-
1
-
-
0030879482
-
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
-
Albrecht, U., Sutcliffe, J. S., Cattanach, B. M., Beechey, C. V., Armstrong, D., Eichele, G., and Beaudet, A. L. (1997). Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nat. Genet. 17, 75-8.
-
(1997)
Nat. Genet.
, vol.17
, pp. 75-78
-
-
Albrecht, U.1
Sutcliffe, J.S.2
Cattanach, B.M.3
Beechey, C.V.4
Armstrong, D.5
Eichele, G.6
Beaudet, A.L.7
-
2
-
-
0028950336
-
Analysis of different inheritance patterns in pre-eclampsia/eclampsia syndrome
-
Arngrimsson, R., Bjornsson, H., and Geirsson, R. T. (1995). Analysis of different inheritance patterns in pre-eclampsia/eclampsia syndrome. Hypertension in Pregnancy 14, 27-38.
-
(1995)
Hypertension in Pregnancy
, vol.14
, pp. 27-38
-
-
Arngrimsson, R.1
Bjornsson, H.2
Geirsson, R.T.3
-
3
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei, M. S., Zemel, S., and Tilghman, S. (1991). Parental imprinting of the mouse H19 gene. Nature 351, 153-5.
-
(1991)
Nature
, vol.351
, pp. 153-155
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.3
-
4
-
-
0027437280
-
Normal phenotype with paternal uniparental isodisomy for chromosome 21
-
Blouin, J-L., Avramopoulos, D., Pangalos, C., and Antonarakis, S. E. (1993). Normal phenotype with paternal uniparental isodisomy for chromosome 21. Am. J. Hum. Genet. 53, 1074-8.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 1074-1078
-
-
Blouin, J.-L.1
Avramopoulos, D.2
Pangalos, C.3
Antonarakis, S.E.4
-
5
-
-
0023180369
-
Pre-eclampsia and trisomy 13: A possible association
-
Boyd, P. A., Lindenbaum, R. H., and Redman, C. (1987). Pre-eclampsia and trisomy 13: a possible association. Lancet 425-7.
-
(1987)
Lancet
, pp. 425-427
-
-
Boyd, P.A.1
Lindenbaum, R.H.2
Redman, C.3
-
6
-
-
0025727201
-
Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome
-
Brockdorff, N., Ashworth, A., Kay, G., Cooper, P., Smith, S., McCabe, V. M., Norris, D. P., Penny, G. D., Patel, D., and Rastan, S. (1991). Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome. Nature 351, 329-31.
-
(1991)
Nature
, vol.351
, pp. 329-331
-
-
Brockdorff, N.1
Ashworth, A.2
Kay, G.3
Cooper, P.4
Smith, S.5
McCabe, V.M.6
Norris, D.P.7
Penny, G.D.8
Patel, D.9
Rastan, S.10
-
7
-
-
0025961771
-
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome
-
Brown, C. J., Ballabio, A., Rupert, J. L., Lafreniere, R. G., Grompe, M., Tonlorenzi, R., and Willard, H. F. (1991). A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome. Nature 349, 38-44.
-
(1991)
Nature
, vol.349
, pp. 38-44
-
-
Brown, C.J.1
Ballabio, A.2
Rupert, J.L.3
Lafreniere, R.G.4
Grompe, M.5
Tonlorenzi, R.6
Willard, H.F.7
-
8
-
-
0028939902
-
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
-
Buiting, K., Saitoh, S., Grow, S., Dittrich, B., Schwarz, S., Nicholls, R. D. and 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
Grow, S.3
Dittrich, B.4
Schwarz, S.5
Nicholls, R.D.6
Horsthemke, B.7
-
10
-
-
0016607485
-
Chromosome imprinting and the mammalian X chromosome
-
Chandra, H. S., and Brown, S. W. (1975). Chromosome imprinting and the mammalian X chromosome. Nature 253, 165-8.
-
(1975)
Nature
, vol.253
, pp. 165-168
-
-
Chandra, H.S.1
Brown, S.W.2
-
11
-
-
0022446516
-
Genetics of hypertension in pregnancy: Possible single gene control of pre-eclampsia in the descendants of eclamptic women
-
Chesley, L. C., and Cooper, D. W. (1986). Genetics of hypertension in pregnancy: possible single gene control of pre-eclampsia in the descendants of eclamptic women. Br. J. Obstet. Gynaecol. 93, 898-908.
-
(1986)
Br. J. Obstet. Gynaecol.
, vol.93
, pp. 898-908
-
-
Chesley, L.C.1
Cooper, D.W.2
-
12
-
-
0014333853
-
The familial factor in toxemia of pregnancy
-
Chesley, L. C., Annitto, J. E., and Cosgrove, R. A. (1968). The familial factor in toxemia of pregnancy. J. Obstet. Gynaecol. 32, 303-11.
-
(1968)
J. Obstet. Gynaecol.
, vol.32
, pp. 303-311
-
-
Chesley, L.C.1
Annitto, J.E.2
Cosgrove, R.A.3
-
13
-
-
0018587820
-
Genetic control of severe pre-eclampsia
-
Cooper, D. W., and Liston, W. A. (1979). Genetic control of severe pre-eclampsia. J. Med. Genet. 16, 409-16.
-
(1979)
J. Med. Genet.
, vol.16
, pp. 409-416
-
-
Cooper, D.W.1
Liston, W.A.2
-
14
-
-
0027241658
-
Genetics of pre-eclampsia
-
Cooper, D. W., Brenneke, S. P., and Wilton, A. (1993a). Genetics of pre-eclampsia. Hypertension in Pregnancy 12, 1-23.
-
(1993)
Hypertension in Pregnancy
, vol.12
, pp. 1-23
-
-
Cooper, D.W.1
Brenneke, S.P.2
Wilton, A.3
-
15
-
-
0000095385
-
X-inactivation in marsupials and monotremes
-
Cooper, D. W., Johnston, P. G., Watson, J. M., and Graves, J. A. M. (1993b). X-inactivation in marsupials and monotremes. Seminars in Developmental Biology 4, 117-128.
-
(1993)
Seminars in Developmental Biology
, vol.4
, pp. 117-128
-
-
Cooper, D.W.1
Johnston, P.G.2
Watson, J.M.3
Graves, J.A.M.4
-
16
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor 2 gene
-
de Chiara, T. M., Robertson, E. J., and Efstradiatis, A. (1991). Parental imprinting of the mouse insulin-like growth factor 2 gene. Cell 64, 849-59.
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
De Chiara, T.M.1
Robertson, E.J.2
Efstradiatis, A.3
-
17
-
-
0026700732
-
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes
-
Driscoll, D. J., Water, M. F., Williams, C. A., Zori, R. T., Glenn, C. C., Avidano, K. M., and Nicholls, R. D. (1992). A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes. Genomics 13, 917-24.
-
(1992)
Genomics
, vol.13
, pp. 917-924
-
-
Driscoll, D.J.1
Water, M.F.2
Williams, C.A.3
Zori, R.T.4
Glenn, C.C.5
Avidano, K.M.6
Nicholls, R.D.7
-
18
-
-
0028815477
-
Genomic imprinting of Mash2, a mouse gene required for trophoblast development
-
Guillemot, F., Caspary, T., Tilghman, S. M., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., Anderson, D. J., Joyner, A. L., Rossant, J., and Nagy, A. (1995). Genomic imprinting of Mash2, a mouse gene required for trophoblast development. Nature Genet. 9, 235-41.
-
(1995)
Nature Genet.
, vol.9
, pp. 235-241
-
-
Guillemot, F.1
Caspary, T.2
Tilghman, S.M.3
Copeland, N.G.4
Gilbert, D.J.5
Jenkins, N.A.6
Anderson, D.J.7
Joyner, A.L.8
Rossant, J.9
Nagy, A.10
-
19
-
-
0027714649
-
Genetic conflicts in human pregnancy
-
Haig, D. (1993). Genetic conflicts in human pregnancy. Q. Rev. Biol. 68, 495-532.
-
(1993)
Q. Rev. Biol.
, vol.68
, pp. 495-532
-
-
Haig, D.1
-
20
-
-
0025681357
-
How imprinting is relevant to human disease
-
Hall, J. G. (1990). How imprinting is relevant to human disease. Development Supplement, pp. 141-8.
-
(1990)
Development Supplement
, pp. 141-148
-
-
Hall, J.G.1
-
21
-
-
0017696835
-
Androgenetic origin of hydatidiform mole
-
Kajii, T., and Ohama, K. (1977). Androgenetic origin of hydatidiform mole. Nature 268, 633-4.
-
(1977)
Nature
, vol.268
, pp. 633-634
-
-
Kajii, T.1
Ohama, K.2
-
22
-
-
0029881013
-
Genomic imprinting and the differential roles of parental genomes in brain development
-
Keverne, E. B., Fuyndele, R., Narasimha, M., Barton, S. C., and Surani, M. A. (1996). Genomic imprinting and the differential roles of parental genomes in brain development. Developments in Brain Research 92, 91.
-
(1996)
Developments in Brain Research
, vol.92
, pp. 91
-
-
Keverne, E.B.1
Fuyndele, R.2
Narasimha, M.3
Barton, S.C.4
Surani, M.A.5
-
23
-
-
0031012849
-
UBE3A/E6-AP mutations cause Angelman syndrome
-
Kishino, T., Lalande, M., and Wagstaff, J. (1997). UBE3A/E6-AP mutations cause Angelman syndrome. Nat. Genet. 15, 70-3.
-
(1997)
Nat. Genet.
, vol.15
, pp. 70-73
-
-
Kishino, T.1
Lalande, M.2
Wagstaff, J.3
-
24
-
-
0027205671
-
Allele-specific replication timing of imprinted gene regions
-
Kitsberg, D., Selig, S., Brandeis, M., Simon, I., Keshet, I, Driscoll, D. J., Nicholls, R. D., and Cedar, H. (1993). Allele-specific replication timing of imprinted gene regions. Nature 364, 459-63.
-
(1993)
Nature
, vol.364
, pp. 459-463
-
-
Kitsberg, D.1
Selig, S.2
Brandeis, M.3
Simon, I.4
Keshet, I.5
Driscoll, D.J.6
Nicholls, R.D.7
Cedar, H.8
-
25
-
-
0028260642
-
Allele-specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosal region
-
Knoll, J. H. M., Cheng, S-D., and Lalande, M. (1994). Allele-specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosal region. Nature Genet. 6, 41-5.
-
(1994)
Nature Genet.
, vol.6
, pp. 41-45
-
-
Knoll, J.H.M.1
Cheng, S.-D.2
Lalande, M.3
-
26
-
-
0029165883
-
An enhancer deletion affects both H19 and IGF2 expression
-
Leighton, P. A., Saam, J. R., Ingram, R. S., Stewart, C. L., and Tilghman, S. M. (1995). An enhancer deletion affects both H19 and IGF2 expression. Genes Dev. 9, 2079-89.
-
(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
-
27
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li, E., Beard, C., and Jaenisch, R. (1993). Role for DNA methylation in genomic imprinting. Nature 366, 362-5.
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
28
-
-
0031031570
-
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelmans syndrome
-
Matsuura, T., Sutcliffe, J. S., Fang, P., Galjaard, R-J., Jing, Y-H., Benton, C. S., Rommens, J. M., and Beaudet, A. L. (1997). De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelmans syndrome. Nat. Genet. 15, 74-7.
-
(1997)
Nat. Genet.
, vol.15
, pp. 74-77
-
-
Matsuura, T.1
Sutcliffe, J.S.2
Fang, P.3
Galjaard, R.-J.4
Jing, Y.-H.5
Benton, C.S.6
Rommens, J.M.7
Beaudet, A.L.8
-
29
-
-
0021139084
-
Completion of mouse embryo-genesis requires both the maternal and paternal genomes
-
McGrath, J., and Solter, D. (1984). Completion of mouse embryo-genesis requires both the maternal and paternal genomes. Cell 37, 179-83.
-
(1984)
Cell
, vol.37
, pp. 179-183
-
-
McGrath, J.1
Solter, D.2
-
30
-
-
0016653984
-
Pre-eclampsia in pregnancies by different fathers: Immunological studies
-
Need, J. A. (1975). Pre-eclampsia in pregnancies by different fathers: Immunological studies. BMJ 1, 548-9.
-
(1975)
BMJ
, vol.1
, pp. 548-549
-
-
Need, J.A.1
-
31
-
-
0027474137
-
Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: A review
-
Nicholls, R. D. (1993). Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review. Am. J. Med. Genet. 46, 16-25.
-
(1993)
Am. J. Med. Genet.
, vol.46
, pp. 16-25
-
-
Nicholls, R.D.1
-
32
-
-
0028276091
-
Pre-eclampsia - 'the disease of theories'
-
Pipkin, F. B., and Rubin, P. C. (1994). Pre-eclampsia - 'the disease of theories'. Br. Med. Bull. 50, 381-96.
-
(1994)
Br. Med. Bull.
, vol.50
, pp. 381-396
-
-
Pipkin, F.B.1
Rubin, P.C.2
-
33
-
-
0021913641
-
Abnormal placentation
-
Robertson, W. B., Bronsens, I., and Landells, W. N. (1985). Abnormal placentation. Obstet. Gynecol. Ann. 14, 411-26.
-
(1985)
Obstet. Gynecol. Ann.
, vol.14
, pp. 411-426
-
-
Robertson, W.B.1
Bronsens, I.2
Landells, W.N.3
-
34
-
-
0026517335
-
Resolution of pre-eclampsia following intrauterine death of one twin
-
Sarhanis, P., and Pugh, D. H. O. (1992). Resolution of pre-eclampsia following intrauterine death of one twin. Br. J. Obstet. Gynaecol. 99, 159-60.
-
(1992)
Br. J. Obstet. Gynaecol.
, vol.99
, pp. 159-160
-
-
Sarhanis, P.1
Pugh, D.H.O.2
-
35
-
-
16944366964
-
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
-
Skuse, D. H., James, R. S., Bishop, D. V. M., Coppin, B., Dalton, P., Aamodt-Leeper, G., Bacarese-Hamilton, M., Creswell, C., McGurk, R., and Jacobs, P. A. (1997). Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 387, 705-8.
-
(1997)
Nature
, vol.387
, pp. 705-708
-
-
Skuse, D.H.1
James, R.S.2
Bishop, D.V.M.3
Coppin, B.4
Dalton, P.5
Aamodt-Leeper, G.6
Bacarese-Hamilton, M.7
Creswell, C.8
McGurk, R.9
Jacobs, P.A.10
-
36
-
-
0025602064
-
Genomic imprinting and development on the mouse
-
Surani, M. A., Kothary, R., Allen, N. D., Singh, P. B., Fundele, R., Ferguson-Smith, A. C., and Barton, S. C. (1990). Genomic imprinting and development on the mouse. Development Supplement, pp. 89-98.
-
(1990)
Development Supplement
, pp. 89-98
-
-
Surani, M.A.1
Kothary, R.2
Allen, N.D.3
Singh, P.B.4
Fundele, R.5
Ferguson-Smith, A.C.6
Barton, S.C.7
-
37
-
-
0019390298
-
The incidence ot severe pre-eclampsia amongst mothers and mothers-in-law of pre-eclamptics and controls
-
Sutherland, A., Cooper, D. W., Howie, P. W., Liston, W. A., and MacGillivray, I. (1981). The incidence ot severe pre-eclampsia amongst mothers and mothers-in-law of pre-eclamptics and controls. Br. J. Obstet. Gynaecol. 88, 785-91.
-
(1981)
Br. J. Obstet. Gynaecol.
, vol.88
, pp. 785-791
-
-
Sutherland, A.1
Cooper, D.W.2
Howie, P.W.3
Liston, W.A.4
MacGillivray, I.5
-
38
-
-
0025954826
-
Pre-eclampsia: Discordance among identical twins
-
Thornton, J. G., and Onwude, J. L. (1991). Pre-eclampsia: discordance among identical twins. BMJ 303, 1241-2.
-
(1991)
BMJ
, vol.303
, pp. 1241-1242
-
-
Thornton, J.G.1
Onwude, J.L.2
-
39
-
-
0345019705
-
Parental imprinting in the mouse
-
The Harvey Society of New York. Wiley-Liss: New York
-
Tilghman, S. M. (1992). Parental imprinting in the mouse. In 'The Harvey Society Lectures, series 87'. (The Harvey Society of New York.) pp. 6-84. (Wiley-Liss: New York.)
-
(1992)
The Harvey Society Lectures, Series 87
, pp. 6-84
-
-
Tilghman, S.M.1
-
40
-
-
0030036331
-
Mapping of the human/mouse imprinted genes IGF2, H19, SNRPN and ZNF127 in marsupials: An indication for possible conserved imprinted clusters
-
Toder, R., Wilcox, S. A., Smithwick, M., and Graves, J. A. M. (1996). Mapping of the human/mouse imprinted genes IGF2, H19, SNRPN and ZNF127 in marsupials: an indication for possible conserved imprinted clusters. Chromosome Res. 4, 295-300.
-
(1996)
Chromosome Res.
, vol.4
, pp. 295-300
-
-
Toder, R.1
Wilcox, S.A.2
Smithwick, M.3
Graves, J.A.M.4
|