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 7069 of 10600

VNTR diversity in Yersinia pestis isolates from an animal challenge study reveals the potential for in vitro mutations during laboratory cultivation.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2016-11-01 | PMID 27664903
Vogler Amy J, Nottingham Roxanne, Busch Joseph D and 8 more
A genetic cluster of patients with variant xeroderma pigmentosum with two different founder mutations.
The British journal of dermatology | 2017-05-01 | PMID 27664908
Munford V, Castro L P, Souto R and 16 more
Genes: POLH
Prefrontal Volume Mediates Effect of COMT Polymorphism on Interference Resolution Capacity in Healthy Male Adults.
Cerebral cortex (New York, N.Y. : 1991) | 2017-11-01 | PMID 27664968
Xu Jiayuan, Qin Wen, Li Qiaojun and 5 more
Genes: COMT
Genome scan reveals selection acting on genes linked to stress response in wild pearl millet.
Molecular ecology | 2016-11-01 | PMID 27664976
Berthouly-Salazar Cécile, Thuillet Anne-Céline, Rhoné Bénédicte and 5 more
Cathepsin A-related arteriopathy with strokes and leukoencephalopathy (CARASAL).
Neurology | 2016-10-25 | PMID 27664989
Bugiani Marianna, Kevelam Sietske H, Bakels Hannah S and 6 more
Genes: CTSA
Prevalence of azole-resistant Aspergillus fumigatus in the environment of Thailand.
Medical mycology | 2017-06-01 | PMID 27664994
Tangwattanachuleeporn Marut, Minarin Nanthakan, Saichan Saranya and 5 more
Genes: ARAF
Traits of eggshells and shell membranes of translucent eggs.
Poultry science | 2017-02-01 | PMID 27665004
Wang De-He, Li Ya-Jie, Liu Long and 5 more
Evaluation of genetic diversity of Saudi native chicken populations using microsatellite markers.
Poultry science | 2017-03-01 | PMID 27665011
Fathi M M, Al-Homidan I, Motawei M I and 2 more
The Conundrum of Heterogeneities in Life History Studies.
Trends in ecology & evolution | 2016-11-01 | PMID 27665020
Cam Emmanuelle, Aubry Lise M, Authier Matthieu
BCR-ABL (Ph)-like acute leukemia-Pathogenesis, diagnosis and therapeutic options.
Blood reviews | 2017-03-01 | PMID 27665024
Ofran Yishai, Izraeli Shai
Genes: BCR
Proteomic comparison of near-isogenic barley (Hordeum vulgare L.) germplasm differing in the allelic state of a major senescence QTL identifies numerous proteins involved in plant pathogen defense.
Plant physiology and biochemistry : PPB | 2016-12-01 | PMID 27665045
Mason Katelyn E, Hilmer Jonathan K, Maaty Walid S and 4 more
Sudden cardiac death: A reappraisal.
Trends in cardiovascular medicine | 2016-11-01 | PMID 27665048
Steinberg Christian, Laksman Zachary W M, Krahn Andrew D
Genes: SCD
Frequency of thiopurine methyltransferase mutation in patients of Mediterranean area with inflammatory bowel disease and autoimmune disorders.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver | 2016-12-01 | PMID 27665263
Di Salvo Angela, Fabiano Carmelo, Mannara Vincenza and 5 more
Genes: TPMT
Molecular analysis reveals the diversity of Hepatozoon species naturally infecting domestic dogs in a northern region of Brazil.
Ticks and tick-borne diseases | 2016-10-01 | PMID 27665264
Gomes Laise de Azevedo, Moraes Pablo Henrique Gonçalves, do Nascimento Luciana de Cássia Silva and 5 more
Pleomorphic adenoma and adenoid cystic carcinoma of salivary glands: E-cadherin immunoexpression and analysis of the CDH1 -160C/A polymorphism.
Archives of oral biology | 2017-01-01 | PMID 27665273
Cavalcante Roberta Barroso, Nonaka Cassiano Francisco Weege, Rabenhorst Silvia Helena Barem and 3 more
Genes: CDH1
A simple method for developing an infectious cDNA clone of Japanese encephalitis virus.
Virus genes | 2017-02-01 | PMID 27665292
Zheng Hao, Zheng Xuchen, Tong Wu and 8 more
The eyespot resistance genes Pch1 and Pch2 of wheat are not homoeoloci.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2017-01-01 | PMID 27665367
Pasquariello M, Ham J, Burt C and 4 more
ASIA syndrome, calcinosis cutis and chronic kidney disease following silicone injections. A case-based review.
Immunologic research | 2016-12-01 | PMID 27665458
Barilaro Giuseppe, Spaziani Testa Claudia, Cacciani Antonella and 3 more
The differential importance of mutations within AmpD in cephalosporin resistance of Enterobacter aerogenes and Enterobacter cloacae.
International journal of antimicrobial agents | 2016-11-01 | PMID 27665520
Babouee Flury Baharak, Ellington Matthew J, Hopkins Katie L and 3 more
Genes: SDS
The R implementation of the CRAN package PATHChange, a tool to study genetic pathway alterations in transcriptomic data.
Computers in biology and medicine | 2016-11-01 | PMID 27665533
Fontoura Carla A R S, Castellani Gastone, Mombach José C M
Defining the performance parameters of a rapid screening tool for myotonic dystrophy type 1 based on triplet-primed PCR and melt curve analysis.
Expert review of molecular diagnostics | 2016-11-01 | PMID 27665623
Lian Mulias, Law Hai-Yang, Lee Caroline G and 1 more
Genes: DMPK
Introduction of novel α1-hemoglobin gene mutation with transfusion-dependent phenotype.
Hematology (Amsterdam, Netherlands) | 2017-04-01 | PMID 27665672
Zekavat Omid Reza, Dehghani Seyed Javad, Imanifard Jaber and 3 more
Gene-gene interactions between DRD3, MRP4 and CYP2B6 polymorphisms and its influence on the pharmacokinetic parameters of efavirenz in HIV infected patients.
Drug metabolism and pharmacokinetics | 2016-10-01 | PMID 27665700
Sánchez-Martín Almudena, Cabrera Figueroa Salvador, Cruz Raquel and 5 more
Genes: DRD3
Whole genome sequencing of Mycobacterium tuberculosis for detection of drug resistance: a systematic review.
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases | 2017-02-01 | PMID 27665704
Papaventsis D, Casali N, Kontsevaya I and 3 more
New SMARCA2 mutation in a patient with Nicolaides-Baraitser syndrome and myoclonic astatic epilepsy.
American journal of medical genetics. Part A | 2017-01-01 | PMID 27665729
Tang S, Hughes E, Lascelles K and 2 more
Genes: SMARCA2
The molecular and phenotypic spectrum of IQSEC2-related epilepsy.
Epilepsia | 2016-11-01 | PMID 27665735
Zerem Ayelet, Haginoya Kazuhiro, Lev Dorit and 26 more
Genes: IQSEC2
Contemporary molecular tests for prognosis and treatment guidance for castration-resistant prostate cancer.
Expert review of molecular diagnostics | 2016-10-01 | PMID 27665838
Buonerba Carlo, Di Lorenzo Giuseppe, Sonpavde Guru
RAD18 polymorphisms are associated with platinum-based chemotherapy toxicity in Chinese patients with non-small cell lung cancer.
Acta pharmacologica Sinica | 2016-11-01 | PMID 27665847
Chu Tian-Qing, Li Rong, Shao Min-Hua and 2 more
Genes: RAD18
Influences of CYP2D6*10 polymorphisms on the pharmacokinetics of iloperidone and its metabolites in Chinese patients with schizophrenia: a population pharmacokinetic analysis.
Acta pharmacologica Sinica | 2016-11-01 | PMID 27665849
Pei Qi, Huang Lu, Huang Jie and 8 more
Association of factor XIII Val34Leu polymorphism and coronary artery disease: A meta-analysis.
Cardiology journal | 2017-01-01 | PMID 27665853
Jung Jae Hyun, Song Gwan Gyu, Kim Jae-Hoon and 2 more
Genes: CAD
The Next Generation of Synthetic Biology Chassis: Moving Synthetic Biology from the Laboratory to the Field.
ACS synthetic biology | 2016-12-16 | PMID 27665861
Adams Bryn L
Apolipoprotein E genotyping using PCR-GoldMag lateral flow assay and its clinical applications.
Molecular medicine reports | 2016-11-01 | PMID 27665864
Lian Ting, Hui Wenli, Li Xianying and 5 more
Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.
International journal of molecular medicine | 2016-11-01 | PMID 27665865
Salvi Alessandro, Giacopuzzi Edoardo, Bardellini Elena and 5 more
Genes: EDAR, EDARADD, MSX1, PAX9
An insertion/deletion polymorphism within the 3'‑untranslated region of COL1A2 confers susceptibility to osteoporosis.
Molecular medicine reports | 2016-11-01 | PMID 27665867
Jiang Zhen-Song, Hao Zhen-Hai
Genes: INS
Common genetic heterogeneity of human interleukin-37 leads to functional variance.
Cellular & molecular immunology | 2017-09-01 | PMID 27665946
Yan Jingjing, Zhang Yuling, Cheng Shimeng and 8 more
New perspectives to the enterotoxigenic E. coli F4 porcine infection model: Susceptibility genotypes in relation to performance, diarrhoea and bacterial shedding.
Veterinary microbiology | 2017-04-01 | PMID 27665990
Roubos-van den Hil Petra J, Litjens Ralph, Oudshoorn Anna-Katharina and 2 more
Using a qualitative approach to conceptualize concerns of patients with neurofibromatosis type 1 associated plexiform neurofibromas (pNF) across the lifespan.
American journal of medical genetics. Part A | 2017-01-01 | PMID 27666129
Lai Jin-Shei, Jensen Sally E, Patel Zabin S and 2 more
Nagashima-type palmoplantar keratosis in a Chinese Han population.
Molecular medicine reports | 2016-11-01 | PMID 27666198
Zhang Jia, Zhang Guolong, Ni Cheng and 4 more
Genes: SERPINB7, AQP5, CSTA, KRT1, KRT9, SLURP1
Genetic variation may explain why females are less susceptible to dental erosion.
European journal of oral sciences | 2016-10-01 | PMID 27666331
Uhlen Marte-Mari, Stenhagen Kjersti R, Dizak Piper M and 4 more
Genes: AMELX, TFIP11, TUFT1
TBCE Mutations Cause Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy.
American journal of human genetics | 2016-10-06 | PMID 27666369
Sferra Antonella, Baillat Gilbert, Rizza Teresa and 23 more
Genes: TBCE
Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy.
American journal of human genetics | 2016-10-06 | PMID 27666370
Flex Elisabetta, Niceta Marcello, Cecchetti Serena and 28 more
Genes: TBCD
Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.
American journal of human genetics | 2016-10-06 | PMID 27666371
Sul Jae Hoon, Cade Brian E, Cho Michael H and 4 more
Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project.
American journal of human genetics | 2016-10-06 | PMID 27666372
Auer Paul L, Reiner Alex P, Wang Gao and 8 more
Biallelic TBCD Mutations Cause Early-Onset Neurodegenerative Encephalopathy.
American journal of human genetics | 2016-10-06 | PMID 27666374
Miyake Noriko, Fukai Ryoko, Ohba Chihiro and 30 more
Genes: TBCD, ARL2, TBCE
HLA-B*40:02 and DRB1*04:03 are risk factors for oxcarbazepine-induced maculopapular eruption.
Epilepsia | 2016-11-01 | PMID 27666425
Moon Jangsup, Kim Tae-Joon, Lim Jung-Ah and 11 more
Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathy.
Annals of neurology | 2016-11-01 | PMID 27666438
Verdura Edgard, Hervé Dominique, Bergametti Françoise and 18 more
Analysis of resistance-associated substitutions in acute hepatitis C virus infection by deep sequencing across six genotypes and three continents.
Journal of viral hepatitis | 2017-01-01 | PMID 27666440
Eltahla A A, Rodrigo C, Betz-Stablein B and 17 more
Determination of restless legs syndrome prevalence in children aged 13-16years in the provincial center of Kayseri.
Brain & development | 2017-02-01 | PMID 27666468
Per Huseyin, Gunay Neslihan, Ismailogullari Sevda and 2 more
A novel missense mutation in the NADPH binding domain of CYBB abolishes the NADPH oxidase activity in a male patient with increased susceptibility to infections.
Microbial pathogenesis | 2016-11-01 | PMID 27666509
Khan Taj Ali, Kalsoom Kalsoom, Iqbal Asif and 9 more
Genes: CYBB, CYBA, NCF1, NCF2, NCF4
Clinical relevance of Helicobacter pylori virulence factors in Iranian patients with gastrointestinal diseases.
Microbial pathogenesis | 2016-11-01 | PMID 27666510
Bagheri Nader, Azadegan-Dehkordi Fatemeh, Rafieian-Kopaei Mahmoud and 3 more
Pro-adhesive phenotype of normal endothelial cells responding to metastatic breast cancer cell conditioned medium is linked to NFκB-mediated transcriptomic regulation.
International journal of oncology | 2016-11-01 | PMID 27666521
Mejía-Rangel Janini, Córdova Emilio, Orozco Lorena and 7 more
Genes: TNF, STAT3
Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotype.
European journal of endocrinology | 2016-11-01 | PMID 27666534
Glaudo Markus, Letz Saskia, Quinkler Marcus and 13 more
ENDOCRINE TUMOURS: Advances in the molecular pathogenesis of thyroid cancer: lessons from the cancer genome.
European journal of endocrinology | 2016-11-01 | PMID 27666535
Riesco-Eizaguirre Garcilaso, Santisteban Pilar
Relationship between polycystic ovary syndrome and ancestry in European Americans.
Fertility and sterility | 2016-12-01 | PMID 27666562
Bjonnes Andrew C, Saxena Richa, Welt Corrine K
Genome-wide nucleotide diversity of hatchery-reared Atlantic and Mediterranean strains of brown trout Salmo trutta compared to wild Mediterranean populations.
Journal of fish biology | 2016-12-01 | PMID 27666575
Leitwein M, Gagnaire P-A, Desmarais E and 4 more
Emergence of Preexisting MET Y1230C Mutation as a Resistance Mechanism to Crizotinib in NSCLC with MET Exon 14 Skipping.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer | 2017-01-01 | PMID 27666659
Ou Sai-Hong Ignatius, Young Lauren, Schrock Alexa B and 5 more
Genes: MET
Molecular screening strategies for NF1-like syndromes with café-au-lait macules (Review).
Molecular medicine reports | 2016-11-01 | PMID 27666661
Zhang Jia, Li Ming, Yao Zhirong
Genes: KIT
[Analysis of association of human 8-oxoguanine giycosylase 1 polymorphism with the susceptibility of laryngeal cancer].
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery | 2016-09-07 | PMID 27666707
Li D P, Huang H, Chai W and 4 more
[Research progress of mutational spectrum and pathophysiology of WFS1 gene in Wolfram syndrome and nonsyndromic low frequency sensorineural hearing loss].
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery | 2016-09-07 | PMID 27666717
Shi S M, Han Y H, Wang H B
Genes: WFS1
Control of Oriented Tissue Growth through Repression of Organ Boundary Genes Promotes Stem Morphogenesis.
Developmental cell | 2016-10-24 | PMID 27666746
Bencivenga Stefano, Serrano-Mislata Antonio, Bush Max and 2 more
Low-grade Schwann cell neoplasms with leptomeningeal dissemination: clinicopathologic and autopsy findings.
Human pathology | 2017-02-01 | PMID 27666764
Rodriguez Erika F, Blakeley Jaishri, Langmead Shannon and 8 more
Clinical significance of BRAF V600E mutational status in capsular nevi of sentinel lymph nodes in patients with primary cutaneous melanoma.
Human pathology | 2017-01-01 | PMID 27666765
Siroy Alan E, Aung Phyu P, Torres-Cabala Carlos A and 6 more
Genes: BRAF, SLN
Dysferlin mutations and mitochondrial dysfunction.
Neuromuscular disorders : NMD | 2016-11-01 | PMID 27666772
Vincent Amy E, Rosa Hannah S, Alston Charlotte L and 6 more
Genes: DYSF
The frequency of late-onset Pompe disease in pediatric patients with limb-girdle muscle weakness and nonspecific hyperCKemia: A multicenter study.
Neuromuscular disorders : NMD | 2016-11-01 | PMID 27666774
Ünver Olcay, Hacıfazlıoğlu Nilüfer Eldeş, Karatoprak Elif and 8 more
Genes: GAA
Muscle MRI in Duchenne muscular dystrophy: Evidence of a distinctive pattern.
Neuromuscular disorders : NMD | 2016-11-01 | PMID 27666775
Polavarapu Kiran, Manjunath Mahadevappa, Preethish-Kumar Veeramani and 6 more
Genes: DMD
Development and Dynamic Regulation of Mitochondrial Network in Human Midbrain Dopaminergic Neurons Differentiated from iPSCs.
Stem cell reports | 2016-10-11 | PMID 27666790
Fang Du, Qing Yu, Yan Shijun and 2 more
Development Refractoriness of MLL-Rearranged Human B Cell Acute Leukemias to Reprogramming into Pluripotency.
Stem cell reports | 2016-10-11 | PMID 27666791
Muñoz-López Alvaro, Romero-Moya Damià, Prieto Cristina and 24 more
Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up.
Movement disorders : official journal of the Movement Disorder Society | 2017-04-01 | PMID 27666935
Zech Michael, Boesch Sylvia, Jochim Angela and 14 more
Genes: ANO3, ADCY5, GCH1, THAP1
The role of electrostatics in TrxR electron transfer mechanism: A computational approach.
Proteins | 2016-12-01 | PMID 27667125
Teixeira Vitor H, Capacho Ana Sofia C, Machuqueiro Miguel
Promoting similarity of model sparsity structures in integrative analysis of cancer genetic data.
Statistics in medicine | 2017-02-10 | PMID 27667129
Huang Yuan, Liu Jin, Yi Huangdi and 2 more
A neonate with a unique non-Down syndrome transient proliferative megakaryoblastic disease.
Pediatric blood & cancer | 2017-03-01 | PMID 27667142
Bertrums Eline J M, Buijs Arjan, van Grotel Martine and 7 more
Genes: GATA1
Complete Genome Sequencing and Comparative Genomic Analysis of the Thermotolerant Acetic Acid Bacterium, Acetobacter pasteurianus SKU1108, Provide a New Insight into Thermotolerance.
Microbes and environments | 2016-12-23 | PMID 27667143
Matsutani Minenosuke, Hirakawa Hideki, Hiraoka Eri and 3 more
Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis.
Blood cells, molecules & diseases | 2016-10-01 | PMID 27667160
Niss Omar, Chonat Satheesh, Dagaonkar Neha and 8 more
Genes: EPB41, SPTA1, SPTB
Next-generation sequencing of hereditary hemochromatosis-related genes: Novel likely pathogenic variants found in the Portuguese population.
Blood cells, molecules & diseases | 2016-10-01 | PMID 27667161
Faria Ricardo, Silva Bruno, Silva Catarina and 9 more
Genes: HFE, HAMP, TFR2, FTL, HJV
The assessment of noncoding variant of PPOX gene in variegate porphyria reveals post-transcriptional role of the 5' untranslated exon 1.
Blood cells, molecules & diseases | 2016-10-01 | PMID 27667166
Fiorentino Valeria, Brancaleoni Valentina, Granata Francesca and 2 more
Genes: PPOX
Non lethal Raine syndrome and differential diagnosis.
European journal of medical genetics | 2016-11-01 | PMID 27667191
Elalaoui Siham Chafai, Al-Sheqaih Nada, Ratbi Ilham and 11 more
Upregulation of INS-IGF2 read-through expression and identification of a novel INS-IGF2 splice variant in insulinomas.
Oncology reports | 2016-11-01 | PMID 27667266
Johannessen Lene E, Panagopoulos Ioannis, Haugvik Sven-Petter and 3 more
Genes: IGF2, INS
[Pedigree survey in a family with hereditary protein S deficiency].
Zhonghua xin xue guan bing za zhi | 2016-09-24 | PMID 27667277
Huang K Y, Kong L Q, Wu Z and 6 more
Genes: PROS1
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.
Human mutation | 2017-01-01 | PMID 27667302
Yokote Koutaro, Chanprasert Sirisak, Lee Lin and 31 more
Genes: WRN
Comparative electrostatic analysis of adenylyl cyclase for isoform dependent regulation properties.
Proteins | 2016-12-01 | PMID 27667304
Tong Rudi, Wade Rebecca C, Bruce Neil J
Genes: RGS2
Why are behavioral and immune traits linked?
Hormones and behavior | 2017-02-01 | PMID 27667337
Lopes Patricia C
Dopa-responsive dystonia or early-onset Parkinson disease - Genotype-phenotype correlation.
Neurologia i neurochirurgia polska | 2000-01-01 | PMID 27667361
Potulska-Chromik Anna, Hoffman-Zacharska Dorota, Łukawska Małgorzata and 1 more
Genes: GCH1
Multi-omics Quantification of Species Variation of Escherichia coli Links Molecular Features with Strain Phenotypes.
Cell systems | 2016-09-28 | PMID 27667363
Monk Jonathan M, Koza Anna, Campodonico Miguel A and 5 more
The Role of Cardiac Magnetic Resonance Imaging in Hypertrophic Cardiomyopathy.
Reviews in cardiovascular medicine | 2016-01-01 | PMID 27667381
Marchesini Marco, Uguccioni Lucia, Parisi Rosario and 5 more
Isolated Left Ventricular Noncompaction Cardiomyopathy: A Transient Disease?
Reviews in cardiovascular medicine | 2016-01-01 | PMID 27667386
Vinardell Juan M, Avila Maria D, Santana Orlando
A real-time study of the interaction of TBP with a TATA box-containing duplex identical to an ancestral or minor allele of human gene LEP or TPI.
Journal of biomolecular structure & dynamics | 2017-11-01 | PMID 27667393
Arkova Olga, Kuznetsov Nikita, Fedorova Olga and 1 more
Genes: TBP, LEP
Investigating the Molecular Mechanisms Behind Uncharacterized Cysteine Losses from Prediction of Their Oxidation State.
Human mutation | 2017-01-01 | PMID 27667481
Raimondi Daniele, Orlando Gabriele, Messens Joris and 1 more
[Causative Genes for Amyotrophic Lateral Sclerosis].
Brain and nerve = Shinkei kenkyu no shinpo | 2016-09-01 | PMID 27667492
Maruyama Hirofumi, Morino Hiroyuki, Kawakami Hideshi
Identification of a novel allele, HLA-A*26:01:01:03N, by full-length genome sequencing.
HLA | 2016-11-01 | PMID 27667496
Park B G, Cho J, Im J and 2 more
Roles of Catalase and Trehalose in the Protection from Hydrogen Peroxide Toxicity in Saccharomyces cerevisiae.
Biocontrol science | 2016-01-01 | PMID 27667523
Nishimoto Takuto, Watanabe Takeru, Furuta Masakazu and 2 more
Systematic Identification of Pharmacological Targets from Small-Molecule Phenotypic Screens.
Cell chemical biology | 2016-10-20 | PMID 27667560
Liu Xueping, Baarsma Hoeke Abele, Thiam Chung Hwee and 9 more
IBS and IBD - separate entities or on a spectrum?
Nature reviews. Gastroenterology & hepatology | 2016-09-26 | PMID 27667579
Spiller Robin, Major Giles
Identification and sequence analysis of a novel HLA-A*33 allele, HLA-A*33:88.
HLA | 2016-11-01 | PMID 27667661
Pei Y F, Huang H N, Li H C and 1 more
Genes: GCG
A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative Phosphorylation.
Cell metabolism | 2016-12-13 | PMID 27667664
Arroyo Jason D, Jourdain Alexis A, Calvo Sarah E and 4 more
Genes: FASTKD2, NGRN, RPUSD3, RPUSD4, TRUB2
Analysis of Positive Selection at Single Nucleotide Polymorphisms Associated with Body Mass Index Does Not Support the "Thrifty Gene" Hypothesis.
Cell metabolism | 2016-10-11 | PMID 27667669
Wang Guanlin, Speakman John R
Genes: LCT
Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior.
Cell | 2016-10-06 | PMID 27667684
Doan Ryan N, Bae Byoung-Il, Cubelos Beatriz and 10 more
Genes: CDKL5, CUX1, GPC4, PTBP2
A Structurally Dynamic Region of the HslU Intermediate Domain Controls Protein Degradation and ATP Hydrolysis.
Structure (London, England : 1993) | 2016-10-04 | PMID 27667691
Baytshtok Vladimir, Fei Xue, Grant Robert A and 2 more
A Phosphomimetic Mutation Stabilizes SOD1 and Rescues Cell Viability in the Context of an ALS-Associated Mutation.
Structure (London, England : 1993) | 2016-11-01 | PMID 27667694
Fay James M, Zhu Cheng, Proctor Elizabeth A and 4 more
Genes: SOD1, DMD
Data-Driven Phenotypic Categorization for Neurobiological Analyses: Beyond DSM-5 Labels.
Biological psychiatry | 2017-03-15 | PMID 27667698
Van Dam Nicholas T, O'Connor David, Marcelle Enitan T and 8 more
Exon Junction Complexes: Supervising the Gene Expression Assembly Line.
Trends in genetics : TIG | 2016-11-01 | PMID 27667727
Boehm Volker, Gehring Niels H