Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7
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[1] T. Eggermann,et al. The centromeric 11p15 imprinting centre is also involved in Silver–Russell syndrome , 2006, Journal of Medical Genetics.
[2] B. Tycko,et al. Imprinted genes in placental growth and obstetric disorders , 2006, Cytogenetic and Genome Research.
[3] Florentia M. Smith,et al. Regulation of growth and metabolism by imprinted genes , 2006, Cytogenetic and Genome Research.
[4] S. Apostolidou,et al. Imprinted genes and their role in human fetal growth , 2006, Cytogenetic and Genome Research.
[5] William Davies,et al. Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice , 2005, Nature Genetics.
[6] E. Maher. Imprinting and assisted reproductive technology. , 2005, Human molecular genetics.
[7] L. Wilkinson,et al. Imprinted Nesp55 Influences Behavioral Reactivity to Novel Environments , 2005, Molecular and Cellular Biology.
[8] G. Shaw,et al. Genomic imprinting of IGF2, p57 KIP2 and PEG1/MEST in a marsupial, the tammar wallaby , 2005, Mechanisms of Development.
[9] B. Tycko,et al. Placental growth retardation due to loss of imprinting of Phlda2 , 2004, Mechanisms of Development.
[10] Josephine Peters,et al. Interactions Between Imprinting Effects in the Mouse , 2004, Genetics.
[11] G. Kelsey,et al. The imprinted signaling protein XLαs is required for postnatal adaptation to feeding , 2004, Nature Genetics.
[12] C. Tohyama,et al. Exposure of Mouse Preimplantation Embryos to 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Alters the Methylation Status of Imprinted Genes H19 and Igf21 , 2004, Biology of reproduction.
[13] B. Joseph,et al. p57Kip2 cooperates with Nurr1 in developing dopamine cells , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[14] E. Maher,et al. Epigenetic risks related to assisted reproductive technologies: epigenetics, imprinting, ART and icebergs? , 2003, Human reproduction.
[15] Shiaoching Gong,et al. A gene expression atlas of the central nervous system based on bacterial artificial chromosomes , 2003, Nature.
[16] Y. Sotomaru,et al. Disruption of imprinting in cloned mouse fetuses from embryonic stem cells. , 2003, Reproduction.
[17] Florentia M. Smith,et al. Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[18] W. Reik,et al. Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) , 2003, Journal of medical genetics.
[19] P. Soloway,et al. Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1 , 2002, Nature Genetics.
[20] W. Reik,et al. Placental-specific IGF-II is a major modulator of placental and fetal growth , 2002, Nature.
[21] B. Tycko,et al. Placental overgrowth in mice lacking the imprinted gene Ipl , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[22] L. Schieve,et al. Low and very low birth weight in infants conceived with use of assisted reproductive technology. , 2002, The New England journal of medicine.
[23] G. Holmes,et al. Neurobehavioral and Electroencephalographic Abnormalities in Ube3a Maternal-Deficient Mice , 2002, Neurobiology of Disease.
[24] M. Surani,et al. Imprinted expression of neuronatin from modified BAC transgenes reveals regulation by distinct and distant enhancers. , 2001, Developmental biology.
[25] J. Killian,et al. Monotreme IGF2 expression and ancestral origin of genomic imprinting. , 2001, The Journal of experimental zoology.
[26] M. Surani,et al. Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome. , 2001, Human molecular genetics.
[27] R. Jaenisch,et al. Non-imprinted Igf2r expression decreases growth and rescues the Tme mutation in mice. , 2001, Development.
[28] M. Oshimura,et al. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome , 2000, Journal of medical genetics.
[29] W. Reik,et al. The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster. , 2005, Human molecular genetics.
[30] A. Feinberg. The two-domain hypothesis in Beckwith-Wiedemann syndrome. , 2000, The Journal of clinical investigation.
[31] C. Cepko,et al. p57(Kip2) regulates progenitor cell proliferation and amacrine interneuron development in the mouse retina. , 2000, Development.
[32] M. Surani,et al. Genomic Imprinting, Mammalian Evolution, and the Mystery of Egg-Laying Mammals , 2000, Cell.
[33] M. Cleary,et al. Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome. , 1999, Genes & development.
[34] M. Surani,et al. A human p57(KIP2) transgene is not activated by passage through the maternal mouse germline. , 1999, Human molecular genetics.
[35] E. Keverne,et al. Regulation of maternal behavior and offspring growth by paternally expressed Peg3. , 1999, Science.
[36] S. Buitendijk. CHILDREN AFTER IN VITRO FERTILIZATION , 1999, International Journal of Technology Assessment in Health Care.
[37] M. Bartolomei,et al. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. , 1998, Genes & development.
[38] M. Azim Surani,et al. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest , 1998, Nature Genetics.
[39] M. Surani. Imprinting and the Initiation of Gene Silencing in the Germ Line , 1998, Cell.
[40] B. Tycko,et al. IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes. , 1998, Human molecular genetics.
[41] S. Grant,et al. A role for the Ras signalling pathway in synaptic transmission and long-term memory , 1997, Nature.
[42] B. Tycko,et al. The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. , 1997, Human molecular genetics.
[43] W. Reik,et al. Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[44] Y. Fukushima,et al. New p57KIP2 mutations in Beckwith-Wiedemann syndrome , 1997, Human Genetics.
[45] B. Tycko,et al. Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors. , 1997, American journal of human genetics.
[46] A. Feinberg,et al. Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome. , 1997, American journal of human genetics.
[47] R. Joshi,et al. Phenotypic alterations in insulin-deficient mutant mice. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[48] S. Elledge,et al. Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome , 1997, Nature.
[49] M. Barbacid,et al. Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development. , 1997, Genes & development.
[50] P. Ye,et al. The role of the insulin-like growth factors in the central nervous system , 1996, Molecular Neurobiology.
[51] Y. Fukushima,et al. An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome , 1996, Nature Genetics.
[52] A. Feinberg,et al. Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[53] A. Ferguson-Smith. Parental Imprinting on Mouse Chromosome 7 , 1996 .
[54] T. Mukai,et al. Genomic imprinting of p57KIP2, a cyclin–dependent kinase inhibitor, in mouse , 1995, Nature Genetics.
[55] S. Elledge,et al. p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. , 1995, Genes & development.
[56] J. Massagué,et al. Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution. , 1995, Genes & development.
[57] L. Powell-Braxton,et al. IGF-I is required for normal embryonic growth in mice. , 1993, Genes & development.
[58] J. Baker,et al. Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r) , 1993, Cell.
[59] V. Beral,et al. Preterm delivery, low birthweight and small-for-gestational-age in liveborn singleton babies resulting from in-vitro fertilization. , 1992, Human reproduction.
[60] H. Werner,et al. Cellular pattern of type-I insulin-like growth factor receptor gene expression during maturation of the rat brain: Comparison with insulin-like growth factors I and II , 1992, Neuroscience.
[61] M. Surani,et al. Embryological and molecular investigations of parental imprinting on mouse chromosome 7 , 1991, Nature.
[62] Chris Graham,et al. Genomic imprinting and the strange case of the insulin-like growth factor II receptor , 1991, Cell.
[63] A. Efstratiadis,et al. Parental imprinting of the mouse insulin-like growth factor II gene , 1991, Cell.
[64] T. Moore,et al. Genomic imprinting in mammalian development: a parental tug-of-war. , 1991, Trends in genetics : TIG.
[65] B. Cattanach,et al. Differential activity of maternally and paternally derived chromosome regions in mice , 1985, Nature.
[66] G. Kelsey,et al. The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding. , 2004, Nature genetics.
[67] Andrew P Feinberg,et al. Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. , 2003, American journal of human genetics.
[68] S. Barton,et al. A transgenic approach to studying imprinted genes: modified BACs and PACs. , 2001, Methods in molecular biology.
[69] K. Nakayama,et al. Mice lacking a CDK inhibitor, p57Kip2, exhibit skeletal abnormalities and growth retardation. , 2000, Journal of biochemistry.
[70] M. O’Neill,et al. Allelic expression of IGF2 in marsupials and birds , 2000, Development Genes and Evolution.
[71] A. Efstratiadis. Genetics of mouse growth. , 1998, The International journal of developmental biology.
[72] A. Joyner,et al. Genomic imprinting of Mash2, a mouse gene required for trophoblast development , 1995, Nature Genetics.
[73] B. Hogan,et al. Manipulating the mouse embryo: A laboratory manual , 1986 .
[74] L. G. Davis,et al. Basic methods in molecular biology , 1986 .