-
1
-
-
0033361765
-
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints
-
Amos-Landgraf, J.M., Y. Ji, W. Gottlieb, T. Depinet, A. Wandstradt, S.B. Cassidy, D.J. Driscoll, P.K. Rogan, S. Schwartz, and R.D. Nicholls. 1999. Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints. Am. J. Hum. Genet. 65: 370-386.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 370-386
-
-
Amos-Landgraf, J.M.1
Ji, Y.2
Gottlieb, W.3
Depinet, T.4
Wandstradt, A.5
Cassidy, S.B.6
Driscoll, D.J.7
Rogan, P.K.8
Schwartz, S.9
Nicholls, R.D.10
-
2
-
-
0022540321
-
CpG-rich islands and the function of DNA methylation
-
Bird, A.P. 1986. CpG-rich islands and the function of DNA methylation. Nature 321: 209-213.
-
(1986)
Nature
, vol.321
, pp. 209-213
-
-
Bird, A.P.1
-
3
-
-
0031444629
-
Inherited interstitial duplications of proximal 15q: Genotype-phenotype correlations
-
Browne, C.E., N.R. Dennis, E. Maher, F.L. Long, J.C. Nicholson, J. Sillibourne, and J.C.K. Barber. 1997. Inherited interstitial duplications of proximal 15q: Genotype-phenotype correlations. Am. J. Hum. Genet. 61: 1342-1352.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 1342-1352
-
-
Browne, C.E.1
Dennis, N.R.2
Maher, E.3
Long, F.L.4
Nicholson, J.C.5
Sillibourne, J.6
Barber, J.C.K.7
-
4
-
-
0031663726
-
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes
-
Buiting, K., S. Gross, Y. Ji, G. Senger, R.D. Nicholls, and B. Horsthemke. 1998. Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes. Cytogenet. Cell Genet. 81: 247-253.
-
(1998)
Cytogenet. Cell Genet.
, vol.81
, pp. 247-253
-
-
Buiting, K.1
Gross, S.2
Ji, Y.3
Senger, G.4
Nicholls, R.D.5
Horsthemke, B.6
-
5
-
-
0001427838
-
Paternal triplication of 15q11-q13 in a hypotonic, developmentally delayed child without Prader-Willi or Angelman syndrome
-
Cassidy, S.B., J. Conroy, L. Becker, and S. Schwartz. 1996. Paternal triplication of 15q11-q13 in a hypotonic, developmentally delayed child without Prader-Willi or Angelman syndrome. Am. J. Med. Genet. 62: 206-207.
-
(1996)
Am. J. Med. Genet.
, vol.62
, pp. 206-207
-
-
Cassidy, S.B.1
Conroy, J.2
Becker, L.3
Schwartz, S.4
-
6
-
-
0032509302
-
Genome sequence of the nematode C. Elegans: A platform for investigating biology
-
published erratum appears in Science 1998 283 35
-
The C. elegans Sequencing Consortium. 1998. Genome sequence of the nematode C. elegans: A platform for investigating biology [published erratum appears in Science 1998 283 35]. Science 282: 2012-2018.
-
(1998)
Science
, vol.282
, pp. 2012-2018
-
-
-
7
-
-
0030881588
-
Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome
-
Chen, K.S., P. Manian, T. Koeuth, L. Potocki, Q. Zhao, A.C. Chinault, C.C. Lee, and J.R. Lupski. 1997. Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome. Nat. Genet. 17: 154-163.
-
(1997)
Nat. Genet.
, vol.17
, pp. 154-163
-
-
Chen, K.S.1
Manian, P.2
Koeuth, T.3
Potocki, L.4
Zhao, Q.5
Chinault, A.C.6
Lee, C.C.7
Lupski, J.R.8
-
8
-
-
0032971379
-
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)
-
Christian, S.L., J.A. Fantes, S.K. Mewborn, B. Huang, and D.H. Ledbetter. 1999. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13). Hum. Mol. Genet. 8: 1025-1037.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1025-1037
-
-
Christian, S.L.1
Fantes, J.A.2
Mewborn, S.K.3
Huang, B.4
Ledbetter, D.H.5
-
9
-
-
0028244102
-
Structural organization of the human type VII collagen gene (COL7A1), composed of more exons than any previously characterized gene
-
Christiano, A.M., G.G. Hoffman, L.C. Chung-Honet, S. Lee, W. Cheng, J. Uitto, and D.S. Greenspan. 1994. Structural organization of the human type VII collagen gene (COL7A1), composed of more exons than any previously characterized gene. Genomics 21: 69-79.
-
(1994)
Genomics
, vol.21
, pp. 69-79
-
-
Christiano, A.M.1
Hoffman, G.G.2
Chung-Honet, L.C.3
Lee, S.4
Cheng, W.5
Uitto, J.6
Greenspan, D.S.7
-
11
-
-
0027231008
-
Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome
-
Clayton-Smirh, J., T. Webb, X.J. Cheng, M.E. Pembrey, and S. Malcolm. 1993a. Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome. J. Med. Genet. 30: 529-531.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 529-531
-
-
Clayton-Smirh, J.1
Webb, T.2
Cheng, X.J.3
Pembrey, M.E.4
Malcolm, S.5
-
12
-
-
0027520382
-
Difference in methylation patterns within the D15S9 region of chromosome 15q11-q13 in first cousins with Angelman syndrome and Prader-Willi syndrome
-
Clayton-Smith, J., D.J. Driscoll, M.F. Waters, T. Webb, T. Andrews, S. Malcolm, M.E. Pembrey, and R.D. Nicholls. 1993b. Difference in methylation patterns within the D15S9 region of chromosome 15q11-q13 in first cousins with Angelman syndrome and Prader-Willi syndrome. Am. J. Med. Genet. 47: 683-686.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 683-686
-
-
Clayton-Smith, J.1
Driscoll, D.J.2
Waters, M.F.3
Webb, T.4
Andrews, T.5
Malcolm, S.6
Pembrey, M.E.7
Nicholls, R.D.8
-
13
-
-
0027373292
-
Structural characterization of the complete human perlecan gene and its promoter
-
Cohen, I.R., S. Grassel, A.D. Murdoch, and R.Y. Iozzo. 1993. Structural characterization of the complete human perlecan gene and its promoter. Proc. Natl. Acad. Sci. 90: 10404-10408.
-
(1993)
Proc. Natl. Acad. Sci.
, vol.90
, pp. 10404-10408
-
-
Cohen, I.R.1
Grassel, S.2
Murdoch, A.D.3
Iozzo, R.Y.4
-
14
-
-
0030950736
-
The organization of the γ-glutamyl transferase genes and other low copy repeats in human chromosome 22q11
-
Collins, J.E., A.J. Mungall, K.L. Badcock, J.M. Fay, and I. Dunham. 1997. The organization of the γ-glutamyl transferase genes and other low copy repeats in human chromosome 22q11. Genome Res. 7: 522-531.
-
(1997)
Genome Res.
, vol.7
, pp. 522-531
-
-
Collins, J.E.1
Mungall, A.J.2
Badcock, K.L.3
Fay, J.M.4
Dunham, I.5
-
15
-
-
79960655760
-
The DNA sequence of human chromosome 22
-
Dunham, I., N. Shimizu, B.A. Roe, S. Chissoe, A.R. Hunt, J.E. Collins, R. Bruskiewich, D.M. Beare, M. Clamp, L.J. Smink et al. 1999. The DNA sequence of human chromosome 22. Nature 402: 489-495.
-
(1999)
Nature
, vol.402
, pp. 489-495
-
-
Dunham, I.1
Shimizu, N.2
Roe, B.A.3
Chissoe, S.4
Hunt, A.R.5
Collins, J.E.6
Bruskiewich, R.7
Beare, D.M.8
Clamp, M.9
Smink, L.J.10
-
16
-
-
0033358588
-
Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome
-
Edelmann, L., R.K. Pandita, and B.E. Morrow. 1999a. Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome. Am. J. Hum. Genet. 64: 1076-1086.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1076-1086
-
-
Edelmann, L.1
Pandita, R.K.2
Morrow, B.E.3
-
17
-
-
0032790898
-
A common molecular basis for rearrangement disorders on chromosome 22q11
-
Edelmann, L., R.K. Pandita, E. Spiteri, B. Funke, R. Goldberg, N. Palanisamy, R.S. Chaganti, E. Magenis, R.J. Shprintzen, and B.E. Morrow. 1999b. A common molecular basis for rearrangement disorders on chromosome 22q11. Hum. Mol. Genet. 8: 1157-1167.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1157-1167
-
-
Edelmann, L.1
Pandita, R.K.2
Spiteri, E.3
Funke, B.4
Goldberg, R.5
Palanisamy, N.6
Chaganti, R.S.7
Magenis, E.8
Shprintzen, R.J.9
Morrow, B.E.10
-
18
-
-
0032428381
-
A model system to study genomic imprinting of human genes
-
Gabriel, J.M., M.J. Higgins, T.C. Gebuhr, T. Shows, S. Saitoh, and R.D. Nicholls. 1998. A model system to study genomic imprinting of human genes. Proc. Natl. Acad. Sci. 95: 14857-14862.
-
(1998)
Proc. Natl. Acad. Sci.
, vol.95
, pp. 14857-14862
-
-
Gabriel, J.M.1
Higgins, M.J.2
Gebuhr, T.C.3
Shows, T.4
Saitoh, S.5
Nicholls, R.D.6
-
19
-
-
0033529801
-
A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and Angelman syndrome
-
Gabriel, J.M., M. Merchant, T. Ohta, Y. Ji, R.G. Caldwell, M.J. Ramsey, J.D. Tucker, R. Longnecker, and R.D. Nicholls. 1999. A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and Angelman syndrome. Proc. Natl. Acad. Sci. 96: 9258-9263.
-
(1999)
Proc. Natl. Acad. Sci.
, 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
-
20
-
-
0033360816
-
The genomic record of Humankind's evolutionary roots
-
Goodman, M. 1999. The genomic record of Humankind's evolutionary roots. Am. J. Hum. Genet. 64: 31-39.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 31-39
-
-
Goodman, M.1
-
21
-
-
0033553403
-
Characterization of the DOC1/APC10 subunit of the yeast and the human anaphase-promoting complex
-
Grossberger, R., C. Gieffers, W. Zachariae, A.V. Podtelejnikov, A. Schleiffer, K. Nasmyth, M. Mann, and J.M. Peters. 1999. Characterization of the DOC1/APC10 subunit of the yeast and the human anaphase-promoting complex. J. Biol. Chem. 274: 14500-14507.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 14500-14507
-
-
Grossberger, R.1
Gieffers, C.2
Zachariae, W.3
Podtelejnikov, A.V.4
Schleiffer, A.5
Nasmyth, K.6
Mann, M.7
Peters, J.M.8
-
22
-
-
0031799965
-
Protein phosphatase 4 is an essential enzyme required for organisation of microtubules at centrosomes in Drosophila embryos
-
Helps, N.R., N.D. Brewis, K. Lineruth, T. Davis, K. Kaiser, and P.T. Cohen. 1998. Protein phosphatase 4 is an essential enzyme required for organisation of microtubules at centrosomes in Drosophila embryos. J. Cell Sci. 111: 1331-1340.
-
(1998)
J. Cell Sci.
, vol.111
, pp. 1331-1340
-
-
Helps, N.R.1
Brewis, N.D.2
Lineruth, K.3
Davis, T.4
Kaiser, K.5
Cohen, P.T.6
-
23
-
-
0031060712
-
Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes
-
Huang, B., J.A. Crolla, S.L. Christian, M.E. Wolf-Ledbetter, M.E. Macha, P.N. Papenhausen, and D.H. Ledbetter. 1997. Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes. Hum. Genet. 99: 11-17.
-
(1997)
Hum. Genet.
, vol.99
, pp. 11-17
-
-
Huang, B.1
Crolla, J.A.2
Christian, S.L.3
Wolf-Ledbetter, M.E.4
Macha, M.E.5
Papenhausen, P.N.6
Ledbetter, D.H.7
-
24
-
-
0033016617
-
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities
-
Ji, Y., M.J. Walkowicz, K. Buiting, D.K. Johnson, R.E. Tarvin, E.M. Rinchik, B. Horsthemke, L. Stubbs, and R.D. Nicholls. 1999. The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities. Hum. Mol. Genet. 8: 533-542.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 533-542
-
-
Ji, Y.1
Walkowicz, M.J.2
Buiting, K.3
Johnson, D.K.4
Tarvin, R.E.5
Rinchik, E.M.6
Horsthemke, B.7
Stubbs, L.8
Nicholls, R.D.9
-
25
-
-
0031803462
-
A map of 75 human ribosomal protein genes
-
Kenmochi, N., T. Kawaguchi, S. Rozen, E. Davis, N. Goodman, T.J. Hudson, T. Tanaka, and D.C. Page. 1998. A map of 75 human ribosomal protein genes. Genome Res. 8: 509-523.
-
(1998)
Genome Res.
, vol.8
, pp. 509-523
-
-
Kenmochi, N.1
Kawaguchi, T.2
Rozen, S.3
Davis, E.4
Goodman, N.5
Hudson, T.J.6
Tanaka, T.7
Page, D.C.8
-
26
-
-
0029931130
-
Structure of mouse type VII collagen reveals evolutionary conservation of functional protein domains and genomic organization
-
Kivirikko, S., K. Li, A.M. Christiano, and J. Uitto. 1996. Structure of mouse type VII collagen reveals evolutionary conservation of functional protein domains and genomic organization. J. Invest. Dermatol. 106: 1300-1306
-
(1996)
J. Invest. Dermatol.
, vol.106
, pp. 1300-1306
-
-
Kivirikko, S.1
Li, K.2
Christiano, A.M.3
Uitto, J.4
-
27
-
-
0028942723
-
Organization and sequence of the human P gene and identification of a new family of transport proteins
-
Lee, S.T., R.D. Nicholls, M.T. Jong, K. Fukai, and R.A. Spritz. 1995. Organization and sequence of the human P gene and identification of a new family of transport proteins. Genomics 26: 354-363.
-
(1995)
Genomics
, vol.26
, pp. 354-363
-
-
Lee, S.T.1
Nicholls, R.D.2
Jong, M.T.3
Fukai, K.4
Spritz, R.A.5
-
28
-
-
13144294984
-
A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice
-
Lehman, A.L., Y. Nakatsu, A. Ching, R.T. Bronson, R.J. Oakey, N. Keipo-Hrynko, J.N. Finger, D. Durham-Pierre, D.B. Horton, J.M. Newton et al. 1998. A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice. Proc. Natl. Acad. Sci. 95: 9436-9441.
-
(1998)
Proc. Natl. Acad. Sci.
, vol.95
, pp. 9436-9441
-
-
Lehman, A.L.1
Nakatsu, Y.2
Ching, A.3
Bronson, R.T.4
Oakey, R.J.5
Keipo-Hrynko, N.6
Finger, J.N.7
Durham-Pierre, D.8
Horton, D.B.9
Newton, J.M.10
-
29
-
-
0032695458
-
Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: A study of 17p11.2 rearrangements associated with CMT1A and HNPP. Hum
-
Lopes, J., S. Tardieu, K. Silander, I. Blair, A. Vandenberghe, F. Palau, M. Ruberg, A. Brice, and E. LeGuern. 1999. Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: A study of 17p11.2 rearrangements associated with CMT1A and HNPP. Hum. Mol. Genet. 8: 2285-2292.
-
(1999)
Mol. Genet.
, vol.8
, pp. 2285-2292
-
-
Lopes, J.1
Tardieu, S.2
Silander, K.3
Blair, I.4
Vandenberghe, A.5
Palau, F.6
Ruberg, M.7
Brice, A.8
LeGuern, E.9
-
30
-
-
0031731487
-
Genomic disorders: Structural features of the genome can lead to DNA rearrangements and human disease traits
-
Lupski, J.R. 1998. Genomic disorders: Structural features of the genome can lead to DNA rearrangements and human disease traits. Trends Genet. 14: 417-422.
-
(1998)
Trends Genet.
, vol.14
, pp. 417-422
-
-
Lupski, J.R.1
-
31
-
-
0029835707
-
Defects in RNA splicing and the consequence of shortened translational reading frames
-
Maquat, L.E. 1996. Defects in RNA splicing and the consequence of shortened translational reading frames. Am. J. Hum. Genet. 59: 279-286.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 279-286
-
-
Maquat, L.E.1
-
32
-
-
8544240102
-
Overview of the yeast genome
-
published erratum appears in Nature 1997, 387: 737
-
Mewes, H.W., K. Albermann, M. Bahr, D. Frishman, A. Gleissner, J. Hani, K. Heumann, K. Kleine, A. Maierl, S.G. Oliver et al. 1997. Overview of the yeast genome [published erratum appears in Nature 1997, 387: 737]. Nature (Suppl.) 387: 7-65.
-
(1997)
Nature
, vol.387
, Issue.SUPPL.
, pp. 7-65
-
-
Mewes, H.W.1
Albermann, K.2
Bahr, M.3
Frishman, D.4
Gleissner, A.5
Hani, J.6
Heumann, K.7
Kleine, K.8
Maierl, A.9
Oliver, S.G.10
-
33
-
-
0032076307
-
Imprinting in Prader-Willi and Angelman syndromes
-
Nicholls, R.D., S. Saitoh, and B. Horsthemke. 1998. Imprinting in Prader-Willi and Angelman syndromes. Trends Genet. 14: 194-200.
-
(1998)
Trends Genet.
, vol.14
, pp. 194-200
-
-
Nicholls, R.D.1
Saitoh, S.2
Horsthemke, B.3
-
34
-
-
0028685657
-
Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1
-
Nomura, N., N. Miyajima, T. Sazuka, A. Tanaka, Y. Kawarabayasi, S. Sato, T. Nagase, N. Seki, K. Ishikawa, and S. Tabata. 1994. Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1. DNA Res. 1: 27-35.
-
(1994)
DNA Res.
, vol.1
, pp. 27-35
-
-
Nomura, N.1
Miyajima, N.2
Sazuka, T.3
Tanaka, A.4
Kawarabayasi, Y.5
Sato, S.6
Nagase, T.7
Seki, N.8
Ishikawa, K.9
Tabata, S.10
-
35
-
-
0028123735
-
Members of a family of Drosophila putative odorant-binding proteins are expressed in different subsets of olfactory hairs
-
Pikielny, C.W., G. Hasan, F. Rouyer, and M. Rosbash. 1994. Members of a family of Drosophila putative odorant-binding proteins are expressed in different subsets of olfactory hairs. Neuron 12: 35-49.
-
(1994)
Neuron
, vol.12
, pp. 35-49
-
-
Pikielny, C.W.1
Hasan, G.2
Rouyer, F.3
Rosbash, M.4
-
36
-
-
0032169436
-
Interstitial duplications of chromosome region 15q11q13: Clinical and molecular characterization
-
Repetto, G.M., L.M. White, P.J. Bader, D. Johnson, and J.H.M. Knoll. 1998. Interstitial duplications of chromosome region 15q11q13: Clinical and molecular characterization. Am. J. Med. Genet. 9: 82-89.
-
(1998)
Am. J. Med. Genet.
, vol.9
, pp. 82-89
-
-
Repetto, G.M.1
White, L.M.2
Bader, P.J.3
Johnson, D.4
Knoll, J.H.M.5
-
37
-
-
0027792161
-
Clinical and molecular analysis of five inv dup(15) patients
-
Robinson, W.P., F. Binkert, R. Gine, C. Vazques, W. Miller, W. Rosenkranz, and A. Schinzel. 1993. Clinical and molecular analysis of five inv dup(15) patients. Eur. J. Hum. Genet. 1: 37-50.
-
(1993)
Eur. J. Hum. Genet.
, vol.1
, pp. 37-50
-
-
Robinson, W.P.1
Binkert, F.2
Gine, R.3
Vazques, C.4
Miller, W.5
Rosenkranz, W.6
Schinzel, A.7
-
38
-
-
0030787047
-
A giant protein that stimulates guanine nucleotide exchange on ARF1 and Rab proteins forms a cytosolic ternary complex with clathrin and Hsp70
-
Rosa, J.L. and M. Barbacid. 1997. A giant protein that stimulates guanine nucleotide exchange on ARF1 and Rab proteins forms a cytosolic ternary complex with clathrin and Hsp70. Oncogene 15: 1-6.
-
(1997)
Oncogene
, vol.15
, pp. 1-6
-
-
Rosa, J.L.1
Barbacid, M.2
-
39
-
-
0029758214
-
p619, a giant protein related to the chromosome condensation regulator RCC1, stimulates guanine nucleotide exchange on ARF1 and Rab proteins
-
published erratum appears in EMBO J. 1996, 15: 5738
-
Rosa, J.L., R.P. Casaroli-Marano, A.J. Buckler, S. Vilaro, and M. Barbacid. 1996. p619, a giant protein related to the chromosome condensation regulator RCC1, stimulates guanine nucleotide exchange on ARF1 and Rab proteins [published erratum appears in EMBO J. 1996, 15: 5738]. EMBO J. 15: 4262-4273.
-
(1996)
EMBO J.
, vol.15
, pp. 4262-4273
-
-
Rosa, J.L.1
Casaroli-Marano, R.P.2
Buckler, A.J.3
Vilaro, S.4
Barbacid, M.5
-
40
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Sambrook, J., E.F. Fritsch, and T. Maniatis. 1989. Molecular cloning: A laboratory manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual, 2nd Ed.
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
41
-
-
0028081050
-
Intrachromosomal triplication of 15q11-q13
-
Schinzel, A.A., L. Brecevic, F. Bernasconi, F. Binkert, F. Berthet, A. Wuilloud, and W.P. Robinson. 1994. Intrachromosomal triplication of 15q11-q13. J. Med. Genet. 31: 798-803.
-
(1994)
J. Med. Genet.
, vol.31
, pp. 798-803
-
-
Schinzel, A.A.1
Brecevic, L.2
Bernasconi, F.3
Binkert, F.4
Berthet, F.5
Wuilloud, A.6
Robinson, W.P.7
-
42
-
-
0033020727
-
Isolation of DNA fragments associated with methylated CpG islands in human adenocarcinomas of the lung using a methylated DNA binding column and denaturing gradient gel electrophoresis
-
Shiraishi, M., Y.H. Chuu, and T. Sekiya. 1999. Isolation of DNA fragments associated with methylated CpG islands in human adenocarcinomas of the lung using a methylated DNA binding column and denaturing gradient gel electrophoresis. Proc. Natl. Acad. Sci. 96: 2913-2918.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 2913-2918
-
-
Shiraishi, M.1
Chuu, Y.H.2
Sekiya, T.3
-
43
-
-
0032831272
-
Molecular characterization of radiation-and chemically-induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice
-
Walkowicz, M., Y. Ji, X. Ren, B. Horsthemke, L.B. Russell, D.K. Johnson, E.M. Rinchik, R.D. Nicholls, and L. Stubbs. 1999. Molecular characterization of radiation-and chemically-induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice. Mamm. Genome 10: 870-878.
-
(1999)
Mamm. Genome
, vol.10
, pp. 870-878
-
-
Walkowicz, M.1
Ji, Y.2
Ren, X.3
Horsthemke, B.4
Russell, L.B.5
Johnson, D.K.6
Rinchik, E.M.7
Nicholls, R.D.8
Stubbs, L.9
-
44
-
-
0031946990
-
Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15
-
Wandstrat, A.E., J. Leana-Cox, L. Jenkins, and S. Schwartz. 1998. Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15. Am. J. Hum. Genet. 62: 925-936.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 925-936
-
-
Wandstrat, A.E.1
Leana-Cox, J.2
Jenkins, L.3
Schwartz, S.4
|