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Items: 1 to 50 of 95

1.

A training program incorporating a diabetes tool to facilitate delivery of quality diabetes care by community pharmacists in Malaysia and Australia.

Ayadurai S, Sunderland B, Tee LB, Hattingh HL.

Pharm Pract (Granada). 2019 Apr-Jun;17(2):1457. doi: 10.18549/PharmPract.2019.2.1457. Epub 2019 Jun 14.

2.

Rapid Detection of Sepsis using CESDA: the Caenorhabditis elegans Sepsis Detection Assay.

Tee LF, Tan TL, Neoh HM, Jamal R.

Rev Soc Bras Med Trop. 2019 Mar 14;52:e20180300. doi: 10.1590/0037-8682-0300-2018.

3.

Does knee position during wound closure alter patella height following total knee arthroplasty?

Clark S, Tee L, Sutherland A.

ANZ J Surg. 2019 Mar;89(3):191-195. doi: 10.1111/ans.15034. Epub 2019 Jan 26.

PMID:
30685890
4.

Extraction and recovery of phytochemical components and antioxidative properties in fruit parts of Dacryodes rostrata influenced by different solvents.

Thavamoney N, Sivanadian L, Tee LH, Khoo HE, Prasad KN, Kong KW.

J Food Sci Technol. 2018 Jul;55(7):2523-2532. doi: 10.1007/s13197-018-3170-6. Epub 2018 May 2.

5.

Structured tool to improve clinical outcomes of type 2 diabetes mellitus patients: A randomized controlled trial.

Ayadurai S, Sunderland VB, Tee LBG, Md Said SN, Hattingh HL.

J Diabetes. 2018 Dec;10(12):965-976. doi: 10.1111/1753-0407.12799. Epub 2018 Jul 18.

PMID:
29877609
6.

Nanopore sequencing and assembly of a human genome with ultra-long reads.

Jain M, Koren S, Miga KH, Quick J, Rand AC, Sasani TA, Tyson JR, Beggs AD, Dilthey AT, Fiddes IT, Malla S, Marriott H, Nieto T, O'Grady J, Olsen HE, Pedersen BS, Rhie A, Richardson H, Quinlan AR, Snutch TP, Tee L, Paten B, Phillippy AM, Simpson JT, Loman NJ, Loose M.

Nat Biotechnol. 2018 Apr;36(4):338-345. doi: 10.1038/nbt.4060. Epub 2018 Jan 29.

7.

Whole Genome Methylation Analysis of Nondysplastic Barrett Esophagus that Progresses to Invasive Cancer.

Dilworth MP, Nieto T, Stockton JD, Whalley CM, Tee L, James JD, Noble F, Underwood TJ, Hallissey MT, Hejmadi R, Trudgill N, Tucker O, Beggs AD.

Ann Surg. 2019 Mar;269(3):479-485. doi: 10.1097/SLA.0000000000002658.

8.

Maintenance of murine platelet homeostasis by the kinase Csk and phosphatase CD148.

Mori J, Nagy Z, Di Nunzio G, Smith CW, Geer MJ, Al Ghaithi R, van Geffen JP, Heising S, Boothman L, Tullemans BME, Correia JN, Tee L, Kuijpers MJE, Harrison P, Heemskerk JWM, Jarvis GE, Tarakhovsky A, Weiss A, Mazharian A, Senis YA.

Blood. 2018 Mar 8;131(10):1122-1144. doi: 10.1182/blood-2017-02-768077. Epub 2018 Jan 4.

9.

Consensus Validation of Simpler™: A Tool to Improve Pharmacist Delivery of Quality, Evidence-Based Diabetes Care.

Ayadurai S, Sunderland VB, Tee LBG, Hattingh HL.

Curr Diabetes Rev. 2018;14(6):565-575. doi: 10.2174/1573399814666171215115239.

PMID:
29243582
10.

Effects of simulated microgravity on gene expression and biological phenotypes of a single generation Caenorhabditis elegans cultured on 2 different media.

Tee LF, Neoh HM, Then SM, Murad NA, Asillam MF, Hashim MH, Nathan S, Jamal R.

Life Sci Space Res (Amst). 2017 Nov;15:11-17. doi: 10.1016/j.lssr.2017.06.002. Epub 2017 Jun 24.

PMID:
29198309
11.

The use of non-prescription medicines during lactation: A qualitative study of community pharmacists' attitudes and perspectives.

Sim TF, Hattingh HL, Sherriff J, Tee LBG.

Res Social Adm Pharm. 2018 May;14(5):464-470. doi: 10.1016/j.sapharm.2017.06.002. Epub 2017 Jun 10.

PMID:
28624292
12.

Valorization of Dacryodes rostrata fruit through the characterization of its oil.

Tee LH, Yang B, Tey BT, Chan ES, Azlan A, Ismail A, Sun J, Lau CY, Palanisamy UD, Ramanan RN, Prasad KN.

Food Chem. 2017 Nov 15;235:257-264. doi: 10.1016/j.foodchem.2017.05.021. Epub 2017 May 5.

PMID:
28554634
13.

Towards the implementation of breastfeeding-related health services in community pharmacies: Pharmacists' perspectives.

Sim TF, Hattingh HL, Sherriff J, Tee LBG.

Res Social Adm Pharm. 2017 Sep - Oct;13(5):980-988. doi: 10.1016/j.sapharm.2017.03.005. Epub 2017 Mar 10.

PMID:
28325528
14.

A Narrative Review of Diabetes Intervention Studies to Explore Diabetes Care Opportunities for Pharmacists.

Ayadurai S, Hattingh HL, Tee LB, Md Said SN.

J Diabetes Res. 2016;2016:5897452. doi: 10.1155/2016/5897452. Epub 2016 May 10. Review.

15.

Magnetic resonance imaging of the fetal brain.

Tee LM, Kan EY, Cheung JC, Leung WC.

Hong Kong Med J. 2016 Jun;22(3):270-8. doi: 10.12809/hkmj154678. Epub 2016 Apr 22. Review.

16.

Erratum to: Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency.

Dang TS, Willet JD, Griffin HR, Morgan NV, O'Boyle G, Arkwright PD, Hughes SM, Abinun M, Tee LJ, Barge D, Engelhardt KR, Jackson M, Cant AJ, Maher ER, Koref MS, Reynard LN, Ali S, Hambleton S.

J Clin Immunol. 2016 Apr;36(3):336-7. doi: 10.1007/s10875-016-0248-7. No abstract available.

17.

Health and population effects of rare gene knockouts in adult humans with related parents.

Narasimhan VM, Hunt KA, Mason D, Baker CL, Karczewski KJ, Barnes MR, Barnett AH, Bates C, Bellary S, Bockett NA, Giorda K, Griffiths CJ, Hemingway H, Jia Z, Kelly MA, Khawaja HA, Lek M, McCarthy S, McEachan R, O'Donnell-Luria A, Paigen K, Parisinos CA, Sheridan E, Southgate L, Tee L, Thomas M, Xue Y, Schnall-Levin M, Petkov PM, Tyler-Smith C, Maher ER, Trembath RC, MacArthur DG, Wright J, Durbin R, van Heel DA.

Science. 2016 Apr 22;352(6284):474-7. doi: 10.1126/science.aac8624. Epub 2016 Mar 3.

18.

Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency.

Dang TS, Willet JD, Griffin HR, Morgan NV, O'Boyle G, Arkwright PD, Hughes SM, Abinun M, Tee LJ, Barge D, Engelhardt KR, Jackson M, Cant AJ, Maher ER, Koref MS, Reynard LN, Ali S, Hambleton S.

J Clin Immunol. 2016 Feb;36(2):117-22. doi: 10.1007/s10875-016-0232-2. Epub 2016 Jan 22. Erratum in: J Clin Immunol. 2016 Apr;36(3):336-7.

19.

Off-target Effects in CRISPR/Cas9-mediated Genome Engineering.

Zhang XH, Tee LY, Wang XG, Huang QS, Yang SH.

Mol Ther Nucleic Acids. 2015 Nov 17;4:e264. doi: 10.1038/mtna.2015.37. Review.

20.

What Do Breastfeeding Women Taking Herbal Galactagogues Perceive of Community Pharmacists' Role in Breastfeeding Support? A Qualitative Study.

Sim TF, Hattingh HL, Sherriff J, Tee LB.

Int J Environ Res Public Health. 2015 Sep 8;12(9):11132-45. doi: 10.3390/ijerph120911132.

21.

The Use, Perceived Effectiveness and Safety of Herbal Galactagogues During Breastfeeding: A Qualitative Study.

Sim TF, Hattingh HL, Sherriff J, Tee LB.

Int J Environ Res Public Health. 2015 Sep 7;12(9):11050-71. doi: 10.3390/ijerph120911050.

22.

Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome.

McKie AB, Alsaedi A, Vogt J, Stuurman KE, Weiss MM, Shakeel H, Tee L, Morgan NV, Nikkels PG, van Haaften G, Park SM, van der Smagt JJ, Bugiani M, Maher ER.

Acta Neuropathol Commun. 2014 Dec 5;2:148. doi: 10.1186/s40478-014-0148-0.

23.

Nutritional compositions and bioactivities of Dacryodes species: a review.

Tee LH, Yang B, Nagendra KP, Ramanan RN, Sun J, Chan ES, Tey BT, Azlan A, Ismail A, Lau CY, Jiang Y.

Food Chem. 2014 Dec 15;165:247-55. doi: 10.1016/j.foodchem.2014.05.084. Epub 2014 May 23. Review.

PMID:
25038673
24.

Perspectives and attitudes of breastfeeding women using herbal galactagogues during breastfeeding: a qualitative study.

Sim TF, Hattingh HL, Sherriff J, Tee LB.

BMC Complement Altern Med. 2014 Jul 2;14:216. doi: 10.1186/1472-6882-14-216.

25.

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects.

Ibrahim A, Kirby G, Hardy C, Dias RP, Tee L, Lim D, Berg J, MacDonald F, Nightingale P, Maher ER.

Clin Epigenetics. 2014 Jun 4;6(1):11. doi: 10.1186/1868-7083-6-11. eCollection 2014.

26.

Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology.

Tee L, Lim DH, Dias RP, Baudement MO, Slater AA, Kirby G, Hancocks T, Stewart H, Hardy C, Macdonald F, Maher ER.

Clin Epigenetics. 2013 Dec 10;5(1):23. doi: 10.1186/1868-7083-5-23.

27.

The use of herbal medicines during breastfeeding: a population-based survey in Western Australia.

Sim TF, Sherriff J, Hattingh HL, Parsons R, Tee LB.

BMC Complement Altern Med. 2013 Nov 13;13:317. doi: 10.1186/1472-6882-13-317.

28.

Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing.

Dias RP, Nightingale P, Hardy C, Kirby G, Tee L, Price S, Macdonald F, Barrett TG, Maher ER.

J Med Genet. 2013 Sep;50(9):635-9. doi: 10.1136/jmedgenet-2013-101693. Epub 2013 Jun 28.

PMID:
23812911
29.

A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver disease.

Morgan NV, Hartley JL, Setchell KD, Simpson MA, Brown R, Tee L, Kirkham S, Pasha S, Trembath RC, Maher ER, Gissen P, Kelly DA.

Orphanet J Rare Dis. 2013 May 16;8:74. doi: 10.1186/1750-1172-8-74.

30.

Analytical performance validation of a coronary heart disease risk assessment multi-analyte proteomic test.

Nolan N, Tee L, Vijayakumar S, Burazor I, Hytopoulos E, Biggs WH 3rd, Beggs M, French C, Harrington DS.

Expert Opin Med Diagn. 2013 Mar;7(2):127-36. doi: 10.1517/17530059.2013.753055. Epub 2012 Dec 11.

PMID:
23530883
31.

A novel wet extrusion technique to fabricate self-assembled microfiber scaffolds for controlled drug delivery.

Lavin DM, Harrison MW, Tee LY, Wei KA, Mathiowitz E.

J Biomed Mater Res A. 2012 Oct;100(10):2793-802. doi: 10.1002/jbm.a.34217. Epub 2012 May 24.

PMID:
22623283
32.

Promoter mutation is a common variant in GJC2-associated Pelizaeus-Merzbacher-like disease.

Meyer E, Kurian MA, Morgan NV, McNeill A, Pasha S, Tee L, Younis R, Norman A, van der Knaap MS, Wassmer E, Trembath RC, Brueton L, Maher ER.

Mol Genet Metab. 2011 Dec;104(4):637-43. doi: 10.1016/j.ymgme.2011.08.032. Epub 2011 Sep 8.

PMID:
21959080
33.

Purification of transcriptionally active multimeric plasmid DNA using zwitterionic detergent and carbonate apatite nano-particles.

Tee LK, Ling CS, Chua MJ, Abdullah S, Rosli R, Chowdhury EH.

Plasmid. 2011 Oct;66(1):38-46. doi: 10.1016/j.plasmid.2011.03.001. Epub 2011 Mar 17.

PMID:
21419794
34.

Antibiogram and heavy metal tolerance of bullfrog bacteria in Malaysia.

Tee LW, Najiah M.

Open Vet J. 2011;1(1):39-45. Epub 2011 Oct 24.

35.

Locus heterogeneity and Knobloch syndrome.

Joyce S, Tee L, Abid A, Khaliq S, Mehdi SQ, Maher ER.

Am J Med Genet A. 2010 Nov;152A(11):2880-1. doi: 10.1002/ajmg.a.33619. No abstract available.

PMID:
20979194
36.
37.

Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy.

Meyer E, Michaelides M, Tee LJ, Robson AG, Rahman F, Pasha S, Luxon LM, Moore AT, Maher ER.

Mol Vis. 2010 Apr 13;16:650-64.

38.

Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome).

Meyer E, Ricketts C, Morgan NV, Morris MR, Pasha S, Tee LJ, Rahman F, Bazin A, Bessières B, Déchelotte P, Yacoubi MT, Al-Adnani M, Marton T, Tannahill D, Trembath RC, Fallet-Bianco C, Cox P, Williams D, Maher ER.

Am J Hum Genet. 2010 Mar 12;86(3):471-8. doi: 10.1016/j.ajhg.2010.02.004. Epub 2010 Mar 4.

39.

Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy).

Hartley JL, Zachos NC, Dawood B, Donowitz M, Forman J, Pollitt RJ, Morgan NV, Tee L, Gissen P, Kahr WH, Knisely AS, Watson S, Chitayat D, Booth IW, Protheroe S, Murphy S, de Vries E, Kelly DA, Maher ER.

Gastroenterology. 2010 Jun;138(7):2388-98, 2398.e1-2. doi: 10.1053/j.gastro.2010.02.010. Epub 2010 Feb 20.

40.

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.

Kurian MA, Zhen J, Cheng SY, Li Y, Mordekar SR, Jardine P, Morgan NV, Meyer E, Tee L, Pasha S, Wassmer E, Heales SJ, Gissen P, Reith ME, Maher ER.

J Clin Invest. 2009 Jun;119(6):1595-603. doi: 10.1172/JCI39060. Epub 2009 May 26.

41.

rAAV.sFlt-1 gene therapy achieves lasting reversal of retinal neovascularization in the absence of a strong immune response to the viral vector.

Lai CM, Estcourt MJ, Wikstrom M, Himbeck RP, Barnett NL, Brankov M, Tee LB, Dunlop SA, Degli-Esposti MA, Rakoczy EP.

Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4279-87. doi: 10.1167/iovs.08-3253. Epub 2009 Apr 8.

PMID:
19357358
42.

Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).

Meyer E, Lim D, Pasha S, Tee LJ, Rahman F, Yates JR, Woods CG, Reik W, Maher ER.

PLoS Genet. 2009 Mar;5(3):e1000423. doi: 10.1371/journal.pgen.1000423. Epub 2009 Mar 20.

43.

Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies.

Lim D, Bowdin SC, Tee L, Kirby GA, Blair E, Fryer A, Lam W, Oley C, Cole T, Brueton LA, Reik W, Macdonald F, Maher ER.

Hum Reprod. 2009 Mar;24(3):741-7. doi: 10.1093/humrep/den406. Epub 2008 Dec 10.

PMID:
19073614
44.

VEGF-induced choroidal damage in a murine model of retinal neovascularisation.

Tee LB, Penrose MA, O'Shea JE, Lai CM, Rakoczy EP, Dunlop SA.

Br J Ophthalmol. 2008 Jun;92(6):832-8. doi: 10.1136/bjo.2007.130898.

PMID:
18523088
45.

Frequency distribution of cytochrome P450 3A4 gene polymorphism in ethnic populations and in transplant recipients.

Zhou X, Barber WH, Moore CK, Tee LY, Aru G, Harrison S, Mangilog B, McDaniel DO.

Res Commun Mol Pathol Pharmacol. 2006;119(1-6):89-104.

PMID:
17974099
46.

Regenerating optic axons restore topography after incomplete optic nerve injury.

Dunlop SA, Tee LB, Goossens MA, Stirling RV, Hool L, Rodger J, Beazley LD.

J Comp Neurol. 2007 Nov 1;505(1):46-57.

PMID:
17729282
47.

Molecular analysis of inflammatory markers in trauma patients at risk of postinjury complications.

McDaniel DO, Hamilton J, Brock M, May W, Calcote L, Tee LY, Vick L, Newman DB, Vick K, Harrison S, Timberlake G, Toevs C.

J Trauma. 2007 Jul;63(1):147-57; discussion 157-8.

PMID:
17622883
48.

Characterisation of a model for retinal neovascularisation. VEGF model characterisation.

van Eeden PE, Tee L, Shen WY, Lukehurst S, Lai CM, Rakoczy PE, Beazley LD, Dunlop SA.

Adv Exp Med Biol. 2006;572:163-8. No abstract available.

PMID:
17249570
49.

Early vascular and neuronal changes in a VEGF transgenic mouse model of retinal neovascularization.

van Eeden PE, Tee LB, Lukehurst S, Lai CM, Rakoczy EP, Beazley LD, Dunlop SA.

Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4638-45.

PMID:
17003462
50.

Clinical and molecular genetic features of ARC syndrome.

Gissen P, Tee L, Johnson CA, Genin E, Caliebe A, Chitayat D, Clericuzio C, Denecke J, Di Rocco M, Fischler B, FitzPatrick D, García-Cazorla A, Guyot D, Jacquemont S, Koletzko S, Leheup B, Mandel H, Sanseverino MT, Houwen RH, McKiernan PJ, Kelly DA, Maher ER.

Hum Genet. 2006 Oct;120(3):396-409. Epub 2006 Aug 1.

PMID:
16896922

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