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Items: 1 to 50 of 76

1.

Altered T-Cell Balance in Lymphoid Organs of a Mouse Model of Colorectal Cancer.

Tanner SM, Daft JG, Hill SA, Martin CA, Lorenz RG.

J Histochem Cytochem. 2016 Dec;64(12):753-767. Epub 2016 Oct 20.

2.

Environmental-mediated intestinal homeostasis in neonatal mice.

Culbreath C, Tanner SM, Yeramilli VA, Berryhill TF, Lorenz RG, Martin CA.

J Surg Res. 2015 Oct;198(2):494-501. doi: 10.1016/j.jss.2015.04.002. Epub 2015 Apr 10.

PMID:
25940157
3.

Pathogenesis of necrotizing enterocolitis: modeling the innate immune response.

Tanner SM, Berryhill TF, Ellenburg JL, Jilling T, Cleveland DS, Lorenz RG, Martin CA.

Am J Pathol. 2015 Jan;185(1):4-16. doi: 10.1016/j.ajpath.2014.08.028. Epub 2014 Nov 4. Review.

4.

Consumption of acidic water alters the gut microbiome and decreases the risk of diabetes in NOD mice.

Wolf KJ, Daft JG, Tanner SM, Hartmann R, Khafipour E, Lorenz RG.

J Histochem Cytochem. 2014 Apr;62(4):237-50. doi: 10.1369/0022155413519650. Epub 2014 Jan 22.

5.

A randomized trial of temazepam versus acetazolamide in high altitude sleep disturbance.

Tanner JB, Tanner SM, Thapa GB, Chang Y, Watson KL, Staunton E, Howarth C, Basnyat B, Harris NS.

High Alt Med Biol. 2013 Sep;14(3):234-9. doi: 10.1089/ham.2013.1023. Epub 2013 Sep 12.

6.

Hereditary intrinsic factor deficiency in chaldeans.

Sturm AC, Baack EC, Armstrong MB, Schiff D, Zia A, Savasan S, de la Chapelle A, Tanner SM.

JIMD Rep. 2013;7:13-8. doi: 10.1007/8904_2012_133. Epub 2012 Mar 18.

7.

Germline allele-specific expression of DAPK1 in chronic lymphocytic leukemia.

Wei QX, Claus R, Hielscher T, Mertens D, Raval A, Oakes CC, Tanner SM, de la Chapelle A, Byrd JC, Stilgenbauer S, Plass C.

PLoS One. 2013;8(1):e55261. doi: 10.1371/journal.pone.0055261. Epub 2013 Jan 28.

8.

Maintenance of host leukocytes in peripheral immune compartments following lethal irradiation and bone marrow reconstitution: implications for graft versus host disease.

Staley EM, Tanner SM, Daft JG, Stanus AL, Martin SM, Lorenz RG.

Transpl Immunol. 2013 Mar;28(2-3):112-9. doi: 10.1016/j.trim.2013.01.001. Epub 2013 Jan 17.

9.

Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.

Tanner SM, Sturm AC, Baack EC, Liyanarachchi S, de la Chapelle A.

Orphanet J Rare Dis. 2012 Aug 28;7:56. doi: 10.1186/1750-1172-7-56.

10.

Altered generation of induced regulatory T cells in the FVB.mdr1a-/- mouse model of colitis.

Tanner SM, Staley EM, Lorenz RG.

Mucosal Immunol. 2013 Mar;6(2):309-23. doi: 10.1038/mi.2012.73. Epub 2012 Aug 8.

11.

Murine P-glycoprotein deficiency alters intestinal injury repair and blunts lipopolysaccharide-induced radioprotection.

Staley EM, Yarbrough VR, Schoeb TR, Daft JG, Tanner SM, Steverson D Jr, Lorenz RG.

Radiat Res. 2012 Sep;178(3):207-16. Epub 2012 Jul 10.

12.

Imerslund-Gräsbeck syndrome: new mutation in amnionless.

Densupsoontorn N, Sanpakit K, Vijarnsorn C, Pattaragarn A, Kangwanpornsiri C, Jatutipsompol C, Tirapongporn H, Jirapinyo P, Shah NP, Sturm AC, Tanner SM.

Pediatr Int. 2012 Jun;54(3):e19-21. doi: 10.1111/j.1442-200X.2011.03482.x. No abstract available.

PMID:
22631584
13.

Acute lymphoblastic leukemia and vitamin B12 deficiency secondary to a gastric intrinsic factor gene mutation.

Zia A, Fışgin T, Sokolowski C, Tanner SM, Savaşan S.

Pediatr Blood Cancer. 2012 Oct;59(4):766-7. doi: 10.1002/pbc.24190. Epub 2012 May 3. No abstract available.

PMID:
22556038
14.

miR-3151 interplays with its host gene BAALC and independently affects outcome of patients with cytogenetically normal acute myeloid leukemia.

Eisfeld AK, Marcucci G, Maharry K, Schwind S, Radmacher MD, Nicolet D, Becker H, Mrózek K, Whitman SP, Metzeler KH, Mendler JH, Wu YZ, Liyanarachchi S, Patel R, Baer MR, Powell BL, Carter TH, Moore JO, Kolitz JE, Wetzler M, Caligiuri MA, Larson RA, Tanner SM, de la Chapelle A, Bloomfield CD.

Blood. 2012 Jul 12;120(2):249-58. doi: 10.1182/blood-2012-02-408492. Epub 2012 Apr 23.

15.

Heritable polymorphism predisposes to high BAALC expression in acute myeloid leukemia.

Eisfeld AK, Marcucci G, Liyanarachchi S, Döhner K, Schwind S, Maharry K, Leffel B, Döhner H, Radmacher MD, Bloomfield CD, Tanner SM, de la Chapelle A.

Proc Natl Acad Sci U S A. 2012 Apr 24;109(17):6668-73. doi: 10.1073/pnas.1203756109. Epub 2012 Apr 9.

16.

Familial peripheral keratopathy without PAX6 mutation.

Smith WM, Lange JM, Sturm AC, Tanner SM, Mauger TF.

Cornea. 2012 Feb;31(2):130-3. doi: 10.1097/ICO.0b013e3182222779.

PMID:
22146551
17.

Juvenile cobalamin deficiency in a 17-year-old child with autonomic dysfunction and skin changes.

Siddiqui AH, Ansari A, Beech CM, Shah NP, Tanner SM, Sarnaik SA.

J Pediatr Hematol Oncol. 2012 Mar;34(2):140-2. doi: 10.1097/MPH.0b013e3182288249.

18.

Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities.

Beech CM, Liyanarachchi S, Shah NP, Sturm AC, Sadiq MF, de la Chapelle A, Tanner SM.

Orphanet J Rare Dis. 2011 Nov 13;6:74. doi: 10.1186/1750-1172-6-74.

19.

Variants in the netrin-1 receptor UNC5C prevent apoptosis and increase risk of familial colorectal cancer.

Coissieux MM, Tomsic J, Castets M, Hampel H, Tuupanen S, Andrieu N, Comeras I, Drouet Y, Lasset C, Liyanarachchi S, Mazelin L, Puisieux A, Saurin JC, Scoazec JY, Wang Q, Aaltonen L, Tanner SM, de la Chapelle A, Bernet A, Mehlen P.

Gastroenterology. 2011 Dec;141(6):2039-46. doi: 10.1053/j.gastro.2011.08.041. Epub 2011 Sep 3.

20.

[Homozygous mutation in the intrinsic factor gene in a child with severe vitamin B12 deficiency].

Leunbach TL, Johansen P, Tanner SM, Gräsbeck R, Helgestad J.

Ugeskr Laeger. 2011 Aug 22;173(34):2047-8. Danish.

PMID:
21867658
21.

Helicobacter felis--associated gastric disease in microbiota-restricted mice.

Schmitz JM, Durham CG, Schoeb TR, Soltau TD, Wolf KJ, Tanner SM, McCracken VJ, Lorenz RG.

J Histochem Cytochem. 2011 Sep;59(9):826-41. doi: 10.1369/0022155411416242.

22.

Critical role for P-glycoprotein expression in hematopoietic cells in the FVB.Mdr1a(-/-) model of colitis.

Staley EM, Dimmitt RA, Schoeb TR, Tanner SM, Lorenz RG.

J Pediatr Gastroenterol Nutr. 2011 Dec;53(6):666-73. doi: 10.1097/MPG.0b013e31822860f1.

23.

Juvenile selective vitamin B₁₂ malabsorption: 50 years after its description-10 years of genetic testing.

Gräsbeck R, Tanner SM.

Pediatr Res. 2011 Sep;70(3):222-8. doi: 10.1203/PDR.0b013e3182242124. Review.

24.

Investigation of the ABC transporter MRP1 in selected patients with presumed defects in vitamin B12 absorption.

Shah NP, Beech CM, Sturm AC, Tanner SM.

Blood. 2011 Apr 21;117(16):4397-8. doi: 10.1182/blood-2010-12-322750. No abstract available.

25.

Allele-specific expression of TGFBR1 in colon cancer patients.

Tomsic J, Guda K, Liyanarachchi S, Hampel H, Natale L, Markowitz SD, Tanner SM, de la Chapelle A.

Carcinogenesis. 2010 Oct;31(10):1800-4. doi: 10.1093/carcin/bgq165. Epub 2010 Aug 12.

26.

Role of postnatal acquisition of the intestinal microbiome in the early development of immune function.

Dimmitt RA, Staley EM, Chuang G, Tanner SM, Soltau TD, Lorenz RG.

J Pediatr Gastroenterol Nutr. 2010 Sep;51(3):262-73. doi: 10.1097/MPG.0b013e3181e1a114.

27.

Vitamin B12 deficiency in a 15-year old boy due to mutations in the intrinsic factor gene, GIF.

Overgaard UM, Tanner SM, Birgens HS.

Br J Haematol. 2010 Aug;150(3):369-71. doi: 10.1111/j.1365-2141.2010.08198.x. Epub 2010 Apr 12. No abstract available.

28.

RelA/p65 functions to maintain cellular senescence by regulating genomic stability and DNA repair.

Wang J, Jacob NK, Ladner KJ, Beg A, Perko JD, Tanner SM, Liyanarachchi S, Fishel R, Guttridge DC.

EMBO Rep. 2009 Nov;10(11):1272-8. doi: 10.1038/embor.2009.197. Epub 2009 Sep 25.

29.

Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients.

Guda K, Natale L, Lutterbaugh J, Wiesner GL, Lewis S, Tanner SM, Tomsic J, Valle L, de la Chapelle A, Elston RC, Willis J, Markowitz SD.

Cancer Res. 2009 Jun 15;69(12):4959-61. doi: 10.1158/0008-5472.CAN-09-0225. Epub 2009 Jun 9.

30.

Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF.

Ament AE, Li Z, Sturm AC, Perko JD, Lawson S, Masterson M, Quadros EV, Tanner SM.

Br J Haematol. 2009 Feb;144(4):622-4. doi: 10.1111/j.1365-2141.2008.07496.x. Epub 2008 Nov 19. No abstract available.

31.

Germline allele-specific expression of TGFBR1 confers an increased risk of colorectal cancer.

Valle L, Serena-Acedo T, Liyanarachchi S, Hampel H, Comeras I, Li Z, Zeng Q, Zhang HT, Pennison MJ, Sadim M, Pasche B, Tanner SM, de la Chapelle A.

Science. 2008 Sep 5;321(5894):1361-5. doi: 10.1126/science.1159397. Epub 2008 Aug 14.

32.

Direct evidence for epithelial-mesenchymal transitions in breast cancer.

Trimboli AJ, Fukino K, de Bruin A, Wei G, Shen L, Tanner SM, Creasap N, Rosol TJ, Robinson ML, Eng C, Ostrowski MC, Leone G.

Cancer Res. 2008 Feb 1;68(3):937-45. doi: 10.1158/0008-5472.CAN-07-2148.

33.

Amnionless (AMN) mutations in Imerslund-Gräsbeck syndrome may be associated with disturbed vitamin B12 transport into the CNS.

Luder AS, Tanner SM, de la Chapelle A, Walter JH.

J Inherit Metab Dis. 2008 Dec;31 Suppl 3:493-6. doi: 10.1007/s10545-007-0760-2. Epub 2008 Jan 7.

PMID:
18181028
34.

Molecular profiling of chronic lymphocytic leukaemia: genetics meets epigenetics to identify predisposing genes.

Plass C, Byrd JC, Raval A, Tanner SM, de la Chapelle A.

Br J Haematol. 2007 Dec;139(5):744-52. Epub 2007 Oct 24. Review.

PMID:
17961188
35.

Imerslund-Gräsbeck syndrome in a 15-year-old German girl caused by compound heterozygous mutations in CUBN.

Hauck FH, Tanner SM, Henker J, Laass MW.

Eur J Pediatr. 2008 Jun;167(6):671-5. Epub 2007 Aug 1.

PMID:
17668238
36.

Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia.

Raval A, Tanner SM, Byrd JC, Angerman EB, Perko JD, Chen SS, Hackanson B, Grever MR, Lucas DM, Matkovic JJ, Lin TS, Kipps TJ, Murray F, Weisenburger D, Sanger W, Lynch J, Watson P, Jansen M, Yoshinaga Y, Rosenquist R, de Jong PJ, Coggill P, Beck S, Lynch H, de la Chapelle A, Plass C.

Cell. 2007 Jun 1;129(5):879-90.

37.

Knee-specific quality-of-life instruments: which ones measure symptoms and disabilities most important to patients?

Tanner SM, Dainty KN, Marx RG, Kirkley A.

Am J Sports Med. 2007 Sep;35(9):1450-8. Epub 2007 May 14.

PMID:
17502427
38.

Reconstruction of the proximal tibiofibular joint: a case report.

Tanner SM, Brinks KF.

Clin J Sport Med. 2007 Jan;17(1):75-7. No abstract available.

PMID:
17304013
39.

Imerslund-Grasbeck syndrome associated with recurrent aphthous stomatitis and defective neutrophil function.

Broides A, Yerushalmi B, Levy R, Hadad N, Kaplun N, Tanner SM, Chapelle Ade L, Levy J.

J Pediatr Hematol Oncol. 2006 Nov;28(11):715-9.

PMID:
17114957
40.

Differential gene expression in patients genetically predisposed to pancreatic cancer.

Zervos EE, Tanner SM, Osborne DA, Bloomston M, Rosemurgy AS, Ellison EC, Melvin WS, de la Chapelle A.

J Surg Res. 2006 Oct;135(2):317-22. Epub 2006 Jun 30.

PMID:
16815451
41.

Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in Jordan.

Al-Alami JR, Tanner SM, Tayeh MK, de la Chapelle A, El-Shanti H.

Saudi Med J. 2005 Jul;26(7):1061-4.

PMID:
16047053
42.

Myopathy with skeletal asymmetry and hemidiaphragm elevation is caused by myotubularin mutations.

Grogan PM, Tanner SM, Ørstavik KH, Knudsen GP, Saperstein DS, Vogel H, Barohn RJ, Herbelin LL, McVey AL, Katz JS.

Neurology. 2005 May 10;64(9):1638-40.

PMID:
15883335
43.

Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo.

He Q, Madsen M, Kilkenney A, Gregory B, Christensen EI, Vorum H, Højrup P, Schäffer AA, Kirkness EF, Tanner SM, de la Chapelle A, Giger U, Moestrup SK, Fyfe JC.

Blood. 2005 Aug 15;106(4):1447-53. Epub 2005 Apr 21.

44.

Baalc, a marker of mesoderm and muscle.

Satoskar AA, Tanner SM, Weinstein M, Qualman SJ, de la Chapelle A.

Gene Expr Patterns. 2005 Apr;5(4):463-73.

PMID:
15749074
45.

Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.

Tanner SM, Li Z, Perko JD, Oner C, Cetin M, Altay C, Yurtsever Z, David KL, Faivre L, Ismail EA, Gräsbeck R, de la Chapelle A.

Proc Natl Acad Sci U S A. 2005 Mar 15;102(11):4130-3. Epub 2005 Feb 28.

46.

Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East.

Tanner SM, Li Z, Bisson R, Acar C, Oner C, Oner R, Cetin M, Abdelaal MA, Ismail EA, Lissens W, Krahe R, Broch H, Gräsbeck R, de la Chapelle A.

Hum Mutat. 2004 Apr;23(4):327-33.

PMID:
15024727
47.

Acute myeloid leukemia with complex karyotypes and abnormal chromosome 21: Amplification discloses overexpression of APP, ETS2, and ERG genes.

Baldus CD, Liyanarachchi S, Mrózek K, Auer H, Tanner SM, Guimond M, Ruppert AS, Mohamed N, Davuluri RV, Caligiuri MA, Bloomfield CD, de la Chapelle A.

Proc Natl Acad Sci U S A. 2004 Mar 16;101(11):3915-20. Epub 2004 Mar 8.

48.

A modified test for patellar instability: the biomechanical basis.

Tanner SM, Garth WP Jr, Soileau R, Lemons JE.

Clin J Sport Med. 2003 Nov;13(6):327-38.

PMID:
14608221
49.

BAALC, a novel marker of human hematopoietic progenitor cells.

Baldus CD, Tanner SM, Kusewitt DF, Liyanarachchi S, Choi C, Caligiuri MA, Bloomfield CD, de la Chapelle A.

Exp Hematol. 2003 Nov;31(11):1051-6.

PMID:
14585369
50.

The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless.

Fyfe JC, Madsen M, Højrup P, Christensen EI, Tanner SM, de la Chapelle A, He Q, Moestrup SK.

Blood. 2004 Mar 1;103(5):1573-9. Epub 2003 Oct 23.

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