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Items: 15


Dasatinib treatment of chronic-phase chronic myeloid leukemia: analysis of responses according to preexisting BCR-ABL mutations.

Müller MC, Cortes JE, Kim DW, Druker BJ, Erben P, Pasquini R, Branford S, Hughes TP, Radich JP, Ploughman L, Mukhopadhyay J, Hochhaus A.

Blood. 2009 Dec 3;114(24):4944-53. doi: 10.1182/blood-2009-04-214221. Epub 2009 Sep 24.


Association between ADAMTS1 matrix metalloproteinase gene variation, coronary heart disease, and benefit of statin therapy.

Sabatine MS, Ploughman L, Simonsen KL, Iakoubova OA, Kirchgessner TG, Ranade K, Tsuchihashi Z, Zerba KE, Long DU, Tong CH, Packard CJ, Pfeffer MA, Devlin JJ, Shepherd J, Campos H, Sacks FM, Braunwald E.

Arterioscler Thromb Vasc Biol. 2008 Mar;28(3):562-7. doi: 10.1161/ATVBAHA.107.156653. Epub 2008 Jan 3.


Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS.

Iakoubova OA, Tong CH, Chokkalingam AP, Rowland CM, Kirchgessner TG, Louie JZ, Ploughman LM, Sabatine MS, Campos H, Catanese JJ, Leong DU, Young BA, Lew D, Tsuchihashi Z, Luke MM, Packard CJ, Zerba KE, Shaw PM, Shepherd J, Devlin JJ, Sacks FM.

Arterioscler Thromb Vasc Biol. 2006 Dec;26(12):2763-8. Epub 2006 Sep 28.


Therapy with efavirenz plus indinavir in patients with extensive prior nucleoside reverse-transcriptase inhibitor experience: a randomized, double-blind, placebo-controlled trial.

Haas DW, Fessel WJ, Delapenha RA, Kessler H, Seekins D, Kaplan M, Ruiz NM, Ploughman LM, Labriola DF, Manion DJ.

J Infect Dis. 2001 Feb 1;183(3):392-400. Epub 2000 Dec 29.


Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome.

Reynolds JE, Marazita ML, Meyer JM, Stevens CA, Eaves LJ, Arnos KS, Ploughman LM, MacLean C, Nance WE, Diehl SR.

Am J Hum Genet. 1996 Feb;58(2):384-92.


Analysis of locus heterogeneity in Waardenburg syndrome types 1 and 2 using highly informative microsatellite markers.

Reynolds JE, Arnos KS, Landa B, Stevens CA, Salbert BA, Wright L, Duke B, Hunt W, Marazita ML, Ploughman L, et al.

Hum Hered. 1995 Sep-Oct;45(5):243-52.


Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.

Marazita ML, Ploughman LM, Rawlings B, Remington E, Arnos KS, Nance WE.

Am J Med Genet. 1993 Jun 15;46(5):486-91.


Heterogeneity testing for Alzheimer's disease within and between data sets.

Miller LL, Ploughman LM, Marazita ML.

Genet Epidemiol. 1993;10(6):443-7.


A new test for linkage in the presence of locus heterogeneity.

MacLean CJ, Ploughman LM, Diehl SR, Kendler KS.

Am J Hum Genet. 1992 Jun;50(6):1259-66.


Estimating the power of a proposed linkage study for a complex genetic trait.

Ploughman LM, Boehnke M.

Am J Hum Genet. 1989 Apr;44(4):543-51.


A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene.

Diehl SR, Boehnke M, Erickson RP, Ploughman LM, Seiler KA, Lieberman JL, Clarke HB, Bruce MA, Schorry EK, Pericak-Vance M, et al.

Am J Hum Genet. 1989 Jan;44(1):33-7.


Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17.

Diehl SR, Boehnke M, Erickson RP, Baxter AB, Bruce MA, Lieberman JL, Platt DJ, Ploughman LM, Seiler KA, Sweet AM, et al.

Genomics. 1987 Dec;1(4):361-3.


Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8.

Diehl SR, Boehnke M, Collins FS, Erickson RP, Karolyi IJ, Ploughman LM, Pericak-Vance MA, Aylsworth AS, Roses AD.

J Med Genet. 1987 Sep;24(9):532-4.


Prolonged mechanical ventilation and intracranial hemorrhage: impact on developmental progress through 18 months in infants weighing 1,200 grams or less at birth.

Bozynski ME, Nelson MN, Matalon TA, O'Donnell KJ, Naughton PM, Vasan U, Meier WA, Ploughman L.

Pediatrics. 1987 May;79(5):670-6.


Severe hypoglycemia during pregnancy: its frequency and predisposing factors in diabetic women.

Rayburn W, Piehl E, Jacober S, Schork A, Ploughman L.

Int J Gynaecol Obstet. 1986 Aug;24(4):263-8.

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