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Items: 1 to 50 of 104

1.

RepSox slows decay of CD34+ acute myeloid leukemia cells and decreases T cell immunoglobulin mucin-3 expression.

Jajosky AN, Coad JE, Vos JA, Martin KH, Senft JR, Wenger SL, Gibson LF.

Stem Cells Transl Med. 2014 Jul;3(7):836-48. doi: 10.5966/sctm.2013-0193. Epub 2014 May 22.

2.

Decreased telomere length in metaphase and interphase cells from newborns with trisomy 21.

Wenger SL, Hansroth J, Shackelford AL.

Gene. 2014 May 25;542(1):87. doi: 10.1016/j.gene.2014.03.019. Epub 2014 Mar 11. No abstract available.

PMID:
24630967
3.

c-MYC Amplification in Acute Myelogenous Leukemia Evolving from Double Minutes (dmins) to Homogeneously Staining Region (hsr).

Sayedian F, Senft JR, Spruill MD, Wenger SL, Vos JA.

J Assoc Genet Technol. 2014;40(2):64-7.

PMID:
26029796
4.

Persistent mosaicism for 12p duplication/triplication chromosome structural abnormality in peripheral blood.

Shackelford AL, Conlin LK, Hummel M, Spinner NB, Wenger SL.

Case Rep Genet. 2013;2013:857926. doi: 10.1155/2013/857926. Epub 2013 Sep 15.

5.
6.
7.

Human telomere length correlates to the size of the associated chromosome arm.

Wise JL, Crout RJ, McNeil DW, Weyant RJ, Marazita ML, Wenger SL.

PLoS One. 2009 Jun 23;4(6):e6013. doi: 10.1371/journal.pone.0006013.

8.

Cryptic subtelomeric rearrangements and X chromosome mosaicism: a study of 565 apparently normal individuals with fluorescent in situ hybridization.

Wise JL, Crout RJ, McNeil DW, Weyant RJ, Marazita ML, Wenger SL.

PLoS One. 2009 Jun 10;4(6):e5855. doi: 10.1371/journal.pone.0005855.

9.

Del(5q) is associated with clinical and histological parameters in small cell neuroendocrine lung carcinoma.

Hartel PH, Shackelford AL, Hartel JV, Wenger SL.

Int J Surg Pathol. 2008 Oct;16(4):419-23. doi: 10.1177/1066896908318935. Epub 2008 May 28.

PMID:
18508840
10.

BRCA1 contributes to cell cycle arrest and chemoresistance in response to the anticancer agent irofulven.

Wiltshire T, Senft J, Wang Y, Konat GW, Wenger SL, Reed E, Wang W.

Mol Pharmacol. 2007 Apr;71(4):1051-60. Epub 2007 Jan 17.

PMID:
17229870
11.

Fanconi anemia D2 protein confers chemoresistance in response to the anticancer agent, irofulven.

Wang Y, Wiltshire T, Senft J, Wenger SL, Reed E, Wang W.

Mol Cancer Ther. 2006 Dec;5(12):3153-61.

12.

The spectrum of WRN mutations in Werner syndrome patients.

Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, Poot M, Rubin CD, Chen DF, Yang CC, Juch H, Dorn T, Spiegel R, Oral EA, Abid M, Battisti C, Lucci-Cordisco E, Neri G, Steed EH, Kidd A, Isley W, Showalter D, Vittone JL, Konstantinow A, Ring J, Meyer P, Wenger SL, von Herbay A, Wollina U, Schuelke M, Huizenga CR, Leistritz DF, Martin GM, Mian IS, Oshima J.

Hum Mutat. 2006 Jun;27(6):558-67.

13.

Molecular characterization of an 11q interstitial deletion in a patient with the clinical features of Jacobsen syndrome.

Wenger SL, Grossfeld PD, Siu BL, Coad JE, Keller FG, Hummel M.

Am J Med Genet A. 2006 Apr 1;140(7):704-8.

PMID:
16502431
14.

Cytogenetic analysis in various tissues of pregnancy loss.

Bennett J, Obringer AC, Williams HJ, Wenger SL.

Genet Med. 2006 Feb;8(2):136. No abstract available.

PMID:
16481899
15.

The Pittsburgh Oral-Facial Cleft study: expanding the cleft phenotype. Background and justification.

Weinberg SM, Neiswanger K, Martin RA, Mooney MP, Kane AA, Wenger SL, Losee J, Deleyiannis F, Ma L, De Salamanca JE, Czeizel AE, Marazita ML.

Cleft Palate Craniofac J. 2006 Jan;43(1):7-20. Review.

PMID:
16405378
16.

Cell death as a possible mechanism for tissue limited mosaicism in Pallister-Killian syndrome.

Tang W, Wenger SL.

J Assoc Genet Technol. 2005;31(4):168-9.

PMID:
16354943
17.

Prenatal detection of deletion 6q13q15 in a complex karyotype.

Yu M, Obringer AC, Fowler MH, Hummel M, Wenger SL.

Prenat Diagn. 2005 Dec;25(12):1084-7. Review.

PMID:
16231325
18.

Comparison of established cell lines at different passages by karyotype and comparative genomic hybridization.

Wenger SL, Senft JR, Sargent LM, Bamezai R, Bairwa N, Grant SG.

Biosci Rep. 2004 Dec;24(6):631-9.

PMID:
16158200
19.

Extra copy of 20q deletion, acute myelomonocytic leukemia (M4) and Niemann-Pick disease.

Wonsettler DM, Chang WW, Wenger SL.

J Assoc Genet Technol. 2005;31(2):55-8.

PMID:
16027483
20.
21.

Acquired Robertsonian translocations in leukemia: two more cases.

Herring DB, Harbert KA, Wenger SL, Ericson SG.

Cancer Genet Cytogenet. 2005 Apr 15;158(2):196-7. No abstract available.

PMID:
15796971
22.

Mosaic ring 12p and total anomalous pulmonary venous return.

Harris DL, Siu BL, Hummel M, Harbert K, Senft J, Sargent L, Wenger SL.

Am J Med Genet A. 2004 Nov 15;131(1):91-3.

PMID:
15389698
23.

Cleft palate in a newborn with duplication 2(q13q23).

Wenger SL, Bleigh OC, Hummel M.

Cleft Palate Craniofac J. 2004 Sep;41(5):568-70.

PMID:
15352858
24.

Partial 7q Isochromosome in Bone Marrow Following Treatment of Hodgkin's Disease.

Grove PS, Auber ML, Wenger SL.

J Assoc Genet Technol. 2003;29(2):64-66.

PMID:
15213420
25.

"Jumping Translocation" Involving 21p in Amniocytes.

Hulley BJ, Bleigh OC, McAdoo SL, Boyd BK, Wenger SL.

J Assoc Genet Technol. 2003;29(3):91. No abstract available.

PMID:
15213416
26.

Prenatal diagnosis of tetrasomy 9p.

Tang W, Boyd BK, Hummel M, Wenger SL.

Am J Med Genet A. 2004 Apr 30;126A(3):328. No abstract available.

PMID:
15054852
27.

Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea.

Voronina VA, Kozhemyakina EA, O'Kernick CM, Kahn ND, Wenger SL, Linberg JV, Schneider AS, Mathers PH.

Hum Mol Genet. 2004 Feb 1;13(3):315-22. Epub 2003 Dec 8.

PMID:
14662654
28.

Screening for cryptic chromosomal abnormalities in patients with mental retardation and dysmorphic facial features using telomere FISH probes.

Hulley BJ, Hummel M, Wenger SL.

Am J Med Genet A. 2003 Mar 15;117A(3):302-3. No abstract available.

PMID:
12599198
29.

Atypical t(15;17)(q13;q12) in a patient with all-trans retinoic acid refractory secondary acute promyelocytic leukemia: a case report and review of the literature.

Kurian S, Hogan TF, Bleigh OC, Dowdy YG, Merghoub T, Pandolfi PP, Wenger SL.

Cancer Genet Cytogenet. 2002 Oct 15;138(2):143-8. Review. Erratum in: Cancer Genet Cytogenet. 2003 May;143(1):92.

PMID:
12505260
30.

Trisomy 8 mosaicism: selective growth advantage of normal cells vs. growth disadvantage of trisomy 8 cells.

Hulley BJ, Hummel M, Cook LL, Boyd BK, Wenger SL.

Am J Med Genet A. 2003 Jan 15;116A(2):144-6.

PMID:
12494432
31.

Maternal cell contamination in an amniotic fluid sample.

McAdoo SL, Bleigh OC, Simmons GM Jr, Wenger SL.

Prenat Diagn. 2002 Aug;22(8):737. No abstract available.

PMID:
12210588
32.

Bone marrow stromal cells regulate caspase 3 activity in leukemic cells during chemotherapy.

Fortney JE, Zhao W, Wenger SL, Gibson LF.

Leuk Res. 2001 Oct;25(10):901-7.

PMID:
11532524
33.

Three-way unbalanced translocation in a mildly dysmorphic mentally retarded child.

Wenger SL, Cutenese C, Hummel M.

Clin Genet. 2001 Feb;59(2):139-40. No abstract available.

PMID:
11260219
34.

Glycogen storage disease type Ia and Sanfilippo syndrome type B in a patient with a balanced translocation.

Wenger SL, McIntire SC, Bansal V, Barranger JA, Higgins J, Balistreri WF, Thompson JN, Deka R.

Clin Genet. 2000 Nov;58(5):409-10. No abstract available.

PMID:
11140844
35.

Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome.

Grant SG, Wenger SL, Latimer JJ, Thull D, Burke LW.

Clin Genet. 2000 Sep;58(3):209-15.

36.

Prenatal detection of trisomy for the entire long arm of chromosome 7.

Ndah BV, Stead JA, Brancazio LR, Hummel M, Wenger SL.

J Med Genet. 2000 Jul;37(7):551-3. No abstract available.

37.

Ring chromosome 1 in a newborn.

Cutenese C, Mullett M, Hummel M, Wenger SL.

Clin Dysmorphol. 2000 Apr;9(2):131-3.

PMID:
10826627
38.

Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s.

Wenger SL, Boone LY, Cummins JH, Del Vecchio MA, Bay CA, Hummel M, Mowery-Rushton PA.

Am J Med Genet. 2000 Apr 24;91(5):351-4.

PMID:
10766997
39.

Spontaneous chromosome breakage in pernicious anemia.

Wenger SL, Orlando SJ.

Clin Nutr. 2000 Dec;19(6):467-8. No abstract available.

PMID:
11104600
40.

Detection of pericentric inversion of X chromosome in a male fetus.

Wenger SL, Cutenese C, Brancazio LR.

Am J Med Genet. 1999 Dec 3;87(4):339-41.

PMID:
10588841
41.

Myeloperoxidase-catalyzed redox-cycling of phenol promotes lipid peroxidation and thiol oxidation in HL-60 cells.

Goldman R, Claycamp GH, Sweetland MA, Sedlov AV, Tyurin VA, Kisin ER, Tyurina YY, Ritov VB, Wenger SL, Grant SG, Kagan VE.

Free Radic Biol Med. 1999 Nov;27(9-10):1050-63.

PMID:
10569638
42.

Tissue culture of human renal epithelial cells using a defined serum-free growth formulation.

Sens DA, Detrisac CJ, Sens MA, Rossi MR, Wenger SL, Todd JH.

Exp Nephrol. 1999 Sep-Dec;7(5-6):344-52.

PMID:
10559632
43.

Relaxation of imprinting in Prader-Willi syndrome.

Rogan PK, Seip JR, White LM, Wenger SL, Steele MW, Sperling MA, Menon R, Knoll JH.

Hum Genet. 1998 Dec;103(6):694-701.

PMID:
9921905
44.

Interstitial deletion 2(p11.2p13): a rare chromosomal abnormality.

Wenger SL, McPherson EW.

Clin Genet. 1997 Jul;52(1):61-2. Review.

PMID:
9272715
45.

Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromes.

Wenger SL, Sell SL, Painter MJ, Steele MW.

Am J Med Genet. 1997 May 16;70(2):150-4.

PMID:
9128934
46.

Molecular and cytogenetic studies of X inactivation in a patient with 46,X,del(X)(q22).

Witchel SF, Wenger SL, Hoffman EP.

J Pediatr Adolesc Gynecol. 1997 May;10(2):78-82.

PMID:
9179806
47.

Terminal 2q deletion--a recognizable syndrome.

Wenger SL, Boone LY, Surti U, Steele MW.

Clin Genet. 1997 Apr;51(4):290. No abstract available.

PMID:
9184258
48.

Interstitial lung disease in an adult with Fanconi anemia: clues to the pathogenesis.

Rubinstein WS, Wenger SL, Hoffman RM, Auerbach AD, Mulvihill JJ.

Am J Med Genet. 1997 Mar 31;69(3):315-9.

PMID:
9096763
49.

Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assay.

Grant SG, Reeger W, Wenger SL.

Genet Test. 1997-1998;1(4):261-7.

PMID:
10464655
50.

Inability to induce fragile sites at CTG repeats in congenital myotonic dystrophy.

Wenger SL, Giangreco CA, Tarleton J, Wessel HB.

Am J Med Genet. 1996 Dec 2;66(1):60-3.

PMID:
8957513

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