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Items: 1 to 20 of 329

1.

Regulation of the DNA Methylation Landscape in Human Somatic Cell Reprogramming by the miR-29 Family.

Hysolli E, Tanaka Y, Su J, Kim KY, Zhong T, Janknecht R, Zhou XL, Geng L, Qiu C, Pan X, Jung YW, Cheng J, Lu J, Zhong M, Weissman SM, Park IH.

Stem Cell Reports. 2016 Jul 12;7(1):43-54. doi: 10.1016/j.stemcr.2016.05.014. Epub 2016 Jun 30.

2.

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.

Li J, Woods SL, Healey S, Beesley J, Chen X, Lee JS, Sivakumaran H, Wayte N, Nones K, Waterfall JJ, Pearson J, Patch AM, Senz J, Ferreira MA, Kaurah P, Mackenzie R, Heravi-Moussavi A, Hansford S, Lannagan TR, Spurdle AB, Simpson PT, da Silva L, Lakhani SR, Clouston AD, Bettington M, Grimpen F, Busuttil RA, Di Costanzo N, Boussioutas A, Jeanjean M, Chong G, Fabre A, Olschwang S, Faulkner GJ, Bellos E, Coin L, Rioux K, Bathe OF, Wen X, Martin HC, Neklason DW, Davis SR, Walker RL, Calzone KA, Avital I, Heller T, Koh C, Pineda M, Rudloff U, Quezado M, Pichurin PN, Hulick PJ, Weissman SM, Newlin A, Rubinstein WS, Sampson JE, Hamman K, Goldgar D, Poplawski N, Phillips K, Schofield L, Armstrong J, Kiraly-Borri C, Suthers GK, Huntsman DG, Foulkes WD, Carneiro F, Lindor NM, Edwards SL, French JD, Waddell N, Meltzer PS, Worthley DL, Schrader KA, Chenevix-Trench G.

Am J Hum Genet. 2016 May 5;98(5):830-42. doi: 10.1016/j.ajhg.2016.03.001. Epub 2016 Apr 14.

PMID:
27087319
3.

A Molecular Chipper technology for CRISPR sgRNA library generation and functional mapping of noncoding regions.

Cheng J, Roden CA, Pan W, Zhu S, Baccei A, Pan X, Jiang T, Kluger Y, Weissman SM, Guo S, Flavell RA, Ding Y, Lu J.

Nat Commun. 2016 Mar 30;7:11178. doi: 10.1038/ncomms11178.

4.

Single-Cell Sequencing for Precise Cancer Research: Progress and Prospects.

Zhang X, Marjani SL, Hu Z, Weissman SM, Pan X, Wu S.

Cancer Res. 2016 Mar 15;76(6):1305-12. doi: 10.1158/0008-5472.CAN-15-1907. Epub 2016 Mar 3. Review.

PMID:
26941284
5.

Evaluation of laboratory perspectives on hereditary cancer panels.

Stoll J, Weissman SM, Hook N, Selkirk C, Johnson AK, Newlin A, Vogel Postula KJ.

Fam Cancer. 2016 Feb 11. [Epub ahead of print]

PMID:
26869169
6.

Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.

Susswein LR, Marshall ML, Nusbaum R, Vogel Postula KJ, Weissman SM, Yackowski L, Vaccari EM, Bissonnette J, Booker JK, Cremona ML, Gibellini F, Murphy PD, Pineda-Alvarez DE, Pollevick GD, Xu Z, Richard G, Bale S, Klein RT, Hruska KS, Chung WK.

Genet Med. 2015 Dec 17. doi: 10.1038/gim.2015.166. [Epub ahead of print]

PMID:
26681312
7.

Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease.

Capuano A, Bucciotti F, Farwell KD, Tippin Davis B, Mroske C, Hulick PJ, Weissman SM, Gao Q, Spessotto P, Colombatti A, Doliana R.

Hum Mutat. 2016 Jan;37(1):84-97. doi: 10.1002/humu.22920. Epub 2015 Nov 4.

8.

Transcriptome Signature and Regulation in Human Somatic Cell Reprogramming.

Tanaka Y, Hysolli E, Su J, Xiang Y, Kim KY, Zhong M, Li Y, Heydari K, Euskirchen G, Snyder MP, Pan X, Weissman SM, Park IH.

Stem Cell Reports. 2015 Jun 9;4(6):1125-39. doi: 10.1016/j.stemcr.2015.04.009. Epub 2015 May 21.

9.

A comparative encyclopedia of DNA elements in the mouse genome.

Yue F, Cheng Y, Breschi A, Vierstra J, Wu W, Ryba T, Sandstrom R, Ma Z, Davis C, Pope BD, Shen Y, Pervouchine DD, Djebali S, Thurman RE, Kaul R, Rynes E, Kirilusha A, Marinov GK, Williams BA, Trout D, Amrhein H, Fisher-Aylor K, Antoshechkin I, DeSalvo G, See LH, Fastuca M, Drenkow J, Zaleski C, Dobin A, Prieto P, Lagarde J, Bussotti G, Tanzer A, Denas O, Li K, Bender MA, Zhang M, Byron R, Groudine MT, McCleary D, Pham L, Ye Z, Kuan S, Edsall L, Wu YC, Rasmussen MD, Bansal MS, Kellis M, Keller CA, Morrissey CS, Mishra T, Jain D, Dogan N, Harris RS, Cayting P, Kawli T, Boyle AP, Euskirchen G, Kundaje A, Lin S, Lin Y, Jansen C, Malladi VS, Cline MS, Erickson DT, Kirkup VM, Learned K, Sloan CA, Rosenbloom KR, Lacerda de Sousa B, Beal K, Pignatelli M, Flicek P, Lian J, Kahveci T, Lee D, Kent WJ, Ramalho Santos M, Herrero J, Notredame C, Johnson A, Vong S, Lee K, Bates D, Neri F, Diegel M, Canfield T, Sabo PJ, Wilken MS, Reh TA, Giste E, Shafer A, Kutyavin T, Haugen E, Dunn D, Reynolds AP, Neph S, Humbert R, Hansen RS, De Bruijn M, Selleri L, Rudensky A, Josefowicz S, Samstein R, Eichler EE, Orkin SH, Levasseur D, Papayannopoulou T, Chang KH, Skoultchi A, Gosh S, Disteche C, Treuting P, Wang Y, Weiss MJ, Blobel GA, Cao X, Zhong S, Wang T, Good PJ, Lowdon RF, Adams LB, Zhou XQ, Pazin MJ, Feingold EA, Wold B, Taylor J, Mortazavi A, Weissman SM, Stamatoyannopoulos JA, Snyder MP, Guigo R, Gingeras TR, Gilbert DM, Hardison RC, Beer MA, Ren B; Mouse ENCODE Consortium.

Nature. 2014 Nov 20;515(7527):355-64. doi: 10.1038/nature13992.

10.

Co-detection and sequencing of genes and transcripts from the same single cells facilitated by a microfluidics platform.

Han L, Zi X, Garmire LX, Wu Y, Weissman SM, Pan X, Fan R.

Sci Rep. 2014 Sep 26;4:6485. doi: 10.1038/srep06485.

11.

Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.

Selkirk CG, Vogel KJ, Newlin AC, Weissman SM, Weiss SM, Wang CH, Hulick PJ.

Fam Cancer. 2014 Dec;13(4):527-36. doi: 10.1007/s10689-014-9741-4.

PMID:
25117502
12.

X Chromosome of female cells shows dynamic changes in status during human somatic cell reprogramming.

Kim KY, Hysolli E, Tanaka Y, Wang B, Jung YW, Pan X, Weissman SM, Park IH.

Stem Cell Reports. 2014 May 15;2(6):896-909. doi: 10.1016/j.stemcr.2014.04.003. eCollection 2014 Jun 3.

13.
14.

Extended lifespan and reduced adiposity in mice lacking the FAT10 gene.

Canaan A, DeFuria J, Perelman E, Schultz V, Seay M, Tuck D, Flavell RA, Snyder MP, Obin MS, Weissman SM.

Proc Natl Acad Sci U S A. 2014 Apr 8;111(14):5313-8. doi: 10.1073/pnas.1323426111. Epub 2014 Mar 24.

15.

Nonstochastic reprogramming from a privileged somatic cell state.

Guo S, Zi X, Schulz VP, Cheng J, Zhong M, Koochaki SH, Megyola CM, Pan X, Heydari K, Weissman SM, Gallagher PG, Krause DS, Fan R, Lu J.

Cell. 2014 Feb 13;156(4):649-62. doi: 10.1016/j.cell.2014.01.020. Epub 2014 Jan 30.

16.

Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2).

Tanaka Y, Kim KY, Zhong M, Pan X, Weissman SM, Park IH.

Hum Mol Genet. 2014 Feb 15;23(4):1045-55. doi: 10.1093/hmg/ddt500. Epub 2013 Oct 15.

17.

Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration.

Zhang Y, Schulz VP, Reed BD, Wang Z, Pan X, Mariani J, Euskirchen G, Snyder MP, Vaccarino FM, Ivanova N, Weissman SM, Szekely AM.

Proc Natl Acad Sci U S A. 2013 Jul 23;110(30):12361-6. doi: 10.1073/pnas.1309725110. Epub 2013 Jul 8.

18.

Robust measurement of telomere length in single cells.

Wang F, Pan X, Kalmbach K, Seth-Smith ML, Ye X, Antumes DM, Yin Y, Liu L, Keefe DL, Weissman SM.

Proc Natl Acad Sci U S A. 2013 May 21;110(21):E1906-12. doi: 10.1073/pnas.1306639110. Epub 2013 May 9.

19.

Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.

Selkirk CG, Weissman SM, Anderson A, Hulick PJ.

Genet Test Mol Biomarkers. 2013 Mar;17(3):219-25. doi: 10.1089/gtmb.2012.0165. Epub 2013 Feb 7.

PMID:
23390885
20.

Cell engineering with synthetic messenger RNA.

Rabinovich PM, Weissman SM.

Methods Mol Biol. 2013;969:3-28. doi: 10.1007/978-1-62703-260-5_1. Review.

PMID:
23296924
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