-
1
-
-
0024543636
-
International Fanconi anemia registry: Relation of clinical symptoms to diepoxybutane sensitivity
-
Auerbach A.D., Rogatko A., Schroeder-Kurth T.M. International Fanconi anemia registry: relation of clinical symptoms to diepoxybutane sensitivity. Blood. 73:1989;391-396.
-
(1989)
Blood
, vol.73
, pp. 391-396
-
-
Auerbach, A.D.1
Rogatko, A.2
Schroeder-Kurth, T.M.3
-
2
-
-
0027213760
-
G2 phase cell cycle disturbance as a manifestation of genetic cell damage
-
Seyschab H., Sun Y., Friedl R., Schindler D., Hoehn H. G2 phase cell cycle disturbance as a manifestation of genetic cell damage. Hum Genet. 92:1993;61-68.
-
(1993)
Hum Genet
, vol.92
, pp. 61-68
-
-
Seyschab, H.1
Sun, Y.2
Friedl, R.3
Schindler, D.4
Hoehn, H.5
-
3
-
-
0019980952
-
The cytogenetic response of Fanconi's anemia lymphoid cell lines to various clastogens
-
Cohen M.M., Fruchtman C.E., Simpson S.D., Martin A.O. The cytogenetic response of Fanconi's anemia lymphoid cell lines to various clastogens. Cytogenet Cell Genet. 34:1982;230-240.
-
(1982)
Cytogenet Cell Genet
, vol.34
, pp. 230-240
-
-
Cohen, M.M.1
Fruchtman, C.E.2
Simpson, S.D.3
Martin, A.O.4
-
4
-
-
0028109326
-
Fanconi anemia and novel strategies for therapy
-
Liu J.M., Buchwald M., Walsh C.E., Young N.S. Fanconi anemia and novel strategies for therapy. Blood. 84:1994;3995-4007.
-
(1994)
Blood
, vol.84
, pp. 3995-4007
-
-
Liu, J.M.1
Buchwald, M.2
Walsh, C.E.3
Young, N.S.4
-
5
-
-
0026878842
-
Evidence for at least four Fanconi anemia genes including FACC on chromosome 9
-
Strathdee C.A., Duncan A.M., Buchwald M. Evidence for at least four Fanconi anemia genes including FACC on chromosome 9. Nat Genet. 1:1992;196-198.
-
(1992)
Nat Genet
, vol.1
, pp. 196-198
-
-
Strathdee, C.A.1
Duncan, A.M.2
Buchwald, M.3
-
6
-
-
0029163523
-
Classification of Fanconi anemia patients by complementation analysis: Evidence for a fifth genetic subtype
-
Joenje H., Lo-ten-Foe J.R., Oostra A.B., van-Berkel C.G., Rooimans M.A., Schroeder-Kurth T., Wegener R.D., Gille J.J., Buchwald M., Arwert F. Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype. Blood. 86:1995;2156-2160.
-
(1995)
Blood
, vol.86
, pp. 2156-2160
-
-
Joenje, H.1
Lo-Ten-Foe, J.R.2
Oostra, A.B.3
Van-Berkel, C.G.4
Rooimans, M.A.5
Schroeder-Kurth, T.6
Wegener, R.D.7
Gille, J.J.8
Buchwald, M.9
Arwert, F.10
-
7
-
-
0026521238
-
Cloning of cDNAs for Fanconi's anemia by functional complementation
-
Strathdee C.A., Gavish H., Shannon W.R., Buchwald M. Cloning of cDNAs for Fanconi's anemia by functional complementation. Nature. 356:1992;763-767.
-
(1992)
Nature
, vol.356
, pp. 763-767
-
-
Strathdee, C.A.1
Gavish, H.2
Shannon, W.R.3
Buchwald, M.4
-
8
-
-
0027215175
-
Cloning and analysis of the murine Fanconi anemia group C cDNA
-
Wevrick R., Clarke C.A., Buchwald M. Cloning and analysis of the murine Fanconi anemia group C cDNA. Hum Mol Genet. 2:1993;655-662.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 655-662
-
-
Wevrick, R.1
Clarke, C.A.2
Buchwald, M.3
-
9
-
-
8944258558
-
Germ cell defects and hematopoietic hypersensitivity to δ-interferon in mice with a targeted disruption of the Fanconi anemia C gene
-
Whitney M.A., Royle G., Low M.J., Kelly M.A., Axthelm M.K., Reifsteck C., Olson S., Braun R.E., Heinrich M.C., Rathbun R.K., Bagby G.C., Grompe M. Germ cell defects and hematopoietic hypersensitivity to δ-interferon in mice with a targeted disruption of the Fanconi anemia C gene. Blood. 88:1996;49-58.
-
(1996)
Blood
, vol.88
, pp. 49-58
-
-
Whitney, M.A.1
Royle, G.2
Low, M.J.3
Kelly, M.A.4
Axthelm, M.K.5
Reifsteck, C.6
Olson, S.7
Braun, R.E.8
Heinrich, M.C.9
Rathbun, R.K.10
Bagby, G.C.11
Grompe, M.12
-
10
-
-
84949193654
-
Diagnosis of Fanconi anemia by diepoxybutane analysis
-
In: Dracopoli NC, Haines JL, Korf BR, Moir DT, Morton CC, Seidman JG, Smith DR, editors. New York, NY: Wiley
-
Auerbach AD. Diagnosis of Fanconi anemia by diepoxybutane analysis. In: Dracopoli NC, Haines JL, Korf BR, Moir DT, Morton CC, Seidman JG, Smith DR, editors. Current Protocols in Human Genetics. New York, NY: Wiley, 1994:8.7.1.
-
(1994)
Current Protocols in Human Genetics
, pp. 871
-
-
Auerbach, A.D.1
-
11
-
-
0029857336
-
Suppression of apoptosis in hematopoietic progenitor cell lines by expression of FAC gene
-
Cumming R.C., Liu J.M., Youssoufian H., Buchwald M. Suppression of apoptosis in hematopoietic progenitor cell lines by expression of FAC gene. Blood. 88:1996;4558-4567.
-
(1996)
Blood
, vol.88
, pp. 4558-4567
-
-
Cumming, R.C.1
Liu, J.M.2
Youssoufian, H.3
Buchwald, M.4
-
12
-
-
0028123475
-
Abnormal lymphokine production: A novel feature of the genetic disease Fanconi anemia. II. In vitro and in vivo spontaneous overproduction of tumor necrosis factor α
-
Rosselli F., Sanceau J., Gluckman E., Wietzerbin J., Moustacchi E. Abnormal lymphokine production: a novel feature of the genetic disease Fanconi anemia. II. In vitro and in vivo spontaneous overproduction of tumor necrosis factor α Blood. 83:1994;1216-1225.
-
(1994)
Blood
, vol.83
, pp. 1216-1225
-
-
Rosselli, F.1
Sanceau, J.2
Gluckman, E.3
Wietzerbin, J.4
Moustacchi, E.5
-
13
-
-
0025006172
-
Physical and laboratory characteristics of heterozygote carriers of the Fanconi aplasia gene
-
Petridou M., Barrett A.J. Physical and laboratory characteristics of heterozygote carriers of the Fanconi aplasia gene. Acta Paediatr Scand. 79:1990;1069-1074.
-
(1990)
Acta Paediatr Scand
, vol.79
, pp. 1069-1074
-
-
Petridou, M.1
Barrett, A.J.2
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