Pathology

E-mail this page

(All fields required)

Please enter a valid email.

Please enter your name.

Please enter a valid email.

Pathology

 

Division Publications

  1. Assa'ad AH, Gupta SK, Collins MH, Thomson M, Heath AT, Smith DA, Perschy TL, Jurgensen CH, Ortega HG, Aceves SS. An antibody against IL-5 reduces numbers of esophageal intraepithelial eosinophils in children with eosinophilic esophagitis. Gastroenterology. 2011; 141:1593-604.
  2. Brown NM, Lindley SL, Witte DP, Setchell KDR. Impact of perinatal exposure to equol enantiomers on reproductive development in rodents. Reproductive Toxicology. 2011; 32:33-42.
  3. Bulmer JN, Burton GJ, Collins S, Cotechini T, Crocker IP, Croy BA, Cvitic S, Desforges M, Deshpande R, Gasperowicz M, Groten T, Haugen G, Hiden U, Host AJ, Jirkovska M, Kiserud T, Konig J, Leach L, Murthi P, Pijnenborg R, Sadekova ON, Salafia CM, Schlabritz-Loutsevitch N, Stanek J, Wallace AE, Westermeier F, Zhang J, Lash GE. IFPA Meeting 2011 workshop report II: Angiogenic signaling and regulation of fetal endothelial function; placental and fetal circulation and growth; spiral artery remodeling. Placenta. 2012; 33 Suppl:S9-S14.
  4. Chamulitrat W, Zhang W, Xu W, Pathil A, Setchell K, Stremmel W. Hepatoprotectant ursodeoxycholyl lysophosphatidylethanolamide increasing phosphatidylcholine levels as a potential therapy of acute liver injury. Front Physiol. 2012; 3:24.
  5. Chen H, Zheng J, Xue L, Meng Y, Wang Y, Zheng B, Fang F, Shi S, Qiu Q, Jiang P, Lu Z, Mo JQ, Lu J, Guan MX. The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigrees. Eur J Hum Genet. 2012; 20:607-12.
  6. Clarkson TB, Utian WH, Barnes S, Gold EB, Basaria SS, Aso T, Kronenberg F, Frankenfeld CL, Cline JMA, Landgren BM, Gallagher JC, Weaver CM, Hodis HN, Brinton RD, Maki PM, Setchell KDR, Setchell DR, Allmen TI, Messina MJ, Shu XO, Ishimi Y, Wong WW, Kim H. The role of soy isoflavones in menopausal health: Report of the North American Menopause Society/Wulf H. Utian Translational Science Symposium in Chicago, IL (October 2010). Menopause. 2011; 18:732-753.
  7. Clerici C, Nardi E, Battezzati PM, Asciutti S, Castellani D, Corazzi N, Giuliano V, Gizzi S, Perriello G, Di Matteo G, Galli F, Setchell KD. Novel soy germ pasta improves endothelial function, blood pressure, and oxidative stress in patients with type 2 diabetes. Diabetes Care. 2011; 34:1946-8.
  8. Coe A, Collins MH, Lawal T, Louden E, Levitt MA, Pena A. Reoperation for Hirschsprung disease: pathology of the resected problematic distal pull-through. Pediatr Dev Pathol. 2012; 15:30-8.
  9. Das A, Green JV, Henson M, DeBurger B, Mortensen J. Cases in Clinical Microbiology. Case Twenty One: A Case of Asymptomatic Pulmonary Nodules. Journal of Continuing Education Topics & Issues. 2012; 14:10-14.
  10. Dickinson SI, Mo J, Cauling HS. Lymphadenopathy with Predominant Follicular Patterns. Non-Neoplastic Hematopathology and Infections. Hoboken, NJ: Wiley-Blackwell; 2012:249-284.
  11. Fernandez NC, Mortensen J. Cases in Clinical Microbiology. Urinary Schistosomiasis: A Rare Cause of Hematuria in the United States. Journal of Continuing Education Topics and Issues. 2012; 14:46-50.
  12. Grom AA, Jordan MB, Mo JQ. Disorders of Macrophages and Dentritic Cells. ACP Medicine Atlas of Dermatology: Cutaneous Manifestations of Systemic Diseases. Hamilton, Ontario: Decker Publishing; 2012.
  13. Henderson CJ, Abonia JP, King EC, Putnam PE, Collins MH, Franciosi JP, Rothenberg ME. Comparative dietary therapy effectiveness in remission of pediatric eosinophilic esophagitis. J Allergy Clin Immunol. 2012; 129:1570-8.
  14. Huang G, Zhao X, Wang L, Elf S, Xu H, Sashida G, Zhang Y, Liu Y, Lee J, Menendez S, Yang Y, Yan X, Zhang P, Tenen DG, Osato M, Hsieh JJD, Nimer SD. The ability of MLL to bind RUNX1 and methylate H3K4 at PU.1 regulatory regions is impaired by MDS/AML-associated RUNX1/AML1 mutations. Blood. 2011; 118:6544-6552.
  15. Huppert JS, Bennett K, Kollar LM, Pattullo L, Mortensen JE. MRSA: rare in the vagina. J Pediatr Adolesc Gynecol. 2011; 24:315-6.
  16. Karakukcu C, Karakukcu M, Unal E, Patiroglu T, Ozdemir MA, Torun YA, Tang PH. Coenzyme Q10 levels in beta-thalassemia and its association with ferritin levels and chelation therapy. Hemoglobin. 2012; 36:219-29.
  17. King BA, Boyd JT, Kingma PS. Pulmonary maturational arrest and death in a patient with pulmonary interstitial glycogenosis. Pediatr Pulmonol. 2011; 46:1142-5.
  18. Kupert E, Anderson M, Liu Y, Succop P, Levin L, Wang J, Wikenheiser-brokamp K, Chen P, Pinney SM, Macdonald T, Dong Z, Starnes S, Lu S. Plasma secretory phospholipase A2-IIa as a potential biomarker for lung cancer in patients with solitary pulmonary nodules. BMC Cancer. 2011; 11:513.
  19. Ladd PE, Emery KH, Salisbury SR, Laor T, Lovell DJ, Bove KE. Juvenile dermatomyositis: correlation of MRI at presentation with clinical outcome. AJR Am J Roentgenol. 2011; 197:W153-8.
  20. Laor T, Stanek J, Leach JL. Diprosopus tetraophthalmus: CT as a complement to autopsy. Br J Radiol. 2012; 85:e10-3.
  21. Levantini E, Lee S, Radomska HS, Hetherington CJ, Alberich-Jorda M, Amabile G, Zhang P, Gonzalez DA, Zhang J, Basseres DS, Wilson NK, Koschmieder S, Huang G, Zhang DE, Ebralidze AK, Bonifer C, Okuno Y, Gottgens B, Tenen DG. RUNX1 regulates the CD34 gene in haematopoietic stem cells by mediating interactions with a distal regulatory element. EMBO Journal. 2011; 30:4059-4070.
  22. Levy M, Trivedi A, Zhang J, Miles L, Mattis AN, Kim GE, Lassman C, Anders RA, Misdraji J, Yerian LM, Xu H, Dhall D, Wang HL. Expression of glypican-3 in undifferentiated embryonal sarcoma and mesenchymal hamartoma of the liver. Hum Pathol. 2012; 43:695-701.
  23. Lu Z, Chen H, Meng Y, Wang Y, Xue L, Zhi S, Qiu Q, Yang L, Mo JQ, Guan MX. The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree. Eur J Hum Genet. 2011; 19:1181-6.
  24. Luo G, Gerrety M, DeBurger B, Pfeffer J, McMasters R, Mortensen J. Cases in Clinical Microbiology. Case Twenty Two: A Disseminated Infection. Journal of Continuing Education Topics and Issues. 2012; 14:22-25.
  25. Maugans T, Sheridan RM, Adams D, Gupta A. Cutaneous vascular anomalies associated with neural tube defects: Nomenclature and pathology revisited. Neurosurgery. 2011; 69:112-118.
  26. Melvin A, Litsky A, Mayerson J, Stringer K, Melvin D, Juncosa-Melvin N. An artificial tendon to connect the quadriceps muscle to the tibia. J Orthop Res. 2011; 29:1775-82.
  27. Miles MV, Miles L, Horn PS, DeGrauw TJ. Enzyme inducing antiepileptic drugs are associated with mitochondrial proliferation and increased cytochrome c oxidase activity in muscle of children with epilepsy. Epilepsy Res. 2012; 98:76-87.
  28. Molho-Pessach V, Rios JJ, Xing C, Setchell KD, Cohen JC, Hobbs HH. Homozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology. Hepatology. 2012; 55:1139-45.
  29. Nkinin SW, Stringer JR, Keely SP, Setchell KDR, Giner JL, Kaneshiro ES. Pneumocystis carinii sterol 14α-demethylase activity in saccharomyces cerevisiae erg11 knockout mutant: Sterol biochemistry. Journal of Eukaryotic Microbiology. 2011; 58:383-392.
  30. O'Leary MF. (2012) Hematocrit. Medscape Reference. .
  31. Pai R, French D, Ma N, Hotzel K, Plise E, Salphati L, Setchell KD, Ware J, Lauriault V, Schutt L, Hartley D, Dambach D. Antibody-mediated inhibition of fibroblast growth factor 19 results in increased bile acids synthesis and ileal malabsorption of bile acids in cynomolgus monkeys. Toxicol Sci. 2012; 126:446-56.
  32. Pardo AC, Do T, Ryder T, Meyer A, Miles L, Wong BL. Combination of steroids and ischial weight-bearing knee ankle foot orthoses in Duchenne's muscular dystrophy prolongs ambulation past 20 years of age--a case report. Neuromuscul Disord. 2011; 21:800-2.
  33. Schroer KT, Gibson AM, Sivaprasad U, Bass SA, Ericksen MB, Wills-Karp M, Lecras T, Fitzpatrick AM, Brown LA, Stringer KF, Hershey GK. Downregulation of glutathione S-transferase pi in asthma contributes to enhanced oxidative stress. J Allergy Clin Immunol. 2011; 128:539-48.
  34. Setchell KD, Brown NM, Zhao X, Lindley SL, Heubi JE, King EC, Messina MJ. Soy isoflavone phase II metabolism differs between rodents and humans: implications for the effect on breast cancer risk. Am J Clin Nutr. 2011; 94:1284-94.
  35. Sheridan RM, Gupta A, Miethke A, Knisely AS, Bove KE. Multiple dysplastic liver nodules in PFIC2 underscore risk for neoplasia associated with functional BSEP deficiency. Am J Surg Pathol. 2012; 36:785-6.
  36. Sheridan RM, Michelfelder EC, Choe KA, Divanovic A, Liu C, Ware S, Stanek J. Ductus arteriosus aneurysm with massive thrombosis of pulmonary artery and fetal hydrops. Pediatr Dev Pathol. 2012; 15:79-85.
  37. Sourris KC, Harcourt BE, Tang PH, Morley AL, Huynh K, Penfold SA, Coughlan MT, Cooper ME, Nguyen TV, Ritchie RH, Forbes JM. Ubiquinone (coenzyme Q10) prevents renal mitochondrial dysfunction in an experimental model of type 2 diabetes. Free Radic Biol Med. 2012; 52:716-23.
  38. Spergel JM, Rothenberg ME, Collins MH, Furuta GT, Markowitz JE, Fuchs G, 3rd, O'Gorman MA, Abonia JP, Young J, Henkel T, Wilkins HJ, Liacouras CA. Reslizumab in children and adolescents with eosinophilic esophagitis: results of a double-blind, randomized, placebo-controlled trial. J Allergy Clin Immunol. 2012; 129:456-63, 463 e1-3.
  39. Stanek J. Utility of diagnosing various histological patterns of diffuse chronic hypoxic placental injury. Pediatr Dev Pathol. 2012; 15:13-23.
  40. Stanek J. Chorionic disk extravillous trophoblasts in placental diagnosis. Am J Clin Pathol. 2011; 136:540-7.
  41. Stanek J, Biesiada J. Sensitivity and specificity of finding of multinucleate trophoblastic giant cells in decidua in placentas from high-risk pregnancies. Hum Pathol. 2012; 43:261-8.
  42. Stanek J, Biesiada J. Clustering of maternal-fetal clinical conditions and outcomes and placental lesions. Am J Obstet Gynecol. 2012; 206:493 e1-8.
  43. Strait RT, Hicks W, Barasa N, Mahler A, Khodoun M, Kohl J, Stringer K, Witte D, Van Rooijen N, Susskind BM, Finkelman FD. MHC class I-specific antibody binding to nonhematopoietic cells drives complement activation to induce transfusion-related acute lung injury in mice. J Exp Med. 2011; 208:2525-44.
  44. Straumann A, Aceves SS, Blanchard C, Collins MH, Furuta GT, Hirano I, Schoepfer AM, Simon D, Simon HU. Pediatric and adult eosinophilic esophagitis: similarities and differences. Allergy. 2012; 67:477-90.
  45. Strother DR, London WB, Schmidt ML, Brodeur GM, Shimada H, Thorner P, Collins MH, Tagge E, Adkins S, Reynolds CP, Murray K, Lavey RS, Matthay KK, Castleberry R, Maris JM, Cohn SL. Outcome after surgery alone or with restricted use of chemotherapy for patients with low-risk neuroblastoma: results of Children's Oncology Group study P9641. J Clin Oncol. 2012; 30:1842-8.
  46. Sun Y, Liou B, Xu YH, Quinn B, Zhang W, Hamler R, Setchell KD, Grabowski GA. Ex vivo and in vivo effects of isofagomine on acid beta-glucosidase variants and substrate levels in Gaucher disease. J Biol Chem. 2012; 287:4275-87.
  47. Tang PH, Miles MV. Measurement of oxidized and reduced coenzyme Q in biological fluids, cells, and tissues: an HPLC-EC method. Methods Mol Biol. 2012; 837:149-68.
  48. Wang L, Gural A, Sun XJ, Zhao X, Perna F, Huang G, Hatlen MA, Vu L, Liu F, Xu H, Asai T, Deblasio T, Menendez S, Voza F, Jiang Y, Cole PA, Zhang J, Melnick A, Roeder RG, Nimer SD. The leukemogenicity of AML1-ETO is dependent on site-specific lysine acetylation. Science. 2011; 333:765-9.
  49. Yan X, Wang X, Wang Z, Sun S, Chen G, He Y, Mo JQ, Li R, Jiang P, Lin Q, Sun M, Li W, Bai Y, Zhang J, Zhu Y, Lu J, Yan Q, Li H, Guan MX. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene. J Med Genet. 2011; 48:682-90.
  50. Yin H, Boyd T, Pacheco MC, Schonfeld D, Bove KE. Rectal biopsy in children with Down syndrome and chronic constipation: Hirschsprung disease vs non-hirschsprung disease. Pediatr Dev Pathol. 2012; 15:87-95.
Please give to Cincinnati Children's.
US News 2013 FooterBest Places to Work Logo

3333 Burnet Avenue, Cincinnati, Ohio 45229-3026 | 1-513-636-4200 | 1-800-344-2462 | TTY:1-513-636-4900

New to Cincinnati Children’s or live outside of the tri-state area? 1-877-881-8479

© 1999-2013 Cincinnati Children's Hospital Medical Center