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Chromosomal autonomy of hMLH1 methylation in colon cancer.
Li H, Myeroff L, Kasturi L, Krumroy L, Schwartz S, Willson JK, Stanbridge E, Casey G, Markowitz S. Li H, et al. Among authors: schwartz s. Oncogene. 2002 Feb 21;21(9):1443-9. doi: 10.1038/sj.onc.1205247. Oncogene. 2002. PMID: 11857087
p53 mutations in bladder carcinoma cell lines.
Cooper MJ, Haluschak JJ, Johnson D, Schwartz S, Morrison LJ, Lippa M, Hatzivassiliou G, Tan J. Cooper MJ, et al. Among authors: schwartz s. Oncol Res. 1994;6(12):569-79. Oncol Res. 1994. PMID: 7787250
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.
Alagramam KN, Yuan H, Kuehn MH, Murcia CL, Wayne S, Srisailpathy CR, Lowry RB, Knaus R, Van Laer L, Bernier FP, Schwartz S, Lee C, Morton CC, Mullins RF, Ramesh A, Van Camp G, Hageman GS, Woychik RP, Smith RJ. Alagramam KN, et al. Among authors: schwartz s. Hum Mol Genet. 2001 Aug 1;10(16):1709-18. doi: 10.1093/hmg/10.16.1709. Hum Mol Genet. 2001. PMID: 11487575
Bascom Headen Palmer, Jr., MD (1889-1954).
Alfonso EC, Schwartz SG, Jacko VA, Clarkson JG. Alfonso EC, et al. Among authors: schwartz sg. Am J Ophthalmol. 2024 Sep 14:S0002-9394(24)00430-6. doi: 10.1016/j.ajo.2024.09.010. Online ahead of print. Am J Ophthalmol. 2024. PMID: 39284483
Kidney Health Monitoring in Neonatal Intensive Care Unit Graduates: A Modified Delphi Consensus Statement.
Starr MC, Harer MW, Steflik HJ, Gorga S, Ambalavanan N, Beck TM, Chaudhry PM, Chmielewski JL, Defreitas MJ, Fuhrman DY, Hanna M, Joseph C, Kwiatkowski DM, Krawczeski CD, Liberio BM, Menon S, Mohamed TH, Rumpel JA, Sanderson KR, Schuh MP, Segar JL, Slagle CL, Soranno DE, Vuong KT, Charlton JR, Gist KM, Askenazi DJ, Selewski DT; Neonatal Kidney Health Consensus Workshop. Starr MC, et al. JAMA Netw Open. 2024 Sep 3;7(9):e2435043. doi: 10.1001/jamanetworkopen.2024.35043. JAMA Netw Open. 2024. PMID: 39269711 Free article.
5,677 results