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Items: 1 to 50 of 58

1.

Methylation-derived Neutrophil-to-Lymphocyte Ratio and Lung Cancer Risk in Heavy Smokers.

Grieshober L, Graw S, Barnett MJ, Thornquist MD, Goodman GE, Chen C, Koestler DC, Marsit CJ, Doherty JA.

Cancer Prev Res (Phila). 2018 Sep 25. doi: 10.1158/1940-6207.CAPR-18-0111. [Epub ahead of print]

PMID:
30254071
2.

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures.

Begay RL, Graw SL, Sinagra G, Asimaki A, Rowland TJ, Slavov DB, Gowan K, Jones KL, Brun F, Merlo M, Miani D, Sweet M, Devaraj K, Wartchow EP, Gigli M, Puggia I, Salcedo EE, Garrity DM, Ambardekar AV, Buttrick P, Reece TB, Bristow MR, Saffitz JE, Mestroni L, Taylor MRG.

JACC Clin Electrophysiol. 2018 Apr;4(4):504-514. doi: 10.1016/j.jacep.2017.12.003. Epub 2018 Feb 2.

3.

Licofelone Enhances the Efficacy of Paclitaxel in Ovarian Cancer by Reversing Drug Resistance and Tumor Stem-like Properties.

Hirst J, Pathak HB, Hyter S, Pessetto ZY, Ly T, Graw S, Koestler DC, Krieg AJ, Roby KF, Godwin AK.

Cancer Res. 2018 Aug 1;78(15):4370-4385. doi: 10.1158/0008-5472.CAN-17-3993. Epub 2018 Jun 11.

PMID:
29891506
4.

Right precordial-directed electrocardiographical markers identify arrhythmogenic right ventricular cardiomyopathy in the absence of conventional depolarization or repolarization abnormalities.

Cortez D, Svensson A, Carlson J, Graw S, Sharma N, Brun F, Spezzacatene A, Mestroni L, Platonov PG.

BMC Cardiovasc Disord. 2017 Oct 13;17(1):261. doi: 10.1186/s12872-017-0696-x.

5.

Sustained O-GlcNAcylation reprograms mitochondrial function to regulate energy metabolism.

Tan EP, McGreal SR, Graw S, Tessman R, Koppel SJ, Dhakal P, Zhang Z, Machacek M, Zachara NE, Koestler DC, Peterson KR, Thyfault JP, Swerdlow RH, Krishnamurthy P, DiTacchio L, Apte U, Slawson C.

J Biol Chem. 2017 Sep 8;292(36):14940-14962. doi: 10.1074/jbc.M117.797944. Epub 2017 Jul 24.

6.

Mitochondrial Genomic Backgrounds Affect Nuclear DNA Methylation and Gene Expression.

Vivian CJ, Brinker AE, Graw S, Koestler DC, Legendre C, Gooden GC, Salhia B, Welch DR.

Cancer Res. 2017 Nov 15;77(22):6202-6214. doi: 10.1158/0008-5472.CAN-17-1473. Epub 2017 Jun 29.

PMID:
28663334
7.

An ensemble-based Cox proportional hazards regression framework for predicting survival in metastatic castration-resistant prostate cancer (mCRPC) patients.

Meier R, Graw S, Usset J, Raghavan R, Dai J, Chalise P, Ellis S, Fridley B, Koestler D.

F1000Res. 2016 Nov 16;5:2677. doi: 10.12688/f1000research.8226.1. eCollection 2016.

8.

Clinical and genetic characterization of adult patients presenting with non-syndromic vascular aneurysms and dissections.

D'Souza RS, Slavov D, Graw S, Jirikowic J, Todd E, Rogers RK, Taylor MR.

Int Angiol. 2017 Oct;36(5):417-427. doi: 10.23736/S0392-9590.17.03757-9. Epub 2017 Jan 31.

PMID:
28139901
9.

digit-a tool for detection and identification of genomic interchromosomal translocations.

Meier R, Graw S, Beyerlein P, Koestler D, Molina JR, Chien J.

Nucleic Acids Res. 2017 May 19;45(9):e72. doi: 10.1093/nar/gkx010.

10.

FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy.

Begay RL, Tharp CA, Martin A, Graw SL, Sinagra G, Miani D, Sweet ME, Slavov DB, Stafford N, Zeller MJ, Alnefaie R, Rowland TJ, Brun F, Jones KL, Gowan K, Mestroni L, Garrity DM, Taylor MR.

JACC Basic Transl Sci. 2016 Aug;1(5):344-359. doi: 10.1016/j.jacbts.2016.05.004. Epub 2016 Jul 27.

11.

Obscurin Variants in Patients With Left Ventricular Noncompaction.

Rowland TJ, Graw SL, Sweet ME, Gigli M, Taylor MR, Mestroni L.

J Am Coll Cardiol. 2016 Nov 15;68(20):2237-2238. doi: 10.1016/j.jacc.2016.08.052. No abstract available.

12.

A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of Cardiomyopathies.

Gigli M, Begay RL, Morea G, Graw SL, Sinagra G, Taylor MR, Granzier H, Mestroni L.

Front Cardiovasc Med. 2016 Jul 21;3:21. doi: 10.3389/fcvm.2016.00021. eCollection 2016. Review.

13.

Genetic knockout of the α7 nicotinic acetylcholine receptor gene alters hippocampal long-term potentiation in a background strain-dependent manner.

Freund RK, Graw S, Choo KS, Stevens KE, Leonard S, Dell'Acqua ML.

Neurosci Lett. 2016 Aug 3;627:1-6. doi: 10.1016/j.neulet.2016.05.043. Epub 2016 May 24.

14.

In Hypertrophic Cardiomyopathy, the Spatial Peaks QRS-T Angle Identifies Those With Sustained Ventricular Arrhythmias.

Cortez D, Graw S, Mestroni L.

Clin Cardiol. 2016 Aug;39(8):459-63. doi: 10.1002/clc.22549. Epub 2016 May 13.

15.

Role of Titin Missense Variants in Dilated Cardiomyopathy.

Begay RL, Graw S, Sinagra G, Merlo M, Slavov D, Gowan K, Jones KL, Barbati G, Spezzacatene A, Brun F, Di Lenarda A, Smith JE, Granzier HL, Mestroni L, Taylor M; Familial Cardiomyopathy Registry.

J Am Heart Assoc. 2015 Nov 13;4(11). pii: e002645. doi: 10.1161/JAHA.115.002645.

16.

Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life-Threatening Arrhythmias.

Spezzacatene A, Sinagra G, Merlo M, Barbati G, Graw SL, Brun F, Slavov D, Di Lenarda A, Salcedo EE, Towbin JA, Saffitz JE, Marcus FI, Zareba W, Taylor MR, Mestroni L; Familial Cardiomyopathy Registry.

J Am Heart Assoc. 2015 Oct 16;4(10):e002149. doi: 10.1161/JAHA.115.002149.

17.

Robust gene expression and mutation analyses of RNA-sequencing of formalin-fixed diagnostic tumor samples.

Graw S, Meier R, Minn K, Bloomer C, Godwin AK, Fridley B, Vlad A, Beyerlein P, Chien J.

Sci Rep. 2015 Jul 23;5:12335. doi: 10.1038/srep12335.

18.

The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function.

Sinkus ML, Graw S, Freedman R, Ross RG, Lester HA, Leonard S.

Neuropharmacology. 2015 Sep;96(Pt B):274-88. doi: 10.1016/j.neuropharm.2015.02.006. Epub 2015 Feb 19. Review.

19.

Danon disease: clinical features, evaluation, and management.

D'souza RS, Levandowski C, Slavov D, Graw SL, Allen LA, Adler E, Mestroni L, Taylor MR.

Circ Heart Fail. 2014 Sep;7(5):843-9. doi: 10.1161/CIRCHEARTFAILURE.114.001105. Review. No abstract available.

20.

Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy.

Brun F, Barnes CV, Sinagra G, Slavov D, Barbati G, Zhu X, Graw SL, Spezzacatene A, Pinamonti B, Merlo M, Salcedo EE, Sauer WH, Taylor MR, Mestroni L; Familial Cardiomyopathy Registry.

J Med Genet. 2014 Oct;51(10):669-76. doi: 10.1136/jmedgenet-2014-102591. Epub 2014 Aug 25.

21.

Pharmacogenetics of heart failure.

Mestroni L, Begay RL, Graw SL, Taylor MR.

Curr Opin Cardiol. 2014 May;29(3):227-34. doi: 10.1097/HCO.0000000000000056. Review.

22.

Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy.

Feldman AM, Begay RL, Knezevic T, Myers VD, Slavov DB, Zhu W, Gowan K, Graw SL, Jones KL, Tilley DG, Coleman RC, Walinsky P, Cheung JY, Mestroni L, Khalili K, Taylor MR.

J Cell Physiol. 2014 Nov;229(11):1697-702. doi: 10.1002/jcp.24615.

23.

Truncations of titin causing dilated cardiomyopathy.

Herman DS, Lam L, Taylor MR, Wang L, Teekakirikul P, Christodoulou D, Conner L, DePalma SR, McDonough B, Sparks E, Teodorescu DL, Cirino AL, Banner NR, Pennell DJ, Graw S, Merlo M, Di Lenarda A, Sinagra G, Bos JM, Ackerman MJ, Mitchell RN, Murry CE, Lakdawala NK, Ho CY, Barton PJ, Cook SA, Mestroni L, Seidman JG, Seidman CE.

N Engl J Med. 2012 Feb 16;366(7):619-28. doi: 10.1056/NEJMoa1110186.

24.

Reduced Chrna7 expression in mice is associated with decreases in hippocampal markers of inhibitory function: implications for neuropsychiatric diseases.

Adams CE, Yonchek JC, Schulz KM, Graw SL, Stitzel J, Teschke PU, Stevens KE.

Neuroscience. 2012 Apr 5;207:274-82. doi: 10.1016/j.neuroscience.2012.01.033. Epub 2012 Jan 25.

25.

Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder.

Graw SL, Swisshelm K, Floyd K, Carstens BJ, Wamboldt MZ, Ross RG, Leonard S.

Mol Cytogenet. 2012 Jan 3;5(1):2. doi: 10.1186/1755-8166-5-2.

26.

Promoter methylation and tissue-specific transcription of the α7 nicotinic receptor gene, CHRNA7.

Canastar A, Logel J, Graw S, Finlay-Schultz J, Osborne C, Palionyte M, Drebing C, Plehaty M, Wilson L, Eyeson R, Leonard S.

J Mol Neurosci. 2012 Jun;47(2):389-400. doi: 10.1007/s12031-011-9663-7. Epub 2011 Nov 4.

PMID:
22052086
27.

Genetic variation in titin in arrhythmogenic right ventricular cardiomyopathy-overlap syndromes.

Taylor M, Graw S, Sinagra G, Barnes C, Slavov D, Brun F, Pinamonti B, Salcedo EE, Sauer W, Pyxaras S, Anderson B, Simon B, Bogomolovas J, Labeit S, Granzier H, Mestroni L.

Circulation. 2011 Aug 23;124(8):876-85. doi: 10.1161/CIRCULATIONAHA.110.005405. Epub 2011 Aug 1.

28.

The chimeric gene CHRFAM7A, a partial duplication of the CHRNA7 gene, is a dominant negative regulator of α7*nAChR function.

Araud T, Graw S, Berger R, Lee M, Neveu E, Bertrand D, Leonard S.

Biochem Pharmacol. 2011 Oct 15;82(8):904-14. doi: 10.1016/j.bcp.2011.06.018. Epub 2011 Jun 28.

29.

Association of the 5'-upstream regulatory region of the alpha7 nicotinic acetylcholine receptor subunit gene (CHRNA7) with schizophrenia.

Stephens SH, Logel J, Barton A, Franks A, Schultz J, Short M, Dickenson J, James B, Fingerlin TE, Wagner B, Hodgkinson C, Graw S, Ross RG, Freedman R, Leonard S.

Schizophr Res. 2009 Apr;109(1-3):102-12. doi: 10.1016/j.schres.2008.12.017. Epub 2009 Jan 31.

30.

Danon disease presenting with dilated cardiomyopathy and a complex phenotype.

Taylor MR, Ku L, Slavov D, Cavanaugh J, Boucek M, Zhu X, Graw S, Carniel E, Barnes C, Quan D, Prall R, Lovell MA, Mierau G, Ruegg P, Mandava N, Bristow MR, Towbin JA, Mestroni L; Familial Cardiomyopathy Registry.

J Hum Genet. 2007;52(10):830-5.

PMID:
17899313
31.

Prevalence of desmin mutations in dilated cardiomyopathy.

Taylor MR, Slavov D, Ku L, Di Lenarda A, Sinagra G, Carniel E, Haubold K, Boucek MM, Ferguson D, Graw SL, Zhu X, Cavanaugh J, Sucharov CC, Long CS, Bristow MR, Lavori P, Mestroni L; Familial Cardiomyopathy Registry; BEST (Beta-Blocker Evaluation of Survival Trial) DNA Bank.

Circulation. 2007 Mar 13;115(10):1244-51. Epub 2007 Feb 26.

PMID:
17325244
32.

Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy.

Taylor MR, Slavov D, Gajewski A, Vlcek S, Ku L, Fain PR, Carniel E, Di Lenarda A, Sinagra G, Boucek MM, Cavanaugh J, Graw SL, Ruegg P, Feiger J, Zhu X, Ferguson DA, Bristow MR, Gotzmann J, Foisner R, Mestroni L; Familial Cardiomyopathy Registry Research Group.

Hum Mutat. 2005 Dec;26(6):566-74.

PMID:
16247757
33.

Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy.

Carniel E, Taylor MR, Sinagra G, Di Lenarda A, Ku L, Fain PR, Boucek MM, Cavanaugh J, Miocic S, Slavov D, Graw SL, Feiger J, Zhu XZ, Dao D, Ferguson DA, Bristow MR, Mestroni L.

Circulation. 2005 Jul 5;112(1):54-9.

PMID:
15998695
34.

BRCA1:185delAG found in the San Luis Valley probably originated in a Jewish founder.

Makriyianni I, Hamel N, Ward S, Foulkes WD, Graw S.

J Med Genet. 2005 May;42(5):e27. No abstract available.

35.

Identification of germline 185delAG BRCA1 mutations in non-Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado.

Mullineaux LG, Castellano TM, Shaw J, Axell L, Wood ME, Diab S, Klein C, Sitarik M, Deffenbaugh AM, Graw SL.

Cancer. 2003 Aug 1;98(3):597-602. Review.

36.

8p23 duplication reconsidered: is it a true euchromatic variant with no clinical manifestation?

Tsai CH, Graw SL, McGavran L.

J Med Genet. 2002 Oct;39(10):769-74. No abstract available.

37.

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, Voullaire L, Lerzo F, Rossi E, Dellavecchia C, Bonaglia MC, Digilio MC, Giannotti A, Marino B, Carrozzo R, Korenberg JR, Danesino C, Sujansky E, Dallapiccola B, Zuffardi O.

Circulation. 2000 Jul 25;102(4):432-7.

PMID:
10908216
38.

Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndrome.

Graw SL, Sample T, Bleskan J, Sujansky E, Patterson D.

Am J Hum Genet. 2000 Mar;66(3):1138-44.

39.

Integration of 30 CA-repeat markers into the cytogenetic, genetic and YAC maps of human chromosome 21.

Bosch A, Guimerà J, Graw S, Gardiner K, Chumakov I, Patterson D, Estivill X.

Eur J Hum Genet. 1996;4(3):135-42.

PMID:
8840113
40.

Molecular analysis and breakpoint definition of a set of human chromosome 21 somatic cell hybrids.

Graw SL, Gardiner K, Hall-Johnson K, Hart I, Joetham A, Walton K, Donaldson D, Patterson D.

Somat Cell Mol Genet. 1995 Nov;21(6):415-28.

PMID:
8600569
41.

YAC analysis and minimal tiling path construction for chromosome 21q.

Gardiner K, Graw S, Ichikawa H, Ohki M, Joetham A, Gervy P, Chumakov I, Patterson D.

Somat Cell Mol Genet. 1995 Nov;21(6):399-414.

PMID:
8600568
42.

A search for genes from the dark band regions of human chromosome 21.

Xu H, Wei H, Tassone F, Graw S, Gardiner K, Weissman SM.

Genomics. 1995 May 1;27(1):1-8.

PMID:
7665155
43.

Cosmid contigs spanning 9q34 including the candidate region for TSC1.

Nahmias J, Hornigold N, Fitzgibbon J, Woodward K, Pilz A, Griffin D, Henske EP, Nakamura Y, Graw S, Florian F, et al.

Eur J Hum Genet. 1995;3(2):65-77.

PMID:
7552144
44.

Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): generation of a 5-cM, > 5 megabase contig on mouse chromosome 1.

Hunter KW, Ontiveros SD, Watson ML, Stanton VP Jr, Gutierrez P, Bhat D, Rochelle J, Graw S, Ton C, Schalling M, et al.

Mamm Genome. 1994 Oct;5(10):597-607.

PMID:
7849394
45.

Identification of human chromosome 9 specific genes using exon amplification.

Church DM, Banks LT, Rogers AC, Graw SL, Housman DE, Gusella JF, Buckler AJ.

Hum Mol Genet. 1993 Nov;2(11):1915-20.

PMID:
7506603
46.

Three dinucleotide repeat polymorphisms on chromosome 9 (D9S200, D9S201, D9S199).

Graw SL, Kwiatkowski DJ.

Hum Mol Genet. 1993 May;2(5):614. No abstract available.

PMID:
8518812
47.

Genetic and physical map of the interferon region on chromosome 9p.

Fountain JW, Karayiorgou M, Taruscio D, Graw SL, Buckler AJ, Ward DC, Dracopoli NC, Housman DE.

Genomics. 1992 Sep;14(1):105-12.

PMID:
1385297
48.

Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome.

Jackson CL, Britt DE, Graw SL, Potts A, Santoro K, Buckler AJ, Housman DE, Mark HF.

Somat Cell Mol Genet. 1992 May;18(3):285-301.

PMID:
1496423
49.

Generation and characterization of a human chromosome 9 cosmid library.

Graw SL, Buckler AJ, Britt DE, Jackson CL, Taruscio D, Baldini A, Ward DC, Housman DE.

Somat Cell Mol Genet. 1992 May;18(3):269-84.

PMID:
1496422
50.

Isolation and characterization of a candidate gene for autosomal-dominant polycystic kidney disease.

Graw SL, Schalling M, Housman D, Callen DF, Klinger K, Landes G, Lerner T.

Contrib Nephrol. 1992;97:110-7. No abstract available.

PMID:
1633711

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