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Items: 43

1.

Corrigendum: Hallmarks of pluripotency.

De Los Angeles A, Ferrari F, Xi R, Fujiwara Y, Benvenisty N, Deng H, Hochedlinger K, Jaenisch R, Lee S, Leitch HG, Lensch MW, Lujan E, Pei D, Rossant J, Wernig M, Park PJ, Daley GQ.

Nature. 2016 Mar 17;531(7594):400. doi: 10.1038/nature16470. Epub 2015 Dec 16. No abstract available.

PMID:
26675727
2.

Hallmarks of pluripotency.

De Los Angeles A, Ferrari F, Xi R, Fujiwara Y, Benvenisty N, Deng H, Hochedlinger K, Jaenisch R, Lee S, Leitch HG, Lensch MW, Lujan E, Pei D, Rossant J, Wernig M, Park PJ, Daley GQ.

Nature. 2015 Sep 24;525(7570):469-78. doi: 10.1038/nature15515. Review. Erratum in: Nature. 2016 Mar 17;531(7594):400.

PMID:
26399828
3.

From stealing fire to cellular reprogramming: a scientific history leading to the 2012 Nobel Prize.

Lensch MW, Mummery CL.

Stem Cell Reports. 2013 Jun 4;1(1):5-17. doi: 10.1016/j.stemcr.2013.05.001. Review.

4.

Pluripotent stem cell models of Shwachman-Diamond syndrome reveal a common mechanism for pancreatic and hematopoietic dysfunction.

Tulpule A, Kelley JM, Lensch MW, McPherson J, Park IH, Hartung O, Nakamura T, Schlaeger TM, Shimamura A, Daley GQ.

Cell Stem Cell. 2013 Jun 6;12(6):727-36. doi: 10.1016/j.stem.2013.04.002. Epub 2013 Apr 18.

5.

Signaling axis involving Hedgehog, Notch, and Scl promotes the embryonic endothelial-to-hematopoietic transition.

Kim PG, Albacker CE, Lu YF, Jang IH, Lim Y, Heffner GC, Arora N, Bowman TV, Lin MI, Lensch MW, De Los Angeles A, Zon LI, Loewer S, Daley GQ.

Proc Natl Acad Sci U S A. 2013 Jan 8;110(2):E141-50. doi: 10.1073/pnas.1214361110. Epub 2012 Dec 12.

6.

An evolving model of hematopoietic stem cell functional identity.

Lensch MW.

Stem Cell Rev Rep. 2012 Jun;8(2):551-60. doi: 10.1007/s12015-012-9347-x. Review.

PMID:
22278132
7.

Donor cell type can influence the epigenome and differentiation potential of human induced pluripotent stem cells.

Kim K, Zhao R, Doi A, Ng K, Unternaehrer J, Cahan P, Huo H, Loh YH, Aryee MJ, Lensch MW, Li H, Collins JJ, Feinberg AP, Daley GQ.

Nat Biotechnol. 2011 Nov 27;29(12):1117-9. doi: 10.1038/nbt.2052. Erratum in: Nat Biotechnol. 2012 Jan;30(1):112.

8.

Public perception of stem cell and genomics research.

Lensch MW.

Genome Med. 2011 Jul 6;3(7):44. doi: 10.1186/gm260. No abstract available.

9.

Investigating monogenic and complex diseases with pluripotent stem cells.

Zhu H, Lensch MW, Cahan P, Daley GQ.

Nat Rev Genet. 2011 Apr;12(4):266-75. doi: 10.1038/nrg2951. Epub 2011 Mar 9. Review.

PMID:
21386866
10.

Induced pluripotent stem cells: opportunities and challenges.

Lensch MW, Rao M.

Regen Med. 2010 Jul;5(4):483-4. doi: 10.2217/rme.10.49. No abstract available.

11.

Reprogramming of T cells from human peripheral blood.

Loh YH, Hartung O, Li H, Guo C, Sahalie JM, Manos PD, Urbach A, Heffner GC, Grskovic M, Vigneault F, Lensch MW, Park IH, Agarwal S, Church GM, Collins JJ, Irion S, Daley GQ.

Cell Stem Cell. 2010 Jul 2;7(1):15-9. doi: 10.1016/j.stem.2010.06.004. No abstract available.

12.

Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage.

Tulpule A, Lensch MW, Miller JD, Austin K, D'Andrea A, Schlaeger TM, Shimamura A, Daley GQ.

Blood. 2010 Apr 29;115(17):3453-62. doi: 10.1182/blood-2009-10-246694. Epub 2010 Jan 20.

13.

Down's syndrome suppression of tumour growth and the role of the calcineurin inhibitor DSCR1.

Baek KH, Zaslavsky A, Lynch RC, Britt C, Okada Y, Siarey RJ, Lensch MW, Park IH, Yoon SS, Minami T, Korenberg JR, Folkman J, Daley GQ, Aird WC, Galdzicki Z, Ryeom S.

Nature. 2009 Jun 25;459(7250):1126-30. doi: 10.1038/nature08062. Epub 2009 May 20.

14.

Biomechanical forces promote embryonic haematopoiesis.

Adamo L, Naveiras O, Wenzel PL, McKinney-Freeman S, Mack PJ, Gracia-Sancho J, Suchy-Dicey A, Yoshimoto M, Lensch MW, Yoder MC, García-Cardeña G, Daley GQ.

Nature. 2009 Jun 25;459(7250):1131-5. doi: 10.1038/nature08073. Epub 2009 May 13.

15.

Cellular reprogramming and pluripotency induction.

Lensch MW.

Br Med Bull. 2009;90:19-35. doi: 10.1093/bmb/ldp011. Epub 2009 Apr 17. Review.

PMID:
19376801
16.

Broader implications of defining standards for the pluripotency of iPSCs.

Daley GQ, Lensch MW, Jaenisch R, Meissner A, Plath K, Yamanaka S.

Cell Stem Cell. 2009 Mar 6;4(3):200-1; author reply 202. doi: 10.1016/j.stem.2009.02.009. No abstract available.

17.

Disease-specific induced pluripotent stem cells.

Park IH, Arora N, Huo H, Maherali N, Ahfeldt T, Shimamura A, Lensch MW, Cowan C, Hochedlinger K, Daley GQ.

Cell. 2008 Sep 5;134(5):877-86. doi: 10.1016/j.cell.2008.07.041. Epub 2008 Aug 7.

18.

Teratoma formation assays with human embryonic stem cells: a rationale for one type of human-animal chimera.

Lensch MW, Schlaeger TM, Zon LI, Daley GQ.

Cell Stem Cell. 2007 Sep 13;1(3):253-8. doi: 10.1016/j.stem.2007.07.019. Epub 2007 Aug 23.

19.

Looking into the future of cell-based therapy.

Lensch MW, West JA.

South Med J. 2008 Jan;101(1):79-82. doi: 10.1097/SMJ.0b013e31815d4201.

PMID:
18176297
20.

Reprogramming of human somatic cells to pluripotency with defined factors.

Park IH, Zhao R, West JA, Yabuuchi A, Huo H, Ince TA, Lerou PH, Lensch MW, Daley GQ.

Nature. 2008 Jan 10;451(7175):141-6. Epub 2007 Dec 23.

PMID:
18157115
21.

The terminology of teratocarcinomas and teratomas.

Lensch MW, Ince TA.

Nat Biotechnol. 2007 Nov;25(11):1211; author reply 1211-2. No abstract available.

PMID:
17989663
22.

Current prospects for the generation of patient-specific pluripotent cells from adult tissues.

Agarwal S, Lensch MW, Daley GQ.

Regen Med. 2007 Sep;2(5):743-52. No abstract available.

23.

Hemogenic endothelial progenitor cells isolated from human umbilical cord blood.

Wu X, Lensch MW, Wylie-Sears J, Daley GQ, Bischoff J.

Stem Cells. 2007 Nov;25(11):2770-6. Epub 2007 Jul 19.

24.

Pluripotent stem cells and their niches.

Lensch MW, Daheron L, Schlaeger TM.

Stem Cell Rev. 2006;2(3):185-201. Review.

PMID:
17625255
25.

Human embryonic stem cells flock together.

Lensch MW, Daley GQ.

Nat Biotechnol. 2007 Jul;25(7):748-50. No abstract available.

PMID:
17621300
26.

Science aside: the trajectory of embryonic stem cell research in the USA.

Schlaeger TM, Lensch MW, Taylor PL.

Drug Discov Today. 2007 Apr;12(7-8):269-71. Epub 2007 Mar 1. No abstract available.

PMID:
17395086
27.

Scientific and clinical opportunities for modeling blood disorders with embryonic stem cells.

Lensch MW, Daley GQ.

Blood. 2006 Apr 1;107(7):2605-12. Epub 2005 Dec 6. Review.

28.

High-efficiency RNA interference in human embryonic stem cells.

Zaehres H, Lensch MW, Daheron L, Stewart SA, Itskovitz-Eldor J, Daley GQ.

Stem Cells. 2005 Mar;23(3):299-305.

29.

LIF/STAT3 signaling fails to maintain self-renewal of human embryonic stem cells.

Dahéron L, Opitz SL, Zaehres H, Lensch MW, Andrews PW, Itskovitz-Eldor J, Daley GQ.

Stem Cells. 2004;22(5):770-8. Erratum in: Stem Cells. 2007 Dec;25(12):3273. Lensch, William M [corrected to Lensch, M William].

30.

Origins of mammalian hematopoiesis: in vivo paradigms and in vitro models.

Lensch MW, Daley GQ.

Curr Top Dev Biol. 2004;60:127-96. Review.

PMID:
15094298
31.

Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia.

Lensch MW, Tischkowitz M, Christianson TA, Reifsteck CA, Speckhart SA, Jakobs PM, O'Dwyer ME, Olson SB, Le Beau MM, Hodgson SV, Mathew CG, Larson RA, Bagby GC Jr.

Blood. 2003 Jul 1;102(1):7-16. Epub 2003 Mar 13.

PMID:
12637330
32.

The Fanconi anemia group C gene product: signaling functions in hematopoietic cells.

Fagerlie S, Lensch MW, Pang Q, Bagby GC Jr.

Exp Hematol. 2001 Dec;29(12):1371-81. Review. No abstract available.

PMID:
11750095
33.

Selective pressure as an essential force in molecular evolution of myeloid leukemic clones: a view from the window of Fanconi anemia.

Lensch MW, Rathbun RK, Olson SB, Jones GR, Bagby GC Jr.

Leukemia. 1999 Nov;13(11):1784-9. Review.

34.

Clinical and molecular analysis in Joubert syndrome.

Pellegrino JE, Lensch MW, Muenke M, Chance PF.

Am J Med Genet. 1997 Oct 3;72(1):59-62.

PMID:
9295076
35.

Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A.

Graf WD, Chance PF, Lensch MW, Eng LJ, Lipe HP, Bird TD.

Cancer. 1996 Apr 1;77(7):1356-62.

PMID:
8608515
36.

Analysis of the CMT1A-REP repeat: mapping crossover breakpoints in CMT1A and HNPP.

Kiyosawa H, Lensch MW, Chance PF.

Hum Mol Genet. 1995 Dec;4(12):2327-34.

PMID:
8634706
37.

New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease.

Bone LJ, Dahl N, Lensch MW, Chance PF, Kelly T, Le Guern E, Magi S, Parry G, Shapiro H, Wang S, et al.

Neurology. 1995 Oct;45(10):1863-6.

PMID:
7477983
38.

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders.

Chance PF, Lensch MW, Lipe H, Brown RH Sr, Brown RH Jr, Bird TD.

Neurology. 1994 Dec;44(12):2253-7.

PMID:
7991108
39.

Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17.

Chance PF, Abbas N, Lensch MW, Pentao L, Roa BB, Patel PI, Lupski JR.

Hum Mol Genet. 1994 Feb;3(2):223-8.

PMID:
8004087
40.

Connexin mutations in X-linked Charcot-Marie-Tooth disease.

Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, Paul DL, Chen K, Lensch MW, Chance PF, Fischbeck KH.

Science. 1993 Dec 24;262(5142):2039-42.

PMID:
8266101
41.

DNA deletion associated with hereditary neuropathy with liability to pressure palsies.

Chance PF, Alderson MK, Leppig KA, Lensch MW, Matsunami N, Smith B, Swanson PD, Odelberg SJ, Disteche CM, Bird TD.

Cell. 1993 Jan 15;72(1):143-51.

PMID:
8422677
42.

Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1A.

Chance PF, Bird TD, Matsunami N, Lensch MW, Brothman AR, Feldman GM.

Neurology. 1992 Dec;42(12):2295-9.

PMID:
1461382
43.

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

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