IL-10 and integrin signaling pathways are associated with head and neck cancer progression.
BMC genomics | 2016-01-08 | PMID 26747525
Bornstein Sophia, Schmidt Mark, Choonoo Gabrielle and 5 more
Genes: CTCF, HRH4, LEP, PAGE4, PAGE5, SMTNL1, VTN
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.
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Publications
Page 6747 of 10600
Cellular phenotyping of chronic rhinosinusitis with nasal polyps.
Rhinology | 2016-06-01 | PMID 26747641
Lou Hongfei, Meng Yifan, Piao Yingshi and 4 more
Identification of a triacylglycerol lipase in the diatom Phaeodactylum tricornutum.
Biochimica et biophysica acta | 2016-03-01 | PMID 26747649
Barka Frederik, Angstenberger Max, Ahrendt Tilman and 3 more
Transcriptional Regulation of miR-31 by Oncogenic KRAS Mediates Metastatic Phenotypes by Repressing RASA1.
Molecular cancer research : MCR | 2016-03-01 | PMID 26747707
Kent Oliver A, Mendell Joshua T, Rottapel Robert
Genes: KRAS, RASA1, ELK1
Genetic control of bone mass.
Molecular and cellular endocrinology | 2016-09-05 | PMID 26747728
Boudin Eveline, Fijalkowski Igor, Hendrickx Gretl and 1 more
Heritability and reliability of automatically segmented human hippocampal formation subregions.
NeuroImage | 2016-03-01 | PMID 26747746
Whelan Christopher D, Hibar Derrek P, van Velzen Laura S and 16 more
Association of ATG5 Gene Polymorphisms With Behçet's Disease and ATG10 Gene Polymorphisms With VKH Syndrome in a Chinese Han Population.
Investigative ophthalmology & visual science | 2015-12-01 | PMID 26747760
Zheng Minming, Yu Hongsong, Zhang Lijun and 4 more
Genes: ATG5, ATG10, ATG7, DAP, IRGM, TSC1, ULK1
Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet Genes.
Investigative ophthalmology & visual science | 2015-12-01 | PMID 26747767
Sun Wenmin, Huang Li, Xu Yan and 7 more
Genes: FBN1, GNAT1, OPA1, PAX2, PRPH2, RPGR, TSPAN12
Predicting the genetic consequences of future climate change: The power of coupling spatial demography, the coalescent, and historical landscape changes.
American journal of botany | 2016-01-01 | PMID 26747843
Brown Jason L, Weber Jennifer J, Alvarado-Serrano Diego F and 3 more
Knockdown Resistance (kdr) Mutations in Indian Anopheles stephensi (Diptera: Culicidae) Populations.
Journal of medical entomology | 2016-03-01 | PMID 26747858
Dykes Cherry L, Das Manoj K, Eapen Alex and 5 more
Genes: DDT
The role of enterocyte defects in the pathogenesis of congenital diarrheal disorders.
Disease models & mechanisms | 2016-01-01 | PMID 26747865
Overeem Arend W, Posovszky Carsten, Rings Edmond H M M and 2 more
The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders.
Disease models & mechanisms | 2016-01-01 | PMID 26747866
Fieten Hille, Gill Yadvinder, Martin Alan J and 18 more
Tauroursodeoxycholic acid prevents hearing loss and hair cell death in Cdh23(erl/erl) mice.
Neuroscience | 2016-03-01 | PMID 26748055
Hu J, Xu M, Yuan J and 4 more
Molecular testing for familial hypercholesterolaemia-associated mutations in a UK-based cohort: development of an NGS-based method and comparison with multiplex polymerase chain reaction and oligonucleotide arrays.
Annals of clinical biochemistry | 2016-11-01 | PMID 26748104
Reiman Anne, Pandey Sarojini, Lloyd Kate L and 7 more
Comparative characterization of botulinum neurotoxin subtypes F1 and F7 featuring differential substrate recognition and cleavage mechanisms.
Toxicon : official journal of the International Society on Toxinology | 2016-03-01 | PMID 26748154
Guo Jiubiao, Chan Edward Wai Chi, Chen Sheng
Genes: VAMP2
Fetal Rat Gubernaculum Mesenchymal Cells Adopt Myogenic and Myofibroblast-Like Phenotypes.
The Journal of urology | 2016-07-01 | PMID 26748163
Robbins Alan K, Mateson Abigail B, Khandha Ashutosh and 4 more
Genes: PAX7
Mutation spectrum of POLE and POLD1 mutations in South East Asian women presenting with grade 3 endometrioid endometrial carcinomas.
Gynecologic oncology | 2016-04-01 | PMID 26748215
Wong Adele, Kuick Chik Hong, Wong Wai Loong and 11 more
Genes: POLE, POLD1, SEA
Efficacy of a Gluten-Free Diet in Subjects With Irritable Bowel Syndrome-Diarrhea Unaware of Their HLA-DQ2/8 Genotype.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association | 2016-05-01 | PMID 26748221
Aziz Imran, Trott Nick, Briggs Rebecca and 3 more
mTOR inhibitor temsirolimus and MEK1/2 inhibitor U0126 promote chromosomal instability and cell type-dependent phenotype changes of glioblastoma cells.
Gene | 2016-03-15 | PMID 26748241
Stepanenko A A, Andreieva S V, Korets K V and 4 more
Biophysical changes of ATP binding pocket may explain loss of kinase activity in mutant DAPK3 in cancer: A molecular dynamic simulation analysis.
Gene | 2016-04-10 | PMID 26748242
Agarwal Tarun, Annamalai Nithyanan, Maiti Tapas Kumar and 1 more
Genes: DAPK3
Association between the surfactant protein D (SFTPD) gene and subclinical carotid artery atherosclerosis.
Atherosclerosis | 2016-03-01 | PMID 26748346
Sorensen Grith L, Bladbjerg Else Marie, Steffensen Rudi and 4 more
Genes: SFTPD
Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis.
Rheumatology (Oxford, England) | 2016-05-01 | PMID 26748351
Tsang-A-Sjoe Michel W P, Nagelkerke Sietse Q, Bultink Irene E M and 11 more
Genes: CNR1
Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome.
Clinical immunology (Orlando, Fla.) | 2016-02-01 | PMID 26748374
Colobran Roger, Álvarez de la Campa Elena, Soler-Palacín Pere and 4 more
Genes: FOXP3
Low frequency of broadly neutralizing HIV antibodies during chronic infection even in quaternary epitope targeting antibodies containing large numbers of somatic mutations.
Molecular immunology | 2016-02-01 | PMID 26748387
Hicar Mark D, Chen Xuemin, Kalams Spyros A and 5 more
GRP-3 and KAPP, encoding interactors of WAK1, negatively affect defense responses induced by oligogalacturonides and local response to wounding.
Journal of experimental botany | 2016-03-01 | PMID 26748394
Gramegna Giovanna, Modesti Vanessa, Savatin Daniel V and 3 more
Genes: GRP
The Impact of Magnetic Resonance Enterography and Capsule Endoscopy on the Re-classification of Disease in Patients with Known Crohn's Disease: A Prospective Israeli IBD Research Nucleus (IIRN) Study.
Journal of Crohn's & colitis | 2016-05-01 | PMID 26748404
Greener Tomer, Klang Eyal, Yablecovitch Doron and 13 more
Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing.
Clinical genetics | 2016-06-01 | PMID 26748417
Mouden C, Dubourg C, Carré W and 10 more
Genes: DISP1, SHH
Functionalities of expressed messenger RNAs revealed from mutant phenotypes.
Wiley interdisciplinary reviews. RNA | 2016-07-01 | PMID 26748449
Liao Ben-Yang, Weng Meng-Pin
Cytomolecular characterization and origin of de novo formed maize B chromosome variants.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology | 2016-05-01 | PMID 26748511
Cheng Ya-Ming, Feng Ying-Ru, Lin Yao-Pin and 1 more
Genomic Signatures of Selective Pressures and Introgression from Archaic Hominins at Human Innate Immunity Genes.
American journal of human genetics | 2016-01-07 | PMID 26748513
Deschamps Matthieu, Laval Guillaume, Fagny Maud and 5 more
Genes: STAT1, TLR1, TLR10, TLR6, TRAF3
Introgression of Neandertal- and Denisovan-like Haplotypes Contributes to Adaptive Variation in Human Toll-like Receptors.
American journal of human genetics | 2016-01-07 | PMID 26748514
Dannemann Michael, Andrés Aida M, Kelso Janet
Genes: TLR1, TLR10, TLR6
Genotype Imputation with Millions of Reference Samples.
American journal of human genetics | 2016-01-07 | PMID 26748515
Browning Brian L, Browning Sharon R
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.
American journal of human genetics | 2016-01-07 | PMID 26748517
Kochinke Korinna, Zweier Christiane, Nijhof Bonnie and 10 more
Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos.
American journal of human genetics | 2016-01-07 | PMID 26748518
Conomos Matthew P, Laurie Cecelia A, Stilp Adrienne M and 34 more
Association of COL4A1 gene polymorphisms with cerebral palsy in a Chinese Han population.
Clinical genetics | 2016-08-01 | PMID 26748532
Bi D, Wang H, Shang Q and 10 more
Kinetic and structural characterization of amyloid-β peptide hydrolysis by human angiotensin-1-converting enzyme.
The FEBS journal | 2016-03-01 | PMID 26748546
Larmuth Kate M, Masuyer Geoffrey, Douglas Ross G and 3 more
Genes: ACE
The evolution of sperm competition genes: The effect of mating system on levels of genetic variation within and between species.
Evolution; international journal of organic evolution | 2016-02-01 | PMID 26748568
Dapper Amy L, Wade Michael J
Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS.
Pediatric transplantation | 2016-03-01 | PMID 26748574
Saida Satoshi, Umeda Katsutsugu, Yasumi Takahiro and 6 more
Genes: GATA2
Truncation and microdeletion of EVC/EVC2 with missense mutation of EFCAB7 in Ellis-van Creveld syndrome.
Congenital anomalies | 2016-09-01 | PMID 26748586
Nguyen Tran Quynh Nhu, Saitoh Makiko, Trinh Huu Tung and 6 more
Genes: EVC, EVC2, EFCAB7
Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disorders.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society | 2016-03-01 | PMID 26748598
de Goede Christian, Yue Wyatt W, Yan Guanhua and 7 more
Genes: RABL6
Founder effect is responsible for the p.Leu131Phe heparin-binding-site antithrombin mutation common in Hungary: phenotype analysis in a large cohort.
Journal of thrombosis and haemostasis : JTH | 2016-04-01 | PMID 26748602
Gindele R, Oláh Z, Ilonczai P and 9 more
Genes: SERPINC1
The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA.
Clinical genetics | 2016-10-01 | PMID 26748608
Cetin H, Wöhrer A, Rittelmeyer I and 5 more
Genes: LAMP2
Adaptation of Escherichia coli to glucose promotes evolvability in lactose.
Evolution; international journal of organic evolution | 2016-02-01 | PMID 26748670
Phillips Kelly N, Castillo Gerardo, Wünsche Andrea and 1 more
CDR3β sequence motifs regulate autoreactivity of human invariant NKT cell receptors.
Journal of autoimmunity | 2016-04-01 | PMID 26748722
Chamoto Kenji, Guo Tingxi, Imataki Osamu and 8 more
Regulation of cell reversal frequency in Myxococcus xanthus requires the balanced activity of CheY-like domains in FrzE and FrzZ.
Molecular microbiology | 2016-04-01 | PMID 26748740
Kaimer Christine, Zusman David R
Mutational spectrum of Korean patients with corneal dystrophy.
Clinical genetics | 2016-06-01 | PMID 26748743
Chae H, Kim M, Kim Y and 8 more
Genes: SCD, TGFBI
Genome Editing in Human Pluripotent Stem Cells: Approaches, Pitfalls, and Solutions.
Cell stem cell | 2016-01-07 | PMID 26748756
Hendriks William T, Warren Curtis R, Cowan Chad A
Prognostic significance of CpG island methylator phenotype in surgically resected small cell lung carcinoma.
Cancer science | 2016-03-01 | PMID 26748784
Saito Yuichi, Nagae Genta, Motoi Noriko and 10 more
Genes: TRADD
α-1,3-Glucanase: present situation and prospect of research.
World journal of microbiology & biotechnology | 2016-02-01 | PMID 26748807
Suyotha Wasana, Yano Shigekazu, Wakayama Mamoru
Pleiotropy and the low cost of individual traits promote cooperation.
Evolution; international journal of organic evolution | 2016-02-01 | PMID 26748821
Mitri Sara, Foster Kevin R
MDM2 Associates with Polycomb Repressor Complex 2 and Enhances Stemness-Promoting Chromatin Modifications Independent of p53.
Molecular cell | 2016-01-07 | PMID 26748827
Wienken Magdalena, Dickmanns Antje, Nemajerova Alice and 11 more
Genes: MDM2, RNF2
Evidence that Environmental Heterogeneity Maintains a Detoxifying Enzyme Polymorphism in Drosophila melanogaster.
Current biology : CB | 2016-01-25 | PMID 26748852
Chakraborty Mahul, Fry James D
Spleen enlargement is a risk factor for thrombosis in essential thrombocythemia: Evaluation on 1,297 patients.
American journal of hematology | 2016-03-01 | PMID 26748894
Andriani Alessandro, Latagliata Roberto, Anaclerico Barbara and 20 more
Mutational pattern of a sample from a critical branching population.
Journal of mathematical biology | 2016-09-01 | PMID 26748918
Delaporte Cécile, Achaz Guillaume, Lambert Amaury
Systematic Review of Modelling Approaches for the Cost Effectiveness of Hepatitis C Treatment with Direct-Acting Antivirals.
PharmacoEconomics | 2016-06-01 | PMID 26748919
Chhatwal Jagpreet, He Tianhua, Lopez-Olivo Maria A
Germline BAP1 mutations misreported as somatic based on tumor-only testing.
Familial cancer | 2016-04-01 | PMID 26748926
Abdel-Rahman Mohamed H, Rai Karan, Pilarski Robert and 2 more
Genes: BAP1
The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety.
Familial cancer | 2016-04-01 | PMID 26748927
Sermijn Erica, Delesie Liesbeth, Deschepper Ellen and 4 more
Genes: BRCA1
Antibody humanization by molecular dynamics simulations-in-silico guided selection of critical backmutations.
Journal of molecular recognition : JMR | 2016-06-01 | PMID 26748949
Margreitter Christian, Mayrhofer Patrick, Kunert Renate and 1 more
5'UTR +24T>C CR2 is not associated with nasopharyngeal carcinoma development in the North Region of Portugal.
Oral diseases | 2016-05-01 | PMID 26748973
Sousa H, Bastos M J, Ribeiro J and 4 more
Inter and intra-population phenotypic and genotypic structuring in the European whitefish Coregonus lavaretus, a rare freshwater fish in Scotland.
Journal of fish biology | 2016-02-01 | PMID 26748995
Adams C E, Bean C W, Dodd J A and 8 more
Genes: FST
De novo development and characterization of polymorphic microsatellite markers in a schilbid catfish, Silonia silondia (Hamilton, 1822) and their validation for population genetic studies.
Molecular biology reports | 2016-02-01 | PMID 26748998
Mandal Sangeeta, Jena J K, Singh Rajeev K and 5 more
Genes: FST
Role of gene expression profiling in defining indeterminate thyroid nodules in addition to BRAF analysis.
Cancer cytopathology | 2016-05-01 | PMID 26749005
Borrelli Nicla, Ugolini Clara, Giannini Riccardo and 7 more
Genes: BRAF
Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention.
Epilepsia | 2016-01-01 | PMID 26749013
Goldman Alica M, Behr Elijah R, Semsarian Christopher and 3 more
ERBB-2 overexpression as a risk factor for malignant phaeochromocytomas and paraganglinomas.
Clinical endocrinology | 2016-06-01 | PMID 26749044
Wang Weiqing, Zhong Xu, Ye Lei and 9 more
The pathological effects of connexin 26 variants related to hearing loss by in silico and in vitro analysis.
Human genetics | 2016-03-01 | PMID 26749107
Kim Hui Ram, Oh Se-Kyung, Lee Eun-Shil and 7 more
Genes: GJB2
Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome.
American journal of medical genetics. Part A | 2016-03-01 | PMID 26749132
Wilson Brian T, Lochan Anneline, Stark Zornitza and 1 more
Genes: ERCC6, ERCC8
Disruptive selection without genome-wide evolution across a migratory divide.
Molecular ecology | 2016-06-01 | PMID 26749140
von Rönn Jan A C, Shafer Aaron B A, Wolf Jochen B W
Genes: BUB1
ATP-binding cassette transporter 1 (ABCA1) deficiency decreases platelet reactivity and reduces thromboxane A2 production independently of hematopoietic ABCA1.
Journal of thrombosis and haemostasis : JTH | 2016-03-01 | PMID 26749169
Lhermusier T, Severin S, Van Rothem J and 9 more
Genes: ABCA1
Global deletion of Panx3 produces multiple phenotypic effects in mouse humeri and femora.
Journal of anatomy | 2016-05-01 | PMID 26749194
Caskenette Deidre, Penuela Silvia, Lee Vanessa and 4 more
Proptosis, Micrognathia, Low Set Ear and Chest Deformity in a Patient with Extra Marker Chromosome 22.
Acta medica Iranica | 2015-12-01 | PMID 26749236
Mosallanejad Asieh, Sayarifard Fatemeh, Hosseinverdi Sima and 3 more
Disease-Causing SDHAF1 Mutations Impair Transfer of Fe-S Clusters to SDHB.
Cell metabolism | 2016-02-09 | PMID 26749241
Maio Nunziata, Ghezzi Daniele, Verrigni Daniela and 7 more
Genes: SDHB, SDHAF1, HSPA9, ISCU, LONP1, SDHA
Genotype/phenotype correlation in a female patient with 21q22.3 and 12p13.33 duplications.
American journal of medical genetics. Part A | 2016-04-01 | PMID 26749249
Mekkawy Mona K, Mazen Inas M, Kamel Alaa K and 2 more
Cell adhesion and polarity in squamous cell carcinoma of the lung.
The Journal of pathology | 2016-04-01 | PMID 26749265
Bonastre Ester, Brambilla Elisabeth, Sanchez-Cespedes Montse
MicroRNA-378-mediated suppression of Runx1 alleviates the aggressive phenotype of triple-negative MDA-MB-231 human breast cancer cells.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2016-07-01 | PMID 26749280
Browne Gillian, Dragon Julie A, Hong Deli and 10 more
Investigation of FIH-1 and SOCS3 expression in KRAS mutant and wild-type patients with colorectal cancer.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2016-07-01 | PMID 26749281
Vakil Ladan, Najafipour Reza, Rakhshani Nasser and 3 more
Genes: KRAS, SOCS3, APC
Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV.
American journal of human genetics | 2016-01-07 | PMID 26749307
Duyzend Michael H, Nuttle Xander, Coe Bradley P and 4 more
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.
American journal of human genetics | 2016-01-07 | PMID 26749308
Turner Tychele N, Hormozdiari Fereydoun, Duyzend Michael H and 21 more
Genes: CANX, DISC1, DSCAM, MBD5, PRKCA, RBFOX1, SAE1
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2.
American journal of human genetics | 2016-01-07 | PMID 26749309
Davidson Alice E, Liskova Petra, Evans Cerys J and 23 more
Genes: OVOL2, ZEB1
Cardiac function in BRCA1/2 mutation carriers with history of breast cancer treated with anthracyclines.
Breast cancer research and treatment | 2016-01-01 | PMID 26749359
Barac Ana, Lynce Filipa, Smith Karen L and 11 more
Genes: BRCA1, GLS
Does kinship affect spatial organization in a small and isolated population of a solitary felid: The Eurasian lynx?
Integrative zoology | 2016-09-01 | PMID 26749400
Schmidt Krzysztof, Davoli Francesca, Kowalczyk Rafał and 1 more
Isolation, Characterization and Virulence Potential of Tenacibaculum dicentrarchi in Salmonid Cultures in Chile.
Transboundary and emerging diseases | 2016-04-01 | PMID 26749435
Avendaño-Herrera R, Irgang R, Sandoval C and 6 more
The association between codon72 polymorphism of p53 gene and the risk of endometrial cancer: an updating meta-analysis.
Archives of gynecology and obstetrics | 2016-08-01 | PMID 26749437
Lin Xinzi, Hou Dabiao, Huang Chenlingzi and 1 more
The Structure of a BamA-BamD Fusion Illuminates the Architecture of the β-Barrel Assembly Machine Core.
Structure (London, England : 1993) | 2016-02-02 | PMID 26749448
Bergal Hans Thor, Hopkins Alex Hunt, Metzner Sandra Ines and 1 more
Polymorphisms in methylenetetrahydrofolate reductase and cystathionine beta-synthase in oral cancer - a case-control study in southeastern Brazilians.
Brazilian journal of otorhinolaryngology | 2000-01-01 | PMID 26749456
Barbosa Andressa, Dos Santos Marcelo, de Podestá José Roberto Vasconcelos and 4 more
Genes: MTHFR, CBS
Novel copy number variants and major limb reduction malformation: Report of three cases.
American journal of medical genetics. Part A | 2016-05-01 | PMID 26749485
Shamseldin Hanan E, Anazi Shams, Wakil Salma M and 7 more
Genes: LMBR1, RAC1, TBX3, TBX5
Acquired C797S Mutation upon Treatment with a T790M-Specific Third-Generation EGFR Inhibitor (HM61713) in Non-Small Cell Lung Cancer.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer | 2016-04-01 | PMID 26749488
Song Haa-Na, Jung Ki Sun, Yoo Kwai Han and 11 more
Genes: EGFR
Prader-Willi Syndrome: A spectrum of anatomical and clinical features.
Clinical anatomy (New York, N.Y.) | 2016-07-01 | PMID 26749552
Hurren Bradley J, Flack Natasha A M S
Microvirga massiliensis sp. nov., the human commensal with the largest genome.
MicrobiologyOpen | 2016-04-01 | PMID 26749561
Caputo Aurélia, Lagier Jean-Christophe, Azza Saïd and 4 more
Dendritic cells: phenotypic and functional heterogeneity.
Italian journal of anatomy and embryology = Archivio italiano di anatomia ed embriologia | 2014-01-01 | PMID 26749691
Silvano Angela
[LEFT VENTRICULAR NON-COMPACTION].
Lijecnicki vjesnik | 2000-01-01 | PMID 26749956
Božić Ivo, Jurišić Zrinka, Božić Dorotea and 3 more
Advances in Exploring the Role of Micrornas in Inflammatory Bowel Disease.
MicroRNA (Shariqah, United Arab Emirates) | 2016-01-01 | PMID 26750140
Ciccacci Cinzia, Politi Cristina, Novelli Giuseppe and 1 more
Functional and prognostic relevance of -173 G/C gene polymorphism of macrophage migration inhibitory factor in sepsis patients in Egyptian intensive care units.
Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit | 2015-12-13 | PMID 26750167
Meawed T E, Mansour M A, Mansour S A and 3 more
Genes: MIF
A human monoclonal antibody against HPV16 recognizes an immunodominant and neutralizing epitope partially overlapping with that of H16.V5.
Scientific reports | 2016-01-11 | PMID 26750243
Xia Lin, Xian Yangfei, Wang Daning and 11 more
REPLACR-mutagenesis, a one-step method for site-directed mutagenesis by recombineering.
Scientific reports | 2016-01-11 | PMID 26750263
Trehan Ashutosh, Kiełbus Michał, Czapinski Jakub and 3 more
Changes in pathogenicity and immunogenicity of Mycoplasma mycoides subsp. mycoides strains revealed by comparative genomics analysis.
Scientific reports | 2016-01-11 | PMID 26750304
Li Yuan, Wang Yang, Wang Rui and 11 more
The association between the serotonin and dopamine neurotransmitters and personality traits.
Epidemiology and psychiatric sciences | 2016-04-01 | PMID 26750396
Delvecchio G, Bellani M, Altamura A C and 1 more
Genes: DRD2, DRD4, HTT
The variation in the eating quality of beef from different sexes and breed classes cannot be completely explained by carcass measurements.
Animal : an international journal of animal bioscience | 2016-06-01 | PMID 26750424
Bonny S P F, Hocquette J-F, Pethick D W and 6 more
Stomatin-like protein 2 overexpression in papillary thyroid carcinoma is significantly associated with high-risk clinicopathological parameters and BRAFV600E mutation.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica | 2016-04-01 | PMID 26750533
Bartolome Aleksandar, Boskovic Srdjan, Paunovic Ivan and 2 more
Genes: BRAF
1,25D3 prevents CD8(+)Tc2 skewing and asthma development through VDR binding changes to the Cyp11a1 promoter.
Nature communications | 2016-01-11 | PMID 26750596
Schedel Michaela, Jia Yi, Michel Sven and 12 more
Genes: VDR
Dual Function of DNA Sequences: Protein-Coding Sequences Function as Transcriptional Enhancers.
Perspectives in biology and medicine | 2015-01-01 | PMID 26750601
Hirsch Naama, Birnbaum Ramon Y