-
1
-
-
0021810948
-
The mosaic genome of warm-blooded vertebrates
-
Bernardi G, Olofsson B, Filipski J, Zerial M, Salinas J, Cuny G, Meunier-Rotival M, Rodier F (1985) The mosaic genome of warm-blooded vertebrates. Science 228:953-958
-
(1985)
Science
, vol.228
, pp. 953-958
-
-
Bernardi, G.1
Olofsson, B.2
Filipski, J.3
Zerial, M.4
Salinas, J.5
Cuny, G.6
Meunier-Rotival, M.7
Rodier, F.8
-
2
-
-
0029564970
-
Localisation of STCH to human chromosome 21q11.1
-
Brodsky G, Otterson GA, Parry BB, Hart I, Patterson D, Kaye FJ (1995) Localisation of STCH to human chromosome 21q11.1. Genomics 30:627-628.
-
(1995)
Genomics
, vol.30
, pp. 627-628
-
-
Brodsky, G.1
Otterson, G.A.2
Parry, B.B.3
Hart, I.4
Patterson, D.5
Kaye, F.J.6
-
3
-
-
0026607209
-
Walking, cloning and mapping with yeast artificial chromosomes: A contig encompassing D21S13 and D21S16
-
Butler R, Ogilvie DJ, Elvin P, Riley JH, Finniear RS, Slynn G, Morten JEN, Markham AF, Anand R (1992) Walking, cloning and mapping with yeast artificial chromosomes: a contig encompassing D21S13 and D21S16. Genomics 12:42-51
-
(1992)
Genomics
, vol.12
, pp. 42-51
-
-
Butler, R.1
Ogilvie, D.J.2
Elvin, P.3
Riley, J.H.4
Finniear, R.S.5
Slynn, G.6
Morten, J.E.N.7
Markham, A.F.8
Anand, R.9
-
4
-
-
0029121358
-
Nuclear factor RIP140 modulates transcriptional activation by the estrogen receptor
-
Cavailles V, Dauvois S, L'Horset F, Lopez G, Hoare S, Kushner PJ, Parker MG (1995) Nuclear factor RIP140 modulates transcriptional activation by the estrogen receptor. EMBO J 14:3741-3751
-
(1995)
EMBO J
, vol.14
, pp. 3741-3751
-
-
Cavailles, V.1
Dauvois, S.2
L'Horset, F.3
Lopez, G.4
Hoare, S.5
Kushner, P.J.6
Parker, M.G.7
-
5
-
-
0029894792
-
The yeast genome project: What did we learn?
-
Dujon B (1996) The yeast genome project: what did we learn? Trends Genet 12:263-270
-
(1996)
Trends Genet
, vol.12
, pp. 263-270
-
-
Dujon, B.1
-
6
-
-
0030560766
-
Base composition and gene distribution: Critical patterns in mammalian genome organization
-
Gardiner K (1996) Base composition and gene distribution: critical patterns in mammalian genome organization. Trends Genet 12:519-524
-
(1996)
Trends Genet
, vol.12
, pp. 519-524
-
-
Gardiner, K.1
-
7
-
-
0025369193
-
A compositional map of human chromosome 21
-
Gardiner K, Aissani B, Bernardi G (1990) A compositional map of human chromosome 21. EMBO J 9:1853-1858
-
(1990)
EMBO J
, vol.9
, pp. 1853-1858
-
-
Gardiner, K.1
Aissani, B.2
Bernardi, G.3
-
8
-
-
0024559652
-
Predisposing locus for Alzheimer disease on chromosome 21
-
Goate AM, Owen MJ, James LA, Mullan MJ, Rossor MN, Haynes AR, Farrall M, Lai LYC, Roques P, Williamson R, Hardy JA (1989) Predisposing locus for Alzheimer disease on chromosome 21. Lancet i:352-355
-
(1989)
Lancet
, vol.1
, pp. 352-355
-
-
Goate, A.M.1
Owen, M.J.2
James, L.A.3
Mullan, M.J.4
Rossor, M.N.5
Haynes, A.R.6
Farrall, M.7
Lai, L.Y.C.8
Roques, P.9
Williamson, R.10
Hardy, J.A.11
-
9
-
-
0029791627
-
The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndrome
-
Katsanis N, Fisher EMC (1996) The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndrome. Hum Genet 98:497-499
-
(1996)
Hum Genet
, vol.98
, pp. 497-499
-
-
Katsanis, N.1
Fisher, E.M.C.2
-
10
-
-
0030200739
-
Paralogy mapping: Identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH loci
-
Katsanis N, Fitzgibbon J, Fisher EMC (1996) Paralogy mapping: identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH loci. Genomics 35:101-108
-
(1996)
Genomics
, vol.35
, pp. 101-108
-
-
Katsanis, N.1
Fitzgibbon, J.2
Fisher, E.M.C.3
-
11
-
-
0029850086
-
RIP-140 interacts with multiple nuclear receptors by means of two distinct sites
-
L'Horset F, Dauvois S, Heery DM, Cavailles V, Parker MG (1996) RIP-140 interacts with multiple nuclear receptors by means of two distinct sites. Mol Cell Biol 16:6029-6036
-
(1996)
Mol Cell Biol
, vol.16
, pp. 6029-6036
-
-
L'Horset, F.1
Dauvois, S.2
Heery, D.M.3
Cavailles, V.4
Parker, M.G.5
-
12
-
-
0026066608
-
PBX2 and PBX3, new homeobox genes with extensive homology to the human proto-oncogene PBX1
-
Monica K, Galini N, Nourse J, Saltman D, Cleary ML (1991) PBX2 and PBX3, new homeobox genes with extensive homology to the human proto-oncogene PBX1. Mol Cell Biol 11:6149-6157
-
(1991)
Mol Cell Biol
, vol.11
, pp. 6149-6157
-
-
Monica, K.1
Galini, N.2
Nourse, J.3
Saltman, D.4
Cleary, M.L.5
-
13
-
-
0028231476
-
An integrated YAC-overlup and "cosmid-pocket" map of the human chromosome 21
-
Nizetic D, Gellen L, Hamvas RMJ, Mott R, Grigoriev A, Vatcheva R, Zehetner G, Yaspo ML, Dutriaux A, Lopes C, Delabar J-M, Broeckhoven CV, Potier M-C, Lehrach H (1994) An integrated YAC-overlup and "cosmid-pocket" map of the human chromosome 21. Hum Mol Genet 3:759-770
-
(1994)
Hum Mol Genet
, vol.3
, pp. 759-770
-
-
Nizetic, D.1
Gellen, L.2
Hamvas, R.M.J.3
Mott, R.4
Grigoriev, A.5
Vatcheva, R.6
Zehetner, G.7
Yaspo, M.L.8
Dutriaux, A.9
Lopes, C.10
Delabar, J.-M.11
Broeckhoven, C.V.12
Potier, M.-C.13
Lehrach, H.14
-
14
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense mutations in a novel gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
Rogaev EI, Sherringlon R, Rogaeva EA, Levesque G, Ikeda M, Liang Y, Chi H, Li J, Holman K, Tsuda T, Mar L, Sorbi S, Naemias S, Piacentini S, Amaducci L, Chumakov I, Cohen D, Lannfelt L, Fraser PE, Rommens JM. St. George-Hyslop PH (1995) Familial Alzheimer's disease in kindreds with missense mutations in a novel gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature 376:775-778
-
(1995)
Nature
, vol.376
, pp. 775-778
-
-
Rogaev, E.I.1
Sherringlon, R.2
Rogaeva, E.A.3
Levesque, G.4
Ikeda, M.5
Liang, Y.6
Chi, H.7
Li, J.8
Holman, K.9
Tsuda, T.10
Mar, L.11
Sorbi, S.12
Naemias, S.13
Piacentini, S.14
Amaducci, L.15
Chumakov, I.16
Cohen, D.17
Lannfelt, L.18
Fraser, P.E.19
Rommens, J.M.20
St George-Hyslop, P.H.21
more..
-
15
-
-
0031569390
-
Analysis of the 5′ sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease
-
Rogaev EI, Sherrington R, Wu C, Levesque G, Liang Y, Rogaeva EA, Ikeda M, Holman K, Lin C, Lukiw WJ, De long PH, Fraser PE, Rommens JM, St. George-Hyslop P (1997) Analysis of the 5′ sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease. Genomics 40:415-424
-
(1997)
Genomics
, vol.40
, pp. 415-424
-
-
Rogaev, E.I.1
Sherrington, R.2
Wu, C.3
Levesque, G.4
Liang, Y.5
Rogaeva, E.A.6
Ikeda, M.7
Holman, K.8
Lin, C.9
Lukiw, W.J.10
De Long, P.H.11
Fraser, P.E.12
Rommens, J.M.13
St George-Hyslop, P.14
-
16
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early onset Alzheimer's disease
-
Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, Ikeda M, Chi H, Li J, Holman K, Tsuda T, Mar L, Foncin JF, Bruni AC, Montesi MP, Sorbi S, Rainero I, Pinessi L, Nee L, Chumakov I, Pollen D, Bookes A, Sanscau P, Polinsky RJ, Wasko W, DaSilva HAR, Haines JL, Pericak-Vance MA, Tanzi R, Roses AD, Fraser PE, Rommens JM, St. George-Hyslop PH (1995) Cloning of a gene bearing missense mutations in early onset Alzheimer's disease. Nature 375:754-760
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Li, J.8
Holman, K.9
Tsuda, T.10
Mar, L.11
Foncin, J.F.12
Bruni, A.C.13
Montesi, M.P.14
Sorbi, S.15
Rainero, I.16
Pinessi, L.17
Nee, L.18
Chumakov, I.19
Pollen, D.20
Bookes, A.21
Sanscau, P.22
Polinsky, R.J.23
Wasko, W.24
DaSilva, H.A.R.25
Haines, J.L.26
Pericak-Vance, M.A.27
Tanzi, R.28
Roses, A.D.29
Fraser, P.E.30
Rommens, J.M.31
St George-Hyslop, P.H.32
more..
-
17
-
-
0029057946
-
Report of the Fifth International Workshop on Human Chromosome 21 Mapping 1994
-
Shimizu N, Antonarakis S, Van Broeckhoven C, Patterson D, Gardiner K, Nizetic D, Creau N, Delabar J-M, Korenberg J, Reeves R, Doering J, Ritter O, Cuticcia J (1995) Report of the Fifth International Workshop on Human Chromosome 21 Mapping 1994. Cytogenet Cell Genet 70:147-182
-
(1995)
Cytogenet Cell Genet
, vol.70
, pp. 147-182
-
-
Shimizu, N.1
Antonarakis, S.2
Van Broeckhoven, C.3
Patterson, D.4
Gardiner, K.5
Nizetic, D.6
Creau, N.7
Delabar, J.-M.8
Korenberg, J.9
Reeves, R.10
Doering, J.11
Ritter, O.12
Cuticcia, J.13
-
18
-
-
0023103748
-
The genetic defect causing familial Alzheimer's disease maps to chromosome 21
-
St. George-Hyslop PH, Tanzi RE, Polinsky PJ, Haines JL, Nee L, Watkins PC, Myers RH, Feldman RG, Pollen D, Drachman D, Growdon J, Bruni A, Foncin J, Salmon D, Frommelt P, Amaducci L, Sorbi S, Piacentini S, Stewart GD, Hobbs WJ, Connealy PM, Gusella JF (1987) The genetic defect causing familial Alzheimer's disease maps to chromosome 21. Science 235:885-890
-
(1987)
Science
, vol.235
, pp. 885-890
-
-
St George-Hyslop, P.H.1
Tanzi, R.E.2
Polinsky, P.J.3
Haines, J.L.4
Nee, L.5
Watkins, P.C.6
Myers, R.H.7
Feldman, R.G.8
Pollen, D.9
Drachman, D.10
Growdon, J.11
Bruni, A.12
Foncin, J.13
Salmon, D.14
Frommelt, P.15
Amaducci, L.16
Sorbi, S.17
Piacentini, S.18
Stewart, G.D.19
Hobbs, W.J.20
Connealy, P.M.21
Gusella, J.F.22
more..
-
19
-
-
0027032695
-
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14
-
St. George-Hyslop PH, Haines JL, Rogaev EI, Motilla M, Vaula G, Pericak-Vance MA, Foncin JF, Montesi MP, Bruni AC, Sorbi S, Rainero I, Pinessi L, Pollen D, Polinsky RJ, Nee L, Kennedy J, Macciardi F, Rogaeva EA, Liang Y, Alexandrova N, Lukiw W, Schlumpf K, Tanzi RE, Tsuda T, Farrer L, Cantu J, Duara R, Amaducci L, Bergamini L, Gusella JF, Roses AD, Crapper McLachlan D (1992) Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. Nat Genet 2:330-334
-
(1992)
Nat Genet
, vol.2
, pp. 330-334
-
-
St George-Hyslop, P.H.1
Haines, J.L.2
Rogaev, E.I.3
Motilla, M.4
Vaula, G.5
Pericak-Vance, M.A.6
Foncin, J.F.7
Montesi, M.P.8
Bruni, A.C.9
Sorbi, S.10
Rainero, I.11
Pinessi, L.12
Pollen, D.13
Polinsky, R.J.14
Nee, L.15
Kennedy, J.16
Macciardi, F.17
Rogaeva, E.A.18
Liang, Y.19
Alexandrova, N.20
Lukiw, W.21
Schlumpf, K.22
Tanzi, R.E.23
Tsuda, T.24
Farrer, L.25
Cantu, J.26
Duara, R.27
Amaducci, L.28
Bergamini, L.29
Gusella, J.F.30
Roses, A.D.31
Crapper McLachlan, D.32
more..
-
20
-
-
0028883252
-
Molecular genetics of Alzheimer's disease
-
Van Broeckhoven CL (1995) Molecular genetics of Alzheimer's disease. Eur Neurol 35:8-19
-
(1995)
Eur Neurol
, vol.35
, pp. 8-19
-
-
Van Broeckhoven, C.L.1
|