
Genes: ANTXR1
Prenatal maternal depression and child serotonin transporter linked polymorphic region (5-HTTLPR) and dopamine receptor D4 (DRD4) genotype predict negative emotionality from 3 to 36 months.
Development and psychopathology | 2017-08-01 | PMID 27427178
Green Cathryn Gordon, Babineau Vanessa, Jolicoeur-Martineau Alexia and 14 more
Genes: DRD4
Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing.
International journal of laboratory hematology | 2016-12-01 | PMID 27427187
Del Orbe Barreto R, Arrizabalaga B, De la Hoz A B and 7 more
Genes: ADAMTS13, ANK1, EPB41, GPI, GSS, HBB, SPTB, TPI1
Whole-genome sequencing to determine transmission of Neisseria gonorrhoeae: an observational study.
The Lancet. Infectious diseases | 2016-11-01 | PMID 27427203
De Silva Dilrini, Peters Joanna, Cole Kevin and 15 more
Molecular Basis for Redox Activation of Epidermal Growth Factor Receptor Kinase.
Cell chemical biology | 2016-07-21 | PMID 27427230
Truong Thu H, Ung Peter Man-Un, Palde Prakash B and 3 more
Genes: EGFR
Evidence-Based and Quantitative Prioritization of Tool Compounds in Phenotypic Drug Discovery.
Cell chemical biology | 2016-07-21 | PMID 27427232
Wang Yuan, Cornett Allen, King Fred J and 5 more
Asymmetric dimethylarginine (ADMA): will be or will not be a new revolutionary biomarker of bronchial asthma?
Minerva medica | 2015-10-01 | PMID 27427261
Calabrese C, Carpagnano G E, Patella V and 2 more
Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL.
Scientific reports | 2016-07-18 | PMID 27427275
Dawidowska Małgorzata, Kosmalska Maria, Sędek Łukasz and 17 more
Genes: VDR
Helicobacter pylori resistance to clarithromycin in Reunion Island.
Medecine et maladies infectieuses | 2016-10-01 | PMID 27427280
Zemali N, Guillemot G, Jaubert J and 7 more
Is deafness mutation screening required in cystic fibrosis patients?
Paediatric respiratory reviews | 2016-08-01 | PMID 27427311
Abusamra Rania, McShane Donna
A novel polymorphism in protein kinase AMP-activated catalytic subunit alpha 2 (PRKAA2) is associated with type 2 diabetes in the Han Chinese population.
Journal of diabetes | 2017-06-01 | PMID 27427333
Shen Ji-Zhong, Ge Wei-Hong, Fang Yun and 1 more
Genes: PRKAA2
Computational analysis and enzyme assay of inhibitor response to disease single nucleotide polymorphisms (SNPs) in lipoprotein lipase.
Journal of bioinformatics and computational biology | 2016-10-01 | PMID 27427383
He Deyong, Huang Ling, Xu Yaping and 2 more
Genes: LPL
Cancer-associated isocitrate dehydrogenase mutations induce mitochondrial DNA instability.
Human molecular genetics | 2016-08-15 | PMID 27427385
Kingsbury Joanne M, Shamaprasad Nachiketha, Billmyre R Blake and 2 more
Genes: IDH1, IDH2
Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
Human molecular genetics | 2016-08-15 | PMID 27427386
Jiang Pingping, Liang Min, Zhang Chaofan and 10 more
TLR7 rs2897827 Polymorphism Affects TLR7 Gene mRNA Expression and Serum Apolipoprotein A1 Level of Ischemic Stroke Patients in a Chinese Han Population.
Journal of molecular neuroscience : MN | 2016-07-01 | PMID 27427388
Gu Lian, Zhou Jinying, Tan Jinjing and 5 more
Genes: TLR7
Avenues to autoimmune arthritis triggered by diverse remote inflammatory challenges.
Journal of autoimmunity | 2016-09-01 | PMID 27427404
Chevalier Nina, Tan Jian K, Mason Linda J and 9 more
Mendelian randomization study of adiposity-related traits and risk of breast, ovarian, prostate, lung and colorectal cancer.
International journal of epidemiology | 2016-06-01 | PMID 27427428
Gao Chi, Patel Chirag J, Michailidou Kyriaki and 19 more
Relative profile analysis of molecular markers for identification and genetic discrimination of loaches (Pisces, Nemacheilidae).
Comptes rendus biologies | 2000-01-01 | PMID 27427438
Patil Tejas Suresh, Tamboli Asif Shabodin, Patil Swapnil Mahadeo and 3 more
Mutation-Induced Population Shift in the MexR Conformational Ensemble Disengages DNA Binding: A Novel Mechanism for MarR Family Derepression.
Structure (London, England : 1993) | 2016-08-02 | PMID 27427478
Anandapadamanaban Madhanagopal, Pilstål Robert, Andresen Cecilia and 4 more