| scholarly article | Q13442814 |
| P50 | author | Azim Surani | Q793786 |
| Rosalind John | Q52693633 | ||
| Simon J. Tunster | Q55816320 | ||
| P2093 | author name string | Sheila C Barton | |
| Michelle D Wood | |||
| Stuart C Andrews | |||
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| The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis | Q24318274 | ||
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| Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15 | Q24568014 | ||
| Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19 | Q24615581 | ||
| Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) | Q24678681 | ||
| New p57KIP2 mutations in Beckwith-Wiedemann syndrome | Q28252299 | ||
| Genomic imprinting in mammalian development: a parental tug-of-war | Q28278146 | ||
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| p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene | Q28300451 | ||
| p57(Kip2) cooperates with Nurr1 in developing dopamine cells | Q28587845 | ||
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| Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans | Q28594559 | ||
| A gene expression atlas of the central nervous system based on bacterial artificial chromosomes | Q29617753 | ||
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| Children after in vitro fertilization. An overview of the literature | Q33688184 | ||
| Imprinted Nesp55 influences behavioral reactivity to novel environments | Q33724476 | ||
| Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome | Q33927299 | ||
| Genomic imprinting, mammalian evolution, and the mystery of egg-laying mammals. | Q33967141 | ||
| Monotreme IGF2 expression and ancestral origin of genomic imprinting | Q34085483 | ||
| Placental-specific IGF-II is a major modulator of placental and fetal growth. | Q34135795 | ||
| Differential activity of maternally and paternally derived chromosome regions in mice | Q34198480 | ||
| Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice | Q34420540 | ||
| Interactions between imprinting effects in the mouse | Q34567123 | ||
| Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism | Q35167917 | ||
| Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome | Q35209963 | ||
| Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. | Q35211749 | ||
| Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors | Q35249129 | ||
| Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome | Q35249196 | ||
| Imprinting and assisted reproductive technology. | Q36088926 | ||
| Imprinted genes and their role in human fetal growth. | Q36436584 | ||
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| Regulation of growth and metabolism by imprinted genes | Q36436592 | ||
| Phenotypic alterations in insulin-deficient mutant mice. | Q36766264 | ||
| The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome | Q37004473 | ||
| Genomic imprinting and the strange case of the insulin-like growth factor II receptor | Q37165552 | ||
| Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse | Q38291049 | ||
| Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
| Preterm delivery, low birthweight and small-for-gestational-age in liveborn singleton babies resulting from in-vitro fertilization | Q38977654 | ||
| The role of the insulin-like growth factors in the central nervous system | Q41301869 | ||
| IGF-I is required for normal embryonic growth in mice | Q41510465 | ||
| A role for the Ras signalling pathway in synaptic transmission and long-term memory | Q42833586 | ||
| The two-domain hypothesis in Beckwith-Wiedemann syndrome | Q43204600 | ||
| Non-imprinted Igf2r expression decreases growth and rescues the Tme mutation in mice. | Q43580738 | ||
| Exposure of mouse preimplantation embryos to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) alters the methylation status of imprinted genes H19 and Igf2. | Q44762564 | ||
| The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding. | Q44992718 | ||
| Low and very low birth weight in infants conceived with use of assisted reproductive technology | Q47191285 | ||
| A human p57(KIP2) transgene is not activated by passage through the maternal mouse germline | Q47915161 | ||
| Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest | Q48016474 | ||
| Regulation of maternal behavior and offspring growth by paternally expressed Peg3. | Q48243147 | ||
| 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. | Q48549457 | ||
| A transgenic approach to studying imprinted genes: modified BACs and PACs | Q48555883 | ||
| Imprinted expression of neuronatin from modified BAC transgenes reveals regulation by distinct and distant enhancers | Q48560971 | ||
| Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome. | Q48561025 | ||
| Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice | Q48661423 | ||
| Disruption of imprinting in cloned mouse fetuses from embryonic stem cells. | Q52099573 | ||
| p57(Kip2) regulates progenitor cell proliferation and amacrine interneuron development in the mouse retina. | Q52166705 | ||
| Imprinting and the initiation of gene silencing in the germ line. | Q52187741 | ||
| Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development. | Q52195138 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Embryological and molecular investigations of parental imprinting on mouse chromosome 7. | Q55052972 | ||
| The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster | Q58134238 | ||
| Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome | Q58236969 | ||
| Allelic expression of IGF2 in marsupials and birds | Q73285233 | ||
| Mice lacking a CDK inhibitor, p57Kip2, exhibit skeletal abnormalities and growth retardation | Q73580769 | ||
| Genetics of mouse growth | Q77684683 | ||
| Epigenetic risks related to assisted reproductive technologies: epigenetics, imprinting, ART and icebergs? | Q79330767 | ||
| Placental growth retardation due to loss of imprinting of Phlda2 | Q80489018 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 53 | |
| P577 | publication date | 2007-05-21 | |
| P1433 | published in | BMC Developmental Biology | Q15761839 |
| P1476 | title | Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. | |
| P478 | volume | 7 |
| Q48238419 | A p57 conditional mutant allele that allows tracking of p57-expressing cells |
| Q64889113 | Abundances of placental imprinted genes CDKN1C, PHLDA2 and IGF-2 are related to low birth weight and early catch-up growth in full-term infants born small for gestational age. |
| Q36808158 | An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs |
| Q38030489 | Attention-deficit/hyperactivity disorder genomics: update for clinicians |
| Q34551069 | Autonomous silencing of the imprinted Cdkn1c gene in stem cells |
| Q34442748 | BACs as tools for the study of genomic imprinting |
| Q38089794 | Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth |
| Q30356916 | Behavioural abnormalities in a novel mouse model for Silver Russell Syndrome. |
| Q35952569 | Cdkn1c Boosts the Development of Brown Adipose Tissue in a Murine Model of Silver Russell Syndrome |
| Q33997704 | Characterisation of marsupial PHLDA2 reveals eutherian specific acquisition of imprinting |
| Q38600504 | Dopaminergic and behavioral changes in a loss-of-imprinting model of Cdkn1c |
| Q38108660 | Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness |
| Q35599540 | Dysregulation of methylation and expression of imprinted genes in oocytes and reproductive tissues in mice of advanced maternal age |
| Q33862459 | Early life protein restriction alters dopamine circuitry. |
| Q36834411 | Epigenetic Characterization of CDKN1C in Placenta Samples from Non-syndromic Intrauterine Growth Restriction. |
| Q38554712 | Epigenetic alterations in sperm associated with male infertility |
| Q28505485 | Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome |
| Q33321972 | Forced expression of the cell cycle inhibitor p57Kip2 in cardiomyocytes attenuates ischemia-reperfusion injury in the mouse heart |
| Q38346535 | Gene expression profiles of single human mature oocytes in relation to age. |
| Q37715275 | Genomic imprinting in development, growth, behavior and stem cells |
| Q64083257 | Human iPSC-derived MSCs (iMSCs) from aged individuals acquire a rejuvenation signature |
| Q33409828 | Imprinted CDKN1C is a tumor suppressor in rhabdoid tumor and activated by restoration of SMARCB1 and histone deacetylase inhibitors |
| Q92563376 | Imprinted Cdkn1c genomic locus cell-autonomously promotes cell survival in cerebral cortex development |
| Q37033645 | Knockdown of CDKN1C (p57(kip2)) and PHLDA2 results in developmental changes in bovine pre-implantation embryos |
| Q58745215 | Loss of Imprinting of Protects against Age and Diet-Induced Obesity |
| Q39388927 | Mutations in the PCNA-binding site of CDKN1C inhibit cell proliferation by impairing the entry into S phase |
| Q28512786 | MyoD regulates p57kip2 expression by interacting with a distant cis-element and modifying a higher order chromatin structure |
| Q81152665 | Neonatal diabetes mellitus |
| Q35737547 | Partial Loss of Genomic Imprinting Reveals Important Roles for Kcnq1 and Peg10 Imprinted Domains in Placental Development |
| Q28591355 | Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction |
| Q36214670 | Placental 5-methylcytosine and 5-hydroxymethylcytosine patterns associate with size at birth |
| Q47959137 | Placental Expressions of CDKN1C and KCNQ1OT1 in Monozygotic Twins with Selective Intrauterine Growth Restriction. |
| Q35949579 | Placental expression of imprinted genes varies with sampling site and mode of delivery. |
| Q33523010 | Postnatal survival of mice with maternal duplication of distal chromosome 7 induced by a Igf2/H19 imprinting control region lacking insulator function |
| Q33575632 | Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome |
| Q37988364 | Specific changes in the expression of imprinted genes in prostate cancer--implications for cancer progression and epigenetic regulation |
| Q52356855 | Territorial Behavior and Social Stability in the Mouse Require Correct Expression of Imprinted Cdkn1c. |
| Q28593841 | The imprinted Phlda2 gene modulates a major endocrine compartment of the placenta to regulate placental demands for maternal resources |
| Q28512597 | The imprinted Phlda2 gene regulates extraembryonic energy stores |
| Q37278762 | The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann region |
| Q36970312 | The molecular genetics of adrenocortical carcinoma |
| Q36392021 | Two distinct mechanisms of silencing by the KvDMR1 imprinting control region |
| Q34488451 | Upregulation of imprinted genes in mice: an insight into the intensity of gene expression and the evolution of genomic imprinting |
| Q37634526 | Visualizing Changes in Cdkn1c Expression Links Early-Life Adversity to Imprint Mis-regulation in Adults |
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