| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1998PNAS...95.1102M |
| P356 | DOI | 10.1073/PNAS.95.3.1102 |
| P932 | PMC publication ID | 18687 |
| P698 | PubMed publication ID | 9448292 |
| P5875 | ResearchGate publication ID | 13783004 |
| P50 | author | Takashi Kohda | Q47296669 |
| P2093 | author name string | M A Surani | |
| S C Barton | |||
| F Ishino | |||
| T Kaneko-Ishino | |||
| H Hasegawa | |||
| N Miyoshi | |||
| Y Kuroiwa | |||
| H Yonekawa | |||
| T Kawabe | |||
| H Shitara | |||
| P2860 | cites work | Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons | Q48045480 |
| Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain | Q48045492 | ||
| De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome | Q48056435 | ||
| Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein. | Q48066774 | ||
| Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization | Q48071136 | ||
| Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting | Q48084682 | ||
| Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method | Q48086267 | ||
| The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain | Q48630943 | ||
| Manipulations of genetic constitution by nuclear transplantation | Q49159148 | ||
| Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome. | Q52037305 | ||
| Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain. | Q52204453 | ||
| A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. | Q52241373 | ||
| Alternative pathway of insulin signalling in mice with targeted disruption of the IRS-1 gene. | Q52507538 | ||
| Insulin resistance and growth retardation in mice lacking insulin receptor substrate-1. | Q52512624 | ||
| Somatic overgrowth associated with overexpression of insulin-like growth factor II. | Q52519232 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome | Q58236969 | ||
| Mouse chromosome 11 | Q60719580 | ||
| A new genetic concept: uniparental disomy and its potential effect, isodisomy | Q70656134 | ||
| Time of initiation and site of action of the mouse chromosome 11 imprinting effects | Q71441501 | ||
| Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation | Q71953304 | ||
| Detection of K-ras mutation in sputum by mutant-allele-specific amplification (MASA) | Q72800053 | ||
| Parental imprinting of the mouse H19 gene | Q22122365 | ||
| UBE3A/E6-AP mutations cause Angelman syndrome | Q24311799 | ||
| Human PEG1/MEST, an imprinted gene on chromosome 7 | Q24322948 | ||
| Grb-IR: a SH2-domain-containing protein that binds to the insulin receptor and inhibits its function | Q24563627 | ||
| Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS) | Q24635921 | ||
| Comparative mapping of the imprinted U2afbpL gene on mouse chromosome 11 and human chromosome 5 | Q28240346 | ||
| Interaction of a GRB-IR splice variant (a human GRB10 homolog) with the insulin and insulin-like growth factor I receptors. Evidence for a role in mitogenic signaling | Q28289183 | ||
| p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene | Q28300451 | ||
| Assignment of growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12 | Q28306122 | ||
| The adapter protein Grb10 associates preferentially with the insulin receptor as compared with the IGF-I receptor in mouse fibroblasts | Q28591965 | ||
| Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r) | Q29619910 | ||
| Allele-specific enzymatic amplification of beta-globin genomic DNA for diagnosis of sickle cell anemia | Q33850554 | ||
| Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis | Q34056205 | ||
| Differential activity of maternally and paternally derived chromosome regions in mice | Q34198480 | ||
| Completion of mouse embryogenesis requires both the maternal and paternal genomes | Q34267351 | ||
| Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1. | Q34373639 | ||
| Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse. | Q34634517 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| A new imprinted gene cloned by a methylation-sensitive genome scanning method | Q35017116 | ||
| Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus | Q35196278 | ||
| Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation | Q35889650 | ||
| The cloning of Grb10 reveals a new family of SH2 domain proteins | Q36701969 | ||
| 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 | ||
| Signal transmission by the insulin-like growth factors | Q38297337 | ||
| Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
| Uniparental disomy (UPD). Genomic imprinting and a case for new genetics (prenatal and clinical implications: the "Likon" concept). | Q38457936 | ||
| Genomic imprinting and genetic disorders in man. | Q38753070 | ||
| Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. | Q41066237 | ||
| Effects of an Igf1 gene null mutation on mouse reproduction | Q42523453 | ||
| Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region | Q44185908 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Silver-Russell syndrome | Q2142496 |
| P304 | page(s) | 1102-1107 | |
| P577 | publication date | 1998-02-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene | |
| P478 | volume | 95 |
| Q24652620 | A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10 |
| Q35221526 | A survey for novel imprinted genes in the mouse placenta by mRNA-seq |
| Q48016474 | Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest |
| Q31147226 | Antisense transcripts with FANTOM2 clone set and their implications for gene regulation |
| Q36783148 | Could epigenetics play a role in the developmental origins of health and disease? |
| Q31742998 | DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts |
| Q73764736 | Disruption of imprinted expression of U2afbp-rs/U2af1-rs1 gene in mouse parthenogenetic fetuses |
| Q52006521 | Disruption of parental-specific expression of imprinted genes in uniparental fetuses. |
| Q35167917 | Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism |
| Q77892020 | Do we understand the evolution of genomic imprinting? |
| Q34146198 | Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome |
| Q74560571 | Effects of fibroblast growth factor 2 and insulin-like growth factor II on the development of parthenogenetic mouse embryos in vitro |
| Q82457009 | Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes |
| Q51953583 | Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient. |
| Q48003531 | Genomic imprinting is disrupted in interspecific Peromyscus hybrids |
| Q36083462 | Genomic imprinting: cis-acting sequences and regional control |
| Q33603375 | Genomic imprinting: concept and clinical consequences |
| Q33541538 | Genomic imprinting: implications for human disease |
| Q37172147 | Genomic organization and control of the grb7 gene family |
| Q35563158 | Grb10 adapter protein as regulator of insulin‐like growth factor receptor signaling |
| Q36131371 | Grb10 and Grb14: enigmatic regulators of insulin action--and more? |
| Q24554440 | Grb10, a positive, stimulatory signaling adapter in platelet-derived growth factor BB-, insulin-like growth factor I-, and insulin-mediated mitogenesis |
| Q28283759 | Grb10/GrbIR as an in vivo substrate of Tec tyrosine kinase |
| Q40642763 | Growth factor receptor-binding protein 10 (Grb10) as a partner of phosphatidylinositol 3-kinase in metabolic insulin action |
| Q41471062 | High throughput sequencing identifies an imprinted gene, Grb10, associated with the pluripotency state in nuclear transfer embryonic stem cells |
| Q34994392 | Identification of novel imprinted genes in a genome-wide screen for maternal methylation. |
| Q34939534 | Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2. |
| Q33852775 | Imprinted genes as potential genetic and epigenetic toxicologic targets |
| Q52094982 | Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis. |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q34142141 | Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome |
| Q39733758 | Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites. |
| Q32058435 | Inhibition of hGrb10 binding to the insulin receptor by functional domain-mediated oligomerization |
| Q34567123 | Interactions between imprinting effects in the mouse |
| Q39252372 | Lmx1a is an activator of Rgs4 and Grb10 and is responsible for the correct specification of rostral and medial mdDA neurons. |
| Q37645483 | Long-term effect of in vitro culture of mouse embryos with serum on mRNA expression of imprinting genes, development, and behavior. |
| Q28603472 | Mammalian-specific genomic functions: Newly acquired traits generated by genomic imprinting and LTR retrotransposon-derived genes in mammals |
| Q48906893 | Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome. |
| Q47172204 | Maternally-inherited Grb10 reduces placental size and efficiency |
| Q35950176 | Mice with a disruption of the imprinted Grb10 gene exhibit altered body composition, glucose homeostasis, and insulin signaling during postnatal life |
| Q47864302 | Mit1/Lb9 and Copg2, new members of mouse imprinted genes closely linked to Peg1/Mest(1). |
| Q35639252 | Monoallelic loss of the imprinted gene Grb10 promotes tumor formation in irradiated Nf1+/- mice. |
| Q48382320 | Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3. |
| Q28742324 | Novel retrotransposed imprinted locus identified at human 6p25 |
| Q53427610 | Polymorphisms, genomic imprinting and cancer susceptibility. |
| Q36349366 | Predicting aberrant CpG island methylation |
| Q50651510 | Russell-Silver Syndrome in a Nigerian infant with intrauterine growth retardation. |
| Q35655481 | Sex-specific genetic architecture of human fatness in Chinese: the SAPPHIRe Study. |
| Q34465575 | Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions |
| Q37512434 | Susceptibility to astrocytoma in mice mutant for Nf1 and Trp53 is linked to chromosome 11 and subject to epigenetic effects |
| Q39968376 | Systemic and maxillofacial characteristics of 11 Japanese children with Russell-Silver syndrome |
| Q57278462 | Síndrome de Silver-Russell: relato de caso |
| Q64929446 | Technical advances contribute to the study of genomic imprinting. |
| Q43564874 | The BPS domain of Grb10 inhibits the catalytic activity of the insulin and IGF1 receptors |
| Q24682781 | The Grb10/Nedd4 complex regulates ligand-induced ubiquitination and stability of the insulin-like growth factor I receptor |
| Q36417552 | The PcG gene Sfmbt2 is paternally expressed in extraembryonic tissues |
| Q35001114 | The Russell-Silver syndrome: a case report and brief review of the literature |
| Q34992967 | The genetics of the Silver-Russell syndrome |
| Q37152145 | Transcript- and tissue-specific imprinting of a tumour suppressor gene |
| Q33939124 | Tumour suppressor activity of human imprinted gene PEG3 in a glioma cell line |
| Q24803027 | Tyrosine kinase signalling in breast cancer: modulation of tyrosine kinase signalling in human breast cancer through altered expression of signalling intermediates |
| Q77531407 | Unregulated expression of the imprinted genes H19 and Igf2r in mouse uniparental fetuses |
| Q52566160 | Widespread disruption of genomic imprinting in adult interspecies mouse (Mus) hybrids. |
| Q28508597 | mGrb10 interacts with Nedd4 |
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