-
1
-
-
0020687919
-
Retinoblastoma: Diagnosis and treatment
-
Balmer A., Gaillioud C. Retinoblastoma. diagnosis and treatment Dev Ophthalmol. 7:1983;36-100.
-
(1983)
Dev Ophthalmol
, vol.7
, pp. 36-100
-
-
Balmer, A.1
Gaillioud, C.2
-
2
-
-
0027297105
-
Molecular mechanism of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma
-
Hogg A., Bia B., Onadim Z., Cowell J.K. Molecular mechanism of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma. Proc Natl Acad Sci U S A. 90:1993;7351-7355.
-
(1993)
Proc Natl Acad Sci U S a
, vol.90
, pp. 7351-7355
-
-
Hogg, A.1
Bia, B.2
Onadim, Z.3
Cowell, J.K.4
-
3
-
-
0027504088
-
Antioncogenes and human cancer
-
Knudson A.G. Antioncogenes and human cancer. Proc Natl Acad Sci U S A. 90:1993;10914-10921.
-
(1993)
Proc Natl Acad Sci U S a
, vol.90
, pp. 10914-10921
-
-
Knudson, A.G.1
-
4
-
-
0017819319
-
Retinoblastoma: A prototypic hereditary neoplasm
-
Knudson A.G. Retinoblastoma. a prototypic hereditary neoplasm Sem Oncol. 5:1978;57.
-
(1978)
Sem Oncol
, vol.5
, pp. 57
-
-
Knudson, A.G.1
-
5
-
-
0023261635
-
The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity
-
Lee W.H., Shew J.Y., Hong F.D., Sery T.W., Donoso L.A., Young L.J., Brookstein R., Lee E.Y. The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity. Nature. 329:1987;642-645.
-
(1987)
Nature
, vol.329
, pp. 642-645
-
-
Lee, W.H.1
Shew, J.Y.2
Hong, F.D.3
Sery, T.W.4
Donoso, L.A.5
Young, L.J.6
Brookstein, R.7
Lee, E.Y.8
-
6
-
-
0027251051
-
Complete genomic sequence of the human retinoblastoma susceptibility gene
-
Toguchida J., McGee T.L., Paterson J.C., Eagle J.R., Tucker S., Yandell D.W. Complete genomic sequence of the human retinoblastoma susceptibility gene. Genomics. 17:1993;535-543.
-
(1993)
Genomics
, vol.17
, pp. 535-543
-
-
Toguchida, J.1
McGee, T.L.2
Paterson, J.C.3
Eagle, J.R.4
Tucker, S.5
Yandell, D.W.6
-
7
-
-
0028970779
-
Germline mutations in the RB1 gene in patients with hereditary retinoblastoma
-
Liu Z., Song Y., Bia B., Cowell J.K. Germline mutations in the RB1 gene in patients with hereditary retinoblastoma. Genes Chromosom Cancer. 14:1995;277-284.
-
(1995)
Genes Chromosom Cancer
, vol.14
, pp. 277-284
-
-
Liu, Z.1
Song, Y.2
Bia, B.3
Cowell, J.K.4
-
8
-
-
0022446922
-
Cytogenetic analysis using quantitative highly sensitive fluorescence hybridization
-
Pinkel D., Straume T., Gray J.W. Cytogenetic analysis using quantitative highly sensitive fluorescence hybridization. Proc Natl Acad Sci U S A. 83:1986;2934-2938.
-
(1986)
Proc Natl Acad Sci U S a
, vol.83
, pp. 2934-2938
-
-
Pinkel, D.1
Straume, T.2
Gray, J.W.3
-
9
-
-
0026673160
-
Detection of retinoblastoma gene copy number in metaphase chromosomes and interphase nuclei by fluorescence in situ hybridization
-
Kallioniemi A., Kaliioniemi O.P., Waldman F.M., Chen L.C., Yu L.C., Fung Y.K., Smith H.S., Pinkel D., Gray J.W. Detection of retinoblastoma gene copy number in metaphase chromosomes and interphase nuclei by fluorescence in situ hybridization. Cytogenet Cell Genet. 60:1992;190-193.
-
(1992)
Cytogenet Cell Genet
, vol.60
, pp. 190-193
-
-
Kallioniemi, A.1
Kaliioniemi, O.P.2
Waldman, F.M.3
Chen, L.C.4
Yu, L.C.5
Fung, Y.K.6
Smith, H.S.7
Pinkel, D.8
Gray, J.W.9
-
10
-
-
0021369015
-
Homozygosity of chromosome 13 in retinoblastoma
-
Dryja T.P., Cavenee W.K., White R., Rapaport J.M., Petersen R., Albert D.M., Bruns G.A. Homozygosity of chromosome 13 in retinoblastoma. N Engl J Med. 310:1984;550-553.
-
(1984)
N Engl J Med
, vol.310
, pp. 550-553
-
-
Dryja, T.P.1
Cavenee, W.K.2
White, R.3
Rapaport, J.M.4
Petersen, R.5
Albert, D.M.6
Bruns, G.A.7
-
11
-
-
0028914616
-
Karyotypic heterogeneity and its relation to labeling index in interphase breast tumor cells
-
Balázs M., Matsumura K., Moore D., Pinkel D., Gray J.W., Waldman F.M. Karyotypic heterogeneity and its relation to labeling index in interphase breast tumor cells. Cytometry. 20:1995;62-73.
-
(1995)
Cytometry
, vol.20
, pp. 62-73
-
-
Balázs, M.1
Matsumura, K.2
Moore, D.3
Pinkel, D.4
Gray, J.W.5
Waldman, F.M.6
-
13
-
-
0024384616
-
Structure and partial genomic sequence of the human retinoblastoma susceptibility gene
-
McGee T.L., Yandell D.W., Dryja T.P. Structure and partial genomic sequence of the human retinoblastoma susceptibility gene. Gene. 80:1989;119-128.
-
(1989)
Gene
, vol.80
, pp. 119-128
-
-
McGee, T.L.1
Yandell, D.W.2
Dryja, T.P.3
-
14
-
-
0342598381
-
Identification of mutations in the retinoblastoma gene
-
F.E. Cotter. Totowa, NJ: Humana Press Inc
-
Hogg A. Identification of mutations in the retinoblastoma gene. Cotter F.E. Methods in Molecular Medicine. Molecular Diagnosis of Cancer:1996;123-140 Humana Press Inc, Totowa, NJ.
-
(1996)
Methods in Molecular Medicine: Molecular Diagnosis of Cancer
, pp. 123-140
-
-
Hogg, A.1
-
15
-
-
0024756969
-
Rapid and sensitive detection of point mutations and DNA polymorphysms using the polymerase chain reaction
-
Orita M., Suzuki Y., Sekiya T., Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphysms using the polymerase chain reaction. Genomics. 5:1989;874-879.
-
(1989)
Genomics
, vol.5
, pp. 874-879
-
-
Orita, M.1
Suzuki, Y.2
Sekiya, T.3
Hayashi, K.4
-
16
-
-
0027193630
-
The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitution
-
Sheffield V.C., Beck J.S., Kwitek A.E., Sandstrom D.W., Stone E.M. The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitution. Genomics. 16:1993;325-332.
-
(1993)
Genomics
, vol.16
, pp. 325-332
-
-
Sheffield, V.C.1
Beck, J.S.2
Kwitek, A.E.3
Sandstrom, D.W.4
Stone, E.M.5
-
17
-
-
0020627270
-
A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q
-
Motegi T., Kaga M., Yanagawa Y., Kadowaki H., Watanabe K., Inoue A., Komatsu M., Minoda K. A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q. Hum Genet. 64:1983;160-162.
-
(1983)
Hum Genet
, vol.64
, pp. 160-162
-
-
Motegi, T.1
Kaga, M.2
Yanagawa, Y.3
Kadowaki, H.4
Watanabe, K.5
Inoue, A.6
Komatsu, M.7
Minoda, K.8
-
18
-
-
0029093470
-
Immunohistochemical evidence of neuronal and glial differentiation in retinoblastoma
-
Xu K.P., Liu S.L., Ni C. Immunohistochemical evidence of neuronal and glial differentiation in retinoblastoma. Br J Ophthalmol. 79:1995;771-776.
-
(1995)
Br J Ophthalmol
, vol.79
, pp. 771-776
-
-
Xu, K.P.1
Liu, S.L.2
Ni, C.3
-
19
-
-
0030722735
-
Incomplete penetrance of familial retinoblastoma linked to germ-line mutations that result in partial loss of RB function
-
Otterson G.A., Chen W.D., Coxon A.Y., Khleif S.N., Kaye F.J. Incomplete penetrance of familial retinoblastoma linked to germ-line mutations that result in partial loss of RB function. Proc Natl Acad Sci U S A. 94:1994;12036-12040.
-
(1994)
Proc Natl Acad Sci U S a
, vol.94
, pp. 12036-12040
-
-
Otterson, G.A.1
Chen, W.D.2
Coxon, A.Y.3
Khleif, S.N.4
Kaye, F.J.5
-
20
-
-
0027478499
-
The effect of formalin fixation on DNA and the extraction of high-molecular-weight DNA from fixed and embedded tissues
-
Koshiba M., Ogawa K., Hamazaki S., Sugiyama T., Ogawa O., Kitajima T. The effect of formalin fixation on DNA and the extraction of high-molecular-weight DNA from fixed and embedded tissues. Pathol Res Pract. 189:1993;66-72.
-
(1993)
Pathol Res Pract
, vol.189
, pp. 66-72
-
-
Koshiba, M.1
Ogawa, K.2
Hamazaki, S.3
Sugiyama, T.4
Ogawa, O.5
Kitajima, T.6
-
22
-
-
0030248583
-
Constitutional nonsense germline mutations in the RB1 gene detected in patients with early onset unilateral retinoblastoma
-
Cowell J.K., Cragg H. Constitutional nonsense germline mutations in the RB1 gene detected in patients with early onset unilateral retinoblastoma. Eur J Cancer. 32A:1996;1749-1752.
-
(1996)
Eur J Cancer
, vol.32
, pp. 1749-1752
-
-
Cowell, J.K.1
Cragg, H.2
-
23
-
-
0018642114
-
Genetics of retinoblastoma
-
Vogel F. Genetics of retinoblastoma. Hum Genet. 52:1979;1-54.
-
(1979)
Hum Genet
, vol.52
, pp. 1-54
-
-
Vogel, F.1
-
24
-
-
0026757785
-
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene
-
Munier F., Spence M.A., Pescia G., Balmer A., Gallioud C., Thonney F., van Melle G., Rutz H.P. Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene. Hum Genet. 89:1992;508-512.
-
(1992)
Hum Genet
, vol.89
, pp. 508-512
-
-
Munier, F.1
Spence, M.A.2
Pescia, G.3
Balmer, A.4
Gallioud, C.5
Thonney, F.6
Van Melle, G.7
Rutz, H.P.8
-
25
-
-
0024835010
-
Oncogenic point mutations in the human retinoblastoma gene: Their application to genetic counseling
-
Yandell D.W., Campbell T.A., Dayton S.H., Petersen R., Walton D., Little J.B., McConkie-Rosell A., Buckley E.G., Dryja T.P. Oncogenic point mutations in the human retinoblastoma gene. their application to genetic counseling New Engl J Med. 321:1989;1689-1695.
-
(1989)
New Engl J Med
, vol.321
, pp. 1689-1695
-
-
Yandell, D.W.1
Campbell, T.A.2
Dayton, S.H.3
Petersen, R.4
Walton, D.5
Little, J.B.6
McConkie-Rosell, A.7
Buckley, E.G.8
Dryja, T.P.9
-
26
-
-
0020518746
-
Expression of recessive alleles by chromosomal mechanism in retinoblastoma
-
Cavenee W.K., Dryja T.P., Phillips R.A., Benedict W.F., Godbout R., Gallie B.L., Murphee A.L., Strong L.C., White R.L. Expression of recessive alleles by chromosomal mechanism in retinoblastoma. Nature. 305:1983;779-784.
-
(1983)
Nature
, vol.305
, pp. 779-784
-
-
Cavenee, W.K.1
Dryja, T.P.2
Phillips, R.A.3
Benedict, W.F.4
Godbout, R.5
Gallie, B.L.6
Murphee, A.L.7
Strong, L.C.8
White, R.L.9
-
27
-
-
0030881844
-
Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma
-
Lohmann D.R., Gerick M., Brandt B., Oelschlager U., Lorenz B., Passarge E., Horshemke B. Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma. Am J Hum Genet. 61:1997;282-294.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 282-294
-
-
Lohmann, D.R.1
Gerick, M.2
Brandt, B.3
Oelschlager, U.4
Lorenz, B.5
Passarge, E.6
Horshemke, B.7
-
28
-
-
0028970779
-
Germline mutations in the RB1 gene in patients with hereditary retinoblastoma
-
Liu Z., Song Y., Bia B., Cowell J.K. Germline mutations in the RB1 gene in patients with hereditary retinoblastoma. Genes Chromosom Cancer. 14:1995;277-284.
-
(1995)
Genes Chromosom Cancer
, vol.14
, pp. 277-284
-
-
Liu, Z.1
Song, Y.2
Bia, B.3
Cowell, J.K.4
-
29
-
-
0021739401
-
Second nonocular tumors in retinoblastoma survivors: Are they radiation induced?
-
Abramson D.H., Ellsworth R.M., Kitchin F.D., Tung G. Second nonocular tumors in retinoblastoma survivors. are they radiation induced? Ophthalmology. 91:1984;1351-1355.
-
(1984)
Ophthalmology
, vol.91
, pp. 1351-1355
-
-
Abramson, D.H.1
Ellsworth, R.M.2
Kitchin, F.D.3
Tung, G.4
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