-
1
-
-
0030846298
-
Tying it all together: Epigenetics, genetics, cell cycle, and cancer
-
Baylin SB (1997): Tying it all together: Epigenetics, genetics, cell cycle, and cancer. Science 277:1948-1949.
-
(1997)
Science
, vol.277
, pp. 1948-1949
-
-
Baylin, S.B.1
-
2
-
-
0000077851
-
Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly
-
Beckwith J (1969): Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly. Birth Defects: Original Articles Series 5:188-196.
-
(1969)
Birth Defects: Original Articles Series
, vol.5
, pp. 188-196
-
-
Beckwith, J.1
-
3
-
-
0019005172
-
Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling
-
Berry AC, Belton EM, Chantler C (1980): Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling. J Med Genet 17:136-8.
-
(1980)
J Med Genet
, vol.17
, pp. 136-138
-
-
Berry, A.C.1
Belton, E.M.2
Chantler, C.3
-
4
-
-
10144256266
-
Skewed X-inactivation in sporadic Beckwith-Wiedemann patients
-
Philadelphia, PA
-
Bird L, Naumova A, Feinberg A, Grundy P, Henry I, Junien C, Newsham I, Weksberg R, Sapienza C (1995): Skewed X-inactivation in sporadic Beckwith-Wiedemann patients. International Conference on Molecular and Clinical Genetics of Childhood Renal Tumors, Philadelphia, PA.
-
(1995)
International Conference on Molecular and Clinical Genetics of Childhood Renal Tumors
-
-
Bird, L.1
Naumova, A.2
Feinberg, A.3
Grundy, P.4
Henry, I.5
Junien, C.6
Newsham, I.7
Weksberg, R.8
Sapienza, C.9
-
5
-
-
0029806141
-
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
-
Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W (1996): Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway. Hum Mol Genet 5:2027-2032.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 2027-2032
-
-
Brown, K.W.1
Villar, A.J.2
Bickmore, W.3
Clayton-Smith, J.4
Catchpoole, D.5
Maher, E.R.6
Reik, W.7
-
6
-
-
0028939902
-
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
-
Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls R, Horsthemke B (1995): Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet 9:395-400.
-
(1995)
Nat Genet
, vol.9
, pp. 395-400
-
-
Buiting, K.1
Saitoh, S.2
Gross, S.3
Dittrich, B.4
Schwartz, S.5
Nicholls, R.6
Horsthemke, B.7
-
8
-
-
0026685962
-
Loss of heterozygosity mapping in Wilms' tumor indicates the involvement of three distinct regions and a limited role for non-dysjunction or mitotic recombination
-
Coppes MJ, Bonetta L, Huang A, Hoban P, Chilton-MacNeill S, Campbell CE, Weksberg R, Yeger H, Reeve AE, Williams BR (1992): Loss of heterozygosity mapping in Wilms' tumor indicates the involvement of three distinct regions and a limited role for non-dysjunction or mitotic recombination. Genes Chromosomes Cancer 5:326-334.
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 326-334
-
-
Coppes, M.J.1
Bonetta, L.2
Huang, A.3
Hoban, P.4
Chilton-MacNeill, S.5
Campbell, C.E.6
Weksberg, R.7
Yeger, H.8
Reeve, A.E.9
Williams, B.R.10
-
9
-
-
0025320906
-
A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting
-
DeChiara TM, Efstratiadis A, Robertson EJ (1990): A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature 345:78-80.
-
(1990)
Nature
, vol.345
, pp. 78-80
-
-
DeChiara, T.M.1
Efstratiadis, A.2
Robertson, E.J.3
-
10
-
-
10144234124
-
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
-
Dittrich B, Buiting K, Korn B, Rickard S, Buxton J, Saitoh S, Nicholls RD, Poustka A, Winterpacht A, Zabel B, Horsthemke B (1996): Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene [see comments]. Nat Genet 14:163-170.
-
(1996)
Nat Genet
, vol.14
, pp. 163-170
-
-
Dittrich, B.1
Buiting, K.2
Korn, B.3
Rickard, S.4
Buxton, J.5
Saitoh, S.6
Nicholls, R.D.7
Poustka, A.8
Winterpacht, A.9
Zabel, B.10
Horsthemke, B.11
-
11
-
-
0030053512
-
High incidence of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas: Uncoupling of H19 and IGF2 expression and biallelic hypomethylation of H19
-
Douc-Rasy S, Barrois M, Fogel S, Ahomadegbe JC, Stehelin D, Coll J, Riou G (1996): High incidence of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas: Uncoupling of H19 and IGF2 expression and biallelic hypomethylation of H19. Oncogene 12:423-430.
-
(1996)
Oncogene
, vol.12
, pp. 423-430
-
-
Douc-Rasy, S.1
Barrois, M.2
Fogel, S.3
Ahomadegbe, J.C.4
Stehelin, D.5
Coll, J.6
Riou, G.7
-
12
-
-
0030660180
-
Mouse mutant embryos overexpressing IF-11 exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes
-
Eggenschwiler J, Ludwig T, Fisher P, Leighton PA, Tilghman SM, Efstratiadis A (1997): Mouse mutant embryos overexpressing IF-11 exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes. Genes Dev 11:3128-3142.
-
(1997)
Genes Dev
, vol.11
, pp. 3128-3142
-
-
Eggenschwiler, J.1
Ludwig, T.2
Fisher, P.3
Leighton, P.A.4
Tilghman, S.M.5
Efstratiadis, A.6
-
13
-
-
0028006662
-
Parental imprinting and the IGF2 gene
-
Ekstrom TJ (1994): Parental imprinting and the IGF2 gene. Horm Res 42:176-181.
-
(1994)
Horm Res
, vol.42
, pp. 176-181
-
-
Ekstrom, T.J.1
-
14
-
-
0031014601
-
A 5′ differentially methylated sequence and the 3' flanking region are necessary for H19 transgene imprinting
-
Elson DA, Bartolomei MS (1997): A 5′ differentially methylated sequence and the 3' flanking region are necessary for H19 transgene imprinting. Mol Cell Biol 17:309-317.
-
(1997)
Mol Cell Biol
, vol.17
, pp. 309-317
-
-
Elson, D.A.1
Bartolomei, M.S.2
-
15
-
-
0027442239
-
Tumor-suppressor activity of H19 RNA
-
Hao Y, Crenshaw T, Moulton T, Newcomb E, Tycko B (1993): Tumor-suppressor activity of H19 RNA. Nature 365:764-767.
-
(1993)
Nature
, vol.365
, pp. 764-767
-
-
Hao, Y.1
Crenshaw, T.2
Moulton, T.3
Newcomb, E.4
Tycko, B.5
-
16
-
-
0029248581
-
Loss of imprinting in choriocarcinoma
-
Hashimoto K, Azuma C, Koyama M, Ohashi K, Kamiura S, Nobunaga T, Kimura T, Tokugawa Y, Kanai T, Saji F (1995): Loss of imprinting in choriocarcinoma [letter]. Nat Genet 9:109-110.
-
(1995)
Nat Genet
, vol.9
, pp. 109-110
-
-
Hashimoto, K.1
Azuma, C.2
Koyama, M.3
Ohashi, K.4
Kamiura, S.5
Nobunaga, T.6
Kimura, T.7
Tokugawa, Y.8
Kanai, T.9
Saji, F.10
-
17
-
-
16044364516
-
KIP2 is mutated in Beckwith-Wiedemann syndrome
-
KIP2 is mutated in Beckwith-Wiedemann syndrome [see comments], Nat Genet 14:171-173.
-
(1996)
Nat Genet
, vol.14
, pp. 171-173
-
-
Hatada, I.1
Ohashi, H.2
Fukushima, Y.3
Kaneko, Y.4
Inoue, M.5
Komoto, Y.6
Okada, A.7
Ohishi, S.8
Nabetani, A.9
Morisaki, H.10
Nakayama, M.11
Niikawa, N.12
Mukai, T.13
-
18
-
-
0031284743
-
KIP2 mutations in Wiedemann-Beckwith syndrome
-
KIP2 mutations in Wiedemann-Beckwith syndrome. Hum Genet 100:681-683.
-
(1997)
Hum Genet
, vol.100
, pp. 681-683
-
-
Hatada, I.1
Nabetani, A.2
Morisaki, H.3
Xin, Z.4
Ohishi, S.5
Tonoki, H.6
Niikawa, N.7
Inoue, M.8
Komoto, Y.9
Okada, A.10
Steichen, E.11
Ohashi, H.12
Fukushima, Y.13
Nakayama, M.14
Mukai, T.15
-
19
-
-
0024232789
-
Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome
-
Henry I, Jeanpierre M, Barichard F, Serre JL, Mallet J, Turleau C, de Grouchy J, Junien C (1988): Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome. Ann Genet 31:216-220.
-
(1988)
Ann Genet
, vol.31
, pp. 216-220
-
-
Henry, I.1
Jeanpierre, M.2
Barichard, F.3
Serre, J.L.4
Mallet, J.5
Turleau, C.6
De Grouchy, J.7
Junien, C.8
-
20
-
-
0025738681
-
Uniparental paternal disomy in a genetic cancer-predisposion syndrome
-
Henry I, Bonaiti-Pellie C, Chehensse V, Beldjord C, Schwartz C, Utermann G, Junien C (1991): Uniparental paternal disomy in a genetic cancer-predisposion syndrome. Nature 351:665-667.
-
(1991)
Nature
, vol.351
, pp. 665-667
-
-
Henry, I.1
Bonaiti-Pellie, C.2
Chehensse, V.3
Beldjord, C.4
Schwartz, C.5
Utermann, G.6
Junien, C.7
-
21
-
-
0031001346
-
Xist has properties of the X-chromosome inactivation centre
-
Herzing L, Romer J, Horn J, Ashworth A (1997): Xist has properties of the X-chromosome inactivation centre. Nat Genet 386:272-275.
-
(1997)
Nat Genet
, vol.386
, pp. 272-275
-
-
Herzing, L.1
Romer, J.2
Horn, J.3
Ashworth, A.4
-
22
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
Hoovers JMN, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, Ivens A, Westerveld A, Little P, Mannens M, Feinberg AP (1995): Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc Natl Acad Sci USA 92:12456-12460.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 12456-12460
-
-
Hoovers, J.M.N.1
Kalikin, L.M.2
Johnson, L.A.3
Alders, M.4
Redeker, B.5
Law, D.J.6
Bliek, J.7
Steenman, M.8
Benedict, M.9
Wiegant, J.10
Lengauer, C.11
Taillon-Miller, P.12
Schlessinger, D.13
Edwards, M.C.14
Elledge, S.J.15
Ivens, A.16
Westerveld, A.17
Little, P.18
Mannens, M.19
Feinberg, A.P.20
more..
-
23
-
-
0015295131
-
Mutation and cancer: A model for Wilms' tumor of the kidney
-
Knudson AG, Strong LC (1972): Mutation and cancer: A model for Wilms' tumor of the kidney. J Natl Cancer Inst 48:313-324.
-
(1972)
J Natl Cancer Inst
, vol.48
, pp. 313-324
-
-
Knudson, A.G.1
Strong, L.C.2
-
24
-
-
0024517062
-
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5
-
Koufos A, Grundy P, Morgan K, Aleck KA, Hadro T, Lampkin BC, Kalbakji A, Cavenee WK (1989): Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Am J Hum Genet 44:711-719.
-
(1989)
Am J Hum Genet
, vol.44
, pp. 711-719
-
-
Koufos, A.1
Grundy, P.2
Morgan, K.3
Aleck, K.A.4
Hadro, T.5
Lampkin, B.C.6
Kalbakji, A.7
Cavenee, W.K.8
-
25
-
-
0028575985
-
Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality
-
Lau MM, Stewart CE, Liu Z, Bhatt H, Rotwein P, Stewart CL (1994): Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality. Genes Dev 8: 2953-2963.
-
(1994)
Genes Dev
, vol.8
, pp. 2953-2963
-
-
Lau, M.M.1
Stewart, C.E.2
Liu, Z.3
Bhatt, H.4
Rotwein, P.5
Stewart, C.L.6
-
26
-
-
0030895047
-
Long-range cis effects of ectopic X-inactivation centres on a mouse autosome
-
Lee J, Jaenisch R (1997): Long-range cis effects of ectopic X-inactivation centres on a mouse autosome. Nat Genet 386:275-279.
-
(1997)
Nat Genet
, vol.386
, pp. 275-279
-
-
Lee, J.1
Jaenisch, R.2
-
28
-
-
0031046285
-
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
-
Lee MP, Hu RJ, Johnson LA, Feinberg AP (1997b): Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nat Genet 15: 181-185.
-
(1997)
Nat Genet
, vol.15
, pp. 181-185
-
-
Lee, M.P.1
Hu, R.J.2
Johnson, L.A.3
Feinberg, A.P.4
-
29
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton PA, Ingram RS, Eggenschwiler J, Efstratiadis A, Tilghman SM (1995a): Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature 375:34-39.
-
(1995)
Nature
, vol.375
, pp. 34-39
-
-
Leighton, P.A.1
Ingram, R.S.2
Eggenschwiler, J.3
Efstratiadis, A.4
Tilghman, S.M.5
-
30
-
-
0029165883
-
An enhancer deletion affects both 1119 and IGF2 expression
-
Leighton PA, Saam JR, Ingram RS, Stewart CL, Tilghman SM (1995b): An enhancer deletion affects both 1119 and IGF2 expression. Genes Dev 9:2079-2089.
-
(1995)
Genes Dev
, vol.9
, pp. 2079-2089
-
-
Leighton, P.A.1
Saam, J.R.2
Ingram, R.S.3
Stewart, C.L.4
Tilghman, S.M.5
-
31
-
-
0030029694
-
Two pairs of male monozygotic twins discordant for Wiedemann-Beckwith syndrome
-
Leonard NJ, Bernier FP, Rudd N, Machin GA, Bamforth F, Bamforth S, Grundy P, Johnson C (1996): Two pairs of male monozygotic twins discordant for Wiedemann-Beckwith syndrome. Am J Med Genet 61: 253-257.
-
(1996)
Am J Med Genet
, vol.61
, pp. 253-257
-
-
Leonard, N.J.1
Bernier, F.P.2
Rudd, N.3
Machin, G.A.4
Bamforth, F.5
Bamforth, S.6
Grundy, P.7
Johnson, C.8
-
32
-
-
0029122489
-
Expression, promoter usage and parental imprinting status of insulin-like growth factor II (IGF2) in human hepatoblastoma: Uncoupling of IGF2 and H19 imprinting
-
Li X, Adam G, Cui H, Sandstedt B, Ohlsson R, Ekstrom TJ (1995): Expression, promoter usage and parental imprinting status of insulin-like growth factor II (IGF2) in human hepatoblastoma: Uncoupling of IGF2 and H19 imprinting. Oncogene 11:221-229.
-
(1995)
Oncogene
, vol.11
, pp. 221-229
-
-
Li, X.1
Adam, G.2
Cui, H.3
Sandstedt, B.4
Ohlsson, R.5
Ekstrom, T.J.6
-
33
-
-
0029670454
-
Expression levels of the insulin-like growth factor-II gene (IGF2) in the human liver: Developmental relationships of the four promoters
-
Li X, Cui H, Sandstedt B, Nordlinder H, Larsson E, Ekstrom TJ (1996): Expression levels of the insulin-like growth factor-II gene (IGF2) in the human liver: Developmental relationships of the four promoters. J Endocrinol 149:117-124.
-
(1996)
J Endocrinol
, vol.149
, pp. 117-124
-
-
Li, X.1
Cui, H.2
Sandstedt, B.3
Nordlinder, H.4
Larsson, E.5
Ekstrom, T.J.6
-
34
-
-
15144361057
-
Disrupted IGF2 promoter control by silencing of promoter P1 in human hepatocellular carcinoma
-
Li X, Nong Z, Ekstrom C, Larsson E, Nordlinder H, Hofmann WJ, Trautwein C, Odenthal M, Dienes HP, Ekstrom TJ, Schirmacher P (1997): Disrupted IGF2 promoter control by silencing of promoter P1 in human hepatocellular carcinoma. Cancer Res 57:2048-2054.
-
(1997)
Cancer Res
, vol.57
, pp. 2048-2054
-
-
Li, X.1
Nong, Z.2
Ekstrom, C.3
Larsson, E.4
Nordlinder, H.5
Hofmann, W.J.6
Trautwein, C.7
Odenthal, M.8
Dienes, H.P.9
Ekstrom, T.J.10
Schirmacher, P.11
-
35
-
-
0023748884
-
Absence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome
-
Litz CE, Taylor KA, Qiu JS, Pescovitz OH, de Martinville B (1988): Absence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome. Am J Med Genet 30:821-833.
-
(1988)
Am J Med Genet
, vol.30
, pp. 821-833
-
-
Litz, C.E.1
Taylor, K.A.2
Qiu, J.S.3
Pescovitz, O.H.4
De Martinville, B.5
-
36
-
-
0030950759
-
An imprinting element from the mouse H19 locus functions as a silencer in Drosophila
-
Lyko F, Brenton JD, Surani MA, Paro R (1997): An imprinting element from the mouse H19 locus functions as a silencer in Drosophila. Nat Genet 16:171-173.
-
(1997)
Nat Genet
, vol.16
, pp. 171-173
-
-
Lyko, F.1
Brenton, J.D.2
Surani, M.A.3
Paro, R.4
-
37
-
-
0024212964
-
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumors
-
Mannens M (1988): Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumors. Hum Genet 81:41-48.
-
(1988)
Hum Genet
, vol.81
, pp. 41-48
-
-
Mannens, M.1
-
38
-
-
0028988159
-
KIP2, a structurally distinct member of the p21cip1 Cdk inhibitor family, is a candidate tumor suppressor gene
-
KIP2, a structurally distinct member of the p21cip1 Cdk inhibitor family, is a candidate tumor suppressor gene. Genes Dev 9:650-662.
-
(1995)
Genes Dev
, vol.9
, pp. 650-662
-
-
Matsuoka, S.1
Edwards, M.C.2
Bai, C.3
Parker, S.4
Zhang, P.5
Baldini, A.6
Harper, J.W.7
Elledge, S.J.8
-
39
-
-
0029939816
-
Somatic overgrowth associated with overexpression of insulin-like growth factor II
-
Morison IM, Becroft DM, Taniguchi T, Woods CG, Reeve AE (1996): Somatic overgrowth associated with overexpression of insulin-like growth factor II. Nat Med 2:311-316.
-
(1996)
Nat Med
, vol.2
, pp. 311-316
-
-
Morison, I.M.1
Becroft, D.M.2
Taniguchi, T.3
Woods, C.G.4
Reeve, A.E.5
-
40
-
-
0026559276
-
Beckwith-Wiedemann syndrome: A demonstration of the mechanisms responsible for the excess of transmitting females
-
Moutou C, Junien C, Henry I, Bonaïti-Pellié C (1992): Beckwith-Wiedemann syndrome: A demonstration of the mechanisms responsible for the excess of transmitting females [see comments]. J Med Genet 29:217-220.
-
(1992)
J Med Genet
, vol.29
, pp. 217-220
-
-
Moutou, C.1
Junien, C.2
Henry, I.3
Bonaïti-Pellié, C.4
-
41
-
-
0029742296
-
Genomic imprinting: Significance in development and diseases and the molecular mechanisms
-
Nakao M, Sasaki H (1996): Genomic imprinting: Significance in development and diseases and the molecular mechanisms. J Biochem 120:467-473.
-
(1996)
J Biochem
, vol.120
, pp. 467-473
-
-
Nakao, M.1
Sasaki, H.2
-
42
-
-
0031054075
-
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
-
Neyroud N, Tesson F, Denjoy I, Leibovici M, Donger C, Barhanin J, Faure S, Gary F, Coumel P, Petit C, Schwartz K, Guicheney P (1997): A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome [see comments]. Nat Genet 15:186-189.
-
(1997)
Nat Genet
, vol.15
, pp. 186-189
-
-
Neyroud, N.1
Tesson, F.2
Denjoy, I.3
Leibovici, M.4
Donger, C.5
Barhanin, J.6
Faure, S.7
Gary, F.8
Coumel, P.9
Petit, C.10
Schwartz, K.11
Guicheney, P.12
-
43
-
-
0028209550
-
New insights reveal complex mechanisms involved in genomic imprinting
-
Nicholls RD (1994): New insights reveal complex mechanisms involved in genomic imprinting [editorial; comment]. Am J Hum Genet 54:733-740.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 733-740
-
-
Nicholls, R.D.1
-
44
-
-
0026773169
-
Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11
-
Nystrom A, Cheetham JE, Engstrom W, Schofield PN (1992): Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11. Eur J Pediatr 151:511-514.
-
(1992)
Eur J Pediatr
, vol.151
, pp. 511-514
-
-
Nystrom, A.1
Cheetham, J.E.2
Engstrom, W.3
Schofield, P.N.4
-
45
-
-
0027422302
-
Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumor and gigantism
-
Ogawa O, Becroft DM, Morison IM, Eccles MR, Skeen JE, Mauger DC, Reeve AE (1993): Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumor and gigantism. Nat Genet 5:408-412.
-
(1993)
Nat Genet
, vol.5
, pp. 408-412
-
-
Ogawa, O.1
Becroft, D.M.2
Morison, I.M.3
Eccles, M.R.4
Skeen, J.E.5
Mauger, D.C.6
Reeve, A.E.7
-
46
-
-
0028089079
-
Overlapping patterns of IGF2 and H19 expression during human development: Biallelic IGF2 expression correlates with a lack of H19 expression
-
Ohlsson R, Hedborg F, Holmgren L, Walsh C, Ekstrom TJ (1994): Overlapping patterns of IGF2 and H19 expression during human development: Biallelic IGF2 expression correlates with a lack of H19 expression. Development 120:361-368.
-
(1994)
Development
, vol.120
, pp. 361-368
-
-
Ohlsson, R.1
Hedborg, F.2
Holmgren, L.3
Walsh, C.4
Ekstrom, T.J.5
-
47
-
-
0023011534
-
An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13-pter: Correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome
-
Okano YOY, Yamamoto H, Hase Y, Tsuruhara T, Fujita H (1986): An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13-pter: Correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome. Jpn J Hum Genet 31:365-372.
-
(1986)
Jpn J Hum Genet
, vol.31
, pp. 365-372
-
-
Okano, Y.O.Y.1
Yamamoto, H.2
Hase, Y.3
Tsuruhara, T.4
Fujita, H.5
-
48
-
-
0030610260
-
KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors
-
KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors. Am J Hum Genet 61:295-303.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 295-303
-
-
O'Keefe, D.1
Dao, D.2
Zhao, L.3
Sanderson, R.4
Warburton, D.5
Weiss, L.6
Anyane-Yeboa, K.7
Tycko, B.8
-
49
-
-
0023891637
-
Wiedemann-Beckwith syndrome in apparently discordant monozygotic twins
-
Olney AH, Buehler BA, Waziri M (1988): Wiedemann-Beckwith syndrome in apparently discordant monozygotic twins. Am J Med Genet 29:491-499.
-
(1988)
Am J Med Genet
, vol.29
, pp. 491-499
-
-
Olney, A.H.1
Buehler, B.A.2
Waziri, M.3
-
50
-
-
0028964550
-
Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome
-
Orstavik RE, Tommerup N, Eiklid K, Orstavik KH (1995): Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome. Am J Med Genet 56: 210-214.
-
(1995)
Am J Med Genet
, vol.56
, pp. 210-214
-
-
Orstavik, R.E.1
Tommerup, N.2
Eiklid, K.3
Orstavik, K.H.4
-
51
-
-
0022910322
-
Wiedemann-Beckwith syndrome: Presentation of clinical and cytogenetic data on 22 new cases and review of the literature
-
Pettenati MJ, Haines JL, Higgins RR, Wappner RS, Palmer CG, Weaver DD (1986): Wiedemann-Beckwith syndrome: Presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Hum Genet 74:143-154.
-
(1986)
Hum Genet
, vol.74
, pp. 143-154
-
-
Pettenati, M.J.1
Haines, J.L.2
Higgins, R.R.3
Wappner, R.S.4
Palmer, C.G.5
Weaver, D.D.6
-
52
-
-
13344261391
-
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
-
Pilia G, Hughes-Benzie RM, MacKenzie A, Baybayan P, Chen EY, Huber R, Neri G, Cao A, Forabosco A, Schlessinger D (1996): Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome [see comments]. Nat Genet 12:241-247.
-
(1996)
Nat Genet
, vol.12
, pp. 241-247
-
-
Pilia, G.1
Hughes-Benzie, R.M.2
MacKenzie, A.3
Baybayan, P.4
Chen, E.Y.5
Huber, R.6
Neri, G.7
Cao, A.8
Forabosco, A.9
Schlessinger, D.10
-
53
-
-
0024518392
-
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15
-
Ping AJ, Reeve AE, Law DJ, Young MR, Boehnke M, Feinberg AP (1989): Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am J Hum Genet 44:720-723.
-
(1989)
Am J Hum Genet
, vol.44
, pp. 720-723
-
-
Ping, A.J.1
Reeve, A.E.2
Law, D.J.3
Young, M.R.4
Boehnke, M.5
Feinberg, A.P.6
-
55
-
-
0030856668
-
Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome
-
Reik W, Maher ER (1997): Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome. Trends Genet 13:330-334.
-
(1997)
Trends Genet
, vol.13
, pp. 330-334
-
-
Reik, W.1
Maher, E.R.2
-
56
-
-
0001811034
-
General principles of the epidemiology of childhood cancer
-
Pizzo PA, Poplack D (eds): Philadelphia: Lippincott-Raven Publishers
-
Robison L (1997): General principles of the epidemiology of childhood cancer. In Pizzo PA, Poplack D (eds): "Principles and Practice of Pediatric Oncology." Philadelphia: Lippincott-Raven Publishers, pp 1-10.
-
(1997)
Principles and Practice of Pediatric Oncology
, pp. 1-10
-
-
Robison, L.1
-
57
-
-
0030823992
-
Paternally inherited duplications of Ilpl5.5 and Beckwith-Wiedemann syndrome
-
Slavotinek A, Gaunt L, Donnai D (1997): Paternally inherited duplications of Ilpl5.5 and Beckwith-Wiedemann syndrome. J Med Genet 34:819-826.
-
(1997)
J Med Genet
, vol.34
, pp. 819-826
-
-
Slavotinek, A.1
Gaunt, L.2
Donnai, D.3
-
58
-
-
0030960876
-
OCI-5/rat glypican-3 binds to fibroblast growth factor-2 but not to insulin-like growth factor-2
-
Song HH, Shi W, Filmus J (1996): OCI-5/rat glypican-3 binds to fibroblast growth factor-2 but not to insulin-like growth factor-2. J Biol Chem 272:7574-7577.
-
(1996)
J Biol Chem
, vol.272
, pp. 7574-7577
-
-
Song, H.H.1
Shi, W.2
Filmus, J.3
-
59
-
-
0029985838
-
Genomic imprinting in tumors
-
Squire J, Shear D (eds): "Gene Rearrangements and Cancer," New York: Academic Press
-
Squire J, Weksberg R (1995): Genomic imprinting in tumors. In Squire J, Shear D (eds): "Gene Rearrangements and Cancer," Vol. 7. Seminars in Cancer Biology. New York: Academic Press, pp 41-47.
-
(1995)
Seminars in Cancer Biology
, vol.7
, pp. 41-47
-
-
Squire, J.1
Weksberg, R.2
-
60
-
-
0030735169
-
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome
-
Sun FI, Dean WL, Kelsey G, Allen NA, Reik W (1997): Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. Nature 389:809-815.
-
(1997)
Nature
, vol.389
, pp. 809-815
-
-
Sun, F.I.1
Dean, W.L.2
Kelsey, G.3
Allen, N.A.4
Reik, W.5
-
61
-
-
0029092413
-
Altered specificity of IGF2 promoter imprinting during fetal development and onset of Wilms tumor
-
Taniguchi T, Schofield AE, Scarlett JL, Morison IM, Sullivan MJ, Reeve AE (1995a): Altered specificity of IGF2 promoter imprinting during fetal development and onset of Wilms tumor. Oncogene 11:751-756.
-
(1995)
Oncogene
, vol.11
, pp. 751-756
-
-
Taniguchi, T.1
Schofield, A.E.2
Scarlett, J.L.3
Morison, I.M.4
Sullivan, M.J.5
Reeve, A.E.6
-
62
-
-
0028935017
-
Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor
-
Taniguchi T, Sullivan MJ, Ogawa O, Reeve AE (1995b): Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor. Proc Natl Acad Sci USA 92:2159-2163.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 2159-2163
-
-
Taniguchi, T.1
Sullivan, M.J.2
Ogawa, O.3
Reeve, A.E.4
-
64
-
-
0030989158
-
Altered transcriptional regulation of the insulin-like growth factor 2 gene in human hepatocellular carcinoma
-
Uchida K, Kondo M, Takeda S, Osada H, Takahashi T, Nakao A, Takahashi T (1997): Altered transcriptional regulation of the insulin-like growth factor 2 gene in human hepatocellular carcinoma. Mol Carcinog 18:193-198.
-
(1997)
Mol Carcinog
, vol.18
, pp. 193-198
-
-
Uchida, K.1
Kondo, M.2
Takeda, S.3
Osada, H.4
Takahashi, T.5
Nakao, A.6
Takahashi, T.7
-
65
-
-
0029931018
-
Alterations in the promoter-specific imprinting of the insulin-like growth factor-II gene in Wilms' tumor
-
Vu TH, Hoffman A (1996): Alterations in the promoter-specific imprinting of the insulin-like growth factor-II gene in Wilms' tumor. J Biol Chem 271:9014-9023.
-
(1996)
J Biol Chem
, vol.271
, pp. 9014-9023
-
-
Vu, T.H.1
Hoffman, A.2
-
66
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT (1996): Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 12:17-23.
-
(1996)
Nat Genet
, vol.12
, pp. 17-23
-
-
Wang, Q.1
Curran, M.E.2
Splawski, I.3
Burn, T.C.4
Millholland, J.M.5
VanRaay, T.J.6
Shen, J.7
Timothy, K.W.8
Vincent, G.M.9
De Jager, T.10
Schwartz, P.J.11
Toubin, J.A.12
Moss, A.J.13
Atkinson, D.L.14
Landes, G.M.15
Connors, T.D.16
Keating, M.T.17
-
67
-
-
0025633055
-
Molecular characterization of Beckwith-Wiedemann syndrome (WBS) patients with partial duplication of chromosome lip excludes the gene MYOD1 from the WBS region
-
Weksberg R, Glaves M, Teshima I, Waziri M, Patil S, Williams BR (1990): Molecular characterization of Beckwith-Wiedemann syndrome (WBS) patients with partial duplication of chromosome lip excludes the gene MYOD1 from the WBS region. Genomics 8:693-698.
-
(1990)
Genomics
, vol.8
, pp. 693-698
-
-
Weksberg, R.1
Glaves, M.2
Teshima, I.3
Waziri, M.4
Patil, S.5
Williams, B.R.6
-
68
-
-
0027420362
-
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
-
Weksberg R, Shen DR, Fei YL, Song QL, Squire J (1993a): Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nat Genet 5:143-150.
-
(1993)
Nat Genet
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei, Y.L.3
Song, Q.L.4
Squire, J.5
-
69
-
-
0027289089
-
Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (WBS) phenotype refines the localization and suggests the gene for WBS is imprinted
-
Weksberg R, Teshima I, Williams BR, Greenberg CR, Pueschel SM, Chernos JE, Fowlow SB, Hoyme E, Anderson IJ, Whiteman DA (1993b): Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (WBS) phenotype refines the localization and suggests the gene for WBS is imprinted. Hum Mol Genet 2:549-556.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 549-556
-
-
Weksberg, R.1
Teshima, I.2
Williams, B.R.3
Greenberg, C.R.4
Pueschel, S.M.5
Chernos, J.E.6
Fowlow, S.B.7
Hoyme, E.8
Anderson, I.J.9
Whiteman, D.A.10
-
70
-
-
0029848437
-
Molecular biology of Beckwith-Wiedemann syndrome
-
Weksberg R, Squire JA (1996): Molecular biology of Beckwith-Wiedemann syndrome. Med Pediatr Oncol 27:462-469.
-
(1996)
Med Pediatr Oncol
, vol.27
, pp. 462-469
-
-
Weksberg, R.1
Squire, J.A.2
-
71
-
-
76549164702
-
Complexe malformatif familial avec hernie ombilicale et macroglossie: Un syndrome nouveau?
-
Wiedemann HR (1964): Complexe malformatif familial avec hernie ombilicale et macroglossie: Un syndrome nouveau? J Génét Hum 13:223-232.
-
(1964)
J Génét Hum
, vol.13
, pp. 223-232
-
-
Wiedemann, H.R.1
-
72
-
-
34250134720
-
Tumors and hemihypertrophy associated with the Wiedemann-Beckwith syndrome
-
Wiedemann HR (1983): Tumors and hemihypertrophy associated with the Wiedemann-Beckwith syndrome. Eur J Pediatr 141:129.
-
(1983)
Eur J Pediatr
, vol.141
, pp. 129
-
-
Wiedemann, H.R.1
-
74
-
-
0028229910
-
Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma
-
Zhan S, Shapiro DN, Helman LJ (1994): Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma. J Clin Invest 94:445-448.
-
(1994)
J Clin Invest
, vol.94
, pp. 445-448
-
-
Zhan, S.1
Shapiro, D.N.2
Helman, L.J.3
-
75
-
-
0029588595
-
Loss of imprinting of IGF2 in Ewing's sarcoma
-
Zhan S, Shapiro DN, Helman LJ (1995): Loss of imprinting of IGF2 in Ewing's sarcoma. Oncogene 11:2503-2507.
-
(1995)
Oncogene
, vol.11
, pp. 2503-2507
-
-
Zhan, S.1
Shapiro, D.N.2
Helman, L.J.3
-
76
-
-
1842335753
-
KIP2 indicates a role in Beckwith-Wiedemann syndrome
-
KIP2 indicates a role in Beckwith-Wiedemann syndrome. Nature 387:151-158.
-
(1997)
Nature
, vol.387
, pp. 151-158
-
-
Zhang, P.1
Liegeois, N.J.2
Wong, C.3
Finegold, M.4
Hou, H.5
Thompson, J.C.6
Silverman, A.7
Harper, J.W.8
DePinho, R.A.9
Elledge, S.J.10
|