Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 34

1.

Tracking Cancer Evolution Reveals Constrained Routes to Metastases: TRACERx Renal.

Turajlic S, Xu H, Litchfield K, Rowan A, Chambers T, Lopez JI, Nicol D, O'Brien T, Larkin J, Horswell S, Stares M, Au L, Jamal-Hanjani M, Challacombe B, Chandra A, Hazell S, Eichler-Jonsson C, Soultati A, Chowdhury S, Rudman S, Lynch J, Fernando A, Stamp G, Nye E, Jabbar F, Spain L, Lall S, Guarch R, Falzon M, Proctor I, Pickering L, Gore M, Watkins TBK, Ward S, Stewart A, DiNatale R, Becerra MF, Reznik E, Hsieh JJ, Richmond TA, Mayhew GF, Hill SM, McNally CD, Jones C, Rosenbaum H, Stanislaw S, Burgess DL, Alexander NR, Swanton C; PEACE; TRACERx Renal Consortium.

Cell. 2018 Apr 19;173(3):581-594.e12. doi: 10.1016/j.cell.2018.03.057. Epub 2018 Apr 12.

2.

Targeted Bisulfite Sequencing Using the SeqCap Epi Enrichment System.

Wendt J, Rosenbaum H, Richmond TA, Jeddeloh JA, Burgess DL.

Methods Mol Biol. 2018;1708:383-405. doi: 10.1007/978-1-4939-7481-8_20.

PMID:
29224155
3.

LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice.

Geister KA, Brinkmeier ML, Cheung LY, Wendt J, Oatley MJ, Burgess DL, Kozloff KM, Cavalcoli JD, Oatley JM, Camper SA.

PLoS Genet. 2015 Oct 23;11(10):e1005569. doi: 10.1371/journal.pgen.1005569. eCollection 2015 Oct.

4.

Genetic perturbation of the maize methylome.

Li Q, Eichten SR, Hermanson PJ, Zaunbrecher VM, Song J, Wendt J, Rosenbaum H, Madzima TF, Sloan AE, Huang J, Burgess DL, Richmond TA, McGinnis KM, Meeley RB, Danilevskaya ON, Vaughn MW, Kaeppler SM, Jeddeloh JA, Springer NM.

Plant Cell. 2014 Dec;26(12):4602-16. doi: 10.1105/tpc.114.133140. Epub 2014 Dec 19.

5.

Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.

Bainbridge MN, Wang M, Wu Y, Newsham I, Muzny DM, Jefferies JL, Albert TJ, Burgess DL, Gibbs RA.

Genome Biol. 2011 Jul 25;12(7):R68. doi: 10.1186/gb-2011-12-7-r68.

6.

Whole exome capture in solution with 3 Gbp of data.

Bainbridge MN, Wang M, Burgess DL, Kovar C, Rodesch MJ, D'Ascenzo M, Kitzman J, Wu YQ, Newsham I, Richmond TA, Jeddeloh JA, Muzny D, Albert TJ, Gibbs RA.

Genome Biol. 2010;11(6):R62. doi: 10.1186/gb-2010-11-6-r62. Epub 2010 Jun 17.

7.

A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment.

Price MG, Yoo JW, Burgess DL, Deng F, Hrachovy RA, Frost JD Jr, Noebels JL.

J Neurosci. 2009 Jul 8;29(27):8752-63. doi: 10.1523/JNEUROSCI.0915-09.2009.

8.

Shoulder resurfacing.

Burgess DL, McGrath MS, Bonutti PM, Marker DR, Delanois RE, Mont MA.

J Bone Joint Surg Am. 2009 May;91(5):1228-38. doi: 10.2106/JBJS.H.01082. Review.

PMID:
19411474
9.
10.

Neonatal epilepsy syndromes and GEFS+: mechanistic considerations.

Burgess DL.

Epilepsia. 2005;46 Suppl 10:51-8. Review.

12.

Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions.

Meisler MH, Plummer NW, Burgess DL, Buchner DA, Sprunger LK.

Genetica. 2004 Sep;122(1):37-45. Review.

13.

Expression of apoptosis inhibitor protein Mcl1 linked to neuroprotection in CNS neurons.

Mori M, Burgess DL, Gefrides LA, Foreman PJ, Opferman JT, Korsmeyer SJ, Cavalheiro EA, Naffah-Mazzacoratti MG, Noebels JL.

Cell Death Differ. 2004 Nov;11(11):1223-33.

14.
15.

Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome.

Heilstedt HA, Burgess DL, Anderson AE, Chedrawi A, Tharp B, Lee O, Kashork CD, Starkey DE, Wu YQ, Noebels JL, Shaffer LG, Shapira SK.

Epilepsia. 2001 Sep;42(9):1103-11.

16.
17.
18.

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T.

Nat Genet. 2000 Oct;26(2):191-4.

PMID:
11017075
19.

Calcium channel defects in models of inherited generalized epilepsy.

Burgess DL, Noebels JL.

Epilepsia. 2000 Aug;41(8):1074-5. Review. No abstract available.

20.

Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.

Burgess DL, Matsuura T, Ashizawa T, Noebels JL.

Epilepsia. 2000 Jan;41(1):24-7.

21.
22.

Single gene defects in mice: the role of voltage-dependent calcium channels in absence models.

Burgess DL, Noebels JL.

Epilepsy Res. 1999 Sep;36(2-3):111-22. Review.

PMID:
10515159
23.

Voltage-dependent calcium channel mutations in neurological disease.

Burgess DL, Noebels JL.

Ann N Y Acad Sci. 1999 Apr 30;868:199-212. Review.

PMID:
10414295
24.

beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain.

Burgess DL, Biddlecome GH, McDonough SI, Diaz ME, Zilinski CA, Bean BP, Campbell KP, Noebels JL.

Mol Cell Neurosci. 1999 Apr;13(4):293-311.

PMID:
10328888
25.

Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A.

Plummer NW, Galt J, Jones JM, Burgess DL, Sprunger LK, Kohrman DC, Meisler MH.

Genomics. 1998 Dec 1;54(2):287-96.

PMID:
9828131
26.
27.

Dlgh1, a mouse homolog of the drosophila discs-large gene, is located on chromosome 16.

Burgess DL, Rafael JA, Meisler MH, Chamberlain JS.

Mamm Genome. 1996 Aug;7(8):623-4. No abstract available.

PMID:
8678991
28.

Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.

Griffith AJ, Burgess DL, Kohrman DC, Yu J, Blaschak J, Blanton SH, Boehnke M, Hecht JT, Overhauser J, Meisler MH.

Genomics. 1996 Jun 15;34(3):299-303.

PMID:
8786128
29.

Location of the 9257 and ataxia mutations on mouse chromosome 18.

Griffith AJ, Radice GL, Burgess DL, Kohrman DC, Hansen GM, Justice MJ, Johnson KR, Davisson MT, Meisler MH.

Mamm Genome. 1996 Jun;7(6):417-9.

30.

Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'.

Burgess DL, Kohrman DC, Galt J, Plummer NW, Jones JM, Spear B, Meisler MH.

Nat Genet. 1995 Aug;10(4):461-5.

PMID:
7670495
31.

Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15.

Kohrman DC, Plummer NW, Schuster T, Jones JM, Jang W, Burgess DL, Galt J, Spear BT, Meisler MH.

Genomics. 1995 Mar 20;26(2):171-7.

PMID:
7601440
32.

Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalities.

Ting CN, Kohrman D, Burgess DL, Boyle A, Altschuler RA, Gholizadeh G, Samuelson LC, Jang W, Meisler MH.

Genetics. 1994 Jan;136(1):247-54.

33.

Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20.

Ting CN, Burgess DL, Chamberlain JS, Keith TP, Falls K, Meisler MH.

Genomics. 1993 Jun;16(3):698-706.

Supplemental Content

Loading ...
Support Center