-
1
-
-
0027183013
-
Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines
-
Almeida A, Kokalj-Vokac N, Lefrancois D, Viegas-Péquignot E, Jeanpierre M, Dutrillaux B, Malfoy B: Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines. Hum Genet 91:538-546 (1993).
-
(1993)
Hum Genet
, vol.91
, pp. 538-546
-
-
Almeida, A.1
Kokalj-Vokac, N.2
Lefrancois, D.3
Viegas-Péquignot, E.4
Jeanpierre, M.5
Dutrillaux, B.6
Malfoy, B.7
-
2
-
-
0029026984
-
ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): Investigation of heterochromatin abnormalities and review of clinical outcome
-
Brown DC, Grace E, Summer AT, Edmunds AT, Ellis PM: ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome. Hum Genet 96:411-416 (1995).
-
(1995)
Hum Genet
, vol.96
, pp. 411-416
-
-
Brown, D.C.1
Grace, E.2
Summer, A.T.3
Edmunds, A.T.4
Ellis, P.M.5
-
3
-
-
0023890497
-
Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9. and 16
-
Carpenter NJ, Fillpovich A, Blaese RM, Carey TL, Berkel AI: Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9. and 16. J Ped 112:757-760 (1988).
-
(1988)
J Ped
, vol.112
, pp. 757-760
-
-
Carpenter, N.J.1
Fillpovich, A.2
Blaese, R.M.3
Carey, T.L.4
Berkel, A.I.5
-
4
-
-
0020489781
-
Amount and distribution of 5-methylcytosine in human DNA from different types of tissues or cells
-
Ehrlich M, Gama-Sosa M, Huang L-H, Midgett RM, Kuo KC, McCune RA, Gehrke C: Amount and distribution of 5-methylcytosine in human DNA from different types of tissues or cells. Nucl Acids Res 10:2709-2721 (1982).
-
(1982)
Nucl Acids Res
, vol.10
, pp. 2709-2721
-
-
Ehrlich, M.1
Gama-Sosa, M.2
Huang, L.-H.3
Midgett, R.M.4
Kuo, K.C.5
McCune, R.A.6
Gehrke, C.7
-
5
-
-
0025346267
-
Fragility of the centromeric region of chromosome 1 associated with combined immunodeficiency in siblings: A recessively inherited entity?
-
Fasth A, Forestier E, Holmberg E, Holmgren G, Nordenson I, Soderstrom T, Wahlstrom J: Fragility of the centromeric region of chromosome 1 associated with combined immunodeficiency in siblings: a recessively inherited entity? Acta Paediatr Scand 79:605-612 (1990).
-
(1990)
Acta Paediatr Scand
, vol.79
, pp. 605-612
-
-
Fasth, A.1
Forestier, E.2
Holmberg, E.3
Holmgren, G.4
Nordenson, I.5
Soderstrom, T.6
Wahlstrom, J.7
-
6
-
-
0019434304
-
Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency
-
Fryns JP, Azou M, Jacken J, Eggermont E, Pedersen JC, Van den Berghe H: Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency. Hum Genet 57:108-110 (1981).
-
(1981)
Hum Genet
, vol.57
, pp. 108-110
-
-
Fryns, J.P.1
Azou, M.2
Jacken, J.3
Eggermont, E.4
Pedersen, J.C.5
Van Den Berghe, H.6
-
7
-
-
0021101229
-
The 5-methylcytosine content of DNA from human tumors
-
Gama-Sosa MA, Slagel VA, Trewyn RW, Oxenhandler R, Kuo KC, Gehrke CW, Ehrlich M: The 5-methylcytosine content of DNA from human tumors. Nucl Acids Res 11:6883-6894 (1983a).
-
(1983)
Nucl Acids Res
, vol.11
, pp. 6883-6894
-
-
Gama-Sosa, M.A.1
Slagel, V.A.2
Trewyn, R.W.3
Oxenhandler, R.4
Kuo, K.C.5
Gehrke, C.W.6
Ehrlich, M.7
-
8
-
-
0021111964
-
The 5-methylcytosine content of highly repeated sequences in human DNA
-
Gama-Sosa MA, Wang RY-H, Kuo KC, Gehrke CW, Ehrlich M: The 5-methylcytosine content of highly repeated sequences in human DNA. Nucl Acids Res 11:3087-3095 (1983b).
-
(1983)
Nucl Acids Res
, vol.11
, pp. 3087-3095
-
-
Gama-Sosa, M.A.1
Wang, R.Y.-H.2
Kuo, K.C.3
Gehrke, C.W.4
Ehrlich, M.5
-
9
-
-
0028947749
-
The effects of 5-azacytidine and 5-azadeoxycytidine on chromosome structure and function: Implications for methylation-associated cellular processes
-
Haaf T: The effects of 5-azacytidine and 5-azadeoxycytidine on chromosome structure and function: implications for methylation-associated cellular processes. Pharmac Ther 65:19-46 (1995).
-
(1995)
Pharmac Ther
, vol.65
, pp. 19-46
-
-
Haaf, T.1
-
10
-
-
0025979413
-
Chromosome topology in mammalian interphase nuclei
-
Haaf T, Schmid M: Chromosome topology in mammalian interphase nuclei. Exp Cell Res 192:325-332 (1991).
-
(1991)
Exp Cell Res
, vol.192
, pp. 325-332
-
-
Haaf, T.1
Schmid, M.2
-
11
-
-
0033603240
-
Sir-Ku-itous routes to make ends meet
-
Haber JE: Sir-Ku-itous routes to make ends meet. Cell 97:829-832 (1999).
-
(1999)
Cell
, vol.97
, pp. 829-832
-
-
Haber, J.E.1
-
13
-
-
0030988255
-
Preferential induction of chromosome 1 multi-branched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidine
-
Hernandez R, Frady A, Zhang X-Y, Varela M, Ehrlich M: Preferential induction of chromosome 1 multi-branched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidine. Cytogenet Cell Genet 76:196-201 (1997).
-
(1997)
Cytogenet Cell Genet
, vol.76
, pp. 196-201
-
-
Hernandez, R.1
Frady, A.2
Zhang, X.-Y.3
Varela, M.4
Ehrlich, M.5
-
14
-
-
0000038810
-
Selective somatic pairing and fragility at 1q12 in a boy with common variable immunodeficiency
-
Hulten M: Selective somatic pairing and fragility at 1q12 in a boy with common variable immunodeficiency. Clin Genet 14:294 (1978).
-
(1978)
Clin Genet
, vol.14
, pp. 294
-
-
Hulten, M.1
-
16
-
-
0028650742
-
Human satellite 2 and 3
-
Jeanpierre M: Human satellite 2 and 3. A Rev Genet 37:163-171 (1994).
-
(1994)
A Rev Genet
, vol.37
, pp. 163-171
-
-
Jeanpierre, M.1
-
17
-
-
0027286618
-
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome
-
Jeanpierre M, Turleau C, Aurias A, Prieur M, Ledeist F, Fischer A, Viegas-Péquignot E: An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. Hum Molec Genet 2:731-735 (1993).
-
(1993)
Hum Molec Genet
, vol.2
, pp. 731-735
-
-
Jeanpierre, M.1
Turleau, C.2
Aurias, A.3
Prieur, M.4
Ledeist, F.5
Fischer, A.6
Viegas-Péquignot, E.7
-
18
-
-
0030867514
-
DNA demethylation and pericentromeric rearrangements of chromosome 1
-
Ji W, Hernandez R, Zhang X-Y, Qu G, Frady A, Varela M, Ehrlich M: DNA demethylation and pericentromeric rearrangements of chromosome 1. Mutation Res 379:33-41 (1997).
-
(1997)
Mutation Res
, vol.379
, pp. 33-41
-
-
Ji, W.1
Hernandez, R.2
Zhang, X.-Y.3
Qu, G.4
Frady, A.5
Varela, M.6
Ehrlich, M.7
-
19
-
-
0034162852
-
Whole-genome methylation scan in ICF syndrome: Hypomethylation of non-satellite DNA repeats D4Z4 and NBL2
-
in press
-
Kondo T, Comenge Y, Bobek MP, Kuick R, Lamb B, Zhu X, Narayan A, Bourc'his D, Viegas-Péquinot E, Ehrlich M, Hanash S: Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2. Hum Mol Gen: in press (2000).
-
(2000)
Hum Mol Gen
-
-
Kondo, T.1
Comenge, Y.2
Bobek, M.P.3
Kuick, R.4
Lamb, B.5
Zhu, X.6
Narayan, A.7
Bourc'his, D.8
Viegas-Péquinot, E.9
Ehrlich, M.10
Hanash, S.11
-
20
-
-
0019202657
-
Quantitative reversed-phase high performance liquid chromatographic determination of major and modified deoxyribonucleosides in DNA
-
Kuo KC, McCune RA, Gehrke CW, Midgett R, Ehrlich M: Quantitative reversed-phase high performance liquid chromatographic determination of major and modified deoxyribonucleosides in DNA. Nucl Acids Res 8:4763-4776 (1980).
-
(1980)
Nucl Acids Res
, vol.8
, pp. 4763-4776
-
-
Kuo, K.C.1
McCune, R.A.2
Gehrke, C.W.3
Midgett, R.4
Ehrlich, M.5
-
21
-
-
0032947095
-
Suppression of intrachromosomal gene conversion in mammalian cells by small degrees of sequence divergence
-
Lukacsovich T, Waldman AS: Suppression of intrachromosomal gene conversion in mammalian cells by small degrees of sequence divergence. Genetics 151:1559-1568 (1999).
-
(1999)
Genetics
, vol.151
, pp. 1559-1568
-
-
Lukacsovich, T.1
Waldman, A.S.2
-
22
-
-
0026564948
-
Interphase cytogenetics of the ICF syndrome
-
Maraschio P, Cortinovis M, Dainotti E, Tupler R, Tiepolo L: Interphase cytogenetics of the ICF syndrome. Ann hum Genet 56:273-278 (1992).
-
(1992)
Ann Hum Genet
, vol.56
, pp. 273-278
-
-
Maraschio, P.1
Cortinovis, M.2
Dainotti, E.3
Tupler, R.4
Tiepolo, L.5
-
23
-
-
0030825508
-
Chromosomal imbalance maps of malignant solid tumors: A cytogenetic survey of 3185 neoplasms
-
Mertens F, Johansson B, Hoglund M, Mitelman F: Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms. Cancer Res 57:2765-2780 (1997).
-
(1997)
Cancer Res
, vol.57
, pp. 2765-2780
-
-
Mertens, F.1
Johansson, B.2
Hoglund, M.3
Mitelman, F.4
-
24
-
-
0030969206
-
Alpha-satellite DNA methylation in normal individuals and in ICF patients: Heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues
-
Miniou P, Jeanpierre M, Bourc'his D, Coutinho Barbosa AC, Blanquet V, Viegas-Péquignot E: Alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues. Hum Genet 99:738-745 (1997).
-
(1997)
Hum Genet
, vol.99
, pp. 738-745
-
-
Miniou, P.1
Jeanpierre, M.2
Bourc'his, D.3
Coutinho Barbosa, A.C.4
Blanquet, V.5
Viegas-Péquignot, E.6
-
25
-
-
0023616290
-
Human chromosome-specific repetitive DNA sequences: Novel markers for genetic analysis
-
Moyzis RK, Albright KL, Bartholdi MF, Cram LS, Deaven LL, Hildebrand CE, Joste NE, Longmire JL, Meyne J, Schwarzacher-Robinson T: Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis. Chromosoma 95:375-386 (1987).
-
(1987)
Chromosoma
, vol.95
, pp. 375-386
-
-
Moyzis, R.K.1
Albright, K.L.2
Bartholdi, M.F.3
Cram, L.S.4
Deaven, L.L.5
Hildebrand, C.E.6
Joste, N.E.7
Longmire, J.L.8
Meyne, J.9
Schwarzacher-Robinson, T.10
-
26
-
-
0031816567
-
Hypomethylation of pericentromeric DNA in breast adenocarcinomas
-
Narayan A, Ji W, Zhang X-Y, Marrogi A, Graff JR, Baylin SB, Ehrlich M: Hypomethylation of pericentromeric DNA in breast adenocarcinomas. Int J Cancer 77:833-838 (1998).
-
(1998)
Int J Cancer
, vol.77
, pp. 833-838
-
-
Narayan, A.1
Ji, W.2
Zhang, X.-Y.3
Marrogi, A.4
Graff, J.R.5
Baylin, S.B.6
Ehrlich, M.7
-
27
-
-
0033615717
-
DNA methyltransferases Dnmt 3a and Dnmt 3b are essential for de novo methylation and mammalian development
-
Okano M, Bell DW, Haber DA, Li E: DNA methyltransferases Dnmt 3a and Dnmt 3b are essential for de novo methylation and mammalian development. Cell 98:247-257 (1999).
-
(1999)
Cell
, vol.98
, pp. 247-257
-
-
Okano, M.1
Bell, D.W.2
Haber, D.A.3
Li, E.4
-
28
-
-
0001992028
-
Satellite DNA hypomethylation vs. overall genomic hypomethylation in ovarian epithelial tumors of different malignant potential
-
Qu G, Dubeau L, Narayan A, Yu M, Ehrlich M: Satellite DNA hypomethylation vs. overall genomic hypomethylation in ovarian epithelial tumors of different malignant potential. Mut Res 423:91-101 (1999a).
-
(1999)
Mut Res
, vol.423
, pp. 91-101
-
-
Qu, G.1
Dubeau, L.2
Narayan, A.3
Yu, M.4
Ehrlich, M.5
-
29
-
-
0033081639
-
Frequent hypomethylation in Wilms tumors of pericentromeric DNA in chromosomes 1 and 16
-
Qu G, Grundy PE, Narayan A, Ehrlich M: Frequent hypomethylation in Wilms tumors of pericentromeric DNA in chromosomes 1 and 16. Cancer Genet Cytogenet 109:34-39 (1999b).
-
(1999)
Cancer Genet Cytogenet
, vol.109
, pp. 34-39
-
-
Qu, G.1
Grundy, P.E.2
Narayan, A.3
Ehrlich, M.4
-
30
-
-
0032030675
-
Jumping translocations of chromosome 1q in multiple myeloma: Evidence for a mechanism involving decondensation of pericentromeric heterochromatin
-
Sawyer J, Tricot G, Mattox S, Jagannath S, Barlogie B: Jumping translocations of chromosome 1q in multiple myeloma: evidence for a mechanism involving decondensation of pericentromeric heterochromatin. Blood 91:1732-1741 (1998).
-
(1998)
Blood
, vol.91
, pp. 1732-1741
-
-
Sawyer, J.1
Tricot, G.2
Mattox, S.3
Jagannath, S.4
Barlogie, B.5
-
31
-
-
0028908387
-
Chromosome instability in ICF syndrome: Formation of micronuclei from multibranched chromosome 1 demonstrated by fluorescence in situ hybridization
-
Sawyer JR, Swanson CM, Wheeler G, Cunniff C: Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosome 1 demonstrated by fluorescence in situ hybridization. Am J med Genet 56:203-209 (1995).
-
(1995)
Am J Med Genet
, vol.56
, pp. 203-209
-
-
Sawyer, J.R.1
Swanson, C.M.2
Wheeler, G.3
Cunniff, C.4
-
32
-
-
0027989585
-
ICF syndrome: A new case and review of the literature
-
Smeets DFCM, Moog U, Weemaes CMR, Vaes-Peeters G, Merkx GFM, Niehof JP, Hamers G: ICF syndrome: a new case and review of the literature. Hum Genet 94:240-246 (1994).
-
(1994)
Hum Genet
, vol.94
, pp. 240-246
-
-
Smeets, D.F.C.M.1
Moog, U.2
Weemaes, C.M.R.3
Vaes-Peeters, G.4
Merkx, G.F.M.5
Niehof, J.P.6
Hamers, G.7
-
33
-
-
0030700397
-
Influence of ATM function on telomere metabolism
-
Smilenov LB, Morgan SE, Mellado W, Sawant SG, Kastan MB, Pandita TK: Influence of ATM function on telomere metabolism. Oncogene 15:2659-2665 (1997).
-
(1997)
Oncogene
, vol.15
, pp. 2659-2665
-
-
Smilenov, L.B.1
Morgan, S.E.2
Mellado, W.3
Sawant, S.G.4
Kastan, M.B.5
Pandita, T.K.6
-
34
-
-
0031688264
-
A FISH study of chromosome fusion in the ICF syndrome: Involvement of paracentric heterochromatin but not of the centromeres themselves
-
Sumner AT, Mitchell AR, Ellis PM: A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves. J Med Genet 35:833-835 (1998).
-
(1998)
J Med Genet
, vol.35
, pp. 833-835
-
-
Sumner, A.T.1
Mitchell, A.R.2
Ellis, P.M.3
-
35
-
-
0018672228
-
Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency
-
Tiepolo L, Maraschio P, Gimelli G, Cuoco C, Gargani GF, Romano C: Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency. Hum Genet 51:127-137 (1979).
-
(1979)
Hum Genet
, vol.51
, pp. 127-137
-
-
Tiepolo, L.1
Maraschio, P.2
Gimelli, G.3
Cuoco, C.4
Gargani, G.F.5
Romano, C.6
-
36
-
-
9344242353
-
A methylated human 9-kb repetitive sequence on acrocentric chromosomes is homologous to a subtelomeric repeat in chimpanzees
-
USA
-
Thoraval D, Asakawa J, Kodaira M, Chang C, Radany E, Kuick R, Lamb B, Richardson B, Neel JV, Glover T, Hanash S: A methylated human 9-kb repetitive sequence on acrocentric chromosomes is homologous to a subtelomeric repeat in chimpanzees. Proc natl Acad Sci, USA 93:4442-4447 (1996).
-
(1996)
Proc Natl Acad Sci
, vol.93
, pp. 4442-4447
-
-
Thoraval, D.1
Asakawa, J.2
Kodaira, M.3
Chang, C.4
Radany, E.5
Kuick, R.6
Lamb, B.7
Richardson, B.8
Neel, J.V.9
Glover, T.10
Hanash, S.11
-
37
-
-
0023636489
-
Triradial configurations indicate that expression of the fragile site at Xq27 is non-lethal
-
Tommerup N: Triradial configurations indicate that expression of the fragile site at Xq27 is non-lethal. Ann Genet 30:231-232 (1987).
-
(1987)
Ann Genet
, vol.30
, pp. 231-232
-
-
Tommerup, N.1
-
38
-
-
0024344545
-
Multi-branched chromosomes in the ICF syndrome: Immunodeficiency, centromeric instability, and facial anomalies
-
Turleau C, Cabanis M-O, Girault D, Ledeist F, Mettey R, Puissant H, Marguerite P, de Grouchy J: Multi-branched chromosomes in the ICF syndrome: Immunodeficiency, centromeric instability, and facial anomalies. Am J med Genet 32:420-424 (1989).
-
(1989)
Am J Med Genet
, vol.32
, pp. 420-424
-
-
Turleau, C.1
Cabanis, M.-O.2
Girault, D.3
Ledeist, F.4
Mettey, R.5
Puissant, H.6
Marguerite, P.7
De Grouchy, J.8
-
39
-
-
0023414542
-
Chromosome-specific alpha satellite DNA from human chromosome 1: Hierarchical structure and genomic organization of polymorphic domain spanning several hundred kilobase pairs of centromeric DNA
-
Waye JS, Durfy SJ, Pinkel D, Kenwrick S, Patterson M, Davies KE, Willard HF: Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of polymorphic domain spanning several hundred kilobase pairs of centromeric DNA. Genomics 1:43-51 (1987).
-
(1987)
Genomics
, vol.1
, pp. 43-51
-
-
Waye, J.S.1
Durfy, S.J.2
Pinkel, D.3
Kenwrick, S.4
Patterson, M.5
Davies, K.E.6
Willard, H.F.7
-
40
-
-
0033547330
-
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
-
Xu G, Bestor TH, Bourc'his D, Hsieh C, Tommerup N, Hulten M, Qu S, Russo JJ, Viegas-Péquignot E: Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. Nature 401:187-191 (1999).
-
(1999)
Nature
, vol.401
, pp. 187-191
-
-
Xu, G.1
Bestor, T.H.2
Bourc'his, D.3
Hsieh, C.4
Tommerup, N.5
Hulten, M.6
Qu, S.7
Russo, J.J.8
Viegas-Péquignot, E.9
-
41
-
-
0030968564
-
Barriers to recombination between closely related bacteria: Muts and RecBCD inhibit recombination between Salmonella typhimurium and Salmonella typhi
-
USA
-
Zahrt TC, Maloy S: Barriers to recombination between closely related bacteria: MutS and RecBCD inhibit recombination between Salmonella typhimurium and Salmonella typhi. Proc natl Acad Sci, USA 94:9786-9791 (1997).
-
(1997)
Proc Natl Acad Sci
, vol.94
, pp. 9786-9791
-
-
Zahrt, T.C.1
Maloy, S.2
|