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Items: 1 to 50 of 155

1.

Islet cells share promoter hypomethylation independently of expression, but exhibit cell-type-specific methylation in enhancers.

Neiman D, Moss J, Hecht M, Magenheim J, Piyanzin S, Shapiro AMJ, de Koning EJP, Razin A, Cedar H, Shemer R, Dor Y.

Proc Natl Acad Sci U S A. 2017 Dec 19;114(51):13525-13530. doi: 10.1073/pnas.1713736114. Epub 2017 Dec 4.

2.

Annotating the genome by DNA methylation.

Cedar H, Razin A.

Int J Dev Biol. 2017;61(3-4-5):137-148. doi: 10.1387/ijdb.160270hc.

3.

Automated circuit fabrication and direct characterization of carbon nanotube vibrations.

Zeevi G, Shlafman M, Tabachnik T, Rogachevsky Z, Rechnitz S, Goldshtein I, Shlafman S, Gordon N, Alchanati G, Itzhak M, Moshe Y, Hajaj EM, Nir H, Milyutin Y, Izraeli TY, Razin A, Shtempluck O, Kotchtakov V, Yaish YE.

Nat Commun. 2016 Jul 11;7:12153. doi: 10.1038/ncomms12153.

4.

Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study.

Cheishvili D, Maayan C, Holzer N, Tsenter J, Lax E, Petropoulos S, Razin A.

J Mol Neurosci. 2016 Jul;59(3):382-91. doi: 10.1007/s12031-016-0760-5. Epub 2016 Apr 30.

PMID:
27129499
5.

Identification of tissue-specific cell death using methylation patterns of circulating DNA.

Lehmann-Werman R, Neiman D, Zemmour H, Moss J, Magenheim J, Vaknin-Dembinsky A, Rubertsson S, Nellgård B, Blennow K, Zetterberg H, Spalding K, Haller MJ, Wasserfall CH, Schatz DA, Greenbaum CJ, Dorrell C, Grompe M, Zick A, Hubert A, Maoz M, Fendrich V, Bartsch DK, Golan T, Ben Sasson SA, Zamir G, Razin A, Cedar H, Shapiro AM, Glaser B, Shemer R, Dor Y.

Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):E1826-34. doi: 10.1073/pnas.1519286113. Epub 2016 Mar 14.

6.

Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation.

Lefler S, Cohen MA, Kantor G, Cheishvili D, Even A, Birger A, Turetsky T, Gil Y, Even-Ram S, Aizenman E, Bashir N, Maayan C, Razin A, Reubinoff BE, Weil M.

PLoS One. 2015 Oct 5;10(10):e0138807. doi: 10.1371/journal.pone.0138807. eCollection 2015.

7.

IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation.

Cheishvili D, Dietrich P, Maayan C, Even A, Weil M, Dragatsis I, Razin A.

PLoS One. 2014 Apr 23;9(4):e94612. doi: 10.1371/journal.pone.0094612. eCollection 2014.

8.

Dynamic changes in IKBKAP mRNA levels during crisis of familial dysautonomia patients.

Cheishvili D, Laiba E, Rekhtman D, Claman A, Razin A, Maayan C.

Auton Neurosci. 2014 Feb;180:59-65. doi: 10.1016/j.autneu.2013.10.009. Epub 2013 Nov 1.

PMID:
24268683
9.

Gate-induced modification of water adsorption on dielectrics probed by EFM and carbon nanotube FETs.

Pascal-Levy Y, Shifman E, Pal-Chowdhury M, Hajaj EM, Shtempluck O, Razin A, Kochetkov V, Yaish YE.

Chemphyschem. 2012 Dec 21;13(18):4202-6. doi: 10.1002/cphc.201200628. Epub 2012 Nov 20.

PMID:
23165969
10.

Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains.

Rabinovitz S, Kaufman Y, Ludwig G, Razin A, Shemer R.

Proc Natl Acad Sci U S A. 2012 May 8;109(19):7403-8. doi: 10.1073/pnas.1116661109. Epub 2012 Apr 23.

11.

IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomia.

Cheishvili D, Maayan C, Cohen-Kupiec R, Lefler S, Weil M, Ast G, Razin A.

Hum Mol Genet. 2011 Apr 15;20(8):1585-94. doi: 10.1093/hmg/ddr036. Epub 2011 Jan 27.

PMID:
21273291
12.

Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain.

Kaufman Y, Heled M, Perk J, Razin A, Shemer R.

Proc Natl Acad Sci U S A. 2009 Jun 23;106(25):10242-7. doi: 10.1073/pnas.0902087106. Epub 2009 Jun 8.

13.

MeCP2 involvement in the regulation of neuronal alpha-tubulin production.

Abuhatzira L, Shemer R, Razin A.

Hum Mol Genet. 2009 Apr 15;18(8):1415-23. doi: 10.1093/hmg/ddp048. Epub 2009 Jan 27.

PMID:
19174478
14.

MeCP2 deficiency in the brain decreases BDNF levels by REST/CoREST-mediated repression and increases TRKB production.

Abuhatzira L, Makedonski K, Kaufman Y, Razin A, Shemer R.

Epigenetics. 2007 Oct-Dec;2(4):214-22. Epub 2007 Oct 29.

PMID:
18075316
15.
16.

The Prader-Willi/Angelman imprinted domain and its control center.

Kantor B, Shemer R, Razin A.

Cytogenet Genome Res. 2006;113(1-4):300-5.

PMID:
16575193
17.

Steps in the study of DNA methylation from phiX174 to genomic imprinting.

Razin A.

Cell Mol Life Sci. 2005 Oct;62(19-20):2147-9. No abstract available.

PMID:
16143822
18.

Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosis.

Abuhatzira L, Makedonski K, Galil YP, Gak E, Ben Zeev B, Razin A, Shemer R.

Hum Genet. 2005 Oct;118(1):91-8. Epub 2005 Oct 28.

PMID:
16133181
19.

DNA methylation in epigenetic control of gene expression.

Razin A, Kantor B.

Prog Mol Subcell Biol. 2005;38:151-67. Review.

PMID:
15881894
20.

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.

Makedonski K, Abuhatzira L, Kaufman Y, Razin A, Shemer R.

Hum Mol Genet. 2005 Apr 15;14(8):1049-58. Epub 2005 Mar 9.

PMID:
15757975
21.

Establishing the epigenetic status of the Prader-Willi/Angelman imprinting center in the gametes and embryo.

Kantor B, Kaufman Y, Makedonski K, Razin A, Shemer R.

Hum Mol Genet. 2004 Nov 15;13(22):2767-79. Epub 2004 Sep 14.

PMID:
15367489
22.

Control elements within the PWS/AS imprinting box and their function in the imprinting process.

Kantor B, Makedonski K, Green-Finberg Y, Shemer R, Razin A.

Hum Mol Genet. 2004 Apr 1;13(7):751-62. Epub 2004 Feb 12.

PMID:
14962980
23.
24.

Characterization of the human Snrpn minimal promoter and cis elements within it.

Green Finberg Y, Kantor B, Hershko AY, Razin A.

Gene. 2003 Jan 30;304:201-6.

PMID:
12568729
25.

Methylation of HoxA5 and HoxB5 and its relevance to expression during mouse development.

Hershko AY, Kafri T, Fainsod A, Razin A.

Gene. 2003 Jan 2;302(1-2):65-72.

PMID:
12527197
26.

The imprinting mechanism of the Prader-Willi/Angelman regional control center.

Perk J, Makedonski K, Lande L, Cedar H, Razin A, Shemer R.

EMBO J. 2002 Nov 1;21(21):5807-14.

27.

Migration and pension.

Razin A, Sadka E.

NBER Work Pap Ser. 1998 Nov;(6778):20 p.

PMID:
12179493
28.

The mouse Snrpn minimal promoter and its human orthologue: activity and imprinting.

Hershko AY, Finberg Y, Kantor B, Shemer R, Razin A.

Genes Cells. 2001 Nov;6(11):967-75.

29.

The imprinting box of the Prader-Willi/Angelman syndrome domain.

Shemer R, Hershko AY, Perk J, Mostoslavsky R, Tsuberi B, Cedar H, Buiting K, Razin A.

Nat Genet. 2000 Dec;26(4):440-3.

PMID:
11101841
30.

Imprinted methylation and its effect on expression of the mouse Zfp127 gene.

Hershko A, Razin A, Shemer R.

Gene. 1999 Jul 8;234(2):323-7.

PMID:
10395905
31.

Epigenetic control of gene expression.

Razin A, Shemer R.

Results Probl Cell Differ. 1999;25:189-204. Review. No abstract available.

PMID:
10339747
32.

The imprinting box of the mouse Igf2r gene.

Birger Y, Shemer R, Perk J, Razin A.

Nature. 1999 Jan 7;397(6714):84-8.

PMID:
9892358
33.
34.

Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern.

Shemer R, Birger Y, Riggs AD, Razin A.

Proc Natl Acad Sci U S A. 1997 Sep 16;94(19):10267-72.

35.
36.

DNA demethylation in vitro: involvement of RNA.

Weiss A, Keshet I, Razin A, Cedar H.

Cell. 1996 Sep 6;86(5):709-18. Erratum in: Cell 1998 Nov 13;95(4):following 573.

37.

Dynamic methylation adjustment and counting as part of imprinting mechanisms.

Shemer R, Birger Y, Dean WL, Reik W, Riggs AD, Razin A.

Proc Natl Acad Sci U S A. 1996 Jun 25;93(13):6371-6.

38.
39.
40.

Utilitarian tradeoff between population growth and income growth.

Razin A, Yuen C.

J Popul Econ. 1995;8(1):81-7.

PMID:
12289751
41.

DNA methylation in early development.

Razin A, Shemer R.

Hum Mol Genet. 1995;4 Spec No:1751-5. Review.

PMID:
8541875
42.

Sp1 elements protect a CpG island from de novo methylation.

Brandeis M, Frank D, Keshet I, Siegfried Z, Mendelsohn M, Nemes A, Temper V, Razin A, Cedar H.

Nature. 1994 Sep 29;371(6496):435-8.

PMID:
8090226
43.

DNA methylation and genomic imprinting.

Razin A, Cedar H.

Cell. 1994 May 20;77(4):473-6. Review. No abstract available.

PMID:
8187170
44.

DNA methylation from embryo to adult.

Razin A, Kafri T.

Prog Nucleic Acid Res Mol Biol. 1994;48:53-81. Review. No abstract available.

PMID:
7938554
45.

Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo.

Kafri T, Gao X, Razin A.

Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10558-62.

46.

Histone H1-mediated inhibition of transcription initiation of methylated templates in vitro.

Levine A, Yeivin A, Ben-Asher E, Aloni Y, Razin A.

J Biol Chem. 1993 Oct 15;268(29):21754-9.

47.

The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.

Brandeis M, Kafri T, Ariel M, Chaillet JR, McCarrey J, Razin A, Cedar H.

EMBO J. 1993 Sep;12(9):3669-77.

48.

Probing CpG methylation at CACGTG with BbrPI restriction enzyme.

Kafri T, Hershko A, Razin A.

Nucleic Acids Res. 1993 Jun 25;21(12):2950. No abstract available.

49.

Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

Stöger R, Kubicka P, Liu CG, Kafri T, Razin A, Cedar H, Barlow DP.

Cell. 1993 Apr 9;73(1):61-71.

PMID:
8462104
50.

Anderson's disease: no linkage to the apo B locus.

Strich D, Goldstein R, Phillips A, Shemer R, Goldberg Y, Razin A, Freier S.

J Pediatr Gastroenterol Nutr. 1993 Apr;16(3):257-64.

PMID:
8492252

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