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Items: 1 to 50 of 115

1.

Genetic variation in dopamine neurotransmission and motor development of infants born extremely-low-birthweight.

Worley G, Erickson SW, Gustafson KE, Nikolova YS, Ashley-Koch AE, Belsky DW, Goldstein RF, Page GP, Cotten CM; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network.

Dev Med Child Neurol. 2019 Nov 6. doi: 10.1111/dmcn.14383. [Epub ahead of print]

PMID:
31691959
2.

Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study.

Cintho Ozahata M, Page GP, Guo Y, Ferreira JE, Dinardo CL, Carneiro-Proietti ABF, Loureiro P, Mota RA, Rodrigues DOW, Belisario AR, Maximo C, Flor-Park MV, Custer B, Kelly S, Sabino EC; International Component of the NHLBI Recipient Epidemiology and Donor Evaluation Study (REDS-III).

J Sex Med. 2019 Dec;16(12):1988-1999. doi: 10.1016/j.jsxm.2019.09.012. Epub 2019 Oct 24.

PMID:
31668730
3.

Sex hormone intake in female blood donors: impact on haemolysis during cold storage and regulation of erythrocyte calcium influx by progesterone.

Fang F, Hazegh K, Sinchar D, Guo Y, Page GP, Mast AE, Kleinman S, Busch MP, Kanias T.

Blood Transfus. 2019 Jul;17(4):263-273. doi: 10.2450/2019.0053-19.

4.

In response.

Page GP, Brambilla DJ.

Transfusion. 2019 Aug;59(8):2750-2751. doi: 10.1111/trf.15418. No abstract available.

PMID:
31374152
5.

Iron status and risk factors for iron depletion in a racially/ethnically diverse blood donor population.

Spencer BR, Guo Y, Cable RG, Kiss JE, Busch MP, Page GP, Endres-Dighe SM, Kleinman S, Glynn SA, Mast AE; National Heart, Lung, and Blood Institute Recipient Epidemiology and Donor Evaluation Study-III (REDS-III).

Transfusion. 2019 Oct;59(10):3146-3156. doi: 10.1111/trf.15448. Epub 2019 Jul 18.

PMID:
31318071
6.

Piloting and implementation of quality assessment and quality control procedures in RBC-Omics: a large multi-center study of red blood cell hemolysis during storage.

Stone M, Keating SM, Kanias T, Lanteri MC, Lebedeva M, Sinchar D, Hampton D, Jakub A, Rychka V, Brewer G, Bakkour S, Gefter N, Murcia K, Page GP, Endres-Dighe S, Bialkowski W, Fu X, Zimring J, Raife TJ, Kleinman S, Gladwin MT, Busch MP; National Heart, Lung, and Blood Institute Recipient Epidemiology Donor Evaluation Study III (REDS-III) Program.

Transfusion. 2019 Jan;59(1):57-66. doi: 10.1111/trf.15099. Epub 2018 Dec 19.

PMID:
30566231
7.

Genetic variants associated with patent ductus arteriosus in extremely preterm infants.

Dagle JM, Ryckman KK, Spracklen CN, Momany AM, Cotten CM, Levy J, Page GP, Bell EF, Carlo WA, Shankaran S, Goldberg RN, Ehrenkranz RA, Tyson JE, Stoll BJ, Murray JC; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network.

J Perinatol. 2019 Mar;39(3):401-408. doi: 10.1038/s41372-018-0285-6. Epub 2018 Dec 5.

PMID:
30518802
8.

Frequent blood donations alter susceptibility of red blood cells to storage- and stress-induced hemolysis.

Kanias T, Stone M, Page GP, Guo Y, Endres-Dighe SM, Lanteri MC, Spencer BR, Cable RG, Triulzi DJ, Kiss JE, Murphy EL, Kleinman S, Gladwin MT, Busch MP, Mast AE; NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III Program.

Transfusion. 2019 Jan;59(1):67-78. doi: 10.1111/trf.14998. Epub 2018 Nov 26.

PMID:
30474858
9.

Development and evaluation of a transfusion medicine genome wide genotyping array.

Guo Y, Busch MP, Seielstad M, Endres-Dighe S, Westhoff CM, Keating B, Hoppe C, Bordbar A, Custer B, Butterworth AS, Kanias T, Mast AE, Kleinman S, Lu Y, Page GP; National Heart, Lung, and Blood Institute Recipient Epidemiology Donor Evaluation Study (REDS)-III.

Transfusion. 2019 Jan;59(1):101-111. doi: 10.1111/trf.15012. Epub 2018 Nov 20.

PMID:
30456907
10.

Intradonor reproducibility and changes in hemolytic variables during red blood cell storage: results of recall phase of the REDS-III RBC-Omics study.

Lanteri MC, Kanias T, Keating S, Stone M, Guo Y, Page GP, Brambilla DJ, Endres-Dighe SM, Mast AE, Bialkowski W, D'Andrea P, Cable RG, Spencer BR, Triulzi DJ, Murphy EL, Kleinman S, Gladwin MT, Busch MP; NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III Program.

Transfusion. 2019 Jan;59(1):79-88. doi: 10.1111/trf.14987. Epub 2018 Nov 8.

PMID:
30408207
11.

Blood, sweat, and tears: Red Blood Cell-Omics study objectives, design, and recruitment activities.

Endres-Dighe SM, Guo Y, Kanias T, Lanteri M, Stone M, Spencer B, Cable RG, Kiss JE, Kleinman S, Gladwin MT, Brambilla DJ, D'Andrea P, Triulzi DJ, Mast AE, Page GP, Busch MP; NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III Program.

Transfusion. 2019 Jan;59(1):46-56. doi: 10.1111/trf.14971. Epub 2018 Sep 28.

PMID:
30267427
12.

Clinical and genetic ancestry profile of a large multi-centre sickle cell disease cohort in Brazil.

Carneiro-Proietti ABF, Kelly S, Miranda Teixeira C, Sabino EC, Alencar CS, Capuani L, Salomon Silva TP, Araujo A, Loureiro P, Máximo C, Lobo C, Flor-Park MV, Rodrigues DOW, Mota RA, Gonçalez TT, Hoppe C, Ferreira JE, Ozahata M, Page GP, Guo Y, Preiss LR, Brambilla D, Busch MP, Custer B; International Component of the NHLBI Recipient Epidemiology and Donor Evaluation Study (REDS-III).

Br J Haematol. 2018 Sep;182(6):895-908. doi: 10.1111/bjh.15462. Epub 2018 Jul 19.

PMID:
30027669
13.

Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8.

Jilling T, Ambalavanan N, Cotten CM, Martin CA, Maheshwari A, Schibler K, Levy J, Page GP.

Pediatr Res. 2018 May;83(5):943-953. doi: 10.1038/pr.2018.33. Epub 2018 May 16.

14.

Genomewide association study of HLA alloimmunization in previously pregnant blood donors.

Seielstad M, Page GP, Gaddis N, Lanteri M, Lee TH, Kakaiya R, Barcellos LF, Criswell LA, Triulzi D, Norris PJ, Busch MP; NHLBI REDS-III Study Investigators.

Transfusion. 2018 Feb;58(2):402-412. doi: 10.1111/trf.14402. Epub 2017 Nov 22.

15.

Ethnicity, sex, and age are determinants of red blood cell storage and stress hemolysis: results of the REDS-III RBC-Omics study.

Kanias T, Lanteri MC, Page GP, Guo Y, Endres SM, Stone M, Keating S, Mast AE, Cable RG, Triulzi DJ, Kiss JE, Murphy EL, Kleinman S, Busch MP, Gladwin MT.

Blood Adv. 2017 Jun 27;1(15):1132-1141. doi: 10.1182/bloodadvances.2017004820.

16.

KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex.

Johnson EO, Hancock DB, Levy JL, Gaddis NC, Page GP, Glasheen C, Saccone NL, Bierut LJ, Kral AH.

Addict Biol. 2016 Nov;21(6):1217-1232. doi: 10.1111/adb.12286. Epub 2015 Jul 23.

17.

Replication of ZNF804A gene variant associations with risk of heroin addiction.

Hancock DB, Levy JL, Gaddis NC, Glasheen C, Saccone NL, Page GP, Bierut LJ, Kral AH, Johnson EO.

Genes Brain Behav. 2015 Nov;14(8):635-40. doi: 10.1111/gbb.12254. Epub 2015 Oct 20.

18.

Cis-Expression Quantitative Trait Loci Mapping Reveals Replicable Associations with Heroin Addiction in OPRM1.

Hancock DB, Levy JL, Gaddis NC, Glasheen C, Saccone NL, Page GP, Hulse GK, Wildenauer D, Kelty EA, Schwab SG, Degenhardt L, Martin NG, Montgomery GW, Attia J, Holliday EG, McEvoy M, Scott RJ, Bierut LJ, Nelson EC, Kral AH, Johnson EO.

Biol Psychiatry. 2015 Oct 1;78(7):474-84. doi: 10.1016/j.biopsych.2015.01.003. Epub 2015 Jan 29.

19.

Genetic contributions to urgency urinary incontinence in women.

Richter HE, Whitehead N, Arya L, Ridgeway B, Allen-Brady K, Norton P, Sung V, Shepherd JP, Komesu Y, Gaddis N, Fraser MO, Tan-Kim J, Meikle S, Page GP; Pelvic Floor Disorders Network.

J Urol. 2015 Jun;193(6):2020-7. doi: 10.1016/j.juro.2014.12.023. Epub 2014 Dec 15.

20.

Integrated genomic analyses in bronchopulmonary dysplasia.

Ambalavanan N, Cotten CM, Page GP, Carlo WA, Murray JC, Bhattacharya S, Mariani TJ, Cuna AC, Faye-Petersen OM, Kelly D, Higgins RD; Genomics and Cytokine Subcommittees of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network.

J Pediatr. 2015 Mar;166(3):531-7.e13. doi: 10.1016/j.jpeds.2014.09.052. Epub 2014 Nov 6.

21.

Imputation across genotyping arrays for genome-wide association studies: assessment of bias and a correction strategy.

Johnson EO, Hancock DB, Levy JL, Gaddis NC, Saccone NL, Bierut LJ, Page GP.

Hum Genet. 2013 May;132(5):509-22. doi: 10.1007/s00439-013-1266-7. Epub 2013 Jan 22.

22.

Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation births.

Boghossian NS, Page GP, Bell EF, Stoll BJ, Murray JC, Cotten CM, Shankaran S, Walsh MC, Laptook AR, Newman NS, Hale EC, McDonald SA, Das A, Higgins RD; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network.

J Pediatr. 2013 Jun;162(6):1120-4, 1124.e1. doi: 10.1016/j.jpeds.2012.11.089. Epub 2013 Jan 13.

23.

Assessment of genotype imputation performance using 1000 Genomes in African American studies.

Hancock DB, Levy JL, Gaddis NC, Bierut LJ, Saccone NL, Page GP, Johnson EO.

PLoS One. 2012;7(11):e50610. doi: 10.1371/journal.pone.0050610. Epub 2012 Nov 30.

24.

MEK inhibition exhibits efficacy in human and mouse neurofibromatosis tumors.

Jessen WJ, Miller SJ, Jousma E, Wu J, Rizvi TA, Brundage ME, Eaves D, Widemann B, Kim MO, Dombi E, Sabo J, Hardiman Dudley A, Niwa-Kawakita M, Page GP, Giovannini M, Aronow BJ, Cripe TP, Ratner N.

J Clin Invest. 2013 Jan;123(1):340-7. doi: 10.1172/JCI60578. Epub 2012 Dec 10.

25.

Karyotype versus microarray testing for genetic abnormalities after stillbirth.

Reddy UM, Page GP, Saade GR, Silver RM, Thorsten VR, Parker CB, Pinar H, Willinger M, Stoll BJ, Heim-Hall J, Varner MW, Goldenberg RL, Bukowski R, Wapner RJ, Drews-Botsch CD, O'Brien BM, Dudley DJ, Levy B; NICHD Stillbirth Collaborative Research Network.

N Engl J Med. 2012 Dec 6;367(23):2185-93. doi: 10.1056/NEJMoa1201569.

26.

Overexpression of CONSTANS homologs CO1 and CO2 fails to alter normal reproductive onset and fall bud set in woody perennial poplar.

Hsu CY, Adams JP, No K, Liang H, Meilan R, Pechanova O, Barakat A, Carlson JE, Page GP, Yuceer C.

PLoS One. 2012;7(9):e45448. doi: 10.1371/journal.pone.0045448. Epub 2012 Sep 19.

27.

PTX3 genetic variation and dizygotic twinning in the Gambia: could pleiotropy with innate immunity explain common dizygotic twinning in Africa?

Sirugo G, Edwards DR, Ryckman KK, Bisseye C, White MJ, Kebbeh B, Morris GA, Adegbola RA, Tacconelli A, Predazzi IM, Novelli G, Vannberg FO, Odunsi K, Page GP, Williams SM.

Ann Hum Genet. 2012 Nov;76(6):454-63. doi: 10.1111/j.1469-1809.2012.00723.x. Epub 2012 Jul 27.

28.

Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability.

Cope N, Eicher JD, Meng H, Gibson CJ, Hager K, Lacadie C, Fulbright RK, Constable RT, Page GP, Gruen JR.

Neuroimage. 2012 Oct 15;63(1):148-56. doi: 10.1016/j.neuroimage.2012.06.037. Epub 2012 Jun 27.

29.

The role of DNA microarrays in the evaluation of fetal death.

Reddy UM, Page GP, Saade GR.

Prenat Diagn. 2012 Apr;32(4):371-5. doi: 10.1002/pd.3825.

PMID:
22467168
30.

Accurate and flexible power calculations on the spot: Applications to genomic research.

Tiwari HK, Birkner T, Moondan A, Zhang S, Page GP, Patki A, Allison DB.

Stat Interface. 2011;4(3):353-358.

31.

Plant-based FRET biosensor discriminates environmental zinc levels.

Adams JP, Adeli A, Hsu CY, Harkess RL, Page GP, Depamphilis CW, Schultz EB, Yuceer C.

Plant Biotechnol J. 2012 Feb;10(2):207-16. doi: 10.1111/j.1467-7652.2011.00656.x. Epub 2011 Sep 13.

32.

FLOWERING LOCUS T duplication coordinates reproductive and vegetative growth in perennial poplar.

Hsu CY, Adams JP, Kim H, No K, Ma C, Strauss SH, Drnevich J, Vandervelde L, Ellis JD, Rice BM, Wickett N, Gunter LE, Tuskan GA, Brunner AM, Page GP, Barakat A, Carlson JE, DePamphilis CW, Luthe DS, Yuceer C.

Proc Natl Acad Sci U S A. 2011 Jun 28;108(26):10756-61. doi: 10.1073/pnas.1104713108. Epub 2011 Jun 8.

33.

Poplar maintains zinc homeostasis with heavy metal genes HMA4 and PCS1.

Adams JP, Adeli A, Hsu CY, Harkess RL, Page GP, dePamphilis CW, Schultz EB, Yuceer C.

J Exp Bot. 2011 Jul;62(11):3737-52. doi: 10.1093/jxb/err025. Epub 2011 Apr 19.

34.

A dyslexia-associated variant in DCDC2 changes gene expression.

Meng H, Powers NR, Tang L, Cope NA, Zhang PX, Fuleihan R, Gibson C, Page GP, Gruen JR.

Behav Genet. 2011 Jan;41(1):58-66. doi: 10.1007/s10519-010-9408-3. Epub 2010 Nov 2.

35.

Gene expression analysis identifies potential biomarkers of neurofibromatosis type 1 including adrenomedullin.

Hummel TR, Jessen WJ, Miller SJ, Kluwe L, Mautner VF, Wallace MR, Lázaro C, Page GP, Worley PF, Aronow BJ, Schorry EK, Ratner N.

Clin Cancer Res. 2010 Oct 15;16(20):5048-57. doi: 10.1158/1078-0432.CCR-10-0613. Epub 2010 Aug 25.

36.

The association between the rs2234693 and rs9340799 estrogen receptor alpha gene polymorphisms and risk factors for cardiovascular disease: a review.

Casazza K, Page GP, Fernandez JR.

Biol Res Nurs. 2010 Jul;12(1):84-97. doi: 10.1177/1099800410371118.

PMID:
20702456
37.

The MicroArray Quality Control (MAQC)-II study of common practices for the development and validation of microarray-based predictive models.

Shi L, Campbell G, Jones WD, Campagne F, Wen Z, Walker SJ, Su Z, Chu TM, Goodsaid FM, Pusztai L, Shaughnessy JD Jr, Oberthuer A, Thomas RS, Paules RS, Fielden M, Barlogie B, Chen W, Du P, Fischer M, Furlanello C, Gallas BD, Ge X, Megherbi DB, Symmans WF, Wang MD, Zhang J, Bitter H, Brors B, Bushel PR, Bylesjo M, Chen M, Cheng J, Cheng J, Chou J, Davison TS, Delorenzi M, Deng Y, Devanarayan V, Dix DJ, Dopazo J, Dorff KC, Elloumi F, Fan J, Fan S, Fan X, Fang H, Gonzaludo N, Hess KR, Hong H, Huan J, Irizarry RA, Judson R, Juraeva D, Lababidi S, Lambert CG, Li L, Li Y, Li Z, Lin SM, Liu G, Lobenhofer EK, Luo J, Luo W, McCall MN, Nikolsky Y, Pennello GA, Perkins RG, Philip R, Popovici V, Price ND, Qian F, Scherer A, Shi T, Shi W, Sung J, Thierry-Mieg D, Thierry-Mieg J, Thodima V, Trygg J, Vishnuvajjala L, Wang SJ, Wu J, Wu Y, Xie Q, Yousef WA, Zhang L, Zhang X, Zhong S, Zhou Y, Zhu S, Arasappan D, Bao W, Lucas AB, Berthold F, Brennan RJ, Buness A, Catalano JG, Chang C, Chen R, Cheng Y, Cui J, Czika W, Demichelis F, Deng X, Dosymbekov D, Eils R, Feng Y, Fostel J, Fulmer-Smentek S, Fuscoe JC, Gatto L, Ge W, Goldstein DR, Guo L, Halbert DN, Han J, Harris SC, Hatzis C, Herman D, Huang J, Jensen RV, Jiang R, Johnson CD, Jurman G, Kahlert Y, Khuder SA, Kohl M, Li J, Li L, Li M, Li QZ, Li S, Li Z, Liu J, Liu Y, Liu Z, Meng L, Madera M, Martinez-Murillo F, Medina I, Meehan J, Miclaus K, Moffitt RA, Montaner D, Mukherjee P, Mulligan GJ, Neville P, Nikolskaya T, Ning B, Page GP, Parker J, Parry RM, Peng X, Peterson RL, Phan JH, Quanz B, Ren Y, Riccadonna S, Roter AH, Samuelson FW, Schumacher MM, Shambaugh JD, Shi Q, Shippy R, Si S, Smalter A, Sotiriou C, Soukup M, Staedtler F, Steiner G, Stokes TH, Sun Q, Tan PY, Tang R, Tezak Z, Thorn B, Tsyganova M, Turpaz Y, Vega SC, Visintainer R, von Frese J, Wang C, Wang E, Wang J, Wang W, Westermann F, Willey JC, Woods M, Wu S, Xiao N, Xu J, Xu L, Yang L, Zeng X, Zhang J, Zhang L, Zhang M, Zhao C, Puri RK, Scherf U, Tong W, Wolfinger RD; MAQC Consortium.

Nat Biotechnol. 2010 Aug;28(8):827-38. doi: 10.1038/nbt.1665. Epub 2010 Jul 30.

38.

Identification of quantitative trait loci underlying proteome variation in human lymphoblastoid cells.

Garge N, Pan H, Rowland MD, Cargile BJ, Zhang X, Cooley PC, Page GP, Bunger MK.

Mol Cell Proteomics. 2010 Jul;9(7):1383-99. doi: 10.1074/mcp.M900378-MCP200. Epub 2010 Feb 23.

39.

Genetical toxicogenomics in Drosophila identifies master-modulatory loci that are regulated by developmental exposure to lead.

Ruden DM, Chen L, Possidente D, Possidente B, Rasouli P, Wang L, Lu X, Garfinkel MD, Hirsch HV, Page GP.

Neurotoxicology. 2009 Nov;30(6):898-914. doi: 10.1016/j.neuro.2009.08.011. Epub 2009 Sep 6.

40.

Massively parallel resequencing of the isogenic Drosophila melanogaster strain w(1118); iso-2; iso-3 identifies hotspots for mutations in sensory perception genes.

Platts AE, Land SJ, Chen L, Page GP, Rasouli P, Wang L, Lu X, Ruden DM.

Fly (Austin). 2009 Jul-Sep;3(3):192-203. Epub 2009 Jul 23.

41.

Genetic aspects of behavioral neurotoxicology.

Levin ED, Aschner M, Heberlein U, Ruden D, Welsh-Bohmer KA, Bartlett S, Berger K, Chen L, Corl AB, Eddins D, French R, Hayden KM, Helmcke K, Hirsch HV, Linney E, Lnenicka G, Page GP, Possidente D, Possidente B, Kirshner A.

Neurotoxicology. 2009 Sep;30(5):741-53. doi: 10.1016/j.neuro.2009.07.014. Epub 2009 Jul 30.

42.

Urinary peptidome may predict renal function decline in type 1 diabetes and microalbuminuria.

Merchant ML, Perkins BA, Boratyn GM, Ficociello LH, Wilkey DW, Barati MT, Bertram CC, Page GP, Rovin BH, Warram JH, Krolewski AS, Klein JB.

J Am Soc Nephrol. 2009 Sep;20(9):2065-74. doi: 10.1681/ASN.2008121233. Epub 2009 Jul 30.

43.

Gene expression profiling of aging in multiple mouse strains: identification of aging biomarkers and impact of dietary antioxidants.

Park SK, Kim K, Page GP, Allison DB, Weindruch R, Prolla TA.

Aging Cell. 2009 Aug;8(4):484-95. doi: 10.1111/j.1474-9726.2009.00496.x. Epub 2009 Jun 25.

44.

Transcriptional reprogramming of gene expression in bovine somatic cell chromatin transfer embryos.

Rodriguez-Osorio N, Wang Z, Kasinathan P, Page GP, Robl JM, Memili E.

BMC Genomics. 2009 Apr 24;10:190. doi: 10.1186/1471-2164-10-190.

45.

Two-stage genome-wide association study identifies integrin beta 5 as having potential role in bull fertility.

Feugang JM, Kaya A, Page GP, Chen L, Mehta T, Hirani K, Nazareth L, Topper E, Gibbs R, Memili E.

BMC Genomics. 2009 Apr 24;10:176. doi: 10.1186/1471-2164-10-176.

46.

Correlation of microRNA levels during hypoxia with predicted target mRNAs through genome-wide microarray analysis.

Guimbellot JS, Erickson SW, Mehta T, Wen H, Page GP, Sorscher EJ, Hong JS.

BMC Med Genomics. 2009 Mar 25;2:15. doi: 10.1186/1755-8794-2-15.

47.

Identification of molecular distinctions between normal breast-associated fibroblasts and breast cancer-associated fibroblasts.

Sadlonova A, Bowe DB, Novak Z, Mukherjee S, Duncan VE, Page GP, Frost AR.

Cancer Microenviron. 2009 Dec;2(1):9-21. doi: 10.1007/s12307-008-0017-0. Epub 2009 Mar 18.

48.

Single nucleotide polymorphisms affect both cis- and trans-eQTLs.

Chen L, Page GP, Mehta T, Feng R, Cui X.

Genomics. 2009 Jun;93(6):501-8. doi: 10.1016/j.ygeno.2009.01.011. Epub 2009 Feb 25.

49.

Repeatability of published microarray gene expression analyses.

Ioannidis JP, Allison DB, Ball CA, Coulibaly I, Cui X, Culhane AC, Falchi M, Furlanello C, Game L, Jurman G, Mangion J, Mehta T, Nitzberg M, Page GP, Petretto E, van Noort V.

Nat Genet. 2009 Feb;41(2):149-55. doi: 10.1038/ng.295. Epub 2008 Jan 28.

PMID:
19174838
50.

Cross-chip probe matching tool: A web-based tool for linking microarray probes within and across plant species.

Ghanekar R, Srinivasasainagendra V, Page GP.

Int J Plant Genomics. 2008;2008:451327. doi: 10.1155/2008/451327. Epub 2008 Oct 21.

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