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Items: 30


Eat, Sleep, Console Approach: A Family-Centered Model for the Treatment of Neonatal Abstinence Syndrome.

Grisham LM, Stephen MM, Coykendall MR, Kane MF, Maurer JA, Bader MY.

Adv Neonatal Care. 2019 Apr;19(2):138-144. doi: 10.1097/ANC.0000000000000581. Review.


The suitcase simulation: an effective and inexpensive psychiatric nursing teaching activity.

Masters JC, Kane MF, Pike ME.

J Psychosoc Nurs Ment Health Serv. 2014 Aug;52(8):39-44. doi: 10.3928/02793695-20140619-01. Epub 2014 Jun 26.


An amino terminal phosphorylation motif regulates intranuclear compartmentalization of Olig2 in neural progenitor cells.

Meijer DH, Sun Y, Liu T, Kane MF, Alberta JA, Adelmant G, Kupp R, Marto JA, Rowitch DH, Nakatani Y, Stiles CD, Mehta S.

J Neurosci. 2014 Jun 18;34(25):8507-18. doi: 10.1523/JNEUROSCI.0309-14.2014.


Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2.

Meijer DH, Kane MF, Mehta S, Liu H, Harrington E, Taylor CM, Stiles CD, Rowitch DH.

Nat Rev Neurosci. 2012 Dec;13(12):819-31. doi: 10.1038/nrn3386. Review.


The central nervous system-restricted transcription factor Olig2 opposes p53 responses to genotoxic damage in neural progenitors and malignant glioma.

Mehta S, Huillard E, Kesari S, Maire CL, Golebiowski D, Harrington EP, Alberta JA, Kane MF, Theisen M, Ligon KL, Rowitch DH, Stiles CD.

Cancer Cell. 2011 Mar 8;19(3):359-71. doi: 10.1016/j.ccr.2011.01.035.


Phosphorylation state of Olig2 regulates proliferation of neural progenitors.

Sun Y, Meijer DH, Alberta JA, Mehta S, Kane MF, Tien AC, Fu H, Petryniak MA, Potter GB, Liu Z, Powers JF, Runquist IS, Rowitch DH, Stiles CD.

Neuron. 2011 Mar 10;69(5):906-17. doi: 10.1016/j.neuron.2011.02.005.


Approaching a complete repository of sequence-verified protein-encoding clones for Saccharomyces cerevisiae.

Hu Y, Rolfs A, Bhullar B, Murthy TV, Zhu C, Berger MF, Camargo AA, Kelley F, McCarron S, Jepson D, Richardson A, Raphael J, Moreira D, Taycher E, Zuo D, Mohr S, Kane MF, Williamson J, Simpson A, Bulyk ML, Harlow E, Marsischky G, Kolodner RD, LaBaer J.

Genome Res. 2007 Apr;17(4):536-43. Epub 2007 Feb 23.


Mutation in Rpa1 results in defective DNA double-strand break repair, chromosomal instability and cancer in mice.

Wang Y, Putnam CD, Kane MF, Zhang W, Edelmann L, Russell R, Carrión DV, Chin L, Kucherlapati R, Kolodner RD, Edelmann W.

Nat Genet. 2005 Jul;37(7):750-5. Epub 2005 Jun 19.


Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility.

Wei K, Clark AB, Wong E, Kane MF, Mazur DJ, Parris T, Kolas NK, Russell R, Hou H Jr, Kneitz B, Yang G, Kunkel TA, Kolodner RD, Cohen PE, Edelmann W.

Genes Dev. 2003 Mar 1;17(5):603-14.


Haploinsufficiency of Flap endonuclease (Fen1) leads to rapid tumor progression.

Kucherlapati M, Yang K, Kuraguchi M, Zhao J, Lia M, Heyer J, Kane MF, Fan K, Russell R, Brown AM, Kneitz B, Edelmann W, Kolodner RD, Lipkin M, Kucherlapati R.

Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):9924-9. Epub 2002 Jul 15.


MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice.

Kneitz B, Cohen PE, Avdievich E, Zhu L, Kane MF, Hou H Jr, Kolodner RD, Kucherlapati R, Pollard JW, Edelmann W.

Genes Dev. 2000 May 1;14(9):1085-97.


Germ-line msh6 mutations in colorectal cancer families.

Kolodner RD, Tytell JD, Schmeits JL, Kane MF, Gupta RD, Weger J, Wahlberg S, Fox EA, Peel D, Ziogas A, Garber JE, Syngal S, Anton-Culver H, Li FP.

Cancer Res. 1999 Oct 15;59(20):5068-74.


Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer.

Verma L, Kane MF, Brassett C, Schmeits J, Evans DG, Kolodner RD, Maher ER.

J Med Genet. 1999 Sep;36(9):678-82.


Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma.

Herman JG, Umar A, Polyak K, Graff JR, Ahuja N, Issa JP, Markowitz S, Willson JK, Hamilton SR, Kinzler KW, Kane MF, Kolodner RD, Vogelstein B, Kunkel TA, Baylin SB.

Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6870-5.


Mutation in the mismatch repair gene Msh6 causes cancer susceptibility.

Edelmann W, Yang K, Umar A, Heyer J, Lau K, Fan K, Liedtke W, Cohen PE, Kane MF, Lipford JR, Yu N, Crouse GF, Pollard JW, Kunkel T, Lipkin M, Kolodner R, Kucherlapati R.

Cell. 1997 Nov 14;91(4):467-77.


A human compound heterozygote for two MLH1 missense mutations.

Hackman P, Tannergård P, Osei-Mensa S, Chen J, Kane MF, Kolodner R, Lambert B, Hellgren D, Lindblom A.

Nat Genet. 1997 Oct;17(2):135-6. No abstract available.


Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2.

Tishkoff DX, Boerger AL, Bertrand P, Filosi N, Gaida GM, Kane MF, Kolodner RD.

Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7487-92.


Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines.

Kane MF, Loda M, Gaida GM, Lipman J, Mishra R, Goldman H, Jessup JM, Kolodner R.

Cancer Res. 1997 Mar 1;57(5):808-11.


Low frequency of hMSH2 mutations in Swedish HNPCC families.

Wahlberg SS, Nyström-Lahti M, Kane MF, Kolodner RD, Peltomäki P, Lindblom A.

Int J Cancer. 1997 Feb 20;74(1):134-7. No abstract available.


Saccharomyces cerevisiae MSH2, a mispaired base recognition protein, also recognizes Holliday junctions in DNA.

Alani E, Lee S, Kane MF, Griffith J, Kolodner RD.

J Mol Biol. 1997 Jan 24;265(3):289-301.


hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6.

Acharya S, Wilson T, Gradia S, Kane MF, Guerrette S, Marsischky GT, Kolodner R, Fishel R.

Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13629-34.


Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families.

Tonin P, Weber B, Offit K, Couch F, Rebbeck TR, Neuhausen S, Godwin AK, Daly M, Wagner-Costalos J, Berman D, Grana G, Fox E, Kane MF, Kolodner RD, Krainer M, Haber DA, Struewing JP, Warner E, Rosen B, Lerman C, Peshkin B, Norton L, Serova O, Foulkes WD, Garber JE, et al.

Nat Med. 1996 Nov;2(11):1179-83. Review. No abstract available.


Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair.

Marsischky GT, Filosi N, Kane MF, Kolodner R.

Genes Dev. 1996 Feb 15;10(4):407-20.


Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas.

Børresen AL, Lothe RA, Meling GI, Lystad S, Morrison P, Lipford J, Kane MF, Rognum TO, Kolodner RD.

Hum Mol Genet. 1995 Nov;4(11):2065-72.


Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations.

Kolodner RD, Hall NR, Lipford J, Kane MF, Morrison PT, Finan PJ, Burn J, Chapman P, Earabino C, Merchant E, et al.

Cancer Res. 1995 Jan 15;55(2):242-8.


Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations.

Kolodner RD, Hall NR, Lipford J, Kane MF, Rao MR, Morrison P, Wirth L, Finan PJ, Burn J, Chapman P.

Genomics. 1994 Dec;24(3):516-26. Erratum in: Genomics 1995 Aug 10;28(3):613.


Human mismatch repair genes and their association with hereditary non-polyposis colon cancer.

Kolodner RD, Hall NR, Lipford J, Kane MF, Rao MR, Morrison P, Wirth L, Finan PJ, Burn J, Chapman P, et al.

Cold Spring Harb Symp Quant Biol. 1994;59:331-8. Review. No abstract available.


Hemifacial hypertrophy affecting the maxillary dentition. Report of a case.

Kogon SL, Jarvis AM, Daley TD, Kane MF.

Oral Surg Oral Med Oral Pathol. 1984 Nov;58(5):549-53.


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