-
2
-
-
0023277545
-
Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction
-
2. Chomczynski, P., and Sacchi, N. (1987). Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162: 156-159.
-
(1987)
Anal. Biochem.
, vol.162
, pp. 156-159
-
-
Chomczynski, P.1
Sacchi, N.2
-
3
-
-
0027158855
-
Parental genomic imprinting of the human IGF2 gene
-
3. Giannoukakis, N., Deal, C., Paquette, J., Goodyer, C. G., and Polychronakos, C. (1993). Parental genomic imprinting of the human IGF2 gene. Nature Genet. 4: 98-101.
-
(1993)
Nature Genet.
, vol.4
, pp. 98-101
-
-
Giannoukakis, N.1
Deal, C.2
Paquette, J.3
Goodyer, C.G.4
Polychronakos, C.5
-
4
-
-
0027169927
-
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients
-
4. Glenn, C. C., Nicholls, R. D., Robinson, W. P., Saitoh, S., Niikawa, N., Schinzel, A., Horsthemke, B., and Driscoll, D. J. (1993). Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients. Hum. Mol. Genet. 2: 1377-1382.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1377-1382
-
-
Glenn, C.C.1
Nicholls, R.D.2
Robinson, W.P.3
Saitoh, S.4
Niikawa, N.5
Schinzel, A.6
Horsthemke, B.7
Driscoll, D.J.8
-
5
-
-
0029114716
-
Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization
-
5. Kaneko-Ishino, T., Kuroiwa, Y., Miyoshi, N., Kohda, T., Suzuki, R., Yokoyama, M., Viville, S., Barton, S. C., Ishino, F., and Surani, M. A. (1995). Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nature Genet. 11: 52-59.
-
(1995)
Nature Genet.
, vol.11
, pp. 52-59
-
-
Kaneko-Ishino, T.1
Kuroiwa, Y.2
Miyoshi, N.3
Kohda, T.4
Suzuki, R.5
Yokoyama, M.6
Viville, S.7
Barton, S.C.8
Ishino, F.9
Surani, M.A.10
-
6
-
-
0028914364
-
Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
-
6. Kotzot, D., Schmitt, S., Bernasconi, F., Robinson, W. P., Lurie, I. W., Ilyina, H., Méhes, K., Hamel, B. C. J., Otten, B. J., Hergersberg, M., Werder, E., Shoenle, E., and Schinzel, A. (1995). Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. Hum. Mol. Genet. 4: 583-587.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 583-587
-
-
Kotzot, D.1
Schmitt, S.2
Bernasconi, F.3
Robinson, W.P.4
Lurie, I.W.5
Ilyina, H.6
Méhes, K.7
Hamel, B.C.J.8
Otten, B.J.9
Hergersberg, M.10
Werder, E.11
Shoenle, E.12
Schinzel, A.13
-
7
-
-
0028105734
-
Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome
-
7. Kubota, T., Saitoh, S., Matsumoto, T., Narahara, K., Fukushima, Y., Jinno, Y., and Niikawa, N. (1994). Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome. Am. J. Med. Genet. 49:378-383.
-
(1994)
Am. J. Med. Genet.
, vol.49
, pp. 378-383
-
-
Kubota, T.1
Saitoh, S.2
Matsumoto, T.3
Narahara, K.4
Fukushima, Y.5
Jinno, Y.6
Niikawa, N.7
-
8
-
-
0027290868
-
Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes
-
8. Nicholls, R. D. (1993). Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes. Curr. Opin. Genet. Dev. 3: 445-456.
-
(1993)
Curr. Opin. Genet. Dev.
, vol.3
, pp. 445-456
-
-
Nicholls, R.D.1
-
9
-
-
0021809891
-
Origin of immature teratoma of the ovary
-
9. Ohma, K., Nomura, K., Okamoto, E., Fukuda, Y., Ihara, T., and Fujiwara, A. (1985). Origin of immature teratoma of the ovary. Am. J. Obstet. Gynecol. 152: 896-900.
-
(1985)
Am. J. Obstet. Gynecol.
, vol.152
, pp. 896-900
-
-
Ohma, K.1
Nomura, K.2
Okamoto, E.3
Fukuda, Y.4
Ihara, T.5
Fujiwara, A.6
-
10
-
-
0028289468
-
Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome
-
10. Reed, M. L., and Leff, S. E. (1994). Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome. Nature Genet. 6: 163-167.
-
(1994)
Nature Genet.
, vol.6
, pp. 163-167
-
-
Reed, M.L.1
Leff, S.E.2
-
11
-
-
0027439329
-
A novel mesoderm-specific cDNA isolated from a mouse embryonal carcinoma cell line
-
11. Sado, T., Nakajima, N., Tada, M., and Takagi, N. (1993). A novel mesoderm-specific cDNA isolated from a mouse embryonal carcinoma cell line. Dev. Growth Differ. 35: 551-560.
-
(1993)
Dev. Growth Differ.
, vol.35
, pp. 551-560
-
-
Sado, T.1
Nakajima, N.2
Tada, M.3
Takagi, N.4
-
12
-
-
0025200279
-
R-banding and nonisotopic in situ hybridization: Precise localization of the human type II collagen gene (COL2A1)
-
12. Takahashi, E., Hori, T., O'connell, P., Leppert, M., and White, R. (1990). R-banding and nonisotopic in situ hybridization: Precise localization of the human type II collagen gene (COL2A1). Hum. Genet. 86: 14-16.
-
(1990)
Hum. Genet.
, vol.86
, pp. 14-16
-
-
Takahashi, E.1
Hori, T.2
O'connell, P.3
Leppert, M.4
White, R.5
-
13
-
-
0018136630
-
Androgenesis as a course of hydatidiform mole
-
13. Wake, N., Takagi, N., and Sasaki, M. (1978). Androgenesis as a course of hydatidiform mole. Natl. Cancer Inst. 60: 51-57.
-
(1978)
Natl. Cancer Inst.
, vol.60
, pp. 51-57
-
-
Wake, N.1
Takagi, N.2
Sasaki, M.3
-
14
-
-
0029916644
-
The mouse gene for P1MCM3 protein involved in DNA replication maps to bands A3-A5 on chromosome 1 by fluorescence in situ hybridization
-
14. Yoshida, I., Kimura, H., and Takagi, N. (1996). The mouse gene for P1MCM3 protein involved in DNA replication maps to bands A3-A5 on chromosome 1 by fluorescence in situ hybridization. Genomics 32: 483-484.
-
(1996)
Genomics
, vol.32
, pp. 483-484
-
-
Yoshida, I.1
Kimura, H.2
Takagi, N.3
-
15
-
-
0027496294
-
Imprinting of human H19: Allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching
-
15. Zhang, Y., Shields, T., Crenshaw, T., Hao, Y., Moulton, T., and Tycko, B. (1993). Imprinting of human H19: Allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching. Am. J. Hum. Genet. 53: 113-124.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 113-124
-
-
Zhang, Y.1
Shields, T.2
Crenshaw, T.3
Hao, Y.4
Moulton, T.5
Tycko, B.6
|