-
2
-
-
38949105879
-
Phenotype and course of Hutchinson-Gilford progeria syndrome
-
Merideth MA, Gordon LB, Clauss S, Sachdev V, Smith AC, Perry MB, Brewer CC, Zalewski C, Kim HJ, Solomon B, Brooks BP, Gerber LH, Turner ML, Domingo DL, Hart TC, Graf J, Reynolds JC, Gropman A, Yanovski JA, Gerhard-Herman M, Collins FS, Nabel EG, Cannon RO 3rd, Gahl WA, Introne WJ. Phenotype and course of Hutchinson-Gilford progeria syndrome. N Engl J Med. 2008;358:592-604. doi: 10.1056/NEJMoa0706898.
-
(2008)
N Engl J Med.
, vol.358
, pp. 592-604
-
-
Merideth, M.A.1
Gordon, L.B.2
Clauss, S.3
Sachdev, V.4
Smith, A.C.5
Perry, M.B.6
Brewer, C.C.7
Zalewski, C.8
Kim, H.J.9
Solomon, B.10
Brooks, B.P.11
Gerber, L.H.12
Turner, M.L.13
Domingo, D.L.14
Hart, T.C.15
Graf, J.16
Reynolds, J.C.17
Gropman, A.18
Yanovski, J.A.19
Gerhard-Herman, M.20
Collins, F.S.21
Nabel, E.G.22
Cannon, R.O.23
Gahl, W.A.24
Introne, W.J.25
more..
-
3
-
-
84903775962
-
Impact of farnesylation inhibitors on survival in Hutchinson-Gilford progeria syndrome
-
Progeria Clinical Trials Collaborative
-
Gordon LB, Massaro J, D'Agostino RB Sr, Campbell SE, Brazier J, Brown WT, Kleinman ME, Kieran MW; Progeria Clinical Trials Collaborative. Impact of farnesylation inhibitors on survival in Hutchinson-Gilford progeria syndrome. Circulation. 2014;130:27-34. doi: 10.1161/CIRCULATIONAHA.113.008285.
-
(2014)
Circulation
, vol.130
, pp. 27-34
-
-
Gordon, L.B.1
Massaro, J.2
D'Agostino, R.B.3
Campbell, S.E.4
Brazier, J.5
Brown, W.T.6
Kleinman, M.E.7
Kieran, M.W.8
-
4
-
-
10744229294
-
Lamin A truncation in Hutchinson-Gilford progeria
-
De Sandre-Giovannoli A, Bernard R, Cau P, Navarro C, Amiel J, Boccaccio I, Lyonnet S, Stewart CL, Munnich A, Le Merrer M, Lévy N. Lamin A truncation in Hutchinson-Gilford progeria. Science. 2003;300:2055. doi: 10.1126/science.1084125.
-
(2003)
Science.
, vol.300
, pp. 2055
-
-
De Sandre-Giovannoli, A.1
Bernard, R.2
Cau, P.3
Navarro, C.4
Amiel, J.5
Boccaccio, I.6
Lyonnet, S.7
Stewart, C.L.8
Munnich, A.9
Le Merrer, M.10
Lévy, N.11
-
5
-
-
0037673950
-
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome
-
Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature. 2003;423:293-298. doi: 10.1038/nature01629.
-
(2003)
Nature
, vol.423
, pp. 293-298
-
-
Eriksson, M.1
Brown, W.T.2
Gordon, L.B.3
Glynn, M.W.4
Singer, J.5
Scott, L.6
Erdos, M.R.7
Robbins, C.M.8
Moses, T.Y.9
Berglund, P.10
Dutra, A.11
Pak, E.12
Durkin, S.13
Csoka, A.B.14
Boehnke, M.15
Glover, T.W.16
Collins, F.S.17
-
6
-
-
33745915850
-
Nuclear lamins: Laminopathies and their role in premature ageing
-
Broers JL, Ramaekers FC, Bonne G, Yaou RB, Hutchison CJ. Nuclear lamins: laminopathies and their role in premature ageing. Physiol Rev. 2006;86:967-1008. doi: 10.1152/physrev. 00047.2005.
-
(2006)
Physiol Rev.
, vol.86
, pp. 967-1008
-
-
Broers, J.L.1
Ramaekers, F.C.2
Bonne, G.3
Yaou, R.B.4
Hutchison, C.J.5
-
7
-
-
0028118904
-
The processing pathway of prelamin A
-
Sinensky M, Fantle K, Trujillo M, McLain T, Kupfer A, Dalton M. The processing pathway of prelamin A. J Cell Sci. 1994;107(pt 1):61-67.
-
(1994)
J Cell Sci.
, vol.107
, pp. 61-67
-
-
Sinensky, M.1
Fantle, K.2
Trujillo, M.3
McLain, T.4
Kupfer, A.5
Dalton, M.6
-
8
-
-
2942643923
-
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome
-
Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, Gruenbaum Y, Khuon S, Mendez M, Varga R, Collins FS. Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA. 2004;101:8963-8968. doi: 10.1073/pnas.0402943101.
-
(2004)
Proc Natl Acad Sci USA.
, vol.101
, pp. 8963-8968
-
-
Goldman, R.D.1
Shumaker, D.K.2
Erdos, M.R.3
Eriksson, M.4
Goldman, A.E.5
Gordon, L.B.6
Gruenbaum, Y.7
Khuon, S.8
Mendez, M.9
Varga, R.10
Collins, F.S.11
-
9
-
-
30844467746
-
Lipid posttranslational modifications. Farnesyl transferase inhibitors
-
Basso AD, Kirschmeier P, Bishop WR. Lipid posttranslational modifications. Farnesyl transferase inhibitors. J Lipid Res. 2006;47:15-31. doi: 10.1194/jlr.R500012-JLR200.
-
(2006)
J Lipid Res.
, vol.47
, pp. 15-31
-
-
Basso, A.D.1
Kirschmeier, P.2
Bishop, W.R.3
-
10
-
-
84897510867
-
Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with Hutchinson-Gilford progeria syndrome
-
Blondel S, Jaskowiak AL, Egesipe AL, Le Corf A, Navarro C, Cordette V, Martinat C, Laabi Y, Djabali K, de Sandre-Giovannoli A, Levy N, Peschanski M, Nissan X. Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with Hutchinson-Gilford progeria syndrome. Stem Cells Transl Med. 2014;3:510-519. doi: 10.5966/sctm.2013-0168.
-
(2014)
Stem Cells Transl Med.
, vol.3
, pp. 510-519
-
-
Blondel, S.1
Jaskowiak, A.L.2
Egesipe, A.L.3
Le Corf, A.4
Navarro, C.5
Cordette, V.6
Martinat, C.7
Laabi, Y.8
Djabali, K.9
De Sandre-Giovannoli, A.10
Levy, N.11
Peschanski, M.12
Nissan, X.13
-
11
-
-
22544440839
-
Blocking protein farnesyltransferase improves nuclear blebbing in mouse fibroblasts with a targeted Hutchinson-Gilford progeria syndrome mutation
-
Yang SH, Bergo MO, Toth JI, Qiao X, Hu Y, Sandoval S, Meta M, Bendale P, Gelb MH, Young SG, Fong LG. Blocking protein farnesyltransferase improves nuclear blebbing in mouse fibroblasts with a targeted Hutchinson-Gilford progeria syndrome mutation. Proc Natl Acad Sci USA. 2005;102:10291-10296. doi: 10.1073/pnas.0504641102.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, pp. 10291-10296
-
-
Yang, S.H.1
Bergo, M.O.2
Toth, J.I.3
Qiao, X.4
Hu, Y.5
Sandoval, S.6
Meta, M.7
Bendale, P.8
Gelb, M.H.9
Young, S.G.10
Fong, L.G.11
-
12
-
-
27544498316
-
Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition
-
Glynn MW, Glover TW. Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition. Hum Mol Genet. 2005;14:2959-2969. doi: 10.1093/hmg/ddi326.
-
(2005)
Hum Mol Genet.
, vol.14
, pp. 2959-2969
-
-
Glynn, M.W.1
Glover, T.W.2
-
13
-
-
24644520772
-
Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome
-
Capell BC, Erdos MR, Madigan JP, Fiordalisi JJ, Varga R, Conneely KN, Gordon LB, Der CJ, Cox AD, Collins FS. Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA. 2005;102:12879-12884. doi: 10.1073/pnas.0506001102.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, pp. 12879-12884
-
-
Capell, B.C.1
Erdos, M.R.2
Madigan, J.P.3
Fiordalisi, J.J.4
Varga, R.5
Conneely, K.N.6
Gordon, L.B.7
Der, C.J.8
Cox, A.D.9
Collins, F.S.10
-
14
-
-
57349159315
-
A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model
-
Capell BC, Olive M, Erdos MR, Cao K, Faddah DA, Tavarez UL, Conneely KN, Qu X, San H, Ganesh SK, Chen X, Avallone H, Kolodgie FD, Virmani R, Nabel EG, Collins FS. A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model. Proc Natl Acad Sci USA. 2008;105:15902-15907. doi: 10.1073/pnas.0807840105.
-
(2008)
Proc Natl Acad Sci USA.
, vol.105
, pp. 15902-15907
-
-
Capell, B.C.1
Olive, M.2
Erdos, M.R.3
Cao, K.4
Faddah, D.A.5
Tavarez, U.L.6
Conneely, K.N.7
Qu, X.8
San, H.9
Ganesh, S.K.10
Chen, X.11
Avallone, H.12
Kolodgie, F.D.13
Virmani, R.14
Nabel, E.G.15
Collins, F.S.16
-
15
-
-
33645060977
-
A protein farnesyltransferase inhibitor ameliorates disease in a mouse model of progeria
-
Fong LG, Frost D, Meta M, Qiao X, Yang SH, Coffinier C, Young SG. A protein farnesyltransferase inhibitor ameliorates disease in a mouse model of progeria. Science. 2006;311:1621-1623. doi: 10.1126/science.1124875.
-
(2006)
Science
, vol.311
, pp. 1621-1623
-
-
Fong, L.G.1
Frost, D.2
Meta, M.3
Qiao, X.4
Yang, S.H.5
Coffinier, C.6
Young, S.G.7
-
16
-
-
33746715642
-
A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation
-
Yang SH, Meta M, Qiao X, Frost D, Bauch J, Coffinier C, Majumdar S, Bergo MO, Young SG, Fong LG. A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation. J Clin Invest. 2006;116:2115-2121. doi: 10.1172/JCI28968.
-
(2006)
J Clin Invest.
, vol.116
, pp. 2115-2121
-
-
Yang, S.H.1
Meta, M.2
Qiao, X.3
Frost, D.4
Bauch, J.5
Coffinier, C.6
Majumdar, S.7
Bergo, M.O.8
Young, S.G.9
Fong, L.G.10
-
17
-
-
84867380060
-
Clinical trial of a farnesyltransferase inhibitor in children with Hutchinson-Gilford progeria syndrome
-
Gordon LB, Kleinman ME, Miller DT, Neuberg DS, Giobbie-Hurder A, Gerhard-Herman M, Smoot LB, Gordon CM, Cleveland R, Snyder BD, Fligor B, Bishop WR, Statkevich P, Regen A, Sonis A, Riley S, Ploski C, Correia A, Quinn N, Ullrich NJ, Nazarian A, Liang MG, Huh SY, Schwartzman A, Kieran MW. Clinical trial of a farnesyltransferase inhibitor in children with Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA. 2012;109:16666-16671. doi: 10.1073/pnas.1202529109.
-
(2012)
Proc Natl Acad Sci USA.
, vol.109
, pp. 16666-16671
-
-
Gordon, L.B.1
Kleinman, M.E.2
Miller, D.T.3
Neuberg, D.S.4
Giobbie-Hurder, A.5
Gerhard-Herman, M.6
Smoot, L.B.7
Gordon, C.M.8
Cleveland, R.9
Snyder, B.D.10
Fligor, B.11
Bishop, W.R.12
Statkevich, P.13
Regen, A.14
Sonis, A.15
Riley, S.16
Ploski, C.17
Correia, A.18
Quinn, N.19
Ullrich, N.J.20
Nazarian, A.21
Liang, M.G.22
Huh, S.Y.23
Schwartzman, A.24
Kieran, M.W.25
more..
-
18
-
-
84881307604
-
Neurologic features of Hutchinson-Gilford progeria syndrome after lonafarnib treatment
-
Ullrich NJ, Kieran MW, Miller DT, Gordon LB, Cho YJ, Silvera VM, Giobbie-Hurder A, Neuberg D, Kleinman ME. Neurologic features of Hutchinson-Gilford progeria syndrome after lonafarnib treatment. Neurology. 2013;81:427-430. doi: 10.1212/WNL.0b013e31829d85c0.
-
(2013)
Neurology.
, vol.81
, pp. 427-430
-
-
Ullrich, N.J.1
Kieran, M.W.2
Miller, D.T.3
Gordon, L.B.4
Cho, Y.J.5
Silvera, V.M.6
Giobbie-Hurder, A.7
Neuberg, D.8
Kleinman, M.E.9
-
19
-
-
46849106102
-
Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging
-
Varela I, Pereira S, Ugalde AP, Navarro CL, Suárez MF, Cau P, Cadinanõs J, Osorio FG, Foray N, Cobo J, de Carlos F, Lévy N, Freije JM, López-Otín C. Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging. Nat Med. 2008;14:767-772. doi: 10.1038/nm1786.
-
(2008)
Nat Med.
, vol.14
, pp. 767-772
-
-
Varela, I.1
Pereira, S.2
Ugalde, A.P.3
Navarro, C.L.4
Suárez, M.F.5
Cau, P.6
Cadinanõs, J.7
Osorio, F.G.8
Foray, N.9
Cobo, J.10
De Carlos, F.11
Lévy, N.12
Freije, J.M.13
López-Otín, C.14
-
20
-
-
35148831133
-
Disease progression in Hutchinson-Gilford progeria syndrome: Impact on growth and development
-
Gordon LB, McCarten KM, Giobbie-Hurder A, Machan JT, Campbell SE, Berns SD, Kieran MW. Disease progression in Hutchinson-Gilford progeria syndrome: impact on growth and development. Pediatrics. 2007;120:824-833. doi: 10.1542/peds.2007-1357.
-
(2007)
Pediatrics.
, vol.120
, pp. 824-833
-
-
Gordon, L.B.1
McCarten, K.M.2
Giobbie-Hurder, A.3
MacHan, J.T.4
Campbell, S.E.5
Berns, S.D.6
Kieran, M.W.7
-
21
-
-
83655167073
-
Mechanisms of premature vascular aging in children with Hutchinson-Gilford progeria syndrome
-
Gerhard-Herman M, Smoot LB, Wake N, Kieran MW, Kleinman ME, Miller DT, Schwartzman A, Giobbie-Hurder A, Neuberg D, Gordon LB. Mechanisms of premature vascular aging in children with Hutchinson-Gilford progeria syndrome. Hypertension. 2012;59:92-97. doi: 10.1161/HYPERTENSIONAHA.111.180919.
-
(2012)
Hypertension.
, vol.59
, pp. 92-97
-
-
Gerhard-Herman, M.1
Smoot, L.B.2
Wake, N.3
Kieran, M.W.4
Kleinman, M.E.5
Miller, D.T.6
Schwartzman, A.7
Giobbie-Hurder, A.8
Neuberg, D.9
Gordon, L.B.10
-
22
-
-
84866729769
-
A prospective study of radiographic manifestations in Hutchinson-Gilford progeria syndrome
-
Cleveland RH, Gordon LB, Kleinman ME, Miller DT, Gordon CM, Snyder BD, Nazarian A, Giobbie-Hurder A, Neuberg D, Kieran MW. A prospective study of radiographic manifestations in Hutchinson-Gilford progeria syndrome. Pediatr Radiol. 2012;42:1089-1098. doi: 10.1007/s00247-012-2423-1.
-
(2012)
Pediatr Radiol.
, vol.42
, pp. 1089-1098
-
-
Cleveland, R.H.1
Gordon, L.B.2
Kleinman, M.E.3
Miller, D.T.4
Gordon, C.M.5
Snyder, B.D.6
Nazarian, A.7
Giobbie-Hurder, A.8
Neuberg, D.9
Kieran, M.W.10
-
23
-
-
79959494879
-
Hutchinson-Gilford progeria is a skeletal dysplasia
-
Gordon CM, Gordon LB, Snyder BD, Nazarian A, Quinn N, Huh S, Giobbie-Hurder A, Neuberg D, Cleveland R, Kleinman M, Miller DT, Kieran MW. Hutchinson-Gilford progeria is a skeletal dysplasia. J Bone Miner Res. 2011;26:1670-1679. doi: 10.1002/jbmr.392.
-
(2011)
J Bone Miner Res.
, vol.26
, pp. 1670-1679
-
-
Gordon, C.M.1
Gordon, L.B.2
Snyder, B.D.3
Nazarian, A.4
Quinn, N.5
Huh, S.6
Giobbie-Hurder, A.7
Neuberg, D.8
Cleveland, R.9
Kleinman, M.10
Miller, D.T.11
Kieran, M.W.12
-
24
-
-
34547659068
-
Phase i and pharmacokinetic study of the oral farnesyltransferase inhibitor lonafarnib administered twice daily to pediatric patients with advanced central nervous system tumors using a modified continuous reassessment method: A Pediatric Brain Tumor Consortium Study
-
Kieran MW, Packer RJ, Onar A, Blaney SM, Phillips P, Pollack IF, Geyer JR, Gururangan S, Banerjee A, Goldman S, Turner CD, Belasco JB, Broniscer A, Zhu Y, Frank E, Kirschmeier P, Statkevich P, Yver A, Boyett JM, Kun LE. Phase I and pharmacokinetic study of the oral farnesyltransferase inhibitor lonafarnib administered twice daily to pediatric patients with advanced central nervous system tumors using a modified continuous reassessment method: a Pediatric Brain Tumor Consortium Study. J Clin Oncol. 2007;25:3137-3143. doi: 10.1200/JCO.2006.09.4243.
-
(2007)
J Clin Oncol.
, vol.25
, pp. 3137-3143
-
-
Kieran, M.W.1
Packer, R.J.2
Onar, A.3
Blaney, S.M.4
Phillips, P.5
Pollack, I.F.6
Geyer, J.R.7
Gururangan, S.8
Banerjee, A.9
Goldman, S.10
Turner, C.D.11
Belasco, J.B.12
Broniscer, A.13
Zhu, Y.14
Frank, E.15
Kirschmeier, P.16
Statkevich, P.17
Yver, A.18
Boyett, J.M.19
Kun, L.E.20
more..
-
25
-
-
34547605714
-
Acute phase response and mineral status following low dose intravenous zoledronic acid in children
-
Munns CF, Rajab MH, Hong J, Briody J, Högler W, McQuade M, Little DG, Cowell CT. Acute phase response and mineral status following low dose intravenous zoledronic acid in children. Bone. 2007;41:366-370. doi: 10.1016/j.bone.2007.05.002.
-
(2007)
Bone.
, vol.41
, pp. 366-370
-
-
Munns, C.F.1
Rajab, M.H.2
Hong, J.3
Briody, J.4
Högler, W.5
McQuade, M.6
Little, D.G.7
Cowell, C.T.8
-
26
-
-
67650901821
-
An echolucent carotid artery intima-media complex is a new and independent predictor of mortality in an elderly male cohort
-
Wohlin M, Sundström J, Andrén B, Larsson A, Lind L. An echolucent carotid artery intima-media complex is a new and independent predictor of mortality in an elderly male cohort. Atherosclerosis. 2009;205:486-491. doi: 10.1016/j.atherosclerosis. 2009.01.032.
-
(2009)
Atherosclerosis.
, vol.205
, pp. 486-491
-
-
Wohlin, M.1
Sundström, J.2
Andrén, B.3
Larsson, A.4
Lind, L.5
-
27
-
-
78650995671
-
A human iPSC model of Hutchinson Gilford progeria reveals vascular smooth muscle and mesenchymal stem cell defects
-
Zhang J, Lian Q, Zhu G, Zhou F, Sui L, Tan C, Mutalif RA, Navasankari R, Zhang Y, Tse HF, Stewart CL, Colman A. A human iPSC model of Hutchinson Gilford progeria reveals vascular smooth muscle and mesenchymal stem cell defects. Cell Stem Cell. 2011;8:31-45. doi: 10.1016/j.stem.2010.12.002.
-
(2011)
Cell Stem Cell.
, vol.8
, pp. 31-45
-
-
Zhang, J.1
Lian, Q.2
Zhu, G.3
Zhou, F.4
Sui, L.5
Tan, C.6
Mutalif, R.A.7
Navasankari, R.8
Zhang, Y.9
Tse, H.F.10
Stewart, C.L.11
Colman, A.12
-
28
-
-
84879297808
-
Defective extracellular pyrophosphate metabolism promotes vascular calcification in a mouse model of Hutchinson-Gilford progeria syndrome that is ameliorated on pyrophosphate treatment
-
Villa-Bellosta R, Rivera-Torres J, Osorio FG, Acín-Pérez R, Enriquez JA, López-Otín C, Andrés V. Defective extracellular pyrophosphate metabolism promotes vascular calcification in a mouse model of Hutchinson-Gilford progeria syndrome that is ameliorated on pyrophosphate treatment. Circulation. 2013;127:2442-2451. doi: 10.1161/CIRCULATIONAHA.112.000571.
-
(2013)
Circulation.
, vol.127
, pp. 2442-2451
-
-
Villa-Bellosta, R.1
Rivera-Torres, J.2
Osorio, F.G.3
Acín-Pérez, R.4
Enriquez, J.A.5
López-Otín, C.6
Andrés, V.7
-
29
-
-
43149124203
-
Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing
-
Scaffidi P, Misteli T. Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing. Nat Cell Biol. 2008;10:452-459. doi: 10.1038/ncb1708.
-
(2008)
Nat Cell Biol.
, vol.10
, pp. 452-459
-
-
Scaffidi, P.1
Misteli, T.2
-
30
-
-
0031920748
-
Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: A national study
-
Block GA, Hulbert-Shearon TE, Levin NW, Port FK. Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: a national study. Am J Kidney Dis. 1998;31:607-617.
-
(1998)
Am J Kidney Dis.
, vol.31
, pp. 607-617
-
-
Block, G.A.1
Hulbert-Shearon, T.E.2
Levin, N.W.3
Port, F.K.4
-
31
-
-
84977615740
-
The decisionmaking process and criteria in selecting candidate drugs for progeria clinical trials
-
[published online ahead of print May 26 2016] Accessed May 17, 2016
-
Gordon LB, Kleinman ME, Kieran MW, Misteli T. The decisionmaking process and criteria in selecting candidate drugs for progeria clinical trials [published online ahead of print May 26, 2016]. EMBO J. doi: 10.15252/emmm.201606280. http://embomolmed.embopress.org/content/early/2016/05/26/emmm.201606280.long. Accessed May 17, 2016.
-
EMBO J
-
-
Gordon, L.B.1
Kleinman, M.E.2
Kieran, M.W.3
Misteli, T.4
|