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Items: 1 to 50 of 68

1.

Disruption of chromatin organisation causes MEF2C gene overexpression in intellectual disability: a case report.

Yauy K, Schneider A, Ng BL, Gaillard JB, Sati S, Coubes C, Wells C, Tournaire M, Guignard T, Bouret P, Geneviève D, Puechberty J, Pellestor F, Gatinois V.

BMC Med Genomics. 2019 Aug 2;12(1):116. doi: 10.1186/s12920-019-0558-8.

2.

Derivation and maintenance of mouse haploid embryonic stem cells.

Elling U, Woods M, Forment JV, Fu B, Yang F, Ng BL, Vicente JR, Adams DJ, Doe B, Jackson SP, Penninger JM, Balmus G.

Nat Protoc. 2019 Jul;14(7):1991-2014. doi: 10.1038/s41596-019-0169-z. Epub 2019 Jun 3.

PMID:
31160788
3.

Automating the Shared Resource Laboratory Using Computer Scripts: A Case Report.

Hall C, Brown L, Graham J, Thompson S, Ng BL.

Cytometry A. 2019 Jul;95(7):797-802. doi: 10.1002/cyto.a.23775. Epub 2019 Apr 29.

4.

Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis.

Petljak M, Alexandrov LB, Brammeld JS, Price S, Wedge DC, Grossmann S, Dawson KJ, Ju YS, Iorio F, Tubio JMC, Koh CC, Georgakopoulos-Soares I, Rodríguez-Martín B, Otlu B, O'Meara S, Butler AP, Menzies A, Bhosle SG, Raine K, Jones DR, Teague JW, Beal K, Latimer C, O'Neill L, Zamora J, Anderson E, Patel N, Maddison M, Ng BL, Graham J, Garnett MJ, McDermott U, Nik-Zainal S, Campbell PJ, Stratton MR.

Cell. 2019 Mar 7;176(6):1282-1294.e20. doi: 10.1016/j.cell.2019.02.012.

5.

Chromosome Analysis Using Benchtop Flow Analysers and High Speed Cell Sorters.

Ng BL, Fu B, Graham J, Hall C, Thompson S.

Cytometry A. 2019 Mar;95(3):323-331. doi: 10.1002/cyto.a.23692. Epub 2018 Dec 17.

6.

Relationship Between Sequence Homology, Genome Architecture, and Meiotic Behavior of the Sex Chromosomes in North American Voles.

Dumont BL, Williams CL, Ng BL, Horncastle V, Chambers CL, McGraw LA, Adams D, Mackay TFC, Breen M.

Genetics. 2018 Sep;210(1):83-97. doi: 10.1534/genetics.118.301182. Epub 2018 Jul 12.

7.

Chromosomal breaks at FRA18C: association with reduced DOK6 expression, altered oncogenic signaling and increased gastric cancer survival.

Leong SH, Lwin KM, Lee SS, Ng WH, Ng KM, Tan SY, Ng BL, Carter NP, Tang C, Lian Kon O.

NPJ Precis Oncol. 2017 May 1;1(1):9. doi: 10.1038/s41698-017-0012-3. eCollection 2017.

8.

Clinical utility of MRI and SPECT in the diagnosis of cognitive impairment referred to memory clinic.

Guinane J, Ng BL.

Int Psychogeriatr. 2018 May;30(5):611-617. doi: 10.1017/S1041610217001624. Epub 2017 Sep 7.

PMID:
28879819
9.

Prompt use of mechanical cardiopulmonary resuscitation in out-of-hospital cardiac arrest: the MECCA study report.

Anantharaman V, Ng BL, Ang SH, Lee CY, Leong SH, Ong ME, Chua SJ, Rabind AC, Anjali NB, Hao Y.

Singapore Med J. 2017 Jul;58(7):424-431. doi: 10.11622/smedj.2017071.

10.

Evolutionary dynamics of Anolis sex chromosomes revealed by sequencing of flow sorting-derived microchromosome-specific DNA.

Kichigin IG, Giovannotti M, Makunin AI, Ng BL, Kabilov MR, Tupikin AE, Barucchi VC, Splendiani A, Ruggeri P, Rens W, O'Brien PC, Ferguson-Smith MA, Graphodatsky AS, Trifonov VA.

Mol Genet Genomics. 2016 Oct;291(5):1955-66. doi: 10.1007/s00438-016-1230-z. Epub 2016 Jul 18.

PMID:
27431992
11.

New insights into sex chromosome evolution in anole lizards (Reptilia, Dactyloidae).

Giovannotti M, Trifonov VA, Paoletti A, Kichigin IG, O'Brien PC, Kasai F, Giovagnoli G, Ng BL, Ruggeri P, Cerioni PN, Splendiani A, Pereira JC, Olmo E, Rens W, Caputo Barucchi V, Ferguson-Smith MA.

Chromosoma. 2017 Mar;126(2):245-260. doi: 10.1007/s00412-016-0585-6. Epub 2016 Mar 22.

PMID:
27001473
12.

Inhibition of isoprenylcysteine carboxylmethyltransferase augments BCR-ABL1 tyrosine kinase inhibition-induced apoptosis in chronic myeloid leukemia.

Sun WT, Xiang W, Ng BL, Asari K, Bunte RM, Casey PJ, Wang M, Chuah C.

Exp Hematol. 2016 Mar;44(3):189-93.e2. doi: 10.1016/j.exphem.2015.12.002. Epub 2015 Dec 17.

PMID:
26706195
13.

The pig X and Y Chromosomes: structure, sequence, and evolution.

Skinner BM, Sargent CA, Churcher C, Hunt T, Herrero J, Loveland JE, Dunn M, Louzada S, Fu B, Chow W, Gilbert J, Austin-Guest S, Beal K, Carvalho-Silva D, Cheng W, Gordon D, Grafham D, Hardy M, Harley J, Hauser H, Howden P, Howe K, Lachani K, Ellis PJ, Kelly D, Kerry G, Kerwin J, Ng BL, Threadgold G, Wileman T, Wood JM, Yang F, Harrow J, Affara NA, Tyler-Smith C.

Genome Res. 2016 Jan;26(1):130-9. doi: 10.1101/gr.188839.114. Epub 2015 Nov 11.

14.

Identification of disrupted AUTS2 and EPHA6 genes by array painting in a patient carrying a de novo balanced translocation t(3;7) with intellectual disability and neurodevelopment disorder.

Schneider A, Puechberty J, Ng BL, Coubes C, Gatinois V, Tournaire M, Girard M, Dumont B, Bouret P, Magnetto J, Baghdadli A, Pellestor F, Geneviève D.

Am J Med Genet A. 2015 Dec;167A(12):3031-7. doi: 10.1002/ajmg.a.37350. Epub 2015 Sep 3.

PMID:
26333717
15.

Post-operative survival following metastasectomy for patients receiving BRAF inhibitor therapy is associated with duration of pre-operative treatment and elective indication.

He M, Lovell J, Ng BL, Spillane J, Speakman D, Henderson MA, Shackleton M, Gyorki DE.

J Surg Oncol. 2015 Jun;111(8):980-4. doi: 10.1002/jso.23938. Epub 2015 Jun 17.

PMID:
26080731
16.

A First Generation Comparative Chromosome Map between Guinea Pig (Cavia porcellus) and Humans.

Romanenko SA, Perelman PL, Trifonov VA, Serdyukova NA, Li T, Fu B, O'Brien PC, Ng BL, Nie W, Liehr T, Stanyon R, Graphodatsky AS, Yang F.

PLoS One. 2015 May 26;10(5):e0127937. doi: 10.1371/journal.pone.0127937. eCollection 2015.

17.

A high-throughput in vivo micronucleus assay for genome instability screening in mice.

Balmus G, Karp NA, Ng BL, Jackson SP, Adams DJ, McIntyre RE.

Nat Protoc. 2015 Jan;10(1):205-15. doi: 10.1038/nprot.2015.010. Epub 2014 Dec 31.

18.

A nucleotide signature for identification of Aglaia stellatopilosa Pannell.

Ng BL, Omarzuki M, Lau GS, Pannell CM, Yeo TC.

Mol Biotechnol. 2014 Jul;56(7):671-9. doi: 10.1007/s12033-014-9746-0.

PMID:
24623047
19.

Chromosomal evolution among leaf-nosed nectarivorous bats--evidence from cross-species chromosome painting (Phyllostomidae, Chiroptera).

Sotero-Caio CG, Volleth M, Gollahon LS, Fu B, Cheng W, Ng BL, Yang F, Baker RJ.

BMC Evol Biol. 2013 Dec 26;13:276. doi: 10.1186/1471-2148-13-276.

20.

Tracking chromosome evolution in southern African gerbils using flow-sorted chromosome paints.

Knight LI, Ng BL, Cheng W, Fu B, Yang F, Rambau RV.

Cytogenet Genome Res. 2013;139(4):267-75. doi: 10.1159/000350696. Epub 2013 May 4.

21.

Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome.

Gribble SM, Wiseman FK, Clayton S, Prigmore E, Langley E, Yang F, Maguire S, Fu B, Rajan D, Sheppard O, Scott C, Hauser H, Stephens PJ, Stebbings LA, Ng BL, Fitzgerald T, Quail MA, Banerjee R, Rothkamm K, Tybulewicz VL, Fisher EM, Carter NP.

PLoS One. 2013 Apr 15;8(4):e60482. doi: 10.1371/journal.pone.0060482. Print 2013.

22.

Genetic basis of Y-linked hearing impairment.

Wang Q, Xue Y, Zhang Y, Long Q, Asan, Yang F, Turner DJ, Fitzgerald T, Ng BL, Zhao Y, Chen Y, Liu Q, Yang W, Han D, Quail MA, Swerdlow H, Burton J, Fahey C, Ning Z, Hurles ME, Carter NP, Yang H, Tyler-Smith C.

Am J Hum Genet. 2013 Feb 7;92(2):301-6. doi: 10.1016/j.ajhg.2012.12.015. Epub 2013 Jan 24.

23.

Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer.

Murchison EP, Schulz-Trieglaff OB, Ning Z, Alexandrov LB, Bauer MJ, Fu B, Hims M, Ding Z, Ivakhno S, Stewart C, Ng BL, Wong W, Aken B, White S, Alsop A, Becq J, Bignell GR, Cheetham RK, Cheng W, Connor TR, Cox AJ, Feng ZP, Gu Y, Grocock RJ, Harris SR, Khrebtukova I, Kingsbury Z, Kowarsky M, Kreiss A, Luo S, Marshall J, McBride DJ, Murray L, Pearse AM, Raine K, Rasolonjatovo I, Shaw R, Tedder P, Tregidgo C, Vilella AJ, Wedge DC, Woods GM, Gormley N, Humphray S, Schroth G, Smith G, Hall K, Searle SM, Carter NP, Papenfuss AT, Futreal PA, Campbell PJ, Yang F, Bentley DR, Evers DJ, Stratton MR.

Cell. 2012 Feb 17;148(4):780-91. doi: 10.1016/j.cell.2011.11.065.

24.

Management of chronic kidney disease in the elderly.

Ng BL, Anpalahan M.

Intern Med J. 2011 Nov;41(11):761-8. doi: 10.1111/j.1445-5994.2011.02590.x. Review.

PMID:
22077944
25.

Molecular cytogenetic characterization of the genome organization of the 6-banded armadillo (Euphractus sexcinctus).

Liu Y, Ye J, Fu B, Ng BL, Wang J, Su W, Yang F, Nie W.

Cytogenet Genome Res. 2011;132(1-2):31-40. doi: 10.1159/000318706. Epub 2010 Aug 17.

PMID:
20720395
26.

Anti-N-methyl-D-aspartate receptor encephalitis in a young woman with an ovarian tumour.

Lo JW, Leung EY, Ng BL, Fu MH, Yip KK, Chan RT, Chang CM.

Hong Kong Med J. 2010 Aug;16(4):313-6.

27.

Reprogramming of T cells to natural killer-like cells upon Bcl11b deletion.

Li P, Burke S, Wang J, Chen X, Ortiz M, Lee SC, Lu D, Campos L, Goulding D, Ng BL, Dougan G, Huntly B, Gottgens B, Jenkins NA, Copeland NG, Colucci F, Liu P.

Science. 2010 Jul 2;329(5987):85-9. doi: 10.1126/science.1188063. Epub 2010 Jun 10.

28.

Laser excitation power and the flow cytometric resolution of complex karyotypes.

Ng BL, Carter NP.

Cytometry A. 2010 Jun;77(6):585-8. doi: 10.1002/cyto.a.20904.

29.

Development of quantitative-fluorescence polymerase chain reaction for the rapid prenatal diagnosis of common chromosomal aneuploidies in 1,000 samples in Singapore.

Baig S, Ho SS, Ng BL, Chiu L, Koay ES, Leow GH, Gole L, Kothandaraman N, Chan J, Sun X, Chan YH, Rauff M, Su LL, Biswas A, Choolani M.

Singapore Med J. 2010 Apr;51(4):343-8.

30.

Array painting: a protocol for the rapid analysis of aberrant chromosomes using DNA microarrays.

Gribble SM, Ng BL, Prigmore E, Fitzgerald T, Carter NP.

Nat Protoc. 2009;4(12):1722-36. doi: 10.1038/nprot.2009.183. Epub 2009 Nov 5.

31.

Human Y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree.

Xue Y, Wang Q, Long Q, Ng BL, Swerdlow H, Burton J, Skuce C, Taylor R, Abdellah Z, Zhao Y; Asan, MacArthur DG, Quail MA, Carter NP, Yang H, Tyler-Smith C.

Curr Biol. 2009 Sep 15;19(17):1453-7. doi: 10.1016/j.cub.2009.07.032. Epub 2009 Aug 27.

32.

De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal age.

Thomas NS, Morris JK, Baptista J, Ng BL, Crolla JA, Jacobs PA.

J Med Genet. 2010 Feb;47(2):112-5. doi: 10.1136/jmg.2009.069716. Epub 2009 Jul 27.

PMID:
19638350
33.

Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.

Gill HK, Parsons SR, Spalluto C, Davies AF, Knorz VJ, Burlinson CE, Ng BL, Carter NP, Ogilvie CM, Wilson DI, Roberts RG.

Eur J Hum Genet. 2009 Nov;17(11):1423-31. doi: 10.1038/ejhg.2009.91. Epub 2009 May 27.

34.

Avian comparative genomics: reciprocal chromosome painting between domestic chicken (Gallus gallus) and the stone curlew (Burhinus oedicnemus, Charadriiformes)--an atypical species with low diploid number.

Nie W, O'Brien PC, Ng BL, Fu B, Volobouev V, Carter NP, Ferguson-Smith MA, Yang F.

Chromosome Res. 2009;17(1):99-113. doi: 10.1007/s10577-009-9021-6. Epub 2009 Jan 27.

35.

Refining quantitative fluorescent polymerase chain reaction for prenatal detection of X chromosomal anomalies in the major Southeast Asian populations.

Gole L, Adrianne F, Ee AM, Ng BL, Baig S, Koay E, Biswas A, Choolani M.

Singapore Med J. 2008 Dec;49(12):1025-8.

36.

Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes.

Howarth KD, Blood KA, Ng BL, Beavis JC, Chua Y, Cooke SL, Raby S, Ichimura K, Collins VP, Carter NP, Edwards PA.

Oncogene. 2008 May 22;27(23):3345-59. Epub 2007 Dec 17.

37.

Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12.

Menten B, Buysse K, Vermeulen S, Meersschaut V, Vandesompele J, Ng BL, Carter NP, Mortier GR, Speleman F.

Eur J Med Genet. 2007 Nov-Dec;50(6):446-54. Epub 2007 Aug 6.

38.

Definition of the zebrafish genome using flow cytometry and cytogenetic mapping.

Freeman JL, Adeniyi A, Banerjee R, Dallaire S, Maguire SF, Chi J, Ng BL, Zepeda C, Scott CE, Humphray S, Rogers J, Zhou Y, Zon LI, Carter NP, Yang F, Lee C.

BMC Genomics. 2007 Jun 27;8:195.

39.

Antiadhesive property of microalgal polysaccharide extract on the binding of Helicobacter pylori to gastric mucin.

Loke MF, Lui SY, Ng BL, Gong M, Ho B.

FEMS Immunol Med Microbiol. 2007 Jul;50(2):231-8. Epub 2007 May 22.

40.

Flow analysis and sorting of microchromosomes (<3 Mb).

Ng BL, Yang F, Carter NP.

Cytometry A. 2007 Jun;71(6):410-3.

41.

Ultra-high resolution array painting facilitates breakpoint sequencing.

Gribble SM, Kalaitzopoulos D, Burford DC, Prigmore E, Selzer RR, Ng BL, Matthews NS, Porter KM, Curley R, Lindsay SJ, Baptista J, Richmond TA, Carter NP.

J Med Genet. 2007 Jan;44(1):51-8. Epub 2006 Sep 13.

42.

Factors affecting flow karyotype resolution.

Ng BL, Carter NP.

Cytometry A. 2006 Sep 1;69(9):1028-36.

43.

Expression of mammalian GPCRs in C. elegans generates novel behavioural responses to human ligands.

Teng MS, Dekkers MP, Ng BL, Rademakers S, Jansen G, Fraser AG, McCafferty J.

BMC Biol. 2006 Jul 20;4:22.

44.

Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.

Fauth C, Gribble SM, Porter KM, Codina-Pascual M, Ng BL, Kraus J, Uhrig S, Leifheit J, Haaf T, Fiegler H, Carter NP, Speicher MR.

Hum Genet. 2006 Mar;119(1-2):145-53. Epub 2006 Jan 3.

PMID:
16395598
45.

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

Rickman L, Fiegler H, Shaw-Smith C, Nash R, Cirigliano V, Voglino G, Ng BL, Scott C, Whittaker J, Adinolfi M, Carter NP, Bobrow M.

J Med Genet. 2006 Apr;43(4):353-61. Epub 2005 Sep 30.

46.

The RASSF1A isoform of RASSF1 promotes microtubule stability and suppresses tumorigenesis.

van der Weyden L, Tachibana KK, Gonzalez MA, Adams DJ, Ng BL, Petty R, Venkitaraman AR, Arends MJ, Bradley A.

Mol Cell Biol. 2005 Sep;25(18):8356-67.

47.

Non-invasive prenatal diagnosis of fetal gender using real-time polymerase chain reaction amplification of SRY in maternal plasma.

Ho SS, Damayanti Z, Chua WY, Ng BL, Peh CM, Biswas A, Choolani M.

Ann Acad Med Singapore. 2004 Sep;33(5 Suppl):S61-2. No abstract available.

PMID:
15651212
48.

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.

Gribble SM, Prigmore E, Burford DC, Porter KM, Ng BL, Douglas EJ, Fiegler H, Carr P, Kalaitzopoulos D, Clegg S, Sandstrom R, Temple IK, Youings SA, Thomas NS, Dennis NR, Jacobs PA, Crolla JA, Carter NP.

J Med Genet. 2005 Jan;42(1):8-16.

49.

BRCTx is a novel, highly conserved RAD18-interacting protein.

Adams DJ, van der Weyden L, Gergely FV, Arends MJ, Ng BL, Tannahill D, Kanaar R, Markus A, Morris BJ, Bradley A.

Mol Cell Biol. 2005 Jan;25(2):779-88.

50.

Corrosion behaviour of high copper dental amalgams.

Yap AU, Ng BL, Blackwood DJ.

J Oral Rehabil. 2004 Jun;31(6):595-9.

PMID:
15189319

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