-
1
-
-
84995191751
-
Puppet children: A report of three cases
-
Angelman H. Puppet children: A report of three cases. Dev. Med. Neurol. 7:1965;681-688.
-
(1965)
Dev. Med. Neurol.
, vol.7
, pp. 681-688
-
-
Angelman, H.1
-
3
-
-
0031638515
-
The host defence function of genomic methylation patterns
-
Bestor T. H. The host defence function of genomic methylation patterns. Novartis Found. Symp. 214:1998;187-195.
-
(1998)
Novartis Found. Symp.
, vol.214
, pp. 187-195
-
-
Bestor, T.H.1
-
4
-
-
0022540321
-
CpG-rich islands and the function of DNA methylation
-
Bird A. P. CpG-rich islands and the function of DNA methylation. Nature. 321:1986;209-213.
-
(1986)
Nature
, vol.321
, pp. 209-213
-
-
Bird, A.P.1
-
5
-
-
0033531134
-
The imprinting box of the mouse Igf2r gene
-
Birger Y., Shemer R., Perk J., Razin A. The imprinting box of the mouse Igf2r gene. Nature. 397:1999;84-88.
-
(1999)
Nature
, vol.397
, pp. 84-88
-
-
Birger, Y.1
Shemer, R.2
Perk, J.3
Razin, A.4
-
6
-
-
0032714383
-
The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region
-
Boccaccio I., Glatt-Deeley H., Watrin F., Roeckel N., Lalande M., Muscatelli F. The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Hum. Mol. Genet. 8:1999;2497-2505.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 2497-2505
-
-
Boccaccio, I.1
Glatt-Deeley, H.2
Watrin, F.3
Roeckel, N.4
Lalande, M.5
Muscatelli, F.6
-
7
-
-
0028104109
-
Sp1 elements protect a CpG island from de novo methylation
-
Brandeis M., Frank D., Keshet I., Siegfried Z., Mendelsohn M., Nemes A., Temper V., Razin A., Cedar H. Sp1 elements protect a CpG island from de novo methylation. Nature. 371:1994;435-438.
-
(1994)
Nature
, vol.371
, pp. 435-438
-
-
Brandeis, M.1
Frank, D.2
Keshet, I.3
Siegfried, Z.4
Mendelsohn, M.5
Nemes, A.6
Temper, V.7
Razin, A.8
Cedar, H.9
-
8
-
-
0027738562
-
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene
-
Buiting K., Dittrich B., Groß S., Greger V., Lalande M., Robinson W., Mutirangura A., Ledbetter D., Horsthemke B. Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene. Hum. Mol. Genet. 2:1993;1991-1994.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1991-1994
-
-
Buiting, K.1
Dittrich, B.2
Groß, S.3
Greger, V.4
Lalande, M.5
Robinson, W.6
Mutirangura, A.7
Ledbetter, D.8
Horsthemke, B.9
-
9
-
-
0032231460
-
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: Implications for imprint-switch models, genetic counseling and prenatal diagnosis
-
Buiting K., Dittrich B., Groß S., Lich C., Färber C., Buchholz T., Smith E., Reis A., Bürger J., Nöthen M. M., Barth-Witte U., Janssen B., Abeliovich D., Lerer I., van den Ouweland A. M. W., Halley D. J. J., Schrander-Stumpel C., Smeets H., Meinecke P., Malcom S., Gardner A., Lalande M., Nicholls R. D., Friend K., Schulze A., Matthijs G., Kokkonen H., Hilbert P., Maldergem L. V., Glover G., Carbonell P., Willems P., Gillessen-Kaesbach G., Horsthemke B. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: Implications for imprint-switch models, genetic counseling and prenatal diagnosis. Am. J. Hum. Genet. 63:1998;170-180.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 170-180
-
-
Buiting, K.1
Dittrich, B.2
Groß, S.3
Lich, C.4
Färber, C.5
Buchholz, T.6
Smith, E.7
Reis, A.8
Bürger, J.9
Nöthen, M.M.10
Barth-Witte, U.11
Janssen, B.12
Abeliovich, D.13
Lerer, I.14
Van Den Ouweland, A.M.W.15
Halley, D.J.J.16
Schrander-Stumpel, C.17
Smeets, H.18
Meinecke, P.19
Malcom, S.20
Gardner, A.21
Lalande, M.22
Nicholls, R.D.23
Friend, K.24
Schulze, A.25
Matthijs, G.26
Kokkonen, H.27
Hilbert, P.28
Maldergem, L.V.29
Glover, G.30
Carbonell, P.31
Willems, P.32
Gillessen-Kaesbach, G.33
Horsthemke, B.34
more..
-
10
-
-
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. D., Horsthemke B. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat. Genet. 9:1995;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.D.6
Horsthemke, B.7
-
11
-
-
0029120391
-
Cleavage site determinants in the mammalian polyadenylation signal
-
Chen F., MacDonald C. C., Wilusz J. Cleavage site determinants in the mammalian polyadenylation signal. Nucleic Acids Res. 14:1995;2614-2620.
-
(1995)
Nucleic Acids Res.
, vol.14
, pp. 2614-2620
-
-
Chen, F.1
MacDonald, C.C.2
Wilusz, J.3
-
12
-
-
0027317479
-
Demethylation of somatic and testis-specific histone H2A and H2B genes in F9 embryonal carcinoma cells
-
Choi Y. C., Chae C. B. Demethylation of somatic and testis-specific histone H2A and H2B genes in F9 embryonal carcinoma cells. Mol. Cell. Biol. 13:1993;5538-5548.
-
(1993)
Mol. Cell. Biol.
, vol.13
, pp. 5538-5548
-
-
Choi, Y.C.1
Chae, C.B.2
-
13
-
-
0029979781
-
Molecular cloning of mouse somatic and testis-specific H2B histone genes containing a methylated CpG island
-
Choi Y. C., Gu W., Hecht N. B., Feinberg A. P., Chae C. B. Molecular cloning of mouse somatic and testis-specific H2B histone genes containing a methylated CpG island. DNA Cell Biol. 15:1996;495-504.
-
(1996)
DNA Cell Biol.
, vol.15
, pp. 495-504
-
-
Choi, Y.C.1
Gu, W.2
Hecht, N.B.3
Feinberg, A.P.4
Chae, C.B.5
-
14
-
-
0027741188
-
Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region
-
Dittrich B., Buiting K., Groß S., Horsthemke B. Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region. Hum. Mol. Genet. 2:1993;1995-1999.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1995-1999
-
-
Dittrich, B.1
Buiting, K.2
Groß, S.3
Horsthemke, B.4
-
15
-
-
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 R. D., Poustka A., Winterpacht A., Zabel B., Horsthemke B. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene. Nat. Genet. 14:1996;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
-
16
-
-
0025322399
-
Sex difference in methylation of single copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting and origin of CpG mutations
-
Driscoll D. J., Migeon B. R. Sex difference in methylation of single copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting and origin of CpG mutations. Somat. Cell Mol. Genet. 16:1990;267-282.
-
(1990)
Somat. Cell Mol. Genet.
, vol.16
, pp. 267-282
-
-
Driscoll, D.J.1
Migeon, B.R.2
-
17
-
-
17144438935
-
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC micodeletion
-
Färber C., Dittrich B., Buiting K., Horsthemke B. The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC micodeletion. Hum. Mol. Genet. 2:1999;337-343.
-
(1999)
Hum. Mol. Genet.
, vol.2
, pp. 337-343
-
-
Färber, C.1
Dittrich, B.2
Buiting, K.3
Horsthemke, B.4
-
19
-
-
0033545993
-
An imprinted, mammalian bicistronic transcript encodes two independent proteins
-
Gray T. A., Saitoh S., Nicholls R. D. An imprinted, mammalian bicistronic transcript encodes two independent proteins. Proc. Natl. Acad. Sci. USA. 96:1999;5616-5621.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 5616-5621
-
-
Gray, T.A.1
Saitoh, S.2
Nicholls, R.D.3
-
21
-
-
0023194745
-
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus
-
Horsthemke B., Greger V., Barnert H. J., Höpping W., Passarge E. Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus. Hum. Genet. 76:1987;257-261.
-
(1987)
Hum. Genet.
, vol.76
, pp. 257-261
-
-
Horsthemke, B.1
Greger, V.2
Barnert, H.J.3
Höpping, W.4
Passarge, E.5
-
22
-
-
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., Roëckel N., Taviaux S., Lefranc J.-L., Cau P., Berta P., Lalande M., Muscatelli F. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nat. Genet. 17:1997;357-361.
-
(1997)
Nat. 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
Roëckel, N.7
Taviaux, S.8
Lefranc, J.-L.9
Cau, P.10
Berta, P.11
Lalande, M.12
Muscatelli, F.13
-
23
-
-
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. C., Carey A. H., Caldwell K. A., Lau M. H., Handel M. A., Driscoll D. J., Stewart C. L., Rinchik E. M., Nicholls R. D. Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region. Hum. Mol. Genet. 8:1999a;795-803.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 795-803
-
-
Jong, M.T.C.1
Carey, A.H.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
-
24
-
-
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. C., Gray T. A., Ji Y., Glenn C. C., Saitoh S., Driscoll D. J., Nicholls R. D. A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region. Hum. Mol. Genet. 8:1999b;783-793.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 783-793
-
-
Jong, M.T.C.1
Gray, T.A.2
Ji, Y.3
Glenn, C.C.4
Saitoh, S.5
Driscoll, D.J.6
Nicholls, R.D.7
-
25
-
-
0031012849
-
UBE3A/E6-AP mutations cause Angelman syndrome
-
Kishino T., Lalande M., Wagstaff J. UBE3A/E6-AP mutations cause Angelman syndrome. Nat. Genet. 15:1997;70-73.
-
(1997)
Nat. Genet.
, vol.15
, pp. 70-73
-
-
Kishino, T.1
Lalande, M.2
Wagstaff, J.3
-
26
-
-
0027018063
-
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region
-
Leff S. E., Brannan C. I., Reed M. L., Özcelik T., Francke U., Copeland N. G., Jenkins N. A. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nat. Genet. 2:1992;259-264.
-
(1992)
Nat. Genet.
, vol.2
, pp. 259-264
-
-
Leff, S.E.1
Brannan, C.I.2
Reed, M.L.3
Özcelik, T.4
Francke, U.5
Copeland, N.G.6
Jenkins, N.A.7
-
27
-
-
0030773594
-
The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse
-
MacDonald H., Wevrick R. The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum. Mol. Genet. 11:1997;1873-1878.
-
(1997)
Hum. Mol. Genet.
, vol.11
, pp. 1873-1878
-
-
MacDonald, H.1
Wevrick, R.2
-
28
-
-
0031031570
-
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
-
Matsuura T., Sutcliffe J. S., Fang P., Galjaard R. J., Jiang Y. H., Benton C. S., Rommens J. M., Beaudet A. L. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome. Nat. Genet. 15:1997;74-77.
-
(1997)
Nat. Genet.
, vol.15
, pp. 74-77
-
-
Matsuura, T.1
Sutcliffe, J.S.2
Fang, P.3
Galjaard, R.J.4
Jiang, Y.H.5
Benton, C.S.6
Rommens, J.M.7
Beaudet, A.L.8
-
29
-
-
0032076307
-
Imprinting in Prader-Willi and Angelman syndromes
-
Nicholls R. D., Saitoh S., Horsthemke B. Imprinting in Prader-Willi and Angelman syndromes. Trends Genet. 14:1998;194-200.
-
(1998)
Trends Genet.
, vol.14
, pp. 194-200
-
-
Nicholls, R.D.1
Saitoh, S.2
Horsthemke, B.3
-
30
-
-
0027026716
-
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region
-
Ozcelik T., Leff S., Robinson W., Donlon T., Lalande M., Sanjines E., Schinzel A., Francke U. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region. Nat. Genet. 2:1992;265-269.
-
(1992)
Nat. Genet.
, vol.2
, pp. 265-269
-
-
Ozcelik, T.1
Leff, S.2
Robinson, W.3
Donlon, T.4
Lalande, M.5
Sanjines, E.6
Schinzel, A.7
Francke, U.8
-
31
-
-
0000927260
-
Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myotonieartigem Zustand im Neugeborenenalter
-
Prader A., Labhart A., Willi H. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myotonieartigem Zustand im Neugeborenenalter. Schweiz. Med. Wochenschr. 86:1956;1260-1261.
-
(1956)
Schweiz. Med. Wochenschr.
, vol.86
, pp. 1260-1261
-
-
Prader, A.1
Labhart, A.2
Willi, H.3
-
32
-
-
0028286005
-
DNA methylation and genomic imprinting
-
Razin A., Cedar H. DNA methylation and genomic imprinting. Cell. 77:1994;473-476.
-
(1994)
Cell
, vol.77
, pp. 473-476
-
-
Razin, A.1
Cedar, H.2
-
34
-
-
0031228039
-
The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain
-
Rougeulle C., Glatt H., Lalande M. The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. Nat. Genet. 17:1997;14-15.
-
(1997)
Nat. Genet.
, vol.17
, pp. 14-15
-
-
Rougeulle, C.1
Glatt, H.2
Lalande, M.3
-
35
-
-
0032500826
-
Germ cell-specific enhancer activity of a repeated element in a variable region of the mouse genome
-
Sage J., Martin L., Rassoulzadegan M., Cuzin F. Germ cell-specific enhancer activity of a repeated element in a variable region of the mouse genome. Gene. 221:1998;85-92.
-
(1998)
Gene
, vol.221
, pp. 85-92
-
-
Sage, J.1
Martin, L.2
Rassoulzadegan, M.3
Cuzin, F.4
-
36
-
-
0031055875
-
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patiens with an imprinting mutation
-
Saitoh S., Buiting K., Cassidy S. B., Conroy J. M., Driscoll D. J., Gabriel J., Gillessen-Kaesbach G., Glenn C. C., Greenswag L. R., Horsthemke B., Kondo I., Kuwajima K., Niikawa N., Rogan P. K., Schwartz S., Seip J., Williams C. A., Nicholls R. D. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patiens with an imprinting mutation. Am. J. Med. Genet. 68:1997;195-206.
-
(1997)
Am. J. Med. Genet.
, vol.68
, pp. 195-206
-
-
Saitoh, S.1
Buiting, K.2
Cassidy, S.B.3
Conroy, J.M.4
Driscoll, D.J.5
Gabriel, J.6
Gillessen-Kaesbach, G.7
Glenn, C.C.8
Greenswag, L.R.9
Horsthemke, B.10
Kondo, I.11
Kuwajima, K.12
Niikawa, N.13
Rogan, P.K.14
Schwartz, S.15
Seip, J.16
Williams, C.A.17
Nicholls, R.D.18
-
37
-
-
0030179993
-
Transcriptional promiscuity in testes
-
Schmidt E. E. Transcriptional promiscuity in testes. Curr. Biol. 6:1996;768-769.
-
(1996)
Curr. Biol.
, vol.6
, pp. 768-769
-
-
Schmidt, E.E.1
-
38
-
-
0032992224
-
DNA methylation represses transcription in vivo
-
Siegfried Z., Eden S., Mendelsohn M., Feng X., Tsuberi B-Z., Cedar H. DNA methylation represses transcription in vivo. Nat. Genet. 22:1999;203-206.
-
(1999)
Nat. Genet.
, vol.22
, pp. 203-206
-
-
Siegfried, Z.1
Eden, S.2
Mendelsohn, M.3
Feng, X.4
Tsuberi, B.-Z.5
Cedar, H.6
-
39
-
-
0030890115
-
The E6-AP ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region
-
Sutcliffe J. S., Jiang Y., Galjaard R.-J., Matsuura T., Fang P., Kubota T., Christian S. L., Bressler J., Cattanach B., Ledbetter D. H., Beaudet A. L. The E6-AP ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region. Genome Res. 7:1997;368-377.
-
(1997)
Genome Res.
, vol.7
, pp. 368-377
-
-
Sutcliffe, J.S.1
Jiang, Y.2
Galjaard, R.-J.3
Matsuura, T.4
Fang, P.5
Kubota, T.6
Christian, S.L.7
Bressler, J.8
Cattanach, B.9
Ledbetter, D.H.10
Beaudet, A.L.11
-
40
-
-
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., Beaudet A. L. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nat. Genet. 8:1994;52-58.
-
(1994)
Nat. 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
-
41
-
-
0026705292
-
Demonstration of a testis-specific trans-acting factor Tet-1 in vitro that binds to the promoter of the mouse protamine 1 gene
-
Tamura T., Makino Y., Mikoshiba K., Muramatsu M. Demonstration of a testis-specific trans-acting factor Tet-1 in vitro that binds to the promoter of the mouse protamine 1 gene. J. Biol. Chem. 267:1992;4327-4332.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 4327-4332
-
-
Tamura, T.1
Makino, Y.2
Mikoshiba, K.3
Muramatsu, M.4
-
42
-
-
0031230614
-
Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain
-
Vu T. H., Hoffman A. R. Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain. Nat. Genet. 17:1997;12-13.
-
(1997)
Nat. Genet.
, vol.17
, pp. 12-13
-
-
Vu, T.H.1
Hoffman, A.R.2
-
43
-
-
0033536040
-
r protein of the cleavage stimulation factor are expressed in mouse male germ cells
-
r protein of the cleavage stimulation factor are expressed in mouse male germ cells. Proc. Natl. Acad. Sci. USA. 96:1999;6763-6768.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 6763-6768
-
-
Wallace, A.M.1
Dass, B.2
Ravnik, S.E.3
Tonk, V.4
Jenkins, N.A.5
Gilbert, D.J.6
Copeland, N.G.7
MacDonald, C.C.8
-
44
-
-
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., Roëckel N., Lacroix L., Mignon C., Mattei M.-G., Disteche C., Muscatelli F. 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. 5:1997;324-332.
-
(1997)
Eur. J. Hum. Genet.
, vol.5
, pp. 324-332
-
-
Watrin, F.1
Roëckel, N.2
Lacroix, L.3
Mignon, C.4
Mattei, M.-G.5
Disteche, C.6
Muscatelli, F.7
-
45
-
-
0031040496
-
An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene
-
Wevrick R., Francke U. An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene. Hum. Mol. Genet. 6:1997;325-332.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 325-332
-
-
Wevrick, R.1
Francke, U.2
-
46
-
-
0028124726
-
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
-
Wevrick R., Kerns J. A., Francke U. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum. Mol. Genet. 3:1994;1877-1882.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1877-1882
-
-
Wevrick, R.1
Kerns, J.A.2
Francke, U.3
-
47
-
-
0025338173
-
How the messenger got its tail: Addition of poly(A) in the nucleus
-
Wickens M. How the messenger got its tail: Addition of poly(A) in the nucleus. Trends Biochem. Sci. 15:1990;277-281.
-
(1990)
Trends Biochem. Sci.
, vol.15
, pp. 277-281
-
-
Wickens, M.1
-
48
-
-
0028969404
-
Angelman syndrome: A consensus for diagnostic criteria
-
Williams C. A., Angelman H., Clayton-Smith J., Driscoll D. J., Hendrickson J. E., Knoll J. H. M., Magenis R. E., Schinzel A., Wagstaff J., Whidden E. M., Zori R. T. Angelman syndrome: A consensus for diagnostic criteria. Am. J. Med. Genet. 56:1995;237-238.
-
(1995)
Am. J. Med. Genet.
, vol.56
, pp. 237-238
-
-
Williams, C.A.1
Angelman, H.2
Clayton-Smith, J.3
Driscoll, D.J.4
Hendrickson, J.E.5
Knoll, J.H.M.6
Magenis, R.E.7
Schinzel, A.8
Wagstaff, J.9
Whidden, E.M.10
Zori, R.T.11
-
49
-
-
0027957814
-
Testis-specific and ubiquitous proteins bind to functionally important regions of the mouse protamine-1 promoter
-
Zambrowicz B. P., Palmiter R. D. Testis-specific and ubiquitous proteins bind to functionally important regions of the mouse protamine-1 promoter. Biol. Reprod. 50:1994;65-72.
-
(1994)
Biol. Reprod.
, vol.50
, pp. 65-72
-
-
Zambrowicz, B.P.1
Palmiter, R.D.2
-
50
-
-
0027198863
-
Analysis of the mouse protamine 1 promoter in transgenic mice
-
Zambrowicz B. P., Harendza C. J., Zimmermann J. W., Brinster R. L., Palmiter R. D. Analysis of the mouse protamine 1 promoter in transgenic mice. Proc. Natl. Acad. Sci. USA. 90:1993;5071-5075.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 5071-5075
-
-
Zambrowicz, B.P.1
Harendza, C.J.2
Zimmermann, J.W.3
Brinster, R.L.4
Palmiter, R.D.5
-
51
-
-
0031927957
-
A gene-specific promoter in transgenic mice directs testis-specific demethylation prior to transcriptional activation in vivo
-
Zhang L. P., Stroud J. C., Walter C. A., Adrian G. S., McCarrey J. R. A gene-specific promoter in transgenic mice directs testis-specific demethylation prior to transcriptional activation in vivo. Biol. Reprod. 59:1998a;284-292.
-
(1998)
Biol. Reprod.
, vol.59
, pp. 284-292
-
-
Zhang, L.P.1
Stroud, J.C.2
Walter, C.A.3
Adrian, G.S.4
McCarrey, J.R.5
-
52
-
-
0031979512
-
Expression of germ cell nuclear factor (GCNF/RTR) during spermatogenesis
-
Zhang Y. L., Akmal K. M., Tsuruta J. K., Shang Q., Hirose T., Jetten A. M., Kim K. H., O'Brien D. A. Expression of germ cell nuclear factor (GCNF/RTR) during spermatogenesis. Mol. Reprod. Dev. 50:1998b;93-102.
-
(1998)
Mol. Reprod. Dev.
, vol.50
, pp. 93-102
-
-
Zhang, Y.L.1
Akmal, K.M.2
Tsuruta, J.K.3
Shang, Q.4
Hirose, T.5
Jetten, A.M.6
Kim, K.H.7
O'Brien, D.A.8
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