When Is an Endophenotype Useful to Detect Association to a Disease? Exploring the Relationships between Disease Status, Endophenotype and Genetic Polymorphisms.
Human heredity | 2016-01-01 | PMID 27475094
Bureau Alexandre, Croteau Jordie
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 7004 of 10600
Cardiac dysfunction in Pkd1-deficient mice with phenotype rescue by galectin-3 knockout.
Kidney international | 2016-09-01 | PMID 27475230
Balbo Bruno E, Amaral Andressa G, Fonseca Jonathan M and 8 more
Identification of a novel DFA I-producing inulin fructotransferase from Streptomyces davawensis.
International journal of biological macromolecules | 2016-11-01 | PMID 27475232
Zhu Yingying, Yu Shuhuai, Huang Danyang and 3 more
Genes: SDS
Preimplantation maternal stress impairs embryo development by inducing oviductal apoptosis with activation of the Fas system.
Molecular human reproduction | 2016-11-01 | PMID 27475493
Zheng Liang-Liang, Tan Xiu-Wen, Cui Xiang-Zhong and 5 more
Genes: CRH, BDNF
The E3 ubiquitin ligase CHIP selectively regulates mutant epidermal growth factor receptor by ubiquitination and degradation.
Biochemical and biophysical research communications | 2016-10-14 | PMID 27475501
Chung Chaeuk, Yoo Geon, Kim Tackhoon and 15 more
Genes: EGFR
Differences in urbanization degree and consequences on the diversity of conventional vs. rapidly mutating Y-STRs in five municipalities from a small region of the Tyrolean Alps in Austria.
Forensic science international. Genetics | 2016-09-01 | PMID 27475702
Niederstätter Harald, Berger Burkhard, Kayser Manfred and 1 more
Genes: FST
Human blood cell levels of 5-hydroxymethylcytosine (5hmC) decline with age, partly related to acquired mutations in TET2.
Experimental hematology | 2016-11-01 | PMID 27475703
Buscarlet Manuel, Tessier Alain, Provost Sylvie and 2 more
Genes: TET2, IDH1, IDH2, ASXL1
Ivacaftor and symptoms of extra-oesophageal reflux in patients with cystic fibrosis and G551D mutation.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society | 2017-01-01 | PMID 27475719
Zeybel Gemma L, Pearson Jeffrey P, Krishnan Amaran and 11 more
Association between Staphylococcus aureus nasal carriage and disease phenotype in patients affected by systemic lupus erythematosus.
Arthritis research & therapy | 2016-07-30 | PMID 27475749
Conti Fabrizio, Ceccarelli Fulvia, Iaiani Giancarlo and 14 more
Genes: SSB
Why Sexually Selected Weapons Are Not Ornaments.
Trends in ecology & evolution | 2016-10-01 | PMID 27475833
McCullough Erin L, Miller Christine W, Emlen Douglas J
A hybrid agent-based model of the developing mammary terminal end bud.
Journal of theoretical biology | 2016-10-21 | PMID 27475843
Butner Joseph D, Chuang Yao-Li, Simbawa Eman and 4 more
Right ventricular and pulmonary vascular reserve in asymptomatic BMPR2 mutation carriers.
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation | 2017-02-01 | PMID 27475894
Claessen Guido, La Gerche Andre, Petit Thibault and 7 more
Genes: BMPR2
Isolation and characterization of sake yeast mutants with enhanced isoamyl acetate productivity.
Journal of bioscience and bioengineering | 2017-01-01 | PMID 27475923
Takahashi Toshinari, Ohara Yusuke, Sawatari Michiyo and 1 more
Genes: ATF1
Irreversible inhibition of Δ16HER2 is necessary to suppress Δ16HER2-positive breast carcinomas resistant to Lapatinib.
Cancer letters | 2016-10-10 | PMID 27475932
Tilio Martina, Gambini Valentina, Wang Junbiao and 14 more
Phenotypic differences based on staging of Alzheimer's neuropathology in autopsy-confirmed dementia with Lewy bodies.
Parkinsonism & related disorders | 2016-10-01 | PMID 27475955
Peavy Guerry M, Edland Steven D, Toole Belinda M and 3 more
Whole genome sequencing identifies ANXA3 and MTHFR mutations in a large family with an unknown equinus deformity associated genetic disorder.
Molecular biology reports | 2016-10-01 | PMID 27475959
Zhang Zhiqun, Kong Zhuqing, Zhu Miao and 4 more
Genes: ANXA3, MTHFR
Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred.
BMC medical genetics | 2016-07-30 | PMID 27475985
Gradstein Libe, Zolotushko Jenny, Sergeev Yuri V and 9 more
Genes: ERG
Loss of Hes1 expression is associated with poor prognosis in colorectal adenocarcinoma.
Human pathology | 2016-11-01 | PMID 27476040
Ahadi Mahsa, Andrici Juliana, Sioson Loretta and 3 more
Genes: HES1
Neuroimaging genetic analyses of novel candidate genes associated with reading and language.
Brain and language | 2017-09-01 | PMID 27476042
Gialluisi Alessandro, Guadalupe Tulio, Francks Clyde and 1 more
Genes: RBFOX2, FLNC
Is the IL-6 -174G/C Gene Polymorphism Related to the Disease Severity Score in Turkish Children with Familial Mediterranean Fever?
Biochemical genetics | 2016-12-01 | PMID 27476063
Özer Samet, Yilmaz Resul, Sonmezgoz Ergün and 2 more
Value of Genetic Testing for the Prediction of Long-Term Outcome in Patients With Hypertrophic Cardiomyopathy.
The American journal of cardiology | 2016-09-15 | PMID 27476098
van Velzen Hannah G, Vriesendorp Pieter A, Oldenburg Rogier A and 4 more
Genes: SCD
Association of insulin-like growth factor (IGF)-1 gene polymorphisms with plasma levels of IGF-1 and acne severity.
Journal of the American Academy of Dermatology | 2016-10-01 | PMID 27476104
Rahaman Shekh Mohammad Amanur, De Dipankar, Handa Sanjeev and 4 more
Use of the UPOINT Classification in Turkish Chronic Prostatitis or Chronic Pelvic Pain Syndrome Patients.
Urology | 2016-11-01 | PMID 27476153
Arda Ersan, Cakiroglu Basri, Tas Tuncay and 2 more
Integrins AV and B8 Gene Polymorphisms and Risk for Intracerebral Hemorrhage in Greek and Polish Populations.
Neuromolecular medicine | 2017-03-01 | PMID 27476161
Dardiotis Efthimios, Siokas Vasileios, Zafeiridis Tilemachos and 9 more
Genes: ITGAV, ITGB8
Renin-Angiotensin-Aldosterone System Antagonism and Polycystic Kidney Disease Progression.
Nephron | 2016-01-01 | PMID 27476173
Hian Chuan Kai, Lee Chin Liang, Thomas Warren
[Changes in Cell Surface Properties and Biofilm Formation Efficiency in Azospirillum brasilense Sp245 Mutants in the Putative Genes of Lipid Metabolism mmsB1 and fabG1].
Mikrobiologiia | 2000-01-01 | PMID 27476204
Shumilova E, Shelud'ko A V, Filip'echeva Yu A and 4 more
Significant Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association | 2016-11-01 | PMID 27476341
Morimoto Takaaki, Mineharu Yohei, Kobayashi Hatasu and 6 more
Genetic and clinical risk factors of root resorption associated with orthodontic treatment.
American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics | 2016-08-01 | PMID 27476361
Guo Yujiao, He Shushu, Gu Tian and 2 more
Movement disorders in mitochondrial diseases.
Revue neurologique | 2000-01-01 | PMID 27476418
Tranchant C, Anheim M
Genes: SPG7
Hepatitis E in a region of Italy: An emerging autochthonous infection?
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver | 2016-11-01 | PMID 27476463
Tarantino Giuseppe, Bagnarelli Patrizia, Marzioni Marco and 6 more
CB2-63 polymorphism and immune-mediated diseases associated with HCV chronic infection.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver | 2016-11-01 | PMID 27476469
Coppola Nicola, Zampino Rosa, Bellini Giulia and 9 more
Genes: CNR2
[Recent advances in the understanding and treatment of diffuse large B-cell lymphoma].
Orvosi hetilap | 2016-07-01 | PMID 27476519
Gergely Lajos, Illés Árpád
Distinct roles of a tyrosine-associated hydrogen-bond network in fine-tuning the structure and function of heme proteins: two cases designed for myoglobin.
Molecular bioSystems | 2016-10-20 | PMID 27476534
Liao Fei, Yuan Hong, Du Ke-Jie and 5 more
The Genetics of Seasonal Migration and Plumage Color.
Current biology : CB | 2016-08-22 | PMID 27476599
Delmore Kira E, Toews David P L, Germain Ryan R and 2 more
Genes: TYRP1
Biophysical and Population Genetic Models Predict the Presence of "Phantom" Stepping Stones Connecting Mid-Atlantic Ridge Vent Ecosystems.
Current biology : CB | 2016-09-12 | PMID 27476600
Breusing Corinna, Biastoch Arne, Drews Annika and 11 more
Comparison of the genetic variability of Blastocystis subtypes between human carriers from two contrasting climatic regions of México.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2016-10-01 | PMID 27476606
Villegas-Gómez Isaac, Martínez-Hernández Fernando, Urrea-Quezada Alejandro and 7 more
Characterization of novel intragenotype recombination events among norovirus pandemic GII.4 variants.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2016-10-01 | PMID 27476607
Siqueira Jones Anderson Monteiro, Bandeira Renato da Silva, Justino Maria Cleonice Aguiar and 2 more
The copper rush of the nineties.
Metallomics : integrated biometal science | 2016-09-01 | PMID 27476637
Solioz Marc
Spectral sensitivity of guppy visual pigments reconstituted in vitro to resolve association of opsins with cone cell types.
Vision research | 2016-10-01 | PMID 27476645
Kawamura Shoji, Kasagi Satoshi, Kasai Daisuke and 5 more
Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions.
American journal of human genetics | 2016-08-04 | PMID 27476651
Pigors Manuela, Sarig Ofer, Heinz Lisa and 10 more
Genes: SERPINB8
GNA14 Somatic Mutation Causes Congenital and Sporadic Vascular Tumors by MAPK Activation.
American journal of human genetics | 2016-08-04 | PMID 27476652
Lim Young H, Bacchiocchi Antonella, Qiu Jingyao and 10 more
Genes: GNA14, GNA11, GNAQ, HRAS, KRAS, NRAS
Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
American journal of human genetics | 2016-08-04 | PMID 27476653
Adam Ronja, Spier Isabel, Zhao Bixiao and 25 more
Genes: MSH3, APC, MUTYH, NTHL1, PMS2, POLD1, POLE
ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects.
American journal of human genetics | 2016-08-04 | PMID 27476655
Izumi Kosuke, Brett Maggie, Nishi Eriko and 21 more
Genes: ARCN1
Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling.
American journal of human genetics | 2016-08-04 | PMID 27476657
Cetinkaya Arda, Xiong Jingwei Rachel, Vargel İbrahim and 18 more
Genes: ELMO2, RAC1, DOCK1
Epidemiological Profile of Newly Diagnosed HIV-Infected Patients in Northern Paris: A Retrospective Study.
AIDS research and human retroviruses | 2017-01-01 | PMID 27476681
Senard Olivia, Burdet Charles, Visseaux Benoit and 8 more
Association between population structure and allele frequencies of the glycogen synthase 1 mutation in the Austrian Noriker draft horse.
Animal genetics | 2017-02-01 | PMID 27476720
Druml T, Grilz-Seger G, Neuditschko M and 1 more
Genes: GYS1
HLA-C*06:02 Allele and Response to IL-12/23 Inhibition: Results from the Ustekinumab Phase 3 Psoriasis Program.
The Journal of investigative dermatology | 2016-12-01 | PMID 27476722
Li Katherine, Huang C Chris, Randazzo Bruce and 5 more
Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma.
The Journal of investigative dermatology | 2016-12-01 | PMID 27476724
Shi Jianxin, Zhou Weiyin, Zhu Bin and 19 more
Genes: CDK4, PARP1
Metastatic ocular melanoma to the liver exhibits infiltrative and nodular growth patterns.
Human pathology | 2016-11-01 | PMID 27476775
Grossniklaus Hans E, Zhang Qing, You Shuo and 3 more
Genes: BAP1, MMP9
Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 2016-12-01 | PMID 27476799
Nielson Carrie M, Liu Ching-Ti, Smith Albert V and 48 more
Genes: EPHB2, SLC1A3, MAF, AKAP11, TNFRSF11B, TNFSF11, WNT4, ZBTB40
Analysis of Variability in HIV-1 Subtype A Strains in Russia Suggests a Combination of Deep Sequencing and Multitarget RNA Interference for Silencing of the Virus.
AIDS research and human retroviruses | 2017-02-01 | PMID 27476852
Kretova Olga V, Chechetkin Vladimir R, Fedoseeva Daria M and 6 more
Persistence of DNMT3A R882 mutations during remission does not adversely affect outcomes of patients with acute myeloid leukaemia.
British journal of haematology | 2016-10-01 | PMID 27476855
Bhatnagar Bhavana, Eisfeld Ann-Kathrin, Nicolet Deedra and 10 more
Genes: ASXL1, JAK2, TET2
A genome-wide association study of heat stress-associated SNPs in catfish.
Animal genetics | 2017-04-01 | PMID 27476875
Jin Y, Zhou T, Geng X and 7 more
Genes: ANAPC2, CLIC5, DNAJC25, KLHL29, PLCB1, PLCB4, PRPF4, SYNCRIP
Atypical femur fracture in an adolescent boy treated with bisphosphonates for X-linked osteoporosis based on PLS3 mutation.
Bone | 2016-10-01 | PMID 27477003
van de Laarschot Denise M, Zillikens M Carola
Genes: PLS3
Filling the (SR)GAP in Excitatory/Inhibitory Balance.
Neuron | 2016-07-20 | PMID 27477010
Subramanian Jaichandar, Nedivi Elly
Bleeding related to disturbed fibrinolysis.
British journal of haematology | 2016-10-01 | PMID 27477022
Kolev Krasimir, Longstaff Colin
Retarded Embryo Development 1 (RED1) regulates embryo development, seed maturation and plant growth in Arabidopsis.
Journal of genetics and genomics = Yi chuan xue bao | 2016-07-20 | PMID 27477025
Du Qian, Wang Huanzhong
Fatty Acid Diversity is Not Associated with Neutral Genetic Diversity in Native Populations of the Biodiesel Plant Jatropha curcas L.
Chemistry & biodiversity | 2017-01-01 | PMID 27477108
Martínez-Díaz Yesenia, González-Rodríguez Antonio, Rico-Ponce Héctor Rómulo and 3 more
MiR-146a rs2910164 polymorphism increases the risk of digestive system cancer: A meta-analysis.
Clinics and research in hepatology and gastroenterology | 2017-02-01 | PMID 27477122
Xie Wen Qun, Wang Xiao Fan
Genetic correlations and sex-specific adaptation in changing environments.
Evolution; international journal of organic evolution | 2016-10-01 | PMID 27477129
Connallon Tim, Hall Matthew D
Keratinization Disorders and Genetic Aspects in Palmar and Plantar Keratodermas.
Acta dermatovenerologica Croatica : ADC | 2016-06-01 | PMID 27477171
Stypczyńska Ewa, Placek Waldemar, Zegarska Barbara and 1 more
PCSK9 knock-out mice are protected from neointimal formation in response to perivascular carotid collar placement.
Atherosclerosis | 2016-10-01 | PMID 27477186
Ferri Nicola, Marchianò Silvia, Tibolla Gianpaolo and 6 more
Genes: PCSK9, LDLR
Quantitative analysis of B-lymphocyte migration directed by CXCL13.
Integrative biology : quantitative biosciences from nano to macro | 2016-08-08 | PMID 27477203
Liu Xiaji, Asokan Sreeja B, Bear James E and 1 more
Genes: CXCL13
BioVLAB-mCpG-SNP-EXPRESS: A system for multi-level and multi-perspective analysis and exploration of DNA methylation, sequence variation (SNPs), and gene expression from multi-omics data.
Methods (San Diego, Calif.) | 2016-12-01 | PMID 27477210
Chae Heejoon, Lee Sangseon, Seo Seokjun and 4 more
A requirement for cell elongation protein RodZ and cell division proteins FtsN and DedD to maintain the small rod morphology of Escherichia coli at growth temperatures near 8°C.
The Journal of general and applied microbiology | 2016-09-12 | PMID 27477251
Porter T, Frederick D, Johnson E and 1 more
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells.
The Journal of allergy and clinical immunology | 2017-02-01 | PMID 27477328
Chen Hannah H, Händel Norman, Ngeow Joanne and 24 more
Genes: PTEN, FOXP3
Metallothionein Prevents Age-Associated Cardiomyopathy via Inhibiting NF-κB Pathway Activation and Associated Nitrative Damage to 2-OGD.
Antioxidants & redox signaling | 2016-12-10 | PMID 27477335
Cong Weitao, Niu Chao, Lv Lingchun and 12 more
Genes: TNF
Frequency of Calreticulin (CALR) Mutation and Its Clinical Prognostic Significance in Essential Thrombocythemia and Primary Myelofibrosis: A Meta-analysis.
Internal medicine (Tokyo, Japan) | 2016-01-01 | PMID 27477402
Kong Hao, Liu Yancheng, Luo Sai and 2 more
Genes: CALR
Alterations in ribosomal protein L19 that decrease the fidelity of translation.
Biochimie | 2000-01-01 | PMID 27477481
VanNice John, Gregory Steven T, Kamath Divya and 1 more
TNFA gene variants related to the inflammatory status and its association with cellular aging: From the CORDIOPREV study.
Experimental gerontology | 2016-10-01 | PMID 27477483
Rangel-Zúñiga Oriol Alberto, Corina Andreea, Lucena-Porras Beatriz and 14 more
Genes: CRP
Evolutionary characteristics of morbilliviruses during serial passages in vitro: Gradual attenuation of virus virulence.
Comparative immunology, microbiology and infectious diseases | 2016-08-01 | PMID 27477502
Liu Fuxiao, Wu Xiaodong, Li Lin and 3 more
Artifactual mutations resulting from DNA lesions limit detection levels in ultrasensitive sequencing applications.
DNA research : an international journal for rapid publication of reports on genes and genomes | 2016-12-01 | PMID 27477585
Arbeithuber Barbara, Makova Kateryna D, Tiemann-Boege Irene
Genetic diversity of Klebsiella pneumoniae isolates during an outbreak in a non-human primate research colony.
Journal of medical primatology | 2016-12-01 | PMID 27477611
Gozalo Alfonso S, Elkins William R, Lambert Lynn E and 3 more
Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controls.
Parkinsonism & related disorders | 2016-10-01 | PMID 27477622
Zech Michael, Jochim Angela, Boesch Sylvia and 10 more
Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability.
Journal of thrombosis and haemostasis : JTH | 2016-10-01 | PMID 27477789
Jourdy Y, Chatron N, Carage M-L and 7 more
Genes: SOX3, LDOC1, SPANXC
Hamartomatous polyps - a clinical and molecular genetic study.
Danish medical journal | 2016-08-01 | PMID 27477802
Jelsig Anne Marie
Genes: PTEN, SMAD4, ENG
Unravelling 5-oxoprolinuria (pyroglutamic aciduria) due to bi-allelic OPLAH mutations: 20 new mutations in 14 families.
Molecular genetics and metabolism | 2016-09-01 | PMID 27477828
Sass Jörn Oliver, Gemperle-Britschgi Corinne, Tarailo-Graovac Maja and 24 more
Genes: OPLAH
221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative.
Molecular genetics and metabolism | 2016-09-01 | PMID 27477829
Bentler Kristi, Zhai Shaohui, Elsbecker Sara A and 7 more
Genes: ACADM
Nanofiber-mediated microRNA-126 delivery to vascular endothelial cells for blood vessel regeneration.
Acta biomaterialia | 2016-10-01 | PMID 27477849
Zhou Fang, Jia Xiaoling, Yang Yang and 6 more
Molecular characterisation and antifungal susceptibility of clinical Cryptococcus deuterogattii (AFLP6/VGII) isolates from Southern Brazil.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 2016-11-01 | PMID 27477855
Herkert P F, Hagen F, de Oliveira Salvador G L and 7 more
Resistin reinforces interferon λ-3 to eliminate hepatitis C virus with fine-tuning from RETN single-nucleotide polymorphisms.
Scientific reports | 2016-08-01 | PMID 27477870
Chang Ming-Ling, Liang Kung-Hao, Ku Cheng-Lung and 5 more
Genes: RETN, IFNL3
Exploring the origin of the catalytic power and product specificity of SET domain protein methyltransferase.
Molecular bioSystems | 2016-10-20 | PMID 27477893
Lima A H, Alves C N, Prasad R and 1 more
Genes: SET
Engineered Covalent Inactivation of TFIIH-Kinase Reveals an Elongation Checkpoint and Results in Widespread mRNA Stabilization.
Molecular cell | 2016-08-04 | PMID 27477907
Rodríguez-Molina Juan B, Tseng Sandra C, Simonett Shane P and 2 more
A Highly Sensitive and Robust Method for Genome-wide 5hmC Profiling of Rare Cell Populations.
Molecular cell | 2016-08-18 | PMID 27477909
Han Dali, Lu Xingyu, Shih Alan H and 6 more
Hypoxia Promotes Osteogenesis of Human Placental-Derived Mesenchymal Stem Cells.
The Tohoku journal of experimental medicine | 2016-08-01 | PMID 27477937
Gu Qiaoli, Gu Yanzheng, Shi Qin and 1 more
Genes: MSC
Susceptibility of Pigs to Zoonotic Hepatitis E Virus Genotype 3 Isolated from a Wild Boar.
Transboundary and emerging diseases | 2017-10-01 | PMID 27477944
Thiry D, Rose N, Mauroy A and 5 more
The effect of introducing small cavities on the allosteric inhibition of phosphofructokinase from Bacillus stearothermophilus.
Archives of biochemistry and biophysics | 2016-10-01 | PMID 27477958
Whitaker Amy M, Reinhart Gregory D
Clinical Utility of Next-Generation Sequencing for Oncogenic Mutations in Patients with Acute Myeloid Leukemia Undergoing Allogeneic Stem Cell Transplantation.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation | 2016-11-01 | PMID 27478011
Luskin Marlise R, Carroll Martin, Lieberman David and 7 more
Genes: FLT3, NPM1
Alpha-synuclein (SNCA) polymorphisms exert protective effects on memory after mild traumatic brain injury.
Neuroscience letters | 2016-09-06 | PMID 27478013
Shee Kevin, Lucas Alexandra, Flashman Laura A and 6 more
Genes: SNCA
Satb2 Is Required for the Development of a Spinal Exteroceptive Microcircuit that Modulates Limb Position.
Neuron | 2016-08-17 | PMID 27478017
Hilde Kathryn L, Levine Ariel J, Hinckley Christopher A and 8 more
Expression of C1ql3 in Discrete Neuronal Populations Controls Efferent Synapse Numbers and Diverse Behaviors.
Neuron | 2016-09-07 | PMID 27478018
Martinelli David C, Chew Kylie S, Rohlmann Astrid and 6 more
Discovery of cyclosporine A and its analogs as broad-spectrum anti-influenza drugs with a high in vitro genetic barrier of drug resistance.
Antiviral research | 2016-09-01 | PMID 27478032
Ma Chunlong, Li Fang, Musharrafieh Rami Ghassan and 1 more
High-throughput Phenotyping of Lung Cancer Somatic Mutations.
Cancer cell | 2016-08-08 | PMID 27478040
Berger Alice H, Brooks Angela N, Wu Xiaoyun and 28 more
Genes: EGFR, ARAF, BRAF, ERBB2
Sequencing Structural Variants in Cancer for Precision Therapeutics.
Trends in genetics : TIG | 2016-09-01 | PMID 27478068
Macintyre Geoff, Ylstra Bauke, Brenton James D
Baltic lineage of tick-borne encephalitis virus: A putative evolutionary pathway.
Ticks and tick-borne diseases | 2016-10-01 | PMID 27478072
Kovalev S Y, Mukhacheva T A
Neuraminidase enhances in vitro expansion of human erythroid progenitors.
European cytokine network | 2016-06-01 | PMID 27478075
Bodivit Gwellaouen, Chadebech Philippe, Vigon Isabelle and 4 more
Effect of pro-inflammatory interleukin-17A on epithelial cell phenotype inversion in HK-2 cells in vitro.
European cytokine network | 2016-06-01 | PMID 27478076
Liu Li, Li Fu-Gang, Yang Man and 5 more
Genes: CCK
Identification of Natural Infections in Sheep/Goats with HoBi-like Pestiviruses in China.
Transboundary and emerging diseases | 2016-10-01 | PMID 27478131
Shi H, Kan Y, Yao L and 4 more
Detection of EGFR and KRAS Mutation by Pyrosequencing Analysis in Cytologic Samples of Non-Small Cell Lung Cancer.
Journal of Korean medical science | 2016-08-01 | PMID 27478332
Lee Seung Eun, Lee So-Young, Park Hyung-Kyu and 4 more
Genes: EGFR, KRAS
Skin Barrier Function Is Not Impaired and Kallikrein 7 Gene Polymorphism Is Frequently Observed in Korean X-linked Ichthyosis Patients Diagnosed by Fluorescence in Situ Hybridization and Array Comparative Genomic Hybridization.
Journal of Korean medical science | 2016-08-01 | PMID 27478344
Lee Noo Ri, Yoon Na Young, Jung Minyoung and 6 more
Genes: KLK7, FLG, SPINK5