-
1
-
-
34748925916
-
Association between paternally inherited haplotypes upstream of the insulin gene and umbilical cord IGF-II levels
-
Adkins R.M., Fain J.N., Krushkal J., Klauser C.K., Magann E.F., and Morrison J.C. Association between paternally inherited haplotypes upstream of the insulin gene and umbilical cord IGF-II levels. Pediatr. Res. 62 (2007) 451-455
-
(2007)
Pediatr. Res.
, vol.62
, pp. 451-455
-
-
Adkins, R.M.1
Fain, J.N.2
Krushkal, J.3
Klauser, C.K.4
Magann, E.F.5
Morrison, J.C.6
-
2
-
-
34548406545
-
Insulin is imprinted in the placenta of the marsupial, Macropus eugenii
-
Ager E., Suzuki S., Pask A., Shaw G., Ishino F., and Renfree M.B. Insulin is imprinted in the placenta of the marsupial, Macropus eugenii. Dev. Biol. 309 (2007) 317-328
-
(2007)
Dev. Biol.
, vol.309
, pp. 317-328
-
-
Ager, E.1
Suzuki, S.2
Pask, A.3
Shaw, G.4
Ishino, F.5
Renfree, M.B.6
-
3
-
-
12744254776
-
Prenatal diagnosis of fetal growth restriction
-
Bamberg C., and Kalache K.D. Prenatal diagnosis of fetal growth restriction. Semin. Fetal Neonatal Med. 9 (2004) 387-394
-
(2004)
Semin. Fetal Neonatal Med.
, vol.9
, pp. 387-394
-
-
Bamberg, C.1
Kalache, K.D.2
-
4
-
-
10844241534
-
The developmental origins of chronic adult disease
-
Barker D.J. The developmental origins of chronic adult disease. Acta Paediatr., Suppl. 93 (2004) 26-33
-
(2004)
Acta Paediatr., Suppl.
, vol.93
, pp. 26-33
-
-
Barker, D.J.1
-
5
-
-
28444491805
-
Arterial and venous Doppler in the diagnosis and management of early onset fetal growth restriction
-
Baschat A.A. Arterial and venous Doppler in the diagnosis and management of early onset fetal growth restriction. Early Hum. Dev. 81 (2005) 877-887
-
(2005)
Early Hum. Dev.
, vol.81
, pp. 877-887
-
-
Baschat, A.A.1
-
6
-
-
29344457864
-
Detailed analysis of the methylation patterns of the KvDMR1 imprinting control region of human chromosome 11
-
Beatty L., Weksberg R., and Sadowski P.D. Detailed analysis of the methylation patterns of the KvDMR1 imprinting control region of human chromosome 11. Genomics 87 (2006) 46-56
-
(2006)
Genomics
, vol.87
, pp. 46-56
-
-
Beatty, L.1
Weksberg, R.2
Sadowski, P.D.3
-
7
-
-
0034713375
-
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
-
Bell A.C., and Felsenfeld G. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene. Nature 405 (2000) 482-485
-
(2000)
Nature
, vol.405
, pp. 482-485
-
-
Bell, A.C.1
Felsenfeld, G.2
-
8
-
-
0033529654
-
The protein CTCF is required for the enhancer blocking activity of vertebrate insulators
-
Bell A.C., West A.G., and Felsenfeld G. The protein CTCF is required for the enhancer blocking activity of vertebrate insulators. Cell 98 (1999) 387-396
-
(1999)
Cell
, vol.98
, pp. 387-396
-
-
Bell, A.C.1
West, A.G.2
Felsenfeld, G.3
-
9
-
-
0035910395
-
Insulators and boundaries: versatile regulatory elements in the eukaryotic genome
-
Bell A.C., West A.G., and Felsenfeld G. Insulators and boundaries: versatile regulatory elements in the eukaryotic genome. Science 291 (2001) 447-450
-
(2001)
Science
, vol.291
, pp. 447-450
-
-
Bell, A.C.1
West, A.G.2
Felsenfeld, G.3
-
10
-
-
16644375005
-
Current concepts in intrauterine growth restriction
-
Brodsky D., and Christou H. Current concepts in intrauterine growth restriction. J. Intensive Care Med. 19 (2004) 307-319
-
(2004)
J. Intensive Care Med.
, vol.19
, pp. 307-319
-
-
Brodsky, D.1
Christou, H.2
-
11
-
-
0017697719
-
Fetal growth retardation and the arteries of the placental bed
-
Brosens I., Dixon H.G., and Robertson W.B. Fetal growth retardation and the arteries of the placental bed. Br. J. Obstet. Gynaecol. 84 (1977) 656-663
-
(1977)
Br. J. Obstet. Gynaecol.
, vol.84
, pp. 656-663
-
-
Brosens, I.1
Dixon, H.G.2
Robertson, W.B.3
-
12
-
-
36348970734
-
Examination of IGF2 and H19 loss of imprinting in bladder cancer
-
Byun H.M., Wong H.L., Birnstein E.A., Wolff E.M., Liang G., and Yang A.S. Examination of IGF2 and H19 loss of imprinting in bladder cancer. Cancer Res. 67 (2007) 10753-10758
-
(2007)
Cancer Res.
, vol.67
, pp. 10753-10758
-
-
Byun, H.M.1
Wong, H.L.2
Birnstein, E.A.3
Wolff, E.M.4
Liang, G.5
Yang, A.S.6
-
13
-
-
0031844688
-
Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster
-
Caspary T., Cleary M.A., Baker C.C., Guan X.J., and Tilghman S.M. Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. Mol. Cell. Biol. 18 (1998) 3466-3474
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 3466-3474
-
-
Caspary, T.1
Cleary, M.A.2
Baker, C.C.3
Guan, X.J.4
Tilghman, S.M.5
-
14
-
-
14044261317
-
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster
-
Cerrato F., Sparago A., Matteo I.D., Zou X., Dean W., Sasaki H., Smith P., Genesio R., Bruggemann M., Reik W., and Riccio A. The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster. Hum. Mol. Genet. 14 (2005) 503-511
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 503-511
-
-
Cerrato, F.1
Sparago, A.2
Matteo, I.D.3
Zou, X.4
Dean, W.5
Sasaki, H.6
Smith, P.7
Genesio, R.8
Bruggemann, M.9
Reik, W.10
Riccio, A.11
-
16
-
-
0029794571
-
Birth weight and adult hypertension and obesity in women
-
Curhan G.C., Chertow G.M., Willett W.C., Spiegelman D., Colditz G.A., Manson J.E., Speizer F.E., and Stampfer M.J. Birth weight and adult hypertension and obesity in women. Circulation 94 (1996) 1310-1315
-
(1996)
Circulation
, vol.94
, pp. 1310-1315
-
-
Curhan, G.C.1
Chertow, G.M.2
Willett, W.C.3
Spiegelman, D.4
Colditz, G.A.5
Manson, J.E.6
Speizer, F.E.7
Stampfer, M.J.8
-
17
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
DeChiara T.M., Robertson E.J., and Efstratiadis A. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64 (1991) 849-859
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
DeChiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
18
-
-
0042631444
-
Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5
-
Du M., Beatty L.G., Zhou W., Lew J., Schoenherr C., Weksberg R., and Sadowski P.D. Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5. Hum. Mol. Genet. 12 (2003) 1927-1939
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1927-1939
-
-
Du, M.1
Beatty, L.G.2
Zhou, W.3
Lew, J.4
Schoenherr, C.5
Weksberg, R.6
Sadowski, P.D.7
-
19
-
-
3042520626
-
The KCNQ1OT1 promoter, a key regulator of genomic imprinting in human chromosome 11p15.5
-
Du M., Zhou W., Beatty L.G., Weksberg R., and Sadowski P.D. The KCNQ1OT1 promoter, a key regulator of genomic imprinting in human chromosome 11p15.5. Genomics 84 (2004) 288-300
-
(2004)
Genomics
, vol.84
, pp. 288-300
-
-
Du, M.1
Zhou, W.2
Beatty, L.G.3
Weksberg, R.4
Sadowski, P.D.5
-
20
-
-
33645985511
-
Morphometric placental villous and vascular abnormalities in early- and late-onset pre-eclampsia with and without fetal growth restriction
-
Egbor M., Ansari T., Morris N., Green C.J., and Sibbons P.D. Morphometric placental villous and vascular abnormalities in early- and late-onset pre-eclampsia with and without fetal growth restriction. Bjog 113 (2006) 580-589
-
(2006)
Bjog
, vol.113
, pp. 580-589
-
-
Egbor, M.1
Ansari, T.2
Morris, N.3
Green, C.J.4
Sibbons, P.D.5
-
21
-
-
33745903915
-
Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain
-
Eggermann T., Schonherr N., Meyer E., Obermann C., Mavany M., Eggermann K., Ranke M.B., and Wollmann H.A. Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain. J. Med. Genet. 43 (2006) 615-616
-
(2006)
J. Med. Genet.
, vol.43
, pp. 615-616
-
-
Eggermann, T.1
Schonherr, N.2
Meyer, E.3
Obermann, C.4
Mavany, M.5
Eggermann, K.6
Ranke, M.B.7
Wollmann, H.A.8
-
22
-
-
0034326859
-
Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting [In Process Citation]
-
Engemann S., Strodicke M., Paulsen M., Franck O., Reinhardt R., Lane N., Reik W., and Walter J. Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting [In Process Citation]. Hum. Mol. Genet. 9 (2000) 2691-2706
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2691-2706
-
-
Engemann, S.1
Strodicke, M.2
Paulsen, M.3
Franck, O.4
Reinhardt, R.5
Lane, N.6
Reik, W.7
Walter, J.8
-
23
-
-
0033805576
-
The two-domain hypothesis in Beckwith-Wiedemann syndrome
-
Feinberg A.P. The two-domain hypothesis in Beckwith-Wiedemann syndrome. J. Clin. Invest. 106 (2000) 739-740
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 739-740
-
-
Feinberg, A.P.1
-
24
-
-
0035839064
-
Imprinting and the epigenetic asymmetry between parental genomes
-
Ferguson-Smith A.C., and Surani M.A. Imprinting and the epigenetic asymmetry between parental genomes. Science 293 (2001) 1086-1089
-
(2001)
Science
, vol.293
, pp. 1086-1089
-
-
Ferguson-Smith, A.C.1
Surani, M.A.2
-
25
-
-
0036831864
-
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1
-
Fitzpatrick G.V., Soloway P.D., and Higgins M.J. Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat. Genet. 32 (2002) 426-431
-
(2002)
Nat. Genet.
, vol.32
, pp. 426-431
-
-
Fitzpatrick, G.V.1
Soloway, P.D.2
Higgins, M.J.3
-
26
-
-
0030607605
-
Birthweight, body-mass index in middle age, and incident coronary heart disease
-
Frankel S., Elwood P., Sweetnam P., Yarnell J., and Smith G.D. Birthweight, body-mass index in middle age, and incident coronary heart disease. Lancet 348 (1996) 1478-1480
-
(1996)
Lancet
, vol.348
, pp. 1478-1480
-
-
Frankel, S.1
Elwood, P.2
Sweetnam, P.3
Yarnell, J.4
Smith, G.D.5
-
27
-
-
0019490028
-
Morphological changes of the spiral arteries in the placental bed in relation to pre-eclampsia and fetal growth retardation
-
Gerretsen G., Huisjes H.J., and Elema J.D. Morphological changes of the spiral arteries in the placental bed in relation to pre-eclampsia and fetal growth retardation. Br. J. Obstet. Gynaecol. 88 (1981) 876-881
-
(1981)
Br. J. Obstet. Gynaecol.
, vol.88
, pp. 876-881
-
-
Gerretsen, G.1
Huisjes, H.J.2
Elema, J.D.3
-
28
-
-
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., Barbu V., Danton F., Thibaud N., Le Merrer M., Burglen L., Bertrand A.M., Netchine I., and Le Bouc Y. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nat. Genet. 37 (2005) 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
Barbu, V.6
Danton, F.7
Thibaud, N.8
Le Merrer, M.9
Burglen, L.10
Bertrand, A.M.11
Netchine, I.12
Le Bouc, Y.13
-
29
-
-
0034713275
-
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
-
Hark A.T., Schoenherr C.J., Katz D.J., Ingram R.S., Levorse J.M., and Tilghman S.M. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus. Nature 405 (2000) 486-489
-
(2000)
Nature
, vol.405
, pp. 486-489
-
-
Hark, A.T.1
Schoenherr, C.J.2
Katz, D.J.3
Ingram, R.S.4
Levorse, J.M.5
Tilghman, S.M.6
-
30
-
-
12244288877
-
Characterization and imprinting status of OBPH1/Obph1 gene: implications for an extended imprinting domain in human and mouse
-
Higashimoto K., Soejima H., Yatsuki H., Joh K., Uchiyama M., Obata Y., Ono R., Wang Y., Xin Z., Zhu X., Masuko S., Ishino F., Hatada I., Jinno Y., Iwasaka T., Katsuki T., and Mukai T. Characterization and imprinting status of OBPH1/Obph1 gene: implications for an extended imprinting domain in human and mouse. Genomics 80 (2002) 575-584
-
(2002)
Genomics
, vol.80
, pp. 575-584
-
-
Higashimoto, K.1
Soejima, H.2
Yatsuki, H.3
Joh, K.4
Uchiyama, M.5
Obata, Y.6
Ono, R.7
Wang, Y.8
Xin, Z.9
Zhu, X.10
Masuko, S.11
Ishino, F.12
Hatada, I.13
Jinno, Y.14
Iwasaka, T.15
Katsuki, T.16
Mukai, T.17
-
31
-
-
0034284693
-
Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
-
Horike S., Mitsuya K., Meguro M., Kotobuki N., Kashiwagi A., Notsu T., Schulz T.C., Shirayoshi Y., and Oshimura M. Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome. Hum. Mol. Genet. 9 (2000) 2075-2083
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2075-2083
-
-
Horike, S.1
Mitsuya, K.2
Meguro, M.3
Kotobuki, N.4
Kashiwagi, A.5
Notsu, T.6
Schulz, T.C.7
Shirayoshi, Y.8
Oshimura, M.9
-
33
-
-
0029043178
-
Establishment of functional imprinting of the H19 gene in human developing placentae
-
Jinno Y., Ikeda Y., Yun K., Maw M., Masuzaki H., Fukuda H., Inuzuka K., Fujishita A., Ohtani Y., Okimoto T., et al. Establishment of functional imprinting of the H19 gene in human developing placentae. Nat. Genet. 10 (1995) 318-324
-
(1995)
Nat. Genet.
, vol.10
, pp. 318-324
-
-
Jinno, Y.1
Ikeda, Y.2
Yun, K.3
Maw, M.4
Masuzaki, H.5
Fukuda, H.6
Inuzuka, K.7
Fujishita, A.8
Ohtani, Y.9
Okimoto, T.10
-
34
-
-
0035172234
-
Regulatory mechanisms at the mouse Igf2/H19 locus
-
Kaffer C.R., Grinberg A., and Pfeifer K. Regulatory mechanisms at the mouse Igf2/H19 locus. Mol. Cell. Biol. 21 (2001) 8189-8196
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 8189-8196
-
-
Kaffer, C.R.1
Grinberg, A.2
Pfeifer, K.3
-
35
-
-
0030846190
-
Oxygen and placental villous development: origins of fetal hypoxia
-
Discussion 623-6
-
Kingdom J.C., and Kaufmann P. Oxygen and placental villous development: origins of fetal hypoxia. Placenta 18 (1997) 613-621 Discussion 623-6
-
(1997)
Placenta
, vol.18
, pp. 613-621
-
-
Kingdom, J.C.1
Kaufmann, P.2
-
36
-
-
33845902840
-
Part 1: a matter of size: evaluating the growth-restricted neonate
-
Lawrence E.J. Part 1: a matter of size: evaluating the growth-restricted neonate. Adv. Neonatal. Care 6 (2006) 313-322
-
(2006)
Adv. Neonatal. Care
, vol.6
, pp. 313-322
-
-
Lawrence, E.J.1
-
37
-
-
0031687985
-
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
-
Lefebvre L., Viville S., Barton S.C., Ishino F., Keverne E.B., and Surani M.A. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat. Genet. 20 (1998) 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
Surani, M.A.6
-
38
-
-
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., Walter J., Higgins M., Feil R., and Reik W. Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. Nat. Genet. 36 (2004) 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
Walter, J.6
Higgins, M.7
Feil, R.8
Reik, W.9
-
39
-
-
0033537716
-
Regulation of maternal behavior and offspring growth by paternally expressed Peg3
-
Li L., Keverne E.B., Aparicio S.A., Ishino F., Barton S.C., and Surani M.A. Regulation of maternal behavior and offspring growth by paternally expressed Peg3. Science 284 (1999) 330-333
-
(1999)
Science
, vol.284
, pp. 330-333
-
-
Li, L.1
Keverne, E.B.2
Aparicio, S.A.3
Ishino, F.4
Barton, S.C.5
Surani, M.A.6
-
40
-
-
0030056272
-
Relation of size at birth to non-insulin dependent diabetes and insulin concentrations in men aged 50-60 years
-
Lithell H.O., McKeigue P.M., Berglund L., Mohsen R., Lithell U.B., and Leon D.A. Relation of size at birth to non-insulin dependent diabetes and insulin concentrations in men aged 50-60 years. Bmj 312 (1996) 406-410
-
(1996)
Bmj
, vol.312
, pp. 406-410
-
-
Lithell, H.O.1
McKeigue, P.M.2
Berglund, L.3
Mohsen, R.4
Lithell, U.B.5
Leon, D.A.6
-
41
-
-
0033975096
-
Beckwith-Wiedemann syndrome: imprinting in clusters revisited
-
Maher E.R., and Reik W. Beckwith-Wiedemann syndrome: imprinting in clusters revisited. J. Clin. Invest. 105 (2000) 247-252
-
(2000)
J. Clin. Invest.
, vol.105
, pp. 247-252
-
-
Maher, E.R.1
Reik, W.2
-
42
-
-
0029978017
-
Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15
-
Matsuoka S., Thompson J.S., Edwards M.C., Bartletta J.M., Grundy P., Kalikin L.M., Harper J.W., Elledge S.J., and Feinberg A.P. Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15. Proc. Natl. Acad. Sci. U. S. A. 93 (1996) 3026-3030
-
(1996)
Proc. Natl. Acad. Sci. U. S. A.
, vol.93
, pp. 3026-3030
-
-
Matsuoka, S.1
Thompson, J.S.2
Edwards, M.C.3
Bartletta, J.M.4
Grundy, P.5
Kalikin, L.M.6
Harper, J.W.7
Elledge, S.J.8
Feinberg, A.P.9
-
43
-
-
33748279806
-
Fetal growth compromise: definitions, standards, and classification
-
Maulik D. Fetal growth compromise: definitions, standards, and classification. Clin. Obstet. Gynecol. 49 (2006) 214-218
-
(2006)
Clin. Obstet. Gynecol.
, vol.49
, pp. 214-218
-
-
Maulik, D.1
-
44
-
-
33748265885
-
Fetal growth restriction: the etiology
-
Maulik D. Fetal growth restriction: the etiology. Clin. Obstet. Gynecol. 49 (2006) 228-235
-
(2006)
Clin. Obstet. Gynecol.
, vol.49
, pp. 228-235
-
-
Maulik, D.1
-
45
-
-
1342344900
-
Aspects of human fetoplacental vasculogenesis and angiogenesis. III. Changes in complicated pregnancies
-
Mayhew T.M., Charnock-Jones D.S., and Kaufmann P. Aspects of human fetoplacental vasculogenesis and angiogenesis. III. Changes in complicated pregnancies. Placenta 25 (2004) 127-139
-
(2004)
Placenta
, vol.25
, pp. 127-139
-
-
Mayhew, T.M.1
Charnock-Jones, D.S.2
Kaufmann, P.3
-
46
-
-
0033594375
-
Birth weight in relation to morbidity and mortality among newborn infants
-
McIntire D.D., Bloom S.L., Casey B.M., and Leveno K.J. Birth weight in relation to morbidity and mortality among newborn infants. N. Engl. J. Med. 340 (1999) 1234-1238
-
(1999)
N. Engl. J. Med.
, vol.340
, pp. 1234-1238
-
-
McIntire, D.D.1
Bloom, S.L.2
Casey, B.M.3
Leveno, K.J.4
-
47
-
-
33645902182
-
Unbalanced placental expression of imprinted genes in human intrauterine growth restriction
-
McMinn J., Wei M., Schupf N., Cusmai J., Johnson E.B., Smith A.C., Weksberg R., Thaker H.M., and Tycko B. Unbalanced placental expression of imprinted genes in human intrauterine growth restriction. Placenta 27 (2006) 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
Smith, A.C.6
Weksberg, R.7
Thaker, H.M.8
Tycko, B.9
-
48
-
-
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 M.P., Katoh M., Schulz T.C., Kugoh H., Yoshida M.A., Niikawa N., Feinberg A.P., and Oshimura M. LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. Hum. Mol. Genet. 8 (1999) 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
Kugoh, H.6
Yoshida, M.A.7
Niikawa, N.8
Feinberg, A.P.9
Oshimura, M.10
-
49
-
-
33646265537
-
Limited evolutionary conservation of imprinting in the human placenta
-
Monk D., Arnaud P., Apostolidou S., Hills F.A., Kelsey G., Stanier P., Feil R., and Moore G.E. Limited evolutionary conservation of imprinting in the human placenta. Proc. Natl. Acad. Sci. U. S. A. 103 (2006) 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
Stanier, P.6
Feil, R.7
Moore, G.E.8
-
50
-
-
0035153058
-
Evidence that insulin is imprinted in the human yolk sac
-
Moore G.E., Abu-Amero S.N., Bell G., Wakeling E.L., Kingsnorth A., Stanier P., Jauniaux E., and Bennett S.T. Evidence that insulin is imprinted in the human yolk sac. Diabetes 50 (2001) 199-203
-
(2001)
Diabetes
, vol.50
, pp. 199-203
-
-
Moore, G.E.1
Abu-Amero, S.N.2
Bell, G.3
Wakeling, E.L.4
Kingsnorth, A.5
Stanier, P.6
Jauniaux, E.7
Bennett, S.T.8
-
51
-
-
0035680734
-
An intragenic methylated region in the imprinted Igf2 gene augments transcription
-
Murrell A., Heeson S., Bowden L., Constancia M., Dean W., Kelsey G., and Reik W. An intragenic methylated region in the imprinted Igf2 gene augments transcription. EMBO Rep. 2 (2001) 1101-1106
-
(2001)
EMBO Rep.
, vol.2
, pp. 1101-1106
-
-
Murrell, A.1
Heeson, S.2
Bowden, L.3
Constancia, M.4
Dean, W.5
Kelsey, G.6
Reik, W.7
-
52
-
-
34547764390
-
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver Syndrome: clinical scoring system and epigenetic-phenotypic correlations
-
Netchine I., Rossignol S., Dufourg M.N., Azzi S., Rousseau A., Perin L., Houang M., Steunou V., Esteva B., Thibaud N., Demay M.C., Danton F., Petriczko E., Bertrand A.M., Heinrichs C., Carel J.C., Loeuille G.A., Pinto G., Jacquemont M.L., Gicquel C., Cabrol S., and Le Bouc Y. 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver Syndrome: clinical scoring system and epigenetic-phenotypic correlations. J. Clin. Endocrinol. Metab. 92 (2007) 3148-3154
-
(2007)
J. Clin. Endocrinol. Metab.
, vol.92
, pp. 3148-3154
-
-
Netchine, I.1
Rossignol, S.2
Dufourg, M.N.3
Azzi, S.4
Rousseau, A.5
Perin, L.6
Houang, M.7
Steunou, V.8
Esteva, B.9
Thibaud, N.10
Demay, M.C.11
Danton, F.12
Petriczko, E.13
Bertrand, A.M.14
Heinrichs, C.15
Carel, J.C.16
Loeuille, G.A.17
Pinto, G.18
Jacquemont, M.L.19
Gicquel, C.20
Cabrol, S.21
Le Bouc, Y.22
more..
-
53
-
-
0036590151
-
Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools
-
Norton N., Williams N., Williams H., Spurlock G., Kirov G., Morris D., Hoogendoorn B., Owen M., and O'Donovan M. Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Hum. Genet. 110 (2002) 471-478
-
(2002)
Hum. Genet.
, vol.110
, pp. 471-478
-
-
Norton, N.1
Williams, N.2
Williams, H.3
Spurlock, G.4
Kirov, G.5
Morris, D.6
Hoogendoorn, B.7
Owen, M.8
O'Donovan, M.9
-
54
-
-
2642531190
-
A nearly continuous measure of birth weight for gestational age using a United States national reference
-
Oken E., Kleinman K.P., Rich-Edwards J., and Gillman M.W. A nearly continuous measure of birth weight for gestational age using a United States national reference. BMC Pediatr. 3 (2003) 6
-
(2003)
BMC Pediatr.
, vol.3
, pp. 6
-
-
Oken, E.1
Kleinman, K.P.2
Rich-Edwards, J.3
Gillman, M.W.4
-
55
-
-
0021989517
-
Risk factors associated with small-for-dates and large-for-dates infants
-
Ounsted M., Moar V.A., and Scott A. Risk factors associated with small-for-dates and large-for-dates infants. Br. J. Obstet. Gynaecol. 92 (1985) 226-232
-
(1985)
Br. J. Obstet. Gynaecol.
, vol.92
, pp. 226-232
-
-
Ounsted, M.1
Moar, V.A.2
Scott, A.3
-
56
-
-
33748257606
-
Perinatal outcome and later implications of intrauterine growth restriction
-
Pallotto E.K., and Kilbride H.W. Perinatal outcome and later implications of intrauterine growth restriction. Clin. Obstet. Gynecol. 49 (2006) 257-269
-
(2006)
Clin. Obstet. Gynecol.
, vol.49
, pp. 257-269
-
-
Pallotto, E.K.1
Kilbride, H.W.2
-
57
-
-
0031750223
-
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5
-
Paulsen M., Davies K.R., Bowden L.M., Villar A.J., Franck O., Fuermann M., Dean W.L., Moore T.F., Rodrigues N., Davies K.E., Hu R.J., Feinberg A.P., Maher E.R., Reik W., and Walter J. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. Hum. Mol. Genet. 7 (1998) 1149-1159
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1149-1159
-
-
Paulsen, M.1
Davies, K.R.2
Bowden, L.M.3
Villar, A.J.4
Franck, O.5
Fuermann, M.6
Dean, W.L.7
Moore, T.F.8
Rodrigues, N.9
Davies, K.E.10
Hu, R.J.11
Feinberg, A.P.12
Maher, E.R.13
Reik, W.14
Walter, J.15
-
59
-
-
18244421874
-
The insulin gene is transcribed in the human thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes
-
Pugliese A., Zeller M., Fernandez Jr. A., Zalcberg L.J., Bartlett R.J., Ricordi C., Pietropaolo M., Eisenbarth G.S., Bennett S.T., and Patel D.D. The insulin gene is transcribed in the human thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes. Nat. Genet. 15 (1997) 293-297
-
(1997)
Nat. Genet.
, vol.15
, pp. 293-297
-
-
Pugliese, A.1
Zeller, M.2
Fernandez Jr., A.3
Zalcberg, L.J.4
Bartlett, R.J.5
Ricordi, C.6
Pietropaolo, M.7
Eisenbarth, G.S.8
Bennett, S.T.9
Patel, D.D.10
-
60
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier S., Johnson L.A., Dobry C.J., Ping A.J., Grundy P.E., and Feinberg A.P. Relaxation of imprinted genes in human cancer. Nature 362 (1993) 747-749
-
(1993)
Nature
, vol.362
, pp. 747-749
-
-
Rainier, S.1
Johnson, L.A.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
61
-
-
17044420868
-
Placental diagnostic criteria and clinical correlation-a workshop report
-
Redline R.W., Heller D., Keating S., and Kingdom J. Placental diagnostic criteria and clinical correlation-a workshop report. Placenta 26 Suppl A (2005) S114-S117
-
(2005)
Placenta
, vol.26
, Issue.SUPPL. A
-
-
Redline, R.W.1
Heller, D.2
Keating, S.3
Kingdom, J.4
-
62
-
-
0035234557
-
Genomic imprinting: parental influence on the genome
-
Reik W., and Walter J. Genomic imprinting: parental influence on the genome. Nat. Rev., Genet. 2 (2001) 21-32
-
(2001)
Nat. Rev., Genet.
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
63
-
-
0030786426
-
Birth weight and risk of cardiovascular disease in a cohort of women followed up since 1976
-
Rich-Edwards J.W., Stampfer M.J., Manson J.E., Rosner B., Hankinson S.E., Colditz G.A., Willett W.C., and Hennekens C.H. Birth weight and risk of cardiovascular disease in a cohort of women followed up since 1976. Bmj 315 (1997) 396-400
-
(1997)
Bmj
, vol.315
, pp. 396-400
-
-
Rich-Edwards, J.W.1
Stampfer, M.J.2
Manson, J.E.3
Rosner, B.4
Hankinson, S.E.5
Colditz, G.A.6
Willett, W.C.7
Hennekens, C.H.8
-
64
-
-
37549048600
-
Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development
-
Rivera R.M., Stein P., Weaver J.R., Mager J., Schultz R.M., and Bartolomei M.S. Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development. Hum. Mol. Genet. 17 (2008) 1-14
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1-14
-
-
Rivera, R.M.1
Stein, P.2
Weaver, J.R.3
Mager, J.4
Schultz, R.M.5
Bartolomei, M.S.6
-
65
-
-
4444337502
-
Mathematics of quantitative kinetic PCR and the application of standard curves
-
Rutledge R.G., and Cote C. Mathematics of quantitative kinetic PCR and the application of standard curves. Nucleic Acids Res. 31 (2003) e93
-
(2003)
Nucleic Acids Res.
, vol.31
-
-
Rutledge, R.G.1
Cote, C.2
-
66
-
-
0028818850
-
Intrauterine growth restriction in infants of less than thirty-two weeks' gestation: associated placental pathologic features
-
Salafia C.M., Minior V.K., Pezzullo J.C., Popek E.J., Rosenkrantz T.S., and Vintzileos A.M. Intrauterine growth restriction in infants of less than thirty-two weeks' gestation: associated placental pathologic features. Am. J. Obstet. Gynecol. 173 (1995) 1049-1057
-
(1995)
Am. J. Obstet. Gynecol.
, vol.173
, pp. 1049-1057
-
-
Salafia, C.M.1
Minior, V.K.2
Pezzullo, J.C.3
Popek, E.J.4
Rosenkrantz, T.S.5
Vintzileos, A.M.6
-
67
-
-
0038104379
-
Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions
-
Sandovici I., Leppert M., Hawk P.R., Suarez A., Linares Y., and Sapienza C. Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions. Hum. Mol. Genet. 12 (2003) 1569-1578
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1569-1578
-
-
Sandovici, I.1
Leppert, M.2
Hawk, P.R.3
Suarez, A.4
Linares, Y.5
Sapienza, C.6
-
68
-
-
0023607414
-
Regulation of human IGF-II transcription in fetal and adult tissues
-
Schofield P.N., and Tate V.E. Regulation of human IGF-II transcription in fetal and adult tissues. Development 101 (1987) 793-803
-
(1987)
Development
, vol.101
, pp. 793-803
-
-
Schofield, P.N.1
Tate, V.E.2
-
69
-
-
0019140071
-
Ultrastructural abnormalities of placental villi in placentae from pregnancies complicated by intrauterine fetal growth retardation: their relationship to decidual spiral arterial lesions
-
Sheppard B.L., and Bonnar J. Ultrastructural abnormalities of placental villi in placentae from pregnancies complicated by intrauterine fetal growth retardation: their relationship to decidual spiral arterial lesions. Placenta 1 (1980) 145-156
-
(1980)
Placenta
, vol.1
, pp. 145-156
-
-
Sheppard, B.L.1
Bonnar, J.2
-
70
-
-
0019453778
-
An ultrastructural study of utero-placental spiral arteries in hypertensive and normotensive pregnancy and fetal growth retardation
-
Sheppard B.L., and Bonnar J. An ultrastructural study of utero-placental spiral arteries in hypertensive and normotensive pregnancy and fetal growth retardation. Br. J. Obstet. Gynaecol. 88 (1981) 695-705
-
(1981)
Br. J. Obstet. Gynaecol.
, vol.88
, pp. 695-705
-
-
Sheppard, B.L.1
Bonnar, J.2
-
71
-
-
0037075032
-
The non-coding Air RNA is required for silencing autosomal imprinted genes
-
Sleutels F., Zwart R., and Barlow D.P. The non-coding Air RNA is required for silencing autosomal imprinted genes. Nature 415 (2002) 810-813
-
(2002)
Nature
, vol.415
, pp. 810-813
-
-
Sleutels, F.1
Zwart, R.2
Barlow, D.P.3
-
72
-
-
0033529207
-
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome
-
Smilinich N.J., Day C.D., Fitzpatrick G.V., Caldwell G.M., Lossie A.C., Cooper P.R., Smallwood A.C., Joyce J.A., Schofield P.N., Reik W., Nicholls R.D., Weksberg R., Driscoll D.J., Maher E.R., Shows T.B., and Higgins M.J. A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 8064-8069
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 8064-8069
-
-
Smilinich, N.J.1
Day, C.D.2
Fitzpatrick, G.V.3
Caldwell, G.M.4
Lossie, A.C.5
Cooper, P.R.6
Smallwood, A.C.7
Joyce, J.A.8
Schofield, P.N.9
Reik, W.10
Nicholls, R.D.11
Weksberg, R.12
Driscoll, D.J.13
Maher, E.R.14
Shows, T.B.15
Higgins, M.J.16
-
73
-
-
4444365791
-
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome
-
Sparago A., Cerrato F., Vernucci M., Ferrero G.B., Silengo M.C., and Riccio A. Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome. Nat. Genet. 36 (2004) 958-960
-
(2004)
Nat. Genet.
, vol.36
, pp. 958-960
-
-
Sparago, A.1
Cerrato, F.2
Vernucci, M.3
Ferrero, G.B.4
Silengo, M.C.5
Riccio, A.6
-
74
-
-
0030735169
-
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome [see comments]
-
Sun F.L., Dean W.L., Kelsey G., Allen N.D., and Reik W. Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome [see comments]. Nature 389 (1997) 809-815
-
(1997)
Nature
, vol.389
, pp. 809-815
-
-
Sun, F.L.1
Dean, W.L.2
Kelsey, G.3
Allen, N.D.4
Reik, W.5
-
75
-
-
0032878170
-
Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation
-
Tanaka M., Puchyr M., Gertsenstein M., Harpal K., Jaenisch R., Rossant J., and Nagy A. Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation. Mech. Dev. 87 (1999) 129-142
-
(1999)
Mech. Dev.
, vol.87
, pp. 129-142
-
-
Tanaka, M.1
Puchyr, M.2
Gertsenstein, M.3
Harpal, K.4
Jaenisch, R.5
Rossant, J.6
Nagy, A.7
-
76
-
-
0033593288
-
The sins of the fathers and mothers: genomic imprinting in mammalian development
-
Tilghman S.M. The sins of the fathers and mothers: genomic imprinting in mammalian development. Cell 96 (1999) 185-193
-
(1999)
Cell
, vol.96
, pp. 185-193
-
-
Tilghman, S.M.1
-
77
-
-
0036323502
-
Physiological functions of imprinted genes
-
Tycko B., and Morison I.M. Physiological functions of imprinted genes. J. Cell. Physiol. 192 (2002) 245-258
-
(2002)
J. Cell. Physiol.
, vol.192
, pp. 245-258
-
-
Tycko, B.1
Morison, I.M.2
-
78
-
-
0031018819
-
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus
-
Vafiadis P., Bennett S.T., Todd J.A., Nadeau J., Grabs R., Goodyer C.G., Wickramasinghe S., Colle E., and Polychronakos C. Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus. Nat. Genet. 15 (1997) 289-292
-
(1997)
Nat. Genet.
, vol.15
, pp. 289-292
-
-
Vafiadis, P.1
Bennett, S.T.2
Todd, J.A.3
Nadeau, J.4
Grabs, R.5
Goodyer, C.G.6
Wickramasinghe, S.7
Colle, E.8
Polychronakos, C.9
-
79
-
-
0029560183
-
Repression of promoters for the mouse insulin-like growth factor II-encoding gene (Igf-2) by products of the Wilms' tumour suppressor gene wt1
-
Ward A., Pooler J.A., Miyagawa K., Duarte A., Hastie N.D., and Caricasole A. Repression of promoters for the mouse insulin-like growth factor II-encoding gene (Igf-2) by products of the Wilms' tumour suppressor gene wt1. Gene 167 (1995) 239-243
-
(1995)
Gene
, vol.167
, pp. 239-243
-
-
Ward, A.1
Pooler, J.A.2
Miyagawa, K.3
Duarte, A.4
Hastie, N.D.5
Caricasole, A.6
-
80
-
-
0037389185
-
Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development
-
Weksberg R., Smith A.C., Squire J., and Sadowski P. Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development. Hum. Mol. Genet. 12 Spec No 1 (2003) R61-R68
-
(2003)
Hum. Mol. Genet.
, vol.12
, Issue.Spec No 1
-
-
Weksberg, R.1
Smith, A.C.2
Squire, J.3
Sadowski, P.4
-
81
-
-
0029881592
-
Regulation of insulin-like growth factor II P3 promotor by p53: a potential mechanism for tumorigenesis
-
Zhang L., Kashanchi F., Zhan Q., Zhan S., Brady J.N., Fornace A.J., Seth P., and Helman L.J. Regulation of insulin-like growth factor II P3 promotor by p53: a potential mechanism for tumorigenesis. Cancer Res. 56 (1996) 1367-1373
-
(1996)
Cancer Res.
, vol.56
, pp. 1367-1373
-
-
Zhang, L.1
Kashanchi, F.2
Zhan, Q.3
Zhan, S.4
Brady, J.N.5
Fornace, A.J.6
Seth, P.7
Helman, L.J.8
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