-
1
-
-
0033593288
-
The sins of the fathers and mothers: Genomic imprinting in mammalian development
-
Tilghman SM. The sins of the fathers and mothers: genomic imprinting in mammalian development. Cell 1999;96:185-93.
-
(1999)
Cell
, vol.96
, pp. 185-193
-
-
Tilghman, S.M.1
-
2
-
-
0035234557
-
Genomic imprinting: Parental influence on the genome
-
Reik W, Walter J. Genomic imprinting: parental influence on the genome. Nat Rev Genet 2001;2:21-32.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
3
-
-
7344254106
-
A catalogue of imprinted genes and parent-of-origin effects in humans and animals
-
Morison IM, Reeve AE. A catalogue of imprinted genes and parent-of-origin effects in humans and animals. Hum Mol Genet 1998;7:1599-609.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1599-1609
-
-
Morison, I.M.1
Reeve, A.E.2
-
4
-
-
0035894625
-
The role of tissue-specific imprinting as a source of phenotypic heterogeneity in human disease
-
Weinstein LS. The role of tissue-specific imprinting as a source of phenotypic heterogeneity in human disease. Biol Psychiatry 2001;50:927-31.
-
(2001)
Biol Psychiatry
, vol.50
, pp. 927-931
-
-
Weinstein, L.S.1
-
5
-
-
0034235175
-
Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion
-
Blagitko N, Mergenthaler S, Schultz U, Wollmann HA, Craigen W, Eggermann T, Ropers HH, Kaischeuer VM. Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet 2000;9:1587-95.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1587-1595
-
-
Blagitko, N.1
Mergenthaler, S.2
Schultz, U.3
Wollmann, H.A.4
Craigen, W.5
Eggermann, T.6
Ropers, H.H.7
Kaischeuer, V.M.8
-
6
-
-
18444412259
-
Asb4, Ata3, and Dcn are novel imprinted genes identified by high-throughput screening using RIKEN cDNA microarray
-
Mizuno Y, Sotamaru Y, Katsuzawa Y, Kono T, Meguro M, Oshimura M, Kawai J, Tomaru Y, Kiyosawa H, Nikaido I, Amanuma H, Hayashizaki Y, Okazaki Y. Asb4, Ata3, and Dcn are novel imprinted genes identified by high-throughput screening using RIKEN cDNA microarray. Biochem Biophys Res Commun 2002;290:1499-505.
-
(2002)
Biochem Biophys Res Commun
, vol.290
, pp. 1499-1505
-
-
Mizuno, Y.1
Sotamaru, Y.2
Katsuzawa, Y.3
Kono, T.4
Meguro, M.5
Oshimura, M.6
Kawai, J.7
Tomaru, Y.8
Kiyosawa, H.9
Nikaido, I.10
Amanuma, H.11
Hayashizaki, Y.12
Okazaki, Y.13
-
7
-
-
0242432463
-
Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a
-
Yamasaki K, Joh K, Ohta T, Masuzaki H, Ishimaru T, Mukai T, Niikawa N, Ogawa M, Wagstaff J, Kishino T. Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a. Hum Mol Genet 2003;12:837-47.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 837-847
-
-
Yamasaki, K.1
Joh, K.2
Ohta, T.3
Masuzaki, H.4
Ishimaru, T.5
Mukai, T.6
Niikawa, N.7
Ogawa, M.8
Wagstaff, J.9
Kishino, T.10
-
8
-
-
0037447101
-
Gatm, a creatine synthesis enzyme, is imprinted in mouse placenta
-
Sandell LL, Guan XJ, Ingram R, Tilghman SM. Gatm, a creatine synthesis enzyme, is imprinted in mouse placenta. Proc Natl Acad Sci U S A 2003;100:4622-27.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 4622-4627
-
-
Sandell, L.L.1
Guan, X.J.2
Ingram, R.3
Tilghman, S.M.4
-
9
-
-
0038246289
-
Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal, region of chromosome 6
-
Hoshiya H, Meguro M, Kashiwagi A, Okita C, Oshimura M. Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal, region of chromosome 6. J Hum Genet 2003;48:208-11.
-
(2003)
J Hum Genet
, vol.48
, pp. 208-211
-
-
Hoshiya, H.1
Meguro, M.2
Kashiwagi, A.3
Okita, C.4
Oshimura, M.5
-
10
-
-
0031952115
-
Imprinting of mouse Kvlqt1 is developmentally regulated
-
Gould TD, Pfeifer K. Imprinting of mouse Kvlqt1 is developmentally regulated. Hum Mol Genet 1998;7:483-7.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 483-487
-
-
Gould, T.D.1
Pfeifer, K.2
-
11
-
-
18744429099
-
Strain-dependent developmental, relaxation of imprinting of an endogenous mouse gene, Kvlqt1
-
Jiang S, Hemann MA, Lee MP, Feinberg AP. Strain-dependent developmental, relaxation of imprinting of an endogenous mouse gene, Kvlqt1. Genomics 1998;53:395-9.
-
(1998)
Genomics
, vol.53
, pp. 395-399
-
-
Jiang, S.1
Hemann, M.A.2
Lee, M.P.3
Feinberg, A.P.4
-
12
-
-
0345628008
-
Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain
-
Bunzel R, Blumcke I, Cichon S, Normann S, Schramm J, Propping P, Nothen MM. Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain. Brain Res Mol Brain Res 1998;59:90-2.
-
(1998)
Brain Res Mol Brain Res
, vol.59
, pp. 90-92
-
-
Bunzel, R.1
Blumcke, I.2
Cichon, S.3
Normann, S.4
Schramm, J.5
Propping, P.6
Nothen, M.M.7
-
13
-
-
0034811734
-
Epigenetic heterogeneity at imprinted loci in normal populations
-
Sokatani T, Wei M, Katoh M, Okita C, Wada D, Mitsuya K, Meguro M, Ikeguchi M, Ito H, Tycko B, Oshimura M. Epigenetic heterogeneity at imprinted loci in normal populations. Biochem Biophys Res Commun 2001;283:1124-30.
-
(2001)
Biochem Biophys Res Commun
, vol.283
, pp. 1124-1130
-
-
Sokatani, T.1
Wei, M.2
Katoh, M.3
Okita, C.4
Wada, D.5
Mitsuya, K.6
Meguro, M.7
Ikeguchi, M.8
Ito, H.9
Tycko, B.10
Oshimura, M.11
-
14
-
-
0038756128
-
Human chromosome 7: DNA sequence and biology
-
Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R, Zhang J, Hudek AK, Li M, Haddad M, Duggan GE, Fernandez BA, Kanematsu E, Gentles S, Christopoulos CC, Choufani S, Kwasnicka D, Zheng XH, Lai Z, Nusskern D, Zhang Q, Gu Z, Lu F, Zeesman S, Nowaczyk MJ, Teshima I, Chitayat D, Shuman C, Weksberg R, Zackai EH, Grebe TA, Cox SR, Kirkpatrick SJ, Rahman N, Friedman JM, Heng HH, Pelicci PG, Lo-Coco F, Belloni E, Shaffer LG, Pober B, Morton CC, Gusella JF, Bruns GA, Korf BR, Quade BJ, Ligon AH, Ferguson H, Higgins AW, Leach NT, Herrick SR, Lemyre E, Farra CG, Kim HG, Summers AM, Gripp KW, Roberts W, Szatmari P, Winsor EJ, Grzeschik KH, Teebi A, Minassian BA, Kere J, Armengol L, Pujana MA, Estivill X, Wilson MD, Koop BF, Tosi S, Moore GE, Boright AP, Zlotorynski E, Kerem B, Kroisel PM, Petek E, Oscier DG, Mould SJ, Dohner H, Dohner K, Rommens JM, Vincent JB, Venter JC, Li PW, Mural RJ, Adams MD, Tsui LC. Human chromosome 7: DNA sequence and biology. Science 2003;300:767-72.
-
(2003)
Science
, vol.300
, pp. 767-772
-
-
Scherer, S.W.1
Cheung, J.2
MacDonald, J.R.3
Osborne, L.R.4
Nakabayashi, K.5
Herbrick, J.A.6
Carson, A.R.7
Parker-Katiraee, L.8
Skaug, J.9
Khaja, R.10
Zhang, J.11
Hudek, A.K.12
Li, M.13
Haddad, M.14
Duggan, G.E.15
Fernandez, B.A.16
Kanematsu, E.17
Gentles, S.18
Christopoulos, C.C.19
Choufani, S.20
Kwasnicka, D.21
Zheng, X.H.22
Lai, Z.23
Nusskern, D.24
Zhang, Q.25
Gu, Z.26
Lu, F.27
Zeesman, S.28
Nowaczyk, M.J.29
Teshima, I.30
Chitayat, D.31
Shuman, C.32
Weksberg, R.33
Zackai, E.H.34
Grebe, T.A.35
Cox, S.R.36
Kirkpatrick, S.J.37
Rahman, N.38
Friedman, J.M.39
Heng, H.H.40
Pelicci, P.G.41
Lo-Coco, F.42
Belloni, E.43
Shaffer, L.G.44
Pober, B.45
Morton, C.C.46
Gusella, J.F.47
Bruns, G.A.48
Korf, B.R.49
Quade, B.J.50
Ligon, A.H.51
Ferguson, H.52
Higgins, A.W.53
Leach, N.T.54
Herrick, S.R.55
Lemyre, E.56
Farra, C.G.57
Kim, H.G.58
Summers, A.M.59
Gripp, K.W.60
Roberts, W.61
Szatmari, P.62
Winsor, E.J.63
Grzeschik, K.H.64
Teebi, A.65
Minassian, B.A.66
Kere, J.67
Armengol, L.68
Pujana, M.A.69
Estivill, X.70
Wilson, M.D.71
Koop, B.F.72
Tosi, S.73
Moore, G.E.74
Boright, A.P.75
Zlotorynski, E.76
Kerem, B.77
Kroisel, P.M.78
Petek, E.79
Oscier, D.G.80
Mould, S.J.81
Dohner, H.82
Dohner, K.83
Rommens, J.M.84
Vincent, J.B.85
Venter, J.C.86
Li, P.W.87
Mural, R.J.88
Adams, M.D.89
Tsui, L.C.90
more..
-
15
-
-
0034002072
-
Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: Identification by a subtractive screen of novel uniparental fibroblast lines
-
Piras G, El-Kharroubi A, Kozlov S, Escalante-Alcalde D, Hernandez L, Copeland NG, Gilbert DJ, Jenkins NA, Stewart CL. Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines. Mol Cell Biol 2000;20:3308-15.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 3308-3315
-
-
Piras, G.1
El-Kharroubi, A.2
Kozlov, S.3
Escalante-Alcalde, D.4
Hernandez, L.5
Copeland, N.G.6
Gilbert, D.J.7
Jenkins, N.A.8
Stewart, C.L.9
-
16
-
-
17944378309
-
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome
-
Zimprich A, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, Scheidtmann K, Kern P, Winkelmann J, Muller-Myhsok B, Riedel L, Bauer M, Muller T, Castro M, Meitinger T, Strom T-M, Gasser T. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Nat Genet 2001;29:66-9.
-
(2001)
Nat Genet
, vol.29
, pp. 66-69
-
-
Zimprich, A.1
Grabowski, M.2
Asmus, F.3
Naumann, M.4
Berg, D.5
Bertram, M.6
Scheidtmann, K.7
Kern, P.8
Winkelmann, J.9
Muller-Myhsok, B.10
Riedel, L.11
Bauer, M.12
Muller, T.13
Castro, M.14
Meitinger, T.15
Strom, T.-M.16
Gasser, T.17
-
17
-
-
0037301222
-
The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted
-
Grabowski M, Zimprich A, Lorenz-Depiereux B, Kalscheuer V, Asmus F, Gasser T, Meitinger T, Strom TM. The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted. Eur J Hum Genet 2003;11:138-44.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 138-144
-
-
Grabowski, M.1
Zimprich, A.2
Lorenz-Depiereux, B.3
Kalscheuer, V.4
Asmus, F.5
Gasser, T.6
Meitinger, T.7
Strom, T.M.8
-
18
-
-
0036916437
-
Evidence that paternal expression or the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystania
-
Muller B, Hedrich K, Kock N, Dragasevic N, Svetel M, Garrels J, Landt O, Nitschke M, Pramstaller PP, Reik W, Schwinger E, Sperner J, Ozelius L, Kostic V, Klein C. Evidence that paternal expression or the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystania. Am J Hum Genet 2002;71:1303-11.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1303-1311
-
-
Muller, B.1
Hedrich, K.2
Kock, N.3
Dragasevic, N.4
Svetel, M.5
Garrels, J.6
Landt, O.7
Nitschke, M.8
Pramstaller, P.P.9
Reik, W.10
Schwinger, E.11
Sperner, J.12
Ozelius, L.13
Kostic, V.14
Klein, C.15
-
19
-
-
0035870563
-
A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21
-
Ono R, Kobayashi S, Wagatsuma H, Aisaka K, Kohda T, Kaneko-Ishino T, Ishino F. A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21. Genomics 2001;73:232-7.
-
(2001)
Genomics
, vol.73
, pp. 232-237
-
-
Ono, R.1
Kobayashi, S.2
Wagatsuma, H.3
Aisaka, K.4
Kohda, T.5
Kaneko-Ishino, T.6
Ishino, F.7
-
20
-
-
0038824784
-
Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6
-
Ono R, Shiura H, Aburatoni A, Kohda T, Kaneko-Ishino T, Ishino F. Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6. Genome Res 2003;13:1696-705.
-
(2003)
Genome Res
, vol.13
, pp. 1696-1705
-
-
Ono, R.1
Shiura, H.2
Aburatoni, A.3
Kohda, T.4
Kaneko-Ishino, T.5
Ishino, F.6
-
21
-
-
0038362419
-
A new imprinted cluster on the human chromosome 7q21-q31 identified by human-mouse monochromosomal hybrids
-
Okita C, Meguro M, Hoshiya H, Haruta M, Sakamota Y, Oshimura M. A new imprinted cluster on the human chromosome 7q21-q31 identified by human-mouse monochromosomal hybrids. Genomics 2003;81:556-9.
-
(2003)
Genomics
, vol.81
, pp. 556-559
-
-
Okita, C.1
Meguro, M.2
Hoshiya, H.3
Haruta, M.4
Sakamota, Y.5
Oshimura, M.6
-
22
-
-
0030682482
-
Neurabin: A novel neural tissue-specific actin filament-binding protein involved in neurite formation
-
Nakanishi H, Obaishi H, Satoh A, Wada M, Mandai K, Satoh K, Nishioka H, Matsuura Y, Mizoguchi A, Takai Y. Neurabin: a novel neural tissue-specific actin filament-binding protein involved in neurite formation. J Cell Biol 1997;139:951-61.
-
(1997)
J Cell Biol
, vol.139
, pp. 951-961
-
-
Nakanishi, H.1
Obaishi, H.2
Satoh, A.3
Wada, M.4
Mandai, K.5
Satoh, K.6
Nishioka, H.7
Matsuura, Y.8
Mizoguchi, A.9
Takai, Y.10
-
23
-
-
0032493285
-
Neurabin is a synoptic protein linking p70 S6 kinase and the neuronal cytoskeleton
-
Burnett PE, Blackshaw S, Lai MM, Qureshi IA, Burnett AF, Sabatini DM, Snyder SH. Neurabin is a synoptic protein linking p70 S6 kinase and the neuronal cytoskeleton. Proc Natl Acad Sci U S A 1998;95:8351-6.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 8351-8356
-
-
Burnett, P.E.1
Blackshaw, S.2
Lai, M.M.3
Qureshi, I.A.4
Burnett, A.F.5
Sabatini, D.M.6
Snyder, S.H.7
-
24
-
-
0033613083
-
Regulation of neurabin I interaction with protein phosphatase 1 by phosphorylation
-
McAvoy T, Allen PB, Obaishi H, Nakanishi H, Takai Y, Greengard P, Nairn AC, Hemmings HC Jr. Regulation of neurabin I interaction with protein phosphatase 1 by phosphorylation. Biochemistry 1999;38:12943-9.
-
(1999)
Biochemistry
, vol.38
, pp. 12943-12949
-
-
McAvoy, T.1
Allen, P.B.2
Obaishi, H.3
Nakanishi, H.4
Takai, Y.5
Greengard, P.6
Nairn, A.C.7
Hemmings Jr., H.C.8
-
25
-
-
0036269244
-
Targeting protein phosphatase 1 (PP1) to the actin cytoskeleton: The neurabin I/PP1 complex regulates cell morphology
-
Oliver CJ, Terry-Lorenzo RT, Elliott E, Bloomer WA, Li S, Brautigan DL, Colbran RJ, Shenolikar S. Targeting protein phosphatase 1 (PP1) to the actin cytoskeleton: the neurabin I/PP1 complex regulates cell morphology. Mol Cell Biol 2002;22:4690-701.
-
(2002)
Mol Cell Biol
, vol.22
, pp. 4690-4701
-
-
Oliver, C.J.1
Terry-Lorenzo, R.T.2
Elliott, E.3
Bloomer, W.A.4
Li, S.5
Brautigan, D.L.6
Colbran, R.J.7
Shenolikar, S.8
-
26
-
-
0035139220
-
The neuronal Rho-GEF Kalirin-7 interacts with PDZ domain-containing proteins and regulates dendritic morphogenesis
-
Penzes P, Johnson RC, Sattler R, Zhang X, Huganir RL, Kambampati V, Mains RE, Eipper BA. The neuronal Rho-GEF Kalirin-7 interacts with PDZ domain-containing proteins and regulates dendritic morphogenesis. Neuron 2001;29:229-42.
-
(2001)
Neuron
, vol.29
, pp. 229-242
-
-
Penzes, P.1
Johnson, R.C.2
Sattler, R.3
Zhang, X.4
Huganir, R.L.5
Kambampati, V.6
Mains, R.E.7
Eipper, B.A.8
-
27
-
-
0033570129
-
Direct interaction of the trans-Golgi network membrane protein TGN38 with the F-actin binding protein neurabin
-
Stephens DJ, Banting G. Direct interaction of the trans-Golgi network membrane protein TGN38 with the F-actin binding protein neurabin. J Biol Chem 1999;274:30080-6.
-
(1999)
J Biol Chem
, vol.274
, pp. 30080-30086
-
-
Stephens, D.J.1
Banting, G.2
-
29
-
-
0035231999
-
Genomic imprinting and the maternal brain
-
Keverne EB. Genomic imprinting and the maternal brain. Prog Brain Res 2001;133:279-85.
-
(2001)
Prog Brain Res
, vol.133
, pp. 279-285
-
-
Keverne, E.B.1
-
30
-
-
18244389962
-
Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome
-
Nakabayashi K, Fernandez BA, Teshima I, Shuman C, Proud VK, Curry CJ, Chitayat D, Grebe T, Ming J, Oshimura M, Meguro M, Mitsuya K, Deb-Rinker P, Herbrick JA, Weksberg R, Scherer SW. Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome. Genomics 2002;79:186-96.
-
(2002)
Genomics
, vol.79
, pp. 186-196
-
-
Nakabayashi, K.1
Fernandez, B.A.2
Teshima, I.3
Shuman, C.4
Proud, V.K.5
Curry, C.J.6
Chitayat, D.7
Grebe, T.8
Ming, J.9
Oshimura, M.10
Meguro, M.11
Mitsuya, K.12
Deb-Rinker, P.13
Herbrick, J.A.14
Weksberg, R.15
Scherer, S.W.16
-
31
-
-
0027478216
-
A mouse model of greig cephalopalysyndactyly syndrome: The extra-toesJ mutation contains an intragenic deletion of the Gli3 gene
-
Hui CC, Joyner AL. A mouse model of greig cephalopalysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene. Nat Genet 1993;3:241-6.
-
(1993)
Nat Genet
, vol.3
, pp. 241-246
-
-
Hui, C.C.1
Joyner, A.L.2
-
32
-
-
0036590151
-
Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools
-
Norton H, Williams NM, Williams HJ, Spurlock G, Kirov G, Morris DW, Hoogendoor B, Owen MJ, O'Donovan MC. Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Hum Genet 2002;110:471-8.
-
(2002)
Hum Genet
, vol.110
, pp. 471-478
-
-
Norton, H.1
Williams, N.M.2
Williams, H.J.3
Spurlock, G.4
Kirov, G.5
Morris, D.W.6
Hoogendoor, B.7
Owen, M.J.8
O'Donovan, M.C.9
-
33
-
-
0033042181
-
An analysis of the distribution of hetero- And isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands
-
Preece MA, Abu-Amero SN, Ali Z, Abu-Amero KK, Wakeling EL, Stanier P, Moore GE. An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands. J Med Genet 1999;36:457-60.
-
(1999)
J Med Genet
, vol.36
, pp. 457-460
-
-
Preece, M.A.1
Abu-Amero, S.N.2
Ali, Z.3
Abu-Amero, K.K.4
Wakeling, E.L.5
Stanier, P.6
Moore, G.E.7
-
34
-
-
0033061081
-
Bau, a splice form of Neurabin-I that interacts with the tumor suppressor Bin1, inhibits malignant cell transformation
-
Duhadaway J, Rowe F, Elliott K, Mao NC, Prendergast GC. Bau, a splice form of Neurabin-I that interacts with the tumor suppressor Bin1, inhibits malignant cell transformation. Cell Adhes Commun 1999;7:99-110.
-
(1999)
Cell Adhes Commun
, vol.7
, pp. 99-110
-
-
Duhadaway, J.1
Rowe, F.2
Elliott, K.3
Mao, N.C.4
Prendergast, G.C.5
-
35
-
-
17744380449
-
Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools
-
Hoogendoorn B, Norton N, Kirov G, Williams N, Hamshere ML, Spurlock G, Austin J, Stephens MK, Buckland PR, Owen MJ, O'Donovan MC. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Hum Genet 2000;107:488-93.
-
(2000)
Hum Genet
, vol.107
, pp. 488-493
-
-
Hoogendoorn, B.1
Norton, N.2
Kirov, G.3
Williams, N.4
Hamshere, M.L.5
Spurlock, G.6
Austin, J.7
Stephens, M.K.8
Buckland, P.R.9
Owen, M.J.10
O'Donovan, M.C.11
-
36
-
-
0036962761
-
Evaluation of a potential epigenetic biomarker by quantitative methyl-single nucleotide polymorphism analysis
-
Uhlmann K, Brinckmann A, Toliat MR, Ritter H, Nurnberg P. Evaluation of a potential epigenetic biomarker by quantitative methyl-single nucleotide polymorphism analysis. Electrophoresis 2002;23:4072-9.
-
(2002)
Electrophoresis
, vol.23
, pp. 4072-4079
-
-
Uhlmann, K.1
Brinckmann, A.2
Toliat, M.R.3
Ritter, H.4
Nurnberg, P.5
-
37
-
-
0035034656
-
Molecular regulation of tongue and craniofacial muscle differentiation
-
Shuler CF, Dalrymple KR. Molecular regulation of tongue and craniofacial muscle differentiation. Crit Rev Oral Biol Med 2001;12:3-17.
-
(2001)
Crit Rev Oral Biol Med
, vol.12
, pp. 3-17
-
-
Shuler, C.F.1
Dalrymple, K.R.2
-
38
-
-
0037096159
-
Involvement of protein phosphatase-1-mediated MARCKS translocation in myogenic differentiation of embryonic muscle cells
-
Kim SS, Kim JH, Lee SH, Chung SS, Bang OS, Park D, Chung CH. Involvement of protein phosphatase-1-mediated MARCKS translocation in myogenic differentiation of embryonic muscle cells. J Cell Sci 2002;115:2465-73.
-
(2002)
J Cell Sci
, vol.115
, pp. 2465-2473
-
-
Kim, S.S.1
Kim, J.H.2
Lee, S.H.3
Chung, S.S.4
Bang, O.S.5
Park, D.6
Chung, C.H.7
-
39
-
-
0024152982
-
Differential imprinting and expression of maternal and paternal genomes
-
Solter D. Differential imprinting and expression of maternal and paternal genomes. Annu Rev Genet 1988;22:127-46.
-
(1988)
Annu Rev Genet
, vol.22
, pp. 127-146
-
-
Solter, D.1
-
40
-
-
0026428611
-
Emoryological and molecular investigations of parental imprinting on mouse chromosome 7
-
Ferguson-Smith AC, Cattanach BM, Barton SC, Beechey CV, Surani MA. Emoryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature 1991;351:667-70.
-
(1991)
Nature
, vol.351
, pp. 667-670
-
-
Ferguson-Smith, A.C.1
Cattanach, B.M.2
Barton, S.C.3
Beechey, C.V.4
Surani, M.A.5
-
41
-
-
0026761039
-
Parthenogenetic stem cells in postnatal mouse chimeras
-
Jagerbauer EM, Fraser A, Herbst EW, Kothary R, Fundele R. Parthenogenetic stem cells in postnatal mouse chimeras. Development 1992;116:95-102.
-
(1992)
Development
, vol.116
, pp. 95-102
-
-
Jagerbauer, E.M.1
Fraser, A.2
Herbst, E.W.3
Kothary, R.4
Fundele, R.5
-
42
-
-
0024345884
-
Systematic elimination of parthenogenetic cells in mouse chimeras
-
Fundele R, Norris ML, Barton SC, Reik W, Surani MA. Systematic elimination of parthenogenetic cells in mouse chimeras. Development 1989;106:29-35.
-
(1989)
Development
, vol.106
, pp. 29-35
-
-
Fundele, R.1
Norris, M.L.2
Barton, S.C.3
Reik, W.4
Surani, M.A.5
-
43
-
-
0024400009
-
Systematic non-uniform distribution of parthenogenetic cells in adult mouse chimaeras
-
Nagy A, Sass M, Markkula M. Systematic non-uniform distribution of parthenogenetic cells in adult mouse chimaeras. Development 1989;106:321-4.
-
(1989)
Development
, vol.106
, pp. 321-324
-
-
Nagy, A.1
Sass, M.2
Markkula, M.3
-
44
-
-
0025186754
-
Temporal and spatial selection against parthenogenetic cells during development of fetal chimeras
-
Fundele RH, Norris ML, Barton SC, Fehlau M, Hewlett SK, Mills WE, Surani MA. Temporal and spatial selection against parthenogenetic cells during development of fetal chimeras. Development 1990;108:203-11.
-
(1990)
Development
, vol.108
, pp. 203-211
-
-
Fundele, R.H.1
Norris, M.L.2
Barton, S.C.3
Fehlau, M.4
Hewlett, S.K.5
Mills, W.E.6
Surani, M.A.7
|