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Items: 1 to 50 of 231

1.

Solvent Dependent Spin-Crossover and Photomagnetic Properties in an Imidazolylimine FeII Complex.

Archer RJ, Scott HS, Polson MIJ, Mathonière C, Rouzières M, Clérac R, Kruger PE.

Chem Asian J. 2019 Jul 1;14(13):2225-2229. doi: 10.1002/asia.201900522. Epub 2019 Jun 11.

PMID:
31090192
2.

The mutational burden of therapy-related myeloid neoplasms is similar to primary myelodysplastic syndrome but has a distinctive distribution.

Singhal D, Wee LYA, Kutyna MM, Chhetri R, Geoghegan J, Schreiber AW, Feng J, Wang PP, Babic M, Parker WT, Hiwase S, Edwards S, Moore S, Branford S, Kuzmanovic T, Singhal N, Gowda R, Brown AL, Arts P, To LB, Bardy PG, Lewis ID, D'Andrea RJ, Maciejewski JP, Scott HS, Hahn CN, Hiwase DK.

Leukemia. 2019 May 14. doi: 10.1038/s41375-019-0479-8. [Epub ahead of print]

PMID:
31089247
3.

Genomic subtyping and therapeutic targeting of acute erythroleukemia.

Iacobucci I, Wen J, Meggendorfer M, Choi JK, Shi L, Pounds SB, Carmichael CL, Masih KE, Morris SM, Lindsley RC, Janke LJ, Alexander TB, Song G, Qu C, Li Y, Payne-Turner D, Tomizawa D, Kiyokawa N, Valentine M, Valentine V, Basso G, Locatelli F, Enemark EJ, Kham SKY, Yeoh AEJ, Ma X, Zhou X, Sioson E, Rusch M, Ries RE, Stieglitz E, Hunger SP, Wei AH, To LB, Lewis ID, D'Andrea RJ, Kile BT, Brown AL, Scott HS, Hahn CN, Marlton P, Pei D, Cheng C, Loh ML, Ebert BL, Meshinchi S, Haferlach T, Mullighan CG.

Nat Genet. 2019 Apr;51(4):694-704. doi: 10.1038/s41588-019-0375-1. Epub 2019 Mar 29.

PMID:
30926971
4.

A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia.

Cheah JJC, Brown AL, Schreiber AW, Feng J, Babic M, Moore S, Young CC, Fine M, Phillips K, Guandalini M, Wilson P, Poplawski N, Hahn CN, Scott HS.

Haematologica. 2019 Jul;104(7):e318-e321. doi: 10.3324/haematol.2018.207316. Epub 2019 Mar 28. No abstract available.

5.

Gene and protein expression profiles of JAK-STAT signalling pathway in the developing brain of the Ts1Cje down syndrome mouse model.

Lee HC, Md Yusof HH, Leong MP, Zainal Abidin S, Seth EA, Hewitt CA, Vidyadaran S, Nordin N, Scott HS, Cheah PS, Ling KH.

Int J Neurosci. 2019 Sep;129(9):871-881. doi: 10.1080/00207454.2019.1580280. Epub 2019 Feb 22.

PMID:
30775947
6.

Expression Profiling of Notch Signalling Pathway and Gamma-Secretase Activity in the Brain of Ts1Cje Mouse Model of Down Syndrome.

Yusof HH, Lee HC, Seth EA, Wu X, Hewitt CA, Scott HS, Cheah PS, Li YM, Chau DM, Ling KH.

J Mol Neurosci. 2019 Apr;67(4):632-642. doi: 10.1007/s12031-019-01275-2. Epub 2019 Feb 13.

PMID:
30758748
7.

A supramolecular porous material comprising Fe(ii) mesocates.

Wilson BH, Scott HS, Qazvini OT, Telfer SG, Mathonière C, Clérac R, Kruger PE.

Chem Commun (Camb). 2018 Nov 27;54(95):13391-13394. doi: 10.1039/c8cc07227b.

PMID:
30421754
8.

Genetic Testing in Endocrinology.

De Sousa SM, Hardy TS, Scott HS, Torpy DJ.

Clin Biochem Rev. 2018 Feb;39(1):17-28. Review.

9.

Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease.

Branford S, Wang P, Yeung DT, Thomson D, Purins A, Wadham C, Shahrin NH, Marum JE, Nataren N, Parker WT, Geoghegan J, Feng J, Shanmuganathan N, Mueller MC, Dietz C, Stangl D, Donaldson Z, Altamura H, Georgievski J, Braley J, Brown A, Hahn C, Walker I, Kim SH, Choi SY, Park SH, Kim DW, White DL, Yong ASM, Ross DM, Scott HS, Schreiber AW, Hughes TP.

Blood. 2018 Aug 30;132(9):948-961. doi: 10.1182/blood-2018-02-832253. Epub 2018 Jul 2.

PMID:
29967129
10.

Varied spin crossover behaviour in a family of dinuclear Fe(ii) triple helicate complexes.

Archer RJ, Scott HS, Polson MIJ, Williamson BE, Mathonière C, Rouzières M, Clérac R, Kruger PE.

Dalton Trans. 2018 Jun 19;47(24):7965-7974. doi: 10.1039/c8dt01567h.

PMID:
29862409
11.

Extending the Duluth Model to Workplace Bullying: A Modification and Adaptation of the Workplace Power-Control Wheel.

Scott HS.

Workplace Health Saf. 2018 Sep;66(9):444-452. doi: 10.1177/2165079917750934. Epub 2018 Mar 27.

PMID:
29582701
12.

ASXL1 and BIM germ line variants predict response and identify CML patients with the greatest risk of imatinib failure.

Marum JE, Yeung DT, Purins L, Reynolds J, Parker WT, Stangl D, Wang PPS, Price DJ, Tuke J, Schreiber AW, Scott HS, Hughes TP, Branford S.

Blood Adv. 2017 Jul 31;1(18):1369-1381. doi: 10.1182/bloodadvances.2017006825. eCollection 2017 Aug 8.

13.

ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II).

De Sousa SMC, Stowasser M, Feng J, Schreiber AW, Wang P, Hahn CN, Gordon RD, Torpy DJ, Scott HS, Gagliardi L.

J Hum Hypertens. 2017 Dec;31(12):857-859. doi: 10.1038/jhh.2017.71. Epub 2017 Oct 12. No abstract available.

PMID:
29022889
14.

Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient.

Venugopal P, Moore S, Lawrence DM, George AJ, Hannan RD, Bray SC, To LB, D'Andrea RJ, Feng J, Tirimacco A, Yeoman AL, Young CC, Fine M, Schreiber AW, Hahn CN, Barnett C, Saxon B, Scott HS.

Haematologica. 2017 Dec;102(12):e506-e509. doi: 10.3324/haematol.2017.166678. Epub 2017 Sep 29. No abstract available.

15.

Clinical implications of transient myeloproliferative disorder in a neonate without Down syndrome features.

Carruthers V, Nicola M, Venugopal P, Hahn CN, Scott HS, Revesz T.

J Paediatr Child Health. 2017 Oct;53(10):1018-1020. doi: 10.1111/jpc.13628. Epub 2017 Jul 4. No abstract available.

PMID:
28675575
16.

A four-gene LincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients.

Beck D, Thoms JAI, Palu C, Herold T, Shah A, Olivier J, Boelen L, Huang Y, Chacon D, Brown A, Babic M, Hahn C, Perugini M, Zhou X, Huntly BJ, Schwarzer A, Klusmann JH, Berdel WE, Wörmann B, Büchner T, Hiddemann W, Bohlander SK, To LB, Scott HS, Lewis ID, D'Andrea RJ, Wong JWH, Pimanda JE.

Leukemia. 2018 Feb;32(2):263-272. doi: 10.1038/leu.2017.210. Epub 2017 Jul 4.

PMID:
28674423
17.

Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes.

Chong CE, Venugopal P, Stokes PH, Lee YK, Brautigan PJ, Yeung DTO, Babic M, Engler GA, Lane SW, Klingler-Hoffmann M, Matthews JM, D'Andrea RJ, Brown AL, Hahn CN, Scott HS.

Leukemia. 2018 Jan;32(1):194-202. doi: 10.1038/leu.2017.196. Epub 2017 Jun 23.

18.

Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 2 and Related Disorders.

Evans DGR, Salvador H, Chang VY, Erez A, Voss SD, Druker H, Scott HS, Tabori U.

Clin Cancer Res. 2017 Jun 15;23(12):e54-e61. doi: 10.1158/1078-0432.CCR-17-0590. Review.

19.

Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 1.

Evans DGR, Salvador H, Chang VY, Erez A, Voss SD, Schneider KW, Scott HS, Plon SE, Tabori U.

Clin Cancer Res. 2017 Jun 15;23(12):e46-e53. doi: 10.1158/1078-0432.CCR-17-0589. Review.

20.

Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders.

Walsh MF, Chang VY, Kohlmann WK, Scott HS, Cunniff C, Bourdeaut F, Molenaar JJ, Porter CC, Sandlund JT, Plon SE, Wang LL, Savage SA.

Clin Cancer Res. 2017 Jun 1;23(11):e23-e31. doi: 10.1158/1078-0432.CCR-17-0465. Review.

21.

Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions.

Porter CC, Druley TE, Erez A, Kuiper RP, Onel K, Schiffman JD, Wolfe Schneider K, Scollon SR, Scott HS, Strong LC, Walsh MF, Nichols KE.

Clin Cancer Res. 2017 Jun 1;23(11):e14-e22. doi: 10.1158/1078-0432.CCR-17-0428. Review.

22.

A novel, somatic, transforming mutation in the extracellular domain of Epidermal Growth Factor Receptor identified in myeloproliferative neoplasm.

Casolari DA, Nguyen T, Butcher CM, Iarossi DG, Hahn CN, Bray SC, Neufing P, Parker WT, Feng J, Maung KZY, Wee A, Vidovic L, Kok CH, Bardy PG, Branford S, Lewis ID, Lane SW, Scott HS, Ross DM, D'Andrea RJ.

Sci Rep. 2017 May 26;7(1):2467. doi: 10.1038/s41598-017-02655-7.

23.

Myeloid neoplasms with germline DDX41 mutation.

Cheah JJC, Hahn CN, Hiwase DK, Scott HS, Brown AL.

Int J Hematol. 2017 Aug;106(2):163-174. doi: 10.1007/s12185-017-2260-y. Epub 2017 May 25. Review.

PMID:
28547672
24.

T cell receptor assessment in autoimmune disease requires access to the most adjacent immunologically active organ.

Oftedal BE, Ardesjö Lundgren B, Hamm D, Gan PY, Holdsworth SR, Hahn CN, Schreiber AW, Scott HS.

J Autoimmun. 2017 Jul;81:24-33. doi: 10.1016/j.jaut.2017.03.002. Epub 2017 Mar 18.

25.

Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumours.

De Sousa SMC, McCabe MJ, Wu K, Roscioli T, Gayevskiy V, Brook K, Rawlings L, Scott HS, Thompson TJ, Earls P, Gill AJ, Cowley MJ, Dinger ME, McCormack AI.

Eur J Endocrinol. 2017 May;176(5):635-644. doi: 10.1530/EJE-16-0944. Epub 2017 Feb 20.

PMID:
28220018
26.

Targeted pharmacotherapy after somatic cancer mutation screening.

Polasek TM, Ambler K, Scott HS, Sorich MJ, Kaub PA, Rowland A, Wiese MD, Kichenadasse G.

Version 2. F1000Res. 2016 Jun 30 [revised 2016 Jan 1];5:1551. doi: 10.12688/f1000research.9040.2. eCollection 2016.

27.

Highly Selective Separation of C2H2 from CO2 by a New Dichromate-Based Hybrid Ultramicroporous Material.

Scott HS, Shivanna M, Bajpai A, Madden DG, Chen KJ, Pham T, Forrest KA, Hogan A, Space B, Perry Iv JJ, Zaworotko MJ.

ACS Appl Mater Interfaces. 2017 Oct 4;9(39):33395-33400. doi: 10.1021/acsami.6b15250. Epub 2017 Jan 27.

PMID:
28128918
28.

Flue-gas and direct-air capture of CO2 by porous metal-organic materials.

Madden DG, Scott HS, Kumar A, Chen KJ, Sanii R, Bajpai A, Lusi M, Curtin T, Perry JJ, Zaworotko MJ.

Philos Trans A Math Phys Eng Sci. 2017 Jan 13;375(2084). pii: 20160025.

29.

Towards an understanding of the propensity for crystalline hydrate formation by molecular compounds.

Bajpai A, Scott HS, Pham T, Chen KJ, Space B, Lusi M, Perry ML, Zaworotko MJ.

IUCrJ. 2016 Oct 18;3(Pt 6):430-439. eCollection 2016 Nov 1.

30.
31.

A network-biology perspective of microRNA function and dysfunction in cancer.

Bracken CP, Scott HS, Goodall GJ.

Nat Rev Genet. 2016 Dec;17(12):719-732. doi: 10.1038/nrg.2016.134. Epub 2016 Oct 31. Review.

PMID:
27795564
32.

Crystal engineering of a family of hybrid ultramicroporous materials based upon interpenetration and dichromate linkers.

Scott HS, Ogiwara N, Chen KJ, Madden DG, Pham T, Forrest K, Space B, Horike S, Perry Iv JJ, Kitagawa S, Zaworotko MJ.

Chem Sci. 2016 Aug 1;7(8):5470-5476. doi: 10.1039/c6sc01385f. Epub 2016 May 10.

33.

Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome Sequencing.

Barnett CP, Nataren NJ, Klingler-Hoffmann M, Schwarz Q, Chong CE, Lee YK, Bruno DL, Lipsett J, McPhee AJ, Schreiber AW, Feng J, Hahn CN, Scott HS.

Hum Mutat. 2016 Sep;37(9):955-63. doi: 10.1002/humu.23032. Epub 2016 Jul 11.

PMID:
27323706
34.

Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implications.

Gagliardi L, Burt MG, Feng J, Poplawski NK, Scott HS.

Clin Endocrinol (Oxf). 2016 Sep;85(3):495-7. doi: 10.1111/cen.13104. Epub 2016 Jun 10. No abstract available.

PMID:
27177819
35.

Apparent 'JAK2-negative' polycythaemia vera due to compound mutations in exon 14.

Tiong IS, Casolari DA, Moore S, Nguyen T, Van Velzen MJM, Zantomio D, Scott HS, D'Andrea RJ, Hahn CN, Ross DM.

Br J Haematol. 2017 Jul;178(2):333-336. doi: 10.1111/bjh.14126. Epub 2016 May 2. No abstract available.

PMID:
27136492
36.

In depth analysis of the Sox4 gene locus that consists of sense and natural antisense transcripts.

Ling KH, Brautigan PJ, Moore S, Fraser R, Leong MP, Leong JW, Zainal Abidin S, Lee HC, Cheah PS, Raison JM, Babic M, Lee YK, Daish T, Mattiske DM, Mann JR, Adelson DL, Thomas PQ, Hahn CN, Scott HS.

Data Brief. 2016 Feb 17;7:282-90. doi: 10.1016/j.dib.2016.01.045. eCollection 2016 Jun.

37.

Derivation of an endogenous small RNA from double-stranded Sox4 sense and natural antisense transcripts in the mouse brain.

Ling KH, Brautigan PJ, Moore S, Fraser R, Cheah PS, Raison JM, Babic M, Lee YK, Daish T, Mattiske DM, Mann JR, Adelson DL, Thomas PQ, Hahn CN, Scott HS.

Genomics. 2016 Mar;107(2-3):88-99. doi: 10.1016/j.ygeno.2016.01.006. Epub 2016 Jan 21.

38.

Correction: HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse.

Lim SL, Qu ZP, Kortschak RD, Lawrence DM, Geoghegan J, Hempfling AL, Bergmann M, Goodnow CC, Ormandy CJ, Wong L, Mann J, Scott HS, Jamsai D, Adelson DL, O'Bryan MK.

PLoS Genet. 2015 Dec 29;11(12):e1005782. doi: 10.1371/journal.pgen.1005782. eCollection 2015 Dec. No abstract available.

39.

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.

Lewinsohn M, Brown AL, Weinel LM, Phung C, Rafidi G, Lee MK, Schreiber AW, Feng J, Babic M, Chong CE, Lee Y, Yong A, Suthers GK, Poplawski N, Altree M, Phillips K, Jaensch L, Fine M, D'Andrea RJ, Lewis ID, Medeiros BC, Pollyea DA, King MC, Walsh T, Keel S, Shimamura A, Godley LA, Hahn CN, Churpek JE, Scott HS.

Blood. 2016 Feb 25;127(8):1017-23. doi: 10.1182/blood-2015-10-676098. Epub 2015 Dec 28.

40.

Delayed diagnosis leading to accelerated-phase chronic eosinophilic leukemia due to a cytogenetically cryptic, imatinib-responsive TNIP1-PDFGRB fusion gene.

Ross DM, Altamura HK, Hahn CN, Nicola M, Yeoman AL, Holloway MR, Geoghegan J, Feng J, Schreiber AW, Branford S, Moore S, Scott HS.

Leukemia. 2016 Jun;30(6):1402-5. doi: 10.1038/leu.2015.301. Epub 2015 Oct 27. No abstract available.

PMID:
26503642
41.

HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse.

Lim SL, Qu ZP, Kortschak RD, Lawrence DM, Geoghegan J, Hempfling AL, Bergmann M, Goodnow CC, Ormandy CJ, Wong L, Mann J, Scott HS, Jamsai D, Adelson DL, O'Bryan MK.

PLoS Genet. 2015 Oct 23;11(10):e1005620. doi: 10.1371/journal.pgen.1005620. eCollection 2015 Oct. Erratum in: PLoS Genet. 2015 Dec;11(12):e1005782.

42.

Transcriptional profiling of the postnatal brain of the Ts1Cje mouse model of Down syndrome.

Tan KL, Ling KH, Hewitt CA, Cheah PS, Simpson K, Gordon L, Pritchard MA, Smyth GK, Thomas T, Scott HS.

Genom Data. 2014 Oct 2;2:314-7. doi: 10.1016/j.gdata.2014.09.009. eCollection 2014 Dec.

43.

Novel mode of 2-fold interpenetration observed in a primitive cubic network of formula [Ni(1,2-bis(4-pyridyl)acetylene)2(Cr2O7)]n.

Scott HS, Bajpai A, Chen KJ, Pham T, Space B, Perry JJ 4th, Zaworotko MJ.

Chem Commun (Camb). 2015 Oct 14;51(80):14832-5. doi: 10.1039/c5cc05866j.

PMID:
26307270
44.

Presentation of m.3243A>G (MT-TL1; tRNALeu) variant with focal neurology in infancy.

Mordaunt DA, McIntyre LC, Salvemini H, Ibrahim A, Bratkovic D, Ketteridge D, Scott HS, Kassahn KS, Smith N.

Am J Med Genet A. 2015 Nov;167A(11):2697-701. doi: 10.1002/ajmg.a.37161. Epub 2015 Aug 20.

PMID:
26289840
45.

Double-walled pyr topology networks from a novel fluoride-bridged heptanuclear metal cluster.

Chen KJ, Perry Iv JJ, Scott HS, Yang QY, Zaworotko MJ.

Chem Sci. 2015 Aug 1;6(8):4784-4789. doi: 10.1039/c5sc01515d. Epub 2015 May 22.

46.

GATA2 is required for lymphatic vessel valve development and maintenance.

Kazenwadel J, Betterman KL, Chong CE, Stokes PH, Lee YK, Secker GA, Agalarov Y, Demir CS, Lawrence DM, Sutton DL, Tabruyn SP, Miura N, Salminen M, Petrova TV, Matthews JM, Hahn CN, Scott HS, Harvey NL.

J Clin Invest. 2015 Aug 3;125(8):2979-94. doi: 10.1172/JCI78888. Epub 2015 Jul 27.

47.

Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics.

Hu Z, Scott HS, Qin G, Zheng G, Chu X, Xie L, Adelson DL, Oftedal BE, Venugopal P, Babic M, Hahn CN, Zhang B, Wang X, Li N, Wei C.

Sci Rep. 2015 Jul 9;5:10940. doi: 10.1038/srep10940.

48.

Allan-Herndon-Dudley syndrome with unusual profound sensorineural hearing loss.

Gagliardi L, Nataren N, Feng J, Schreiber AW, Hahn CN, Conwell LS, Coman D, Scott HS.

Am J Med Genet A. 2015 Aug;167A(8):1872-6. doi: 10.1002/ajmg.a.37075. Epub 2015 Apr 6.

PMID:
25850411
49.

A tale of two siblings: two cases of AML arising from a single pre-leukemic DNMT3A mutant clone.

Hahn CN, Ross DM, Feng J, Beligaswatte A, Hiwase DK, Parker WT, Ho M, Zawitkowski M, Ambler KL, Cheetham GD, Lee YK, Babic M, Butcher CM, Engler GA, Brown AL, D'Andrea RJ, Lewis ID, Schreiber AW, To LB, Scott HS.

Leukemia. 2015 Oct;29(10):2101-4. doi: 10.1038/leu.2015.67. Epub 2015 Mar 9. No abstract available.

50.

Characterisation of a compound in-cis GATA2 germline mutation in a pedigree presenting with myelodysplastic syndrome/acute myeloid leukemia with concurrent thrombocytopenia.

Hahn CN, Brautigan PJ, Chong CE, Janssan A, Venugopal P, Lee Y, Tims AE, Horwitz MS, Klingler-Hoffmann M, Scott HS.

Leukemia. 2015 Aug;29(8):1795-7. doi: 10.1038/leu.2015.40. Epub 2015 Feb 13. No abstract available.

PMID:
25676417

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