-
1
-
-
12644266319
-
Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence
-
Weeda G., Donker I., de Wit J., Morreau H., Janssens R., Vissers C. J., Nigg A., Van Steeg H., Bootsma D., Hoeijmakers J. H. J., Disruption of mouse Ercc1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence. Current Biology 1997 7 6 427 439 2-s2.0-12644266319 (Pubitemid 27274796)
-
(1997)
Current Biology
, vol.7
, Issue.6
, pp. 427-439
-
-
Weeda, G.1
Donker, I.2
De Wit, J.3
Morreau, H.4
Janssens, R.5
Vissers, C.J.6
Nigg, A.7
Van Steeg, H.8
Bootsma, D.9
Hoeijmakers, J.H.J.10
-
2
-
-
79960394750
-
Physiological consequences of defects in Ercc1 -XPF DNA repair endonuclease
-
2-s2.0-79960394750 10.1016/j.dnarep.2011.04.026
-
Gregg S. Q., Robinson A. R., Niedernhofer L. J., Physiological consequences of defects in Ercc1 -XPF DNA repair endonuclease. DNA Repair 2011 10 7 781 791 2-s2.0-79960394750 10.1016/j.dnarep.2011.04.026
-
(2011)
DNA Repair
, vol.10
, Issue.7
, pp. 781-791
-
-
Gregg, S.Q.1
Robinson, A.R.2
Niedernhofer, L.J.3
-
3
-
-
33749838920
-
Mice with skin-specific DNA repair gene (Ercc1) inactivation are hypersensitive to ultraviolet irradiation-induced skin cancer and show more rapid actinic progression
-
DOI 10.1038/sj.onc.1209642, PII 1209642
-
Doig J., Anderson C., Lawrence N. J., Selfridge J., Brownstein D. G., Melton D. W., Mice with skin-specific DNA repair gene (Ercc1) inactivation are hypersensitive to ultraviolet irradiation-induced skin cancer and show more rapid actinic progression. Oncogene 2006 25 47 6229 6238 2-s2.0-33749838920 10.1038/sj.onc.1209642 (Pubitemid 44564740)
-
(2006)
Oncogene
, vol.25
, Issue.47
, pp. 6229-6238
-
-
Doig, J.1
Anderson, C.2
Lawrence, N.J.3
Selfridge, J.4
Brownstein, D.G.5
Melton, D.W.6
-
4
-
-
0027378895
-
Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaning
-
DOI 10.1038/ng1193-217
-
McWhir J., Selfridge J., Harrison D. J., Squires S., Melton D. W., Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaning. Nature Genetics 1993 5 3 217 224 2-s2.0-0027378895 10.1038/ng1193-217 (Pubitemid 23330382)
-
(1993)
Nature Genetics
, vol.5
, Issue.3
, pp. 217-224
-
-
McWhir, J.1
Selfridge, J.2
Harrison, D.J.3
Squires, S.4
Melton, D.W.5
-
5
-
-
15444370725
-
-/- mice
-
DOI 10.1038/sj.emboj.7600542
-
-/- mice. EMBO Journal 2005 24 4 861 871 2-s2.0-15444370725 10.1038/sj.emboj.7600542 (Pubitemid 40396114)
-
(2005)
EMBO Journal
, vol.24
, Issue.4
, pp. 861-871
-
-
Prasher, J.M.1
Lalai, A.S.2
Heijmans-Antonissen, C.3
Ploemacher, R.E.4
Hoeijmakers, J.H.J.5
Touw, I.P.6
Niedernhofer, L.J.7
-
6
-
-
0035890270
-
The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells
-
DOI 10.1093/emboj/20.22.6540
-
Niedernhofer L. J., Essers J., Weeda G., Beverloo B., De Wit J., Muijtjens M., Odijk H., Hoeijmakers J. H. J., Kanaar R., The structure-specific endonuclease Ercc1 -Xpf is required for targeted gene replacement in embryonic stem cells. EMBO Journal 2001 20 22 6540 6549 2-s2.0-0035890270 10.1093/emboj/20.22.6540 (Pubitemid 33078726)
-
(2001)
EMBO Journal
, vol.20
, Issue.22
, pp. 6540-6549
-
-
Niedernhofer, L.J.1
Essers, J.2
Weeda, G.3
Beverloo, B.4
De Wit, J.5
Muijtjens, M.6
Odijk, H.7
Hoeijmakers, J.H.J.8
Kanaar, R.9
-
7
-
-
0035818496
-
Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum group A and Cockayne syndrome group B DNA repair genes
-
DOI 10.1073/pnas.231329598
-
Murai M., Enokido Y., Inamura N., Yoshino M., Nakatsu Y., Van Der Horst G. T. J., Hoeijmakers J. H. J., Tanaka K., Hatanaka H., Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum group A and Cockayne syndrome group B DNA repair genes. Proceedings of the National Academy of Sciences of the United States of America 2001 98 23 13379 13384 2-s2.0-0035818496 10.1073/pnas.231329598 (Pubitemid 33051371)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.23
, pp. 13379-13384
-
-
Murai, M.1
Enokido, Y.2
Inamura, N.3
Yoshino, M.4
Nakatsu, Y.5
Van Der Horst, G.T.J.6
Hoeijmakers, J.H.J.7
Tanaka, K.8
Hatanaka, H.9
-
8
-
-
67349287384
-
Persistent transcription-blocking DNA lesions trigger somatic growth attenuation associated with longevity
-
2-s2.0-67349287384 10.1038/ncb1866
-
Garinis G. A., Uittenboogaard L. M., Stachelscheid H., Fousteri M., van Ijcken W., Breit T. M., van Steeg H., Mullenders L. H. F., van der Horst G. T. J., Brüning J. C., Niessen C. M., Hoeijmakers J. H. J., Schumacher B., Persistent transcription-blocking DNA lesions trigger somatic growth attenuation associated with longevity. Nature Cell Biology 2009 11 5 604 615 2-s2.0-67349287384 10.1038/ncb1866
-
(2009)
Nature Cell Biology
, vol.11
, Issue.5
, pp. 604-615
-
-
Garinis, G.A.1
Uittenboogaard, L.M.2
Stachelscheid, H.3
Fousteri, M.4
Van Ijcken, W.5
Breit, T.M.6
Van Steeg, H.7
Mullenders, L.H.F.8
Van Der Horst, G.T.J.9
Brüning, J.C.10
Niessen, C.M.11
Hoeijmakers, J.H.J.12
Schumacher, B.13
-
9
-
-
33846030099
-
Impaired genome maintenance suppresses the growth hormone-insulin-like growth factor 1 axis in mice with cockayne syndrome
-
article e2 2-s2.0-33846030099
-
van der Pluijm I., Garinis G. A., Brandt R. M. C., Gorgels T. G. M. F., Wijnhoven S. W., Diderich K. E. M., De Wit J., Mitchell J. R., Van Oostrom C., Beems R., Niedernhofer L. J., Velasco S., Friedberg E. C., Tanaka K., Van Steeg H., Hoeijmakers J. H. J., Van Der Horst G. T. J., Impaired genome maintenance suppresses the growth hormone-insulin-like growth factor 1 axis in mice with cockayne syndrome. PLoS Biology 2007 5 1, article e2 2-s2.0-33846030099
-
(2007)
PLoS Biology
, vol.5
, Issue.1
-
-
Van Der Pluijm, I.1
Garinis, G.A.2
Brandt, R.M.C.3
Gorgels, T.G.M.F.4
Wijnhoven, S.W.5
Diderich, K.E.M.6
De Wit, J.7
Mitchell, J.R.8
Van Oostrom, C.9
Beems, R.10
Niedernhofer, L.J.11
Velasco, S.12
Friedberg, E.C.13
Tanaka, K.14
Van Steeg, H.15
Hoeijmakers, J.H.J.16
Van Der Horst, G.T.J.17
-
10
-
-
0032052129
-
Assessment of mitomycin C sensitivity in Fanconi anemia complementation group C gene (Fac) knock-out mouse cells
-
PII S0925571098000127
-
Otsuki T., Wang J., Demuth I., Digweed M., Liu J. M., Assessment of mitomycin C sensitivity in Fanconi anemia complementation group C gene (Fac) knock-out mouse cells. International Journal of Hematology 1998 67 3 243 248 2-s2.0-0032052129 (Pubitemid 28257136)
-
(1998)
International Journal of Hematology
, vol.67
, Issue.3
, pp. 243-248
-
-
Otsuki, T.1
Wang, J.2
Demuth, I.3
Digweed, M.4
Liu, J.M.5
-
11
-
-
71949083551
-
XPF- Ercc1 participates in the Fanconi anemia pathway of cross-link repair
-
2-s2.0-71949083551 10.1128/MCB.00086-09
-
Bhagwat N., Olsen A. L., Wang A. T., Hanada K., Stuckert P., Kanaar R., D'Andrea A., Niedernhofer L. J., McHugh P. J., XPF- Ercc1 participates in the Fanconi anemia pathway of cross-link repair. Molecular and Cellular Biology 2009 29 24 6427 6437 2-s2.0-71949083551 10.1128/MCB.00086-09
-
(2009)
Molecular and Cellular Biology
, vol.29
, Issue.24
, pp. 6427-6437
-
-
Bhagwat, N.1
Olsen, A.L.2
Wang, A.T.3
Hanada, K.4
Stuckert, P.5
Kanaar, R.6
D'Andrea, A.7
Niedernhofer, L.J.8
McHugh, P.J.9
-
12
-
-
82755184119
-
The Fanconi anaemia pathway orchestrates incisions at sites of crosslinked DNA
-
Crossan G. P., Patel K. J., The Fanconi anaemia pathway orchestrates incisions at sites of crosslinked DNA. The Journal of Pathology 2012 226 2 326 337
-
(2012)
The Journal of Pathology
, vol.226
, Issue.2
, pp. 326-337
-
-
Crossan, G.P.1
Patel, K.J.2
-
13
-
-
51649100722
-
Ercc1 is required for FANCD2 focus formation
-
2-s2.0-51649100722 10.1016/j.ymgme.2008.06.009
-
McCabe K. M., Hemphill A., Akkari Y., Jakobs P. M., Pauw D., Olson S. B., Moses R. E., Grompe M., Ercc1 is required for FANCD2 focus formation. Molecular Genetics and Metabolism 2008 95 1-2 66 73 2-s2.0-51649100722 10.1016/j.ymgme.2008.06.009
-
(2008)
Molecular Genetics and Metabolism
, vol.95
, Issue.1-2
, pp. 66-73
-
-
McCabe, K.M.1
Hemphill, A.2
Akkari, Y.3
Jakobs, P.M.4
Pauw, D.5
Olson, S.B.6
Moses, R.E.7
Grompe, M.8
-
14
-
-
79251624412
-
Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia
-
2-s2.0-79251624412 10.1038/ng.752
-
Crossan G. P., van der Weyden L., Rosado I. V., Langevin F., Gaillard P. H. L., McIntyre R. E., Gallagher F., Kettunen M. I., Lewis D. Y., Brindle K., Arends M. J., Adams D. J., Patel K. J., Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia. Nature Genetics 2011 43 2 147 152 2-s2.0-79251624412 10.1038/ng.752
-
(2011)
Nature Genetics
, vol.43
, Issue.2
, pp. 147-152
-
-
Crossan, G.P.1
Van Der Weyden, L.2
Rosado, I.V.3
Langevin, F.4
Gaillard, P.H.L.5
McIntyre, R.E.6
Gallagher, F.7
Kettunen, M.I.8
Lewis, D.Y.9
Brindle, K.10
Arends, M.J.11
Adams, D.J.12
Patel, K.J.13
-
15
-
-
20944451595
-
-/- stem/progenitor cells predisposes cells to undergo apoptosis, and surviving stem/progenitor cells display cytogenetic abnormalities and an increased risk of malignancy
-
DOI 10.1182/blood-2004-06-2483
-
-/- stem/progenitor cells predisposes cells to undergo apoptosis, and surviving stem/progenitor cells display cytogenetic abnormalities and an increased risk of malignancy. Blood 2005 105 9 3465 3471 2-s2.0-20944451595 10.1182/blood-2004-06-2483 (Pubitemid 40628187)
-
(2005)
Blood
, vol.105
, Issue.9
, pp. 3465-3471
-
-
Li, X.1
Le Beau, M.M.2
Ciccone, S.3
Yang, F.-C.4
Freie, B.5
Chen, S.6
Yuan, J.7
Hong, P.8
Orazi, A.9
Haneline, L.S.10
Clapp, D.W.11
-
16
-
-
67650451108
-
Fanconi anemia and its diagnosis
-
2-s2.0-67650451108 10.1016/j.mrfmmm.2009.01.013
-
Auerbach A. D., Fanconi anemia and its diagnosis. Mutation Research 2009 668 1-2 4 10 2-s2.0-67650451108 10.1016/j.mrfmmm.2009.01.013
-
(2009)
Mutation Research
, vol.668
, Issue.1-2
, pp. 4-10
-
-
Auerbach, A.D.1
-
17
-
-
0027326213
-
Molecular cloning and characterization of mouse TIE and TEK receptor tyrosine kinase genes and their expression in hematopoietic stem cells
-
DOI 10.1006/bbrc.1993.2045
-
Iwama A., Hamaguchi I., Hashiyama M., Murayama Y., Yasunaga K., Suda T., Molecular cloning and characterization of mouse TIE and TEK receptor tyrosine kinase genes and their expression in hematopoietic stem cells. Biochemical and Biophysical Research Communications 1993 195 1 301 309 2-s2.0-0027326213 10.1006/bbrc.1993.2045 (Pubitemid 23266532)
-
(1993)
Biochemical and Biophysical Research Communications
, vol.195
, Issue.1
, pp. 301-309
-
-
Iwama, A.1
Hamaguchi, I.2
Hashiyama, M.3
Murayama, Y.4
Yasunaga, K.5
Suda, T.6
-
18
-
-
0031903227
-
Characterization of TEK receptor tyrosine kinase and its ligands, Angiopoietins, in human hematopoietic progenitor cells
-
DOI 10.1093/intimm/10.8.1217
-
Sato A., Iwama A., Takakura N., Nishio H., Yancopoulos G. D., Suda T., Characterization of TEK receptor tyrosine kinase and its ligands, Angiopoietins, in human hematopoietic progenitor cells. International Immunology 1998 10 8 1217 1227 2-s2.0-0031903227 10.1093/intimm/10.8.1217 (Pubitemid 28362697)
-
(1998)
International Immunology
, vol.10
, Issue.8
, pp. 1217-1227
-
-
Sato, A.1
Iwama, A.2
Takakura, N.3
Nishio, H.4
Yancopoulos, G.D.5
Suda, T.6
-
19
-
-
0035911253
-
Conditional vascular cell adhesion molecule 1 deletion in mice: Impaired lymphocyte migration to bone marrow
-
DOI 10.1084/jem.193.6.741
-
Koni P. A., Joshi S. K., Temann U. A., Olson D., Burkly L., Flavell R. A., Conditional vascular cell adhesion molecule 1 deletion in mice: impaired lymphocyte migration to bone marrow. Journal of Experimental Medicine 2001 193 6 741 754 2-s2.0-0035911253 10.1084/jem.193.6.741 (Pubitemid 32524467)
-
(2001)
Journal of Experimental Medicine
, vol.193
, Issue.6
, pp. 741-753
-
-
Koni, P.A.1
Joshi, S.K.2
Temann, U.-A.3
Olson, D.4
Burkly, L.5
Flavell, R.A.6
-
20
-
-
34548817270
-
Toxicity of ligand-dependent Cre recombinases and generation of a conditional Cre deleter mouse allowing mosaic recombination in peripheral tissues
-
DOI 10.1152/physiolgenomics.00019.2007
-
Hameyer D., Loonstra A., Eshkind L., Schmitt S., Antunes C., Groen A., Bindels E., Jonkers J., Krimpenfort P., Meuwissen R., Rijswijk L., Bex A., Berns A., Bockamp E., Toxicity of ligand-dependent Cre recombinases and generation of a conditional Cre deleter mouse allowing mosaic recombination in peripheral tissues. Physiological Genomics 2007 31 1 32 41 2-s2.0-34548817270 10.1152/physiolgenomics.00019.2007 (Pubitemid 47443846)
-
(2007)
Physiological Genomics
, vol.31
, Issue.1
, pp. 32-41
-
-
Hameyer, D.1
Loonstra, A.2
Eshkind, L.3
Schmitt, S.4
Antunes, C.5
Groen, A.6
Bindels, E.7
Jonkers, J.8
Krimpenfort, P.9
Meuwissen, R.10
Rijswijk, L.11
Bex, A.12
Berns, A.13
Bockamp, E.14
-
21
-
-
84856404122
-
A mouse model of accelerated liver aging due to a defect in DNA repair
-
Gregg S. Q., Gutierrez V., Robinson A. R., A mouse model of accelerated liver aging due to a defect in DNA repair. Hepatology 2012 55 2 609 621
-
(2012)
Hepatology
, vol.55
, Issue.2
, pp. 609-621
-
-
Gregg, S.Q.1
Gutierrez, V.2
Robinson, A.R.3
-
22
-
-
78549289930
-
Lineage-instructive function of C/EBP α in multipotent hematopoietic cells and early thymic progenitors
-
2-s2.0-78549289930 10.1182/blood-2010-03-275404
-
Wölfler A., Danen-van Oorschot A. A., Haanstra J. R., Valkhof M., Bodner C., Vroegindeweij E., Van Strien P., Novak A., Cupedo T., Touw I. P., Lineage-instructive function of C/EBP α in multipotent hematopoietic cells and early thymic progenitors. Blood 2010 116 20 4116 4125 2-s2.0-78549289930 10.1182/blood-2010-03-275404
-
(2010)
Blood
, vol.116
, Issue.20
, pp. 4116-4125
-
-
Wölfler, A.1
Danen-Van Oorschot, A.A.2
Haanstra, J.R.3
Valkhof, M.4
Bodner, C.5
Vroegindeweij, E.6
Van Strien, P.7
Novak, A.8
Cupedo, T.9
Touw, I.P.10
-
23
-
-
67650403821
-
Genotype-phenotype correlations in Fanconi anemia
-
2-s2.0-67650403821 10.1016/j.mrfmmm.2009.05.006
-
Neveling K., Endt D., Hoehn H., Schindler D., Genotype-phenotype correlations in Fanconi anemia. Mutation Research 2009 668 1-2 73 91 2-s2.0-67650403821 10.1016/j.mrfmmm.2009.05.006
-
(2009)
Mutation Research
, vol.668
, Issue.1-2
, pp. 73-91
-
-
Neveling, K.1
Endt, D.2
Hoehn, H.3
Schindler, D.4
-
24
-
-
0032742894
-
+ primitive hematopoietic cells and shows reduced reconstitution ability
-
DOI 10.1016/S0301-472X(99)00102-2, PII S0301472X99001022
-
+ primitive hematopoietic cells and shows reduced reconstitution ability. Experimental Hematology 1999 27 11 1667 1674 2-s2.0-0032742894 10.1016/S0301-472X(99)00102-2 (Pubitemid 29526751)
-
(1999)
Experimental Hematology
, vol.27
, Issue.11
, pp. 1667-1674
-
-
Carreau, M.1
Gan, O.I.2
Liu, L.3
Doedens, M.4
Dick, J.E.5
Buchwald, M.6
-
25
-
-
0032523198
-
Bone marrow failure in the fanconi anemia group C mouse model after DNA damage
-
Carreau M., Gan O. I., Liu L., Doedens M., McKerlie C., Dick J. E., Buchwald M., Bone marrow failure in the Fanconi anemia group C mouse model after DNA damage. Blood 1998 91 8 2737 2744 2-s2.0-0032523198 (Pubitemid 28227523)
-
(1998)
Blood
, vol.91
, Issue.8
, pp. 2737-2744
-
-
Carreau, M.1
Gan, O.I.2
Liu, L.3
Doedens, M.4
McKerlie, C.5
Dick, J.E.6
Buchwald, M.7
-
26
-
-
19944431331
-
Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway
-
DOI 10.1182/blood-2004-05-1852
-
Soulier J., Leblanc T., Larghero J., Dastot H., Shimamura A., Guardiola P., Esperou H., Ferry C., Jubert C., Feugeas J. P., Henri A., Toubert A., Socié G., Baruchel A., Sigaux F., D'Andrea A. D., Gluckman E., Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway. Blood 2005 105 3 1329 1336 2-s2.0-19944431331 10.1182/blood-2004-05-1852 (Pubitemid 40170910)
-
(2005)
Blood
, vol.105
, Issue.3
, pp. 1329-1336
-
-
Soulier, J.1
Leblanc, T.2
Larghero, J.3
Dastot, H.4
Shimamura, A.5
Guardiola, P.6
Esperou, H.7
Ferry, C.8
Jubert, C.9
Feugeas, J.-P.10
Henri, A.11
Toubert, A.12
Socie, G.13
Baruchel, A.14
Sigaux, F.15
D'Andrea, A.D.16
Gluckman, E.17
-
27
-
-
34250007142
-
Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age
-
DOI 10.1038/nature05862, PII NATURE05862
-
Rossi D. J., Bryder D., Seita J., Nussenzweig A., Hoeijmakers J., Weissman I. L., Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age. Nature 2007 447 7145 725 729 2-s2.0-34250007142 10.1038/nature05862 (Pubitemid 46889729)
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 725-729
-
-
Rossi, D.J.1
Bryder, D.2
Seita, J.3
Nussenzweig, A.4
Hoeijmakers, J.5
Weissman, I.L.6
-
28
-
-
34147109207
-
Hematopoietic stem cell aging: Mechanism and consequence
-
DOI 10.1016/j.exger.2006.11.019, PII S0531556506004475
-
Rossi D. J., Bryder D., Weissman I. L., Hematopoietic stem cell aging: mechanism and consequence. Experimental Gerontology 2007 42 5 385 390 2-s2.0-34147109207 10.1016/j.exger.2006.11.019 (Pubitemid 46561181)
-
(2007)
Experimental Gerontology
, vol.42
, pp. 385-390
-
-
Rossi, D.J.1
Bryder, D.2
Weissman, I.L.3
-
29
-
-
79955941129
-
Maintenance of genomic integrity in hematopoietic stem cells
-
2-s2.0-79955941129 10.1007/s12185-011-0793-z
-
Naka K., Hirao A., Maintenance of genomic integrity in hematopoietic stem cells. International Journal of Hematology 2011 93 4 434 439 2-s2.0-79955941129 10.1007/s12185-011-0793-z
-
(2011)
International Journal of Hematology
, vol.93
, Issue.4
, pp. 434-439
-
-
Naka, K.1
Hirao, A.2
-
30
-
-
0025016054
-
Prenatal identification of potential donors for umbilical cord blood transplantation for Fanconi anemia
-
Auerbach A. D., Liu Q., Ghosh R., Pollack M. S., Douglas G. W., Broxmeyer H. E., Prenatal identification of potential donors for umbilical cord blood transplantation for Fanconi anemia. Transfusion 1990 30 8 682 687 2-s2.0-0025016054 (Pubitemid 20361781)
-
(1990)
Transfusion
, vol.30
, Issue.8
, pp. 682-687
-
-
Auerbach, A.D.1
Liu, Q.2
Ghosh, R.3
Pollack, M.S.4
Douglas, G.W.5
Broxmeyer, H.E.6
-
31
-
-
33845993292
-
Stem cell collection and gene transfer in fanconi anemia
-
DOI 10.1038/sj.mt.6300033, PII 6300033
-
Kelly P. F., Radtke S., von Kalle C., Balcik B., Bohn K., Mueller R., Schuesler T., Haren M., Reeves L., Cancelas J. A., Leemhuis T., Harris R., Auerbach A. D., Smith F. O., Davies S. M., Williams D. A., Stem cell collection and gene transfer in Fanconi anemia. Molecular Therapy 2007 15 1 211 219 2-s2.0-33845993292 10.1038/sj.mt.6300033 (Pubitemid 46043667)
-
(2007)
Molecular Therapy
, vol.15
, Issue.1
, pp. 211-219
-
-
Kelly, P.F.1
Radtke, S.2
Von Kalle, C.3
Balcik, B.4
Bohn, K.5
Mueller, R.6
Schuesler, T.7
Haren, M.8
Reeves, L.9
Cancelas, J.A.10
Leemhuis, T.11
Harris, R.12
Auerbach, A.D.13
Smith, F.O.14
Davies, S.M.15
Williams, D.A.16
-
33
-
-
67650627743
-
Mouse models of Fanconi anemia
-
2-s2.0-67650627743 10.1016/j.mrfmmm.2009.03.015
-
Parmar K., D'Andrea A., Niedernhofer L. J., Mouse models of Fanconi anemia. Mutation Research 2009 668 1-2 133 140 2-s2.0-67650627743 10.1016/j.mrfmmm.2009.03.015
-
(2009)
Mutation Research
, vol.668
, Issue.1-2
, pp. 133-140
-
-
Parmar, K.1
D'Andrea, A.2
Niedernhofer, L.J.3
-
34
-
-
62949145716
-
Myelodysplasia and acute leukemia as late complications of marrow failure: Future prospects for leukemia prevention
-
2-s2.0-62949145716 10.1016/j.hoc.2009.01.006
-
Bagby G. C., Meyers G., Myelodysplasia and acute leukemia as late complications of marrow failure: future prospects for leukemia prevention. Hematology/Oncology Clinics of North America 2009 23 2 361 376 2-s2.0-62949145716 10.1016/j.hoc.2009.01.006
-
(2009)
Hematology/Oncology Clinics of North America
, vol.23
, Issue.2
, pp. 361-376
-
-
Bagby, G.C.1
Meyers, G.2
-
35
-
-
0037441757
-
A 20-year perspective on the International Fanconi Anemia Registry (IFAR)
-
DOI 10.1182/blood-2002-07-2170
-
Kutler D. I., Singh B., Satagopan J., Batish S. D., Berwick M., Giampietro P. F., Hanenberg H., Auerbach A. D., A 20-year perspective on the International Fanconi Anemia Registry (IFAR). Blood 2003 101 4 1249 1256 2-s2.0-0037441757 10.1182/blood-2002-07-2170 (Pubitemid 36182492)
-
(2003)
Blood
, vol.101
, Issue.4
, pp. 1249-1256
-
-
Kutler, D.I.1
Singh, B.2
Satagopan, J.3
Batish, S.D.4
Berwick, M.5
Giampietro, P.F.6
Hanenberg, H.7
Auerbach, A.D.8
|