-
1
-
-
0019410039
-
Wiedemann-Beckwith syndrome: Autosomal dominant inheritance in a family
-
Best LG, Hoekstra RE (1981) Wiedemann-Beckwith syndrome: autosomal dominant inheritance in a family. Am J Hum Genet 9:291-299
-
(1981)
Am J Hum Genet
, vol.9
, pp. 291-299
-
-
Best, L.G.1
Hoekstra, R.E.2
-
2
-
-
0027365762
-
Nuclear localization signals (NLS)
-
Boulikas T (1993) Nuclear localization signals (NLS). Crit Revs Eukaryot Gene Expr 3:193-227
-
(1993)
Crit Revs Eukaryot Gene Expr
, vol.3
, pp. 193-227
-
-
Boulikas, T.1
-
3
-
-
0031844688
-
Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster
-
Caspary T, Cleary MA, Baker CC, Guan X-J, Tilghman SM (1998) Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. Mol Cell Biol 18:3466-3474
-
(1998)
Mol Cell Biol
, vol.18
, pp. 3466-3474
-
-
Caspary, T.1
Cleary, M.A.2
Baker, C.C.3
Guan, X.-J.4
Tilghman, S.M.5
-
4
-
-
0027496935
-
The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases
-
Harper JW, Adami GR, Wei N, Keyomarsi K, Elledge SJ (1993) The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases. Cell 75:805-816
-
(1993)
Cell
, vol.75
, pp. 805-816
-
-
Harper, J.W.1
Adami, G.R.2
Wei, N.3
Keyomarsi, K.4
Elledge, S.J.5
-
6
-
-
0028980026
-
KIP2, a cyclin dependent kinase inhibitor, in mouse
-
KIP2, a cyclin dependent kinase inhibitor, in mouse. Nat Genet 11:204-206
-
(1995)
Nat Genet
, vol.11
, pp. 204-206
-
-
Hatada, I.1
Mukai, T.2
-
9
-
-
0031284743
-
KIP2 mutations in Beckwith-Wiedemann syndrome
-
KIP2 mutations in Beckwith-Wiedemann 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
-
10
-
-
0025738681
-
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
-
Henri I, Bonaiti-Pellie C, Chehensse V, Beldjord C, Schwartz C, Utermann G, Junien C (1991) Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature 351:665-667
-
(1991)
Nature
, vol.351
, pp. 665-667
-
-
Henri, I.1
Bonaiti-Pellie, C.2
Chehensse, V.3
Beldjord, C.4
Schwartz, C.5
Utermann, G.6
Junien, C.7
-
11
-
-
0030934283
-
Induction of the cyclin-dependent kinase inhibitor p21Sdi1/Cip1/Waf1 by nitric oxide-generating vasodilator in vascular smooth muscle cells
-
Ishida A, Sasaguri T, Kosaka C, Nojima H, Ogata J (1997) Induction of the cyclin-dependent kinase inhibitor p21Sdi1/Cip1/Waf1 by nitric oxide-generating vasodilator in vascular smooth muscle cells . J Biol Chem 272:10051-10057
-
(1997)
J Biol Chem
, vol.272
, pp. 10051-10057
-
-
Ishida, A.1
Sasaguri, T.2
Kosaka, C.3
Nojima, H.4
Ogata, J.5
-
12
-
-
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
-
13
-
-
0014949207
-
Cleavage of structural proteins during the assembly of the head of bacteriophage T4
-
Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 277:680-685
-
(1970)
Nature
, vol.277
, pp. 680-685
-
-
Laemmli, U.K.1
-
14
-
-
0028988158
-
KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution
-
KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution. Genes Dev 9:639-649
-
(1995)
Genes Dev
, vol.9
, pp. 639-649
-
-
Lee, M.H.1
Reynisdottir, I.2
Massague, J.3
-
16
-
-
0028316620
-
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
-
Mannens M, Hoovers JMN, Redeker E, Verjaal M, Feinberg AP, Little P, Boavida M, et al (1994) Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. Eur J Hum Genet 2:3-23
-
(1994)
Eur J Hum Genet
, vol.2
, pp. 3-23
-
-
Mannens, M.1
Hoovers, J.M.N.2
Redeker, E.3
Verjaal, M.4
Feinberg, A.P.5
Little, P.6
Boavida, M.7
-
17
-
-
0028988159
-
CIPI Cdk inhibitor family, is a candidate tumor suppressor gene
-
CIPI 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
-
18
-
-
0026573580
-
A general and fast method to generate multiple site directed mutation
-
Mikaelian I, Sergeant A (1992) A general and fast method to generate multiple site directed mutation. Nucleic Acids Res 20:376
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 376
-
-
Mikaelian, I.1
Sergeant, A.2
-
19
-
-
0026559276
-
Beckwith-Wiedemann syndrome: A demonstration of the mechanisms responsible for the excess of transmitting females
-
Moutou C, Junien C, Henry I, Bonaiti-Pellie C (1992) Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females. J Med Genet 29:217-220
-
(1992)
J Med Genet
, vol.29
, pp. 217-220
-
-
Moutou, C.1
Junien, C.2
Henry, I.3
Bonaiti-Pellie, C.4
-
20
-
-
0022470737
-
The Wiedemann-Beckwith syndrome: Pedigree studies on five families. Evidence for autosomal dominant inheritance with variable expressivity
-
Niikawa N, Ishikiriyama S, Takahashi S, Inagawa A, Tonoki H, Ohta Y, Hase N, Kamei T, Kajii T (1986) The Wiedemann-Beckwith syndrome: pedigree studies on five families. Evidence for autosomal dominant inheritance with variable expressivity. Am J Med Genet 24:41-45
-
(1986)
Am J Med Genet
, vol.24
, pp. 41-45
-
-
Niikawa, N.1
Ishikiriyama, S.2
Takahashi, S.3
Inagawa, A.4
Tonoki, H.5
Ohta, Y.6
Hase, N.7
Kamei, T.8
Kajii, T.9
-
21
-
-
0023011534
-
An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13-pter: Correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome
-
Okano Y (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.1
-
22
-
-
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
-
23
-
-
0024518392
-
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.5
-
Ping AJ, Reeve AE, Law DJ, Young MR, Boehnke M, Feinberg AP (1989) Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.5. 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
-
24
-
-
0028176483
-
KIPI, a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitotic signals
-
KIPI, a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitotic signals. Cell 78:59-66
-
(1994)
Cell
, vol.78
, pp. 59-66
-
-
Polyak, K.1
Lee, M.H.2
Erdjument-Bromage, H.3
Koff, A.4
Roberts, J.M.5
Tempst, P.6
Massague, J.7
-
25
-
-
0344506969
-
Chromosome 11 and Beckwith-Wiedemann syndrome
-
Pueschel SM, Padre-Mendoza T (1984) Chromosome 11 and Beckwith-Wiedemann syndrome. J Pediatr 102:873-876
-
(1984)
J Pediatr
, vol.102
, pp. 873-876
-
-
Pueschel, S.M.1
Padre-Mendoza, T.2
-
26
-
-
0030602833
-
Size control: The regulation of cell numbers in animal development
-
Raff MC (1996) Size control: the regulation of cell numbers in animal development. Cell 86:173-175
-
(1996)
Cell
, vol.86
, pp. 173-175
-
-
Raff, M.C.1
-
27
-
-
0030856668
-
Imprinting in clusters: Lesson from Beckwith-Wiedemann syndrome
-
Reik W, Maher ER (1997) Imprinting in clusters: lesson from Beckwith-Wiedemann syndrome. Trends Genet 134:330-335
-
(1997)
Trends Genet
, vol.134
, pp. 330-335
-
-
Reik, W.1
Maher, E.R.2
-
28
-
-
0026347794
-
V. Report of the committee on chromosome and gene loss in human neoplasia
-
Seizinger B, et al (1991) V. Report of the committee on chromosome and gene loss in human neoplasia. Cytogenet Cell Genet 58:1080-1096
-
(1991)
Cytogenet Cell Genet
, vol.58
, pp. 1080-1096
-
-
Seizinger, B.1
-
29
-
-
0028363519
-
P27, a novel inhibitor of G1 cyclin-Cd1 protein kinase activity, is related to p21
-
Toyoshima H, Hunter T (1994) P27, a novel inhibitor of G1 cyclin-Cd1 protein kinase activity, is related to p21. Cell 78:67-74
-
(1994)
Cell
, vol.78
, pp. 67-74
-
-
Toyoshima, H.1
Hunter, T.2
-
31
-
-
0020511170
-
An abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome
-
Waziri M, Patil SR, Hanson JW, Batrley JA (1983) An abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J Pediatr 102:873-876
-
(1983)
J Pediatr
, vol.102
, pp. 873-876
-
-
Waziri, M.1
Patil, S.R.2
Hanson, J.W.3
Batrley, J.A.4
-
32
-
-
34250134720
-
Tumors and hemihypertrophy associated with Wiedemann-Beckwith syndrome
-
Wiedemann HR (1983) Tumors and hemihypertrophy associated with Wiedemann-Beckwith syndrome. Eur J Pediatr 141:129
-
(1983)
Eur J Pediatr
, vol.141
, pp. 129
-
-
Wiedemann, H.R.1
-
34
-
-
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.Z.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, A.R.9
Elledge, S.J.10
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