-
1
-
-
0021139084
-
Completion of mouse embryogenesis requires both the maternal and paternal genomes
-
McGrath J, Solter D (1984) Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell 37: 179-183.
-
(1984)
Cell
, vol.37
, pp. 179-183
-
-
McGrath, J.1
Solter, D.2
-
2
-
-
0021237658
-
Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
-
Surani MA, Barton SC, Norris ML (1984) Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature 308: 548-550.
-
(1984)
Nature
, vol.308
, pp. 548-550
-
-
Surani, M.A.1
Barton, S.C.2
Norris, M.L.3
-
3
-
-
0022391691
-
Differential activity of maternally and paternally derived chromosome regions in mice
-
Cattanach BM, Kirk M (1985) Differential activity of maternally and paternally derived chromosome regions in mice. Nature 315: 496-498.
-
(1985)
Nature
, vol.315
, pp. 496-498
-
-
Cattanach, B.M.1
Kirk, M.2
-
4
-
-
0024440608
-
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome
-
Nicholls RD, Knoll JH, Butler MG, Karam S, Lalande M (1989) Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature 342: 281-285.
-
(1989)
Nature
, vol.342
, pp. 281-285
-
-
Nicholls, R.D.1
Knoll, J.H.2
Butler, M.G.3
Karam, S.4
Lalande, M.5
-
5
-
-
0026098090
-
The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus
-
Barlow DP, Stoger R, Herrmann BG, Saito K, Schweifer N (1991) The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus. Nature 349: 84-87.
-
(1991)
Nature
, vol.349
, pp. 84-87
-
-
Barlow, D.P.1
Stoger, R.2
Herrmann, B.G.3
Saito, K.4
Schweifer, N.5
-
6
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei MS, Zemel S, Tilghman SM (1991) Parental imprinting of the mouse H19 gene. Nature 351: 153-155.
-
(1991)
Nature
, vol.351
, pp. 153-155
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.M.3
-
7
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
DeChiara TM, Robertson EJ, Efstratiadis A (1991) Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64: 849-859.
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
DeChiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
8
-
-
0027172684
-
Parentalorigin- specific epigenetic modification of the mouse H19 gene
-
Ferguson-Smith AC, Sasaki H, Cattanach BM, Surani MA (1993) Parentalorigin- specific epigenetic modification of the mouse H19 gene. Nature 362: 751-755.
-
(1993)
Nature
, vol.362
, pp. 751-755
-
-
Ferguson-Smith, A.C.1
Sasaki, H.2
Cattanach, B.M.3
Surani, M.A.4
-
9
-
-
0034484223
-
The kinship theory of genomic imprinting
-
Haig D (2000) The kinship theory of genomic imprinting. Annu Rev Ecol Syst 31: 9-32.
-
(2000)
Annu Rev Ecol Syst
, vol.31
, pp. 9-32
-
-
Haig, D.1
-
10
-
-
0026428611
-
Embryological and molecular investigations of parental imprinting on mouse chromosome 7
-
Ferguson-Smith AC, Cattanach BM, Barton SC, Beechey CV, Surani MA (1991) Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature 351: 667-670.
-
(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
-
11
-
-
0025320906
-
A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting
-
DeChiara TM, Efstratiadis A, Robertson EJ (1990) A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature 345: 78-80.
-
(1990)
Nature
, vol.345
, pp. 78-80
-
-
DeChiara, T.M.1
Efstratiadis, A.2
Robertson, E.J.3
-
12
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton PA, Ingram RS, Eggenschwiler J, Efstratiadis A, Tilghman SM (1995) Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature 375: 34-39.
-
(1995)
Nature
, vol.375
, pp. 34-39
-
-
Leighton, P.A.1
Ingram, R.S.2
Eggenschwiler, J.3
Efstratiadis, A.4
Tilghman, S.M.5
-
13
-
-
0028575985
-
Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality
-
Lau MM, Stewart CE, Liu Z, Bhatt H, Rotwein P, et al. (1994) Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality. Genes Dev 8: 2953-2963.
-
(1994)
Genes Dev
, vol.8
, pp. 2953-2963
-
-
Lau, M.M.1
Stewart, C.E.2
Liu, Z.3
Bhatt, H.4
Rotwein, P.5
-
14
-
-
0027999284
-
Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene
-
Wang ZQ, Fung MR, Barlow DP, Wagner EF (1994) Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene. Nature 372: 464-467.
-
(1994)
Nature
, vol.372
, pp. 464-467
-
-
Wang, Z.Q.1
Fung, M.R.2
Barlow, D.P.3
Wagner, E.F.4
-
15
-
-
0030221121
-
Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds
-
Ludwig T, Eggenschwiler J, Fisher P, D'Ercole AJ, Davenport ML, et al. (1996) Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds. Dev Biol 177: 517-535.
-
(1996)
Dev Biol
, vol.177
, pp. 517-535
-
-
Ludwig, T.1
Eggenschwiler, J.2
Fisher, P.3
D'Ercole, A.J.4
Davenport, M.L.5
-
16
-
-
0030077356
-
Function of the two mannose 6-phosphate receptors in lysosomal enzyme transport
-
Munier-Lehmann H, Mauxion F, Hoflack B (1996) Function of the two mannose 6-phosphate receptors in lysosomal enzyme transport. Biochem Soc Trans 24: 133-136.
-
(1996)
Biochem Soc Trans
, vol.24
, pp. 133-136
-
-
Munier-Lehmann, H.1
Mauxion, F.2
Hoflack, B.3
-
17
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li E, Beard C, Jaenisch R (1993) Role for DNA methylation in genomic imprinting. Nature 366: 362-365.
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
18
-
-
0028968205
-
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
-
Tremblay KD, Saam JR, Ingram RS, Tilghman SM, Bartolomei MS (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
-
19
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen JL, Duran KL, Bartolomei MS (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
-
20
-
-
0032878252
-
Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor
-
Frevel MA, Sowerby SJ, Petersen GB, Reeve AE (1999) Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor. J Biol Chem 274: 29331-29340.
-
(1999)
J Biol Chem
, vol.274
, pp. 29331-29340
-
-
Frevel, M.A.1
Sowerby, S.J.2
Petersen, G.B.3
Reeve, A.E.4
-
21
-
-
0035393429
-
Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site
-
Cui H, Niemitz EL, Ravenel JD, Onyango P, Brandenburg SA, et al. (2001) Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site. Cancer Res 61: 4947-4950.
-
(2001)
Cancer Res
, vol.61
, pp. 4947-4950
-
-
Cui, H.1
Niemitz, E.L.2
Ravenel, J.D.3
Onyango, P.4
Brandenburg, S.A.5
-
22
-
-
0035510088
-
Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer
-
Takai D, Gonzales FA, Tsai YC, Thayer MJ, Jones PA (2001) Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer. Hum Mol Genet 10: 2619-2626.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2619-2626
-
-
Takai, D.1
Gonzales, F.A.2
Tsai, Y.C.3
Thayer, M.J.4
Jones, P.A.5
-
23
-
-
25144454048
-
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome
-
Gicquel C, Rossignol S, Cabrol S, Houang M, Steunou V, et al. (2005) Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nat Genet 37: 1003-1007.
-
(2005)
Nat Genet
, vol.37
, pp. 1003-1007
-
-
Gicquel, C.1
Rossignol, S.2
Cabrol, S.3
Houang, M.4
Steunou, V.5
-
24
-
-
27244436752
-
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome
-
Cooper WN, Luharia A, Evans GA, Raza H, Haire AC, et al. (2005) Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome. Eur J Hum Genet 13: 1025-1032.
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 1025-1032
-
-
Cooper, W.N.1
Luharia, A.2
Evans, G.A.3
Raza, H.4
Haire, A.C.5
-
25
-
-
33646265537
-
Limited evolutionary conservation of imprinting in the human placenta
-
Monk D, Arnaud P, Apostolidou S, Hills FA, Kelsey G, et al. (2006) Limited evolutionary conservation of imprinting in the human placenta. Proc Natl Acad Sci U S A 103: 6623-6628.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 6623-6628
-
-
Monk, D.1
Arnaud, P.2
Apostolidou, S.3
Hills, F.A.4
Kelsey, G.5
-
26
-
-
56149111804
-
Identification of the human homolog of the imprinted mouse Air non-coding RNA
-
Yotova IY, Vlatkovic IM, Pauler FM, Warczok KE, Ambros PF, et al. (2008) Identification of the human homolog of the imprinted mouse Air non-coding RNA. Genomics 92: 464-473.
-
(2008)
Genomics
, vol.92
, pp. 464-473
-
-
Yotova, I.Y.1
Vlatkovic, I.M.2
Pauler, F.M.3
Warczok, K.E.4
Ambros, P.F.5
-
27
-
-
67651091794
-
Placental efficiency and adaptation: Endocrine regulation
-
Fowden AL, Sferruzzi-Perri AN, Coan PM, Constancia M, Burton GJ (2009) Placental efficiency and adaptation: Endocrine regulation. J Physiol 587: 3459-3472.
-
(2009)
J Physiol
, vol.587
, pp. 3459-3472
-
-
Fowden, A.L.1
Sferruzzi-Perri, A.N.2
Coan, P.M.3
Constancia, M.4
Burton, G.J.5
-
28
-
-
33847191352
-
Control of human trophoblast function
-
Lunghi L, Ferretti ME, Medici S, Biondi C, Vesce F (2007) Control of human trophoblast function. Reprod Biol Endocrinol 5: 6.
-
(2007)
Reprod Biol Endocrinol
, vol.5
, pp. 6
-
-
Lunghi, L.1
Ferretti, M.E.2
Medici, S.3
Biondi, C.4
Vesce, F.5
-
29
-
-
0036549899
-
Cytokines of the placenta and extra-placental membranes: Roles and regulation during human pregnancy and parturition
-
Bowen JM, Chamley L, Keelan JA, Mitchell MD (2002) Cytokines of the placenta and extra-placental membranes: roles and regulation during human pregnancy and parturition. Placenta 23: 257-273.
-
(2002)
Placenta
, vol.23
, pp. 257-273
-
-
Bowen, J.M.1
Chamley, L.2
Keelan, J.A.3
Mitchell, M.D.4
-
31
-
-
0142150078
-
Apoptosis of extravillous trophoblast cells limits the trophoblast invasion in uterine but not in tubal pregnancy during first trimester
-
von Rango U, Krusche CA, Kertschanska S, Alfer J, Kaufmann P, et al. (2003) Apoptosis of extravillous trophoblast cells limits the trophoblast invasion in uterine but not in tubal pregnancy during first trimester. Placenta 24: 929-940.
-
(2003)
Placenta
, vol.24
, pp. 929-940
-
-
von Rango, U.1
Krusche, C.A.2
Kertschanska, S.3
Alfer, J.4
Kaufmann, P.5
-
33
-
-
69949111772
-
Differential expression of imprinted genes in normal and IUGR human placentas
-
Diplas AI, Lambertini L, Lee MJ, Sperling R, Lee YL, et al. (2009) Differential expression of imprinted genes in normal and IUGR human placentas. Epigenetics 4.
-
(2009)
Epigenetics
, pp. 4
-
-
Diplas, A.I.1
Lambertini, L.2
Lee, M.J.3
Sperling, R.4
Lee, Y.L.5
-
34
-
-
0041896849
-
Placental-fetal interrelationship in IUGR fetuses-a review
-
Pardi G, Marconi AM, Cetin I (2002) Placental-fetal interrelationship in IUGR fetuses-a review. Placenta 23 Suppl A: S136-S141.
-
(2002)
Placenta
, vol.23
, Issue.SUPPL. A
-
-
Pardi, G.1
Marconi, A.M.2
Cetin, I.3
-
35
-
-
0345451625
-
Genomic imprinting, development and disease-is preeclampsia caused by a maternally imprinted gene?
-
Graves JA (1998) Genomic imprinting, development and disease-is preeclampsia caused by a maternally imprinted gene? Reprod Fertil Dev 10: 23-29.
-
(1998)
Reprod Fertil Dev
, vol.10
, pp. 23-29
-
-
Graves, J.A.1
-
36
-
-
4344708984
-
The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas
-
Oudejans CB, Mulders J, Lachmeijer AM, van DM, Konst AA, et al. (2004) The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas. Mol Hum Reprod 10: 589-598.
-
(2004)
Mol Hum Reprod
, vol.10
, pp. 589-598
-
-
Oudejans, C.B.1
Mulders, J.2
Lachmeijer, A.M.3
van, D.M.4
Konst, A.A.5
-
37
-
-
67349262027
-
CDKN1C mutations in HELLP/preeclamptic mothers of Beckwith- Wiedemann Syndrome (BWS) patients
-
Romanelli V, Belinchon A, Campos-Barros A, Heath KE, Garcia-Minaur S, et al. (2009) CDKN1C mutations in HELLP/preeclamptic mothers of Beckwith- Wiedemann Syndrome (BWS) patients. Placenta 30: 551-554.
-
(2009)
Placenta
, vol.30
, pp. 551-554
-
-
Romanelli, V.1
Belinchon, A.2
Campos-Barros, A.3
Heath, K.E.4
Garcia-Minaur, S.5
-
38
-
-
0033694908
-
p57(Kip2) regulates the proper development of labyrinthine and spongiotrophoblasts
-
Takahashi K, Kobayashi T, Kanayama N (2000) p57(Kip2) regulates the proper development of labyrinthine and spongiotrophoblasts. Mol Hum Reprod 6: 1019-1025.
-
(2000)
Mol Hum Reprod
, vol.6
, pp. 1019-1025
-
-
Takahashi, K.1
Kobayashi, T.2
Kanayama, N.3
-
39
-
-
0036924244
-
Deficiency in p57Kip2 expression induces preeclampsia-like symptoms in mice
-
Kanayama N, Takahashi K, Matsuura T, Sugimura M, Kobayashi T, et al. (2002) Deficiency in p57Kip2 expression induces preeclampsia-like symptoms in mice. Mol Hum Reprod 8: 1129-1135.
-
(2002)
Mol Hum Reprod
, vol.8
, pp. 1129-1135
-
-
Kanayama, N.1
Takahashi, K.2
Matsuura, T.3
Sugimura, M.4
Kobayashi, T.5
-
40
-
-
33847295115
-
STOX1 is not imprinted and is not likely to be involved in preeclampsia
-
Iglesias-Platas I, Monk D, Jebbink J, Buimer M, Boer K, et al. (2007) STOX1 is not imprinted and is not likely to be involved in preeclampsia. Nat Genet 39: 279-280.
-
(2007)
Nat Genet
, vol.39
, pp. 279-280
-
-
Iglesias-Platas, I.1
Monk, D.2
Jebbink, J.3
Buimer, M.4
Boer, K.5
-
41
-
-
33947398439
-
Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight
-
Apostolidou S, bu-Amero S, O'Donoghue K, Frost J, Olafsdottir O, et al. (2007) Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight. J Mol Med 85: 379-387.
-
(2007)
J Mol Med
, vol.85
, pp. 379-387
-
-
Apostolidou, S.1
bu-Amero, S.2
O'Donoghue, K.3
Frost, J.4
Olafsdottir, O.5
-
42
-
-
33645902182
-
Unbalanced placental expression of imprinted genes in human intrauterine growth restriction
-
McMinn J, Wei M, Schupf N, Cusmai J, Johnson EB, et al. (2006) Unbalanced placental expression of imprinted genes in human intrauterine growth restriction. Placenta 27: 540-549.
-
(2006)
Placenta
, vol.27
, pp. 540-549
-
-
McMinn, J.1
Wei, M.2
Schupf, N.3
Cusmai, J.4
Johnson, E.B.5
-
43
-
-
0033986515
-
Expression of the imprinted genes MEST/Mest in human and murine placenta suggests a role in angiogenesis
-
Mayer W, Hemberger M, Frank HG, Grummer R, Winterhager E, et al. (2000) Expression of the imprinted genes MEST/Mest in human and murine placenta suggests a role in angiogenesis. Dev Dyn 217: 1-10.
-
(2000)
Dev Dyn
, vol.217
, pp. 1-10
-
-
Mayer, W.1
Hemberger, M.2
Frank, H.G.3
Grummer, R.4
Winterhager, E.5
-
44
-
-
0035168178
-
A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver- Russell syndrome delimits a candidate gene region
-
Hannula K, Lipsanen-Nyman M, Kontiokari T, Kere J (2001) A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver- Russell syndrome delimits a candidate gene region. Am J Hum Genet 68: 247-253.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 247-253
-
-
Hannula, K.1
Lipsanen-Nyman, M.2
Kontiokari, T.3
Kere, J.4
-
45
-
-
0031687985
-
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
-
Lefebvre L, Viville S, Barton SC, Ishino F, Keverne EB, et al. (1998) Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet 20: 163-169.
-
(1998)
Nat Genet
, vol.20
, pp. 163-169
-
-
Lefebvre, L.1
Viville, S.2
Barton, S.C.3
Ishino, F.4
Keverne, E.B.5
-
46
-
-
68049112640
-
Reciprocal imprinting of human GRB10 in placental trophoblast and brain: Evolutionary conservation of reversed allelic expression
-
Monk D, Arnaud P, Frost J, Hills FA, Stanier P, et al. (2009) Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression. Hum Mol Genet.
-
(2009)
Hum Mol Genet
-
-
Monk, D.1
Arnaud, P.2
Frost, J.3
Hills, F.A.4
Stanier, P.5
-
47
-
-
0033940412
-
Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome
-
Monk D, Wakeling EL, Proud V, Hitchins M, bu-Amero SN, et al. (2000) Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome. Am J Hum Genet 66: 36-46.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 36-46
-
-
Monk, D.1
Wakeling, E.L.2
Proud, V.3
Hitchins, M.4
bu-Amero, S.N.5
-
48
-
-
42049087364
-
The genetic aetiology of Silver-Russell syndrome
-
Abu-Amero S, Monk D, Frost J, Preece M, Stanier P, et al. (2008) The genetic aetiology of Silver-Russell syndrome. J Med Genet 45: 193-199.
-
(2008)
J Med Genet
, vol.45
, pp. 193-199
-
-
Abu-Amero, S.1
Monk, D.2
Frost, J.3
Preece, M.4
Stanier, P.5
-
49
-
-
0037816227
-
Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism
-
Charalambous M, Smith FM, Bennett WR, Crew TE, Mackenzie F, et al. (2003) Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism. Proc Natl Acad Sci U S A 100: 8292-8297.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 8292-8297
-
-
Charalambous, M.1
Smith, F.M.2
Bennett, W.R.3
Crew, T.E.4
Mackenzie, F.5
-
50
-
-
70450224442
-
Maternally-inherited Grb10 reduces placental size and efficiency
-
Charalambous M, Cowley M, Geoghegan F, Smith FM, Radford EJ, et al. (2010) Maternally-inherited Grb10 reduces placental size and efficiency. Dev Biol 337: 1-8.
-
(2010)
Dev Biol
, vol.337
, pp. 1-8
-
-
Charalambous, M.1
Cowley, M.2
Geoghegan, F.3
Smith, F.M.4
Radford, E.J.5
-
51
-
-
0037182866
-
Placental-specific IGF-II is a major modulator of placental and fetal growth
-
Constancia M, Hemberger M, Hughes J, Dean W, Ferguson-Smith A, et al. (2002) Placental-specific IGF-II is a major modulator of placental and fetal growth. Nature 417: 945-948.
-
(2002)
Nature
, vol.417
, pp. 945-948
-
-
Constancia, M.1
Hemberger, M.2
Hughes, J.3
Dean, W.4
Ferguson-Smith, A.5
-
52
-
-
33645820241
-
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human
-
Monk D, Sanches R, Arnaud P, Apostolidou S, Hills FA, et al. (2006) Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human. Hum Mol Genet 15: 1259-1269.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1259-1269
-
-
Monk, D.1
Sanches, R.2
Arnaud, P.3
Apostolidou, S.4
Hills, F.A.5
-
53
-
-
2542555066
-
Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta
-
Sibley CP, Coan PM, Ferguson-Smith AC, Dean W, Hughes J, et al. (2004) Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta. Proc Natl Acad Sci U S A 101: 8204-8208.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 8204-8208
-
-
Sibley, C.P.1
Coan, P.M.2
Ferguson-Smith, A.C.3
Dean, W.4
Hughes, J.5
-
54
-
-
30044432595
-
Adaptation of nutrient supply to fetal demand in the mouse involves interaction between the Igf2 gene and placental transporter systems
-
Constancia M, Angiolini E, Sandovici I, Smith P, Smith R, et al. (2005) Adaptation of nutrient supply to fetal demand in the mouse involves interaction between the Igf2 gene and placental transporter systems. Proc Natl Acad Sci U S A 102: 19219-19224.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 19219-19224
-
-
Constancia, M.1
Angiolini, E.2
Sandovici, I.3
Smith, P.4
Smith, R.5
-
55
-
-
18444364959
-
Placental overgrowth in mice lacking the imprinted gene Ipl
-
Frank D, Fortino W, Clark L, Musalo R, Wang W, et al. (2002) Placental overgrowth in mice lacking the imprinted gene Ipl. Proc Natl Acad Sci U S A 99: 7490-7495.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 7490-7495
-
-
Frank, D.1
Fortino, W.2
Clark, L.3
Musalo, R.4
Wang, W.5
-
56
-
-
73549090111
-
The imprinted Phlda2 gene regulates extraembryonic energy stores
-
Tunster SJ, Tycko B, John RM (2010) The imprinted Phlda2 gene regulates extraembryonic energy stores. Mol Cell Biol 30: 295-306.
-
(2010)
Mol Cell Biol
, vol.30
, pp. 295-306
-
-
Tunster, S.J.1
Tycko, B.2
John, R.M.3
-
57
-
-
9644266664
-
Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation
-
Lewis A, Mitsuya K, Umlauf D, Smith P, Dean W, et al. (2004) Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. Nat Genet 36: 1291-1295.
-
(2004)
Nat Genet
, vol.36
, pp. 1291-1295
-
-
Lewis, A.1
Mitsuya, K.2
Umlauf, D.3
Smith, P.4
Dean, W.5
-
58
-
-
9644281546
-
Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes
-
Umlauf D, Goto Y, Cao R, Cerqueira F, Wagschal A, et al. (2004) Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes. Nat Genet 36: 1296-1300.
-
(2004)
Nat Genet
, vol.36
, pp. 1296-1300
-
-
Umlauf, D.1
Goto, Y.2
Cao, R.3
Cerqueira, F.4
Wagschal, A.5
-
59
-
-
33747674520
-
Characterization of the placenta specific bovine mammalian achaete scute-like homologue 2 (Mash2) gene
-
Arnold DR, Lefebvre R, Smith LC (2006) Characterization of the placenta specific bovine mammalian achaete scute-like homologue 2 (Mash2) gene. Placenta 27: 1124-1131.
-
(2006)
Placenta
, vol.27
, pp. 1124-1131
-
-
Arnold, D.R.1
Lefebvre, R.2
Smith, L.C.3
-
60
-
-
0028815477
-
Genomic imprinting of Mash2, a mouse gene required for trophoblast development
-
Guillemot F, Caspary T, Tilghman SM, Copeland NG, Gilbert DJ, et al. (1995) Genomic imprinting of Mash2, a mouse gene required for trophoblast development. Nat Genet 9: 235-242.
-
(1995)
Nat Genet
, vol.9
, pp. 235-242
-
-
Guillemot, F.1
Caspary, T.2
Tilghman, S.M.3
Copeland, N.G.4
Gilbert, D.J.5
-
61
-
-
0030955563
-
Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development
-
Yan Y, Frisen J, Lee MH, Massague J, Barbacid M (1997) Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development. Genes Dev 11: 973-983.
-
(1997)
Genes Dev
, vol.11
, pp. 973-983
-
-
Yan, Y.1
Frisen, J.2
Lee, M.H.3
Massague, J.4
Barbacid, M.5
-
62
-
-
16044364516
-
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
-
Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, et al. (1996) An imprinted gene p57KIP2 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
-
63
-
-
0034530186
-
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
-
Engel JR, Smallwood A, Harper A, Higgins MJ, Oshimura M, et al. (2000) Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome. JMed Genet 37: 921-926.
-
(2000)
JMed Genet
, vol.37
, pp. 921-926
-
-
Engel, J.R.1
Smallwood, A.2
Harper, A.3
Higgins, M.J.4
Oshimura, M.5
-
64
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, et al. (1996) Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 12: 17-23.
-
(1996)
Nat Genet
, vol.12
, pp. 17-23
-
-
Wang, Q.1
Curran, M.E.2
Splawski, I.3
Burn, T.C.4
Millholland, J.M.5
-
65
-
-
0031046285
-
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
-
Lee MP, Hu RJ, Johnson LA, Feinberg AP (1997) Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nat Genet 15: 181-185.
-
(1997)
Nat Genet
, vol.15
, pp. 181-185
-
-
Lee, M.P.1
Hu, R.J.2
Johnson, L.A.3
Feinberg, A.P.4
-
66
-
-
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 MP, Katoh M, Schulz TC, et al. (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
-
67
-
-
0036831864
-
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1
-
Fitzpatrick GV, Soloway PD, Higgins MJ (2002) Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat Genet 32: 426-431.
-
(2002)
Nat Genet
, vol.32
, pp. 426-431
-
-
Fitzpatrick, G.V.1
Soloway, P.D.2
Higgins, M.J.3
-
68
-
-
33646598385
-
Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes
-
Mancini-DiNardo D, Steele SJ, Levorse JM, Ingram RS, Tilghman SM (2006) Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes. Genes Dev 20: 1268-1282.
-
(2006)
Genes Dev
, vol.20
, pp. 1268-1282
-
-
Mancini-DiNardo, D.1
Steele, S.J.2
Levorse, J.M.3
Ingram, R.S.4
Tilghman, S.M.5
-
69
-
-
38049045084
-
Two distinct mechanisms of silencing by the KvDMR1 imprinting control region
-
Shin JY, Fitzpatrick GV, Higgins MJ (2008) Two distinct mechanisms of silencing by the KvDMR1 imprinting control region. Embo J 27: 168-178.
-
(2008)
Embo J
, vol.27
, pp. 168-178
-
-
Shin, J.Y.1
Fitzpatrick, G.V.2
Higgins, M.J.3
-
70
-
-
33846818301
-
A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA
-
Green K, Lewis A, Dawson C, Dean W, Reinhart B, et al. (2007) A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA. Mamm Genome 18: 32-42.
-
(2007)
Mamm Genome
, vol.18
, pp. 32-42
-
-
Green, K.1
Lewis, A.2
Dawson, C.3
Dean, W.4
Reinhart, B.5
-
71
-
-
3042584653
-
Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting
-
Kaneda M, Okano M, Hata K, Sado T, Tsujimoto N, et al. (2004) Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting. Nature 429: 900-903.
-
(2004)
Nature
, vol.429
, pp. 900-903
-
-
Kaneda, M.1
Okano, M.2
Hata, K.3
Sado, T.4
Tsujimoto, N.5
-
72
-
-
55349100420
-
Polycomb group proteins Ezh2 and Rnf2 direct genomic contraction and imprinted repression in early mouse embryos
-
Terranova R, Yokobayashi S, Stadler MB, Otte AP, van LM, et al. (2008) Polycomb group proteins Ezh2 and Rnf2 direct genomic contraction and imprinted repression in early mouse embryos. Dev Cell 15: 668-679.
-
(2008)
Dev Cell
, vol.15
, pp. 668-679
-
-
Terranova, R.1
Yokobayashi, S.2
Stadler, M.B.3
Otte, A.P.4
van, L.M.5
-
73
-
-
60149092541
-
The long noncoding RNA Kcnq1ot1 organises a lineage-specific nuclear domain for epigenetic gene silencing
-
Redrup L, Branco MR, Perdeaux ER, Krueger C, Lewis A, et al. (2009) The long noncoding RNA Kcnq1ot1 organises a lineage-specific nuclear domain for epigenetic gene silencing. Development 136: 525-530.
-
(2009)
Development
, vol.136
, pp. 525-530
-
-
Redrup, L.1
Branco, M.R.2
Perdeaux, E.R.3
Krueger, C.4
Lewis, A.5
-
74
-
-
0035217664
-
Evolution of the placenta and fetal membranes seen in the light of molecular phylogenetics
-
Carter AM (2001) Evolution of the placenta and fetal membranes seen in the light of molecular phylogenetics. Placenta 22: 800-807.
-
(2001)
Placenta
, vol.22
, pp. 800-807
-
-
Carter, A.M.1
-
75
-
-
34047190806
-
Animal models of human placentation-a review
-
Carter AM (2007) Animal models of human placentation-a review. Placenta 28 Suppl A: S41-S47.
-
(2007)
Placenta
, vol.28
, Issue.SUPPL. A
-
-
Carter, A.M.1
-
76
-
-
60249094325
-
Reasons for diversity of placental structure
-
Enders AC (2009) Reasons for diversity of placental structure. Placenta 30 Suppl A: S15-S18.
-
(2009)
Placenta
, vol.30
, Issue.SUPPL. A
-
-
Enders, A.C.1
-
77
-
-
33845360672
-
Origin and characteristics of glycogen cells in the developing murine placenta
-
Coan PM, Conroy N, Burton GJ, Ferguson-Smith AC (2006) Origin and characteristics of glycogen cells in the developing murine placenta. Dev Dyn 235: 3280-3294.
-
(2006)
Dev Dyn
, vol.235
, pp. 3280-3294
-
-
Coan, P.M.1
Conroy, N.2
Burton, G.J.3
Ferguson-Smith, A.C.4
-
79
-
-
33947714583
-
New light on early post-implantation pregnancy in the mouse: Roles for insulin-like growth factor-II (IGF-II)?
-
Pringle KG, Roberts CT (2007) New light on early post-implantation pregnancy in the mouse: roles for insulin-like growth factor-II (IGF-II)? Placenta 28: 286-297.
-
(2007)
Placenta
, vol.28
, pp. 286-297
-
-
Pringle, K.G.1
Roberts, C.T.2
-
80
-
-
0032949412
-
Microsatellites indicate a high frequency of multiple paternity in Apodemus (Rodentia)
-
Baker RJ, Makova KD, Chesser RK (1999) Microsatellites indicate a high frequency of multiple paternity in Apodemus (Rodentia). Mol Ecol 8: 107-111.
-
(1999)
Mol Ecol
, vol.8
, pp. 107-111
-
-
Baker, R.J.1
Makova, K.D.2
Chesser, R.K.3
-
81
-
-
33750216517
-
The frequency of multiple paternity suggests that sperm competition is common in house mice (Mus domesticus)
-
Dean MD, Ardlie KG, Nachman MW (2006) The frequency of multiple paternity suggests that sperm competition is common in house mice (Mus domesticus). Mol Ecol 15: 4141-4151.
-
(2006)
Mol Ecol
, vol.15
, pp. 4141-4151
-
-
Dean, M.D.1
Ardlie, K.G.2
Nachman, M.W.3
-
82
-
-
0033020682
-
Multiple paternity and genomic imprinting
-
Haig D (1999) Multiple paternity and genomic imprinting. Genetics 151: 1229-1231.
-
(1999)
Genetics
, vol.151
, pp. 1229-1231
-
-
Haig, D.1
-
83
-
-
0027941535
-
Essential role of Mash-2 in extraembryonic development
-
Guillemot F, Nagy A, Auerbach A, Rossant J, Joyner AL (1994) Essential role of Mash-2 in extraembryonic development. Nature 371: 333-336.
-
(1994)
Nature
, vol.371
, pp. 333-336
-
-
Guillemot, F.1
Nagy, A.2
Auerbach, A.3
Rossant, J.4
Joyner, A.L.5
-
84
-
-
0035985843
-
The human ASCL2 gene escaping genomic imprinting and its expression pattern
-
Miyamoto T, Hasuike S, Jinno Y, Soejima H, Yun K, et al. (2002) The human ASCL2 gene escaping genomic imprinting and its expression pattern. J Assist Reprod Genet 19: 240-244.
-
(2002)
J Assist Reprod Genet
, vol.19
, pp. 240-244
-
-
Miyamoto, T.1
Hasuike, S.2
Jinno, Y.3
Soejima, H.4
Yun, K.5
-
85
-
-
38349113485
-
Monoallelic expression of nine imprinted genes in the sheep embryo occurs after the blastocyst stage
-
Thurston A, Taylor J, Gardner J, Sinclair KD, Young LE (2008) Monoallelic expression of nine imprinted genes in the sheep embryo occurs after the blastocyst stage. Reproduction 135: 29-40.
-
(2008)
Reproduction
, vol.135
, pp. 29-40
-
-
Thurston, A.1
Taylor, J.2
Gardner, J.3
Sinclair, K.D.4
Young, L.E.5
-
86
-
-
42349091015
-
Genomic evolution of the placenta using co-option and duplication and divergence
-
Knox K, Baker JC (2008) Genomic evolution of the placenta using co-option and duplication and divergence. Genome Res 18: 695-705.
-
(2008)
Genome Res
, vol.18
, pp. 695-705
-
-
Knox, K.1
Baker, J.C.2
-
87
-
-
0033865243
-
Identification of a methylation imprint mark within the mouse Gnas locus
-
Liu J, Yu S, Litman D, Chen W, Weinstein LS (2000) Identification of a methylation imprint mark within the mouse Gnas locus. Mol Cell Biol 20: 5808-5817.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 5808-5817
-
-
Liu, J.1
Yu, S.2
Litman, D.3
Chen, W.4
Weinstein, L.S.5
-
88
-
-
3543036987
-
The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding
-
Plagge A, Gordon E, Dean W, Boiani R, Cinti S, et al. (2004) The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding. Nat Genet 36: 818-826.
-
(2004)
Nat Genet
, vol.36
, pp. 818-826
-
-
Plagge, A.1
Gordon, E.2
Dean, W.3
Boiani, R.4
Cinti, S.5
-
89
-
-
0028301177
-
Developmental regulation of genomic imprinting of the IGF2 gene in human liver
-
Davies SM (1994) Developmental regulation of genomic imprinting of the IGF2 gene in human liver. Cancer Res 54: 2560-2562.
-
(1994)
Cancer Res
, vol.54
, pp. 2560-2562
-
-
Davies, S.M.1
-
90
-
-
0025958320
-
Genomic imprinting in mammalian development: A parental tug-of-war
-
Moore T, Haig D (1991) Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet 7: 45-49.
-
(1991)
Trends Genet
, vol.7
, pp. 45-49
-
-
Moore, T.1
Haig, D.2
-
91
-
-
43549091117
-
Intergenerational obesity involves both the father and the mother
-
Cole TJ, Power C, Moore GE (2008) Intergenerational obesity involves both the father and the mother. Am J Clin Nutr 87: 1535-1536.
-
(2008)
Am J Clin Nutr
, vol.87
, pp. 1535-1536
-
-
Cole, T.J.1
Power, C.2
Moore, G.E.3
-
92
-
-
50249110937
-
Evolution of genomic imprinting with biparental care: Implications for Prader-Willi and Angelman syndromes
-
Ubeda F (2008) Evolution of genomic imprinting with biparental care: implications for Prader-Willi and Angelman syndromes. PLoS Biol 6: e208.
-
(2008)
PLoS Biol
, vol.6
-
-
Ubeda, F.1
-
93
-
-
0028964548
-
Clinical profile of Angelman syndrome at different ages
-
Buntinx IM, Hennekam RC, Brouwer OF, Stroink H, Beuten J, et al. (1995) Clinical profile of Angelman syndrome at different ages. Am J Med Genet 56: 176-183.
-
(1995)
Am J Med Genet
, vol.56
, pp. 176-183
-
-
Buntinx, I.M.1
Hennekam, R.C.2
Brouwer, O.F.3
Stroink, H.4
Beuten, J.5
-
94
-
-
0037738698
-
Prader-Willi syndrome and the evolution of human childhood
-
Haig D, Wharton R (2003) Prader-Willi syndrome and the evolution of human childhood. Am J Hum Biol 15: 320-329.
-
(2003)
Am J Hum Biol
, vol.15
, pp. 320-329
-
-
Haig, D.1
Wharton, R.2
-
95
-
-
44349191455
-
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
-
Sahoo T, del GD, German JR, Shinawi M, Peters SU, et al. (2008) Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster. Nat Genet 40: 719-721.
-
(2008)
Nat Genet
, vol.40
, pp. 719-721
-
-
Sahoo, T.1
del, G.D.2
German, J.R.3
Shinawi, M.4
Peters, S.U.5
-
96
-
-
37749004050
-
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation
-
Skryabin BV, Gubar LV, Seeger B, Pfeiffer J, Handel S, et al. (2007) Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation. PLoS Genet 3: e235.
-
(2007)
PLoS Genet
, vol.3
-
-
Skryabin, B.V.1
Gubar, L.V.2
Seeger, B.3
Pfeiffer, J.4
Handel, S.5
-
97
-
-
45849144806
-
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
-
Ding F, Li HH, Zhang S, Solomon NM, Camper SA, et al. (2008) SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. PLoS ONE 3: e1709.
-
(2008)
PLoS ONE
, vol.3
-
-
Ding, F.1
Li, H.H.2
Zhang, S.3
Solomon, N.M.4
Camper, S.A.5
-
98
-
-
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, Schulz U, Wollmann HA, Craigen W, et al. (2000) Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet 9: 1587-1595.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1587-1595
-
-
Blagitko, N.1
Mergenthaler, S.2
Schulz, U.3
Wollmann, H.A.4
Craigen, W.5
-
99
-
-
0035131431
-
Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome
-
Hitchins MP, Monk D, Bell GM, Ali Z, Preece MA, et al. (2001) Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome. Eur J Hum Genet 9: 82-90.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 82-90
-
-
Hitchins, M.P.1
Monk, D.2
Bell, G.M.3
Ali, Z.4
Preece, M.A.5
-
100
-
-
0038364061
-
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark
-
Arnaud P, Monk D, Hitchins M, Gordon E, Dean W, et al. (2003) Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark. Hum Mol Genet 12: 1005-1019.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1005-1019
-
-
Arnaud, P.1
Monk, D.2
Hitchins, M.3
Gordon, E.4
Dean, W.5
-
101
-
-
34547888298
-
Mice with a disruption of the imprinted Grb10 gene exhibit altered body composition, glucose homeostasis, and insulin signaling during postnatal life
-
Smith FM, Holt LJ, Garfield AS, Charalambous M, Koumanov F, et al. (2007) Mice with a disruption of the imprinted Grb10 gene exhibit altered body composition, glucose homeostasis, and insulin signaling during postnatal life. Mol Cell Biol 27: 5871-5886.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 5871-5886
-
-
Smith, F.M.1
Holt, L.J.2
Garfield, A.S.3
Charalambous, M.4
Koumanov, F.5
-
102
-
-
61449215237
-
Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: Implications for the evolution of imprinting
-
da Rocha ST, Charalambous M, Lin SP, Gutteridge I, Ito Y, et al. (2009) Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: implications for the evolution of imprinting. PLoS Genet 5: e1000392.
-
(2009)
PLoS Genet
, vol.5
-
-
da Rocha, S.T.1
Charalambous, M.2
Lin, S.P.3
Gutteridge, I.4
Ito, Y.5
-
103
-
-
0036318227
-
Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity
-
Moon YS, Smas CM, Lee K, Villena JA, Kim KH, et al. (2002) Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity. Mol Cell Biol 22: 5585-5592.
-
(2002)
Mol Cell Biol
, vol.22
, pp. 5585-5592
-
-
Moon, Y.S.1
Smas, C.M.2
Lee, K.3
Villena, J.A.4
Kim, K.H.5
-
104
-
-
17744391429
-
Co-evolution of X-chromosome inactivation and imprinting in mammals
-
Reik W, Lewis A (2005) Co-evolution of X-chromosome inactivation and imprinting in mammals. Nat Rev Genet 6: 403-410.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 403-410
-
-
Reik, W.1
Lewis, A.2
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