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Items: 35

1.

A new data effort to inform career choices in biomedicine.

Blank R, Daniels RJ, Gilliland G, Gutmann A, Hawgood S, Hrabowski FA, Pollack ME, Price V, Reif LR, Schlissel MS.

Science. 2017 Dec 15;358(6369):1388-1389. doi: 10.1126/science.aar4638. No abstract available.

PMID:
29242335
2.

Effect of instructions on EMG during the bench press in trained and untrained males.

Daniels RJ, Cook SB.

Hum Mov Sci. 2017 Oct;55:182-188. doi: 10.1016/j.humov.2017.08.010. Epub 2017 Aug 24.

PMID:
28841536
3.

A generation at risk: young investigators and the future of the biomedical workforce.

Daniels RJ.

Proc Natl Acad Sci U S A. 2015 Jan 13;112(2):313-8. doi: 10.1073/pnas.1418761112. Epub 2015 Jan 5.

4.

Will the age of austerity save the NHS?

Daniels RJ.

Br J Gen Pract. 2014 Feb;64(619):70. doi: 10.3399/bjgp14X677022. No abstract available.

5.

The Friends of the Axon, the Schwann Cell, and Jack Griffin.

Daniels RJ.

J Peripher Nerv Syst. 2012 Dec;17 Suppl 3:2. doi: 10.1111/j.1529-8027.2012.00422.x. No abstract available.

PMID:
23279423
6.

Academic medical centers--organizational integration and discipline through contractual and firm models.

Daniels RJ, Carson LD.

JAMA. 2011 Nov 2;306(17):1912-3. doi: 10.1001/jama.2011.1606. No abstract available.

PMID:
22045769
7.

Sustaining biodiversity in ancient tropical countryside.

Ranganathan J, Daniels RJ, Chandran MD, Ehrlich PR, Daily GC.

Proc Natl Acad Sci U S A. 2008 Nov 18;105(46):17852-4. doi: 10.1073/pnas.0808874105. Epub 2008 Nov 3.

8.

SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data.

Price TS, Regan R, Mott R, Hedman A, Honey B, Daniels RJ, Smith L, Greenfield A, Tiganescu A, Buckle V, Ventress N, Ayyub H, Salhan A, Pedraza-Diaz S, Broxholme J, Ragoussis J, Higgs DR, Flint J, Knight SJ.

Nucleic Acids Res. 2005 Jun 16;33(11):3455-64. Print 2005.

9.

The human GPI1 gene is required for efficient glycosylphosphatidylinositol biosynthesis.

Tiede A, Daniels RJ, Higgs DR, Mehrein Y, Schmidt RE, Schubert J.

Gene. 2001 Jun 27;271(2):247-54.

PMID:
11418246
10.

Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects.

Horsley SW, Daniels RJ, Anguita E, Raynham HA, Peden JF, Villegas A, Vickers MA, Green S, Waye JS, Chui DH, Ayyub H, MacCarthy AB, Buckle VJ, Gibbons RJ, Kearney L, Higgs DR.

Eur J Hum Genet. 2001 Mar;9(3):217-25.

11.

Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the alpha globin cluster.

Flint J, Tufarelli C, Peden J, Clark K, Daniels RJ, Hardison R, Miller W, Philipsen S, Tan-Un KC, McMorrow T, Frampton J, Alter BP, Frischauf AM, Higgs DR.

Hum Mol Genet. 2001 Feb 15;10(4):371-82.

PMID:
11157800
12.

Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16.

Daniels RJ, Peden JF, Lloyd C, Horsley SW, Clark K, Tufarelli C, Kearney L, Buckle VJ, Doggett NA, Flint J, Higgs DR.

Hum Mol Genet. 2001 Feb 15;10(4):339-52.

PMID:
11157797
13.

Serotonin syndrome due to venlafaxine overdose.

Daniels RJ.

J Accid Emerg Med. 1998 Sep;15(5):333-4.

14.

Maternal mosaicism for a second mutational event in a type I spinal muscular atrophy family.

Campbell L, Daniels RJ, Dubowitz V, Davies KE.

Am J Hum Genet. 1998 Jul;63(1):37-44.

15.

An unusual cause of rib fracture following a road traffic accident.

Daniels RJ, Fulcher RA.

J Accid Emerg Med. 1997 Mar;14(2):113-4.

16.

Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele.

Daniels RJ, Campbell L, Rodrigues NR, Francis MJ, Morrison KE, McLean M, MacKenzie A, Ignatius J, Dubowitz V, Davies KE.

J Med Genet. 1995 Feb;32(2):93-6.

17.

Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q.

Dubowitz V, Daniels RJ, Davies KE.

Neuromuscul Disord. 1995 Jan;5(1):25-9. No abstract available.

PMID:
7719137
18.

Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13.

Theodosiou AM, Morrison KE, Nesbit AM, Daniels RJ, Campbell L, Francis MJ, Christodoulou Z, Davies KE.

Am J Hum Genet. 1994 Dec;55(6):1209-17.

19.

An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.

Mérette C, Brzustowicz LM, Daniels RJ, Davies KE, Gilliam TC, Melki J, Munnich A, Pericak-Vance MA, Siddique T, Voosen B, et al.

Genomics. 1994 May 1;21(1):27-33.

PMID:
8088801
20.

Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at D5S681.

Morrison KE, Daniels RJ, Campbell L, McPherson J, Davies KE.

Hum Mol Genet. 1993 Oct;2(10):1753. No abstract available.

PMID:
8268953
21.

Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA).

Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Grewal PK, Dennis C, Buckle V, Ignatius J, Dubowitz V, et al.

Hum Genet. 1993 Sep;92(2):133-8.

PMID:
8370578
22.

A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13.

Francis MJ, Morrison KE, Campbell L, Grewal PK, Christodoulou Z, Daniels RJ, Monaco AP, Frischauf AM, McPherson J, Wasmuth J, et al.

Hum Mol Genet. 1993 Aug;2(8):1161-7.

PMID:
8401497
23.

Complete and partial XY sex reversal associated with terminal deletion of 10q: report of 2 cases and literature review.

Wilkie AO, Campbell FM, Daubeney P, Grant DB, Daniels RJ, Mullarkey M, Affara NA, Fitchett M, Huson SM.

Am J Med Genet. 1993 Jun 15;46(5):597-600. Review.

PMID:
8322827
24.

On the relationship between bird and woody plant species diversity in the Uttara Kannada district of south India.

Daniels RJ, Joshi NV, Gadgil M.

Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5311-5.

25.

High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.

Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Buckle VJ, Davies KE.

Am J Hum Genet. 1992 Mar;50(3):520-7.

26.

Prenatal prediction of spinal muscular atrophy.

Daniels RJ, Suthers GK, Morrison KE, Thomas NH, Francis MJ, Mathew CG, Loughlin S, Heiberg A, Wood D, Dubowitz V, et al.

J Med Genet. 1992 Mar;29(3):165-70.

27.

Linkage analysis of spinal muscular atrophy.

Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K, et al.

Genomics. 1992 Feb;12(2):335-9.

PMID:
1346777
28.

Molecular studies of spinal muscular atrophy.

Davies KE, Thomas NH, Daniels RJ, Dubowitz V.

Neuromuscul Disord. 1991;1(2):83-5. Review.

PMID:
1822785
29.

Characterization of deletions in the dystrophin gene giving mild phenotypes.

Love DR, Flint TJ, Marsden RF, Bloomfield JF, Daniels RJ, Forrest SM, Gabrielli O, Giorgi P, Novelli G, Davies KE.

Am J Med Genet. 1990 Sep;37(1):136-42.

PMID:
2240031
30.

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.

Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y, et al.

Nature. 1990 Jun 28;345(6278):823-5.

PMID:
1972783
31.

Liquid chromatographic method for quantitation of glyphosate and metabolite residues in organic and mineral soils, stream sediments, and hardwood foliage.

Thompson DG, Cowell JE, Daniels RJ, Staznik B, MacDonald LM.

J Assoc Off Anal Chem. 1989 Mar-Apr;72(2):355-60.

PMID:
2708285
32.

Studies on the rate of efflux of cholesterol from cultured human skin fibroblasts.

Daniels RJ, Guertler LS, Parker TS, Steinberg D.

J Biol Chem. 1981 May 25;256(10):4978-83.

33.

The production, recovery, and purification of 172Hf for utilization in nuclear medicine as the generator of 172Lu.

Daniels RJ, Grant PM, O'Brien HA Jr.

Int J Nucl Med Biol. 1978 Mar;5(1):11-7. No abstract available.

PMID:
659056
34.

Pathologic scar formation. Morphologic and biochemical correlates.

Knapp TR, Daniels RJ, Kaplan EN.

Am J Pathol. 1977 Jan;86(1):47-70.

35.

Granulosa-cell carcinoma of ovary.

Daniels RJ.

Proc R Soc Med. 1966 Sep;59(9):835. No abstract available.

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