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    Results: 15

    1.

    Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for Lynch syndrome.

    Zighelboim I, Powell MA, Babb SA, Whelan AJ, Schmidt AP, Clendenning M, Senter L, Thibodeau SN, de la Chapelle A, Goodfellow PJ.

    Fam Cancer. 2009;8(4):501-4. Epub 2009 Aug 12.PMID: 19672700 [PubMed - in process]Related articlesFree article

    2.

    Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis.

    Walsh MD, Buchanan DD, Walters R, Roberts A, Arnold S, McKeone D, Clendenning M, Ruszkiewicz AR, Jenkins MA, Hopper JL, Goldblatt J, George J, Suthers GK, Phillips K, Young GP, Macrae F, Drini M, Woods MO, Parry S, Jass JR, Young JP.

    Fam Cancer. 2009;8(4):313-23. Epub 2009 Feb 25.PMID: 19241144 [PubMed - in process]Related articles

    3.

    Feasibility of screening for Lynch syndrome among patients with colorectal cancer.

    Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Clendenning M, Sotamaa K, Prior T, Westman JA, Panescu J, Fix D, Lockman J, LaJeunesse J, Comeras I, de la Chapelle A.

    J Clin Oncol. 2008 Dec 10;26(35):5783-8. Epub 2008 Sep 22.PMID: 18809606 [PubMed - indexed for MEDLINE]Related articles

    4.

    The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.

    Senter L, Clendenning M, Sotamaa K, Hampel H, Green J, Potter JD, Lindblom A, Lagerstedt K, Thibodeau SN, Lindor NM, Young J, Winship I, Dowty JG, White DM, Hopper JL, Baglietto L, Jenkins MA, de la Chapelle A.

    Gastroenterology. 2008 Aug;135(2):419-28. Epub 2008 May 2.PMID: 18602922 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Origins and prevalence of the American Founder Mutation of MSH2.

    Clendenning M, Baze ME, Sun S, Walsh K, Liyanarachchi S, Fix D, Schunemann V, Comeras I, Deacon M, Lynch JF, Gong G, Thomas BC, Thibodeau SN, Lynch HT, Hampel H, de la Chapelle A.

    Cancer Res. 2008 Apr 1;68(7):2145-53.PMID: 18381419 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Café-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2.

    Jackson CC, Holter S, Pollett A, Clendenning M, Chou S, Senter L, Ramphal R, Gallinger S, Boycott K.

    Pediatr Blood Cancer. 2008 Jun;50(6):1268-70.PMID: 18273873 [PubMed - indexed for MEDLINE]Related articles

    7.

    A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.

    Clendenning M, Senter L, Hampel H, Robinson KL, Sun S, Buchanan D, Walsh MD, Nilbert M, Green J, Potter J, Lindblom A, de la Chapelle A.

    J Med Genet. 2008 Jun;45(6):340-5. Epub 2008 Jan 4.PMID: 18178629 [PubMed - indexed for MEDLINE]Related articles

    8.

    Multifocal anaplastic astrocytoma in a patient with hereditary colorectal cancer, transcobalamin II deficiency, agenesis of the corpus callosum, mental retardation, and inherited PMS2 mutation.

    Gururangan S, Frankel W, Broaddus R, Clendenning M, Senter L, McDonald M, Eastwood J, Reardon D, Vredenburgh J, Quinn J, Friedman HS.

    Neuro Oncol. 2008 Feb;10(1):93-7. Epub 2007 Nov 9.PMID: 17993636 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients.

    Hampel H, Panescu J, Lockman J, Sotamaa K, Fix D, Comeras I, LaJeunesse J, Nakagawa H, Westman JA, Prior TW, Clendenning M, de la Chapelle A, Frankel W, Penzone P, Cohn DE, Copeland L, Eaton L, Fowler J, Lombardi J, Dunn P, Bell J, Reid G, Lewandowski G, Vaccarello L.

    Cancer Res. 2007 Oct 1;67(19):9603. No abstract available. PMID: 17909073 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.

    Lagerstedt Robinson K, Liu T, Vandrovcova J, Halvarsson B, Clendenning M, Frebourg T, Papadopoulos N, Kinzler KW, Vogelstein B, Peltomäki P, Kolodner RD, Nilbert M, Lindblom A.

    J Natl Cancer Inst. 2007 Feb 21;99(4):291-9.PMID: 17312306 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.

    Hampel H, Frankel W, Panescu J, Lockman J, Sotamaa K, Fix D, Comeras I, La Jeunesse J, Nakagawa H, Westman JA, Prior TW, Clendenning M, Penzone P, Lombardi J, Dunn P, Cohn DE, Copeland L, Eaton L, Fowler J, Lewandowski G, Vaccarello L, Bell J, Reid G, de la Chapelle A.

    Cancer Res. 2006 Aug 1;66(15):7810-7.PMID: 16885385 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Long-range PCR facilitates the identification of PMS2-specific mutations.

    Clendenning M, Hampel H, LaJeunesse J, Lindblom A, Lockman J, Nilbert M, Senter L, Sotamaa K, de la Chapelle A.

    Hum Mutat. 2006 May;27(5):490-5. Erratum in: Hum Mutat. 2006 Nov;27(11):1155. PMID: 16619239 [PubMed - indexed for MEDLINE]Related articles

    13.

    COM184: a polymorphic microsatellite marker for CKB on chicken chromosome 5.

    Clendenning M, Bumstead N.

    Anim Genet. 2001 Apr;32(2):119. No abstract available. PMID: 11421956 [PubMed - indexed for MEDLINE]Related articles

    14.

    Topiramate and hepatotoxicity.

    Doan RJ, Clendenning M.

    Can J Psychiatry. 2000 Dec;45(10):937-8. No abstract available. PMID: 11190367 [PubMed - indexed for MEDLINE]Related articles

    15.

    The effect of a target date based utilization review program on length of stay.

    Clendenning MK, Wolfe H, Shuman LJ, Huber GA.

    Med Care. 1976 Sep;14(9):751-64.PMID: 787698 [PubMed - indexed for MEDLINE]Related articles

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