-
1
-
-
0030458551
-
Parental imprinting and human disease
-
Lalande, M. (1997) Parental imprinting and human disease. Annu. Rev. Genet., 30, 173-195.
-
(1997)
Annu. Rev. Genet.
, vol.30
, pp. 173-195
-
-
Lalande, M.1
-
2
-
-
0030726998
-
Prader-Willi syndrome
-
Cassidy, S.B. (1997) Prader-Willi syndrome. J. Med. Genet., 34, 917-923.
-
(1997)
J. Med. Genet.
, vol.34
, pp. 917-923
-
-
Cassidy, S.B.1
-
3
-
-
0032103697
-
Imprinting in Angelman and Prader-Willi syndromes
-
Jiang, Y., Tsai, T.F., Bressler, J. and Beaudet, A.L. (1998) Imprinting in Angelman and Prader-Willi syndromes. Curr. Opin. Genet. Dev., 8, 334-342.
-
(1998)
Curr. Opin. Genet. Dev.
, vol.8
, pp. 334-342
-
-
Jiang, Y.1
Tsai, T.F.2
Bressler, J.3
Beaudet, A.L.4
-
4
-
-
0030833487
-
Imprinting mutations on human chromosome 15
-
Horsthemke, B., Dittrich, B. and Buiting, K. (1997) Imprinting mutations on human chromosome 15. Hum. Mutat., 10, 329-337.
-
(1997)
Hum. Mutat.
, vol.10
, pp. 329-337
-
-
Horsthemke, B.1
Dittrich, B.2
Buiting, K.3
-
5
-
-
0033073395
-
Imprinting-mutation mechanisms in Prader-Willi syndrome
-
Ohta, T., Gray, T.A., Rogan, P.K., Buiting, K., Gabriel, J.M., Saitoh, S., Muralidhar, B., Bilienska, B., Krajewska-Walasek, M., Driscoll, D.J., Horsthemke, B., Butler, M.G. and Nicholls, R.D. (1999) Imprinting-mutation mechanisms in Prader-Willi syndrome. Am. J. Hum. Genet., 64, 397-413.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 397-413
-
-
Ohta, T.1
Gray, T.A.2
Rogan, P.K.3
Buiting, K.4
Gabriel, J.M.5
Saitoh, S.6
Muralidhar, B.7
Bilienska, B.8
Krajewska-Walasek, M.9
Driscoll, D.J.10
Horsthemke, B.11
Butler, M.G.12
Nicholls, R.D.13
-
6
-
-
0030052505
-
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene
-
Glenn, C.C., Saitoh, S., Jong, M.T.C., Filbrandt, M.M., Surti, U., Driscoll, D.J. and Nicholls, R.D. (1996) Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene. Am. J. Hum. Genet., 58, 335-346.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 335-346
-
-
Glenn, C.C.1
Saitoh, S.2
Jong, M.T.C.3
Filbrandt, M.M.4
Surti, U.5
Driscoll, D.J.6
Nicholls, R.D.7
-
7
-
-
0033545993
-
An imprinted, mammalian bicistronic transcript encodes two independent proteins
-
Gray, T.A., Saitoh, S. and Nicholls, R.D. (1999) An imprinted, mammalian bicistronic transcript encodes two independent proteins. Proc. Natl Acad. Sci. USA, 96, 5616-5621.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 5616-5621
-
-
Gray, T.A.1
Saitoh, S.2
Nicholls, R.D.3
-
8
-
-
0032896919
-
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region
-
Jong, M.T., Gray, T.A., Ji, Y., Glenn, C.C., Saitoh, S., Driscoll, D.J. and Nicholls, R.D. (1999) A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region. Hum. Mol. Genet., 8, 783-793.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 783-793
-
-
Jong, M.T.1
Gray, T.A.2
Ji, Y.3
Glenn, C.C.4
Saitoh, S.5
Driscoll, D.J.6
Nicholls, R.D.7
-
9
-
-
16944363776
-
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
-
Jay, P., Rougeulle, C., Massacrier, A., Moncla, A., Mattei, M.G., Malzac, P., Roeckel, N., Taviaux, S., Lefranc, J.L., Cau, P., Berta, P., Lalande, M. and Muscatelli, F. (1997) The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nature Genet., 17, 357-361.
-
(1997)
Nature Genet.
, vol.17
, pp. 357-361
-
-
Jay, P.1
Rougeulle, C.2
Massacrier, A.3
Moncla, A.4
Mattei, M.G.5
Malzac, P.6
Roeckel, N.7
Taviaux, S.8
Lefranc, J.L.9
Cau, P.10
Berta, P.11
Lalande, M.12
Muscatelli, F.13
-
10
-
-
0030773594
-
The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse
-
MacDonald, H.R. and Wevrick, R. (1997) The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum. Mol. Genet., 6, 1873-1878.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1873-1878
-
-
MacDonald, H.R.1
Wevrick, R.2
-
11
-
-
0028124726
-
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
-
Wevrick, R., Kerns, J. and Francke, U. (1994) Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum. Mol. Genet., 3, 1877-1882.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1877-1882
-
-
Wevrick, R.1
Kerns, J.2
Francke, U.3
-
12
-
-
0028133293
-
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
-
Sutcliffe, J.S., Nakao, M., Christian, S., Orstavik, K.H., Tommerup, N., Ledbetter, D.H. and Beaudet, A.L. (1994) Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nature Genet., 8, 52-58.
-
(1994)
Nature Genet.
, vol.8
, pp. 52-58
-
-
Sutcliffe, J.S.1
Nakao, M.2
Christian, S.3
Orstavik, K.H.4
Tommerup, N.5
Ledbetter, D.H.6
Beaudet, A.L.7
-
13
-
-
0027018063
-
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome
-
Leff, S.E., Brannan, C.I., Reed, M.L., Ozcekik, T., Francke, U., Copeland, N.G. and Jenkins, N.A. (1992) Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome. Nature Genet., 2, 259-250.
-
(1992)
Nature Genet.
, vol.2
, pp. 259-1250
-
-
Leff, S.E.1
Brannan, C.I.2
Reed, M.L.3
Ozcekik, T.4
Francke, U.5
Copeland, N.G.6
Jenkins, N.A.7
-
14
-
-
0030776554
-
The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region
-
Watrin, F., Roeckel, N., Lacroix, L., Mignon, C., Mattei, M.G., Disteche, C. and Muscatelli, F. (1997) The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region. Eur. J. Hum. Genet., 5, 324-332.
-
(1997)
Eur. J. Hum. Genet.
, vol.5
, pp. 324-332
-
-
Watrin, F.1
Roeckel, N.2
Lacroix, L.3
Mignon, C.4
Mattei, M.G.5
Disteche, C.6
Muscatelli, F.7
-
15
-
-
0032897757
-
Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region
-
Jong, M.T., Carey, A.M., Caldwell, K.A., Lau, M.H., Handel, M.A., Driscoll, D.J., Stewart, C.L., Rinchik, E.M. and Nicholls, R.D. (1999) Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region. Hum. Mol. Genet., 8. 795-803.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 795-803
-
-
Jong, M.T.1
Carey, A.M.2
Caldwell, K.A.3
Lau, M.H.4
Handel, M.A.5
Driscoll, D.J.6
Stewart, C.L.7
Rinchik, E.M.8
Nicholls, R.D.9
-
16
-
-
0031040496
-
An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene
-
Wevrick, R. and Francke, U. (1997) An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene. Hum. Mol. Genet., 6, 325-332.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 325-332
-
-
Wevrick, R.1
Francke, U.2
-
17
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprinting-centre mutations
-
Yang, T., Adamson, T.E., Resnick, J.L., Leff, S., Wevrick, R., Francke, U., Jenkins, N.A., Copeland, N.G. and Brannan, C.I. (1998) A mouse model for Prader-Willi syndrome imprinting-centre mutations. Nature Genet., 19, 25-31.
-
(1998)
Nature Genet.
, vol.19
, pp. 25-31
-
-
Yang, T.1
Adamson, T.E.2
Resnick, J.L.3
Leff, S.4
Wevrick, R.5
Francke, U.6
Jenkins, N.A.7
Copeland, N.G.8
Brannan, C.I.9
-
18
-
-
0032837539
-
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome
-
Tsai, T.F., Jiang, Y., Bressler, J., Armstrong, D. and Beaudet, A.L. (1999) Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome. Hum. Mol. Genet., 8, 1357-1364.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1357-1364
-
-
Tsai, T.F.1
Jiang, Y.2
Bressler, J.3
Armstrong, D.4
Beaudet, A.L.5
-
19
-
-
0032963667
-
Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome
-
Tsai, T.F., Armstrong, D. and Beaudet, A.L. (1999) Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome. Nature Genet., 22, 15-16.
-
(1999)
Nature Genet.
, vol.22
, pp. 15-16
-
-
Tsai, T.F.1
Armstrong, D.2
Beaudet, A.L.3
-
20
-
-
0030627982
-
Neural network prediction of translation initiation sites in eukaryote perspectives for EST and genome analysis
-
Pedersen, A.G. and Nielsen, H. (1997) Neural network prediction of translation initiation sites in eukaryote perspectives for EST and genome analysis. ISMB, 5, 226-233.
-
(1997)
ISMB
, vol.5
, pp. 226-233
-
-
Pedersen, A.G.1
Nielsen, H.2
-
21
-
-
0029809212
-
Comparative analysis of 1196 orthologous mouse and human full-length mRNA and protein sequences
-
Makalowski, W., Zhang, J. and Boguski, M.S. (1996) Comparative analysis of 1196 orthologous mouse and human full-length mRNA and protein sequences. Genome Res., 6, 846-857.
-
(1996)
Genome Res.
, vol.6
, pp. 846-857
-
-
Makalowski, W.1
Zhang, J.2
Boguski, M.S.3
-
22
-
-
0028851082
-
Characteristics of imprinted genes
-
Erratum (1995) Nature Genet., 9, 451
-
Neumann, B., Kubicka, P. and Barlow, D.P. (1995) Characteristics of imprinted genes. Nature Genet., 9, 12-13 [Erratum (1995) Nature Genet., 9, 451].
-
(1995)
Nature Genet.
, vol.9
, pp. 12-13
-
-
Neumann, B.1
Kubicka, P.2
Barlow, D.P.3
-
23
-
-
0028788194
-
AU-rich elements: Characterization and importance in mRNA degradation
-
Chen, C.Y. and Shyu, A.B. (1995) AU-rich elements: characterization and importance in mRNA degradation. Trends Biochem. Sci., 20, 465-470.
-
(1995)
Trends Biochem. Sci.
, vol.20
, pp. 465-470
-
-
Chen, C.Y.1
Shyu, A.B.2
-
24
-
-
0033566760
-
A new MAGE gene with ubiquitous expression does not code for known MAGE antigens recognized by T cells
-
Lucas, S., Brasseur, F. and Boon, T. (1999) A new MAGE gene with ubiquitous expression does not code for known MAGE antigens recognized by T cells. Cancer Res., 59, 4100-4103.
-
(1999)
Cancer Res.
, vol.59
, pp. 4100-4103
-
-
Lucas, S.1
Brasseur, F.2
Boon, T.3
-
25
-
-
0031762651
-
Imprinting mechanisms
-
Constancia, M., Pickard, B., Kelsey, G. and Reik, W. (1998) Imprinting mechanisms. Genome Res., 8, 881-900.
-
(1998)
Genome Res.
, vol.8
, pp. 881-900
-
-
Constancia, M.1
Pickard, B.2
Kelsey, G.3
Reik, W.4
-
26
-
-
0031469678
-
Genomic imprinting: A chromatin connection
-
Feil, R. and Kelsey, G. (1997) Genomic imprinting: a chromatin connection. Am. J. Hum. Genet., 61, 1213-1219.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 1213-1219
-
-
Feil, R.1
Kelsey, G.2
-
27
-
-
0031964697
-
Necdin, a postmitotic neuron-specific growth suppressor, interacts with viral transforming proteins and cellular transcription factor E2FI
-
Taniura, H., Taniguchi, N., Hara, M. and Yoshikawa, K. (1998) Necdin, a postmitotic neuron-specific growth suppressor, interacts with viral transforming proteins and cellular transcription factor E2FI. J. Biol. Chem., 273, 720-728.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 720-728
-
-
Taniura, H.1
Taniguchi, N.2
Hara, M.3
Yoshikawa, K.4
-
28
-
-
0033522919
-
Physical and functional interactions of neuronal growth suppressor Necdin with p53
-
Taniura, H., Matsumoto, K. and Yoshikawa, K. (1999) Physical and functional interactions of neuronal growth suppressor Necdin with p53. J. Biol. Chem., 274, 16242-16248.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 16242-16248
-
-
Taniura, H.1
Matsumoto, K.2
Yoshikawa, K.3
-
29
-
-
0033556347
-
A new family of mouse genes homologous to the human MAGE genes
-
De Plaen, E., De Backer, O., Arnaud, D., Bonjean, B., Chomez, P., Martelange, V., Avner, P., Baldacci, P., Babinet, C., Hwang, S.Y., Knowles, B. and Boon, T. (1999) A new family of mouse genes homologous to the human MAGE genes. Genomics, 55, 176-184.
-
(1999)
Genomics
, vol.55
, pp. 176-184
-
-
De Plaen, E.1
De Backer, O.2
Arnaud, D.3
Bonjean, B.4
Chomez, P.5
Martelange, V.6
Avner, P.7
Baldacci, P.8
Babinet, C.9
Hwang, S.Y.10
Knowles, B.11
Boon, T.12
-
30
-
-
0031937488
-
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb
-
Christian, S.L., Bhatt, N.K., Martin, S.A., Sutcliffe, J.S., Kubota, T., Huang, B., Mutirangura, A., Chinault, A.C., Beaudet, A.L. and Ledbetter, D.H. (1998) Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb. Genome Res., 8, 146-157.
-
(1998)
Genome Res.
, vol.8
, pp. 146-157
-
-
Christian, S.L.1
Bhatt, N.K.2
Martin, S.A.3
Sutcliffe, J.S.4
Kubota, T.5
Huang, B.6
Mutirangura, A.7
Chinault, A.C.8
Beaudet, A.L.9
Ledbetter, D.H.10
-
31
-
-
0027017879
-
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
-
Cattanach, B.M., Barr, J.A., Evans, E.P., Burtenshaw, M., Beechey, C.V., Leff, S.E., Brannan, C.I., Copeland, N.G., Jenkins, N.A. and Jones, J. (1992) A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. Nature Genet., 2, 270-274.
-
(1992)
Nature Genet.
, vol.2
, pp. 270-274
-
-
Cattanach, B.M.1
Barr, J.A.2
Evans, E.P.3
Burtenshaw, M.4
Beechey, C.V.5
Leff, S.E.6
Brannan, C.I.7
Copeland, N.G.8
Jenkins, N.A.9
Jones, J.10
-
32
-
-
0033529801
-
A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and Angelman syndromes
-
Gabriel, J.M., Merchant, M., Ohta, T., Ji, Y., Caldwell, R.G., Ramsey, M.J., Tucker, J.D., Longnecker, R. and Nicholls, R.D. (1999) A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and Angelman syndromes. Proc. Natl Acad. Sci. USA, 96, 9258-9263.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 9258-9263
-
-
Gabriel, J.M.1
Merchant, M.2
Ohta, T.3
Ji, Y.4
Caldwell, R.G.5
Ramsey, M.J.6
Tucker, J.D.7
Longnecker, R.8
Nicholls, R.D.9
-
33
-
-
0026703169
-
Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector
-
Shizuya, H., Birren, B., Kim, U.J., Mancino, V., Slepak, T., Tachiiri, Y. and Simon, M. (1992) Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector. Proc. Natl Acad. Sci. USA, 89, 8794-8797.
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.89
, pp. 8794-8797
-
-
Shizuya, H.1
Birren, B.2
Kim, U.J.3
Mancino, V.4
Slepak, T.5
Tachiiri, Y.6
Simon, M.7
|