M. William Lensch
M. William Lensch
Chief of Staff, Office of the Dean, Harvard Medical School
Bekræftet mail på hms.harvard.edu - Startside
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Reprogramming of human somatic cells to pluripotency with defined factors
IH Park, R Zhao, JA West, A Yabuuchi, H Huo, TA Ince, PH Lerou, ...
Nature 451 (7175), 141-146, 2007
33662007
Disease-specific induced pluripotent stem cells
IH Park, N Arora, H Huo, N Maherali, T Ahfeldt, A Shimamura, MW Lensch, ...
cell 134 (5), 877-886, 2008
24382008
Connexin mutations in X-linked Charcot-Marie-Tooth disease
J Bergoffen, SS Scherer, S Wang, MO Scott, LJ Bone, DL Paul, K Chen, ...
Science 262 (5142), 2039-2042, 1993
12441993
DNA deletion associated with hereditary neuropathy with liability to pressure palsies
PF Chance, MK Alderson, KA Leppig, MW Lensch, N Matsunami, B Smith, ...
Cell 72 (1), 143-151, 1993
8801993
Donor cell type can influence the epigenome and differentiation potential of human induced pluripotent stem cells
K Kim, R Zhao, A Doi, K Ng, J Unternaehrer, P Cahan, H Hongguang, ...
Nature biotechnology 29 (12), 1117-1119, 2011
5592011
Biomechanical forces promote embryonic haematopoiesis
L Adamo, O Naveiras, PL Wenzel, S McKinney-Freeman, PJ Mack, ...
Nature 459 (7250), 1131-1135, 2009
4692009
Down's syndrome suppression of tumour growth and the role of the calcineurin inhibitor DSCR1
KH Baek, A Zaslavsky, RC Lynch, C Britt, Y Okada, RJ Siarey, MW Lensch, ...
Nature 459 (7250), 1126-1130, 2009
3522009
Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11. 2 associated with Charcot–Marie–Tooth 1A
N Matsunami, B Smith, L Ballard, MW Lensch, M Robertson, H Albertsen, ...
Nature genetics 1 (3), 176-179, 1992
3441992
Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
PF Chance, N Abbas, MW Lensch, L Pentao, BB Roa, PI Patel, JR Lupski
Human Molecular Genetics 3 (2), 223-228, 1994
3431994
High‐efficiency RNA interference in human embryonic stem cells
H Zaehres, MW Lensch, L Daheron, SA Stewart, J Itskovitz‐Eldor, ...
Stem Cells 23 (3), 299-305, 2005
3402005
Reprogramming of T cells from human peripheral blood
YH Loh, O Hartung, H Li, C Guo, JM Sahalie, PD Manos, A Urbach, ...
Cell stem cell 7 (1), 15, 2010
3202010
Hallmarks of pluripotency
A De Los Angeles, F Ferrari, R Xi, Y Fujiwara, N Benvenisty, H Deng, ...
Nature 525 (7570), 469-478, 2015
2922015
Teratoma formation assays with human embryonic stem cells: a rationale for one type of human-animal chimera
MW Lensch, TM Schlaeger, LI Zon, GQ Daley
Cell Stem Cell 1 (3), 253-258, 2007
1552007
Severe vincristine neuropathy in charcot‐marie‐tooth disease type 1A
WD Graf, PF Chance, MW Lensch, LJ Eng, HP Lipe, TD Bird
Cancer 77 (7), 1356-1362, 1996
1371996
Broader implications of defining standards for the pluripotency of iPSCs.
GQ Daley, MW Lensch, R Jaenisch, A Meissner, K Plath, S Yamanaka
Cell Stem Cell 4 (3), 200, 2009
1342009
Investigating monogenic and complex diseases with pluripotent stem cells
H Zhu, MW Lensch, P Cahan, GQ Daley
Nature Reviews Genetics 12 (4), 266-275, 2011
1142011
Trisomy 17p associated with Charcot‐Marie‐Tooth neuropathy type 1A phenotype Evidence for gene dosage as a mechanism in CMT1A
PF Chance, TD Bird, N Matsunami, MW Lensch, AR Brothman, ...
Neurology 42 (12), 2295-2295, 1992
1081992
The terminology of teratocarcinomas and teratomas
MW Lensch, TA Ince
Nature biotechnology 25 (11), 1211-1211, 2007
97*2007
Pluripotent stem cells and their niches
MW Lensch, L Daheron, TM Schlaeger
Stem cell reviews 2 (3), 185-201, 2006
892006
Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage
A Tulpule, MW Lensch, JD Miller, K Austin, A D'Andrea, TM Schlaeger, ...
Blood 115 (17), 3453-3462, 2010
882010
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Artikler 1–20