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Items: 41

1.

Analysis of spinal and muscle pathology in transgenic mice overexpressing wild-type and ALS-linked mutant MATR3.

Moloney C, Rayaprolu S, Howard J, Fromholt S, Brown H, Collins M, Cabrera M, Duffy C, Siemienski Z, Miller D, Borchelt DR, Lewis J.

Acta Neuropathol Commun. 2018 Dec 19;6(1):137. doi: 10.1186/s40478-018-0631-0.

2.

Partial loss of ATP13A2 causes selective gliosis independent of robust lipofuscinosis.

Rayaprolu S, Seven YB, Howard J, Duffy C, Altshuler M, Moloney C, Giasson BI, Lewis J.

Mol Cell Neurosci. 2018 Oct;92:17-26. doi: 10.1016/j.mcn.2018.05.009. Epub 2018 Jun 1.

PMID:
29859891
3.

Retraction Note: Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype.

Moloney C, Rayaprolu S, Howard J, Fromholt S, Brown H, Collins M, Cabrera M, Duffy C, Siemienski Z, Miller D, Swanson MS, Notterpek L, Borchelt DR, Lewis J.

Acta Neuropathol Commun. 2017 Dec 13;5(1):97. doi: 10.1186/s40478-017-0502-0.

4.

Serpin-9 and -13 regulate hemolymph proteases during immune responses of Manduca sexta.

He Y, Wang Y, Zhao P, Rayaprolu S, Wang X, Cao X, Jiang H.

Insect Biochem Mol Biol. 2017 Nov;90:71-81. doi: 10.1016/j.ibmb.2017.09.015. Epub 2017 Oct 5.

5.

A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking.

Khare S, Nick JA, Zhang Y, Galeano K, Butler B, Khoshbouei H, Rayaprolu S, Hathorn T, Ranum LPW, Smithson L, Golde TE, Paucar M, Morse R, Raff M, Simon J, Nordenskjöld M, Wirdefeldt K, Rincon-Limas DE, Lewis J, Kaczmarek LK, Fernandez-Funez P, Nick HS, Waters MF.

PLoS One. 2017 May 3;12(5):e0173565. doi: 10.1371/journal.pone.0173565. eCollection 2017.

6.

Soybean peptide fractions inhibit human blood, breast and prostate cancer cell proliferation.

Rayaprolu SJ, Hettiarachchy NS, Horax R, Phillips GK, Mahendran M, Chen P.

J Food Sci Technol. 2017 Jan;54(1):38-44. doi: 10.1007/s13197-016-2426-2. Epub 2017 Jan 13.

7.

Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype.

Moloney C, Rayaprolu S, Howard J, Fromholt S, Brown H, Collins M, Cabrera M, Duffy C, Siemienski Z, Miller D, Swanson MS, Notterpek L, Borchelt DR, Lewis J.

Acta Neuropathol Commun. 2016 Nov 18;4(1):122. doi: 10.1186/s40478-016-0393-5. Retraction in: Acta Neuropathol Commun. 2017 Dec 13;5(1):97.

8.

Protein-rich beverage developed using non-GM soybean (R08-4004) and evaluated for sensory acceptance and shelf-life.

Nguyen Q, Hettiarachchy N, Rayaprolu S, Seo HS, Horax R, Chen P, Kumar TK.

J Food Sci Technol. 2016 Aug;53(8):3271-3281. Epub 2016 Aug 12.

9.

TREM2 p.R47H substitution is not associated with dementia with Lewy bodies.

Walton RL, Soto-Ortolaza AI, Murray ME, Lorenzo-Betancor O, Ogaki K, Heckman MG, Rayaprolu S, Rademakers R, Ertekin-Taner N, Uitti RJ, van Gerpen JA, Wszolek ZK, Smith GE, Kantarci K, Lowe VJ, Parisi JE, Jones DT, Savica R, Graff-Radford J, Knopman DS, Petersen RC, Graff-Radford NR, Ferman TJ, Dickson DW, Boeve BF, Ross OA, Labbé C.

Neurol Genet. 2016 Jul 14;2(4):e85. doi: 10.1212/NXG.0000000000000085. eCollection 2016 Aug.

10.

Bioactivity of a Rice Bran-Derived Peptide and its Sensory Evaluation and Storage Stability in Orange Juice.

Graves AM, Hettiarachchy N, Rayaprolu S, Li R, Horax R, Seo HS.

J Food Sci. 2016 Apr;81(4):H1010-5. doi: 10.1111/1750-3841.13245. Epub 2016 Feb 19.

PMID:
26894442
11.

Heterogeneity of Matrin 3 in the developing and aging murine central nervous system.

Rayaprolu S, D'Alton S, Crosby K, Moloney C, Howard J, Duffy C, Cabrera M, Siemienski Z, Hernandez AR, Gallego-Iradi C, Borchelt DR, Lewis J.

J Comp Neurol. 2016 Oct 1;524(14):2740-52. doi: 10.1002/cne.23986. Epub 2016 Jun 2.

12.

Association of Parkinson disease age of onset with DRD2, DRD3 and GRIN2B polymorphisms.

Hassan A, Heckman MG, Ahlskog JE, Wszolek ZK, Serie DJ, Uitti RJ, van Gerpen JA, Okun MS, Rayaprolu S, Ross OA.

Parkinsonism Relat Disord. 2016 Jan;22:102-5. doi: 10.1016/j.parkreldis.2015.11.016. Epub 2015 Nov 25.

13.

Electrostatic spraying of organic acids on biofilms formed by E. coli O157:H7 and Salmonella Typhimurium on fresh produce.

Almasoud A, Hettiarachchy N, Rayaprolu S, Horax R, Eswaranandam S.

Food Res Int. 2015 Dec;78:27-33. doi: 10.1016/j.foodres.2015.11.012. Epub 2015 Nov 20.

PMID:
28433292
14.

Improved functional properties of glycosylated soy protein isolate using D-glucose and xanthan gum.

Li R, Hettiarachchy N, Rayaprolu S, Davis M, Eswaranandam S, Jha A, Chen P.

J Food Sci Technol. 2015 Sep;52(9):6067-72. doi: 10.1007/s13197-014-1681-3. Epub 2015 Jan 6.

15.

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies.

Labbé C, Ogaki K, Lorenzo-Betancor O, Soto-Ortolaza AI, Walton RL, Rayaprolu S, Fujioka S, Murray ME, Heckman MG, Puschmann A, McCarthy A, Lynch T, Siuda J, Opala G, Rudzinska M, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Sanotsky Y, Rektorová I, McLean PJ, Rademakers R, Ertekin-Taner N, Hassan A, Ahlskog JE, Boeve BF, Petersen RC, Maraganore DM, Adler CH, Ferman TJ, Parisi JE, Graff-Radford NR, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA.

Neurology. 2015 Nov 10;85(19):1680-6. doi: 10.1212/WNL.0000000000001946. Epub 2015 Sep 2. Erratum in: Neurology. 2015 Nov 10;85(19):1728.

16.

Low density lipoprotein receptor related protein 1 and 6 gene variants and ischaemic stroke risk.

Harriott AM, Heckman MG, Rayaprolu S, Soto-Ortolaza AI, Diehl NN, Kanekiyo T, Liu CC, Bu G, Malik R; METASTROKE Consortium, Cole JW, Meschia JF, Ross OA.

Eur J Neurol. 2015 Aug;22(8):1235-41. doi: 10.1111/ene.12735. Epub 2015 May 29.

17.

LRRK2 exonic variants and risk of multiple system atrophy.

Heckman MG, Schottlaender L, Soto-Ortolaza AI, Diehl NN, Rayaprolu S, Ogaki K, Fujioka S, Murray ME, Cheshire WP, Uitti RJ, Wszolek ZK, Farrer MJ, Sailer A, Singleton AB, Chinnery PF, Keogh MJ, Gentleman SM, Holton JL, Aoife K, Mann DM, Al-Sarraj S, Troakes C, Dickson DW, Houlden H, Ross OA.

Neurology. 2014 Dec 9;83(24):2256-61. doi: 10.1212/WNL.0000000000001078. Epub 2014 Nov 5.

18.

Analysis of COQ2 gene in multiple system atrophy.

Ogaki K, Fujioka S, Heckman MG, Rayaprolu S, Soto-Ortolaza AI, Labbé C, Walton RL, Lorenzo-Betancor O, Wang X, Asmann Y, Rademakers R, Graff-Radford N, Uitti R, Cheshire WP, Wszolek ZK, Dickson DW, Ross OA.

Mol Neurodegener. 2014 Nov 5;9:44. doi: 10.1186/1750-1326-9-44.

19.

Functional properties and Angiotensin-I converting enzyme inhibitory activity of soy-whey proteins and fractions.

Lassissi TA, Hettiarachchy NS, Rayaprolu SJ, Kannan A, Davis M.

Food Res Int. 2014 Oct;64:598-602. doi: 10.1016/j.foodres.2014.07.015. Epub 2014 Jul 28.

PMID:
30011693
20.

VPS35 and DNAJC13 disease-causing variants in essential tremor.

Rajput A, Ross JP, Bernales CQ, Rayaprolu S, Soto-Ortolaza AI, Ross OA, van Gerpen J, Uitti RJ, Wszolek ZK, Rajput AH, Vilariño-Güell C.

Eur J Hum Genet. 2015 Jun;23(6):887-8. doi: 10.1038/ejhg.2014.164. Epub 2014 Aug 13.

21.

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data.

Holmes MV, Dale CE, Zuccolo L, Silverwood RJ, Guo Y, Ye Z, Prieto-Merino D, Dehghan A, Trompet S, Wong A, Cavadino A, Drogan D, Padmanabhan S, Li S, Yesupriya A, Leusink M, Sundstrom J, Hubacek JA, Pikhart H, Swerdlow DI, Panayiotou AG, Borinskaya SA, Finan C, Shah S, Kuchenbaecker KB, Shah T, Engmann J, Folkersen L, Eriksson P, Ricceri F, Melander O, Sacerdote C, Gamble DM, Rayaprolu S, Ross OA, McLachlan S, Vikhireva O, Sluijs I, Scott RA, Adamkova V, Flicker L, Bockxmeer FM, Power C, Marques-Vidal P, Meade T, Marmot MG, Ferro JM, Paulos-Pinheiro S, Humphries SE, Talmud PJ, Mateo Leach I, Verweij N, Linneberg A, Skaaby T, Doevendans PA, Cramer MJ, van der Harst P, Klungel OH, Dowling NF, Dominiczak AF, Kumari M, Nicolaides AN, Weikert C, Boeing H, Ebrahim S, Gaunt TR, Price JF, Lannfelt L, Peasey A, Kubinova R, Pajak A, Malyutina S, Voevoda MI, Tamosiunas A, Maitland-van der Zee AH, Norman PE, Hankey GJ, Bergmann MM, Hofman A, Franco OH, Cooper J, Palmen J, Spiering W, de Jong PA, Kuh D, Hardy R, Uitterlinden AG, Ikram MA, Ford I, Hyppönen E, Almeida OP, Wareham NJ, Khaw KT, Hamsten A, Husemoen LL, Tjønneland A, Tolstrup JS, Rimm E, Beulens JW, Verschuren WM, Onland-Moret NC, Hofker MH, Wannamethee SG, Whincup PH, Morris R, Vicente AM, Watkins H, Farrall M, Jukema JW, Meschia J, Cupples LA, Sharp SJ, Fornage M, Kooperberg C, LaCroix AZ, Dai JY, Lanktree MB, Siscovick DS, Jorgenson E, Spring B, Coresh J, Li YR, Buxbaum SG, Schreiner PJ, Ellison RC, Tsai MY, Patel SR, Redline S, Johnson AD, Hoogeveen RC, Hakonarson H, Rotter JI, Boerwinkle E, de Bakker PI, Kivimaki M, Asselbergs FW, Sattar N, Lawlor DA, Whittaker J, Davey Smith G, Mukamal K, Psaty BM, Wilson JG, Lange LA, Hamidovic A, Hingorani AD, Nordestgaard BG, Bobak M, Leon DA, Langenberg C, Palmer TM, Reiner AP, Keating BJ, Dudbridge F, Casas JP; InterAct Consortium.

BMJ. 2014 Jul 10;349:g4164. doi: 10.1136/bmj.g4164.

22.

Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease.

Shannon B, Soto-Ortolaza A, Rayaprolu S, Cannon HD, Labbé C, Benitez BA, Choi J, Lynch T, Boczarska-Jedynak M, Opala G, Krygowska-Wajs A, Barcikowska M, Van Gerpen JA, Uitti RJ, Springer W, Cruchaga C, Wszolek ZK, Ross OA.

Neurobiol Aging. 2014 Aug;35(8):1958.e1-2. doi: 10.1016/j.neurobiolaging.2014.03.004. Epub 2014 Mar 5.

23.

Frequency of APOE, MTHFR and ACE polymorphisms in the Zambian population.

Atadzhanov M, Mwaba MH, Mukomena PN, Lakhi S, Mwaba P, Rayaprolu S, Meschia JF, Ross OA.

BMC Res Notes. 2014 Mar 28;7:194. doi: 10.1186/1756-0500-7-194.

24.

Phenolics and antioxidant activity of Saskatoon berry (Amelanchier alnifolia) pomace extract.

Li R, Hettiarachchy N, Rayaprolu S, Eswaranandam S, Howe B, Davis M, Jha A.

J Med Food. 2014 Mar;17(3):384-92. doi: 10.1089/jmf.2012.0278. Epub 2014 Jan 29.

PMID:
24476215
25.

Association of the APOE, MTHFR and ACE Genes Polymorphisms and Stroke in Zambian Patients.

Atadzhanov M, Mwaba MH, Mukomena PN, Lakhi S, Rayaprolu S, Ross OA, Meschia JF.

Neurol Int. 2013 Nov 11;5(4):e20. doi: 10.4081/ni.2013.e20. eCollection 2013.

26.

GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.

Soto-Ortolaza AI, Heckman MG, Labbé C, Serie DJ, Puschmann A, Rayaprolu S, Strongosky A, Boczarska-Jedynak M, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Lynch T, Uitti RJ, Wszolek ZK, Ross OA.

Am J Neurodegener Dis. 2013 Nov 29;2(4):287-99. eCollection 2013.

27.

Investigating FUS variation in Parkinson's disease.

Labbé C, Rayaprolu S, Soto-Ortolaza A, Ogaki K, Uitti RJ, Wszolek ZK, Ross OA.

Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S147-9. doi: 10.1016/S1353-8020(13)70035-X. Review.

28.

SLC1A2 rs3794087 does not associate with essential tremor.

Ross JP, Rayaprolu S, Bernales CQ, Soto-Ortolaza AI, van Gerpen J, Uitti RJ, Wszolek ZK, Rajput A, Rajput AH, Rajput ML, Ross OA, Vilariño-Güell C.

Neurobiol Aging. 2014 Apr;35(4):935.e9-10. doi: 10.1016/j.neurobiolaging.2013.09.022. Epub 2013 Oct 16.

29.

NOTCH3 variants and risk of ischemic stroke.

Ross OA, Soto-Ortolaza AI, Heckman MG, Verbeeck C, Serie DJ, Rayaprolu S, Rich SS, Nalls MA, Singleton A, Guerreiro R, Kinsella E, Wszolek ZK, Brott TG, Brown RD Jr, Worrall BB, Meschia JF.

PLoS One. 2013 Sep 23;8(9):e75035. doi: 10.1371/journal.pone.0075035. eCollection 2013.

30.

TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease.

Rayaprolu S, Mullen B, Baker M, Lynch T, Finger E, Seeley WW, Hatanpaa KJ, Lomen-Hoerth C, Kertesz A, Bigio EH, Lippa C, Josephs KA, Knopman DS, White CL 3rd, Caselli R, Mackenzie IR, Miller BL, Boczarska-Jedynak M, Opala G, Krygowska-Wajs A, Barcikowska M, Younkin SG, Petersen RC, Ertekin-Taner N, Uitti RJ, Meschia JF, Boylan KB, Boeve BF, Graff-Radford NR, Wszolek ZK, Dickson DW, Rademakers R, Ross OA.

Mol Neurodegener. 2013 Jun 21;8:19. doi: 10.1186/1750-1326-8-19.

31.

Investigating the role of FUS exonic variants in essential tremor.

Labbé C, Soto-Ortolaza AI, Rayaprolu S, Harriott AM, Strongosky AJ, Uitti RJ, Van Gerpen JA, Wszolek ZK, Ross OA.

Parkinsonism Relat Disord. 2013 Aug;19(8):755-7. doi: 10.1016/j.parkreldis.2013.03.005. Epub 2013 Apr 16.

32.

TARDBP mutations in Parkinson's disease.

Rayaprolu S, Fujioka S, Traynor S, Soto-Ortolaza AI, Petrucelli L, Dickson DW, Rademakers R, Boylan KB, Graff-Radford NR, Uitti RJ, Wszolek ZK, Ross OA.

Parkinsonism Relat Disord. 2013 Mar;19(3):312-5. doi: 10.1016/j.parkreldis.2012.11.003. Epub 2012 Dec 8.

33.

Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome.

Dejesus-Hernandez M, Rayaprolu S, Soto-Ortolaza AI, Rutherford NJ, Heckman MG, Traynor S, Strongosky A, Graff-Radford N, Van Gerpen J, Uitti RJ, Shih JJ, Lin SC, Wszolek ZK, Rademakers R, Ross OA.

Parkinsonism Relat Disord. 2013 Feb;19(2):198-201. doi: 10.1016/j.parkreldis.2012.09.013. Epub 2012 Oct 18.

34.

A novel de novo pathogenic mutation in the CACNA1A gene.

Fujioka S, Rayaprolu S, Sundal C, Broderick DF, Langley WA, Shoffner J, Hyams LC, Rademakers R, Graff-Radford NR, Tatum W, Ross OA, Wszolek ZK.

Mov Disord. 2012 Oct;27(12):1578-9. doi: 10.1002/mds.25198. Epub 2012 Oct 4. No abstract available.

35.

Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.

Heckman MG, Soto-Ortolaza AI, Diehl NN, Rayaprolu S, Brott TG, Wszolek ZK, Meschia JF, Ross OA.

Eur J Neurol. 2013 Feb;20(2):300-8. doi: 10.1111/j.1468-1331.2012.03846.x. Epub 2012 Aug 6.

36.

Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype.

Rutherford NJ, Heckman MG, Dejesus-Hernandez M, Baker MC, Soto-Ortolaza AI, Rayaprolu S, Stewart H, Finger E, Volkening K, Seeley WW, Hatanpaa KJ, Lomen-Hoerth C, Kertesz A, Bigio EH, Lippa C, Knopman DS, Kretzschmar HA, Neumann M, Caselli RJ, White CL 3rd, Mackenzie IR, Petersen RC, Strong MJ, Miller BL, Boeve BF, Uitti RJ, Boylan KB, Wszolek ZK, Graff-Radford NR, Dickson DW, Ross OA, Rademakers R.

Neurobiol Aging. 2012 Dec;33(12):2950.e5-7. doi: 10.1016/j.neurobiolaging.2012.07.005. Epub 2012 Jul 26.

37.

Angiogenin variation and Parkinson disease.

Rayaprolu S, Soto-Ortolaza A, Rademakers R, Uitti RJ, Wszolek ZK, Ross OA.

Ann Neurol. 2012 May;71(5):725-7; author reply 727-8. doi: 10.1002/ana.23586. No abstract available.

38.

Recognition of microbial molecular patterns and stimulation of prophenoloxidase activation by a β-1,3-glucanase-related protein in Manduca sexta larval plasma.

Wang Y, Sumathipala N, Rayaprolu S, Jiang H.

Insect Biochem Mol Biol. 2011 May;41(5):322-31. doi: 10.1016/j.ibmb.2011.01.010. Epub 2011 Feb 4.

39.

Functional analysis of four processing products from multiple precursors encoded by a lebocin-related gene from Manduca sexta.

Rayaprolu S, Wang Y, Kanost MR, Hartson S, Jiang H.

Dev Comp Immunol. 2010 Jun;34(6):638-47. doi: 10.1016/j.dci.2010.01.008. Epub 2010 Jan 28.

40.

Solution structure, antibacterial activity, and expression profile of Manduca sexta moricin.

Dai H, Rayaprolu S, Gong Y, Huang R, Prakash O, Jiang H.

J Pept Sci. 2008 Jul;14(7):855-63. doi: 10.1002/psc.1016.

41.

Proteolytic activation of pro-spätzle is required for the induced transcription of antimicrobial peptide genes in lepidopteran insects.

Wang Y, Cheng T, Rayaprolu S, Zou Z, Xia Q, Xiang Z, Jiang H.

Dev Comp Immunol. 2007;31(10):1002-12. Epub 2007 Feb 12.

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