-
1
-
-
0014112634
-
Familiar constitutional panmyelocytopathy, Fanconi's anemia (FA). I. Clinical aspects
-
Fanconi G. Familiar constitutional panmyelocytopathy, Fanconi's anemia (FA). I. Clinical aspects. Semin Hematol 1967; 4:233-40.
-
(1967)
Semin Hematol
, vol.4
, pp. 233-240
-
-
Fanconi, G.1
-
2
-
-
0028944751
-
Fanconi anemia research: Current status and prospects
-
Joenje H, Mathew C, Gluckman E. Fanconi anemia research: current status and prospects. Eur J Cancer 1995; 31A:268-72.
-
(1995)
Eur J Cancer
, vol.31 A
, pp. 268-272
-
-
Joenje, H.1
Mathew, C.2
Gluckman, E.3
-
3
-
-
0023231386
-
Fanconi anemia: Another disease of unusually high prevalence in the Africans population of South Africa
-
Rosendorff J, Berstein R, Macdougall L, Jenkins T. Fanconi anemia: another disease of unusually high prevalence in the Africans population of South Africa. Am J Med Genet 1987; 27:793-7.
-
(1987)
Am J Med Genet
, vol.27
, pp. 793-797
-
-
Rosendorff, J.1
Berstein, R.2
Macdougall, L.3
Jenkins, T.4
-
4
-
-
0025490738
-
The Italian contribution to the study of Fanconi's anemia
-
Sansone R, Sansone G. The Italian contribution to the study of Fanconi's anemia. Pathologica 1990; 82:473-8.
-
(1990)
Pathologica
, vol.82
, pp. 473-478
-
-
Sansone, R.1
Sansone, G.2
-
5
-
-
0344085311
-
Fanconi anemia
-
Scriver C, Beaudet AL, Sly WS, Vallz D, eds. New York: McGraw-Hill
-
Buchwald M, Joenje H, Auerbach AD. Fanconi anemia. In: Scriver C, Beaudet AL, Sly WS, Vallz D, eds. The Metabolic and Molecular Basis of Inherited Disease. 7th ed. New York: McGraw-Hill, 1997.
-
(1997)
The Metabolic and Molecular Basis of Inherited Disease. 7th Ed.
-
-
Buchwald, M.1
Joenje, H.2
Auerbach, A.D.3
-
6
-
-
0001652428
-
The bone marrow failure syndromes
-
Nathan DG, Oski FA, eds. Philadelphia: Saunders
-
Alter BP, Young NS. The bone marrow failure syndromes. In: Nathan DG, Oski FA, eds. Hematology of Infancy and Childhood, I. 4th ed. Philadelphia: Saunders; 1993. p. 216-316.
-
(1993)
Hematology of Infancy and Childhood, I. 4th Ed.
, pp. 216-316
-
-
Alter, B.P.1
Young, N.S.2
-
7
-
-
0028068579
-
Hematologic abnormalities in Fanconi anemia: An International Fanconi Anemia Registry study
-
Butturini A, Gale RP, Verlander PC, Adler-Brecher B, Gillio AP, Auerbach AD. Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study. Blood 1994; 84:1650-5.
-
(1994)
Blood
, vol.84
, pp. 1650-1655
-
-
Butturini, A.1
Gale, R.P.2
Verlander, P.C.3
Adler-Brecher, B.4
Gillio, A.P.5
Auerbach, A.D.6
-
8
-
-
0024543636
-
International Fanconi anemia Registry: Relation of clinical symptoms to diepoxybutane sensitivity
-
Auerbach AD, Rogatko A, Schroeder-Kurth TM. International Fanconi anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity. Blood 1989; 73:391-6.
-
(1989)
Blood
, vol.73
, pp. 391-396
-
-
Auerbach, A.D.1
Rogatko, A.2
Schroeder-Kurth, T.M.3
-
9
-
-
0027445492
-
Fanconi's anemia and its variability
-
Alter BP. Fanconi's anemia and its variability. Br J Haematol 1993; 85:9-14.
-
(1993)
Br J Haematol
, vol.85
, pp. 9-14
-
-
Alter, B.P.1
-
10
-
-
0027298257
-
The need for more accurate and timely diagnosis in Fanconi anemia: A report from the International Fanconi Anemia Registry
-
Giampietro PF, Adler-Brecher B, Verlander PC, Pavlakis SG, Davis JG, Auerbach AD. The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry. Pediatrics 1993; 91:1116-20.
-
(1993)
Pediatrics
, vol.91
, pp. 1116-1120
-
-
Giampietro, P.F.1
Adler-Brecher, B.2
Verlander, P.C.3
Pavlakis, S.G.4
Davis, J.G.5
Auerbach, A.D.6
-
11
-
-
0344374066
-
The association of dyskeratosis congenita and Fanconi anemia
-
Addison M, Rice MS. The association of dyskeratosis congenita and Fanconi anemia. Med J Aust 1965; 1:797-9.
-
(1965)
Med J Aust
, vol.1
, pp. 797-799
-
-
Addison, M.1
Rice, M.S.2
-
12
-
-
0021688628
-
Progressive preleukemia with a chromosomally abnormal clone in a kindred with the Estren-Dameshek variant of Fanconi's anemia
-
Nowell P, Bergman G, Besa E, Wilmoth D, Emanuel B. Progressive preleukemia with a chromosomally abnormal clone in a kindred with the Estren-Dameshek variant of Fanconi's anemia. Blood 1984; 64:1135-8.
-
(1984)
Blood
, vol.64
, pp. 1135-1138
-
-
Nowell, P.1
Bergman, G.2
Besa, E.3
Wilmoth, D.4
Emanuel, B.5
-
13
-
-
0023864689
-
Thrombocytopenia with absent radii. A review of 100 cases
-
Hedberg VA, Lipton JM. Thrombocytopenia with absent radii. A review of 100 cases. Am J Pediatr Hematol Oncol 1988; 10:51-64.
-
(1988)
Am J Pediatr Hematol Oncol
, vol.10
, pp. 51-64
-
-
Hedberg, V.A.1
Lipton, J.M.2
-
14
-
-
0028265083
-
Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome
-
Farrell SA, Paes BA, Lewis ME. Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome. Am J Med Genet 1994; 50:98-9.
-
(1994)
Am J Med Genet
, vol.50
, pp. 98-99
-
-
Farrell, S.A.1
Paes, B.A.2
Lewis, M.E.3
-
15
-
-
0030039981
-
Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome
-
Rossbach Hc, Sutcliffe MJ, Haag MM, Grana NH, Rossi AR, Barbosa JL. Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome. Am J Med Genet 1996; 61:65-7.
-
(1996)
Am J Med Genet
, vol.61
, pp. 65-67
-
-
Rossbach, Hc.1
Sutcliffe, M.J.2
Haag, M.M.3
Grana, N.H.4
Rossi, A.R.5
Barbosa, J.L.6
-
16
-
-
0025959243
-
Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry
-
Auerbach AD, Allen RG. Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry. Cancer Genet Cytogen 1991; 5:1-12.
-
(1991)
Cancer Genet Cytogen
, vol.5
, pp. 1-12
-
-
Auerbach, A.D.1
Allen, R.G.2
-
17
-
-
0015220743
-
Squamous cell carcinomas in Fanconi's anemia
-
Swift M, Zimmerman D, McDonough ER. Squamous cell carcinomas in Fanconi's anemia. JAMA 1971; 216:325-6.
-
(1971)
JAMA
, vol.216
, pp. 325-326
-
-
Swift, M.1
Zimmerman, D.2
McDonough, E.R.3
-
18
-
-
0029013081
-
Squamous cell carcinoma of the tongue in a child with Fanconi anemia: A case report and review of the literature
-
Somers GR, Tabrizi SN, Tiedemann K, Chow CW, Garland SM, Venter DJ. Squamous cell carcinoma of the tongue in a child with Fanconi anemia: a case report and review of the literature. Pediatr Pathol Lab Med 1995; 15:597-607.
-
(1995)
Pediatr Pathol Lab Med
, vol.15
, pp. 597-607
-
-
Somers, G.R.1
Tabrizi, S.N.2
Tiedemann, K.3
Chow, C.W.4
Garland, S.M.5
Venter, D.J.6
-
19
-
-
0029861118
-
Fanconi's anemia and malignancies
-
Alter BP. Fanconi's anemia and malignancies. Am J Hematol 1996; 53:99-110.
-
(1996)
Am J Hematol
, vol.53
, pp. 99-110
-
-
Alter, B.P.1
-
20
-
-
0015891353
-
A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents
-
Sasaky MS, Tonomura A. A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents. Cancer Res 1973; 33:1829-36.
-
(1973)
Cancer Res
, vol.33
, pp. 1829-1836
-
-
Sasaky, M.S.1
Tonomura, A.2
-
21
-
-
0016825649
-
Is Fanconi's anaemia defective in a process essential to repair of DNA cross-link?
-
Sasaky MS. Is Fanconi's anaemia defective in a process essential to repair of DNA cross-link? Nature 1975; 257:501-3.
-
(1975)
Nature
, vol.257
, pp. 501-503
-
-
Sasaky, M.S.1
-
24
-
-
0028831333
-
Bloom's syndrome
-
German J. Bloom's syndrome. Dermatol Clin 1995; 13:7-18.
-
(1995)
Dermatol Clin
, vol.13
, pp. 7-18
-
-
German, J.1
-
25
-
-
0029850732
-
Cockayne syndrome. A primary defect in DNA repair, transcription, both, or neither
-
Friedberg E. Cockayne syndrome. A primary defect in DNA repair, transcription, both, or neither. Bioessays 1996; 18:731-8.
-
(1996)
Bioessays
, vol.18
, pp. 731-738
-
-
Friedberg, E.1
-
26
-
-
0030861685
-
DNA elicases in inherited human disorders
-
Ellis NA. DNA elicases in inherited human disorders. Curr Opin Genet Dev 1997; 7:354-63.
-
(1997)
Curr Opin Genet Dev
, vol.7
, pp. 354-363
-
-
Ellis, N.A.1
-
28
-
-
0017118656
-
Susceptibility of Fanconi's anemia fibroblasts to chromosome damage by carcinogens
-
Auerbach AD, Wolman SR. Susceptibility of Fanconi's anemia fibroblasts to chromosome damage by carcinogens. Nature 1976; 261:494-6.
-
(1976)
Nature
, vol.261
, pp. 494-496
-
-
Auerbach, A.D.1
Wolman, S.R.2
-
29
-
-
0020357892
-
Susceptibility of Fanconi's anemia lymphoblasts to cross-linking and alkylating agents
-
Isida R, Buchwald M. Susceptibility of Fanconi's anemia lymphoblasts to cross-linking and alkylating agents. Cancer Res 1982; 42:4000-6.
-
(1982)
Cancer Res
, vol.42
, pp. 4000-4006
-
-
Isida, R.1
Buchwald, M.2
-
30
-
-
0027468707
-
Chromosome abnormalities in bone marrow of Fanconi anemia patients
-
Berger R, Le Coniat M, Schaison G. Chromosome abnormalities in bone marrow of Fanconi anemia patients. Cancer Genet Cytogenet 1993; 65:47-50.
-
(1993)
Cancer Genet Cytogenet
, vol.65
, pp. 47-50
-
-
Berger, R.1
Le Coniat, M.2
Schaison, G.3
-
31
-
-
0027507581
-
Clonal chromosomal abnormalities in Fanconi's anaemia: What do they really mean?
-
Alter BP, Scalise A, McCombs J, Najfeld V. Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean? Br J Haematol 1993; 85: 627-30.
-
(1993)
Br J Haematol
, vol.85
, pp. 627-630
-
-
Alter, B.P.1
Scalise, A.2
McCombs, J.3
Najfeld, V.4
-
32
-
-
0028198465
-
Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints
-
Fundia A, Gorla N, Larripa I. Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints. Hereditas 1994; 120:47-50.
-
(1994)
Hereditas
, vol.120
, pp. 47-50
-
-
Fundia, A.1
Gorla, N.2
Larripa, I.3
-
33
-
-
0019444973
-
Oxygen-dependence of chromosomal aberrations in Fanconi's anemia
-
Joenje H, Arwert F, Eriksson AW, et al. Oxygen-dependence of chromosomal aberrations in Fanconi's anemia. Nature 1981; 290:142-3.
-
(1981)
Nature
, vol.290
, pp. 142-143
-
-
Joenje, H.1
Arwert, F.2
Eriksson, A.W.3
-
34
-
-
0023685747
-
Fanconi anemia mutation causes cellular susceptibility to ambient oxygen
-
Schindler D, Hoehn H. Fanconi anemia mutation causes cellular susceptibility to ambient oxygen. Am J Hum Genet 1988; 43:429-35.
-
(1988)
Am J Hum Genet
, vol.43
, pp. 429-435
-
-
Schindler, D.1
Hoehn, H.2
-
35
-
-
0002032578
-
Oxygen metabolism and chromosomal breakage in Fanconi anemia
-
Schroeder T, Auerbach AD, Obe G, eds. Berlin: Springer-Verlag
-
Joenje H, Gille JJP. Oxygen metabolism and chromosomal breakage in Fanconi anemia. In: Schroeder T, Auerbach AD, Obe G, eds. Fanconi anemia: clinical, cytogenetic and experimental aspects. Berlin: Springer-Verlag, 1989. p. 174-82.
-
(1989)
Fanconi Anemia: Clinical, Cytogenetic and Experimental Aspects
, pp. 174-182
-
-
Joenje, H.1
Gille, J.J.P.2
-
36
-
-
0030948476
-
In vitro hypersensitivity to oxygen of Fanconi anemia (FA) cells is linked to ex vivo evidence for oxidative stress in FA homozygotes and heterozygotes
-
Pagano G, Korkina LG, Degan P, et al. In vitro hypersensitivity to oxygen of Fanconi anemia (FA) cells is linked to ex vivo evidence for oxidative stress in FA homozygotes and heterozygotes. Blood 1997; 89:1111-2.
-
(1997)
Blood
, vol.89
, pp. 1111-1112
-
-
Pagano, G.1
Korkina, L.G.2
Degan, P.3
-
37
-
-
0020067168
-
Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment
-
Kaiser TN, Lojewki A, Dougherty C, Juergens L, Sahar E, Latt SA. Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment. Cytometry 1982; 2:291-7.
-
(1982)
Cytometry
, vol.2
, pp. 291-297
-
-
Kaiser, T.N.1
Lojewki, A.2
Dougherty, C.3
Juergens, L.4
Sahar, E.5
Latt, S.A.6
-
38
-
-
0020307710
-
The cell cycle of lymphocytes in Fanconi anemia
-
Dutrillaux B, Aurias A, Dutrillaux AM, Buriot D, Prieur M. The cell cycle of lymphocytes in Fanconi anemia. Hum Genet 1982; 62:327-32.
-
(1982)
Hum Genet
, vol.62
, pp. 327-332
-
-
Dutrillaux, B.1
Aurias, A.2
Dutrillaux, A.M.3
Buriot, D.4
Prieur, M.5
-
39
-
-
0027861014
-
Fanconi anemia diagnosis and the diepoxibutane (DEB) test
-
Auerbach AD. Fanconi anemia diagnosis and the diepoxibutane (DEB) test. Exp Hematol 1993; 21:731-3.
-
(1993)
Exp Hematol
, vol.21
, pp. 731-733
-
-
Auerbach, A.D.1
-
40
-
-
0028950319
-
Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia
-
Seyschab H, Friedl R, Sun Y, et al. Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia. Blood 1995; 85:2233-7.
-
(1995)
Blood
, vol.85
, pp. 2233-2237
-
-
Seyschab, H.1
Friedl, R.2
Sun, Y.3
-
41
-
-
0028125830
-
Evaluation of granulocyte-macrophage colony-stimulating factor for treatment of pancytopenia in children with Fanconi anemia
-
Guinan EC, Lopez KD, Huhn RD, Felser JM, Nathan DG. Evaluation of granulocyte-macrophage colony-stimulating factor for treatment of pancytopenia in children with Fanconi anemia. J Pediatr 1994; 124: 144-50.
-
(1994)
J Pediatr
, vol.124
, pp. 144-150
-
-
Guinan, E.C.1
Lopez, K.D.2
Huhn, R.D.3
Felser, J.M.4
Nathan, D.G.5
-
42
-
-
0029844796
-
Prolonged administration of granulocyte colony-stimulating factor (filgrastim) to with Fanconi anemia: A pilot study
-
Rackoff WR, Orazi A, Robinson CA, et al. Prolonged administration of granulocyte colony-stimulating factor (filgrastim) to with Fanconi anemia: a pilot study. Blood 1996; 88:1588-93.
-
(1996)
Blood
, vol.88
, pp. 1588-1593
-
-
Rackoff, W.R.1
Orazi, A.2
Robinson, C.A.3
-
43
-
-
0027305811
-
Hepatic tumours during androgen therapy in Fanconi anaemia
-
Touraine RL, Bertrand Y, Foray P, Gilly J, Philippe N. Hepatic tumours during androgen therapy in Fanconi anaemia. Eur J Pediatr 1993; 152:691-3.
-
(1993)
Eur J Pediatr
, vol.152
, pp. 691-693
-
-
Touraine, R.L.1
Bertrand, Y.2
Foray, P.3
Gilly, J.4
Philippe, N.5
-
44
-
-
0029157355
-
Bone marrow transplantation for Fanconi anemia
-
Gluckman E, Auerbach AD, Horowitz MM, et al. Bone marrow transplantation for Fanconi anemia. Blood 1995; 86:2856-62.
-
(1995)
Blood
, vol.86
, pp. 2856-2862
-
-
Gluckman, E.1
Auerbach, A.D.2
Horowitz, M.M.3
-
46
-
-
0026878842
-
Evidence for at least four Fanconi anemia genes including FACC on chromosome 9
-
Strathdee CA, Duncan AMV, Buchwald M. Evidence for at least four Fanconi anemia genes including FACC on chromosome 9. Nature Genet 1992; 1:196-8:
-
(1992)
Nature Genet
, vol.1
, pp. 196-198
-
-
Strathdee, C.A.1
Duncan, A.M.V.2
Buchwald, M.3
-
47
-
-
0029163523
-
Classification of Fanconi anemia patients by complementation analysis: Evidence for a fifth genetic subtype
-
Joenje H, Lo Ten Foe JR, Oostra AB, et al. Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype. Blood 1995; 86:2156-60.
-
(1995)
Blood
, vol.86
, pp. 2156-2160
-
-
Joenje, H.1
Lo Ten Foe, J.R.2
Oostra, A.B.3
-
48
-
-
16944362011
-
Evidence for at least eight Fanconi anemia genes
-
Joenje H, Oostra A, Wijker M, et al. Evidence for at least eight Fanconi anemia genes. Am J Hum Genet 1997; 61:940-4.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 940-944
-
-
Joenje, H.1
Oostra, A.2
Wijker, M.3
-
49
-
-
0029410634
-
Complementation groups: One or more per gene?
-
Buchwald M. Complementation groups: one or more per gene? Nature Genet 1995; 11:228-30.
-
(1995)
Nature Genet
, vol.11
, pp. 228-230
-
-
Buchwald, M.1
-
50
-
-
0030741287
-
Complementation group assignments in Fanconi anemia fibroblast cell lines from North America
-
Jakobs PM, Fiddler-Odell E, Reifsteck C, Olson S, Moses RE, Grompe M. Complementation group assignments in Fanconi anemia fibroblast cell lines from North America. Somat Cell Mol Genet 1997; 23:1-7.
-
(1997)
Somat Cell Mol Genet
, vol.23
, pp. 1-7
-
-
Jakobs, P.M.1
Fiddler-Odell, E.2
Reifsteck, C.3
Olson, S.4
Moses, R.E.5
Grompe, M.6
-
51
-
-
0029947378
-
Fanconi anaemia in Italy: High prevalence of complementation group A in two geographic clusters
-
Savoia A, Zatterale A, Del Principe D, Joenje H. Fanconi anaemia in Italy: high prevalence of complementation group A in two geographic clusters. Hum Genet 1996; 97:599-603.
-
(1996)
Hum Genet
, vol.97
, pp. 599-603
-
-
Savoia, A.1
Zatterale, A.2
Del Principe, D.3
Joenje, H.4
-
52
-
-
0030023770
-
Fanconi anaemia complementation groups in Germany and the Netherlands
-
European Fanconi Anaemia Research Group
-
Joenje H. European Fanconi Anaemia Research Group. Fanconi anaemia complementation groups in Germany and the Netherlands. Hum Genet 1996; 97:280-2.
-
(1996)
Hum Genet
, vol.97
, pp. 280-282
-
-
Joenje, H.1
-
53
-
-
0028857959
-
Microcell mediated chromosome transfer maps the Fanconi anemia group D gene to chromosome 3p
-
Whitney M, Thayer M, Reifsteck C, et al. Microcell mediated chromosome transfer maps the Fanconi anemia group D gene to chromosome 3p. Nature Genet 1995; 11:341-3.
-
(1995)
Nature Genet
, vol.11
, pp. 341-343
-
-
Whitney, M.1
Thayer, M.2
Reifsteck, C.3
-
54
-
-
0026521238
-
Cloning of cDNAs for Fanconi's anemia by functional complementation
-
Strathedee CA., Gavish H, Shannon WR, Buchwald M. Cloning of cDNAs for Fanconi's anemia by functional complementation. Nature 1992; 356:763-7.
-
(1992)
Nature
, vol.356
, pp. 763-767
-
-
Strathedee, C.A.1
Gavish, H.2
Shannon, W.R.3
Buchwald, M.4
-
55
-
-
0027407408
-
Characterization of the exon structure of the Fanconi anemia group C gene by vectorette PCR
-
Gibson RA, Buchwald M, Roberts RG, Mathew CG. Characterization of the exon structure of the Fanconi anemia group C gene by vectorette PCR. Hum Mol Genet 1993; 2:35-8.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 35-38
-
-
Gibson, R.A.1
Buchwald, M.2
Roberts, R.G.3
Mathew, C.G.4
-
56
-
-
15844386165
-
Mutations of the human homolog of Drosophila patched in nevoid basal cell carcinoma syndrome
-
Hahn H, Wicking C, Zaphiropoulos PG, et al. Mutations of the human homolog of Drosophila patched in nevoid basal cell carcinoma syndrome. Cell 1996; 85: 841-51.
-
(1996)
Cell
, vol.85
, pp. 841-851
-
-
Hahn, H.1
Wicking, C.2
Zaphiropoulos, P.G.3
-
57
-
-
0027215175
-
Cloning and analysis of the murine Fanconi anemia group C cDNA
-
Wevrick C, Clarke CA, Buchwald M. Cloning and analysis of the murine Fanconi anemia group C cDNA. Hum Mol Genet 1993; 2:655-62.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 655-662
-
-
Wevrick, C.1
Clarke, C.A.2
Buchwald, M.3
-
58
-
-
6844257552
-
Cloning of the bovine and rat Fanconi anemia group C cDNA
-
Ching-Ying-Wong J, Alon N, Buchwald M. Cloning of the bovine and rat Fanconi anemia group C cDNA. Mamm Genome 1997; 8:522-5.
-
(1997)
Mamm Genome
, vol.8
, pp. 522-525
-
-
Ching-Ying-Wong, J.1
Alon, N.2
Buchwald, M.3
-
59
-
-
0030293337
-
Positional cloning of the Fanconi anemia group A gene
-
FAB Consortium. Positional cloning of the Fanconi anemia group A gene. Nature Genet 1996; 14:324-8.
-
(1996)
Nature Genet
, vol.14
, pp. 324-328
-
-
-
60
-
-
1842337370
-
Expression of cloning of a cDNA for the major Fanconi anemia gene, FAA
-
Lo Ten Foe JR, Roimans AA, Bosnoyan-Collins L, et al. Expression of cloning of a cDNA for the major Fanconi anemia gene, FAA. Nature Genet 1996; 14:320-3.
-
(1996)
Nature Genet
, vol.14
, pp. 320-323
-
-
Lo Ten Foe, J.R.1
Roimans, A.A.2
Bosnoyan-Collins, L.3
-
61
-
-
0028840709
-
Localization of the Fanconi anemia complementation group A gene to chromosome 16q24.3
-
Pronk JC, Gibson RA, Savoia A, et al. Localization of the Fanconi anemia complementation group A gene to chromosome 16q24.3. Nature Genet 1995; 11:338-40.
-
(1995)
Nature Genet
, vol.11
, pp. 338-340
-
-
Pronk, J.C.1
Gibson, R.A.2
Savoia, A.3
-
62
-
-
0031060706
-
Linkage analysis of Fanconi anemia in Italy and mapping of the complementation group A gene
-
Savoia, Piemontese MR, Savino M, et al. Linkage analysis of Fanconi anemia in Italy and mapping of the complementation group A gene. Hum Genet 1997; 99:93-7.
-
(1997)
Hum Genet
, vol.99
, pp. 93-97
-
-
Savoia1
Piemontese, M.R.2
Savino, M.3
-
63
-
-
17544391773
-
The genomic organization of the Fanconi anemia group A (FAA) gene
-
Ianzano L, d'Apolito M, Centra M, et al. The genomic organization of the Fanconi anemia group A (FAA) gene. Genomics 1997; 41:309-14.
-
(1997)
Genomics
, vol.41
, pp. 309-314
-
-
Ianzano, L.1
D'Apolito, M.2
Centra, M.3
-
64
-
-
0027295719
-
FACC gene mutations and early prenatal diagnosis of Fanconi's anaemia
-
Murer-Orlando M, Llerena JC, Birjandi F, Gibson RA, Mathew CG. FACC gene mutations and early prenatal diagnosis of Fanconi's anaemia. Lancet 1993; 342: 686.
-
(1993)
Lancet
, vol.342
, pp. 686
-
-
Murer-Orlando, M.1
Llerena, J.C.2
Birjandi, F.3
Gibson, R.A.4
Mathew, C.G.5
-
65
-
-
0027299882
-
A nonsense mutation and exon skipping in the Fanconi anaemia group C gene
-
Gibson RA, Hajianpour A, Murer-Orlando M, Buchwald M, Mathew CG. A nonsense mutation and exon skipping in the Fanconi anaemia group C gene. Hum Mol Genet 1993; 2:797-9.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 797-799
-
-
Gibson, R.A.1
Hajianpour, A.2
Murer-Orlando, M.3
Buchwald, M.4
Mathew, C.G.5
-
66
-
-
0027288907
-
A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews
-
Whitney MA, Saito H, Jakobs PM, Gibson RA, Moses RE, Grompe M. A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews. Nature Genet 1993; 4:202-5.
-
(1993)
Nature Genet
, vol.4
, pp. 202-205
-
-
Whitney, M.A.1
Saito, H.2
Jakobs, P.M.3
Gibson, R.A.4
Moses, R.E.5
Grompe, M.6
-
67
-
-
0028231738
-
Mutation analysis of the Fanconi anemia gene FACC
-
Verlander PC, Lin JD, Udono MU, et al. Mutation analysis of the Fanconi anemia gene FACC. Am J Hum Genet 1994; 54:595-601.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 595-601
-
-
Verlander, P.C.1
Lin, J.D.2
Udono, M.U.3
-
68
-
-
19144373220
-
Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia C gene, FAC
-
Lo Ten Foe JR, Rooimans MA, Joenje H, Arwert F. Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia C gene, FAC. Hum Mutat 1996; 7: 264-5.
-
(1996)
Hum Mutat
, vol.7
, pp. 264-265
-
-
Lo Ten Foe, J.R.1
Rooimans, M.A.2
Joenje, H.3
Arwert, F.4
-
69
-
-
0029848631
-
Sequence variations in the Fanconi anaemia gene, FAC: Pathogenicity of 1860insA and R548X and recognition of D195V as a polymorphic variant
-
Lo Ten Foe JR, Barel MT, Thub P, Digweed M, Arwert F, Hoenje H. Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1860insA and R548X and recognition of D195V as a polymorphic variant. Hum Genet 1996; 98:522-3.
-
(1996)
Hum Genet
, vol.98
, pp. 522-523
-
-
Lo Ten Foe, J.R.1
Barel, M.T.2
Thub, P.3
Digweed, M.4
Arwert, F.5
Hoenje, H.6
-
70
-
-
15844403607
-
Novel mutations and polymorphisms in the Fanconi anemia group C gene
-
Gibson RA, Morgan NV, Goldstein LH, et al. Novel mutations and polymorphisms in the Fanconi anemia group C gene. Hum Mutat 1996; 8:140-8.
-
(1996)
Hum Mutat
, vol.8
, pp. 140-148
-
-
Gibson, R.A.1
Morgan, N.V.2
Goldstein, L.H.3
-
71
-
-
26844568343
-
Exon 6 skipping in the Fanconi Anemia C gene associated with a nonsense/missense mutation (775C→T) in exon 5
-
Lo Ten Foe JR, Kruyt FAE, Zweekhoest MBM, et al. Exon 6 skipping in the Fanconi Anemia C gene associated with a nonsense/missense mutation (775C→T) in exon 5. Hum Mutat 1997; 1:525-7.
-
(1997)
Hum Mutat
, vol.1
, pp. 525-527
-
-
Lo Ten Foe, J.R.1
Kruyt, F.A.E.2
Zweekhoest, M.B.M.3
-
72
-
-
0027339986
-
A Leu554-toPro substitution completely abolishes the functional complementing activity of the Fanconi anemia (FACC) protein
-
Gavish H, dos Santos CC, Buchwald M. A Leu554-toPro substitution completely abolishes the functional complementing activity of the Fanconi anemia (FACC) protein. Hum Mol Genet 1993; 2:123-6.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 123-126
-
-
Gavish, H.1
Dos Santos, C.C.2
Buchwald, M.3
-
73
-
-
0028292273
-
The Ashkenazi Jewish Fanconi anemia mutation: Incidence among patients and carrier frequency in the at-risk population
-
Whitney MA, Jakobs P, Kaback M, Moses RE, Grompe M. The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population. Hum Mutat 1994; 3:339-41.
-
(1994)
Hum Mutat
, vol.3
, pp. 339-341
-
-
Whitney, M.A.1
Jakobs, P.2
Kaback, M.3
Moses, R.E.4
Grompe, M.5
-
74
-
-
0028858123
-
Carrier frequency of the IVS4+4A→T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population
-
Verlander PC, Kaporis A, Liu Q, Zhang Q, Seligsohn U, Auerbach AD. Carrier frequency of the IVS4+4A→T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population. Blood 1995; 86:4034-8.
-
(1995)
Blood
, vol.86
, pp. 4034-4038
-
-
Verlander, P.C.1
Kaporis, A.2
Liu, Q.3
Zhang, Q.4
Seligsohn, U.5
Auerbach, A.D.6
-
75
-
-
0031012093
-
VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): Mutations in the FAC gene
-
Cox PM, Gibson RA, Morgan N, Brueton LA. VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): mutations in the FAC gene. Am J Med Genet 1997; 68:86-90.
-
(1997)
Am J Med Genet
, vol.68
, pp. 86-90
-
-
Cox, P.M.1
Gibson, R.A.2
Morgan, N.3
Brueton, L.A.4
-
76
-
-
0029988091
-
Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity
-
Yamashita T, Wu N, Kupfer G, et al. Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity. Blood 1996; 87:4424-32.
-
(1996)
Blood
, vol.87
, pp. 4424-4432
-
-
Yamashita, T.1
Wu, N.2
Kupfer, G.3
-
77
-
-
0030695440
-
Sequence variation in the Fanconi anemia gene FAA
-
Levran O, Erlich T, Magdalena N, et al. Sequence variation in the Fanconi anemia gene FAA. Proc Natl Acad USA 1997; 94:13051-6.
-
(1997)
Proc Natl Acad USA
, vol.94
, pp. 13051-13056
-
-
Levran, O.1
Erlich, T.2
Magdalena, N.3
-
78
-
-
0031440867
-
Mutations of the Fanconi anemia A gene (FAA) in Italian patients
-
Savino M, Ianzano L, Strippoli P, et al. Mutations of the Fanconi anemia A gene (FAA) in Italian patients. Am J Hum Genet 1997; 61:1246-53.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1246-1253
-
-
Savino, M.1
Ianzano, L.2
Strippoli, P.3
-
79
-
-
0013512335
-
Heterogeneous spectrum of mutations in the Fanconi anemia group A gene
-
in press
-
Wijker M, Morgan NV, Herterich S, et al. Heterogeneous spectrum of mutations in the Fanconi anemia group A gene. Eur J Hum Genet 1998; in press.
-
(1998)
Eur J Hum Genet
-
-
Wijker, M.1
Morgan, N.V.2
Herterich, S.3
-
80
-
-
0032144186
-
Fine exon-intron structure of the Fanconi anemia group A (FAA) gen and characterization of two genomic deletions
-
in press
-
Centra M, Memeo E, d'Apolito M, et al. Fine exon-intron structure of the Fanconi anemia group A (FAA) gen and characterization of two genomic deletions. Genomics 1998; in press.
-
(1998)
Genomics
-
-
Centra, M.1
Memeo, E.2
D'Apolito, M.3
-
81
-
-
12644293813
-
Somatic mosaicism in Fanconi anemia: Molecular basis and clinical significance
-
Lo Ten Foe JR, Kwee ML, Rooimans MA, et al. Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance. Eur J Hum Genet 1997; 5:137-48.
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 137-148
-
-
Lo Ten Foe, J.R.1
Kwee, M.L.2
Rooimans, M.A.3
-
82
-
-
0026637764
-
Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): Evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers
-
Klein CJ, Coovert DD, Bulman DE, et al. Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers. Am J Hum Genet 1992; 50:950-9.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 950-959
-
-
Klein, C.J.1
Coovert, D.D.2
Bulman, D.E.3
-
83
-
-
0028859379
-
Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells
-
Ellis NA, Lennon DJ, Proytcheva M, Alhadeff B, Henderson EE, German J. Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells. Am J Hum Genet 1995; 57:1019-27.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1019-1027
-
-
Ellis, N.A.1
Lennon, D.J.2
Proytcheva, M.3
Alhadeff, B.4
Henderson, E.E.5
German, J.6
-
84
-
-
0029902033
-
Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency
-
Hirschhorn R, Ruixi Yang D, PunkJM, Huie ML, Jiang CK, Kurlandsky LE. Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency. Nature Genet 1996; 6:290-5.
-
(1996)
Nature Genet
, vol.6
, pp. 290-295
-
-
Hirschhorn, R.1
Ruixi Yang, D.2
Punk, J.M.3
Huie, M.L.4
Jiang, C.K.5
Kurlandsky, L.E.6
-
85
-
-
0030047192
-
Developmental expression of the Fac gene correlates with congenital defects in Fanconi anemia patients
-
Krasnoshtein F, Buchwald M. Developmental expression of the Fac gene correlates with congenital defects in Fanconi anemia patients. Hum Mol Genet 1996; 5:85-93.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 85-93
-
-
Krasnoshtein, F.1
Buchwald, M.2
-
86
-
-
0029122525
-
Characterization of the 5′ region of the Fanconi anaemia group C (FACC) gene
-
Savoia A, Centra M, Ianzano L, de Cillis GP, Zelante L, Buchwald M. Characterization of the 5′ region of the Fanconi anaemia group C (FACC) gene. Hum Mol Genet 1995; 8:1321-6.
-
(1995)
Hum Mol Genet
, vol.8
, pp. 1321-1326
-
-
Savoia, A.1
Centra, M.2
Ianzano, L.3
De Cillis, G.P.4
Zelante, L.5
Buchwald, M.6
-
87
-
-
0031057961
-
p53 actives Fanconi anemia group C gene expression
-
Liebetrau W, Budde A, Savoia A, Grummt F, Hoehn H. p53 actives Fanconi anemia group C gene expression. Hum Mol Genet 1997; 2:277-83.
-
(1997)
Hum Mol Genet
, vol.2
, pp. 277-283
-
-
Liebetrau, W.1
Budde, A.2
Savoia, A.3
Grummt, F.4
Hoehn, H.5
-
88
-
-
0028275031
-
The Fanconi anemia polypeptide FACC is localized to the cytoplasm
-
Yamashita T, Barber DL, Zhu Y, Wu N, D'Andrea AD. The Fanconi anemia polypeptide FACC is localized to the cytoplasm. Proc Natl Acad Sci USA 1994; 91:6712-6.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6712-6716
-
-
Yamashita, T.1
Barber, D.L.2
Zhu, Y.3
Wu, N.4
D'Andrea, A.D.5
-
89
-
-
0027999023
-
Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells
-
Youssoufian H. Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells. Proc Natl Acad Sci 1994; 91:7975-9.
-
(1994)
Proc Natl Acad Sci
, vol.91
, pp. 7975-7979
-
-
Youssoufian, H.1
-
90
-
-
0028968316
-
Identification of cytosolic proteins that bind to the Fanconi anemia complementation group C polypeptide in vitro. Evidence for a multimeric complex
-
Youssoufian H, Auerbach AD, Verlander PC, Steimle V, Mach B. Identification of cytosolic proteins that bind to the Fanconi anemia complementation group C polypeptide in vitro. Evidence for a multimeric complex. J Biol Chem 1995; 270:9876-82.
-
(1995)
J Biol Chem
, vol.270
, pp. 9876-9882
-
-
Youssoufian, H.1
Auerbach, A.D.2
Verlander, P.C.3
Steimle, V.4
Mach, B.5
-
91
-
-
0029863680
-
Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells
-
Youssoufian H. Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells. J Clin Invest 1996; 97:2003-10.
-
(1996)
J Clin Invest
, vol.97
, pp. 2003-2010
-
-
Youssoufian, H.1
-
92
-
-
0842344634
-
The molecular chaperone GRP94 binds to a central domain within the group C Fanconi anemia protein
-
Hoshino T, Youssoufian H, Wang J, et al. The molecular chaperone GRP94 binds to a central domain within the group C Fanconi anemia protein [abstract]. Blood 1996; 88(Suppl 1):1734a.
-
(1996)
Blood
, vol.88
, Issue.1 SUPPL.
-
-
Hoshino, T.1
Youssoufian, H.2
Wang, J.3
-
93
-
-
0030831350
-
The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2
-
Kupfer GM, Yamashita T, Naf D, Suliman A, Asano S, D'Andrea AD. The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2. Blood 1997; 90:1047-54.
-
(1997)
Blood
, vol.90
, pp. 1047-1054
-
-
Kupfer, G.M.1
Yamashita, T.2
Naf, D.3
Suliman, A.4
Asano, S.5
D'Andrea, A.D.6
-
94
-
-
0030735797
-
Cytoplasmic localization of a functionally active Fanconi anemia group A-green fluorescent protein chimera in human 293 cells
-
Kruyt FAE, Waisfisz Q, Dijkmans LM, et al. Cytoplasmic localization of a functionally active Fanconi anemia group A-green fluorescent protein chimera in human 293 cells. Blood 1997; 90:3288-95.
-
(1997)
Blood
, vol.90
, pp. 3288-3295
-
-
Kruyt, F.A.E.1
Waisfisz, Q.2
Dijkmans, L.M.3
-
95
-
-
0030667925
-
The Fanconi anemia proteins, FAA and FAC, interact to form a nuclear complex
-
Kupfer G, Naf D, Suliman A, Pulsipher M, D'Andrea AD. The Fanconi anemia proteins, FAA and FAC, interact to form a nuclear complex. Nature Genet 1997; 17:487-90.
-
(1997)
Nature Genet
, vol.17
, pp. 487-490
-
-
Kupfer, G.1
Naf, D.2
Suliman, A.3
Pulsipher, M.4
D'Andrea, A.D.5
-
96
-
-
13344278020
-
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia
-
Chen M, Tomkins DJ, Auerbach W, et al. Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia. Nature Genet 1996; 12:448-51.
-
(1996)
Nature Genet
, vol.12
, pp. 448-451
-
-
Chen, M.1
Tomkins, D.J.2
Auerbach, W.3
-
97
-
-
8944258558
-
Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene
-
Whitney MA, Royle G, Low MJ, et al. Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene. Blood 1996; 88:49-58.
-
(1996)
Blood
, vol.88
, pp. 49-58
-
-
Whitney, M.A.1
Royle, G.2
Low, M.J.3
-
98
-
-
0029134016
-
Role of the cyclin-dependent kinase inhibitors in the development of cancer
-
Hirana T, Koeffler HP. Role of the cyclin-dependent kinase inhibitors in the development of cancer. Blood 1995; 86:841-54.
-
(1995)
Blood
, vol.86
, pp. 841-854
-
-
Hirana, T.1
Koeffler, H.P.2
-
99
-
-
0028938554
-
Irreversible repression of DNA synthesis in Fanconi anemia cells is alleviated by the product of a novel cyclin-related gene
-
Digweed M, Gunthert U, Schneider R, Seyschab H, Friedl R, Sperling K. Irreversible repression of DNA synthesis in Fanconi anemia cells is alleviated by the product of a novel cyclin-related gene. Mol Cell Biol 1995; 15:305-14.
-
(1995)
Mol Cell Biol
, vol.15
, pp. 305-314
-
-
Digweed, M.1
Gunthert, U.2
Schneider, R.3
Seyschab, H.4
Friedl, R.5
Sperling, K.6
-
100
-
-
0027977842
-
Repression of Fanconi anemia gene (FACC) expression inhibits growth of hematopoietic progenitor cells
-
Segal GM, Magenis RE, Brown M, et al. Repression of Fanconi anemia gene (FACC) expression inhibits growth of hematopoietic progenitor cells. J Clin Invest 1994; 94:846-52.
-
(1994)
J Clin Invest
, vol.94
, pp. 846-852
-
-
Segal, G.M.1
Magenis, R.E.2
Brown, M.3
-
101
-
-
0025086953
-
p53 function as a cell cycle control in osteosarcoma
-
Diller L, Kassel J, Nelson CE, et al. p53 function as a cell cycle control in osteosarcoma. Mol Cell Biol 1990; 10:5772-81.
-
(1990)
Mol Cell Biol
, vol.10
, pp. 5772-5781
-
-
Diller, L.1
Kassel, J.2
Nelson, C.E.3
-
102
-
-
0026496885
-
A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia telangiectasia
-
Kastan M, Zhan Q, El-Deiry, et al. A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia telangiectasia. Cell 1992; 71:587-97.
-
(1992)
Cell
, vol.71
, pp. 587-597
-
-
Kastan, M.1
Zhan, Q.2
El-Deiry3
-
103
-
-
0030953165
-
Deregulated apoptosis is a hallmark of the Fanconi anemia syndrome
-
Ridet A, Guillouf C, Duchaud E. Deregulated apoptosis is a hallmark of the Fanconi anemia syndrome. Cancer Res 1997; 57:1722-30.
-
(1997)
Cancer Res
, vol.57
, pp. 1722-1730
-
-
Ridet, A.1
Guillouf, C.2
Duchaud, E.3
-
104
-
-
0029857336
-
Suppression of apoptosis in hematopoietic factor-dependent progenitor cell lines by expression of the FAC gene
-
Cumming RC, Liu JM, Youssoufian H, Buchwald M. Suppression of apoptosis in hematopoietic factor-dependent progenitor cell lines by expression of the FAC gene. Blood 1996; 88:4558-67.
-
(1996)
Blood
, vol.88
, pp. 4558-4567
-
-
Cumming, R.C.1
Liu, J.M.2
Youssoufian, H.3
Buchwald, M.4
-
105
-
-
0030063534
-
Fanconi Anemia genes act to suppress a cross-linker-inducible p53-independent apoptosis pathway in lymphoblastoid cell lines
-
Kruyt FA, Dijkmans LM, van den Berg TK, Joenje H. Fanconi Anemia genes act to suppress a cross-linker-inducible p53-independent apoptosis pathway in lymphoblastoid cell lines. Blood 1996; 87:938-48.
-
(1996)
Blood
, vol.87
, pp. 938-948
-
-
Kruyt, F.A.1
Dijkmans, L.M.2
Van Den Berg, T.K.3
Joenje, H.4
-
106
-
-
0029744915
-
The effect of the Fanconi anemia polypeptide, FAC, upon p53 induction and G2 checkpoint regulation
-
Kupfer GM, D'Andrea AD. The effect of the Fanconi anemia polypeptide, FAC, upon p53 induction and G2 checkpoint regulation. Blood 1996; 88:1019-25.
-
(1996)
Blood
, vol.88
, pp. 1019-1025
-
-
Kupfer, G.M.1
D'Andrea, A.D.2
-
107
-
-
0028814071
-
p53-dependent pathway of radio-induced apoptosis is altered in Fanconi anemia
-
Rosselli F, Ridet A, Soussi T, Duchaud E, Alapetite C, Moustacchi E. p53-dependent pathway of radio-induced apoptosis is altered in Fanconi anemia. Oncogene 1995; 10:9-17.
-
(1995)
Oncogene
, vol.10
, pp. 9-17
-
-
Rosselli, F.1
Ridet, A.2
Soussi, T.3
Duchaud, E.4
Alapetite, C.5
Moustacchi, E.6
-
108
-
-
0030845529
-
Inactivation of Fanconi anemia group C gene augments interferon-gamma-induced apoptotic responses in hematopoietic cells
-
Rathbun RK, Faulkner GR, Ostroski MH, et al. Inactivation of Fanconi anemia group C gene augments interferon-gamma-induced apoptotic responses in hematopoietic cells. Blood 1997; 90:974-85.
-
(1997)
Blood
, vol.90
, pp. 974-985
-
-
Rathbun, R.K.1
Faulkner, G.R.2
Ostroski, M.H.3
-
109
-
-
0025059685
-
Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus
-
Papadopulo D, Guillouf C, Mohrenweiser H, Moustacchi E. Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus. Proc Natl Acad Sci USA 1990; 87:8383-7.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 8383-8387
-
-
Papadopulo, D.1
Guillouf, C.2
Mohrenweiser, H.3
Moustacchi, E.4
-
110
-
-
0028821379
-
The molecular mechanism underlying formation of deletions in Fanconi anemia cells may involve a site specific recombination
-
Laquerbe A, Moustacchi E, Fuscoe JC, Papadopoulo D. The molecular mechanism underlying formation of deletions in Fanconi anemia cells may involve a site specific recombination. Proc Natl Acad Sci USA 1995; 92:831-5.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 831-835
-
-
Laquerbe, A.1
Moustacchi, E.2
Fuscoe, J.C.3
Papadopoulo, D.4
-
111
-
-
0030854142
-
Elevated homologous recombination activity in Fanconi anemia fribroblasts
-
Thyagarajan B, Campell C. Elevated homologous recombination activity in Fanconi anemia fribroblasts. J Biol Chem 1997; 272:23328-33.
-
(1997)
J Biol Chem
, vol.272
, pp. 23328-23333
-
-
Thyagarajan, B.1
Campell, C.2
-
112
-
-
0030292447
-
Fanconi anemia forges a novel pathway
-
D'Andrea A. Fanconi anemia forges a novel pathway. Nature Genet 1996; 14:240-2.
-
(1996)
Nature Genet
, vol.14
, pp. 240-242
-
-
D'Andrea, A.1
-
113
-
-
0030884238
-
Molecular biology of Fanconi anemia: Implication for diagnosis and therapy
-
D'Andrea A, Grompe M. Molecular biology of Fanconi anemia: implication for diagnosis and therapy. Blood 1997; 90:1725-36.
-
(1997)
Blood
, vol.90
, pp. 1725-1736
-
-
D'Andrea, A.1
Grompe, M.2
-
114
-
-
0030909989
-
A novel, membrane receptor-based retroviral vector for Fanconi anemia group C gene therapy
-
Machl AW, Planitzer S, Kubbies M. A novel, membrane receptor-based retroviral vector for Fanconi anemia group C gene therapy. Gene Ther 1997; 4:339-45.
-
(1997)
Gene Ther
, vol.4
, pp. 339-345
-
-
Machl, A.W.1
Planitzer, S.2
Kubbies, M.3
-
115
-
-
0030869786
-
Functional correction of Fanconi group A hematopoietic cells by retroviral gene transfer
-
Fu K-L, Lo Ten Foe JR, Joenje H, Rao KW, Liu JM, Walsh CE. Functional correction of Fanconi group A hematopoietic cells by retroviral gene transfer. Blood 1997; 90:3296-303.
-
(1997)
Blood
, vol.90
, pp. 3296-3303
-
-
Fu, K.-L.1
Lo Ten Foe, J.R.2
Joenje, H.3
Rao, K.W.4
Liu, J.M.5
Walsh, C.E.6
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