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Items: 1 to 50 of 133

1.

Profile of Bruce M. Alberts, 2016 Lasker-Koshland Special Achievement Award in Medical Science Awardee.

Tilghman SM.

Proc Natl Acad Sci U S A. 2017 Feb 14;114(7):1439-1441. doi: 10.1073/pnas.1700685114. Epub 2017 Feb 6. No abstract available.

2.

Twists and turns: a scientific journey.

Tilghman SM.

Annu Rev Cell Dev Biol. 2014;30:1-21. doi: 10.1146/annurev-cellbio-100913-013512.

PMID:
25288111
3.

It's all about the talent.

Tilghman SM.

Mol Biol Cell. 2010 Nov 15;21(22):3823. doi: 10.1091/mbc.E10-05-0472. No abstract available.

4.

Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes.

Mancini-Dinardo D, Steele SJ, Levorse JM, Ingram RS, Tilghman SM.

Genes Dev. 2006 May 15;20(10):1268-82.

5.

Phosphoenolpyruvate carboxykinase and the critical role of cataplerosis in the control of hepatic metabolism.

Hakimi P, Johnson MT, Yang J, Lepage DF, Conlon RA, Kalhan SC, Reshef L, Tilghman SM, Hanson RW.

Nutr Metab (Lond). 2005 Nov 21;2:33.

6.

Functional characterization of a novel Ku70/80 pause site at the H19/Igf2 imprinting control region.

Katz DJ, Beer MA, Levorse JM, Tilghman SM.

Mol Cell Biol. 2005 May;25(10):3855-63.

7.

Education. Scientific teaching.

Handelsman J, Ebert-May D, Beichner R, Bruns P, Chang A, DeHaan R, Gentile J, Lauffer S, Stewart J, Tilghman SM, Wood WB.

Science. 2004 Apr 23;304(5670):521-2. No abstract available.

PMID:
15105480
8.

Functional characterization of a testis-specific DNA binding activity at the H19/Igf2 imprinting control region.

Bowman AB, Levorse JM, Ingram RS, Tilghman SM.

Mol Cell Biol. 2003 Nov;23(22):8345-51.

9.

Glyceroneogenesis and the triglyceride/fatty acid cycle.

Reshef L, Olswang Y, Cassuto H, Blum B, Croniger CM, Kalhan SC, Tilghman SM, Hanson RW.

J Biol Chem. 2003 Aug 15;278(33):30413-6. Epub 2003 Jun 4. Review. No abstract available.

10.
11.

Gatm, a creatine synthesis enzyme, is imprinted in mouse placenta.

Sandell LL, Guan XJ, Ingram R, Tilghman SM.

Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4622-7. Epub 2003 Apr 1.

12.

A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer.

Mancini-DiNardo D, Steele SJ, Ingram RS, Tilghman SM.

Hum Mol Genet. 2003 Feb 1;12(3):283-94.

PMID:
12554682
13.

CTCF maintains differential methylation at the Igf2/H19 locus.

Schoenherr CJ, Levorse JM, Tilghman SM.

Nat Genet. 2003 Jan;33(1):66-9. Epub 2002 Dec 2.

PMID:
12461525
14.

Clock regulatory elements control cyclic expression of Lunatic fringe during somitogenesis.

Cole SE, Levorse JM, Tilghman SM, Vogt TF.

Dev Cell. 2002 Jul;3(1):75-84.

15.

Genomic imprinting of a placental lactogen gene in Peromyscus.

Vrana PB, Matteson PG, Schmidt JV, Ingram RS, Joyce A, Prince KL, Dewey MJ, Tilghman SM.

Dev Genes Evol. 2001 Dec;211(11):523-32. Epub 2001 Nov 17.

PMID:
11862458
16.

A human H19 transgene exhibits impaired paternal-specific imprint acquisition and maintenance in mice.

Jones BK, Levorse J, Tilghman SM.

Hum Mol Genet. 2002 Feb 15;11(4):411-8.

PMID:
11854173
17.

Candidate genes required for embryonic development: a comparative analysis of distal mouse chromosome 14 and human chromosome 13q22.

Kurihara LJ, Semenova E, Miller W, Ingram RS, Guan XJ, Tilghman SM.

Genomics. 2002 Feb;79(2):154-61.

PMID:
11829485
18.

A mutation in the peroxisome proliferator-activated receptor gamma-binding site in the gene for the cytosolic form of phosphoenolpyruvate carboxykinase reduces adipose tissue size and fat content in mice.

Olswang Y, Cohen H, Papo O, Cassuto H, Croniger CM, Hakimi P, Tilghman SM, Hanson RW, Reshef L.

Proc Natl Acad Sci U S A. 2002 Jan 22;99(2):625-30. Epub 2002 Jan 15.

19.

Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia.

Kurihara LJ, Kikuchi T, Wada K, Tilghman SM.

Hum Mol Genet. 2001 Sep 1;10(18):1963-70.

PMID:
11555633
20.

Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice.

Cleary MA, van Raamsdonk CD, Levorse J, Zheng B, Bradley A, Tilghman SM.

Nat Genet. 2001 Sep;29(1):78-82.

PMID:
11528397
21.

Optimizing the detection of nascent transcripts by RNA fluorescence in situ hybridization.

van Raamsdonk CD, Tilghman SM.

Nucleic Acids Res. 2001 Apr 15;29(8):E42-2.

22.
23.

Dosage requirement and allelic expression of PAX6 during lens placode formation.

van Raamsdonk CD, Tilghman SM.

Development. 2000 Dec;127(24):5439-48.

24.

The Dlk1 and Gtl2 genes are linked and reciprocally imprinted.

Schmidt JV, Matteson PG, Jones BK, Guan XJ, Tilghman SM.

Genes Dev. 2000 Aug 15;14(16):1997-2002.

25.

Exploring genome space.

Vukmirovic OG, Tilghman SM.

Nature. 2000 Jun 15;405(6788):820-2. Review.

PMID:
10866207
26.

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus.

Hark AT, Schoenherr CJ, Katz DJ, Ingram RS, Levorse JM, Tilghman SM.

Nature. 2000 May 25;405(6785):486-9.

PMID:
10839547
27.

Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus.

Vrana PB, Fossella JA, Matteson P, del Rio T, O'Neill MJ, Tilghman SM.

Nat Genet. 2000 May;25(1):120-4.

PMID:
10802670
28.

Expression and functional analysis of Uch-L3 during mouse development.

Kurihara LJ, Semenova E, Levorse JM, Tilghman SM.

Mol Cell Biol. 2000 Apr;20(7):2498-504.

29.

Spatially restricted hypopigmentation associated with an Ednrbs-modifying locus on mouse chromosome 10.

Rhim H, Dunn KJ, Aronzon A, Mac S, Cheng M, Lamoreux ML, Tilghman SM, Pavan WJ.

Genome Res. 2000 Jan;10(1):17-29.

30.

Allelic expression of IGF2 in marsupials and birds.

O'Neill MJ, Ingram RS, Vrana PB, Tilghman SM.

Dev Genes Evol. 2000 Jan;210(1):18-20.

PMID:
10603082
31.

Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome.

Caspary T, Cleary MA, Perlman EJ, Zhang P, Elledge SJ, Tilghman SM.

Genes Dev. 1999 Dec 1;13(23):3115-24.

32.

The temporal requirement for endothelin receptor-B signalling during neural crest development.

Shin MK, Levorse JM, Ingram RS, Tilghman SM.

Nature. 1999 Dec 2;402(6761):496-501.

PMID:
10591209
33.

Monoallelic expression of reactivated imprinted genes in embryonal carcinoma cell hybrids.

Forejt J, Saam JR, Gregorová S, Tilghman SM.

Exp Cell Res. 1999 Nov 1;252(2):416-22.

PMID:
10527631
34.

Enhancer competition between H19 and Igf2 does not mediate their imprinting.

Schmidt JV, Levorse JM, Tilghman SM.

Proc Natl Acad Sci U S A. 1999 Aug 17;96(17):9733-8.

35.

The sins of the fathers and mothers: genomic imprinting in mammalian development.

Tilghman SM.

Cell. 1999 Jan 22;96(2):185-93. Review. No abstract available.

36.

Genomic imprinting is disrupted in interspecific Peromyscus hybrids.

Vrana PB, Guan XJ, Ingram RS, Tilghman SM.

Nat Genet. 1998 Dec;20(4):362-5. Erratum in: Nat Genet 1999 Feb;21(2):241.

PMID:
9843208
37.

Chromatin conformation of the H19 epigenetic mark.

Hark AT, Tilghman SM.

Hum Mol Genet. 1998 Nov;7(12):1979-85.

PMID:
9811943
38.

Igf2 imprinting does not require its own DNA methylation or H19 RNA.

Jones BK, Levorse JM, Tilghman SM.

Genes Dev. 1998 Jul 15;12(14):2200-7.

39.

Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.

Caspary T, Cleary MA, Baker CC, Guan XJ, Tilghman SM.

Mol Cell Biol. 1998 Jun;18(6):3466-74.

40.
41.

Competitive edge at the imprinted Prader-Willi/Angelman region?

Tilghman SM, Caspary T, Ingram RS.

Nat Genet. 1998 Mar;18(3):206-8. No abstract available.

PMID:
9500535
42.

Location of enhancers is essential for the imprinting of H19 and Igf2 genes.

Webber AL, Ingram RS, Levorse JM, Tilghman SM.

Nature. 1998 Feb 12;391(6668):711-5.

PMID:
9490417
43.

Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes.

Eggenschwiler J, Ludwig T, Fisher P, Leighton PA, Tilghman SM, Efstratiadis A.

Genes Dev. 1997 Dec 1;11(23):3128-42.

44.

Molecular characterization of four induced alleles at the Ednrb locus.

Shin MK, Russell LB, Tilghman SM.

Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13105-10.

45.
46.

Two dominant mutations in the mouse fused gene are the result of transposon insertions.

Vasicek TJ, Zeng L, Guan XJ, Zhang T, Costantini F, Tilghman SM.

Genetics. 1997 Oct;147(2):777-86.

47.

Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans.

Forné T, Oswald J, Dean W, Saam JR, Bailleul B, Dandolo L, Tilghman SM, Walter J, Reik W.

Proc Natl Acad Sci U S A. 1997 Sep 16;94(19):10243-8. Erratum in: Proc Natl Acad Sci U S A 1997 Dec 9;94(25):14211.

48.

The mouse Fused locus encodes Axin, an inhibitor of the Wnt signaling pathway that regulates embryonic axis formation.

Zeng L, Fagotto F, Zhang T, Hsu W, Vasicek TJ, Perry WL 3rd, Lee JJ, Tilghman SM, Gumbiner BM, Costantini F.

Cell. 1997 Jul 11;90(1):181-92.

49.

Genomic imprinting in mammals.

Bartolomei MS, Tilghman SM.

Annu Rev Genet. 1997;31:493-525. Review.

PMID:
9442905
50.

The structural H19 gene is required for transgene imprinting.

Pfeifer K, Leighton PA, Tilghman SM.

Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13876-83.

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