-
1
-
-
0035228079
-
X-chromosome inactivation: Counting, choice and initiation
-
Avner, P. and Heard, E. 2001. X-chromosome inactivation: Counting, choice and initiation. Nat. Rev. Genet. 2: 59-67.
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 59-67
-
-
Avner, P.1
Heard, E.2
-
2
-
-
0034744639
-
Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer
-
Baylin, S.B., Esteller, M., Rountree, M.R., Bachman, K.E., Schuebel, K., and Herman, J.G. 2001. Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer. Hum. Mol. Genet. 10: 687-692.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 687-692
-
-
Baylin, S.B.1
Esteller, M.2
Rountree, M.R.3
Bachman, K.E.4
Schuebel, K.5
Herman, J.G.6
-
4
-
-
0035930660
-
Dnmt3L and the establishment of maternal genomic imprints
-
Bourchis, D., Xu, G.L., Lin, C.S., Bollman, B., and Bestor, T.H. 2001. Dnmt3L and the establishment of maternal genomic imprints, Science 294: 2536-2539.
-
(2001)
Science
, vol.294
, pp. 2536-2539
-
-
Bourchis, D.1
Xu, G.L.2
Lin, C.S.3
Bollman, B.4
Bestor, T.H.5
-
5
-
-
0031844688
-
Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster
-
Caspary, T., Cleary, M.A., Baker, C.C., Guan, X.J., and Tilghman, S.M. 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
-
6
-
-
0034862306
-
Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice
-
Cleary, M.A., van Raamsdonk, C.D., Levorse, J., Zheng, B., Bradley, A,. and Tilghman, S.M. 2001. Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice. Nat. Genet. 29: 78-82.
-
(2001)
Nat. Genet.
, vol.29
, pp. 78-82
-
-
Cleary, M.A.1
van Raamsdonk, C.D.2
Levorse, J.3
Zheng, B.4
Bradley, A.5
Tilghman, S.M.6
-
7
-
-
0031924628
-
IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes
-
Dao, D., Frank, D., Qian, N., O'Keefe, D., Vosatka, R.J., Walsh, C.P., and Tycko, B. 1998. IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes. Hum. Mol. Genet. 7: 597-608.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 597-608
-
-
Dao, D.1
Frank, D.2
Qian, N.3
O'Keefe, D.4
Vosatka, R.J.5
Walsh, C.P.6
Tycko, B.7
-
8
-
-
0034326859
-
Sequence and functional comparison in the Beckwith-Wiedemann region: Implications for a novel imprinting centre and extended imprinting
-
Engemann, S., Strodicke, M., Paulsen, M., Franck, O., Reinhardt, R., Lane, N., Reik, W., and Walter, J. 2000. Sequence and functional comparison in the Beckwith-Wiedemann region: Implications for a novel imprinting centre and extended imprinting. Hum. Mol. Genet. 9: 2691-2706.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2691-2706
-
-
Engemann, S.1
Strodicke, M.2
Paulsen, M.3
Franck, O.4
Reinhardt, R.5
Lane, N.6
Reik, W.7
Walter, J.8
-
9
-
-
0033805576
-
The two-domain hypothesis in Beckwith-Wiedemann syndrome
-
Feinberg, A.P. 2000. The two-domain hypothesis in Beckwith-Wiedemann syndrome. J. Clin. Invest. 106: 739-740.
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 739-740
-
-
Feinberg, A.P.1
-
10
-
-
0035839064
-
Imprinting and the epigenetic asymmetry between parental genomes
-
Ferguson-Smith, A.C. and Surani, M.A. 2001. Imprinting and the epigenetic asymmetry between parental genomes. Science 293: 1086-1089.
-
(2001)
Science
, vol.293
, pp. 1086-1089
-
-
Ferguson-Smith, A.C.1
Surani, M.A.2
-
11
-
-
0031952115
-
Imprinting of mouse Kvlqt1 is developmentally regulated
-
Gould, T.D. and Pfeifer, K. 1998. Imprinting of mouse Kvlqt1 is developmentally regulated. Hum. Mol. Genet. 7: 483-487.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 483-487
-
-
Gould, T.D.1
Pfeifer, K.2
-
12
-
-
0035102797
-
Establishment and maintenance of DNA methylation patterns in mouse Ndn: Implications for maintenance of imprinting in target genes of the imprinting center
-
Hanel, M.L. and Wevrick, R. 2001. Establishment and maintenance of DNA methylation patterns in mouse Ndn: Implications for maintenance of imprinting in target genes of the imprinting center. Mol. Cell Biol. 21: 2384-2392.
-
(2001)
Mol. Cell Biol.
, vol.21
, pp. 2384-2392
-
-
Hanel, M.L.1
Wevrick, R.2
-
13
-
-
0031769152
-
Chromatin conformation of the H19 epigenetic mark
-
Hark, A.T. and Tilghman, S.M. 1998. Chromatin conformation of the H19 epigenetic mark. Hum. Mol. Genet. 7: 1979-1985.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1979-1985
-
-
Hark, A.T.1
Tilghman, S.M.2
-
14
-
-
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
-
15
-
-
16044364516
-
KIP2 is mutated in Beckwith-Wiedemann syndrome
-
KIP2 is mutated in Beckwith-Wiedemann syndrome. 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
-
16
-
-
0034284693
-
Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
-
Horike, S., Mitsuya, K., Meguro, M., Kotobuki, N., Kashiwagi, A., Notsu, T., Schulz, T.C., Shirayoshi, Y., and Oshimura, M. 2000. Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome. Hum. Mol. Genet. 9: 2075-2083.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2075-2083
-
-
Horike, S.1
Mitsuya, K.2
Meguro, M.3
Kotobuki, N.4
Kashiwagi, A.5
Notsu, T.6
Schulz, T.C.7
Shirayoshi, Y.8
Oshimura, M.9
-
17
-
-
0030817976
-
Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19
-
Hu, J.F., Vu, T.H., and Hoffman, A.R. 1997. Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19. J. Biol. Chem. 272: 20715-20720.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 20715-20720
-
-
Hu, J.F.1
Vu, T.H.2
Hoffman, A.R.3
-
19
-
-
0037124080
-
A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator
-
Kanduri, C., Fitzpatrick, G., Mukhopadhyay, R., Kanduri, M., Lobanenkov, V., Higgins, M., and Ohlsson, R. 2002. A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator. J. Biol. Chem. 277: 18106-18110.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 18106-18110
-
-
Kanduri, C.1
Fitzpatrick, G.2
Mukhopadhyay, R.3
Kanduri, M.4
Lobanenkov, V.5
Higgins, M.6
Ohlsson, R.7
-
21
-
-
0033609117
-
Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
-
Lee, M.P., DeBaun, M.R., Mitsuya, K., Galonek, H.L., Brandenburg, S., Oshimura, M., and Feinberg, A.P. 1999. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. Proc. Natl. Acad. Sci. 96: 5203-5208.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 5203-5208
-
-
Lee, M.P.1
DeBaun, M.R.2
Mitsuya, K.3
Galonek, H.L.4
Brandenburg, S.5
Oshimura, M.6
Feinberg, A.P.7
-
22
-
-
0033975096
-
Beckwith-Wiedemann syndrome: Imprinting in clusters revisited
-
Maher E.R. and Reik, W. 2000. Beckwith-Wiedemann syndrome: Imprinting in clusters revisited. J. Clin. Invest. 105: 247-252.
-
(2000)
J. Clin. Invest.
, vol.105
, pp. 247-252
-
-
Maher, E.R.1
Reik, W.2
-
23
-
-
0032813924
-
LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids
-
Mitsuya, K., Meguro, M., Lee, M.P., Katoh, M., Schulz, T.C., Kugoh, H., Yoshida, M.A., Niikawa, N., Feinberg, A.P., and Oshimura, M. 1999. LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. Hum. Mol. Genet. 8: 1209-1217.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1209-1217
-
-
Mitsuya, K.1
Meguro, M.2
Lee, M.P.3
Katoh, M.4
Schulz, T.C.5
Kugoh, H.6
Yoshida, M.A.7
Niikawa, N.8
Feinberg, A.P.9
Oshimura, M.10
-
25
-
-
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
-
26
-
-
0033665147
-
Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain
-
Onyango, P,, Miller, W., Lehoczky, J., Leung, C.T., Birren, B., Wheelan, S., Dewar, K., and Feinberg, A.P. 2000. Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain. Genome Res. 10: 1697-1710.
-
(2000)
Genome Res.
, vol.10
, pp. 1697-1710
-
-
Onyango, P.1
Miller, W.2
Lehoczky, J.3
Leung, C.T.4
Birren, B.5
Wheelan, S.6
Dewar, K.7
Feinberg, A.P.8
-
27
-
-
0032212130
-
Urea improves efficiency of bisulphite-mediated sequencing of 5′-methylcytosine in genomic DNA
-
Paulin, R., Grigg, G.W., Davey, M.W., and Piper, A.A. 1998. Urea improves efficiency of bisulphite-mediated sequencing of 5′-methylcytosine in genomic DNA. Nucleic Acids Res. 26: 5009-5010.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 5009-5010
-
-
Paulin, R.1
Grigg, G.W.2
Davey, M.W.3
Piper, A.A.4
-
28
-
-
0031750223
-
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5
-
Paulsen, M., Davies, K.R., Bowden, L.M., Villar, A.J., Franck, O., Fuermann, M., Dean, W.L., Moore, T.F., Rodrigues, N., Davies, K.E., et. al. 1998. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. Hum. Mol. Genet. 7: 1149-1159.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1149-1159
-
-
Paulsen, M.1
Davies, K.R.2
Bowden, L.M.3
Villar, A.J.4
Franck, O.5
Fuermann, M.6
Dean, W.L.7
Moore, T.F.8
Rodrigues, N.9
Davies, K.E.10
-
29
-
-
0033858005
-
Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse
-
Paulsen, M., El-Maarri, O., Engemann, S., Strodicke, M., Franck, O., Davies, K., Reinhardt, R., Reik, W., and Walter J. 2000. Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse. Hum. Mol. Genet. 9: 1829-1841.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1829-1841
-
-
Paulsen, M.1
El-Maarri, O.2
Engemann, S.3
Strodicke, M.4
Franck, O.5
Davies, K.6
Reinhardt, R.7
Reik, W.8
Walter, J.9
-
30
-
-
9844265406
-
The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis
-
Qian, N., Frank, D., O'Keefe, D., Dao, D., Zhao, L., Yuan, L., Wang, Q., Keating, M., Walsh, C., and Tycko, B. 1997. The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. Hum. Mol. Genet. 6: 2021-2029.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2021-2029
-
-
Qian, N.1
Frank, D.2
O'Keefe, D.3
Dao, D.4
Zhao, L.5
Yuan, L.6
Wang, Q.7
Keating, M.8
Walsh, C.9
Tycko, B.10
-
31
-
-
0025945632
-
DNA methylation and gene expression
-
Razin, A. and Cedar, H. 1991. DNA methylation and gene expression. Microbiol. Rev. 55: 451-458.
-
(1991)
Microbiol. Rev.
, vol.55
, pp. 451-458
-
-
Razin, A.1
Cedar, H.2
-
32
-
-
0030856668
-
Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome
-
Reik, W. and Maher, E.R. 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
-
33
-
-
0035234557
-
Genomic imprinting: Parental influence on the genome
-
Reik, W. and Walter, J. 2001. Genomic imprinting: Parental influence on the genome. Nat. Rev. Genet. 2: 21-32.
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
34
-
-
0004136246
-
-
3rd ed., chapter 17. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Sambrook, J. and Russell, D.W. 2001. Molecular cloning: A laboratory manual, 3rd ed., chapter 17. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(2001)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Russell, D.W.2
-
35
-
-
0033035048
-
In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit
-
Schweizer, J., Zynger, D., and Francke, U. 1999. In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit. Hum. Mol. Genet. 8: 555-566.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 555-566
-
-
Schweizer, J.1
Zynger, D.2
Francke, U.3
-
36
-
-
0030015418
-
Dynamic methylation adjustment and counting as part of imprinting mechanisms
-
Shemer, R., Birger, Y., Dean, W.L., Reik, W., Riggs, A.D., and Razin, A. 1996. Dynamic methylation adjustment and counting as part of imprinting mechanisms. Proc. Natl. Acad. Sci. 93: 6371-6376.
-
(1996)
Proc. Natl. Acad. Sci.
, vol.93
, pp. 6371-6376
-
-
Shemer, R.1
Birger, Y.2
Dean, W.L.3
Reik, W.4
Riggs, A.D.5
Razin, A.6
-
37
-
-
0030886796
-
Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
-
Shemer, R., Birger, Y., Riggs, A.D., and Razin, A. 1997. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Proc. Natl. Acad. Sci. 94: 10267-10272.
-
(1997)
Proc. Natl. Acad. Sci.
, vol.94
, pp. 10267-10272
-
-
Shemer, R.1
Birger, Y.2
Riggs, A.D.3
Razin, A.4
-
38
-
-
0033529207
-
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome
-
Smilinich, N.J., Day, C.D., Fitzpatrick, G.V., Caldwell, G.M., Lossie, A.C., Cooper, P.R., Smallwood, A.C., Joyce, J.A., Schofield, P.N., Reik, W., et. al. 1999. A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. Proc. Natl. Acad. Sci. 96: 8064-8069.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 8064-8069
-
-
Smilinich, N.J.1
Day, C.D.2
Fitzpatrick, G.V.3
Caldwell, G.M.4
Lossie, A.C.5
Cooper, P.R.6
Smallwood, A.C.7
Joyce, J.A.8
Schofield, P.N.9
Reik, W.10
-
39
-
-
0027400888
-
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal
-
Stöger, R., Kubicka, P., Liu, C.G., Kafri, T., Razin, A., Cedar, H., and Barlow, D.P. 1993. Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. Cell 73: 61-71.
-
(1993)
Cell
, vol.73
, pp. 61-71
-
-
Stöger, R.1
Kubicka, P.2
Liu, C.G.3
Kafri, T.4
Razin, A.5
Cedar, H.6
Barlow, D.P.7
-
40
-
-
0030735169
-
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome
-
Sun, F.L., Dean, W.L., Kelsey, G., Allen, N.D., and 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.L.1
Dean, W.L.2
Kelsey, G.3
Allen, N.D.4
Reik, W.5
-
41
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen, J.L., Duran, K.L., and Bartolomei, M.S. 1998. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes & Dev. 12: 3693-3702.
-
(1998)
Genes & Dev.
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
42
-
-
0033593288
-
The sins of the fathers and mothers: Genomic imprinting in mammalian development
-
Tilghman, S.M. 1999. The sins of the fathers and mothers: Genomic imprinting in mammalian development. Cell 96: 185-193.
-
(1999)
Cell
, vol.96
, pp. 185-193
-
-
Tilghman, S.M.1
-
43
-
-
0028968205
-
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
-
Tremblay, K.D., Saam, J.R., Ingram, R.S., Tilghman, S.M., and Bartolomei, M.S. 1995. A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nat. Genet. 9: 407-413.
-
(1995)
Nat. Genet.
, vol.9
, pp. 407-413
-
-
Tremblay, K.D.1
Saam, J.R.2
Ingram, R.S.3
Tilghman, S.M.4
Bartolomei, M.S.5
-
44
-
-
0032528048
-
Bisulphite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene
-
Warnecke, P.M., Mann, J.R., Frommer, M., and Clark, S.J. 1998. Bisulphite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene. Genomics 51: 182-190.
-
(1998)
Genomics
, vol.51
, pp. 182-190
-
-
Warnecke, P.M.1
Mann, J.R.2
Frommer, M.3
Clark, S.J.4
-
45
-
-
0034733229
-
Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: Long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human
-
Yatsuki, H., Watanabe, H., Hattori, M., Joh, K., Soejima, H., Komoda, H., Xin, Z., Zhu, X., Higashimoto, K., Nishimura, M., et al. 2000. Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: Long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human. DNA Res. 7: 195-206.
-
(2000)
DNA Res.
, vol.7
, pp. 195-206
-
-
Yatsuki, H.1
Watanabe, H.2
Hattori, M.3
Joh, K.4
Soejima, H.5
Komoda, H.6
Xin, Z.7
Zhu, X.8
Higashimoto, K.9
Nishimura, M.10
-
46
-
-
0028948179
-
The modified method of two-step differential extraction of sperm and vaginal epithelial cell DNA from vaginal fluid mixed with semen
-
Yoshida, K., Sekiguchi, K., Mizuno, N., Kasai, K., Sakai, I., Sato, H., and Seta, S. 1995. The modified method of two-step differential extraction of sperm and vaginal epithelial cell DNA from vaginal fluid mixed with semen. Forensic Sci. Int. 72: 25-33.
-
(1995)
Forensic Sci. Int.
, vol.72
, pp. 25-33
-
-
Yoshida, K.1
Sekiguchi, K.2
Mizuno, N.3
Kasai, K.4
Sakai, I.5
Sato, H.6
Seta, S.7
-
47
-
-
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
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