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Items: 1 to 20 of 211

1.

Nurses' perceptions, acceptance, and use of a novel in-room pediatric ICU technology: testing an expanded technology acceptance model.

Holden RJ, Asan O, Wozniak EM, Flynn KE, Scanlon MC.

BMC Med Inform Decis Mak. 2016 Nov 15;16(1):145.

2.

In focus in HCB: from cell biology to tissue structure and function.

Asan E.

Histochem Cell Biol. 2016 Dec;146(6):645-646. No abstract available.

PMID:
27796529
3.

Sensory processing sensitivity and serotonin gene variance: Insights into mechanisms shaping environmental sensitivity.

Homberg JR, Schubert D, Asan E, Aron EN.

Neurosci Biobehav Rev. 2016 Dec;71:472-483. doi: 10.1016/j.neubiorev.2016.09.029. Review.

PMID:
27697602
4.

Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.

Xu XJ, Lv F, Liu Y, Wang JY, Ma DD, Asan, Wang JW, Song LJ, Jiang Y, Wang O, Xia WB, Xing XP, Li M.

J Hum Genet. 2016 Aug 25. doi: 10.1038/jhg.2016.109. [Epub ahead of print]

PMID:
27762305
5.

Capturing the patients' voices: Planning for patient-centered electronic health record use.

Asan O, Tyszka J, Fletcher KE.

Int J Med Inform. 2016 Nov;95:1-7. doi: 10.1016/j.ijmedinf.2016.08.002.

PMID:
27697228
6.

Providers' perceived facilitators and barriers to EHR screen sharing in outpatient settings.

Asan O.

Appl Ergon. 2017 Jan;58:301-7. doi: 10.1016/j.apergo.2016.07.005.

PMID:
27633226
7.

Density of acetylcholine esterase (AchE) and tyrosine hydroxylase (TH) containing fibers in the amygdala of roman high- and low-avoidance rats.

Yilmazer-Hanke D, Eliava M, Hanke J, Schwegler H, Asan E.

Neurosci Lett. 2016 Oct 6;632:114-8. doi: 10.1016/j.neulet.2016.08.053.

PMID:
27585749
8.

Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations.

Liang D, Wang Y, Ji X, Hu H, Zhang J, Meng L, Lin Y, Ma D, Jiang T, Jiang H, Asan, Song L, Guo J, Hu P, Xu Z.

Clin Genet. 2016 Aug 5. doi: 10.1111/cge.12844. [Epub ahead of print]

PMID:
27491356
9.

Diaphragmatic Eventration in Sisters with Asparagine Synthetase Deficiency: A Novel Homozygous ASNS Mutation and Expanded Phenotype.

Sun J, McGillivray AJ, Pinner J, Yan Z, Liu F, Bratkovic D, Thompson E, Wei X, Jiang H, Asan, Chopra M.

JIMD Rep. 2016 Jul 27. [Epub ahead of print]

PMID:
27469131
10.

Provider Use of a Novel EHR display in the Pediatric Intensive Care Unit. Large Customizable Interactive Monitor (LCIM).

Asan O, Holden RJ, Flynn KE, Yang Y, Azam L, Scanlon MC.

Appl Clin Inform. 2016 Jul 20;7(3):682-92. doi: 10.4338/ACI-2016-02-RA-0030.

PMID:
27453191
11.

Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations.

Liu Y, Song L, Ma D, Lv F, Xu X, Wang J, Xia W, Jiang Y, Wang O, Song Y, Xing X, Asan, Li M.

Clin Chim Acta. 2016 Oct 1;461:172-80. doi: 10.1016/j.cca.2016.07.012.

PMID:
27450065
12.

Non-Invasive Prenatal Diagnosis of Lethal Skeletal Dysplasia by Targeted Capture Sequencing of Maternal Plasma.

Dan S, Yuan Y, Wang Y, Chen C, Gao C, Yu S, Liu Y, Song W, Asan, Zhu H, Yang L, Deng H, Su Y, Yi X.

PLoS One. 2016 Jul 19;11(7):e0159355. doi: 10.1371/journal.pone.0159355.

13.

Designing Patient-facing Health Information Technologies for the Outpatient Settings: A Literature Review.

Yang Y, Asan O.

J Innov Health Inform. 2016 Apr 6;23(1):185. doi: 10.14236/jhi.v23i1.185.

14.

Initial characterization of a Syap1 knock-out mouse and distribution of Syap1 in mouse brain and cultured motoneurons.

Schmitt D, Funk N, Blum R, Asan E, Andersen L, Rülicke T, Sendtner M, Buchner E.

Histochem Cell Biol. 2016 Oct;146(4):489-512. doi: 10.1007/s00418-016-1457-0.

15.

A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta.

Xu XJ, Lv F, Liu Y, Wang JY, Song YW, Asan, Wang JW, Song LJ, Jiang Y, Wang O, Xia WB, Xing XP, Li M.

Clin Chim Acta. 2016 Sep 1;460:33-9. doi: 10.1016/j.cca.2016.06.011.

PMID:
27312322
16.

A Novel Approach to Assess Motor Outcome of Deep Brain Stimulation Effects in the Hemiparkinsonian Rat: Staircase and Cylinder Test.

Rattka M, Fluri F, Krstić M, Asan E, Volkmann J.

J Vis Exp. 2016 May 31;(111). doi: 10.3791/53951.

PMID:
27284739
17.

Correction: Morphogenesis of the C. elegans Intestine Involves Axon Guidance Genes.

Asan A, Raiders SA, Priess JR.

PLoS Genet. 2016 May 18;12(5):e1006077. doi: 10.1371/journal.pgen.1006077.

18.

Neuregulin-1 Administration Protocols Sufficient for Stimulating Cardiac Regeneration in Young Mice Do Not Induce Somatic, Organ, or Neoplastic Growth.

Ganapathy B, Nandhagopal N, Polizzotti BD, Bennett D, Asan A, Wu Y, Kühn B.

PLoS One. 2016 May 13;11(5):e0155456. doi: 10.1371/journal.pone.0155456.

19.

Targeted sequencing of maternal plasma for haplotype-based noninvasive prenatal testing of spinal muscular atrophy.

Chen M, Lu S, Lai Z, Chen C, Luo K, Yuan Y, Wang Y, Li S, Gao Y, Chen F, Asan, Chen D.

Ultrasound Obstet Gynecol. 2016 Apr 22. doi: 10.1002/uog.15947. [Epub ahead of print]

PMID:
27102838
20.

Morphogenesis of the C. elegans Intestine Involves Axon Guidance Genes.

Asan A, Raiders SA, Priess JR.

PLoS Genet. 2016 Apr 1;12(4):e1005950. doi: 10.1371/journal.pgen.1005950. Erratum in: PLoS Genet. 2016 May;12(5):e1006077.

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