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 7508 of 10600

Genetic variations of bone marrow mesenchymal stromal cells derived from acute leukemia and myelodysplastic syndrome by targeted deep sequencing.
Leukemia research | 2017-11-01 | PMID 28964959
Azuma Kenko, Umezu Tomohiro, Imanishi Satoshi and 5 more
Genes: MSC, ASXL1, FLT3
Association of Single Nucleotide Polymorphism -2548 G/A (rs12112075) of leptin gene with endometrial cancer and uterine leiomyomas.
European journal of obstetrics, gynecology, and reproductive biology | 2017-11-01 | PMID 28964972
Bieńkiewicz Jan, Romanowicz Hanna, Malinowski Andrzej and 1 more
Genes: LEP
A novel PAX9 mutation causing oligodontia.
Archives of oral biology | 2017-12-01 | PMID 28965043
Daw Eiman Mohammed, Saliba Christian, Grech Godfrey and 1 more
Genes: PAX9, MSX1
Rapid identification of an adult plant stripe rust resistance gene in hexaploid wheat by high-throughput SNP array genotyping of pooled extremes.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2018-01-01 | PMID 28965125
Wu Jianhui, Liu Shengjie, Wang Qilin and 6 more
Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients.
Journal of neuro-oncology | 2018-01-01 | PMID 28965162
Jacobs Daniel I, Liu Yanhong, Gabrusiewicz Konrad and 14 more
Genes: MET
Cardiac Arrhythmias Related to Sodium Channel Dysfunction.
Handbook of experimental pharmacology | 2018-01-01 | PMID 28965168
Savio-Galimberti Eleonora, Argenziano Mariana, Antzelevitch Charles
Voltage-Gated Sodium Channel β Subunits and Their Related Diseases.
Handbook of experimental pharmacology | 2018-01-01 | PMID 28965169
Bouza Alexandra A, Isom Lori L
Gating Pore Currents in Sodium Channels.
Handbook of experimental pharmacology | 2018-01-01 | PMID 28965172
Groome J R, Moreau A, Delemotte L
Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) | 2018-02-01 | PMID 28965242
Demircioglu Kılıc Beltinge, Buyukcelik Mithat, Oguzkan Balcı Sibel and 4 more
Genes: INS
Genetic variants of immune-related genes IL17F and IL10 are associated with functional dyspepsia: A case-control study.
Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology | 2017-09-01 | PMID 28965252
Singh Rajan, Ghoshal Uday C, Kumar Sushil and 1 more
Association of Glutathione S-Transferase P-1 (GSTP-1) rs1695 polymorphism with overall survival in glioblastoma patients treated with combined radio-chemotherapy.
Investigational new drugs | 2018-04-01 | PMID 28965273
Pasqualetti Francesco, Gonnelli Alessandra, Cantarella Martina and 15 more
Genes: XRCC3, RAD51, XRCC1
MicroRNA-155 Inhibits Polarization of Macrophages to M2-Type and Suppresses Choroidal Neovascularization.
Inflammation | 2018-02-01 | PMID 28965281
Zhang Pengfei, Wang Hong, Luo Xueting and 8 more
The DRD2 Taq1A A1 Allele May Magnify the Risk of Alzheimer's in Aging African-Americans.
Molecular neurobiology | 2018-07-01 | PMID 28965318
Blum Kenneth, Badgaiyan Rajendra D, Dunston Georgia M and 6 more
Genes: DRD2
The study of familial hypercholesterolemia in Italy: A narrative review.
Atherosclerosis. Supplements | 2017-10-01 | PMID 28965614
Bertolini Stefano, Pisciotta Livia, Fasano Tommaso and 2 more
Genes: LDLR, APOB, PCSK9
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN).
Atherosclerosis. Supplements | 2017-10-01 | PMID 28965615
Averna Maurizio, Cefalù Angelo B, Casula Manuela and 6 more
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study.
Atherosclerosis. Supplements | 2017-10-01 | PMID 28965616
Pirillo Angela, Garlaschelli Katia, Arca Marcello and 5 more
Genes: LDLR, APOB, LDLRAP1, PCSK9, APOE, STAP1
Detection of familial hypercholesterolemia in patients from a general practice database.
Atherosclerosis. Supplements | 2017-10-01 | PMID 28965617
Casula Manuela, Catapano Alberico L, Rossi Bernardi Luigi and 2 more
CD30+ T cell enriched primary cutaneous CD4+ small/medium sized pleomorphic T cell lymphoma: A distinct variant of indolent CD4+ T cell lymphoproliferative disease.
Annals of diagnostic pathology | 2017-10-01 | PMID 28965629
Magro Cynthia M, Olson Luke C, Fulmer Clifton G
Severe Delayed Drug Reactions: Role of Genetics and Viral Infections.
Immunology and allergy clinics of North America | 2017-11-01 | PMID 28965641
Pavlos Rebecca, White Katie D, Wanjalla Celestine and 2 more
A Delicate Connection: c-di-AMP Affects Cell Integrity by Controlling Osmolyte Transport.
Trends in microbiology | 2018-03-01 | PMID 28965724
Commichau Fabian M, Gibhardt Johannes, Halbedel Sven and 2 more
Genomic Selection in Plant Breeding: Methods, Models, and Perspectives.
Trends in plant science | 2017-11-01 | PMID 28965742
Crossa José, Pérez-Rodríguez Paulino, Cuevas Jaime and 14 more
Genomic Patterns of De Novo Mutation in Simplex Autism.
Cell | 2017-10-19 | PMID 28965761
Turner Tychele N, Coe Bradley P, Dickel Diane E and 9 more
Single-Cell Analysis of Human Pancreas Reveals Transcriptional Signatures of Aging and Somatic Mutation Patterns.
Cell | 2017-10-05 | PMID 28965763
Enge Martin, Arda H Efsun, Mignardi Marco and 4 more
Jak1 Integrates Cytokine Sensing to Regulate Hematopoietic Stem Cell Function and Stress Hematopoiesis.
Cell stem cell | 2017-10-05 | PMID 28965767
Kleppe Maria, Spitzer Matthew H, Li Sheng and 13 more
Genes: JAK1
Acanthamoeba keratitis in noncompliant soft contact lenses users: Genotyping and risk factors, a study from Cairo, Egypt.
Journal of infection and public health | 2000-01-01 | PMID 28965795
Taher Eman E, Méabed Eman M H, Abdallah Islam and 1 more
Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2.
American journal of human genetics | 2017-10-05 | PMID 28965844
Maddirevula Sateesh, Coskun Serdar, Alhassan Saad and 6 more
Genes: PATL2
The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs.
American journal of human genetics | 2017-10-05 | PMID 28965845
Loviglio Maria Nicla, Arbogast Thomas, Jønch Aia Elise and 10 more
Genes: LAT, KCTD13, MAPK3, MVP, ZAP70
FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum of Mitochondrial Fe-S-Synthesis Diseases.
American journal of human genetics | 2017-10-05 | PMID 28965846
Paul Antoine, Drecourt Anthony, Petit Floriane and 25 more
Genes: FDXR
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.
American journal of human genetics | 2017-10-05 | PMID 28965848
Demaerel Wolfram, Hestand Matthew S, Vergaelen Elfi and 10 more
Minor spliceosome and disease.
Seminars in cell & developmental biology | 2018-07-01 | PMID 28965864
Verma Bhupendra, Akinyi Maureen V, Norppa Antto J and 1 more
The divergent N-terminal domain of Tim17 is critical for its assembly in the TIM complex in Trypanosoma brucei.
Molecular and biochemical parasitology | 2017-12-01 | PMID 28965880
Weems Ebony, Singha Ujjal K, Smith Joseph T and 1 more
Genes: SDS
Nuclear receptor FXR, bile acids and liver damage: Introducing the progressive familial intrahepatic cholestasis with FXR mutations.
Biochimica et biophysica acta. Molecular basis of disease | 2018-04-01 | PMID 28965883
Cariello Marica, Piccinin Elena, Garcia-Irigoyen Oihane and 2 more
Genes: FGF19
d-Allulose, a stereoisomer of d-fructose, extends Caenorhabditis elegans lifespan through a dietary restriction mechanism: A new candidate dietary restriction mimetic.
Biochemical and biophysical research communications | 2017-12-02 | PMID 28965946
Shintani Tomoya, Sakoguchi Hirofumi, Yoshihara Akihide and 2 more
MENIN loss as a tissue-specific driver of tumorigenesis.
Molecular and cellular endocrinology | 2018-07-05 | PMID 28965973
Li Janet W Y, Hua Xianxin, Reidy-Lagunes Diane and 1 more
Genes: MEN1
Rhabdoid tumor of the liver: Report of 6 pediatric cases treated at a single institute.
Journal of pediatric surgery | 2018-03-01 | PMID 28966010
Cornet Marianna, De Lambert Guénolée, Pariente Danièle and 5 more
Genes: SMARCB1, AFP
Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma.
Cancer cell | 2017-10-09 | PMID 28966033
Mackay Alan, Burford Anna, Carvalho Diana and 60 more
Genes: BCOR
Malaria Epidemiology at the Clone Level.
Trends in parasitology | 2017-12-01 | PMID 28966050
Koepfli Cristian, Mueller Ivo
Adaptive gene profiling of Mycobacterium tuberculosis during sub-lethal kanamycin exposure.
Microbial pathogenesis | 2017-11-01 | PMID 28966063
Habib Zeshan, Xu Weize, Jamal Muhammad and 5 more
Functional validation of Ca2+-binding residues from the crystal structure of the BK ion channel.
Biochimica et biophysica acta. Biomembranes | 2018-04-01 | PMID 28966112
Kshatri Aravind S, Gonzalez-Hernandez Alberto J, Giraldez Teresa
Crohn's Disease Disturbs the Immune Properties of Human Adipose-Derived Stem Cells Related to Inflammasome Activation.
Stem cell reports | 2017-10-10 | PMID 28966116
Serena Carolina, Keiran Noelia, Madeira Ana and 12 more
Phylogeny, biogeography and character evolution in the tribe Desmodieae (Fabaceae: Papilionoideae), with special emphasis on the New Caledonian endemic genera.
Molecular phylogenetics and evolution | 2018-01-01 | PMID 28966123
Jabbour Florian, Gaudeul Myriam, Lambourdière Josie and 4 more
Determination of complete sequence information of the human ABO blood group orthologous gene in pigs and breed difference in blood type frequencies.
Gene | 2018-01-15 | PMID 28966132
Choi Min-Kyeung, Le Minh Thong, Cho Hyesun and 7 more
Genes: ABO
Construction and analysis of protein-protein interaction network correlated with ankylosing spondylitis.
Gene | 2018-01-05 | PMID 28966133
Kanwal Attiya, Fazal Sahar
Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse Clinic.
Behavioural brain research | 2018-10-15 | PMID 28966146
Fuchs Helmut, Aguilar-Pimentel Juan Antonio, Amarie Oana V and 38 more
The deubiquitylating enzyme Ubp12 regulates Rad23-dependent proteasomal degradation.
Journal of cell science | 2017-10-01 | PMID 28966167
Gödderz Daniela, Giovannucci Tatiana A, Laláková Jana and 2 more
Genes: UBA2
Elucidation of the Synthetic Mechanism of Acylceramide, an Essential Lipid for Skin Barrier Function.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan | 2017-01-01 | PMID 28966260
Ohno Yusuke
Genes: PNPLA1, CERS3, ELOVL1, ELOVL4
Diagnostic application of clinical exome sequencing in Leber congenital amaurosis.
Molecular vision | 2017-01-01 | PMID 28966547
Han Jinu, Rim John Hoon, Hwang In Sik and 4 more
Genes: NMNAT1, RPGRIP1, CRX, SPATA7
Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate.
Molecular vision | 2017-01-01 | PMID 28966548
Matovinovic Elizabeth, Kho Pik Fang, Lea Rodney A and 7 more
Genes: DLG2, BANP, RAPSN
The Inter-rater Variability of Clinical Assessment in Post-anoxic Myoclonus.
Tremor and other hyperkinetic movements (New York, N.Y.) | 2017-01-01 | PMID 28966876
van Zijl Jonathan C, Beudel Martijn, Elting Jan-Willem J and 6 more
Genes: PAM
Uncommon somatic mutations in metastatic NUT midline carcinoma.
Tumori | 2017-11-15 | PMID 28967088
Cavalieri Stefano, Stathis Anastasios, Fabbri Alessandra and 6 more
Genes: BRD4, DCC
Association of MNS16A VNTR and hTERT rs2736098: G>A polymorphisms with susceptibility to diffuse large B-cell lymphoma.
Tumori | 2018-06-01 | PMID 28967095
Essa Enas S, Alagizy Hagar A
Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene.
Human mutation | 2018-01-01 | PMID 28967163
Iommarini Luisa, Ghelli Anna, Leone Giulia and 5 more
VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions.
Human mutation | 2018-01-01 | PMID 28967166
Freeman Peter J, Hart Reece K, Gretton Liam J and 2 more
Missense variants in the X-linked gene PRPS1 cause retinal degeneration in females.
Human mutation | 2018-01-01 | PMID 28967191
Fiorentino Alessia, Fujinami Kaoru, Arno Gavin and 15 more
Genes: PRPS1
Tetrazole-Based Probes for Integrated Phenotypic Screening, Affinity-Based Proteome Profiling, and Sensitive Detection of a Cancer Biomarker.
Angewandte Chemie (International ed. in English) | 2017-11-20 | PMID 28967196
Cheng Ke, Lee Jun-Seok, Hao Piliang and 3 more
Genes: ANXA2, FLAD1, NOS2, PDIA3
Supratentorial hemangioblastomas in von Hippel-Lindau wild-type patients - case series and literature review.
The International journal of neuroscience | 2018-03-01 | PMID 28967275
Rocha Luís, Noronha Carolina, Taipa Ricardo and 3 more
Psychotic patients who used cannabis frequently before illness onset have higher genetic predisposition to schizophrenia than those who did not.
Psychological medicine | 2018-01-01 | PMID 28967348
Aas M, Melle I, Bettella F and 9 more
Genes: PGC
Clinical Manifestations Associated With the N-Terminal-Acetyltransferase NAA10 Gene Mutation in a Girl: Ogden Syndrome.
Pediatric neurology | 2017-11-01 | PMID 28967461
Sidhu Mandeep, Brady Lauren, Tarnopolsky Mark and 1 more
Genes: NAA10
Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease.
Neuromuscular disorders : NMD | 2017-11-01 | PMID 28967462
Inal-Gültekin Güldal, Toptaş-Hekimoğlu Bahar, Görmez Zeliha and 16 more
Genes: PYGM
Fibroblast Growth Factor 2 as an Antifibrotic: Antagonism of Myofibroblast Differentiation and Suppression of Pro-Fibrotic Gene Expression.
Cytokine & growth factor reviews | 2017-12-01 | PMID 28967471
Dolivo David M, Larson Sara A, Dominko Tanja
Genes: FGF2
Pulmonary artery hypertension in childhood: The transforming growth factor-β superfamily-related genes.
Pediatrics and neonatology | 2018-04-01 | PMID 28967497
Yuan Shi-Min
Genes: PAH, KCNK3
Tissue-specific genome editing of laminA/C in the posterior silk glands of Bombyx mori.
Journal of genetics and genomics = Yi chuan xue bao | 2017-09-20 | PMID 28967614
Liu Yuanyuan, Ma Sanyuan, Chang Jiasong and 7 more
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society | 2018-01-01 | PMID 28967629
Heimer G, Eyal E, Zhu X and 10 more
Genes: AIFM1
Content of stem tumor CD133+ cells in brain neoplasms of different histological type.
Experimental oncology | 2017-09-01 | PMID 28967635
Lisyaniy N I, Stanetskaya D N, Lisyaniy A N and 1 more
Are CD44+/CD24- cells the assumed cancer stem cells in breast cancer?
Experimental oncology | 2017-09-01 | PMID 28967636
Ryspayeva D E, Smolanka I I, Dudnichenko А S and 5 more
Postnatal extra-embryonic tissues as a source of multiple cell types for regenerative medicine applications.
Experimental oncology | 2017-09-01 | PMID 28967638
Gubar O S, Rodnichenko A E, Vasyliev R G and 2 more
Genes: MSC
Tissue-engineered bone for treatment of combat related limb injuries.
Experimental oncology | 2017-09-01 | PMID 28967639
Vasyliev R G, Oksymets V M, Rodnichenko A E and 4 more
Endometrial stromal cells: isolation, expansion, morphological and functional properties.
Experimental oncology | 2017-09-01 | PMID 28967640
Zlatska A V, Rodnichenko A E, Gubar O S and 3 more
Genes: MSC
Large-scale expansion and characterization of human adult neural crest-derived multipotent stem cells from hair follicle for regenerative medicine applications.
Experimental oncology | 2017-09-01 | PMID 28967641
Vasyliev R G, Rodnichenko A E, Gubar O S and 4 more
Link between embryonic stem cell pluripotency and homologous allelic pairing of Oct4 loci.
Development, growth & differentiation | 2017-10-01 | PMID 28967672
Asaka Masamitsu N, Uranishi Kousuke, Suzuki Ayumu and 3 more
Excessive UDPG resulting from the mutation of UAP1 causes programmed cell death by triggering reactive oxygen species accumulation and caspase-like activity in rice.
The New phytologist | 2018-01-01 | PMID 28967675
Xiao Guiqing, Zhou Jiahao, Lu Xiangyang and 2 more
Genes: UAP1
HUMA: A platform for the analysis of genetic variation in humans.
Human mutation | 2018-01-01 | PMID 28967693
Brown David K, Tastan Bishop Özlem
A SNP uncoupling Mina expression from the TGFβ signaling pathway.
Immunity, inflammation and disease | 2018-03-01 | PMID 28967702
Lian Shang L, Mihi Belgacem, Koyanagi Madoka and 2 more
Pharmacokinetics and Safety of Letermovir Coadministered With Cyclosporine A or Tacrolimus in Healthy Subjects.
Clinical pharmacology in drug development | 2018-01-01 | PMID 28967706
Kropeit Dirk, von Richter Oliver, Stobernack Hans-Peter and 2 more
Effects of seasonal changes in cotton plants on the evolution of resistance to pyramided cotton producing the Bt toxins Cry1Ac and Cry1F in Helicoverpa zea.
Pest management science | 2018-03-01 | PMID 28967711
Carrière Yves, Degain Ben A, Unnithan Gopalan C and 4 more
Reduction in the number of CGG repeats on the FMR1 gene in carriers of genetic disorders versus noncarriers.
JBRA assisted reproduction | 2017-12-01 | PMID 28967713
Peyser Alexandra, Singer Tomer, Mullin Christine and 1 more
Genes: FMR1
Cardiac surgery in the elderly: What goals of care?
Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace | 2017-07-18 | PMID 28967719
Pratesi Alessandra, Orso Francesco, Ghiara Camilla and 5 more
Aurora-A-mediated phosphorylation of LKB1 compromises LKB1/AMPK signaling axis to facilitate NSCLC growth and migration.
Oncogene | 2018-01-25 | PMID 28967900
Zheng X, Chi J, Zhi J and 7 more
Genes: AURKA
A growth hormone receptor SNP promotes lung cancer by impairment of SOCS2-mediated degradation.
Oncogene | 2018-01-25 | PMID 28967904
Chhabra Y, Wong H Y, Nikolajsen L F and 8 more
Genes: SOCS2, GHR, CCND1, EGFR, MYC, SNAI2, TWIST1
Using a novel computational drug-repositioning approach (DrugPredict) to rapidly identify potent drug candidates for cancer treatment.
Oncogene | 2018-01-18 | PMID 28967908
Nagaraj A B, Wang Q Q, Joseph P and 10 more
Inhibition of USP10 induces degradation of oncogenic FLT3.
Nature chemical biology | 2017-12-01 | PMID 28967922
Weisberg Ellen L, Schauer Nathan J, Yang Jing and 25 more
Genes: FLT3, USP10
Transposon Insertion Site Sequencing (TIS-Seq): An Efficient and High-Throughput Method for Determining Transposon Insertion Site(s) and Their Relative Abundances in a PiggyBac Transposon Mutant Pool by Next-Generation Sequencing.
Current protocols in molecular biology | 2017-10-02 | PMID 28967994
Veeranagouda Yaligara, Didier Michel
Chemical Changes during Maize Tissue Aging and Its Relationship with Mediterranean Corn Borer Resistance.
Journal of agricultural and food chemistry | 2017-10-25 | PMID 28968115
López-Malvar Ana, Ordás Bernardo, Souto Carlos and 3 more
Gefitinib Plus Chemotherapy Versus Chemotherapy in Epidermal Growth Factor Receptor Mutation-Positive Non-Small-Cell Lung Cancer Resistant to First-Line Gefitinib (IMPRESS): Overall Survival and Biomarker Analyses.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2017-12-20 | PMID 28968167
Mok Tony S K, Kim Sang-We, Wu Yi-Long and 13 more
Genes: EGFR
Prevalence of COMT Val158Met polymorphism in Eastern UP population.
Cellular and molecular biology (Noisy-le-Grand, France) | 2017-07-31 | PMID 28968204
Kumar P, Yadav U, Rai V
Genes: COMT
Effects of arsenic toxicity on morphological characters in blackgram (Vigna mungo L.) during early growth stage.
Cellular and molecular biology (Noisy-le-Grand, France) | 2017-07-31 | PMID 28968207
Shamim M Z, Pandey A
Association of C677T polymorphism (rs1801133) in MTHFR gene with depression.
Cellular and molecular biology (Noisy-le-Grand, France) | 2017-07-31 | PMID 28968218
Rai V
Genes: MTHFR
Chymotrypsinogen C Genetic Variants, Including c.180TT, Are Strongly Associated With Chronic Pancreatitis in Pediatric Patients.
Journal of pediatric gastroenterology and nutrition | 2017-12-01 | PMID 28968289
Grabarczyk Alicja Monika, Oracz Grzegorz, Wertheim-Tysarowska Katarzyna and 8 more
Genes: CTRC
Influence of catechol-O-methyltransferase Val158Met on fear of pain and placebo analgesia.
Pain | 2018-01-01 | PMID 28968343
Forsberg June T, Gjerstad Johannes, Flaten Magne Arve and 1 more
Genes: COMT
Genomics of parallel adaptation at two timescales in Drosophila.
PLoS genetics | 2017-10-01 | PMID 28968391
Zhao Li, Begun David J
SNPs near the cysteine proteinase cathepsin O gene (CTSO) determine tamoxifen sensitivity in ERα-positive breast cancer through regulation of BRCA1.
PLoS genetics | 2017-10-01 | PMID 28968398
Cairns Junmei, Ingle James N, Wickerham Lawrence D and 3 more
Genes: CTSO, BRCA1
One-carbon genetic variants and the role of MTHFD1 1958G>A in liver and colon cancer risk according to global DNA methylation.
PloS one | 2017-01-01 | PMID 28968444
Moruzzi Sara, Guarini Patrizia, Udali Silvia and 9 more
Genes: MTHFD1, BHMT, DHFR, MTHFR, MTR, MTRR, RFC1, SHMT1
Genetic economy in picornaviruses: Foot-and-mouth disease virus replication exploits alternative precursor cleavage pathways.
PLoS pathogens | 2017-10-01 | PMID 28968463
Herod Morgan R, Gold Sarah, Lasecka-Dykes Lidia and 8 more
Molecular analysis of TSC1 and TSC2 genes and phenotypic correlations in Brazilian families with tuberous sclerosis.
PloS one | 2017-01-01 | PMID 28968464
Rosset Clévia, Vairo Filippo, Bandeira Isabel Cristina and 10 more
Genes: TSC1, TSC2
Effects of glutamate and ivermectin on single glutamate-gated chloride channels of the parasitic nematode H. contortus.
PLoS pathogens | 2017-10-01 | PMID 28968469
Atif Mohammed, Estrada-Mondragon Argel, Nguyen Bindi and 2 more
Esophageal Adenocarcinoma-Derived Extracellular Vesicle MicroRNAs Induce a Neoplastic Phenotype in Gastric Organoids.
Neoplasia (New York, N.Y.) | 2017-11-01 | PMID 28968550
Ke Xiquan, Yan Rong, Sun Zhenguo and 15 more
Genes: AIFM3, PTEN
Association score testing for rare variants and binary traits in family data with shared controls.
Briefings in bioinformatics | 2019-01-18 | PMID 28968627
Saad Mohamad, Wijsman Ellen M
Computational approaches for discovery of mutational signatures in cancer.
Briefings in bioinformatics | 2019-01-18 | PMID 28968631
Baez-Ortega Adrian, Gori Kevin
tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine.
Bioinformatics (Oxford, England) | 2018-01-01 | PMID 28968638
Wei Chih-Hsuan, Phan Lon, Feltz Juliana and 3 more
Genes: MAF
CGmapTools improves the precision of heterozygous SNV calls and supports allele-specific methylation detection and visualization in bisulfite-sequencing data.
Bioinformatics (Oxford, England) | 2018-02-01 | PMID 28968643
Guo Weilong, Zhu Ping, Pellegrini Matteo and 3 more