PubMed Clinical Queries
From PubMed Clinical Queries
PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas
Similarity of the dog and human gut microbiomes in gene content and response to diet. Coelho LP, Kultima JR, Costea PI, Fournier C, Pan Y, Czarnecki-Maulden G, Hayward MR, Forslund SK, Schmidt TSB, Descombes P, et al. Microbiome. 2018 Apr 19; 6(1):72. Epub 2018 Apr 19.
The human clone ST22 SCCmec IV methicillin-resistant Staphylococcus aureus isolated from swine herds and wild primates in Nepal: is man the common source? Roberts MC, Joshi PR, Greninger AL, Melendez D, Paudel S, Acharya M, Bimali NK, Koju NP, No D, Chalise M, et al. FEMS Microbiol Ecol. 2018 May 1; 94(5).
Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers. Pritchard AL, Johansson PA, Nathan V, Howlie M, Symmons J, Palmer JM, Hayward NK. PLoS One. 2018; 13(4):e0194098. Epub 2018 Apr 11.
Recognition of the polycistronic nature of human genes is critical to understanding the genotype-phenotype relationship. Brunet MA, Levesque SA, Hunting DJ, Cohen AA, Roucou X. Genome Res. 2018 Apr 6; . Epub 2018 Apr 6.
New insights into the phylogenetics and population structure of the prairie falcon (Falco mexicanus). Doyle JM, Bell DA, Bloom PH, Emmons G, Fesnock A, Katzner TE, LaPré L, Leonard K, SanMiguel P, Westerman R, et al. BMC Genomics. 2018 Apr 4; 19(1):233. Epub 2018 Apr 4.
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New technologies to uncover the molecular basis of disorders of sex development. Barseghyan H, Délot EC, Vilain E. Mol Cell Endocrinol. 2018 Apr 12; . Epub 2018 Apr 12.
Recognition of the polycistronic nature of human genes is critical to understanding the genotype-phenotype relationship. Brunet MA, Levesque SA, Hunting DJ, Cohen AA, Roucou X. Genome Res. 2018 Apr 6; . Epub 2018 Apr 6.
A Protocol for Epigenetic Imprinting Analysis with RNA-Seq Data. Zou J, Xiang D, Datla R, Wang E. Methods Mol Biol. 2018; 1751:199-208.
Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature. Schwarze K, Buchanan J, Taylor JC, Wordsworth S. Genet Med. 2018 Feb 15; . Epub 2018 Feb 15.
Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants. Finsterer J, Zarrouk-Mahjoub S. Am J Transl Res. 2018; 10(1):13-15. Epub 2018 Jan 15.
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Medical Genetics Topic: All Diagnosis Differential Diagnosis Clinical Description Management Genetic Counseling Molecular Genetics Genetic Testing
Use of Genetic Testing for Primary Immunodeficiency Patients. Heimall JR, Hagin D, Hajjar J, Henrickson SE, Hernandez-Trujillo HS, Tan Y, Kobrynski L, Paris K, Torgerson TR, Verbsky JW, et al. J Clin Immunol. 2018 Apr 19; . Epub 2018 Apr 19.
Patterns of differential gene expression in a cellular model of human islet development, and relationship to type 2 diabetes predisposition. Perez-Alcantara M, Honoré C, Wesolowska-Andersen A, Gloyn AL, McCarthy MI, Hansson M, Beer NL, van de Bunt M. Diabetologia. 2018 Apr 19; . Epub 2018 Apr 19.
A 200K SNP chip reveals a novel Pacific salmon louse genotype linked to differential efficacy of emamectin benzoate. Messmer AM, Leong JS, Rondeau EB, Mueller A, Despins CA, Minkley DR, Kent MP, Lien S, Boyce B, Morrison D, et al. Mar Genomics. 2018 Apr 16; . Epub 2018 Apr 16.
Enabling multiplexed testing of pooled donor cells through whole-genome sequencing. Chan Y, Chan YK, Goodman DB, Guo X, Chavez A, Lim ET, Church GM. Genome Med. 2018 Apr 19; 10(1):31. Epub 2018 Apr 19.
Protracted Outbreak of Salmonella Newport Infections Linked to Ground Beef: Possible Role of Dairy Cows - 21 States, 2016-2017. Marshall KEH, Tewell M, Tecle S, Leeper M, Sinatra J, Kissler B, Fung A, Brown K, Wagner D, Trees E, et al. MMWR Morb Mortal Wkly Rep. 2018 Apr 20; 67(15):443-446. Epub 2018 Apr 20.
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