In silico screening, molecular docking, and molecular dynamics studies of SNP-derived human P5CR mutants.
Journal of biomolecular structure & dynamics | 2017-08-01 | PMID 27677826
Sang Peng, Hu Wei, Ye Yu-Jia and 4 more
Genes: PYCR1
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 7072 of 10600
Mechanics in human fibroblasts and progeria: Lamin A mutation E145K results in stiffening of nuclei.
Journal of molecular recognition : JMR | 2017-02-01 | PMID 27677907
Apte Ketaki, Stick Reimer, Radmacher Manfred
Genes: AFM
ABCC8 Single Nucleotide Polymorphisms are Associated with Cerebral Edema in Severe TBI.
Neurocritical care | 2017-04-01 | PMID 27677908
Jha Ruchira M, Puccio Ava M, Okonkwo David O and 8 more
Genes: ABCC8
Rhinovirus C is associated with wheezing and rhinovirus A is associated with pneumonia in hospitalized children in Morocco.
Journal of medical virology | 2017-04-01 | PMID 27677921
Annamalay Alicia A, Jroundi Imane, Bizzintino Joelene and 11 more
Epidemiology and treatment of relative anemia in children with sickle cell disease in sub-Saharan Africa.
Expert review of hematology | 2016-11-01 | PMID 27677923
Bello-Manga Halima, DeBaun Michael R, Kassim Adetola A
Genes: SCD
Lipoprotein (a) as a cause of cardiovascular disease: insights from epidemiology, genetics, and biology.
Journal of lipid research | 2016-11-01 | PMID 27677946
Nordestgaard Børge G, Langsted Anne
Rare variant association test in family-based sequencing studies.
Briefings in bioinformatics | 2017-11-01 | PMID 27677958
Wang Xuefeng, Zhang Zhenyu, Morris Nathan and 6 more
Role of positron emission tomography imaging in Multiple Endocrine Neoplasia syndromes.
Clinical physiology and functional imaging | 2018-01-01 | PMID 27677981
July Mose, Santhanam Prasanna, Giovanella Luca and 1 more
Ethylene-Regulated Glutamate Dehydrogenase Fine-Tunes Metabolism during Anoxia-Reoxygenation.
Plant physiology | 2016-11-01 | PMID 27677986
Tsai Kuen-Jin, Lin Chih-Yu, Ting Chen-Yun and 1 more
Major prognostic value of complex karyotype in addition to TP53 and IGHV mutational status in first-line chronic lymphocytic leukemia.
Hematological oncology | 2017-12-01 | PMID 27678008
Le Bris Yannick, Struski Stéphanie, Guièze Romain and 7 more
Genes: ATM
Prevalence and molecular characterization of human rhinovirus in stool samples of individuals with and without acute gastroenteritis.
Journal of medical virology | 2017-05-01 | PMID 27678016
Khoonta Prapaporn, Linsuwanon Piyada, Posuwan Nawarat and 3 more
The significance of FOXP1 in diffuse large B-cell lymphoma.
Leukemia & lymphoma | 2017-05-01 | PMID 27678023
Gascoyne Duncan M, Banham Alison H
Genes: FOXP1
Epistasis and Pleiotropy Affect the Modularity of the Genotype-Phenotype Map of Cross-Resistance in HIV-1.
Molecular biology and evolution | 2016-12-01 | PMID 27678053
Polster Robert, Petropoulos Christos J, Bonhoeffer Sebastian and 1 more
Serum Osteopontin Levels Are Decreased in Focal Adenomyosis.
Reproductive sciences (Thousand Oaks, Calif.) | 2017-05-01 | PMID 27678100
Streuli Isabelle, Santulli Pietro, Chouzenoux Sandrine and 2 more
Eliminating hydrolytic activity without affecting the transglycosylation of a GH1 β-glucosidase.
Applied microbiology and biotechnology | 2017-02-01 | PMID 27678115
Lundemo Pontus, Karlsson Eva Nordberg, Adlercreutz Patrick
Atopic Dermatitis Susceptibility Variants in Filaggrin Hitchhike Hornerin Selective Sweep.
Genome biology and evolution | 2016-11-11 | PMID 27678121
Eaaswarkhanth Muthukrishnan, Xu Duo, Flanagan Colin and 5 more
Genes: FLG, HRNR
Reconstructing pedigrees using probabilistic analysis of ISSR amplification.
Journal of theoretical biology | 2017-01-07 | PMID 27678162
Chaumont Loïc, Malécot Valéry, Pymar Richard and 1 more
Senescent Carcinoma-Associated Fibroblasts Upregulate IL8 to Enhance Prometastatic Phenotypes.
Molecular cancer research : MCR | 2017-01-01 | PMID 27678171
Wang Tao, Notta Faiyaz, Navab Roya and 7 more
Clinical and genetic investigation of a Brazilian family with Huntington's disease.
Functional neurology | 2000-01-01 | PMID 27678206
Agostinho L A, Spitz M, Pereira J S and 1 more
Genes: HTT
Molecular characterization of GPR50 gene and study of its comparative genetic variability in sheep breeds adapted to different thermo-contrasting climatic regimens.
International journal of biometeorology | 2017-04-01 | PMID 27678249
Saxena Vijay Kumar, Kumar Davendra, Naqvi S M K
Genes: GPR50
Outcomes of annual surveillance imaging in an adult and paediatric cohort of succinate dehydrogenase B mutation carriers.
Clinical endocrinology | 2017-02-01 | PMID 27678251
Tufton Nicola, Shapiro Lucy, Srirangalingam Umasuthan and 15 more
Genes: SDHB
Amelioration of X-Linked Related Autophagy Failure in Danon Disease With DNA Methylation Inhibitor.
Circulation | 2016-11-01 | PMID 27678261
Ng Kwong-Man, Mok Pamela Y, Butler Amy W and 12 more
Genes: LAMP2
Integration of next-generation sequencing in clinical diagnostic molecular pathology laboratories for analysis of solid tumours; an expert opinion on behalf of IQN Path ASBL.
Virchows Archiv : an international journal of pathology | 2017-01-01 | PMID 27678269
Deans Zandra C, Costa Jose Luis, Cree Ian and 19 more
Drug metabolism by flavin-containing monooxygenases of human and mouse.
Expert opinion on drug metabolism & toxicology | 2017-02-01 | PMID 27678284
Phillips Ian R, Shephard Elizabeth A
Genes: FMO1, FMO5
Pediatric Renal Angiomyolipomas in Tuberous Sclerosis Complex.
The Journal of urology | 2017-02-01 | PMID 27678300
Warncke Jason C, Brodie Katie E, Grantham Erin C and 4 more
Inflammatory bowel disease and airway diseases.
World journal of gastroenterology | 2016-09-14 | PMID 27678355
Vutcovici Maria, Brassard Paul, Bitton Alain
Tumor necrosis factor-α -G308A polymorphism is associated with liver pathological changes in hepatitis C virus patients.
World journal of gastroenterology | 2016-09-14 | PMID 27678360
Bader El Din Noha G, Farouk Sally, El-Shenawy Reem and 7 more
Global epidemiology of hepatitis C virus infection: An up-date of the distribution and circulation of hepatitis C virus genotypes.
World journal of gastroenterology | 2016-09-14 | PMID 27678366
Petruzziello Arnolfo, Marigliano Samantha, Loquercio Giovanna and 2 more
Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients.
Clinica chimica acta; international journal of clinical chemistry | 2016-11-01 | PMID 27678411
Liu Yi, Wang Jiawei, Ma Doudou and 10 more
Genes: IFITM5
The Cohesive Metastasis Phenotype in Human Prostate Cancer.
Biochimica et biophysica acta | 2016-12-01 | PMID 27678419
Harryman William L, Hinton James P, Rubenstein Cynthia P and 5 more
Rapid identification of familial hypercholesterolemia from electronic health records: The SEARCH study.
Journal of clinical lipidology | 2000-01-01 | PMID 27678441
Safarova Maya S, Liu Hongfang, Kullo Iftikhar J
Biomarkers of Response and Resistance to DNA Repair Targeted Therapies.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2016-12-01 | PMID 27678458
Stover Elizabeth H, Konstantinopoulos Panagiotis A, Matulonis Ursula A and 1 more
Genes: ATM, ATR
A Natural Mutation Involving both Pathogenicity and Perithecium Formation in the Fusarium graminearum Species Complex.
G3 (Bethesda, Md.) | 2016-12-07 | PMID 27678518
Suga Haruhisha, Kageyama Koji, Shimizu Masafumi and 1 more
Autosomal and X-Linked Additive Genetic Variation for Lifespan and Aging: Comparisons Within and Between the Sexes in Drosophila melanogaster.
G3 (Bethesda, Md.) | 2016-12-07 | PMID 27678519
Griffin Robert M, Schielzeth Holger, Friberg Urban
Drosophila CG2469 Encodes a Homolog of Human CTR9 and Is Essential for Development.
G3 (Bethesda, Md.) | 2016-12-07 | PMID 27678520
Chaturvedi Dhananjay, Inaba Mayu, Scoggin Shane and 1 more
Genes: CTR9
On Robust Association Testing for Quantitative Traits and Rare Variants.
G3 (Bethesda, Md.) | 2016-12-07 | PMID 27678522
Wei Peng, Cao Ying, Zhang Yiwei and 4 more
X Chromosome Crossover Formation and Genome Stability in Caenorhabditis elegans Are Independently Regulated by xnd-1.
G3 (Bethesda, Md.) | 2016-12-07 | PMID 27678523
McClendon T Brooke, Mainpal Rana, Amrit Francis R G and 3 more
Generation of Full-Length Class I Human Leukocyte Antigen Gene Consensus Sequences for Novel Allele Characterization.
Clinical chemistry | 2016-12-01 | PMID 27679434
Clark Peter M, Duke Jamie L, Ferriola Deborah and 5 more
Genomic diversity of cercarial clones of Himasthla elongata (Trematoda, Echinostomatidae) determined with AFLP technique.
Parasitology research | 2016-12-01 | PMID 27679450
Galaktionov N K, Podgornaya O I, Strelkov P P and 1 more
Discontinuing colchicine in symptomatic carriers for MEFV (Mediterranean FeVer) variants.
Clinical rheumatology | 2017-02-01 | PMID 27679472
Sönmez Hafize Emine, Batu Ezgi Deniz, Bilginer Yelda and 1 more
Genes: MEFV
COEXPEDIA: exploring biomedical hypotheses via co-expressions associated with medical subject headings (MeSH).
Nucleic acids research | 2017-01-04 | PMID 27679477
Yang Sunmo, Kim Chan Yeong, Hwang Sohyun and 4 more
Influenza Research Database: An integrated bioinformatics resource for influenza virus research.
Nucleic acids research | 2017-01-04 | PMID 27679478
Zhang Yun, Aevermann Brian D, Anderson Tavis K and 25 more
Activation of the Wnt/β-catenin pathway is common in wilms tumor, but rarely through β-catenin mutation and APC promoter methylation.
Pediatric surgery international | 2016-12-01 | PMID 27679509
Schweigert Amei, Fischer Carmen, Mayr Doris and 3 more
Genes: APC, AXIN2, CTNNB1
Effect of CYP3A4 genetic polymorphisms on the genotoxicity of 4,4'-methylene-bis(2-chloroaniline)-exposed workers.
Occupational and environmental medicine | 2017-01-01 | PMID 27679675
Wang Chung-Ching, Chen Wei-Liang, Hsiung Chia-Ni and 6 more
Miro phosphorylation sites regulate Parkin recruitment and mitochondrial motility.
Proceedings of the National Academy of Sciences of the United States of America | 2016-10-11 | PMID 27679849
Shlevkov Evgeny, Kramer Tal, Schapansky Jason and 2 more
Genes: PINK1, PTEN
The role of the mtDNA set point in differentiation, development and tumorigenesis.
The Biochemical journal | 2016-10-01 | PMID 27679856
Sun Xin, St John Justin C
IFN-γ Blocks Development of an Asthma Phenotype in Rhinovirus-Infected Baby Mice by Inhibiting Type 2 Innate Lymphoid Cells.
American journal of respiratory cell and molecular biology | 2017-02-01 | PMID 27679954
Han Mingyuan, Hong Jun Young, Jaipalli Suraj and 7 more
Effects of paroxetine on intravaginal ejaculatory latency time in Egyptian patients with lifelong premature ejaculation as a function of serotonin transporter polymorphism.
International journal of impotence research | 2017-01-01 | PMID 27679962
Salem A M, Kamel I I, Rashed L A and 1 more
Identification of a novel HLA-B*50 allele, HLA-B*50:01:08, in a Spanish hematological patient.
HLA | 2016-11-01 | PMID 27679987
Martin-Rodriguez S, Martinez-Carretero C, Llorente-Lumbreras A M and 2 more
Genetic divergence among invasive and native populations of the yellow peacock cichlid Cichla kelberi.
Journal of fish biology | 2016-12-01 | PMID 27679988
Marques A C P B, Franco A C S, Salgueiro F and 2 more
New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy.
Neurogenetics | 2016-10-01 | PMID 27679995
Martín-Hernández Elena, Rodríguez-García María Elena, Camacho Ana and 9 more
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing.
Neurogenetics | 2016-10-01 | PMID 27679996
Kumar Kishore R, Wali G M, Kamate Mahesh and 9 more
Genes: DDHD2, GLB1, PEX16
[Research progress in molecular classification of gastric cancer].
Zhonghua wei chang wai ke za zhi = Chinese journal of gastrointestinal surgery | 2016-09-25 | PMID 27680079
Zhou Menglong, Li Guichao, Zhang Zhen
A case of cerebrotendinous xanthomatosis mimicking the clinical phenotype of mitochondrial disease with a novel frame-shift mutation (c. 43_44 delGG) in CYP27A1 gene exon 1.
Rinsho shinkeigaku = Clinical neurology | 2016-10-28 | PMID 27680221
Koge Junpei, Hayashi Shintaro, Yamaguchi Hiroo and 3 more
The possible roles of B-cell novel protein-1 (BCNP1) in cellular signalling pathways and in cancer.
Journal of cellular and molecular medicine | 2017-03-01 | PMID 27680505
Patel Sapan J, Trivedi Gaurang L, Darie Costel C and 1 more
Genes: AKT2, KRAS, MAPK1
Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I.
Human mutation | 2017-01-01 | PMID 27680507
Xiong Fu, Ji Zhisong, Liu Yanhui and 20 more
Genes: SSUH2
The impact of TP53 mutations and TP53 deletions on survival varies between AML, ALL, MDS and CLL: an analysis of 3307 cases.
Leukemia | 2017-03-01 | PMID 27680515
Stengel A, Kern W, Haferlach T and 3 more
Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation.
European journal of neurology | 2017-01-01 | PMID 27680516
Konno T, Yoshida K, Mizuno T and 8 more
Caveolin 1 Modulates Aldosterone-Mediated Pathways of Glucose and Lipid Homeostasis.
Journal of the American Heart Association | 2016-09-28 | PMID 27680666
Baudrand Rene, Gupta Nidhi, Garza Amanda E and 11 more
Genes: CAV1
Mutations in actin used for structural studies partially disrupt β-thymosin/WH2 domains interaction.
FEBS letters | 2016-10-01 | PMID 27680677
Deville Célia, Girard-Blanc Christine, Assrir Nadine and 6 more
Genome-wide associations for birth weight and correlations with adult disease.
Nature | 2016-10-13 | PMID 27680694
Horikoshi Momoko, Beaumont Robin N, Day Felix R and 160 more
XPO1-dependent nuclear export is a druggable vulnerability in KRAS-mutant lung cancer.
Nature | 2016-10-06 | PMID 27680702
Kim Jimi, McMillan Elizabeth, Kim Hyun Seok and 20 more
Genes: KRAS, XPO1, FSTL5, YAP1, NFKBIA
Genetic diagnosis of familial hypercholesterolaemia using a rapid biochip array assay for 40 common LDLR, APOB and PCSK9 mutations.
Atherosclerosis | 2016-11-01 | PMID 27680772
Martin Rosalind, Latten Mark, Hart Padraig and 6 more
Genes: APOB, LDLR, PCSK9
A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans.
The Journal of clinical endocrinology and metabolism | 2016-11-01 | PMID 27680876
Pazderska Agnieszka, Oftedal Bergithe E, Napier Catherine M and 5 more
Genes: BACH2
Macrophages of genetically characterized familial hypercholesterolaemia patients show up-regulation of LDL-receptor-related proteins.
Journal of cellular and molecular medicine | 2017-03-01 | PMID 27680891
Escate Rafael, Padro Teresa, Borrell-Pages Maria and 4 more
Genes: LDLR, LRP1, LRP5, LRP6
Bacteria Are Smartphones and Mobile Genes Are Apps.
Trends in microbiology | 2016-12-01 | PMID 27680981
Young J Peter W
Enrichment of dissimilatory Fe(III)-reducing bacteria from groundwater of the Siklós BTEX-contaminated site (Hungary).
Folia microbiologica | 2017-01-01 | PMID 27680983
Farkas Milán, Szoboszlay Sándor, Benedek Tibor and 4 more
Bandwagons I, too, have known.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2016-12-01 | PMID 27681088
Bernardo Rex
A novel QTL associated with dwarf bunt resistance in Idaho 444 winter wheat.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2016-12-01 | PMID 27681089
Chen Jianli, Guttieri Mary J, Zhang Junli and 3 more
Heterozygosity for the rs696217 SNP in the Preproghrelin Gene Predicts Weight Loss After Bariatric Surgery in Severely Obese Individuals.
Obesity surgery | 2017-04-01 | PMID 27681093
Vitolo Edoardo, Santini Eleonora, Seghieri Marta and 5 more
Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice.
Journal of virology | 2016-12-01 | PMID 27681129
Jaumain Emilie, Quadrio Isabelle, Herzog Laetitia and 7 more
The Antagonism of HIV-1 Nef to SERINC5 Particle Infectivity Restriction Involves the Counteraction of Virion-Associated Pools of the Restriction Factor.
Journal of virology | 2016-12-01 | PMID 27681140
Trautz Birthe, Pierini Virginia, Wombacher Rebecka and 4 more
Genes: SERINC5, SERINC3
Antagonism of BST-2/Tetherin Is a Conserved Function of the Env Glycoprotein of Primary HIV-2 Isolates.
Journal of virology | 2016-12-15 | PMID 27681141
Chen Chia-Yen, Shingai Masashi, Welbourn Sarah and 4 more
TRIM5α Resistance Escape Mutations in the Capsid Are Transferable between Simian Immunodeficiency Virus Strains.
Journal of virology | 2016-12-15 | PMID 27681142
Wu Fan, Kirmaier Andrea, White Ellen and 10 more
Differentially expressed microRNAs in the corpus cavernosum from a murine model with type 2 diabetes mellitus-associated erectile dysfunction.
Molecular genetics and genomics : MGG | 2016-12-01 | PMID 27681254
Pan Feng, You Jinwei, Liu Yuan and 6 more
How the codfish changed its immune system.
Nature genetics | 2016-09-28 | PMID 27681288
Parham Peter
Uniparental disomy causes deficiencies of vitamin K-dependent proteins.
Journal of thrombosis and haemostasis : JTH | 2016-12-01 | PMID 27681307
Dasi M A, Gonzalez-Conejero R, Izquierdo S and 9 more
Genes: GGCX, VKORC1
Genetic and Biochemical Biomarkers in Canine Glaucoma.
Veterinary pathology | 2017-03-01 | PMID 27681326
Graham K L, McCowan C, White A
Genes: ADAMTS10, ADAMTS17, SRBD1
First report of Escherichia coli co-producing NDM-1 and OXA-232.
Diagnostic microbiology and infectious disease | 2016-12-01 | PMID 27681362
Both Anna, Huang Jiabin, Kaase Martin and 9 more
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease.
Human genetics | 2016-12-01 | PMID 27681385
Ma Lijiang, Bayram Yavuz, McLaughlin Heather M and 25 more
Phylogenetic relationships of D. rudis (Bedriaga, 1886) and D. bithynica(Mehely, 1909) based on microsatellite and mitochondrial DNA in Turkey.
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis | 2017-11-01 | PMID 27681412
Koç Halime, Kutrup Bilal, Eroğlu Oğuzhan and 4 more
Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas.
Cell reports | 2016-09-27 | PMID 27681435
Griffith Obi L, Chan Szeman Ruby, Griffith Malachi and 18 more
Genes: PRLR, STAT3
Estrogen receptor alpha gene ( ESR1) polymorphism can contribute to clinical findings in systemic lupus erythematosus patients.
Lupus | 2017-03-01 | PMID 27681518
Drehmer M N, Andrade D, Pereira I A and 4 more
Genes: ESR1
NRAMP1 gene polymorphisms and cutaneous leishmaniasis: An evaluation on host susceptibility and treatment outcome.
Journal of vector borne diseases | 2000-01-01 | PMID 27681549
Fattahi-Dolatabadi Marzieh, Mousavi Tahereh, Mohammadi-Barzelighi Hajar and 7 more
Loss of ift122, a Retrograde Intraflagellar Transport (IFT) Complex Component, Leads to Slow, Progressive Photoreceptor Degeneration Due to Inefficient Opsin Transport.
The Journal of biological chemistry | 2016-11-18 | PMID 27681595
Boubakri Meriam, Chaya Taro, Hirata Hiromi and 6 more
Heparin Binds Lamprey Angiotensinogen and Promotes Thrombin Inhibition through a Template Mechanism.
The Journal of biological chemistry | 2016-11-25 | PMID 27681598
Wei Hudie, Cai Haiyan, Wu Jiawei and 10 more
Repression of p63 and induction of EMT by mutant Ras in mammary epithelial cells.
Proceedings of the National Academy of Sciences of the United States of America | 2016-10-11 | PMID 27681615
Yoh Kathryn E, Regunath Kausik, Guzman Asja and 6 more
Mutant PFN1 causes ALS phenotypes and progressive motor neuron degeneration in mice by a gain of toxicity.
Proceedings of the National Academy of Sciences of the United States of America | 2016-10-11 | PMID 27681617
Yang Chunxing, Danielson Eric W, Qiao Tao and 4 more
Genes: PFN1
A ring-shaped conduit connects the mother cell and forespore during sporulation in Bacillus subtilis.
Proceedings of the National Academy of Sciences of the United States of America | 2016-10-11 | PMID 27681621
Rodrigues Christopher D A, Henry Xavier, Neumann Emmanuelle and 7 more
Functional receptor molecules CD300lf and CD300ld within the CD300 family enable murine noroviruses to infect cells.
Proceedings of the National Academy of Sciences of the United States of America | 2016-10-11 | PMID 27681626
Haga Kei, Fujimoto Akira, Takai-Todaka Reiko and 7 more
Early somatic mosaicism is a rare cause of long-QT syndrome.
Proceedings of the National Academy of Sciences of the United States of America | 2016-10-11 | PMID 27681629
Priest James Rush, Gawad Charles, Kahlig Kristopher M and 26 more
Characteristics of Japanese aldosterone-producing adenomas with KCNJ5 mutations.
Endocrine journal | 2017-01-30 | PMID 27681703
Okamura Takashi, Nakajima Yasuyo, Katano-Toki Akiko and 16 more
Genes: KCNJ5
Country-specific HPV-related genital disease among men residing in Brazil, Mexico and The United States: The HIM study.
International journal of cancer | 2017-01-15 | PMID 27681815
Sudenga Staci L, Torres B Nelson, Fulp William J and 11 more
Regulation of divalent metal transporter-1 by serine phosphorylation.
The Biochemical journal | 2016-11-15 | PMID 27681840
Seo Young Ah, Kumara Ruvin, Wetli Herbert and 1 more
How close are we to standardised extended RAS gene mutation testing? The UK NEQAS evaluation.
Journal of clinical pathology | 2017-01-01 | PMID 27681846
Richman Susan D, Fairley Jennifer, Butler Rachel and 1 more
Genes: KRAS, NRAS, EGFR
Targeted next-generation sequencing identifies molecular subgroups in squamous cell carcinoma of the head and neck with distinct outcome after concurrent chemoradiation.
Annals of oncology : official journal of the European Society for Medical Oncology | 2016-12-01 | PMID 27681865
Tinhofer I, Stenzinger A, Eder T and 9 more
Genes: KDR, NOTCH1
Dalotuzumab in chemorefractory KRAS exon 2 mutant colorectal cancer: Results from a randomised phase II/III trial.
International journal of cancer | 2017-01-15 | PMID 27681944
Sclafani Francesco, Kim Tae Y, Cunningham David and 16 more
Genes: KRAS, EREG
Molecular and clinical features of KATP -channel neonatal diabetes mellitus in Japan.
Pediatric diabetes | 2017-11-01 | PMID 27681997
Hashimoto Yukiko, Dateki Sumito, Hirose Masakazu and 9 more
Genes: ABCC8, KCNJ11
The T>A (rs11646213) gene polymorphism of cadherin-13 (CDH13) gene is associated with decreased risk of developing hypertension in Mexican population.
Immunobiology | 2017-10-01 | PMID 27682011
Vargas-Alarcon Gilberto, Martinez-Rodriguez Nancy, Velazquez-Cruz Rafael and 7 more
Genes: CDH13
The Molecular Epidemiology and Antimicrobial Resistance of Neisseria gonorrhoeae in Australia: A Nationwide Cross-Sectional Study, 2012.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America | 2016-12-15 | PMID 27682063
Trembizki Ella, Wand Handan, Donovan Basil and 16 more