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Items: 1 to 20 of 4367

1.

Association of HLA-G 3'UTR polymorphisms and haplotypes with severe sepsis in a Brazilian population.

Hahn EC, Báo Zambra FM, Kamada AJ, Delongui F, Carvalho Grion CM, Reiche EMV, Bogo Chies JA.

Hum Immunol. 2017 Sep 20. pii: S0198-8859(17)30493-7. doi: 10.1016/j.humimm.2017.09.002. [Epub ahead of print]

PMID:
28941746
2.

MiR-9, miR-21, and miR-155 as potential biomarkers for HPV positive and negative cervical cancer.

Park S, Eom K, Kim J, Bang H, Wang HY, Ahn S, Kim G, Jang H, Kim S, Lee D, Park KH, Lee H.

BMC Cancer. 2017 Sep 21;17(1):658. doi: 10.1186/s12885-017-3642-5.

PMID:
28934937
3.

Predicting Major Bleeding in Ischemic Stroke Patients With Atrial Fibrillation.

Hilkens NA, Algra A, Greving JP.

Stroke. 2017 Sep 20. pii: STROKEAHA.117.019183. doi: 10.1161/STROKEAHA.117.019183. [Epub ahead of print]

PMID:
28931618
4.

Microarray-based SNP genotyping to identify genetic risk factors of triple-negative breast cancer (TNBC) in South Indian population.

Aravind Kumar M, Singh V, Naushad SM, Shanker U, Lakshmi Narasu M.

Mol Cell Biochem. 2017 Sep 16. doi: 10.1007/s11010-017-3187-6. [Epub ahead of print]

PMID:
28918577
5.

Genetic Test, Risk Prediction, and Counseling.

Wang MH, Weng H.

Adv Exp Med Biol. 2017;1005:21-46. doi: 10.1007/978-981-10-5717-5_2.

PMID:
28916927
6.

Accumulation of minor alleles and risk prediction in schizophrenia.

He P, Lei X, Yuan D, Zhu Z, Huang S.

Sci Rep. 2017 Sep 15;7(1):11661. doi: 10.1038/s41598-017-12104-0.

7.

Shared polymorphisms and modifiable behavior factors for myocardial infarction and high cholesterol in a retrospective population study.

Liang Y, Kelemen A.

Medicine (Baltimore). 2017 Sep;96(37):e7683. doi: 10.1097/MD.0000000000007683.

8.

Editor's Highlight: Nlrp3 Is Required for Inflammatory Changes and Nigral Cell Loss Resulting From Chronic Intragastric Rotenone Exposure in Mice.

Martinez EM, Young AL, Patankar YR, Berwin BL, Wang L, von Herrmann KM, Weier JM, Havrda MC.

Toxicol Sci. 2017 Sep 1;159(1):64-75. doi: 10.1093/toxsci/kfx117.

PMID:
28903492
9.

Improving Disease Prediction by Incorporating Family Disease History in Risk Prediction Models with Large-Scale Genetic Data.

Gim J, Kim W, Kwak SH, Choi H, Park C, Park KS, Kwon S, Park T, Won S.

Genetics. 2017 Sep 12. pii: genetics.300283.2017. doi: 10.1534/genetics.117.300283. [Epub ahead of print]

10.

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.

Wheeler E, Leong A, Liu CT, Hivert MF, Strawbridge RJ, Podmore C, Li M, Yao J, Sim X, Hong J, Chu AY, Zhang W, Wang X, Chen P, Maruthur NM, Porneala BC, Sharp SJ, Jia Y, Kabagambe EK, Chang LC, Chen WM, Elks CE, Evans DS, Fan Q, Giulianini F, Go MJ, Hottenga JJ, Hu Y, Jackson AU, Kanoni S, Kim YJ, Kleber ME, Ladenvall C, Lecoeur C, Lim SH, Lu Y, Mahajan A, Marzi C, Nalls MA, Navarro P, Nolte IM, Rose LM, Rybin DV, Sanna S, Shi Y, Stram DO, Takeuchi F, Tan SP, van der Most PJ, Van Vliet-Ostaptchouk JV, Wong A, Yengo L, Zhao W, Goel A, Martinez Larrad MT, Radke D, Salo P, Tanaka T, van Iperen EPA, Abecasis G, Afaq S, Alizadeh BZ, Bertoni AG, Bonnefond A, Böttcher Y, Bottinger EP, Campbell H, Carlson OD, Chen CH, Cho YS, Garvey WT, Gieger C, Goodarzi MO, Grallert H, Hamsten A, Hartman CA, Herder C, Hsiung CA, Huang J, Igase M, Isono M, Katsuya T, Khor CC, Kiess W, Kohara K, Kovacs P, Lee J, Lee WJ, Lehne B, Li H, Liu J, Lobbens S, Luan J, Lyssenko V, Meitinger T, Miki T, Miljkovic I, Moon S, Mulas A, Müller G, Müller-Nurasyid M, Nagaraja R, Nauck M, Pankow JS, Polasek O, Prokopenko I, Ramos PS, Rasmussen-Torvik L, Rathmann W, Rich SS, Robertson NR, Roden M, Roussel R, Rudan I, Scott RA, Scott WR, Sennblad B, Siscovick DS, Strauch K, Sun L, Swertz M, Tajuddin SM, Taylor KD, Teo YY, Tham YC, Tönjes A, Wareham NJ, Willemsen G, Wilsgaard T, Hingorani AD; EPIC-CVD Consortium; EPIC-InterAct Consortium; Lifelines Cohort Study, Egan J, Ferrucci L, Hovingh GK, Jula A, Kivimaki M, Kumari M, Njølstad I, Palmer CNA, Serrano Ríos M, Stumvoll M, Watkins H, Aung T, Blüher M, Boehnke M, Boomsma DI, Bornstein SR, Chambers JC, Chasman DI, Chen YI, Chen YT, Cheng CY, Cucca F, de Geus EJC, Deloukas P, Evans MK, Fornage M, Friedlander Y, Froguel P, Groop L, Gross MD, Harris TB, Hayward C, Heng CK, Ingelsson E, Kato N, Kim BJ, Koh WP, Kooner JS, Körner A, Kuh D, Kuusisto J, Laakso M, Lin X, Liu Y, Loos RJF, Magnusson PKE, März W, McCarthy MI, Oldehinkel AJ, Ong KK, Pedersen NL, Pereira MA, Peters A, Ridker PM, Sabanayagam C, Sale M, Saleheen D, Saltevo J, Schwarz PE, Sheu WHH, Snieder H, Spector TD, Tabara Y, Tuomilehto J, van Dam RM, Wilson JG, Wilson JF, Wolffenbuttel BHR, Wong TY, Wu JY, Yuan JM, Zonderman AB, Soranzo N, Guo X, Roberts DJ, Florez JC, Sladek R, Dupuis J, Morris AP, Tai ES, Selvin E, Rotter JI, Langenberg C, Barroso I, Meigs JB.

PLoS Med. 2017 Sep 12;14(9):e1002383. doi: 10.1371/journal.pmed.1002383. eCollection 2017 Sep.

11.

Structure and functional impact of seed region variant in MIR-499 gene family in bronchial asthma.

Toraih EA, Hussein MH, Al Ageeli E, Riad E, AbdAllah NB, Helal GM, Fawzy MS.

Respir Res. 2017 Sep 8;18(1):169. doi: 10.1186/s12931-017-0648-0.

12.

Liquid biopsy in patients with hepatocellular carcinoma: Circulating tumor cells and cell-free nucleic acids.

Okajima W, Komatsu S, Ichikawa D, Miyamae M, Ohashi T, Imamura T, Kiuchi J, Nishibeppu K, Arita T, Konishi H, Shiozaki A, Morimura R, Ikoma H, Okamoto K, Otsuji E.

World J Gastroenterol. 2017 Aug 21;23(31):5650-5668. doi: 10.3748/wjg.v23.i31.5650. Review.

13.

Phenotype in combination with genotype improves outcome prediction in acute myeloid leukemia: a report from Children's Oncology Group protocol AAML0531.

Voigt AP, Eidenschink Brodersen L, Alonzo TA, Gerbing RB, Menssen AJ, Wilson ER, Kahwash S, Raimondi SC, Hirsch BA, Gamis AS, Meshinchi S, Wells DA, Loken MR; Children's Oncology Group.

Haematologica. 2017 Sep 7. pii: haematol.2017.169029. doi: 10.3324/haematol.2017.169029. [Epub ahead of print]

14.

Identification of long non-coding RNAs biomarkers associated with progression of endometrial carcinoma and patient outcomes.

Sun Y, Zou X, He J, Mao Y.

Oncotarget. 2017 Apr 30;8(32):52604-52613. doi: 10.18632/oncotarget.17537. eCollection 2017 Aug 8.

15.

Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene.

Dicks E, Song H, Ramus SJ, Oudenhove EV, Tyrer JP, Intermaggio MP, Kar S, Harrington P, Bowtell DD, Group AS, Cicek MS, Cunningham JM, Fridley BL, Alsop J, Jimenez-Linan M, Piskorz A, Goranova T, Kent E, Siddiqui N, Paul J, Crawford R, Poblete S, Lele S, Sucheston-Campbell L, Moysich KB, Sieh W, McGuire V, Lester J, Odunsi K, Whittemore AS, Bogdanova N, Dürst M, Hillemanns P, Karlan BY, Gentry-Maharaj A, Menon U, Tischkowitz M, Levine D, Brenton JD, Dörk T, Goode EL, Gayther SA, Pharoah DPP.

Oncotarget. 2017 Mar 3;8(31):50930-50940. doi: 10.18632/oncotarget.15871. eCollection 2017 Aug 1.

16.

Discovery of mutations in homologous recombination genes in African-American women with breast cancer.

Ding YC, Adamson AW, Steele L, Bailis AM, John EM, Tomlinson G, Neuhausen SL.

Fam Cancer. 2017 Sep 2. doi: 10.1007/s10689-017-0036-4. [Epub ahead of print]

PMID:
28864920
17.

Child neurodevelopmental outcomes following preterm and term birth: What can the placenta tell us?

Hodyl NA, Aboustate N, Bianco-Miotto T, Roberts CT, Clifton VL, Stark MJ.

Placenta. 2017 Sep;57:79-86. doi: 10.1016/j.placenta.2017.06.009. Epub 2017 Jun 15. Review.

PMID:
28864022
18.

Higher-than-expected population prevalence of potentially pathogenic germline TP53 variants in individuals unselected for cancer history.

de Andrade KC, Mirabello L, Stewart DR, Karlins E, Koster R, Wang M, Gapstur SM, Gaudet MM, Freedman ND, Landi MT, Lemonnier N, Hainaut P, Savage SA, Achatz MI.

Hum Mutat. 2017 Sep 1. doi: 10.1002/humu.23320. [Epub ahead of print]

PMID:
28861920
19.

Triplex HRM assay for the simultaneous assessment of IL28B rs12979860, ABCB11 rs2287622, and RNF7 rs16851720 genotypes in chronic hepatitis C patients.

Enache EL, Sin A, Enache LS, Bancu L.

J Mol Diagn. 2017 Aug 28. pii: S1525-1578(17)30299-4. doi: 10.1016/j.jmoldx.2017.07.005. [Epub ahead of print]

PMID:
28860020
20.

The wide spectrum of POT1 gene variants correlates with multiple cancer types.

Calvete O, Garcia-Pavia P, Domínguez F, Bougeard G, Kunze K, Braeuninger A, Teule A, Lasa A, Ramón Y Cajal T, Llort G, Fernández V, Lázaro C, Urioste M, Benitez J.

Eur J Hum Genet. 2017 Aug 30. doi: 10.1038/ejhg.2017.134. [Epub ahead of print]

PMID:
28853721

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