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Items: 40

1.

Genes Linked to Endometriosis by GWAS Are Integral to Cytoskeleton Regulation and Suggests That Mesothelial Barrier Homeostasis Is a Factor in the Pathogenesis of Endometriosis.

Albertsen HM, Ward K.

Reprod Sci. 2017 Jun;24(6):803-811. doi: 10.1177/1933719116660847. Epub 2016 Jul 28. Review.

PMID:
27470151
2.

Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis.

Chettier R, Nelson L, Ogilvie JW, Albertsen HM, Ward K.

PLoS One. 2015 Feb 12;10(2):e0117708. doi: 10.1371/journal.pone.0117708. eCollection 2015.

3.

Endometriosis is associated with rare copy number variants.

Chettier R, Ward K, Albertsen HM.

PLoS One. 2014 Aug 1;9(8):e103968. doi: 10.1371/journal.pone.0103968. eCollection 2014.

4.

Genome-wide association study link novel loci to endometriosis.

Albertsen HM, Chettier R, Farrington P, Ward K.

PLoS One. 2013;8(3):e58257. doi: 10.1371/journal.pone.0058257. Epub 2013 Mar 5.

5.

Oncogenetic tree model of somatic mutations and DNA methylation in colon tumors.

Sweeney C, Boucher KM, Samowitz WS, Wolff RK, Albertsen H, Curtin K, Caan BJ, Slattery ML.

Genes Chromosomes Cancer. 2009 Jan;48(1):1-9. doi: 10.1002/gcc.20614.

6.

The MLH1 -93 G>A promoter polymorphism and genetic and epigenetic alterations in colon cancer.

Samowitz WS, Curtin K, Wolff RK, Albertsen H, Sweeney C, Caan BJ, Ulrich CM, Potter JD, Slattery ML.

Genes Chromosomes Cancer. 2008 Oct;47(10):835-44. doi: 10.1002/gcc.20584.

7.

Pulsed-field gel electrophoresis for long-range restriction mapping.

Gemmill RM, Bolin R, Albertsen H, Tomkins JP, Wing RA.

Curr Protoc Hum Genet. 2002 Feb;Chapter 5:Unit5.1. doi: 10.1002/0471142905.hg0501s31.

PMID:
18428330
8.

Identification of intron/exon boundaries in genomic DNA by inverse PCR.

Albertsen H, Thliveris A.

Curr Protoc Hum Genet. 2001 May;Chapter 6:Unit 6.4. doi: 10.1002/0471142905.hg0604s00.

PMID:
18428300
9.

Deriving probes from large-insert clones by PCR methods.

Albertsen H, Thliveris A, Riley JH, Munroe DJ, Watkins P, Basson CT.

Curr Protoc Hum Genet. 2001 May;Chapter 5:Unit 5.9. doi: 10.1002/0471142905.hg0509s17.

PMID:
18428296
10.

Genetic polymorphisms in one-carbon metabolism: associations with CpG island methylator phenotype (CIMP) in colon cancer and the modifying effects of diet.

Curtin K, Slattery ML, Ulrich CM, Bigler J, Levin TR, Wolff RK, Albertsen H, Potter JD, Samowitz WS.

Carcinogenesis. 2007 Aug;28(8):1672-9. Epub 2007 Apr 21.

11.

APC mutations and other genetic and epigenetic changes in colon cancer.

Samowitz WS, Slattery ML, Sweeney C, Herrick J, Wolff RK, Albertsen H.

Mol Cancer Res. 2007 Feb;5(2):165-70. Epub 2007 Feb 9.

12.

Association of smoking, CpG island methylator phenotype, and V600E BRAF mutations in colon cancer.

Samowitz WS, Albertsen H, Sweeney C, Herrick J, Caan BJ, Anderson KE, Wolff RK, Slattery ML.

J Natl Cancer Inst. 2006 Dec 6;98(23):1731-8.

PMID:
17148775
13.

Diet and lifestyle factor associations with CpG island methylator phenotype and BRAF mutations in colon cancer.

Slattery ML, Curtin K, Sweeney C, Levin TR, Potter J, Wolff RK, Albertsen H, Samowitz WS.

Int J Cancer. 2007 Feb 1;120(3):656-63.

14.

Evaluation of a large, population-based sample supports a CpG island methylator phenotype in colon cancer.

Samowitz WS, Albertsen H, Herrick J, Levin TR, Sweeney C, Murtaugh MA, Wolff RK, Slattery ML.

Gastroenterology. 2005 Sep;129(3):837-45.

PMID:
16143123
15.

Poor survival associated with the BRAF V600E mutation in microsatellite-stable colon cancers.

Samowitz WS, Sweeney C, Herrick J, Albertsen H, Levin TR, Murtaugh MA, Wolff RK, Slattery ML.

Cancer Res. 2005 Jul 15;65(14):6063-9.

16.

Inhibition of DNA methyltransferase stimulates the expression of signal transducer and activator of transcription 1, 2, and 3 genes in colon tumor cells.

Karpf AR, Peterson PW, Rawlins JT, Dalley BK, Yang Q, Albertsen H, Jones DA.

Proc Natl Acad Sci U S A. 1999 Nov 23;96(24):14007-12.

17.

The chromosome location of the human homolog of the mouse mammary tumor-associated gene INT6 and its status in human breast carcinomas.

Miyazaki S, Imatani A, Ballard L, Marchetti A, Buttitta F, Albertsen H, Nevanlinna HA, Gallahan D, Callahan R.

Genomics. 1997 Nov 15;46(1):155-8.

PMID:
9403073
18.

Long-range physical map and deletion characterization of the 1100-kb NotI restriction fragment harboring the APC gene.

Thliveris A, Albertsen H, Tuohy T, Carlson M, Groden J, Joslyn G, Gelbert L, Samowitz W, Spirio L, White R.

Genomics. 1996 Jun 1;34(2):268-70. No abstract available.

PMID:
8661068
19.
20.

Sequence, genomic structure, and chromosomal assignment of human DOC-2.

Albertsen HM, Smith SA, Melis R, Williams B, Holik P, Stevens J, White R.

Genomics. 1996 Apr 15;33(2):207-13.

PMID:
8660969
21.

Isolation of a gene (DLG3) encoding a second member of the discs-large family on chromosome 17q12-q21.

Smith SA, Holik P, Stevens J, Mazoyer S, Melis R, Williams B, White R, Albertsen H.

Genomics. 1996 Jan 15;31(2):145-50.

PMID:
8824795
22.

Loss of chromosome 17 loci in prostate cancer detected by polymerase chain reaction quantitation of allelic markers.

Brothman AR, Steele MR, Williams BJ, Jones E, Odelberg S, Albertsen HM, Jorde LB, Rohr LR, Stephenson RA.

Genes Chromosomes Cancer. 1995 Aug;13(4):278-84.

PMID:
7547636
23.

A gene (DLG2) located at 17q12-q21 encodes a new homologue of the Drosophila tumor suppressor dIg-A.

Mazoyer S, Gayther SA, Nagai MA, Smith SA, Dunning A, van Rensburg EJ, Albertsen H, White R, Ponder BA.

Genomics. 1995 Jul 1;28(1):25-31.

PMID:
7590743
24.

Isolation and mapping of a gene encoding a novel human ADP-ribosylation factor on chromosome 17q12-q21.

Smith SA, Holik PR, Stevens J, Melis R, White R, Albertsen H.

Genomics. 1995 Jul 1;28(1):113-5.

PMID:
7590735
25.

Breakpoint analysis: precise localization of genetic markers by means of nonstatistical computation using relatively few genotypes.

Elsner TI, Albertsen H, Gerken SC, Cartwright P, White R.

Am J Hum Genet. 1995 Feb;56(2):500-7.

26.

A strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels.

Gerken SC, Albertsen H, Elsner T, Ballard L, Holik P, Lawrence E, Moore M, Zhao X, White R.

Am J Hum Genet. 1995 Feb;56(2):484-99.

27.

A physical map and candidate genes in the BRCA1 region on chromosome 17q12-21.

Albertsen HM, Smith SA, Mazoyer S, Fujimoto E, Stevens J, Williams B, Rodriguez P, Cropp CS, Slijepcevic P, Carlson M, et al.

Nat Genet. 1994 Aug;7(4):472-9.

PMID:
7951316
28.

Evidence for involvement of BRCA1 in sporadic breast carcinomas.

Cropp CS, Nevanlinna HA, Pyrhönen S, Stenman UH, Salmikangas P, Albertsen H, White R, Callahan R.

Cancer Res. 1994 May 15;54(10):2548-51.

29.

Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.

Jorde LB, Watkins WS, Carlson M, Groden J, Albertsen H, Thliveris A, Leppert M.

Am J Hum Genet. 1994 May;54(5):884-98.

30.

Localisation of the breast-ovarian cancer susceptibility gene (BRCA1) on 17q12-21 to an interval of < or = 1 cM.

Smith SA, DiCioccio RA, Struewing JP, Easton DF, Gallion HH, Albertsen H, Mazoyer S, Johansson B, Steichen-Gersdorf E, Stratton M, et al.

Genes Chromosomes Cancer. 1994 May;10(1):71-6.

PMID:
7519878
31.

A radiation hybrid map of the BRCA1 region.

O'Connell P, Albertsen H, Matsunami N, Taylor T, Hundley JE, Johnson-Pais TL, Reus B, Lawrence E, Ballard L, White R, et al.

Am J Hum Genet. 1994 Mar;54(3):526-34.

32.

Genetic mapping of the BRCA1 region on chromosome 17q21.

Albertsen H, Plaetke R, Ballard L, Fujimoto E, Connolly J, Lawrence E, Rodriguez P, Robertson M, Bradley P, Milner B, et al.

Am J Hum Genet. 1994 Mar;54(3):516-25.

33.

Polymorphic SSR (simple-sequence-repeat) markers for chromosome 20.

Melis R, Bradley P, Elsner T, Robertson M, Lawrence E, Gerken S, Albertsen H, White R.

Genomics. 1993 Apr;16(1):56-62.

PMID:
8486385
34.

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

Matsunami N, Smith B, Ballard L, Lensch MW, Robertson M, Albertsen H, Hanemann CO, Müller HW, Bird TD, White R, et al.

Nat Genet. 1992 Jun;1(3):176-9.

PMID:
1303231
35.

Identification of deletion mutations and three new genes at the familial polyposis locus.

Joslyn G, Carlson M, Thliveris A, Albertsen H, Gelbert L, Samowitz W, Groden J, Stevens J, Spirio L, Robertson M, et al.

Cell. 1991 Aug 9;66(3):601-13.

PMID:
1678319
36.

Identification and characterization of the familial adenomatous polyposis coli gene.

Groden J, Thliveris A, Samowitz W, Carlson M, Gelbert L, Albertsen H, Joslyn G, Stevens J, Spirio L, Robertson M, et al.

Cell. 1991 Aug 9;66(3):589-600.

PMID:
1651174
37.

Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region.

Alitalo T, Kruse TA, Ahrens P, Albertsen HM, Eriksson AW, de la Chapelle A.

Hum Genet. 1991 Apr;86(6):599-603.

PMID:
1673960
38.

Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents.

Albertsen HM, Abderrahim H, Cann HM, Dausset J, Le Paslier D, Cohen D.

Proc Natl Acad Sci U S A. 1990 Jun;87(11):4256-60.

39.

Improved control of partial DNA restriction enzyme digest in agarose using limiting concentrations of Mg++.

Albertsen HM, Le Paslier D, Abderrahim H, Dausset J, Cann H, Cohen D.

Nucleic Acids Res. 1989 Jan 25;17(2):808. No abstract available.

40.

An anonymous single copy X-chromosome clone, pTAK8, identifies a frequent RFLP at Xp11-q12(HGM8 no. DXS146).

Kruse TA, Ahrens P, Albertsen HM, Jørgensen B, Vestergaard SR.

Nucleic Acids Res. 1986 Feb 25;14(4):1921. No abstract available.

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