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Items: 1 to 20 of 876

1.

Cryptic oxygen cycling in anoxic marine zones.

Garcia-Robledo E, Padilla CC, Aldunate M, Stewart FJ, Ulloa O, Paulmier A, Gregori G, Revsbech NP.

Proc Natl Acad Sci U S A. 2017 Jul 17. pii: 201619844. doi: 10.1073/pnas.1619844114. [Epub ahead of print]

PMID:
28716941
2.

Acoustic Sensing and Ultrasonic Drug Delivery in Multimodal Theranostic Capsule Endoscopy.

Stewart FR, Qiu Y, Lay HS, Newton IP, Cox BF, Al-Rawhani MA, Beeley J, Liu Y, Huang Z, Cumming DRS, Näthke I, Cochran S.

Sensors (Basel). 2017 Jul 3;17(7). pii: E1553. doi: 10.3390/s17071553.

3.

Putative archaeal viruses from the mesopelagic ocean.

Vik DR, Roux S, Brum JR, Bolduc B, Emerson JB, Padilla CC, Stewart FJ, Sullivan MB.

PeerJ. 2017 Jun 15;5:e3428. doi: 10.7717/peerj.3428. eCollection 2017.

4.

Ultrasound capsule endoscopy: sounding out the future.

Cox BF, Stewart F, Lay H, Cummins G, Newton IP, Desmulliez MPY, Steele RJC, Näthke I, Cochran S.

Ann Transl Med. 2017 May;5(9):201. doi: 10.21037/atm.2017.04.21.

5.

The factors affecting lipid profile in adult patients with Mucopolysaccharidosis.

Stepien KM, Stewart FJ, Hendriksz CJ.

Mol Genet Metab Rep. 2017 May 18;12:35-40. doi: 10.1016/j.ymgmr.2017.05.006. eCollection 2017 Sep.

6.

Correction: AAV-mediated expression of anti-tau scFvs decreases tau accumulation in a mouse model of tauopathy.

Ising C, Gallardo G, Leyns CEG, Wong CH, Jiang H, Stewart F, Koscal LJ, Roh J, Robinson GO, Serrano JR, Holtzman DM.

J Exp Med. 2017 Jul 3;214(7):2163. doi: 10.1084/jem.2016212505192017c. Epub 2017 May 23. No abstract available.

7.

Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.

Tatton-Brown K, Loveday C, Yost S, Clarke M, Ramsay E, Zachariou A, Elliott A, Wylie H, Ardissone A, Rittinger O, Stewart F, Temple IK, Cole T; Childhood Overgrowth Collaboration, Mahamdallie S, Seal S, Ruark E, Rahman N.

Am J Hum Genet. 2017 May 4;100(5):725-736. doi: 10.1016/j.ajhg.2017.03.010.

8.

Anti-tau antibody administration increases plasma tau in transgenic mice and patients with tauopathy.

Yanamandra K, Patel TK, Jiang H, Schindler S, Ulrich JD, Boxer AL, Miller BL, Kerwin DR, Gallardo G, Stewart F, Finn MB, Cairns NJ, Verghese PB, Fogelman I, West T, Braunstein J, Robinson G, Keyser J, Roh J, Knapik SS, Hu Y, Holtzman DM.

Sci Transl Med. 2017 Apr 19;9(386). pii: eaal2029. doi: 10.1126/scitranslmed.aal2029.

PMID:
28424326
9.

Shifting microbial communities sustain multiyear iron reduction and methanogenesis in ferruginous sediment incubations.

Bray MS, Wu J, Reed BC, Kretz CB, Belli KM, Simister RL, Henny C, Stewart FJ, DiChristina TJ, Brandes JA, Fowle DA, Crowe SA, Glass JB.

Geobiology. 2017 Apr 17. doi: 10.1111/gbi.12239. [Epub ahead of print]

PMID:
28419718
10.

AAV-mediated expression of anti-tau scFvs decreases tau accumulation in a mouse model of tauopathy.

Ising C, Gallardo G, Leyns CEG, Wong CH, Stewart F, Koscal LJ, Roh J, Robinson GO, Remolina Serrano J, Holtzman DM.

J Exp Med. 2017 May 1;214(5):1227-1238. doi: 10.1084/jem.20162125. Epub 2017 Apr 17. Erratum in: J Exp Med. 2017 May 23;:.

PMID:
28416651
11.

Tracheal tear from blunt neck trauma in children: Diagnosis and management.

Mener DJ, Stewart FD, Tunkel DE.

Int J Pediatr Otorhinolaryngol. 2017 May;96:100-102. doi: 10.1016/j.ijporl.2017.03.010. Epub 2017 Mar 7.

PMID:
28390594
12.

PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features.

Low KJ, Ansari M, Abou Jamra R, Clarke A, El Chehadeh S, FitzPatrick DR, Greenslade M, Henderson A, Hurst J, Keller K, Kuentz P, Prescott T, Roessler F, Selmer KK, Schneider MC, Stewart F, Tatton-Brown K, Thevenon J, Vigeland MD, Vogt J, Willems M, Zonana J, Study DD, Smithson SF.

Eur J Hum Genet. 2017 May;25(5):552-559. doi: 10.1038/ejhg.2017.27. Epub 2017 Mar 22.

13.

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.

Depienne C, Nava C, Keren B, Heide S, Rastetter A, Passemard S, Chantot-Bastaraud S, Moutard ML, Agrawal PB, VanNoy G, Stoler JM, Amor DJ, Billette de Villemeur T, Doummar D, Alby C, Cormier-Daire V, Garel C, Marzin P, Scheidecker S, de Saint-Martin A, Hirsch E, Korff C, Bottani A, Faivre L, Verloes A, Orzechowski C, Burglen L, Leheup B, Roume J, Andrieux J, Sheth F, Datar C, Parker MJ, Pasquier L, Odent S, Naudion S, Delrue MA, Le Caignec C, Vincent M, Isidor B, Renaldo F, Stewart F, Toutain A, Koehler U, Häckl B, von Stülpnagel C, Kluger G, Møller RS, Pal D, Jonson T, Soller M, Verbeek NE, van Haelst MM, de Kovel C, Koeleman B, Monroe G, van Haaften G; DDD Study, Attié-Bitach T, Boutaud L, Héron D, Mignot C.

Hum Genet. 2017 Apr;136(4):463-479. doi: 10.1007/s00439-017-1772-0. Epub 2017 Mar 10.

14.

Multisensory integration in Lepidoptera: Insights into flower-visitor interactions.

Kinoshita M, Stewart FJ, Ômura H.

Bioessays. 2017 Apr;39(4). doi: 10.1002/bies.201600086. Epub 2017 Feb 7. Review.

PMID:
28169433
15.

Clinical and molecular consequences of disease-associated de novo mutations in SATB2.

Bengani H, Handley M, Alvi M, Ibitoye R, Lees M, Lynch SA, Lam W, Fannemel M, Nordgren A, Malmgren H, Kvarnung M, Mehta S, McKee S, Whiteford M, Stewart F, Connell F, Clayton-Smith J, Mansour S, Mohammed S, Fryer A, Morton J; UK10K Consortium, Grozeva D, Asam T, Moore D, Sifrim A, McRae J, Hurles ME, Firth HV, Raymond FL, Kini U, Nellåker C, Ddd Study, FitzPatrick DR.

Genet Med. 2017 Feb 2. doi: 10.1038/gim.2016.211. [Epub ahead of print]

PMID:
28151491
16.

Assessment and validation of a novel angiographic scoring system for peripheral artery disease.

Morris DR, Singh TP, Moxon JV, Smith A, Stewart F, Jones RE, Golledge J.

Br J Surg. 2017 Apr;104(5):544-554. doi: 10.1002/bjs.10460. Epub 2017 Jan 31.

PMID:
28140457
17.

Prevalence and architecture of de novo mutations in developmental disorders.

Deciphering Developmental Disorders Study.

Nature. 2017 Feb 23;542(7642):433-438. doi: 10.1038/nature21062. Epub 2017 Jan 25.

PMID:
28135719
18.

Approaches to male hypogonadism in primary care.

Lawrence KL, Stewart F, Larson BM.

Nurse Pract. 2017 Feb 12;42(2):32-37. doi: 10.1097/01.NPR.0000511774.51873.da.

19.

Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11.

Rea G, Homfray T, Till J, Roses-Noguer F, Buchan RJ, Wilkinson S, Wilk A, Walsh R, John S, McKee S, Stewart FJ, Murday V, Taylor RW, Ashworth M, Baksi AJ, Daubeney P, Prasad S, Barton PJR, Cook SA, Ware JS.

Cold Spring Harb Mol Case Stud. 2017 Jan;3(1):a001271. doi: 10.1101/mcs.a001271.

20.

Sex can affect participation, engagement, and adherence in trials.

Avenell A, Robertson C, Stewart F, Boyers D, Douglas F, Archibald D, van Teijlingen E, Hoddinott P, Boachie C.

BMJ. 2016 Dec 30;355:i6754. doi: 10.1136/bmj.i6754. No abstract available.

PMID:
28039151

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